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Volumn 16, Issue 4, 2017, Pages 580-616

Ferulic Acid and Naturally Occurring Compounds Bearing a Feruloyl Moiety: A Review on Their Structures, Occurrence, and Potential Health Benefits

Author keywords

antioxidant activity; ferulated naturally occurring compounds; ferulic acid; feruloyl moiety; phenolics

Indexed keywords

ANTIOXIDANTS; NEURODEGENERATIVE DISEASES;

EID: 85018784406     PISSN: None     EISSN: 15414337     Source Type: Journal    
DOI: 10.1111/1541-4337.12266     Document Type: Article
Times cited : (119)

References (364)
  • 4
    • 84875232097 scopus 로고    scopus 로고
    • Ferulic acid improves cardiovascular and kidney structure and function in hypertensive rats
    • Alam A, Sernia C, Brown L. 2013. Ferulic acid improves cardiovascular and kidney structure and function in hypertensive rats. J Cardiovasc Pharmacol 61:240–9.
    • (2013) J Cardiovasc Pharmacol , vol.61 , pp. 240-249
    • Alam, A.1    Sernia, C.2    Brown, L.3
  • 5
    • 64749088460 scopus 로고    scopus 로고
    • Protective effect of ferulic acid on 7,12-dimethylbenz[α]anthracene-induced skin carcinogenesis in Swiss albino mice
    • Alias LM, Manoharan S, Vellaichamy L, Balakrishnan S, Ramachandran CR. 2009. Protective effect of ferulic acid on 7,12-dimethylbenz[α]anthracene-induced skin carcinogenesis in Swiss albino mice. Exp Toxicol Pathol 61:205–14.
    • (2009) Exp Toxicol Pathol , vol.61 , pp. 205-214
    • Alias, L.M.1    Manoharan, S.2    Vellaichamy, L.3    Balakrishnan, S.4    Ramachandran, C.R.5
  • 6
    • 11844249939 scopus 로고    scopus 로고
    • Isolation and structural identification of diarabinosyl 8-O-4-dehydrodiferulate from maize bran insoluble fibre
    • Allerdings E, Ralph J, Schatz PF, Gniechwitz D, Steinhart H, Bunzel M. 2005. Isolation and structural identification of diarabinosyl 8-O-4-dehydrodiferulate from maize bran insoluble fibre. Phytochemistry 66:113–24.
    • (2005) Phytochemistry , vol.66 , pp. 113-124
    • Allerdings, E.1    Ralph, J.2    Schatz, P.F.3    Gniechwitz, D.4    Steinhart, H.5    Bunzel, M.6
  • 9
    • 4344692590 scopus 로고    scopus 로고
    • Conformational analysis: a tool for the elucidation of the antioxidant properties of ferulic acid derivatives in membrane models
    • Anselmi C, Centini M, Andreassi M, Buonocore A, Rosa C La, Facino RM, Sega A, Tsuno F. 2004. Conformational analysis: a tool for the elucidation of the antioxidant properties of ferulic acid derivatives in membrane models. J Pharm Biomed Anal 35:1241–9.
    • (2004) J Pharm Biomed Anal , vol.35 , pp. 1241-1249
    • Anselmi, C.1    Centini, M.2    Andreassi, M.3    Buonocore, A.4    La, R.C.5    Facino, R.M.6    Sega, A.7    Tsuno, F.8
  • 10
    • 0034257193 scopus 로고    scopus 로고
    • Oxidative derangement in rat synaptosomes induced by hyperglycemia: restorative effect of dehydroepiandosterone treatment
    • Aragno M, Parola S, Tamagno E. 2000. Oxidative derangement in rat synaptosomes induced by hyperglycemia: restorative effect of dehydroepiandosterone treatment. Biochem Pharmacol 60:389–95.
    • (2000) Biochem Pharmacol , vol.60 , pp. 389-395
    • Aragno, M.1    Parola, S.2    Tamagno, E.3
  • 11
    • 12844272321 scopus 로고    scopus 로고
    • Polyphenols and disease risk in epidemiologic studies
    • Arts I, Hollman P. 2005. Polyphenols and disease risk in epidemiologic studies. Am J Clin Nutr 81:317S–25S.
    • (2005) Am J Clin Nutr , vol.81 , pp. 317S-325S
    • Arts, I.1    Hollman, P.2
  • 13
    • 30644475948 scopus 로고    scopus 로고
    • Plant polyphenols mobilize endogenous copper in human peripheral lymphocytes leading to oxidative DNA breakage: a putative mechanism for anticancer properties
    • Azmi AS, Bhat SH, Hanif S, Hadi SM. 2006. Plant polyphenols mobilize endogenous copper in human peripheral lymphocytes leading to oxidative DNA breakage: a putative mechanism for anticancer properties. FEBS Lett 580:533–8.
    • (2006) FEBS Lett , vol.580 , pp. 533-538
    • Azmi, A.S.1    Bhat, S.H.2    Hanif, S.3    Hadi, S.M.4
  • 16
    • 61849147931 scopus 로고    scopus 로고
    • Ferulic acid and its therapeutic potential as a hormetin for age-related diseases
    • Barone E, Calabrese V, Mancuso C. 2009. Ferulic acid and its therapeutic potential as a hormetin for age-related diseases. Biogerontology 10:97–108.
    • (2009) Biogerontology , vol.10 , pp. 97-108
    • Barone, E.1    Calabrese, V.2    Mancuso, C.3
  • 17
    • 84958243668 scopus 로고    scopus 로고
    • Uses and potential applications of ferulic acid
    • In, Warren B, editor., 1st ed, New York, N.Y, Nova Science Publishers, Inc, p
    • Batista R. 2014. Uses and potential applications of ferulic acid. In: Warren B, editor. Ferulic acid: antioxidant properties, uses and potential health benefits. 1st ed. New York, N.Y.: Nova Science Publishers, Inc. p 39–70.
    • (2014) Ferulic acid: antioxidant properties, uses and potential health benefits , pp. 39-70
    • Batista, R.1
  • 19
    • 84899988992 scopus 로고    scopus 로고
    • Oxidative stress: an essential factor in the pathogenesis of gastrointestinal mucosal diseases
    • Bhattacharyya A, Chattopadhyay R, Mitra S, Crowe SE. 2014. Oxidative stress: an essential factor in the pathogenesis of gastrointestinal mucosal diseases. Physiol Rev 94:329–54.
    • (2014) Physiol Rev , vol.94 , pp. 329-354
    • Bhattacharyya, A.1    Chattopadhyay, R.2    Mitra, S.3    Crowe, S.E.4
  • 21
    • 0032487969 scopus 로고    scopus 로고
    • Identification of flavonol and anthocyanin metabolites in leaves of Petunia “Mitchell” and its LC transgenic
    • Bloor SJ, Bradley JM, Lewis DH, Davies KM. 1998. Identification of flavonol and anthocyanin metabolites in leaves of Petunia “Mitchell” and its LC transgenic. Phytochemistry 49:1427–30.
    • (1998) Phytochemistry , vol.49 , pp. 1427-1430
    • Bloor, S.J.1    Bradley, J.M.2    Lewis, D.H.3    Davies, K.M.4
  • 22
    • 84880902860 scopus 로고    scopus 로고
    • Antibacterial activity and mode of action of ferulic and gallic acids against pathogenic bacteria
    • Borges A, Ferreira C, Saavedra MJ, Simões M. 2013. Antibacterial activity and mode of action of ferulic and gallic acids against pathogenic bacteria. Microb Drug Resist 19:256–65.
    • (2013) Microb Drug Resist , vol.19 , pp. 256-265
    • Borges, A.1    Ferreira, C.2    Saavedra, M.J.3    Simões, M.4
  • 24
    • 0033956066 scopus 로고    scopus 로고
    • A novel acylated flavonol glycoside isolated from Brunfelsia grandiflora ssp. grandiflora. Structure elucidation by gradient accelerated NMR spectroscopy at 14T
    • Brunner G, Burger U, Castioni P, Kapetanidis I, Christen P. 2000. A novel acylated flavonol glycoside isolated from Brunfelsia grandiflora ssp. grandiflora. Structure elucidation by gradient accelerated NMR spectroscopy at 14T. Phytochem Anal 11:29–33.
    • (2000) Phytochem Anal , vol.11 , pp. 29-33
    • Brunner, G.1    Burger, U.2    Castioni, P.3    Kapetanidis, I.4    Christen, P.5
  • 25
    • 1542393782 scopus 로고    scopus 로고
    • Isolation and identification of a ferulic acid dehydrotrimer from saponified maize bran insoluble fiber
    • Bunzel M, Ralph J, Funk C, Steinhart H. 2003. Isolation and identification of a ferulic acid dehydrotrimer from saponified maize bran insoluble fiber. Eur Food Res Technol 217:128–33.
    • (2003) Eur Food Res Technol , vol.217 , pp. 128-133
    • Bunzel, M.1    Ralph, J.2    Funk, C.3    Steinhart, H.4
  • 26
    • 23044505859 scopus 로고    scopus 로고
    • Structural elucidation of new ferulic acid-containing phenolic dimers and trimers isolated from maize bran
    • Bunzel M, Ralph J, Funk C, Steinhart H. 2005. Structural elucidation of new ferulic acid-containing phenolic dimers and trimers isolated from maize bran. Tetrahedron Lett 46:5845–50.
    • (2005) Tetrahedron Lett , vol.46 , pp. 5845-5850
    • Bunzel, M.1    Ralph, J.2    Funk, C.3    Steinhart, H.4
  • 27
    • 33748560454 scopus 로고    scopus 로고
    • Structural identification of dehydrotriferulic and dehydrotetraferulic acids isolated from insoluble maize bran fiber
    • Bunzel M, Ralph J, Brüning P, Steinhart H. 2006. Structural identification of dehydrotriferulic and dehydrotetraferulic acids isolated from insoluble maize bran fiber. J Agric Food Chem 54:6409–18.
    • (2006) J Agric Food Chem , vol.54 , pp. 6409-6418
    • Bunzel, M.1    Ralph, J.2    Brüning, P.3    Steinhart, H.4
  • 28
    • 36048992152 scopus 로고    scopus 로고
    • Cross-linking of arabinoxylans via 8-8-coupled diferulates as demonstrated by isolation and identification of diarabinosyl 8-8(cyclic)-dehydrodiferulate from maize bran
    • Bunzel M, Allerdings E, Ralph J, Steinhart H. 2008. Cross-linking of arabinoxylans via 8-8-coupled diferulates as demonstrated by isolation and identification of diarabinosyl 8-8(cyclic)-dehydrodiferulate from maize bran. J Cereal Sci 47:29–40.
    • (2008) J Cereal Sci , vol.47 , pp. 29-40
    • Bunzel, M.1    Allerdings, E.2    Ralph, J.3    Steinhart, H.4
  • 29
    • 0031453673 scopus 로고    scopus 로고
    • Benzopyranones and ferulic acid derivatives from Antidesma membranaceum
    • Buske A, Schmidt J, Porzel A, Adam G. 1997. Benzopyranones and ferulic acid derivatives from Antidesma membranaceum. Phytochemistry 46:1385–8.
    • (1997) Phytochemistry , vol.46 , pp. 1385-1388
    • Buske, A.1    Schmidt, J.2    Porzel, A.3    Adam, G.4
  • 30
    • 84911917970 scopus 로고
    • Lagotoside: a new phenylpropanoid glycoside from Lagotis stolonifera
    • Çaliş I, Tasdemir D, Wright AD, Sticher O. 1991. Lagotoside: a new phenylpropanoid glycoside from Lagotis stolonifera. Helv Chim Acta 74:1273–7.
    • (1991) Helv Chim Acta , vol.74 , pp. 1273-1277
    • Çaliş, I.1    Tasdemir, D.2    Wright, A.D.3    Sticher, O.4
  • 31
  • 35
    • 41549114478 scopus 로고    scopus 로고
    • D:C-Friedooleanane-type triterpenoids from Lagenaria siceraria and their cytotoxic activity
    • Chen C-R, Chen H-W, Chang C-I. 2008b. D:C-Friedooleanane-type triterpenoids from Lagenaria siceraria and their cytotoxic activity. Chem Pharm Bull (Tokyo) 56:385–8.
    • (2008) Chem Pharm Bull (Tokyo) , vol.56 , pp. 385-388
    • Chen, C.-R.1    Chen, H.-W.2    Chang, C.-I.3
  • 36
    • 40549123329 scopus 로고    scopus 로고
    • Neolignans, a coumarinolignan, lignan derivatives, and a chromene: anti-inflammatory constituents from Zanthoxylum avicennae
    • Chen J-J, Wang T-Y, Hwang T-L. 2008c. Neolignans, a coumarinolignan, lignan derivatives, and a chromene: anti-inflammatory constituents from Zanthoxylum avicennae. J Nat Prod 71:212–7.
    • (2008) J Nat Prod , vol.71 , pp. 212-217
    • Chen, J.-J.1    Wang, T.-Y.2    Hwang, T.-L.3
  • 37
    • 47549115108 scopus 로고    scopus 로고
    • Dihydroagarofuranoid sesquiterpenes, a lignan derivative, a benzenoid, and antitubercular constituents from the stem of Microtropis japonica
    • Chen JJ, Yang CS, Peng CF, Chen IS, Miaw CL. 2008d. Dihydroagarofuranoid sesquiterpenes, a lignan derivative, a benzenoid, and antitubercular constituents from the stem of Microtropis japonica. J Nat Prod 71:1016–21.
    • (2008) J Nat Prod , vol.71 , pp. 1016-1021
    • Chen, J.J.1    Yang, C.S.2    Peng, C.F.3    Chen, I.S.4    Miaw, C.L.5
  • 40
    • 84993960739 scopus 로고    scopus 로고
    • Phytomedicine-modulating oxidative stress and the tumor microenvironment for cancer therapy
    • Cheng Y-T, Yang C-C, Shyur L-F. 2016b. Phytomedicine-modulating oxidative stress and the tumor microenvironment for cancer therapy. Pharmacol Res 114:128–43.
    • (2016) Pharmacol Res , vol.114 , pp. 128-143
    • Cheng, Y.-T.1    Yang, C.-C.2    Shyur, L.-F.3
  • 42
    • 80052909518 scopus 로고    scopus 로고
    • A new ferulic acid ester, a new ellagic acid derivative, and other constituents from Pachycentria formosana: effects on neutrophil pro-inflammatory responses
    • Cho JY, Lee TH, Hwang TL, Yang SZ, Chen IS, Chou TH, Sung PJ, Chen JJ. 2011. A new ferulic acid ester, a new ellagic acid derivative, and other constituents from Pachycentria formosana: effects on neutrophil pro-inflammatory responses. Chem Biodivers 8:1709–16.
    • (2011) Chem Biodivers , vol.8 , pp. 1709-1716
    • Cho, J.Y.1    Lee, T.H.2    Hwang, T.L.3    Yang, S.Z.4    Chen, I.S.5    Chou, T.H.6    Sung, P.J.7    Chen, J.J.8
  • 43
    • 84897555008 scopus 로고    scopus 로고
    • A new neolignan and lignans from the stems of Lindera obtusiloba Blume and their anti-allergic inflammatory effects
    • Choi HG, Choi YH, Kim JH, Kim HH, Kim SH, Kim JA, Lee SM, Na M, Lee SH. 2014. A new neolignan and lignans from the stems of Lindera obtusiloba Blume and their anti-allergic inflammatory effects. Arch Pharm Res 37:467–72.
    • (2014) Arch Pharm Res , vol.37 , pp. 467-472
    • Choi, H.G.1    Choi, Y.H.2    Kim, J.H.3    Kim, H.H.4    Kim, S.H.5    Kim, J.A.6    Lee, S.M.7    Na, M.8    Lee, S.H.9
  • 49
    • 84883161880 scopus 로고    scopus 로고
    • Ferulic acid inhibits the transition of amyloid-β42 monomers to oligomers but accelerates the transition from oligomers to fibrils
    • Cui L, Zhang Y, Cao H, Wang Y, Teng T, Ma G, Li Y, Li K, Zhang Y. 2013. Ferulic acid inhibits the transition of amyloid-β42 monomers to oligomers but accelerates the transition from oligomers to fibrils. J Alzheimers Dis 37:19–28.
    • (2013) J Alzheimers Dis , vol.37 , pp. 19-28
    • Cui, L.1    Zhang, Y.2    Cao, H.3    Wang, Y.4    Teng, T.5    Ma, G.6    Li, Y.7    Li, K.8    Zhang, Y.9
  • 52
    • 77649239042 scopus 로고    scopus 로고
    • Structural characterization and radical scavenging activity of monomeric and dimeric cinnamoyl glucose esters from Petrorhagia velutina leaves
    • D'Abrosca B, Fiorentino A, Ricci A, Scognamiglio M, Pacifico S, Piccolella S, Monaco P. 2010. Structural characterization and radical scavenging activity of monomeric and dimeric cinnamoyl glucose esters from Petrorhagia velutina leaves. Phytochem Lett 3:38–44.
    • (2010) Phytochem Lett , vol.3 , pp. 38-44
    • D'Abrosca, B.1    Fiorentino, A.2    Ricci, A.3    Scognamiglio, M.4    Pacifico, S.5    Piccolella, S.6    Monaco, P.7
  • 53
    • 84859161959 scopus 로고    scopus 로고
    • Polyphenols as antimicrobial agents
    • Daglia M. 2012. Polyphenols as antimicrobial agents. Curr Opin Biotechnol 23:174–81.
    • (2012) Curr Opin Biotechnol , vol.23 , pp. 174-181
    • Daglia, M.1
  • 54
    • 78149448327 scopus 로고    scopus 로고
    • Plant phenolics: extraction, analysis and their antioxidant and anticancer properties
    • Dai J, Mumper RJ. 2010. Plant phenolics: extraction, analysis and their antioxidant and anticancer properties. Molecules 15:7313–52.
    • (2010) Molecules , vol.15 , pp. 7313-7352
    • Dai, J.1    Mumper, R.J.2
  • 56
    • 4444378781 scopus 로고    scopus 로고
    • Antioxidant compounds from Chaerophyllum hirsutum extracts
    • Dall'Acqua S, Innocenti G. 2004. Antioxidant compounds from Chaerophyllum hirsutum extracts. Fitoterapia 75:592–5.
    • (2004) Fitoterapia , vol.75 , pp. 592-595
    • Dall'Acqua, S.1    Innocenti, G.2
  • 58
    • 9444295344 scopus 로고    scopus 로고
    • Anti-cholinergic, cytotoxic and anti-HIV-1 activities of sesquiterpenes and a flavonoid glycoside from the aerial parts of Polygonum viscosum
    • Datta BK, Datta SK, Khan TH, Kundu JK, Rashid MA, Nahar L, Sarker SD. 2004. Anti-cholinergic, cytotoxic and anti-HIV-1 activities of sesquiterpenes and a flavonoid glycoside from the aerial parts of Polygonum viscosum. Pharm Biol 42:18–23.
    • (2004) Pharm Biol , vol.42 , pp. 18-23
    • Datta, B.K.1    Datta, S.K.2    Khan, T.H.3    Kundu, J.K.4    Rashid, M.A.5    Nahar, L.6    Sarker, S.D.7
  • 59
    • 9444259802 scopus 로고    scopus 로고
    • Antioxidant phenylpropanoid esters of triterpenes from Dioclea lasiophylla
    • David J, Barreiros A, David J. 2004. Antioxidant phenylpropanoid esters of triterpenes from Dioclea lasiophylla. Pharm Biol 42:36–8.
    • (2004) Pharm Biol , vol.42 , pp. 36-38
    • David, J.1    Barreiros, A.2    David, J.3
  • 60
    • 0026686439 scopus 로고
    • Plant metabolites. New sesquiterpene and ionone glycosides from Eriobotrya japonica
    • De Tommasi N, Aquino R, De Simone F, Pizza C. 1992. Plant metabolites. New sesquiterpene and ionone glycosides from Eriobotrya japonica. J Nat Prod 55:1025–32.
    • (1992) J Nat Prod , vol.55 , pp. 1025-1032
    • De Tommasi, N.1    Aquino, R.2    De Simone, F.3    Pizza, C.4
  • 61
    • 0003438149 scopus 로고    scopus 로고
    • The mevalonate and methylerythritol phosphate pathways: terpenoids and steroids
    • In, 3rd ed, Chicheste, John Wiley & Sons, Ltd, p
    • Dewick PM. 2009. The mevalonate and methylerythritol phosphate pathways: terpenoids and steroids. In: Medicinal natural products—a biosynthetic approach. 3rd ed. Chicheste: John Wiley & Sons, Ltd. p 187–306.
    • (2009) Medicinal natural products—a biosynthetic approach , pp. 187-306
    • Dewick, P.M.1
  • 62
    • 77954394118 scopus 로고    scopus 로고
    • Identification of ferulate oligomers from corn stover
    • Dobberstein D, Bunzel M. 2010. Identification of ferulate oligomers from corn stover. J Sci Food Agric 90:1802–10.
    • (2010) J Sci Food Agric , vol.90 , pp. 1802-1810
    • Dobberstein, D.1    Bunzel, M.2
  • 64
    • 84959010701 scopus 로고    scopus 로고
    • Targeting inflammatory mediators with ferulic acid, a dietary polyphenol, for the suppression of monosodium urate crystal-induced inflammation in rats
    • Doss HM, Dey C, Sudandiradoss C, Rasool MK. 2016. Targeting inflammatory mediators with ferulic acid, a dietary polyphenol, for the suppression of monosodium urate crystal-induced inflammation in rats. Life Sci 148:201–10.
    • (2016) Life Sci , vol.148 , pp. 201-210
    • Doss, H.M.1    Dey, C.2    Sudandiradoss, C.3    Rasool, M.K.4
  • 65
    • 33745741451 scopus 로고    scopus 로고
    • Antioxidant constituents in the fruits of Luffa cylindrica (L.) Roem
    • Du Q, Xu Y, Li L, Zhao Y, Jerz G, Winterhalter P. 2006. Antioxidant constituents in the fruits of Luffa cylindrica (L.) Roem. J Agric Food Chem 54:4186–90.
    • (2006) J Agric Food Chem , vol.54 , pp. 4186-4190
    • Du, Q.1    Xu, Y.2    Li, L.3    Zhao, Y.4    Jerz, G.5    Winterhalter, P.6
  • 68
    • 34548415505 scopus 로고    scopus 로고
    • New long-chained feruloyl ester from the bark of Cedrelinga catenaeformis
    • El-Seedi HR. 2007. New long-chained feruloyl ester from the bark of Cedrelinga catenaeformis. Chem Nat Compd 43:256–8.
    • (2007) Chem Nat Compd , vol.43 , pp. 256-258
    • El-Seedi, H.R.1
  • 69
    • 0031772604 scopus 로고    scopus 로고
    • Post-infectional metabolites from infected potato tubers
    • Engström K. 1998. Post-infectional metabolites from infected potato tubers. Phytochemistry 49:1585–7.
    • (1998) Phytochemistry , vol.49 , pp. 1585-1587
    • Engström, K.1
  • 70
    • 79955036004 scopus 로고    scopus 로고
    • Effect of ferulic acid and α-tocopherol antioxidants on properties of sodium caseinate edible films
    • Fabra MJ, Hambleton A, Talens P, Debeaufort F, Chiralt A. 2011. Effect of ferulic acid and α-tocopherol antioxidants on properties of sodium caseinate edible films. Food Hydrocolloid 25:1441–7.
    • (2011) Food Hydrocolloid , vol.25 , pp. 1441-1447
    • Fabra, M.J.1    Hambleton, A.2    Talens, P.3    Debeaufort, F.4    Chiralt, A.5
  • 71
    • 84906944148 scopus 로고    scopus 로고
    • Diterpenes and phenolic compounds from Sideritis pullulans
    • Faiella L, Piaz FD, Bader A, Braca A. 2014. Diterpenes and phenolic compounds from Sideritis pullulans. Phytochemistry 106:164–70.
    • (2014) Phytochemistry , vol.106 , pp. 164-170
    • Faiella, L.1    Piaz, F.D.2    Bader, A.3    Braca, A.4
  • 72
    • 77956105776 scopus 로고    scopus 로고
    • Chemical constituents with free-radical-scavenging activities from the stem of Microcos paniculata
    • Fan H, Yang GZ, Zheng T, Mei ZN, Liu XM, Chen Y, Chen S. 2010. Chemical constituents with free-radical-scavenging activities from the stem of Microcos paniculata. Molecules 15:5547–60.
    • (2010) Molecules , vol.15 , pp. 5547-5560
    • Fan, H.1    Yang, G.Z.2    Zheng, T.3    Mei, Z.N.4    Liu, X.M.5    Chen, Y.6    Chen, S.7
  • 74
    • 39549084306 scopus 로고    scopus 로고
    • Antibacterial phenolic components from Eriocaulon buergerianum
    • Fang J-J, Ye G, Chen W-L, Zhao W-M. 2008. Antibacterial phenolic components from Eriocaulon buergerianum. Phytochemistry 69:1279–86.
    • (2008) Phytochemistry , vol.69 , pp. 1279-1286
    • Fang, J.-J.1    Ye, G.2    Chen, W.-L.3    Zhao, W.-M.4
  • 75
    • 84876701861 scopus 로고    scopus 로고
    • Enhanced profiling of flavonol glycosides in the fruits of sea buckthorn (Hippophae rhamnoides)
    • Fang R, Veitch NC, Kite GC, Porter EA, Simmonds, Monique SJ. 2013. Enhanced profiling of flavonol glycosides in the fruits of sea buckthorn (Hippophae rhamnoides). J Agric Food Chem 61:3868–75.
    • (2013) J Agric Food Chem , vol.61 , pp. 3868-3875
    • Fang, R.1    Veitch, N.C.2    Kite, G.C.3    Porter, E.A.4    Simmonds5    Monique, S.J.6
  • 76
  • 78
    • 84941048655 scopus 로고    scopus 로고
    • NMR-based identification of the phenolic profile of fruits of Lycium barbarum (goji berries). Isolation and structural determination of a novel N-feruloyl tyramine dimer as the most abundant antioxidant polyphenol of goji berries
    • Forino M, Tartaglione L, Dell'Aversano C, Ciminiello P. 2016. NMR-based identification of the phenolic profile of fruits of Lycium barbarum (goji berries). Isolation and structural determination of a novel N-feruloyl tyramine dimer as the most abundant antioxidant polyphenol of goji berries. Food Chem 194:1254–9.
    • (2016) Food Chem , vol.194 , pp. 1254-1259
    • Forino, M.1    Tartaglione, L.2    Dell'Aversano, C.3    Ciminiello, P.4
  • 79
    • 33750958329 scopus 로고    scopus 로고
    • New insights on the anticancer properties of dietary polyphenols
    • Fresco P, Borges F, Diniz C, Marques MPM. 2006. New insights on the anticancer properties of dietary polyphenols. Med Res Rev 26:747–66.
    • (2006) Med Res Rev , vol.26 , pp. 747-766
    • Fresco, P.1    Borges, F.2    Diniz, C.3    Marques, M.P.M.4
  • 80
    • 0024308039 scopus 로고
    • Superoxide dismutases. An adaptation to a paramagnetic gas
    • Fridovich I. 1989. Superoxide dismutases. An adaptation to a paramagnetic gas. J Biol Chem 264:7761–76.
    • (1989) J Biol Chem , vol.264 , pp. 7761-7776
    • Fridovich, I.1
  • 81
    • 42149190774 scopus 로고    scopus 로고
    • Oligosaccharide polyester and triterpenoid saponins from the roots of Polygala japonica
    • Fu J, Zuo L, Yang J, Chen R, Zhang D. 2008. Oligosaccharide polyester and triterpenoid saponins from the roots of Polygala japonica. Phytochemistry 69:1617–24.
    • (2008) Phytochemistry , vol.69 , pp. 1617-1624
    • Fu, J.1    Zuo, L.2    Yang, J.3    Chen, R.4    Zhang, D.5
  • 82
    • 12844276122 scopus 로고    scopus 로고
    • Isolation and structural characterisation of 8-O-4/8-O-4- and 8-8/8-O-4-coupled dehydrotriferulic acids from maize bran
    • Funk C, Ralph J, Steinhart H, Bunzel M. 2005. Isolation and structural characterisation of 8-O-4/8-O-4- and 8-8/8-O-4-coupled dehydrotriferulic acids from maize bran. Phytochemistry 66:363–71.
    • (2005) Phytochemistry , vol.66 , pp. 363-371
    • Funk, C.1    Ralph, J.2    Steinhart, H.3    Bunzel, M.4
  • 84
    • 84922471873 scopus 로고    scopus 로고
    • Three new dimers and two monomers of phenolic amides from the fruits of Lycium barbarum and their antioxidant activities
    • Gao K, Ma D, Cheng Y, Tian X, Lu Y, Du X, Tang H, Chen J. 2015. Three new dimers and two monomers of phenolic amides from the fruits of Lycium barbarum and their antioxidant activities. J Agric Food Chem 63:1067–75.
    • (2015) J Agric Food Chem , vol.63 , pp. 1067-1075
    • Gao, K.1    Ma, D.2    Cheng, Y.3    Tian, X.4    Lu, Y.5    Du, X.6    Tang, H.7    Chen, J.8
  • 85
    • 55549135728 scopus 로고    scopus 로고
    • Lignanamides and sesquiterpenoids from stems of Mitrephora thorelii
    • Ge F, Tang C-P, Ye Y. 2008. Lignanamides and sesquiterpenoids from stems of Mitrephora thorelii. Helv Chim Acta 91:1023–30.
    • (2008) Helv Chim Acta , vol.91 , pp. 1023-1030
    • Ge, F.1    Tang, C.-P.2    Ye, Y.3
  • 86
    • 0006025360 scopus 로고    scopus 로고
    • Elucidation of the structure and conformation of red radish (Raphanus sativus) anthocyanins using one-and two-dimensional nuclear magnetic resonance techniques
    • Giusti MM, Ghanadan H, Wrolstad RE. 1998. Elucidation of the structure and conformation of red radish (Raphanus sativus) anthocyanins using one-and two-dimensional nuclear magnetic resonance techniques. J Agric Food Chem 46:4858–63.
    • (1998) J Agric Food Chem , vol.46 , pp. 4858-4863
    • Giusti, M.M.1    Ghanadan, H.2    Wrolstad, R.E.3
  • 89
    • 0035861341 scopus 로고    scopus 로고
    • Two diacylated malvidin glycosides from Petunia hybrida flowers
    • Gonzalez E, Fougerousse A, Brouillard R. 2001. Two diacylated malvidin glycosides from Petunia hybrida flowers. Phytochemistry 58:1257–62.
    • (2001) Phytochemistry , vol.58 , pp. 1257-1262
    • Gonzalez, E.1    Fougerousse, A.2    Brouillard, R.3
  • 90
    • 33646022878 scopus 로고    scopus 로고
    • Newbouldiosides A-C, phenylethanoid glycosides from the stem bark of Newbouldia laevis
    • Gormann R, Kaloga M, Ferreira D, Marais JPJ, Kolodziej H. 2006. Newbouldiosides A-C, phenylethanoid glycosides from the stem bark of Newbouldia laevis. Phytochemistry 67:805–11.
    • (2006) Phytochemistry , vol.67 , pp. 805-811
    • Gormann, R.1    Kaloga, M.2    Ferreira, D.3    Marais, J.P.J.4    Kolodziej, H.5
  • 93
    • 0026688245 scopus 로고
    • Antioxidant potential of ferulic acid
    • Graf E. 1992. Antioxidant potential of ferulic acid. Free Radic Biol Med 13:435–48.
    • (1992) Free Radic Biol Med , vol.13 , pp. 435-448
    • Graf, E.1
  • 94
    • 84915754274 scopus 로고    scopus 로고
    • Chemical constituents with NO production inhibitory and cytotoxic activities from Litsea cubeba
    • Guo Q, Zeng K, Gao X, Zhu Z, Zhang S, Chai X, Tu P. 2015. Chemical constituents with NO production inhibitory and cytotoxic activities from Litsea cubeba. J Nat Med 69:94–9.
    • (2015) J Nat Med , vol.69 , pp. 94-99
    • Guo, Q.1    Zeng, K.2    Gao, X.3    Zhu, Z.4    Zhang, S.5    Chai, X.6    Tu, P.7
  • 96
    • 84937710875 scopus 로고    scopus 로고
    • Two new phenylpropane glycosides from Allium tuberosum Rottler
    • Han SH, Suh WS, Park KJ, Kim KH, Lee KR. 2015a. Two new phenylpropane glycosides from Allium tuberosum Rottler. Arch Pharm Res 38:1312–6.
    • (2015) Arch Pharm Res , vol.38 , pp. 1312-1316
    • Han, S.H.1    Suh, W.S.2    Park, K.J.3    Kim, K.H.4    Lee, K.R.5
  • 98
    • 43349085441 scopus 로고    scopus 로고
    • Dekkera and Brettanomyces growth and utilization of hydroxycinnamic acids in synthetic media
    • Harris V, Ford CM, Jiranek V, Grbin PR. 2008. Dekkera and Brettanomyces growth and utilization of hydroxycinnamic acids in synthetic media. Appl Microbiol Biotechnol 78:997–1006.
    • (2008) Appl Microbiol Biotechnol , vol.78 , pp. 997-1006
    • Harris, V.1    Ford, C.M.2    Jiranek, V.3    Grbin, P.R.4
  • 99
    • 0001476446 scopus 로고
    • Carbohydrate esters of ferulic acid as components of cell-walls of Lolium multiflorum
    • Hartley RD. 1973. Carbohydrate esters of ferulic acid as components of cell-walls of Lolium multiflorum. Phytochemistry 12:661–5.
    • (1973) Phytochemistry , vol.12 , pp. 661-665
    • Hartley, R.D.1
  • 101
    • 0031983023 scopus 로고    scopus 로고
    • Acylated flavonoid glycosides and accompanying phenolics from Licorice
    • Hatano T, Takagi M, Ito H, Yoshida T. 1998. Acylated flavonoid glycosides and accompanying phenolics from Licorice. Phytochemistry 47:287–93.
    • (1998) Phytochemistry , vol.47 , pp. 287-293
    • Hatano, T.1    Takagi, M.2    Ito, H.3    Yoshida, T.4
  • 102
    • 77949918628 scopus 로고    scopus 로고
    • Enzymatic processes involved in the incorporation of hydroxycinnamates into grass cell walls
    • Hatfield RD, Marita JM. 2010. Enzymatic processes involved in the incorporation of hydroxycinnamates into grass cell walls. Phytochem Rev 9:35–45.
    • (2010) Phytochem Rev , vol.9 , pp. 35-45
    • Hatfield, R.D.1    Marita, J.M.2
  • 103
    • 84960978027 scopus 로고    scopus 로고
    • Protective effects of ferulic acid against heat stress-induced intestinal epithelial barrier dysfunction in vitro and in vivo
    • He S, Liu F, Xu L, Yin P, Li D, Mei C, Jiang L, Ma Y, Xu J. 2016. Protective effects of ferulic acid against heat stress-induced intestinal epithelial barrier dysfunction in vitro and in vivo. PLoS One 11:1–15.
    • (2016) PLoS One , vol.11 , pp. 1-15
    • He, S.1    Liu, F.2    Xu, L.3    Yin, P.4    Li, D.5    Mei, C.6    Jiang, L.7    Ma, Y.8    Xu, J.9
  • 104
    • 0032909443 scopus 로고    scopus 로고
    • Iridoid glycosides and phenolic glycosides from Holmskioldia sanguinea
    • Helfrich E, Rimpler H. 1999. Iridoid glycosides and phenolic glycosides from Holmskioldia sanguinea. Phytochemistry 50:619–27.
    • (1999) Phytochemistry , vol.50 , pp. 619-627
    • Helfrich, E.1    Rimpler, H.2
  • 106
    • 0029013573 scopus 로고
    • Inhibitory effect of ferulic acid and isoferulic acid on murine interleukin-8 production in response to influenzavirus infections in vitro and in vivo
    • Hirabayashi T, Ochiai H, Sakai S, Nakajima K, Terasawa K. 1995. Inhibitory effect of ferulic acid and isoferulic acid on murine interleukin-8 production in response to influenzavirus infections in vitro and in vivo. Planta Med 61:221–6.
    • (1995) Planta Med , vol.61 , pp. 221-226
    • Hirabayashi, T.1    Ochiai, H.2    Sakai, S.3    Nakajima, K.4    Terasawa, K.5
  • 107
    • 84977252279 scopus 로고
    • Mittheilungen aus dem chemischen Laboratorium in Innsbruck I)Ueber einige Harze [Zersetzungsproducte derselben durch schmelzendes Kali]
    • Hlasiwetz H, Barth L. 1866. Mittheilungen aus dem chemischen Laboratorium in Innsbruck IUeber einige Harze [Zersetzungsproducte derselben durch schmelzendes Kali]. Eur J Org Chem 138:61–76.
    • (1866) Eur J Org Chem , vol.138 , pp. 61-76
    • Hlasiwetz, H.1    Barth, L.2
  • 109
    • 78650636272 scopus 로고    scopus 로고
    • Aristolactams and alkamides of Aristolochia gigantea
    • Holzbach JC, Lopes LMX. 2010. Aristolactams and alkamides of Aristolochia gigantea. Molecules 15:9462–72.
    • (2010) Molecules , vol.15 , pp. 9462-9472
    • Holzbach, J.C.1    Lopes, L.M.X.2
  • 112
    • 0031869449 scopus 로고    scopus 로고
    • Gmelinosides A-L, twelve acylated iridoid glycosides from Gmelina arborea
    • Hosny M, Rosazza JPN. 1998. Gmelinosides A-L, twelve acylated iridoid glycosides from Gmelina arborea. J Nat Prod 61:734–42.
    • (1998) J Nat Prod , vol.61 , pp. 734-742
    • Hosny, M.1    Rosazza, J.P.N.2
  • 115
    • 0028873242 scopus 로고
    • Five acylated pelargonidin glucosides in the red flowers of Hyacinthus orientalis
    • Hosokawa K, Fukunaga Y, Fukushi E, Kawabata J. 1995. Five acylated pelargonidin glucosides in the red flowers of Hyacinthus orientalis. Phytochemistry 40:567–71.
    • (1995) Phytochemistry , vol.40 , pp. 567-571
    • Hosokawa, K.1    Fukunaga, Y.2    Fukushi, E.3    Kawabata, J.4
  • 116
    • 0036932569 scopus 로고    scopus 로고
    • Bacopaside III, bacopasaponin G, and bacopasides A, B, and C from Bacopa monniera
    • Hou C-C, Lin S-J, Cheng J-T, Hsu F-L. 2002. Bacopaside III, bacopasaponin G, and bacopasides A, B, and C from Bacopa monniera. J Nat Prod 65:1759–63.
    • (2002) J Nat Prod , vol.65 , pp. 1759-1763
    • Hou, C.-C.1    Lin, S.-J.2    Cheng, J.-T.3    Hsu, F.-L.4
  • 117
    • 0028857387 scopus 로고
    • Lignans from the wood of Aralia bipinnata
    • Hsiao J-J, Chiang H-C. 1995. Lignans from the wood of Aralia bipinnata. Phytochemistry 39:899–902.
    • (1995) Phytochemistry , vol.39 , pp. 899-902
    • Hsiao, J.-J.1    Chiang, H.-C.2
  • 118
    • 65749086280 scopus 로고    scopus 로고
    • Acylated stilbene glucosides and further constituents from Acanthopanax brachypus
    • Hu H-B, Zheng X-D, Hu H-S, Li Y. 2009. Acylated stilbene glucosides and further constituents from Acanthopanax brachypus. Helv Chim Acta 92:546–54.
    • (2009) Helv Chim Acta , vol.92 , pp. 546-554
    • Hu, H.-B.1    Zheng, X.-D.2    Hu, H.-S.3    Li, Y.4
  • 119
    • 84906678337 scopus 로고    scopus 로고
    • An unusual piceatannol dimer from Rheum austral D. Don with antioxidant activity
    • Hu L, Chen N-N, Hu Q, Yang C, Yang Q-S, Wang F-F. 2014. An unusual piceatannol dimer from Rheum austral D. Don with antioxidant activity. Molecules 19:11453–64.
    • (2014) Molecules , vol.19 , pp. 11453-11464
    • Hu, L.1    Chen, N.-N.2    Hu, Q.3    Yang, C.4    Yang, Q.-S.5    Wang, F.-F.6
  • 120
    • 84942111087 scopus 로고    scopus 로고
    • Phytoconstituents from the leaves of Dracaena cochinchinensis (Lour.) S. C. Chen
    • Hu L, Wang FF, Wang XH, Yang QS, Xiong Y, Liu WX. 2015. Phytoconstituents from the leaves of Dracaena cochinchinensis (Lour.) S. C. Chen. Biochem Syst Ecol 63:1–5.
    • (2015) Biochem Syst Ecol , vol.63 , pp. 1-5
    • Hu, L.1    Wang, F.F.2    Wang, X.H.3    Yang, Q.S.4    Xiong, Y.5    Liu, W.X.6
  • 121
    • 15544383555 scopus 로고    scopus 로고
    • The chemistry behind antioxidant capacity assays
    • Huang D, Boxin OU, Prior RL. 2005. The chemistry behind antioxidant capacity assays. J Agric Food Chem 53:1841–56.
    • (2005) J Agric Food Chem , vol.53 , pp. 1841-1856
    • Huang, D.1    Boxin, O.U.2    Prior, R.L.3
  • 123
    • 0023790908 scopus 로고
    • Inhibitory effect of curcumin, chlorogenic acid, caffeic acid, and ferulic acid on tumor promotion in mouse skin by 12-O-tetradecanoylphorbol-13-acetate
    • Huang M, Smart RC, Wong C, Huang M, Smart RC, Wong C, Conney AH. 1988. Inhibitory effect of curcumin, chlorogenic acid, caffeic acid, and ferulic acid on tumor promotion in mouse skin by 12-O-tetradecanoylphorbol-13-acetate. Cancer Res 48:5941–6.
    • (1988) Cancer Res , vol.48 , pp. 5941-5946
    • Huang, M.1    Smart, R.C.2    Wong, C.3    Huang, M.4    Smart, R.C.5    Wong, C.6    Conney, A.H.7
  • 124
    • 2142662219 scopus 로고    scopus 로고
    • Phenyl and phenylethyl glycosides from Picrorhiza scrophulariiflora
    • Huang S-X, Liao X, Nie Q-J, Ding L-S, Peng S-L. 2004. Phenyl and phenylethyl glycosides from Picrorhiza scrophulariiflora. Helv Chim Acta 87:598–604.
    • (2004) Helv Chim Acta , vol.87 , pp. 598-604
    • Huang, S.-X.1    Liao, X.2    Nie, Q.-J.3    Ding, L.-S.4    Peng, S.-L.5
  • 126
    • 33750191907 scopus 로고    scopus 로고
    • Anticancer activity of phenolic antioxidants against breast cancer cells and a spontaneous mammary tumor
    • Indap MA, Radhika S, Motiwale L, Rao K. 2006. Anticancer activity of phenolic antioxidants against breast cancer cells and a spontaneous mammary tumor. Indian J Pharm Sci 68:470–4.
    • (2006) Indian J Pharm Sci , vol.68 , pp. 470-474
    • Indap, M.A.1    Radhika, S.2    Motiwale, L.3    Rao, K.4
  • 128
    • 59049104149 scopus 로고    scopus 로고
    • In vitro and in vivo antioxidant properties of ferulic acid: a comparative study with other natural oxidation inhibitors
    • Itagaki S, Kurokawa T, Nakata C, Saito Y, Oikawa S, Kobayashi M, Hirano T, Iseki K. 2009. In vitro and in vivo antioxidant properties of ferulic acid: a comparative study with other natural oxidation inhibitors. Food Chem 114:466–71.
    • (2009) Food Chem , vol.114 , pp. 466-471
    • Itagaki, S.1    Kurokawa, T.2    Nakata, C.3    Saito, Y.4    Oikawa, S.5    Kobayashi, M.6    Hirano, T.7    Iseki, K.8
  • 129
    • 33845446013 scopus 로고    scopus 로고
    • Five new phenylethanoid glycosides from the whole plants of Lamium purpureum L
    • Ito N, Nihei T, Kakuda R, Yaoita Y, Kikuchi M. 2006. Five new phenylethanoid glycosides from the whole plants of Lamium purpureum L. Chem Pharm Bull (Tokyo) 54:1705–8.
    • (2006) Chem Pharm Bull (Tokyo) , vol.54 , pp. 1705-1708
    • Ito, N.1    Nihei, T.2    Kakuda, R.3    Yaoita, Y.4    Kikuchi, M.5
  • 130
    • 0007346535 scopus 로고
    • 6’-O-feruloyl- and 6’-O-sinapoyl-demethylalangisides, tetrahydroisoquinoline-monoterpene glucosides from Alangium platanifolium
    • Itoh A, Tanahashi T, Nagakura N. 1992. 6’-O-feruloyl- and 6’-O-sinapoyl-demethylalangisides, tetrahydroisoquinoline-monoterpene glucosides from Alangium platanifolium. Phytochemistry 31:1037–40.
    • (1992) Phytochemistry , vol.31 , pp. 1037-1040
    • Itoh, A.1    Tanahashi, T.2    Nagakura, N.3
  • 131
    • 0030067507 scopus 로고    scopus 로고
    • Acylated tetrahydroisoquinoline-monoterpene glucosides from Alangium lamarckii
    • Itoh A, Tanahashi T, Nagakura N. 1996. Acylated tetrahydroisoquinoline-monoterpene glucosides from Alangium lamarckii. Phytochemistry 41:651–6.
    • (1996) Phytochemistry , vol.41 , pp. 651-656
    • Itoh, A.1    Tanahashi, T.2    Nagakura, N.3
  • 133
    • 84929751562 scopus 로고    scopus 로고
    • Potentiometric study of antioxidant activity: development and prospects
    • Ivanova AV, Gerasimova EL, Brainina K. 2015. Potentiometric study of antioxidant activity: development and prospects. Crit Rev Anal Chem 45:311–22.
    • (2015) Crit Rev Anal Chem , vol.45 , pp. 311-322
    • Ivanova, A.V.1    Gerasimova, E.L.2    Brainina, K.3
  • 135
    • 1842733098 scopus 로고    scopus 로고
    • Constituents of Asparagus officinalis evaluated for inhibitory activity against cyclooxygenase-2
    • Jang DS, Cuendet M, Fong HHS, Pezzuto JM, Kinghorn AD. 2004. Constituents of Asparagus officinalis evaluated for inhibitory activity against cyclooxygenase-2. J Agric Food Chem 52:2218–22.
    • (2004) J Agric Food Chem , vol.52 , pp. 2218-2222
    • Jang, D.S.1    Cuendet, M.2    Fong, H.H.S.3    Pezzuto, J.M.4    Kinghorn, A.D.5
  • 136
    • 79957606096 scopus 로고    scopus 로고
    • The antiproliferative effect of dietary fiber phenolic compounds ferulic acid and p-coumaric acid on the cell cycle of Caco-2 cells
    • Janicke B, Hegardt C, Krogh M, Onning G, Akesson B, Cirenajwis HM, Oredsson SM. 2011. The antiproliferative effect of dietary fiber phenolic compounds ferulic acid and p-coumaric acid on the cell cycle of Caco-2 cells. Nutr Cancer 63:611–22.
    • (2011) Nutr Cancer , vol.63 , pp. 611-622
    • Janicke, B.1    Hegardt, C.2    Krogh, M.3    Onning, G.4    Akesson, B.5    Cirenajwis, H.M.6    Oredsson, S.M.7
  • 137
    • 33746869949 scopus 로고    scopus 로고
    • Impact of alkyl esters of caffeic and ferulic acids on tumor cell proliferation, cyclooxygenase enzyme, and lipid peroxidation
    • Jayaprakasam B, Vanisree M, Zhang Y, Dewitt DL, Nair MG. 2006. Impact of alkyl esters of caffeic and ferulic acids on tumor cell proliferation, cyclooxygenase enzyme, and lipid peroxidation. J Agric Food Chem 54:5375–81.
    • (2006) J Agric Food Chem , vol.54 , pp. 5375-5381
    • Jayaprakasam, B.1    Vanisree, M.2    Zhang, Y.3    Dewitt, D.L.4    Nair, M.G.5
  • 138
    • 4043052432 scopus 로고    scopus 로고
    • Isolation and identification of 3-methoxy-4-hydroxybenzoic acid and 3-methoxy-4-hydroxycinnamic acid from hot water extracts of Hovenia dulcis Thumb and confirmation of their antioxidative and antimicrobial activity
    • Jeong YC, Jae HM, Keun HP. 2000. Isolation and identification of 3-methoxy-4-hydroxybenzoic acid and 3-methoxy-4-hydroxycinnamic acid from hot water extracts of Hovenia dulcis Thumb and confirmation of their antioxidative and antimicrobial activity. Korean J Food Sci Technol 32:1403–8.
    • (2000) Korean J Food Sci Technol , vol.32 , pp. 1403-1408
    • Jeong, Y.C.1    Jae, H.M.2    Keun, H.P.3
  • 139
    • 0032985471 scopus 로고    scopus 로고
    • Pikuroside: a novel iridoid from Picrorhiza kurroa
    • Jia Q, Hong MF, Minter D. 1999. Pikuroside: a novel iridoid from Picrorhiza kurroa. J Nat Prod 62:901–3.
    • (1999) J Nat Prod , vol.62 , pp. 901-903
    • Jia, Q.1    Hong, M.F.2    Minter, D.3
  • 140
    • 0342802074 scopus 로고
    • Phenylpropanoid and iridoid glycosides from Pedicularis longiflora
    • Jia Z-J, Liu Z-M. 1992. Phenylpropanoid and iridoid glycosides from Pedicularis longiflora. Phytochemistry 31:3125–7.
    • (1992) Phytochemistry , vol.31 , pp. 3125-3127
    • Jia, Z.-J.1    Liu, Z.-M.2
  • 142
    • 84890805249 scopus 로고    scopus 로고
    • Chemical constituents from the stem barks of Garcinia multiflora
    • Jing W, Jiang C, Ji F, Hua H, Li Z. 2013. Chemical constituents from the stem barks of Garcinia multiflora. J Asian Nat Prod Res 15:1152–7.
    • (2013) J Asian Nat Prod Res , vol.15 , pp. 1152-1157
    • Jing, W.1    Jiang, C.2    Ji, F.3    Hua, H.4    Li, Z.5
  • 143
    • 37349104209 scopus 로고    scopus 로고
    • Hypoglycemic effects of a phenolic acid fraction of rice bran and ferulic acid in C57BL/KsJ-db/db mice
    • Jung EH, Kim SR, Hwang IK, Ha TY. 2007. Hypoglycemic effects of a phenolic acid fraction of rice bran and ferulic acid in C57BL/KsJ-db/db mice. J Agric Food Chem 55:9800–4.
    • (2007) J Agric Food Chem , vol.55 , pp. 9800-9804
    • Jung, E.H.1    Kim, S.R.2    Hwang, I.K.3    Ha, T.Y.4
  • 144
    • 55249107556 scopus 로고    scopus 로고
    • A comparative study of the radical-scavenging activity of the phenolcarboxylic acids caffeic acid, p-coumaric acid, chlorogenic acid and ferulic acid, with or without 2-mercaptoethanol, a thiol, using the induction period method
    • Kadoma Y, Fujisawa S. 2008. A comparative study of the radical-scavenging activity of the phenolcarboxylic acids caffeic acid, p-coumaric acid, chlorogenic acid and ferulic acid, with or without 2-mercaptoethanol, a thiol, using the induction period method. Molecules 13:2488–99.
    • (2008) Molecules , vol.13 , pp. 2488-2499
    • Kadoma, Y.1    Fujisawa, S.2
  • 145
    • 0037382196 scopus 로고    scopus 로고
    • Acylated phenolic glycosides from Solenostemma argel
    • Kamel MS. 2003a. Acylated phenolic glycosides from Solenostemma argel. Phytochemistry 62:1247–50.
    • (2003) Phytochemistry , vol.62 , pp. 1247-1250
    • Kamel, M.S.1
  • 146
    • 0038441445 scopus 로고    scopus 로고
    • Flavone C-glycosides from Lupinus hartwegii
    • Kamel MS. 2003b. Flavone C-glycosides from Lupinus hartwegii. Phytochemistry 63:449–52.
    • (2003) Phytochemistry , vol.63 , pp. 449-452
    • Kamel, M.S.1
  • 150
    • 0036264981 scopus 로고    scopus 로고
    • Ferulic acid antioxidant protection against hydroxyl and peroxyl radical oxidation in synaptosomal and neuronal cell culture systems in vitro: structure-activity studies
    • Kanski J, Aksenova M, Stoyanova A, Butterfield DA. 2002. Ferulic acid antioxidant protection against hydroxyl and peroxyl radical oxidation in synaptosomal and neuronal cell culture systems in vitro: structure-activity studies. J Nutr Biochem 13:273–81.
    • (2002) J Nutr Biochem , vol.13 , pp. 273-281
    • Kanski, J.1    Aksenova, M.2    Stoyanova, A.3    Butterfield, D.A.4
  • 151
    • 79952729308 scopus 로고    scopus 로고
    • Dimorphamides A-C, new polyphenolic amides from Atriplex dimorphostagia
    • Karim A, Fatima I, Hussain S, Malik A. 2011. Dimorphamides A-C, new polyphenolic amides from Atriplex dimorphostagia. Helv Chim Acta 94:528–33.
    • (2011) Helv Chim Acta , vol.94 , pp. 528-533
    • Karim, A.1    Fatima, I.2    Hussain, S.3    Malik, A.4
  • 152
    • 84868088837 scopus 로고    scopus 로고
    • Oxidants and antioxidants in the pathogenesis of HIV/AIDS
    • Kashou AH, Agarwal A. 2011. Oxidants and antioxidants in the pathogenesis of HIV/AIDS. Open Reprod Sci J 3:154–61.
    • (2011) Open Reprod Sci J , vol.3 , pp. 154-161
    • Kashou, A.H.1    Agarwal, A.2
  • 153
    • 0027408080 scopus 로고
    • Free radicals as mediators of tissue injury and disease
    • Kehrer JP. 1993. Free radicals as mediators of tissue injury and disease. Crit Rev Toxicol 23:21–48.
    • (1993) Crit Rev Toxicol , vol.23 , pp. 21-48
    • Kehrer, J.P.1
  • 155
    • 84874643105 scopus 로고    scopus 로고
    • Techniques for analysis of plant phenolic compounds
    • Khoddami A, Wilkes MA, Roberts TH. 2013. Techniques for analysis of plant phenolic compounds. Molecules 18:2328–75.
    • (2013) Molecules , vol.18 , pp. 2328-2375
    • Khoddami, A.1    Wilkes, M.A.2    Roberts, T.H.3
  • 156
    • 84865026038 scopus 로고    scopus 로고
    • A new putrescine bisamide phenolic glycoside from the seeds of Lallemantia iberica (M. Bieb.) Fisch. & C. A. Mey
    • Khosravi Dehaghi N, Lai D, Amanzadeh Y, Sadat-Ebrahimi SS, Proksch P. 2012. A new putrescine bisamide phenolic glycoside from the seeds of Lallemantia iberica (M. Bieb.) Fisch. & C. A. Mey. Phytochem Lett 5:643–5.
    • (2012) Phytochem Lett , vol.5 , pp. 643-645
    • Khosravi Dehaghi, N.1    Lai, D.2    Amanzadeh, Y.3    Sadat-Ebrahimi, S.S.4    Proksch, P.5
  • 158
    • 84862796420 scopus 로고    scopus 로고
    • Anti-inflammatory activity of hydroxycinnamic acid derivatives isolated from corn bran in lipopolysaccharide-stimulated Raw 264.7 macrophages
    • Kim EO, Min KJ, Kwon TK, Um BH, Moreau RA, Choi SW. 2012. Anti-inflammatory activity of hydroxycinnamic acid derivatives isolated from corn bran in lipopolysaccharide-stimulated Raw 264.7 macrophages. Food Chem Toxicol 50:1309–16.
    • (2012) Food Chem Toxicol , vol.50 , pp. 1309-1316
    • Kim, E.O.1    Min, K.J.2    Kwon, T.K.3    Um, B.H.4    Moreau, R.A.5    Choi, S.W.6
  • 159
    • 78651080108 scopus 로고    scopus 로고
    • Isolation and identification of sea buckthorn (Hippophae rhamnoides) phenolics with antioxidant activity and α-glucosidase inhibitory effect
    • Kim JS, Kwon YS, Sa YJ, Kim MJ. 2011. Isolation and identification of sea buckthorn (Hippophae rhamnoides) phenolics with antioxidant activity and α-glucosidase inhibitory effect. J Agric Food Chem 59:138–44.
    • (2011) J Agric Food Chem , vol.59 , pp. 138-144
    • Kim, J.S.1    Kwon, Y.S.2    Sa, Y.J.3    Kim, M.J.4
  • 160
    • 84906939882 scopus 로고    scopus 로고
    • Quantitative and pattern recognition analyses of magnoflorine, spinosin, 6’’’-feruloyl spinosin and jujuboside a by HPLC in Zizyphi semen
    • Kim W Il, Zhao BT, Zhang HY, Lee JH, Son JK, Woo MH. 2014. Quantitative and pattern recognition analyses of magnoflorine, spinosin, 6’’’-feruloyl spinosin and jujuboside a by HPLC in Zizyphi semen. Arch Pharm Res 37:1139–47.
    • (2014) Arch Pharm Res , vol.37 , pp. 1139-1147
    • Kim, W.1    Zhao, B.T.2    Zhang, H.Y.3    Lee, J.H.4    Son, J.K.5    Woo, M.H.6
  • 161
    • 0033951830 scopus 로고    scopus 로고
    • Flavonol glycoside gallate and ferulate esters from Persicaria lapathifolia as inhibitors of superoxide production in human monocytes stimulated by unopsonized zymosan
    • Kim Y, Jang DS, Park SH, Yun J, Min BK, Min KR, Lee HK. 2000. Flavonol glycoside gallate and ferulate esters from Persicaria lapathifolia as inhibitors of superoxide production in human monocytes stimulated by unopsonized zymosan. Planta Med 66:72–4.
    • (2000) Planta Med , vol.66 , pp. 72-74
    • Kim, Y.1    Jang, D.S.2    Park, S.H.3    Yun, J.4    Min, B.K.5    Min, K.R.6    Lee, H.K.7
  • 163
    • 0141849446 scopus 로고    scopus 로고
    • Inhibitory phenolic amides on lipopolysaccharide-induced nitric oxide production in RAW 264.7 cells from Beta vulgaris var. cicla seeds
    • Kim Y, Han MS, Lee JS, Kim J, Kim YC. 2003. Inhibitory phenolic amides on lipopolysaccharide-induced nitric oxide production in RAW 264.7 cells from Beta vulgaris var. cicla seeds. Phyther Res 17:983–5.
    • (2003) Phyther Res , vol.17 , pp. 983-985
    • Kim, Y.1    Han, M.S.2    Lee, J.S.3    Kim, J.4    Kim, Y.C.5
  • 164
    • 78249236210 scopus 로고    scopus 로고
    • A feruloyltyramine trimer isolated from potato common scab lesions
    • King RR, Calhoun LA. 2010. A feruloyltyramine trimer isolated from potato common scab lesions. Phytochemistry 71:2187–9.
    • (2010) Phytochemistry , vol.71 , pp. 2187-2189
    • King, R.R.1    Calhoun, L.A.2
  • 165
    • 3042670485 scopus 로고    scopus 로고
    • Iridoid and phenylethyl glycosides from Globularia sintenisii
    • Kirmizibekmez H, Çaliş I, Piacente S, Pizza C. 2004. Iridoid and phenylethyl glycosides from Globularia sintenisii. Helv Chim Acta 87:1172–9.
    • (2004) Helv Chim Acta , vol.87 , pp. 1172-1179
    • Kirmizibekmez, H.1    Çaliş, I.2    Piacente, S.3    Pizza, C.4
  • 168
    • 79952188169 scopus 로고    scopus 로고
    • Acylated flavonol tri- and tetraglycosides in the flavonoid metabolome of Cladrastis kentukea (Leguminosae)
    • Kite GC, Rowe ER, Lewis GP, Veitch NC. 2011. Acylated flavonol tri- and tetraglycosides in the flavonoid metabolome of Cladrastis kentukea (Leguminosae). Phytochemistry 72:372–84.
    • (2011) Phytochemistry , vol.72 , pp. 372-384
    • Kite, G.C.1    Rowe, E.R.2    Lewis, G.P.3    Veitch, N.C.4
  • 169
    • 0034656296 scopus 로고    scopus 로고
    • Echinophyllins C-F, new nitrogen-containing clerodane diterpenoids from Echinodorus macrophyllus
    • Kobayashi J, Sekiguchi M, Shigemori H, Ohsaki A. 2000. Echinophyllins C-F, new nitrogen-containing clerodane diterpenoids from Echinodorus macrophyllus. Tethrahedron Lett 41:2939–43.
    • (2000) Tethrahedron Lett , vol.41 , pp. 2939-2943
    • Kobayashi, J.1    Sekiguchi, M.2    Shigemori, H.3    Ohsaki, A.4
  • 170
    • 55749094483 scopus 로고    scopus 로고
    • New lignan glycosides from Glehnia littoralis
    • Kong WX, Yuan Z. 2008. New lignan glycosides from Glehnia littoralis. Chinese Chem Lett 19:1459–61.
    • (2008) Chinese Chem Lett , vol.19 , pp. 1459-1461
    • Kong, W.X.1    Yuan, Z.2
  • 173
    • 84862025001 scopus 로고    scopus 로고
    • Antioxidative activities and chemical characterization of polysaccharide extracts from the widely used mushrooms Ganoderma applanatum, Ganoderma lucidum, Lentinus edodes and Trametes versicolor
    • Kozarski M, Klaus A, Nikšić M, Vrvić MM, Todorović N, Jakovljević D, Van Griensven LJLD. 2012. Antioxidative activities and chemical characterization of polysaccharide extracts from the widely used mushrooms Ganoderma applanatum, Ganoderma lucidum, Lentinus edodes and Trametes versicolor. J Food Compos Anal 26:144–53.
    • (2012) J Food Compos Anal , vol.26 , pp. 144-153
    • Kozarski, M.1    Klaus, A.2    Nikšić, M.3    Vrvić, M.M.4    Todorović, N.5    Jakovljević, D.6    Van Griensven, L.J.L.D.7
  • 174
    • 84921492626 scopus 로고    scopus 로고
    • Potential applications of ferulic acid from natural sources
    • Kumar N, Pruthi V. 2014. Potential applications of ferulic acid from natural sources. Biotechnol Rep 4:86-93.
    • (2014) Biotechnol Rep , vol.4 , pp. 86-93
    • Kumar, N.1    Pruthi, V.2
  • 175
    • 0043235769 scopus 로고    scopus 로고
    • Biological activity of serotonin conjugates from the seeds of Centaurea nigra
    • Kumarasamy Y, Middleton M, Reid RG, Nahar L, Sarker SD. 2003. Biological activity of serotonin conjugates from the seeds of Centaurea nigra. Fitoterapia 74:609–12.
    • (2003) Fitoterapia , vol.74 , pp. 609-612
    • Kumarasamy, Y.1    Middleton, M.2    Reid, R.G.3    Nahar, L.4    Sarker, S.D.5
  • 176
    • 79955848215 scopus 로고    scopus 로고
    • Chemical constituents and antitubercular activity of Formosan Pisonia umbellifera
    • Kuo H-T, Peng C-F, Huang H-Y, Lin C-H, Chen I-S, Tsai I-L. 2011. Chemical constituents and antitubercular activity of Formosan Pisonia umbellifera. Planta Med 77:736–41.
    • (2011) Planta Med , vol.77 , pp. 736-741
    • Kuo, H.-T.1    Peng, C.-F.2    Huang, H.-Y.3    Lin, C.-H.4    Chen, I.-S.5    Tsai, I.-L.6
  • 177
    • 78651410618 scopus 로고    scopus 로고
    • Chemical constituents of the stems and twigs of Lindera umbellata
    • Kuroda M, Sakurai K, Mimaki Y. 2011. Chemical constituents of the stems and twigs of Lindera umbellata. J Nat Med 65:198–201.
    • (2011) J Nat Med , vol.65 , pp. 198-201
    • Kuroda, M.1    Sakurai, K.2    Mimaki, Y.3
  • 178
    • 0034944951 scopus 로고    scopus 로고
    • An acetylene and a monoterpene glycoside from Adenocaulon himalaicum
    • Kwon HC, Lee KR. 2001. An acetylene and a monoterpene glycoside from Adenocaulon himalaicum. Planta Med 67:482–4.
    • (2001) Planta Med , vol.67 , pp. 482-484
    • Kwon, H.C.1    Lee, K.R.2
  • 181
    • 84947777461 scopus 로고    scopus 로고
    • The molecular events behind ferulic acid mediated modulation of IL-6 expression in LPS-activated Raw 264.7 cells
    • Lampiasi N, Montana G. 2016. The molecular events behind ferulic acid mediated modulation of IL-6 expression in LPS-activated Raw 264.7 cells. Immunobiology 221:486–93.
    • (2016) Immunobiology , vol.221 , pp. 486-493
    • Lampiasi, N.1    Montana, G.2
  • 182
    • 77049122784 scopus 로고    scopus 로고
    • Cholestane glycosides and trihydroxy fatty acids from the rhizomes of Dioscorea septemloba
    • Lee KY, Kim S-H, Jeong EJ, Park JH, Kim SH, Kim YC, Sung SH. 2010a. Cholestane glycosides and trihydroxy fatty acids from the rhizomes of Dioscorea septemloba. Planta Med 76:291–4.
    • (2010) Planta Med , vol.76 , pp. 291-294
    • Lee, K.Y.1    Kim, S.-H.2    Jeong, E.J.3    Park, J.H.4    Kim, S.H.5    Kim, Y.C.6    Sung, S.H.7
  • 183
    • 77954463024 scopus 로고    scopus 로고
    • A new phenylpropane glycoside from the rhizome of Sparganium stoloniferum
    • Lee SY, Choi SU, Lee JH, Lee DU, Lee KR. 2010b. A new phenylpropane glycoside from the rhizome of Sparganium stoloniferum. Arch Pharm Res 33:515–21.
    • (2010) Arch Pharm Res , vol.33 , pp. 515-521
    • Lee, S.Y.1    Choi, S.U.2    Lee, J.H.3    Lee, D.U.4    Lee, K.R.5
  • 184
  • 185
    • 84908119984 scopus 로고    scopus 로고
    • Inhibitory effects of Colocasia esculenta (L.) Schott constituents on aldose reductase
    • Li HM, Hwang SH, Kang BG, Hong JS, Lim SS. 2014a. Inhibitory effects of Colocasia esculenta (L.) Schott constituents on aldose reductase. Molecules 19:13212–24.
    • (2014) Molecules , vol.19 , pp. 13212-13224
    • Li, H.M.1    Hwang, S.H.2    Kang, B.G.3    Hong, J.S.4    Lim, S.S.5
  • 186
    • 61849154111 scopus 로고    scopus 로고
    • Cytotoxicity of cardenolides and cardenolide glycosides from Asclepias curassavica
    • Li JZ, Qing C, Chen CX, Hao XJ, Liu HY. 2009. Cytotoxicity of cardenolides and cardenolide glycosides from Asclepias curassavica. Bioorganic Med Chem Lett 19:1956–9.
    • (2009) Bioorganic Med Chem Lett , vol.19 , pp. 1956-1959
    • Li, J.Z.1    Qing, C.2    Chen, C.X.3    Hao, X.J.4    Liu, H.Y.5
  • 189
    • 0034739169 scopus 로고    scopus 로고
    • Phenylpropanoid glycosides from Scrophularia ningpoensis
    • Li YM, Jiang SH, Gao WY, Zhu DY. 2000. Phenylpropanoid glycosides from Scrophularia ningpoensis. Phytochemistry 54:923–5.
    • (2000) Phytochemistry , vol.54 , pp. 923-925
    • Li, Y.M.1    Jiang, S.H.2    Gao, W.Y.3    Zhu, D.Y.4
  • 190
    • 80051712305 scopus 로고    scopus 로고
    • Antioxidative caffeoylquinic acids and flavonoids from Hemerocallis fulva flowers
    • Lin YL, Lu CK, Huang YJ, Chen HJ. 2011. Antioxidative caffeoylquinic acids and flavonoids from Hemerocallis fulva flowers. J Agric Food Chem 59:8789–95.
    • (2011) J Agric Food Chem , vol.59 , pp. 8789-8795
    • Lin, Y.L.1    Lu, C.K.2    Huang, Y.J.3    Chen, H.J.4
  • 191
    • 0032909766 scopus 로고    scopus 로고
    • Acylated flavonol glycosides from leaves of Stenochlaena palustris
    • Liu H, Orjala J, Sticher O, Rali T. 1999. Acylated flavonol glycosides from leaves of Stenochlaena palustris. J Nat Prod 62:70–5.
    • (1999) J Nat Prod , vol.62 , pp. 70-75
    • Liu, H.1    Orjala, J.2    Sticher, O.3    Rali, T.4
  • 192
    • 55449099620 scopus 로고    scopus 로고
    • Phenylpropanoid esters of rhamnose from Buddleja asiatica
    • Liu Y, Cai X, Li W, Luo X. 2008. Phenylpropanoid esters of rhamnose from Buddleja asiatica. Helv Chim Acta 91:1299–1304.
    • (2008) Helv Chim Acta , vol.91 , pp. 1299-1304
    • Liu, Y.1    Cai, X.2    Li, W.3    Luo, X.4
  • 193
    • 0032897373 scopus 로고    scopus 로고
    • The effects of plant phenolics, caffeic acid, chlorogenic acid and ferulic acid on arylamine N-acetyltransferase activities in human gastrointestinal microflora
    • Lo HH, Chung JG. 1999. The effects of plant phenolics, caffeic acid, chlorogenic acid and ferulic acid on arylamine N-acetyltransferase activities in human gastrointestinal microflora. Anticancer Res 19:133–9.
    • (1999) Anticancer Res , vol.19 , pp. 133-139
    • Lo, H.H.1    Chung, J.G.2
  • 194
    • 67650685220 scopus 로고    scopus 로고
    • Active constituents from Sophora japonica exhibiting cellular tyrosinase inhibition in human epidermal melanocytes
    • Lo YH, Lin RD, Lin YP, Liu YL, Lee MH. 2009. Active constituents from Sophora japonica exhibiting cellular tyrosinase inhibition in human epidermal melanocytes. J Ethnopharmacol 124:625–9.
    • (2009) J Ethnopharmacol , vol.124 , pp. 625-629
    • Lo, Y.H.1    Lin, R.D.2    Lin, Y.P.3    Liu, Y.L.4    Lee, M.H.5
  • 195
    • 0037298781 scopus 로고    scopus 로고
    • Redox-sensitive mechanisms of phytochemical-mediated inhibition of cancer cell proliferation
    • Loo G. 2003. Redox-sensitive mechanisms of phytochemical-mediated inhibition of cancer cell proliferation. J Nutr Biochem 14:64–73.
    • (2003) J Nutr Biochem , vol.14 , pp. 64-73
    • Loo, G.1
  • 196
    • 84860783215 scopus 로고    scopus 로고
    • Studies on the constituents of Cimicifuga foetida collected in Guizhou Province and their cytotoxic activities
    • Lu L, Chen J, Li Y, Qing C, Wang Y, Nian Y, Qiu M. 2012. Studies on the constituents of Cimicifuga foetida collected in Guizhou Province and their cytotoxic activities. Chem Pharm Bull (Tokyo) 60:571–7.
    • (2012) Chem Pharm Bull (Tokyo) , vol.60 , pp. 571-577
    • Lu, L.1    Chen, J.2    Li, Y.3    Qing, C.4    Wang, Y.5    Nian, Y.6    Qiu, M.7
  • 197
    • 84862817930 scopus 로고    scopus 로고
    • Acylated flavonol glycosides from Sedum aizoon
    • Luo Q, Li W, Wu L. 2012. Acylated flavonol glycosides from Sedum aizoon. Chem Nat Compd 48:23–5.
    • (2012) Chem Nat Compd , vol.48 , pp. 23-25
    • Luo, Q.1    Li, W.2    Wu, L.3
  • 198
    • 0036179960 scopus 로고    scopus 로고
    • Lignanamides and nonalkaloidal components of Hyoscyamus niger seeds
    • Ma C-Y, Liu WK, Che C-T. 2002. Lignanamides and nonalkaloidal components of Hyoscyamus niger seeds. J Nat Prod 65:206–9.
    • (2002) J Nat Prod , vol.65 , pp. 206-209
    • Ma, C.-Y.1    Liu, W.K.2    Che, C.-T.3
  • 199
    • 2942751999 scopus 로고    scopus 로고
    • Phenolic acid amides: a new type of DNA strand scission agent from Piper caninum
    • Ma J, Jones SH, Hecht SM. 2004. Phenolic acid amides: a new type of DNA strand scission agent from Piper caninum. Bioorganic Med Chem 12:3885–9.
    • (2004) Bioorganic Med Chem , vol.12 , pp. 3885-3889
    • Ma, J.1    Jones, S.H.2    Hecht, S.M.3
  • 201
    • 84908147297 scopus 로고    scopus 로고
    • Taxiphyllin 6′-O-gallate, actinidioionoside 6’-O-gallate and myricetrin 2″-O-sulfate from the leaves of Syzygium samarangense and their biological activities
    • Mamdouh NS, Sugimoto S, Matsunami K, Otsuka H, Kamel MS. 2014. Taxiphyllin 6′-O-gallate, actinidioionoside 6’-O-gallate and myricetrin 2″-O-sulfate from the leaves of Syzygium samarangense and their biological activities. Chem Pharm Bull (Tokyo) 62:1013–8.
    • (2014) Chem Pharm Bull (Tokyo) , vol.62 , pp. 1013-1018
    • Mamdouh, N.S.1    Sugimoto, S.2    Matsunami, K.3    Otsuka, H.4    Kamel, M.S.5
  • 202
    • 84892632782 scopus 로고    scopus 로고
    • Ferulic acid: pharmacological and toxicological aspects
    • Mancuso C, Santangelo R. 2014. Ferulic acid: pharmacological and toxicological aspects. Food Chem Toxicol 65:185–95.
    • (2014) Food Chem Toxicol , vol.65 , pp. 185-195
    • Mancuso, C.1    Santangelo, R.2
  • 204
    • 44349110091 scopus 로고    scopus 로고
    • Therapeutic effect of ferulic acid, an ethereal fraction of ethanolic extract of seed of Syzygium cumini against streptozotocin-induced diabetes in male rat
    • Mandal S, Barik B, Mallick C, De D, Ghosh D. 2008. Therapeutic effect of ferulic acid, an ethereal fraction of ethanolic extract of seed of Syzygium cumini against streptozotocin-induced diabetes in male rat. Methods Find Exp Clin Pharmacol 30:121–8.
    • (2008) Methods Find Exp Clin Pharmacol , vol.30 , pp. 121-128
    • Mandal, S.1    Barik, B.2    Mallick, C.3    De, D.4    Ghosh, D.5
  • 205
    • 0030949412 scopus 로고    scopus 로고
    • An unusually lipophilic flavonol glycoside from Ranunculus sardous pollen
    • Markham KR, Mitchell KA, Campos M. 1997. An unusually lipophilic flavonol glycoside from Ranunculus sardous pollen. Phytochemistry 45:203–4.
    • (1997) Phytochemistry , vol.45 , pp. 203-204
    • Markham, K.R.1    Mitchell, K.A.2    Campos, M.3
  • 206
    • 84928390457 scopus 로고    scopus 로고
    • Protective effects of ferulic acid and related polyphenols against glyoxal- or methylglyoxal-induced cytotoxicity and oxidative stress in isolated rat hepatocytes
    • Maruf AAl, Lip H, Wong H, O'Brien PJ. 2015. Protective effects of ferulic acid and related polyphenols against glyoxal- or methylglyoxal-induced cytotoxicity and oxidative stress in isolated rat hepatocytes. Chem Biol Interact 234:96–104.
    • (2015) Chem Biol Interact , vol.234 , pp. 96-104
    • Maruf, A.1    Lip, H.2    Wong, H.3    O'Brien, P.J.4
  • 209
    • 14744278639 scopus 로고    scopus 로고
    • Antioxidant activity of the main phenolic compounds isolated from hot pepper fruit (Capsicum annuum L.)
    • Materska M, Perucka I. 2005. Antioxidant activity of the main phenolic compounds isolated from hot pepper fruit (Capsicum annuum L.). J Agric Food Chem 53:1750–6.
    • (2005) J Agric Food Chem , vol.53 , pp. 1750-1756
    • Materska, M.1    Perucka, I.2
  • 210
    • 4444320433 scopus 로고    scopus 로고
    • Ferulic acid: an antioxidant found naturally in plant cell walls and feruloyl esterases involved in its release and their applications
    • Mathew S, Abraham TE. 2004. Ferulic acid: an antioxidant found naturally in plant cell walls and feruloyl esterases involved in its release and their applications. Crit Rev Biotechnol 24:59–83.
    • (2004) Crit Rev Biotechnol , vol.24 , pp. 59-83
    • Mathew, S.1    Abraham, T.E.2
  • 211
    • 78049428270 scopus 로고    scopus 로고
    • Antioxidant and prooxidant nature of hydroxycinnamic acid derivatives ferulic and caffeic acids
    • Maurya DK, Devasagayam TPA. 2010. Antioxidant and prooxidant nature of hydroxycinnamic acid derivatives ferulic and caffeic acids. Food Chem Toxicol 48:3369–73.
    • (2010) Food Chem Toxicol , vol.48 , pp. 3369-3373
    • Maurya, D.K.1    Devasagayam, T.P.A.2
  • 213
    • 10044280297 scopus 로고    scopus 로고
    • A new glucosyl feruloyl quinic acid as a potential marker for roots and rhizomes of goldenseal, Hydrastis canadensis
    • McNamara CE, Perry NB, Follett JM, Parmenter GA, Douglas JA. 2004. A new glucosyl feruloyl quinic acid as a potential marker for roots and rhizomes of goldenseal, Hydrastis canadensis. J Nat Prod 67:1818–22.
    • (2004) J Nat Prod , vol.67 , pp. 1818-1822
    • McNamara, C.E.1    Perry, N.B.2    Follett, J.M.3    Parmenter, G.A.4    Douglas, J.A.5
  • 216
    • 0001781446 scopus 로고
    • Linkage of p-coumaroyl and feruloyl groups to cell-wall polysaccharides of barley straw
    • Mueller-Harvey I, Hartley RD, Harris PJ, Curzon EH. 1986. Linkage of p-coumaroyl and feruloyl groups to cell-wall polysaccharides of barley straw. Carbohydr Res 148:71–85.
    • (1986) Carbohydr Res , vol.148 , pp. 71-85
    • Mueller-Harvey, I.1    Hartley, R.D.2    Harris, P.J.3    Curzon, E.H.4
  • 217
    • 84923108330 scopus 로고    scopus 로고
    • Isolation of flavonoids and triterpenoids from the fruits of Alphitonia neocaledonica and evaluation of their anti-oxidant, antityrosinase and cytotoxic activities
    • Muhammad D, Hubert J, Lalun N, Renault JH, Bobichon H, Nour M, Voutquenne-Nazabadioko L. 2015. Isolation of flavonoids and triterpenoids from the fruits of Alphitonia neocaledonica and evaluation of their anti-oxidant, antityrosinase and cytotoxic activities. Phytochem Anal 26:137–44.
    • (2015) Phytochem Anal , vol.26 , pp. 137-144
    • Muhammad, D.1    Hubert, J.2    Lalun, N.3    Renault, J.H.4    Bobichon, H.5    Nour, M.6    Voutquenne-Nazabadioko, L.7
  • 218
    • 84941259487 scopus 로고    scopus 로고
    • Cholinesterase-inhibitory diterpenoids and chemical constituents from aerial parts of Caryopteris mongolica
    • Murata T, Selenge E, Oikawa S, Ageishi K, Batkhuu J, Sasaki K, Yoshizaki F. 2015. Cholinesterase-inhibitory diterpenoids and chemical constituents from aerial parts of Caryopteris mongolica. J Nat Med 69:471–8.
    • (2015) J Nat Med , vol.69 , pp. 471-478
    • Murata, T.1    Selenge, E.2    Oikawa, S.3    Ageishi, K.4    Batkhuu, J.5    Sasaki, K.6    Yoshizaki, F.7
  • 221
    • 27144528571 scopus 로고    scopus 로고
    • A new phenylethanoid glycoside from Clerodendrum inerme
    • Nan H, Wu J, Zhang S. 2005. A new phenylethanoid glycoside from Clerodendrum inerme. Pharmazie 60:798–9.
    • (2005) Pharmazie , vol.60 , pp. 798-799
    • Nan, H.1    Wu, J.2    Zhang, S.3
  • 222
    • 84938815871 scopus 로고    scopus 로고
    • Ferulic acid exerts its antidiabetic effect by modulating insulin-signalling molecules in the liver of high-fat diet and fructose-induced type-2 diabetic adult male rat
    • Narasimhan A, Chinnaiyan M, Karundevi B. 2015. Ferulic acid exerts its antidiabetic effect by modulating insulin-signalling molecules in the liver of high-fat diet and fructose-induced type-2 diabetic adult male rat. Appl Physiol Nutr Metab 40:769–81.
    • (2015) Appl Physiol Nutr Metab , vol.40 , pp. 769-781
    • Narasimhan, A.1    Chinnaiyan, M.2    Karundevi, B.3
  • 223
    • 0035627251 scopus 로고    scopus 로고
    • Alkamides and phenethyl derivatives from Aristolochia gehrtii
    • Navickiene HMD, Lopes LMX. 2001. Alkamides and phenethyl derivatives from Aristolochia gehrtii. J Braz Chem Soc 12:467–72.
    • (2001) J Braz Chem Soc , vol.12 , pp. 467-472
    • Navickiene, H.M.D.1    Lopes, L.M.X.2
  • 224
    • 0242500948 scopus 로고    scopus 로고
    • Structure–antioxidant activity relationship of ferulic acid derivatives: effect of carbon side chain characteristic groups
    • Nenadis N, Zhang H-Y, Tsimidou MZ. 2003. Structure–antioxidant activity relationship of ferulic acid derivatives: effect of carbon side chain characteristic groups. J Agric Food Chem 51:1874–9.
    • (2003) J Agric Food Chem , vol.51 , pp. 1874-1879
    • Nenadis, N.1    Zhang, H.-Y.2    Tsimidou, M.Z.3
  • 225
  • 226
    • 0032373359 scopus 로고    scopus 로고
    • Kaempferol tetraglucosides from cabbage leaves
    • Nielsen JK, Norbok R, Olsen CE. 1998. Kaempferol tetraglucosides from cabbage leaves. Phytochemistry 49:2171–6.
    • (1998) Phytochemistry , vol.49 , pp. 2171-2176
    • Nielsen, J.K.1    Norbok, R.2    Olsen, C.E.3
  • 227
    • 84958087688 scopus 로고    scopus 로고
    • Screening of ferulic acid related compounds as inhibitors of xanthine oxidase and cyclooxygenase-2 with anti-inflammatory activity
    • Nile SH, Ko EY, Kim DH, Keum Y-S. 2016. Screening of ferulic acid related compounds as inhibitors of xanthine oxidase and cyclooxygenase-2 with anti-inflammatory activity. Rev Bras Farmacogn 26:50–5.
    • (2016) Rev Bras Farmacogn , vol.26 , pp. 50-55
    • Nile, S.H.1    Ko, E.Y.2    Kim, D.H.3    Keum, Y.-S.4
  • 228
    • 0030238154 scopus 로고    scopus 로고
    • Minor hydroxycinnamic acid spermidines from pollen of Quercus dentata
    • Nimtz M, Bokern M, Meurer-Grimes B. 1996. Minor hydroxycinnamic acid spermidines from pollen of Quercus dentata. Phytochemistry 43:487–9.
    • (1996) Phytochemistry , vol.43 , pp. 487-489
    • Nimtz, M.1    Bokern, M.2    Meurer-Grimes, B.3
  • 231
    • 0037471616 scopus 로고    scopus 로고
    • Flavone C-glycoside, phenolic acid, and nitrogen contents in leaves of barley subject to organic fertilization treatments
    • Norbok R, Aaboer DBF, Bleeg IS, Christensen BT, Kondo T, Brandt K. 2003. Flavone C-glycoside, phenolic acid, and nitrogen contents in leaves of barley subject to organic fertilization treatments. J Agric Food Chem 51:809–13.
    • (2003) J Agric Food Chem , vol.51 , pp. 809-813
    • Norbok, R.1    Aaboer, D.B.F.2    Bleeg, I.S.3    Christensen, B.T.4    Kondo, T.5    Brandt, K.6
  • 232
    • 18244369991 scopus 로고    scopus 로고
    • Chemical constituents of Capsicum annuum L var. angulosum, and anti Helicobacter pylori activity
    • Ochi T, Takaishi Y, Shibata H, Higuti T, Kataoka M. 2005. Chemical constituents of Capsicum annuum L var. angulosum, and anti Helicobacter pylori activity. Nat Med 59:76–84.
    • (2005) Nat Med , vol.59 , pp. 76-84
    • Ochi, T.1    Takaishi, Y.2    Shibata, H.3    Higuti, T.4    Kataoka, M.5
  • 233
  • 234
    • 43649105758 scopus 로고    scopus 로고
    • Novel effects of a single administration of ferulic acid on the regulation of blood pressure and the hepatic lipid metabolic profile in stroke-prone spontaneously hypertensive rats
    • Ohsaki AY, Shirakawa H, Koseki T, Komai M. 2008. Novel effects of a single administration of ferulic acid on the regulation of blood pressure and the hepatic lipid metabolic profile in stroke-prone spontaneously hypertensive rats. J Agric Food Chem 56:2825–30.
    • (2008) J Agric Food Chem , vol.56 , pp. 2825-2830
    • Ohsaki, A.Y.1    Shirakawa, H.2    Koseki, T.3    Komai, M.4
  • 235
    • 84897164203 scopus 로고    scopus 로고
    • Anti-inflammatory and anticancer drugs from nature
    • In, Zappia V, Panico S, Russo GL, Budillon A, Ragione FD, editors., New York Springer, p
    • Orlikova B, Legrand N, Panning J, Dicato M, Diederich M. 2014. Anti-inflammatory and anticancer drugs from nature. In: Zappia V, Panico S, Russo GL, Budillon A, Ragione FD, editors. Advances in nutrition and cancer. New York: Springer p 123–43.
    • (2014) Advances in nutrition and cancer , pp. 123-143
    • Orlikova, B.1    Legrand, N.2    Panning, J.3    Dicato, M.4    Diederich, M.5
  • 238
    • 4043115588 scopus 로고    scopus 로고
    • Ferulic acid: pharmaceutical functions, preparation and applications in foods
    • Ou S, Kwok K-C. 2004. Ferulic acid: pharmaceutical functions, preparation and applications in foods. J Sci Food Agric 84:1261–9.
    • (2004) J Sci Food Agric , vol.84 , pp. 1261-1269
    • Ou, S.1    Kwok, K.-C.2
  • 239
    • 34248208519 scopus 로고    scopus 로고
    • Rhusemialins A—C, new cyclolignan esters from the roots of Rhus javanica var. roxburghiana
    • Ouyang MA, Wein Y-S, Su R-K, Kuo Y-H. 2007a. Rhusemialins A—C, new cyclolignan esters from the roots of Rhus javanica var. roxburghiana. Chem Pharm Bull (Tokyo) 55:804–7.
    • (2007) Chem Pharm Bull (Tokyo) , vol.55 , pp. 804-807
    • Ouyang, M.A.1    Wein, Y.-S.2    Su, R.-K.3    Kuo, Y.-H.4
  • 240
    • 34447323353 scopus 로고    scopus 로고
    • Four new lariciresinol-based lignan glycosides from the roots of Rhus javanica var. roxburghiana
    • Ouyang MA, Wein Y-SS, Kuo Y-HH. 2007b. Four new lariciresinol-based lignan glycosides from the roots of Rhus javanica var. roxburghiana. Helv Chim Acta 90:1099–106.
    • (2007) Helv Chim Acta , vol.90 , pp. 1099-1106
    • Ouyang, M.A.1    Wein, Y.-S.S.2    Kuo, Y.-H.H.3
  • 241
    • 34548009315 scopus 로고    scopus 로고
    • Inhibitory activity against tobacco mosaic virus (TMV) replication of pinoresinol and syringaresinol lignans and their glycosides from the root of Rhus javanica var. roxburghiana
    • Ouyang MA, Wein YS, Zhang ZK, Kuo YH. 2007c. Inhibitory activity against tobacco mosaic virus (TMV) replication of pinoresinol and syringaresinol lignans and their glycosides from the root of Rhus javanica var. roxburghiana. J Agric Food Chem 55:6460–5.
    • (2007) J Agric Food Chem , vol.55 , pp. 6460-6465
    • Ouyang, M.A.1    Wein, Y.S.2    Zhang, Z.K.3    Kuo, Y.H.4
  • 242
    • 85006169013 scopus 로고    scopus 로고
    • Characterization and anticancer potential of ferulic acid-loaded chitosan nanoparticles against ME-180 human cervical cancer cell lines
    • Panwar R, Sharma AK, Kaloti M, Dutt D, Pruthi V. 2015. Characterization and anticancer potential of ferulic acid-loaded chitosan nanoparticles against ME-180 human cervical cancer cell lines. Appl Nanosci 5:1–11.
    • (2015) Appl Nanosci , vol.5 , pp. 1-11
    • Panwar, R.1    Sharma, A.K.2    Kaloti, M.3    Dutt, D.4    Pruthi, V.5
  • 243
    • 80052105118 scopus 로고    scopus 로고
    • Feruloyl, caffeoyl, and flavonol glucosides from Equisetum hyemale
    • Park BJ, Tomohiko M. 2011. Feruloyl, caffeoyl, and flavonol glucosides from Equisetum hyemale. Chem Nat Compd 47:363–5.
    • (2011) Chem Nat Compd , vol.47 , pp. 363-365
    • Park, B.J.1    Tomohiko, M.2
  • 244
    • 33845768987 scopus 로고    scopus 로고
    • Integrating cell-signalling pathways with NF-κB and IKK function
    • Perkins ND. 2007. Integrating cell-signalling pathways with NF-κB and IKK function. Nat Rev Mol Cell Biol 8:49–62.
    • (2007) Nat Rev Mol Cell Biol , vol.8 , pp. 49-62
    • Perkins, N.D.1
  • 245
    • 84863722167 scopus 로고    scopus 로고
    • Caffeic acid and ferulic acid inhibit UVA-induced matrix metalloproteinase-1 through regulation of antioxidant defense system in keratinocyte HaCaT cells
    • Pluemsamran T, Onkoksoong T, Panich U. 2012. Caffeic acid and ferulic acid inhibit UVA-induced matrix metalloproteinase-1 through regulation of antioxidant defense system in keratinocyte HaCaT cells. Photochem Photobiol 88:961–8.
    • (2012) Photochem Photobiol , vol.88 , pp. 961-968
    • Pluemsamran, T.1    Onkoksoong, T.2    Panich, U.3
  • 246
    • 84875915456 scopus 로고    scopus 로고
    • Synergistic interaction of ferulic acid with commercial hypoglycemic drugs in streptozotocin induced diabetic rats
    • Prabhakar PK, Prasad R, Ali S, Doble M. 2013. Synergistic interaction of ferulic acid with commercial hypoglycemic drugs in streptozotocin induced diabetic rats. Phytomedicine 20:488–94.
    • (2013) Phytomedicine , vol.20 , pp. 488-494
    • Prabhakar, P.K.1    Prasad, R.2    Ali, S.3    Doble, M.4
  • 247
    • 34548281199 scopus 로고    scopus 로고
    • Ferulic acid inhibits UV-B-induced oxidative stress in human lymphocytes
    • Prasad NR, Ramachandran S, Pugalendi KV, Menon VP. 2007. Ferulic acid inhibits UV-B-induced oxidative stress in human lymphocytes. Nutr Res 27:559–64.
    • (2007) Nutr Res , vol.27 , pp. 559-564
    • Prasad, N.R.1    Ramachandran, S.2    Pugalendi, K.V.3    Menon, V.P.4
  • 248
    • 84874387175 scopus 로고    scopus 로고
    • Highly glycosylated flavonols with an O-linked branched pentasaccharide from Iberis saxatilis (Brassicaceae)
    • Prescott TAK, Kite GC, Porter EA, Veitch NC. 2013. Highly glycosylated flavonols with an O-linked branched pentasaccharide from Iberis saxatilis (Brassicaceae). Phytochemistry 88:85–91.
    • (2013) Phytochemistry , vol.88 , pp. 85-91
    • Prescott, T.A.K.1    Kite, G.C.2    Porter, E.A.3    Veitch, N.C.4
  • 250
    • 29244453190 scopus 로고    scopus 로고
    • Hydroxycinnamoyl conjugates from the roots of Achillea holosericea Sibth. et Sm
    • Radulović N, Stojanović G, Asakawa Y. 2006. Hydroxycinnamoyl conjugates from the roots of Achillea holosericea Sibth. et Sm. Biochem Syst Ecol 34:83–7.
    • (2006) Biochem Syst Ecol , vol.34 , pp. 83-87
    • Radulović, N.1    Stojanović, G.2    Asakawa, Y.3
  • 252
    • 33745044318 scopus 로고
    • Identification and synthesis of new ferulic acid dehydrodimers present in grass cell walls
    • Ralph J, Quideau S, Grabber JH, Hatfield RD. 1994. Identification and synthesis of new ferulic acid dehydrodimers present in grass cell walls. J Chem Soc Perkin Trans 1 1:3485–98.
    • (1994) J Chem Soc Perkin Trans 1 , vol.1 , pp. 3485-3498
    • Ralph, J.1    Quideau, S.2    Grabber, J.H.3    Hatfield, R.D.4
  • 254
    • 0005993665 scopus 로고
    • A furanocoumarin glucoside from stembark of Skimmia japonica
    • Reisch J, Achenbach SH. 1992. A furanocoumarin glucoside from stembark of Skimmia japonica. Phytochemistry 31:4376–7.
    • (1992) Phytochemistry , vol.31 , pp. 4376-4377
    • Reisch, J.1    Achenbach, S.H.2
  • 255
    • 84879625087 scopus 로고    scopus 로고
    • Comparison of the protective effects of ferulic acid and its drug-containing plasma on primary cultured neonatal rat cardiomyocytes with hypoxia/reoxygenation injury
    • Ren C, Bao Y, Meng X, Diao Y, Kang T. 2013. Comparison of the protective effects of ferulic acid and its drug-containing plasma on primary cultured neonatal rat cardiomyocytes with hypoxia/reoxygenation injury. Pharmacogn Mag 9:202–9.
    • (2013) Pharmacogn Mag , vol.9 , pp. 202-209
    • Ren, C.1    Bao, Y.2    Meng, X.3    Diao, Y.4    Kang, T.5
  • 257
    • 0038408778 scopus 로고    scopus 로고
    • Phenolic acids in foods: an overview of analytical methodology
    • Robbins RJ. 2003. Phenolic acids in foods: an overview of analytical methodology. J Agric Food Chem 51:2866–87.
    • (2003) J Agric Food Chem , vol.51 , pp. 2866-2887
    • Robbins, R.J.1
  • 258
    • 15244352099 scopus 로고    scopus 로고
    • Review of methods to determine chain-breaking antioxidant activity in food
    • Roginsky V, Lissi EA. 2005. Review of methods to determine chain-breaking antioxidant activity in food. Food Chem 92:235–54.
    • (2005) Food Chem , vol.92 , pp. 235-254
    • Roginsky, V.1    Lissi, E.A.2
  • 260
    • 84885666131 scopus 로고    scopus 로고
    • Treatment with ferulic acid to rats with streptozotocin-induced diabetes: effects on oxidative stress, pro-inflammatory cytokines, and apoptosis in the pancreatic β cell
    • Roy S, Metya SK, Sannigrahi S, Rahaman N, Ahmed F. 2013. Treatment with ferulic acid to rats with streptozotocin-induced diabetes: effects on oxidative stress, pro-inflammatory cytokines, and apoptosis in the pancreatic β cell. Endocrine 44:369–79.
    • (2013) Endocrine , vol.44 , pp. 369-379
    • Roy, S.1    Metya, S.K.2    Sannigrahi, S.3    Rahaman, N.4    Ahmed, F.5
  • 261
    • 84896466421 scopus 로고    scopus 로고
    • Isolation and absolute configuration of boehmenan from Durio affinis Becc
    • Rudiyansyah M, Mudianta IW, Garson MJ. 2014. Isolation and absolute configuration of boehmenan from Durio affinis Becc. Rec Nat Prod 8:195–8.
    • (2014) Rec Nat Prod , vol.8 , pp. 195-198
    • Rudiyansyah, M.1    Mudianta, I.W.2    Garson, M.J.3
  • 262
    • 78650219690 scopus 로고    scopus 로고
    • Antimicrobial activity of phenolics and glucosinolate hydrolysis products and their synergy with streptomycin against pathogenic bacteria
    • Saavedra MJ, Borges A, Dias C, Aires A, Bennett RN, Rosa ES, Simões M. 2010. Antimicrobial activity of phenolics and glucosinolate hydrolysis products and their synergy with streptomycin against pathogenic bacteria. Med Chem (Los Angeles) 6:174–83.
    • (2010) Med Chem (Los Angeles) , vol.6 , pp. 174-183
    • Saavedra, M.J.1    Borges, A.2    Dias, C.3    Aires, A.4    Bennett, R.N.5    Rosa, E.S.6    Simões, M.7
  • 263
    • 84886909657 scopus 로고    scopus 로고
    • Antifungal cinnamic acid derivatives from Persian leek (Allium ampeloprasum subsp. persicum)
    • Sadeghi M, Zolfaghari B, Senatore M, Lanzotti V. 2013. Antifungal cinnamic acid derivatives from Persian leek (Allium ampeloprasum subsp. persicum). Phytochem Lett 6:360–3.
    • (2013) Phytochem Lett , vol.6 , pp. 360-363
    • Sadeghi, M.1    Zolfaghari, B.2    Senatore, M.3    Lanzotti, V.4
  • 264
    • 84866003070 scopus 로고    scopus 로고
    • Effect of ferulic acid from Hibiscus mutabilis on filarial parasite Setaria cervi: molecular and biochemical approaches
    • Saini P, Gayen P, Nayak A, Kumar D, Mukherjee N, Pal BC, Babu SPS. 2012. Effect of ferulic acid from Hibiscus mutabilis on filarial parasite Setaria cervi: molecular and biochemical approaches. Parasitol Intl 61:520–31.
    • (2012) Parasitol Intl , vol.61 , pp. 520-531
    • Saini, P.1    Gayen, P.2    Nayak, A.3    Kumar, D.4    Mukherjee, N.5    Pal, B.C.6    Babu, S.P.S.7
  • 265
    • 57049154634 scopus 로고    scopus 로고
    • Tetra-acylated cyanidin 3-sophoroside-5-glucosides from the flowers of Iberis umbellata L. (Cruciferae)
    • Saito N, Tatsuzawa F, Suenaga E, Toki K, Shinoda K, Shigihara A, Honda T. 2008. Tetra-acylated cyanidin 3-sophoroside-5-glucosides from the flowers of Iberis umbellata L. (Cruciferae). Phytochemistry 69:3139–50.
    • (2008) Phytochemistry , vol.69 , pp. 3139-3150
    • Saito, N.1    Tatsuzawa, F.2    Suenaga, E.3    Toki, K.4    Shinoda, K.5    Shigihara, A.6    Honda, T.7
  • 266
    • 80053634349 scopus 로고    scopus 로고
    • The blue anthocyanin pigments from the blue flowers of Heliophila coronopifolia L. (Brassicaceae)
    • Saito N, Tatsuzawa F, Toki K, Shinoda K, Shigihara A, Honda T. 2011. The blue anthocyanin pigments from the blue flowers of Heliophila coronopifolia L. (Brassicaceae). Phytochemistry 72:2219–29.
    • (2011) Phytochemistry , vol.72 , pp. 2219-2229
    • Saito, N.1    Tatsuzawa, F.2    Toki, K.3    Shinoda, K.4    Shigihara, A.5    Honda, T.6
  • 267
    • 33746513213 scopus 로고    scopus 로고
    • Secondary metabolites from Opuntia ficus indica var. saboten
    • Saleem M, Kim HJ, Han CK, Jin C, Lee YS. 2006. Secondary metabolites from Opuntia ficus indica var. saboten. Phytochemistry 67:1390–4.
    • (2006) Phytochemistry , vol.67 , pp. 1390-1394
    • Saleem, M.1    Kim, H.J.2    Han, C.K.3    Jin, C.4    Lee, Y.S.5
  • 268
    • 0028096212 scopus 로고
    • Lipid hydroperoxides induce apoptosis in T cells displaying a HIV-associated glutathione peroxidase deficiency
    • Sandstrom PA, Tebbey PW, Cleave S Van, Buttke TM. 1994. Lipid hydroperoxides induce apoptosis in T cells displaying a HIV-associated glutathione peroxidase deficiency. J Biol Chem 269:798–801.
    • (1994) J Biol Chem , vol.269 , pp. 798-801
    • Sandstrom, P.A.1    Tebbey, P.W.2    Van Cleave, S.3    Buttke, T.M.4
  • 269
    • 0036583439 scopus 로고    scopus 로고
    • New phenylethanoid glycosides from Veronica pectinata var. glandulosa and their free radical scavenging activities
    • Saracoglu I, Harput US, Inoue M, Ogihara Y. 2002. New phenylethanoid glycosides from Veronica pectinata var. glandulosa and their free radical scavenging activities. Chem Pharm Bull (Tokyo) 50:665–8.
    • (2002) Chem Pharm Bull (Tokyo) , vol.50 , pp. 665-668
    • Saracoglu, I.1    Harput, U.S.2    Inoue, M.3    Ogihara, Y.4
  • 270
    • 4544286091 scopus 로고    scopus 로고
    • Acylated flavonoids and phenol glycosides from Veronica thymoides subsp. pseudocinerea
    • Saracoglu I, Varel M, Harput US, Nagatsu A. 2004. Acylated flavonoids and phenol glycosides from Veronica thymoides subsp. pseudocinerea. Phytochemistry 65:2379–85.
    • (2004) Phytochemistry , vol.65 , pp. 2379-2385
    • Saracoglu, I.1    Varel, M.2    Harput, U.S.3    Nagatsu, A.4
  • 272
    • 0033059228 scopus 로고    scopus 로고
    • Ferulic acid and diferulic acids as components of sugar-beet pectins and maize bran heteroxylans
    • Saulnier L, Thibault JF. 1999. Ferulic acid and diferulic acids as components of sugar-beet pectins and maize bran heteroxylans. J Sci Food Agric 79:396–402.
    • (1999) J Sci Food Agric , vol.79 , pp. 396-402
    • Saulnier, L.1    Thibault, J.F.2
  • 274
    • 3843110296 scopus 로고    scopus 로고
    • Isolation and identification of novel pyranoanthocyanins from black carrot (Daucus carota L.) juice
    • Schwarz M, Wray V, Winterhalter P. 2004. Isolation and identification of novel pyranoanthocyanins from black carrot (Daucus carota L.) juice. J Agric Food Chem 52:5095–101.
    • (2004) J Agric Food Chem , vol.52 , pp. 5095-5101
    • Schwarz, M.1    Wray, V.2    Winterhalter, P.3
  • 275
    • 84938058205 scopus 로고    scopus 로고
    • Anti-hyperglycemic activity of polyphenols isolated from barnyard millet (Echinochloa utilis L.) and their role inhibiting α-glucosidase
    • Seo KH, Ra JE, Lee SJ, Lee JH, Kim SR, Lee JH, Seo WD. 2015. Anti-hyperglycemic activity of polyphenols isolated from barnyard millet (Echinochloa utilis L.) and their role inhibiting α-glucosidase. J Korean Soc Appl Biol Chem 58:571–9.
    • (2015) J Korean Soc Appl Biol Chem , vol.58 , pp. 571-579
    • Seo, K.H.1    Ra, J.E.2    Lee, S.J.3    Lee, J.H.4    Kim, S.R.5    Lee, J.H.6    Seo, W.D.7
  • 277
    • 84861716494 scopus 로고    scopus 로고
    • Potent and selective butyrylcholinesterase inhibitors from Ficus foveolata
    • Sermboonpaisarn T, Sawasdee P. 2012. Potent and selective butyrylcholinesterase inhibitors from Ficus foveolata. Fitoterapia 83:780–4.
    • (2012) Fitoterapia , vol.83 , pp. 780-784
    • Sermboonpaisarn, T.1    Sawasdee, P.2
  • 278
    • 84937422538 scopus 로고    scopus 로고
    • Ferulic acid: a hope for Alzheimer's disease therapy from plants
    • Sgarbossa A, Giacomazza D, Di Carlo M. 2015. Ferulic acid: a hope for Alzheimer's disease therapy from plants. Nutrients 7:5764–82.
    • (2015) Nutrients , vol.7 , pp. 5764-5782
    • Sgarbossa, A.1    Giacomazza, D.2    Di Carlo, M.3
  • 279
    • 77949915823 scopus 로고    scopus 로고
    • Hydroxycinnamates and their in vitro and in vivo antioxidant activities
    • Shahidi F, Chandrasekara A. 2010. Hydroxycinnamates and their in vitro and in vivo antioxidant activities. Phytochem Rev 9:147–70.
    • (2010) Phytochem Rev , vol.9 , pp. 147-170
    • Shahidi, F.1    Chandrasekara, A.2
  • 281
    • 84867356278 scopus 로고    scopus 로고
    • Isolation and characterization of five glycerol esters from wuhan propolis and their potential anti-inflammatory properties
    • Shi H, Yang H, Zhang X, Sheng Y, Huang H, Yu L. 2012. Isolation and characterization of five glycerol esters from wuhan propolis and their potential anti-inflammatory properties. J Agric Food Chem 60:10041–7.
    • (2012) J Agric Food Chem , vol.60 , pp. 10041-10047
    • Shi, H.1    Yang, H.2    Zhang, X.3    Sheng, Y.4    Huang, H.5    Yu, L.6
  • 282
    • 33744948895 scopus 로고    scopus 로고
    • New phenolic glycosides from Clematis mandshurica
    • Shi S, Jiang D, Dong C, Tu P. 2006. New phenolic glycosides from Clematis mandshurica. Helv Chim Acta 89:1023–9.
    • (2006) Helv Chim Acta , vol.89 , pp. 1023-1029
    • Shi, S.1    Jiang, D.2    Dong, C.3    Tu, P.4
  • 283
    • 77957130409 scopus 로고    scopus 로고
    • Dietary phytophenols act as scavengers of reducing radicals
    • Shi Y, Yao S, Jia Z, Lin N, Zheng R. 2011. Dietary phytophenols act as scavengers of reducing radicals. Food Chem 124:1322–7.
    • (2011) Food Chem , vol.124 , pp. 1322-1327
    • Shi, Y.1    Yao, S.2    Jia, Z.3    Lin, N.4    Zheng, R.5
  • 284
    • 0031081078 scopus 로고    scopus 로고
    • Two phenylpropanoid glycosides from Sparganium stoloniferum
    • Shirota O, Sekita S, Satake M. 1997. Two phenylpropanoid glycosides from Sparganium stoloniferum. Phytochemistry 44:695–8.
    • (1997) Phytochemistry , vol.44 , pp. 695-698
    • Shirota, O.1    Sekita, S.2    Satake, M.3
  • 286
    • 84887430026 scopus 로고    scopus 로고
    • Chemical composition and antinociceptive, anti-inflammatory and antiviral activities of Gallesia gorazema (Phytolaccaceae), a potential candidate for novel anti-herpetic phytomedicines
    • Silva Júnior AJ, Campos-Buzzi F de, Romanos MTV, Wagner TM, Guimarães AF, de PC, Filho VC, Batista R. 2013. Chemical composition and antinociceptive, anti-inflammatory and antiviral activities of Gallesia gorazema (Phytolaccaceae), a potential candidate for novel anti-herpetic phytomedicines. J Ethnopharmacol 150:595–600.
    • (2013) J Ethnopharmacol , vol.150 , pp. 595-600
    • Silva Júnior, A.J.1    de Campos-Buzzi, F.2    Romanos, M.T.V.3    Wagner, T.M.4    Guimarães, A.F.5    de, P.C.6    Filho, V.C.7    Batista, R.8
  • 288
    • 0038814320 scopus 로고    scopus 로고
    • Why whole grains are protective: biological mechanisms
    • Slavin JL. 2003. Why whole grains are protective: biological mechanisms. Soc Proc Nutr 12:129–34.
    • (2003) Soc Proc Nutr , vol.12 , pp. 129-134
    • Slavin, J.L.1
  • 289
    • 0001917552 scopus 로고
    • Occurrence and nature of ferulic acid substitution of cell-wall polysaccharides in graminaceous plants
    • Smith MM, Hartley RD. 1983. Occurrence and nature of ferulic acid substitution of cell-wall polysaccharides in graminaceous plants. Carbohydr Res 118:65–80.
    • (1983) Carbohydr Res , vol.118 , pp. 65-80
    • Smith, M.M.1    Hartley, R.D.2
  • 290
    • 78651445048 scopus 로고    scopus 로고
    • Effect of oryzanol and ferulic acid on the glucose metabolism of mice fed with a high-fat diet
    • Son MJ, Rico CW, Nam SH, Kang MY. 2011. Effect of oryzanol and ferulic acid on the glucose metabolism of mice fed with a high-fat diet. J Food Sci 76:H7–10.
    • (2011) J Food Sci , vol.76 , pp. H7-10
    • Son, M.J.1    Rico, C.W.2    Nam, S.H.3    Kang, M.Y.4
  • 291
    • 84959132460 scopus 로고    scopus 로고
    • Cytoprotective mechanism of ferulic acid against high glucose-induced oxidative stress in cardiomyocytes and hepatocytes
    • Song Y, Wen L, Sun J, Bai W, Jiao R, Hu Y, Peng X, He Y, Ou S. 2016. Cytoprotective mechanism of ferulic acid against high glucose-induced oxidative stress in cardiomyocytes and hepatocytes. Food Nutr Res 60:1–12.
    • (2016) Food Nutr Res , vol.60 , pp. 1-12
    • Song, Y.1    Wen, L.2    Sun, J.3    Bai, W.4    Jiao, R.5    Hu, Y.6    Peng, X.7    He, Y.8    Ou, S.9
  • 292
    • 3242786334 scopus 로고    scopus 로고
    • Phenylpropanoid derivatives from edible canna, Canna edulis
    • Sook Yun Y, Satake M, Katsuki S, Kunugi A. 2004. Phenylpropanoid derivatives from edible canna, Canna edulis. Phytochemistry 65:2167–71.
    • (2004) Phytochemistry , vol.65 , pp. 2167-2171
    • Sook Yun, Y.1    Satake, M.2    Katsuki, S.3    Kunugi, A.4
  • 293
    • 34247230858 scopus 로고    scopus 로고
    • Ferulic acid: therapeutic potential through its antioxidant property
    • Srinivasan M, Sudheer AR, Menon VP. 2007a. Ferulic acid: therapeutic potential through its antioxidant property. J Clin Biochem Nutr 40:92–100.
    • (2007) J Clin Biochem Nutr , vol.40 , pp. 92-100
    • Srinivasan, M.1    Sudheer, A.R.2    Menon, V.P.3
  • 296
    • 0035191299 scopus 로고    scopus 로고
    • Alfalfa (Medicago sativa L.) flavonoids. 2. Tricin and chrysoeriol glycosides from aerial parts
    • Stochmal A, Simonet AM, Macias FA, Oleszek W. 2001a. Alfalfa (Medicago sativa L.) flavonoids. 2. Tricin and chrysoeriol glycosides from aerial parts. J Agric Food Chem 49:5310–4.
    • (2001) J Agric Food Chem , vol.49 , pp. 5310-5314
    • Stochmal, A.1    Simonet, A.M.2    Macias, F.A.3    Oleszek, W.4
  • 299
    • 85022208188 scopus 로고    scopus 로고
    • Soy protein isolate/poly (vinyl alcohol) films with IPN structure by crosslinkage of ferulic acid
    • Su J-F, Wang Y-Y, Han S, Zhang X-L. 2016. Soy protein isolate/poly (vinyl alcohol) films with IPN structure by crosslinkage of ferulic acid. J Res Updates Polym Sci 5:114-7.
    • (2016) J Res Updates Polym Sci , vol.5 , pp. 114-117
    • Su, J.-F.1    Wang, Y.-Y.2    Han, S.3    Zhang, X.-L.4
  • 300
    • 37149024116 scopus 로고    scopus 로고
    • Influence of ferulic acid on nicotine-induced lipid peroxidation, DNA damage and inflammation in experimental rats as compared to N-acetylcysteine
    • Sudheer AR, Muthukumaran S, Devipriya N, Devaraj H, Menon VP. 2008. Influence of ferulic acid on nicotine-induced lipid peroxidation, DNA damage and inflammation in experimental rats as compared to N-acetylcysteine. Toxicology 243:317–29.
    • (2008) Toxicology , vol.243 , pp. 317-329
    • Sudheer, A.R.1    Muthukumaran, S.2    Devipriya, N.3    Devaraj, H.4    Menon, V.P.5
  • 301
    • 0010064853 scopus 로고
    • Phenolic glycosides from Osmanthus asiaticus
    • Sugiyama M, Kikuchi M. 1991. Phenolic glycosides from Osmanthus asiaticus. Phytochemistry 30:3147–9.
    • (1991) Phytochemistry , vol.30 , pp. 3147-3149
    • Sugiyama, M.1    Kikuchi, M.2
  • 302
    • 13644265462 scopus 로고    scopus 로고
    • Ferulic acid ethyl ester protects neurons against amyloid β-peptide(1-42)-induced oxidative stress and neurotoxicity: relationship to antioxidant activity
    • Sultana R, Ravagna A, Mohmmad-Abdul H, Calabrese V, Butterfield DA. 2005. Ferulic acid ethyl ester protects neurons against amyloid β-peptide(1-42)-induced oxidative stress and neurotoxicity: relationship to antioxidant activity. J Neurochem 92:749–58.
    • (2005) J Neurochem , vol.92 , pp. 749-758
    • Sultana, R.1    Ravagna, A.2    Mohmmad-Abdul, H.3    Calabrese, V.4    Butterfield, D.A.5
  • 303
    • 0036117412 scopus 로고    scopus 로고
    • Short- and long-term effects of ferulic acid on blood pressure in spontaneously hypertensive rats
    • Suzuki A, Kagawa D, Fujii A, Ochiai R, Tokimitsu I, Saito I. 2002. Short- and long-term effects of ferulic acid on blood pressure in spontaneously hypertensive rats. Am J Hypertens 15:351–7.
    • (2002) Am J Hypertens , vol.15 , pp. 351-357
    • Suzuki, A.1    Kagawa, D.2    Fujii, A.3    Ochiai, R.4    Tokimitsu, I.5    Saito, I.6
  • 305
    • 85028113078 scopus 로고    scopus 로고
    • Flavonol glycosides of Pseudodrynaria coronans and their antioxidant activity
    • Tai Z, Zhang F, Cai L, Shi J, Cao Q, Ding Z. 2012. Flavonol glycosides of Pseudodrynaria coronans and their antioxidant activity. Chem Nat Compd 48:221–4.
    • (2012) Chem Nat Compd , vol.48 , pp. 221-224
    • Tai, Z.1    Zhang, F.2    Cai, L.3    Shi, J.4    Cao, Q.5    Ding, Z.6
  • 306
    • 84859914035 scopus 로고    scopus 로고
    • Potent α-glucosidase inhibitors from safflower (Carthamus tinctorius L.) seed
    • Takahashi T, Miyazawa M. 2012. Potent α-glucosidase inhibitors from safflower (Carthamus tinctorius L.) seed. Phyther Res 26:722–6.
    • (2012) Phyther Res , vol.26 , pp. 722-726
    • Takahashi, T.1    Miyazawa, M.2
  • 308
    • 79958856102 scopus 로고    scopus 로고
    • Vitamin C as an antioxidant supplement in women's health: a myth in need of urgent burial
    • Talaulikar VS, Manyonda IT. 2011. Vitamin C as an antioxidant supplement in women's health: a myth in need of urgent burial. Eur J Obstet Gynecol Reprod Biol 157:10–3.
    • (2011) Eur J Obstet Gynecol Reprod Biol , vol.157 , pp. 10-13
    • Talaulikar, V.S.1    Manyonda, I.T.2
  • 309
    • 33645755408 scopus 로고    scopus 로고
    • Antitrypanosomal and antileishmanial activities of flavonoids and their analogues: in vitro, in vivo, structure-activity relationship, and quantitative structure-activity relationship studies
    • Tasdemir D, Kaiser M, Brun R, Yardley V, Schmidt TJ, Tosun F, Rüedi P. 2006. Antitrypanosomal and antileishmanial activities of flavonoids and their analogues: in vitro, in vivo, structure-activity relationship, and quantitative structure-activity relationship studies. Antimicrob Agents Chemother 50:1352–64.
    • (2006) Antimicrob Agents Chemother , vol.50 , pp. 1352-1364
    • Tasdemir, D.1    Kaiser, M.2    Brun, R.3    Yardley, V.4    Schmidt, T.J.5    Tosun, F.6    Rüedi, P.7
  • 311
    • 84900311641 scopus 로고    scopus 로고
    • Acylated cyanidin 3-sambubioside-5-glucosides from the purple-violet flowers of Matthiola longipetala subsp. bicornis (Sm) P. W. Ball. (Brassicaceae)
    • Tatsuzawa F. 2014. Acylated cyanidin 3-sambubioside-5-glucosides from the purple-violet flowers of Matthiola longipetala subsp. bicornis (Sm) P. W. Ball. (Brassicaceae). Phytochem Lett 9:17–21.
    • (2014) Phytochem Lett , vol.9 , pp. 17-21
    • Tatsuzawa, F.1
  • 312
    • 84887029796 scopus 로고    scopus 로고
    • Acylated cyanidin glycosides from the pale-violet flowers of Ionopsidium acaule (Desf.) Rchb. (Brassicaceae)
    • Tatsuzawa F, Takahashi N, Kato K, Shinoda K, Saito N, Honda T. 2014. Acylated cyanidin glycosides from the pale-violet flowers of Ionopsidium acaule (Desf.) Rchb. (Brassicaceae). Phytochem Lett 7:69–76.
    • (2014) Phytochem Lett , vol.7 , pp. 69-76
    • Tatsuzawa, F.1    Takahashi, N.2    Kato, K.3    Shinoda, K.4    Saito, N.5    Honda, T.6
  • 313
    • 0035479734 scopus 로고    scopus 로고
    • Acylated anthocyanidin 3-sophoroside-5-glucosides from Ajuga reptans flowers and the corresponding cell cultures
    • Terahara N, Callebaut A, Ohba R, Nagata T, Ohnishi-Kameyama M, Suzuki M. 2001. Acylated anthocyanidin 3-sophoroside-5-glucosides from Ajuga reptans flowers and the corresponding cell cultures. Phytochemistry 58:493–500.
    • (2001) Phytochemistry , vol.58 , pp. 493-500
    • Terahara, N.1    Callebaut, A.2    Ohba, R.3    Nagata, T.4    Ohnishi-Kameyama, M.5    Suzuki, M.6
  • 314
    • 0036583839 scopus 로고    scopus 로고
    • Flavanone and flavonol glycosides from the leaves of Thevetia peruviana and their HIV-1 reverse transcriptase and HIV-1 integrase inhibitory activities
    • Tewtrakul S, Nakamura N, Hattori M, Fujiwara T, Supavita T. 2002. Flavanone and flavonol glycosides from the leaves of Thevetia peruviana and their HIV-1 reverse transcriptase and HIV-1 integrase inhibitory activities. Chem Pharm Bull (Tokyo) 50:630–5.
    • (2002) Chem Pharm Bull (Tokyo) , vol.50 , pp. 630-635
    • Tewtrakul, S.1    Nakamura, N.2    Hattori, M.3    Fujiwara, T.4    Supavita, T.5
  • 316
    • 78549284021 scopus 로고    scopus 로고
    • Phenolic compounds from the fresh leaves of Eucalyptus maideni
    • Tian LW, Yang CR, Zhang YJ. 2010a. Phenolic compounds from the fresh leaves of Eucalyptus maideni. Helv Chim Acta 93:2194–202.
    • (2010) Helv Chim Acta , vol.93 , pp. 2194-2202
    • Tian, L.W.1    Yang, C.R.2    Zhang, Y.J.3
  • 317
    • 77956689693 scopus 로고    scopus 로고
    • Anti-HBV active flavone glucosides from Euphorbia humifusa Willd
    • Tian Y, Sun LM, Liu XQ, Li B, Wang Q, Dong JX. 2010b. Anti-HBV active flavone glucosides from Euphorbia humifusa Willd. Fitoterapia 81:799–802.
    • (2010) Fitoterapia , vol.81 , pp. 799-802
    • Tian, Y.1    Sun, L.M.2    Liu, X.Q.3    Li, B.4    Wang, Q.5    Dong, J.X.6
  • 318
    • 0025979060 scopus 로고
    • Effects ofphenolcarboxylic acids on superoxide anion and lipid peroxidation induced by superoxide anion
    • Toda S, Kumura M, Ohnishi M. 1991. Effects ofphenolcarboxylic acids on superoxide anion and lipid peroxidation induced by superoxide anion. Planta Med 57:8–10.
    • (1991) Planta Med , vol.57 , pp. 8-10
    • Toda, S.1    Kumura, M.2    Ohnishi, M.3
  • 321
    • 34447332818 scopus 로고    scopus 로고
    • Biologically active natural products from Mongolian medicinal plants Scorzonera divaricata and Scorzonera pseudodivaricata
    • Tsevegsuren N, Edrada R, Lin W, Ebel R, Torre C, Ortlepp S, Wray V, Proksch P. 2007. Biologically active natural products from Mongolian medicinal plants Scorzonera divaricata and Scorzonera pseudodivaricata. J Nat Prod 70:962–7.
    • (2007) J Nat Prod , vol.70 , pp. 962-967
    • Tsevegsuren, N.1    Edrada, R.2    Lin, W.3    Ebel, R.4    Torre, C.5    Ortlepp, S.6    Wray, V.7    Proksch, P.8
  • 322
    • 0033628344 scopus 로고    scopus 로고
    • Effects of caffeic acid, chlorogenic acid and ferulic acid on growth and arylamine N-acetyltransferase activity in Shigella sonnei (group D)
    • Tsou MF, Hung CF, Lu HF, Wu LT, Chang SH, Chang HL, Chen GW, Chung JG. 2000. Effects of caffeic acid, chlorogenic acid and ferulic acid on growth and arylamine N-acetyltransferase activity in Shigella sonnei (group D). Microbios 101:37–46.
    • (2000) Microbios , vol.101 , pp. 37-46
    • Tsou, M.F.1    Hung, C.F.2    Lu, H.F.3    Wu, L.T.4    Chang, S.H.5    Chang, H.L.6    Chen, G.W.7    Chung, J.G.8
  • 323
    • 0142154309 scopus 로고    scopus 로고
    • Induction of rat hepatic and intestinal UDP-glucuronosyltransferases by naturally occurring dietary anticarcinogens
    • Van der Logt EMJ, Roelofs HMJ, Nagengast FM, Peters WH. 2003. Induction of rat hepatic and intestinal UDP-glucuronosyltransferases by naturally occurring dietary anticarcinogens. Carcinogenesis 24:1651–6.
    • (2003) Carcinogenesis , vol.24 , pp. 1651-1656
    • Van der Logt, E.M.J.1    Roelofs, H.M.J.2    Nagengast, F.M.3    Peters, W.H.4
  • 324
    • 0038544209 scopus 로고    scopus 로고
    • Mast cells and oral inflammation
    • Walsh LJ. 2003. Mast cells and oral inflammation. Crit Rev Oral Biol Med 14:188–98.
    • (2003) Crit Rev Oral Biol Med , vol.14 , pp. 188-198
    • Walsh, L.J.1
  • 327
    • 0033995837 scopus 로고    scopus 로고
    • Isolation and structural elucidation of two new glycosides from sage (Salvia officinalis L.)
    • Wang M, Kikuzaki H, Zhu N, Sang S, Nakatani N, Ho CT. 2000. Isolation and structural elucidation of two new glycosides from sage (Salvia officinalis L.). J Agric Food Chem 48:235–8.
    • (2000) J Agric Food Chem , vol.48 , pp. 235-238
    • Wang, M.1    Kikuzaki, H.2    Zhu, N.3    Sang, S.4    Nakatani, N.5    Ho, C.T.6
  • 328
    • 84962062632 scopus 로고    scopus 로고
    • Ferulic acid inhibits proliferation and promotes apoptosis via blockage of PI3K/Akt pathway in osteosarcoma cell
    • Wang T, Gong X, Jiang R, Li H, Du W, Kuang G. 2016. Ferulic acid inhibits proliferation and promotes apoptosis via blockage of PI3K/Akt pathway in osteosarcoma cell. Am J Transl Res 8:968–80.
    • (2016) Am J Transl Res , vol.8 , pp. 968-980
    • Wang, T.1    Gong, X.2    Jiang, R.3    Li, H.4    Du, W.5    Kuang, G.6
  • 329
    • 84883151782 scopus 로고    scopus 로고
    • Tumoral cytotoxic and antioxidative phenylpropanoid glycosides in Smilax riparia A
    • Wang WX, Li TX, Ma H, Zhang JF, Jia AQ. 2013. Tumoral cytotoxic and antioxidative phenylpropanoid glycosides in Smilax riparia A. DC. J Ethnopharmacol 149:527–32.
    • (2013) DC. J Ethnopharmacol , vol.149 , pp. 527-532
    • Wang, W.X.1    Li, T.X.2    Ma, H.3    Zhang, J.F.4    Jia, A.Q.5
  • 330
    • 0034255582 scopus 로고    scopus 로고
    • A new isoflavanone from the stem bark of Erythrina latissima
    • Wanjala CCW, Majinda RRT. 2000. A new isoflavanone from the stem bark of Erythrina latissima. Fitoterapia 71:400–5.
    • (2000) Fitoterapia , vol.71 , pp. 400-405
    • Wanjala, C.C.W.1    Majinda, R.R.T.2
  • 331
    • 84935022761 scopus 로고    scopus 로고
    • Characterization of diferuloylated pectic polysaccharides from quinoa (Chenopodium quinoa WILLD.)
    • Wefers D, Gmeiner BM, Tyl CE, Bunzel M. 2015. Characterization of diferuloylated pectic polysaccharides from quinoa (Chenopodium quinoa WILLD.). Phytochemistry 116:320–8.
    • (2015) Phytochemistry , vol.116 , pp. 320-328
    • Wefers, D.1    Gmeiner, B.M.2    Tyl, C.E.3    Bunzel, M.4
  • 333
    • 0030049032 scopus 로고    scopus 로고
    • Damage to DNA by reactive oxygen and nitrogen species: role in inflammatory disease and progression to cancer
    • Wiseman H, Halliwell B. 1996. Damage to DNA by reactive oxygen and nitrogen species: role in inflammatory disease and progression to cancer. Biochem J 313:17–29.
    • (1996) Biochem J , vol.313 , pp. 17-29
    • Wiseman, H.1    Halliwell, B.2
  • 334
    • 84870247049 scopus 로고    scopus 로고
    • Flavonoid glycosides from the leaves of Allium victorialis var. platyphyllum and their anti-neuroinflammatory effects
    • Woo KW, Moon E, Park SY, Kim SY, Lee KR. 2012. Flavonoid glycosides from the leaves of Allium victorialis var. platyphyllum and their anti-neuroinflammatory effects. Bioorganic Med Chem Lett 22:7465–70.
    • (2012) Bioorganic Med Chem Lett , vol.22 , pp. 7465-7470
    • Woo, K.W.1    Moon, E.2    Park, S.Y.3    Kim, S.Y.4    Lee, K.R.5
  • 335
    • 0026084890 scopus 로고
    • Iridoids from Hedyotis diffusa
    • Wu H, Tao X, Chen Q, Lao X. 1991. Iridoids from Hedyotis diffusa. J Nat Prod 54:254–6.
    • (1991) J Nat Prod , vol.54 , pp. 254-256
    • Wu, H.1    Tao, X.2    Chen, Q.3    Lao, X.4
  • 337
    • 1842636253 scopus 로고    scopus 로고
    • Cytotoxicity of phenylpropanoid esters from the stems of Hibiscus taiwanensis
    • Wu PL, Chuang TH, He CX, Wu TS. 2004. Cytotoxicity of phenylpropanoid esters from the stems of Hibiscus taiwanensis. Bioorganic Med Chem 12:2193–7.
    • (2004) Bioorganic Med Chem , vol.12 , pp. 2193-2197
    • Wu, P.L.1    Chuang, T.H.2    He, C.X.3    Wu, T.S.4
  • 338
    • 33745629851 scopus 로고    scopus 로고
    • Two new benzofurans and other constituents from Ligularia przewalskii
    • Xie WD, Gao X, Shen T, Jia ZJ. 2006. Two new benzofurans and other constituents from Ligularia przewalskii. Pharmazie 61:556–8.
    • (2006) Pharmazie , vol.61 , pp. 556-558
    • Xie, W.D.1    Gao, X.2    Shen, T.3    Jia, Z.J.4
  • 339
    • 67649373036 scopus 로고    scopus 로고
    • New chemical constituents from the rhizomes of Sparganium stoloniferum
    • Xiong Y, Deng K-Z, Guo Y-Q, Gao W-Y, Zhang T-J. 2009. New chemical constituents from the rhizomes of Sparganium stoloniferum. Arch Pharm Res 32:717–20.
    • (2009) Arch Pharm Res , vol.32 , pp. 717-720
    • Xiong, Y.1    Deng, K.-Z.2    Guo, Y.-Q.3    Gao, W.-Y.4    Zhang, T.-J.5
  • 340
    • 46749127109 scopus 로고    scopus 로고
    • Two new flavonol glycosides from Sarcopyramis bodinieri var. delicate
    • Xiu MW, Chun PW, Shou RZ, Qiu Y. 2008. Two new flavonol glycosides from Sarcopyramis bodinieri var. delicate. Molecules 13:1399–405.
    • (2008) Molecules , vol.13 , pp. 1399-1405
    • Xiu, M.W.1    Chun, P.W.2    Shou, R.Z.3    Qiu, Y.4
  • 342
  • 343
    • 0018391572 scopus 로고
    • Action of ferulic acid and its derivatives as antioxidants
    • Yagi K, Ohishi N. 1979. Action of ferulic acid and its derivatives as antioxidants. J Nutr Sci Vitaminol (Tokyo) 25:127–30.
    • (1979) J Nutr Sci Vitaminol (Tokyo) , vol.25 , pp. 127-130
    • Yagi, K.1    Ohishi, N.2
  • 345
    • 84872720134 scopus 로고    scopus 로고
    • Protective effects of ferulic acid in amyloid precursor protein plus presenilin-1 transgenic mouse model of Alzheimer disease
    • Yan J-J, Jung J-S, Kim T-K, Hasan A, Hong C-W, Nam J-S, Song D-K. 2013. Protective effects of ferulic acid in amyloid precursor protein plus presenilin-1 transgenic mouse model of Alzheimer disease. Biol Pharm Bull 36:140–3.
    • (2013) Biol Pharm Bull , vol.36 , pp. 140-143
    • Yan, J.-J.1    Jung, J.-S.2    Kim, T.-K.3    Hasan, A.4    Hong, C.-W.5    Nam, J.-S.6    Song, D.-K.7
  • 347
    • 44149127948 scopus 로고    scopus 로고
    • A new phenylpropanoid glycosides from Paris polyphylla var. yunnanensis
    • Yan L, Gao WY, Zhang Y, Wang Y. 2008. A new phenylpropanoid glycosides from Paris polyphylla var. yunnanensis. Fitoterapia 79:306–7.
    • (2008) Fitoterapia , vol.79 , pp. 306-307
    • Yan, L.1    Gao, W.Y.2    Zhang, Y.3    Wang, Y.4
  • 348
    • 84944061935 scopus 로고    scopus 로고
    • Ferulic acid exerts anti-angiogenic and anti-tumor activity by targeting fibroblast growth factor receptor 1-mediated angiogenesis
    • Yang G-W, Jiang J-S, Lu W-Q. 2015. Ferulic acid exerts anti-angiogenic and anti-tumor activity by targeting fibroblast growth factor receptor 1-mediated angiogenesis. Intl J Mol Sci 16:24011–31.
    • (2015) Intl J Mol Sci , vol.16 , pp. 24011-24031
    • Yang, G.-W.1    Jiang, J.-S.2    Lu, W.-Q.3
  • 349
    • 84862915073 scopus 로고    scopus 로고
    • A new feruloyl tyramine glycoside from the roots of Achyranthes bidentata
    • Yang L, Jiang H, Wang QH, Yang BY, Kuang HX. 2012. A new feruloyl tyramine glycoside from the roots of Achyranthes bidentata. Chin J Nat Med 10:16–9.
    • (2012) Chin J Nat Med , vol.10 , pp. 16-19
    • Yang, L.1    Jiang, H.2    Wang, Q.H.3    Yang, B.Y.4    Kuang, H.X.5
  • 350
    • 84873701506 scopus 로고    scopus 로고
    • Radical scavenging activity and cytotoxicity of active quinic acid derivatives from Scorzonera divaricata roots
    • Yang Y-J, Liu X, Wu H-R, He X-F, Bi Y-R, Zhu Y, Liu Z-L. 2013. Radical scavenging activity and cytotoxicity of active quinic acid derivatives from Scorzonera divaricata roots. Food Chem 138:2057–63.
    • (2013) Food Chem , vol.138 , pp. 2057-2063
    • Yang, Y.-J.1    Liu, X.2    Wu, H.-R.3    He, X.-F.4    Bi, Y.-R.5    Zhu, Y.6    Liu, Z.-L.7
  • 351
    • 81855221938 scopus 로고    scopus 로고
    • Glycosides from the methanol extract of Notopterygium incisum
    • You M, Xiong J, Zhao Y, Cao L, Wu SB, Xia G, Hu JF. 2011. Glycosides from the methanol extract of Notopterygium incisum. Planta Med 77:1939–43.
    • (2011) Planta Med , vol.77 , pp. 1939-1943
    • You, M.1    Xiong, J.2    Zhao, Y.3    Cao, L.4    Wu, S.B.5    Xia, G.6    Hu, J.F.7
  • 353
    • 0027367663 scopus 로고
    • Premnafolioside, a new phenylethanoid, and other phenolic compounds from stems of Premna corymbosa var. obtusifolia
    • Yuasa K, Ide T, Otsuka H. 1993. Premnafolioside, a new phenylethanoid, and other phenolic compounds from stems of Premna corymbosa var. obtusifolia. J Nat Prod 56:1695–9.
    • (1993) J Nat Prod , vol.56 , pp. 1695-1699
    • Yuasa, K.1    Ide, T.2    Otsuka, H.3
  • 354
    • 84946840851 scopus 로고    scopus 로고
    • A new tricyclic alkaloid from Portulaca oleracea L
    • Yue S, Jiao Z, Sun H, Jin T, Xiang L. 2015. A new tricyclic alkaloid from Portulaca oleracea L. Helv Chim Acta 98:961–6.
    • (2015) Helv Chim Acta , vol.98 , pp. 961-966
    • Yue, S.1    Jiao, Z.2    Sun, H.3    Jin, T.4    Xiang, L.5
  • 357
    • 0026562148 scopus 로고
    • Additional bioactive compounds and trilobacin, a novel highly cytotoxic acetogenin, from the bark of Asimina triloba
    • Zhao G, Hui Y, Rupprecht JK, McLaughlin JL, Wood KV. 1992. Additional bioactive compounds and trilobacin, a novel highly cytotoxic acetogenin, from the bark of Asimina triloba. J Nat Prod 55:347–56.
    • (1992) J Nat Prod , vol.55 , pp. 347-356
    • Zhao, G.1    Hui, Y.2    Rupprecht, J.K.3    McLaughlin, J.L.4    Wood, K.V.5
  • 358
    • 41549123951 scopus 로고    scopus 로고
    • Chemistry, natural sources, dietary intake and pharmacokinetic properties of ferulic acid: a review
    • Zhao Z, Moghadasian MH. 2008. Chemistry, natural sources, dietary intake and pharmacokinetic properties of ferulic acid: a review. Food Chem 109:691–702.
    • (2008) Food Chem , vol.109 , pp. 691-702
    • Zhao, Z.1    Moghadasian, M.H.2
  • 359
    • 44949277340 scopus 로고
    • Phenylpropanoid and iridoid glycosides from Pedicularis lasiophrys
    • Zhongjian J, Zimin L, Changzeng W. 1992. Phenylpropanoid and iridoid glycosides from Pedicularis lasiophrys. Phytochemistry 31:263–6.
    • (1992) Phytochemistry , vol.31 , pp. 263-266
    • Zhongjian, J.1    Zimin, L.2    Changzeng, W.3
  • 360
    • 0026280765 scopus 로고    scopus 로고
    • Phenylpropanoid and iridoid glycosides from Pedicularis spicata
    • Zhongjian J, Zimin L, Changzeng W. 1997. Phenylpropanoid and iridoid glycosides from Pedicularis spicata. Phytochemistry 30:3745–7.
    • (1997) Phytochemistry , vol.30 , pp. 3745-3747
    • Zhongjian, J.1    Zimin, L.2    Changzeng, W.3
  • 361
    • 0031731292 scopus 로고    scopus 로고
    • Phenylethanoid glycosides from Digitalis purpurea and Penstemon linarioides with PKCα-inhibitory activity
    • Zhou B-N, Bahler BD, Hofmann GA, Mattern MR, Johnson RK, Kingston DGI. 1998. Phenylethanoid glycosides from Digitalis purpurea and Penstemon linarioides with PKCα-inhibitory activity. J Nat Prod 61:1410–2.
    • (1998) J Nat Prod , vol.61 , pp. 1410-1412
    • Zhou, B.-N.1    Bahler, B.D.2    Hofmann, G.A.3    Mattern, M.R.4    Johnson, R.K.5    Kingston, D.G.I.6
  • 362
    • 70349499193 scopus 로고    scopus 로고
    • Triterpenoids and flavonoids from celery (Apium graveolens)
    • Zhou K, Zhao F, Liu Z, Zhuang Y, Chen L, Qiu F. 2009. Triterpenoids and flavonoids from celery (Apium graveolens). J Nat Prod 72:1563–7.
    • (2009) J Nat Prod , vol.72 , pp. 1563-1567
    • Zhou, K.1    Zhao, F.2    Liu, Z.3    Zhuang, Y.4    Chen, L.5    Qiu, F.6
  • 364
    • 0028212674 scopus 로고
    • Vanicosides A and B, protein kinase C inhibitors from Polygonum pensylvanicum
    • Zimmermann ML, Sneden AT. 1994. Vanicosides A and B, protein kinase C inhibitors from Polygonum pensylvanicum. J Nat Prod 57:236–42.
    • (1994) J Nat Prod , vol.57 , pp. 236-242
    • Zimmermann, M.L.1    Sneden, A.T.2


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