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Volumn , Issue , 2005, Pages 17-32

Sources and chemistry of resveratrol

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EID: 85040146771     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1201/9781420026474     Document Type: Chapter
Times cited : (6)

References (99)
  • 2
    • 0034901818 scopus 로고    scopus 로고
    • Grape extract, resveratrol and its analogs: A review
    • Sovak M, Grape extract, resveratrol and its analogs: a review, J Med Food 4, 93-105, 2001.
    • (2001) J Med Food , vol.4 , pp. 93-105
    • Sovak, M.1
  • 3
    • 0242695672 scopus 로고    scopus 로고
    • Resveratrol: From grapevines to mammalian biology
    • Pervaiz S, Resveratrol: from grapevines to mammalian biology, FASEB J 17, 1975-1985, 2003.
    • (2003) FASEB J , vol.17 , pp. 1975-1985
    • Pervaiz, S.1
  • 4
    • 0028119154 scopus 로고
    • Isolation of resveratrol from Festuca versuta and evidence for the widespread occurrence of this stilbene in the Poaceae
    • Powell RG, TePaske MR, Plattner RD, White JF, and Clement SL, Isolation of resveratrol from Festuca versuta and evidence for the widespread occurrence of this stilbene in the Poaceae, Phytochemistry, 35, 335-338, 1994.
    • (1994) Phytochemistry , vol.35 , pp. 335-338
    • Powell, R.G.1    TePaske, M.R.2    Plattner, R.D.3    White, J.F.4    Clement, S.L.5
  • 9
    • 0000793534 scopus 로고
    • Wood phenolics of Morus species. IV. Phenolics of the heartwood of five Morus species
    • Deshpande VH, Srinivasan R, and Rao AV, Wood phenolics of Morus species. IV. Phenolics of the heartwood of five Morus species, Indian J Chem 13, 453-457, 1975.
    • (1975) Indian J Chem , vol.13 , pp. 453-457
    • Deshpande, V.H.1    Srinivasan, R.2    Rao, A.V.3
  • 10
    • 6944241179 scopus 로고    scopus 로고
    • Liquid chromatography/tandem mass spectrometry of unusual phenols from Yucca schidigera bark: Comparison with other analytical techniques
    • Montoro P, Piacente S, Oleszek W, and Pizza C, Liquid chromatography/tandem mass spectrometry of unusual phenols from Yucca schidigera bark:comparison with other analytical techniques, J Mass Spectrosc 39, 1131-1138, 2004.
    • (2004) J Mass Spectrosc , vol.39 , pp. 1131-1138
    • Montoro, P.1    Piacente, S.2    Oleszek, W.3    Pizza, C.4
  • 11
    • 0038721897 scopus 로고    scopus 로고
    • Inhibition of oxidative stress in blood platelets by different phenolics from Yucca schidigera Roezl. bark
    • Olas B, Wachowicz B, Stochmal A, and Oleszek W, Inhibition of oxidative stress in blood platelets by different phenolics from Yucca schidigera Roezl. bark, Nutrition 19, 633-640, 2003.
    • (2003) Nutrition , vol.19 , pp. 633-640
    • Olas, B.1    Wachowicz, B.2    Stochmal, A.3    Oleszek, W.4
  • 13
    • 3042780522 scopus 로고    scopus 로고
    • Study on chemical constituents in rhizome of Smilax perfoliate
    • Cheng Y, Zhang D, Yu S, and Ding Y, Study on chemical constituents in rhizome of Smilax perfoliate, Zhongguo Zhongyao Zazhi 28, 233-235, 2003.
    • (2003) Zhongguo Zhongyao Zazhi , vol.28 , pp. 233-235
    • Cheng, Y.1    Zhang, D.2    Yu, S.3    Ding, Y.4
  • 14
    • 0001579617 scopus 로고
    • Dihydrostilbene phytoalexins from Dioscorea bulbifera and D. dumentorum
    • Adesanya SA, Ogundana SK, and Roberts MF, Dihydrostilbene phytoalexins from Dioscorea bulbifera and D. dumentorum, Phytochemistry 28, 773-774, 1989.
    • (1989) Phytochemistry , vol.28 , pp. 773-774
    • Adesanya, S.A.1    Ogundana, S.K.2    Roberts, M.F.3
  • 15
    • 0021276662 scopus 로고
    • Use of potato disc and brine shrimp bioassays to detect activity and isolate piceatannol as the 27 antileukemic principle from the seeds of Euphorbia lagascae
    • Ferrigni NR, Mclaughlin JL, Powell RG, and Smith CR, Use of potato disc and brine shrimp bioassays to detect activity and isolate piceatannol as the 27 antileukemic principle from the seeds of Euphorbia lagascae, J Nat Prod 47, 347-349, 1984.
    • (1984) J Nat Prod , vol.47 , pp. 347-349
    • Ferrigni, N.R.1    McLaughlin, J.L.2    Powell, R.G.3    Smith, C.R.4
  • 16
    • 0026344210 scopus 로고
    • Biologically active constituents of Melaleuca leucadendron: Inhibitors of induced histamine release from rat mast cells
    • Tsuruga T, Chun YT, Ebizuka Y, and Sankawa U, Biologically active constituents of Melaleuca leucadendron: inhibitors of induced histamine release from rat mast cells, Chem Pharm Bull 39, 3276-3278, 1991.
    • (1991) Chem Pharm Bull , vol.39 , pp. 3276-3278
    • Tsuruga, T.1    Chun, Y.T.2    Ebizuka, Y.3    Sankawa, U.4
  • 17
    • 0021330526 scopus 로고
    • Physiological activities of 3,30,4,50-tetrahydroxystilbene isolated from the heartwood of Cassia garrettiana Craib
    • Inamori Y, Kato Y, Kubo M, Yasuda M, Baba K, and Kozawa M, Physiological activities of 3,30,4,50-tetrahydroxystilbene isolated from the heartwood of Cassia garrettiana Craib., Chem Pharm Bull 32, 213-218, 1984.
    • (1984) Chem Pharm Bull , vol.32 , pp. 213-218
    • Inamori, Y.1    Kato, Y.2    Kubo, M.3    Yasuda, M.4    Baba, K.5    Kozawa, M.6
  • 18
    • 0033174985 scopus 로고    scopus 로고
    • Anti-platelet aggregation activity of stilbene derivatives from Rheum undulatum
    • Ko S, Lee SM, and Whang WK, Anti-platelet aggregation activity of stilbene derivatives from Rheum undulatum, Arch Pharm Res 22, 401-403, 1999.
    • (1999) Arch Pharm Res , vol.22 , pp. 401-403
    • Ko, S.1    Lee, S.M.2    Whang, W.K.3
  • 20
    • 6944254533 scopus 로고
    • Isolation of 3,4,3,5-tetrahydroxystilbene (piceatannol) from Cassia marginata heartwoood
    • Rao VSS and Rajaduri S, Isolation of 3,4,3,5-tetrahydroxystilbene (piceatannol) from Cassia marginata heartwoood, Aust J Chem 21, 1921-1922, 1968.
    • (1968) Aust J Chem , vol.21 , pp. 1921-1922
    • Rao, V.S.S.1    Rajaduri, S.2
  • 24
    • 0036911164 scopus 로고    scopus 로고
    • Artoindonesianins N and O, new prenylated stilbene and prenylated arylbenzofuran derivatives from Atocarpus gomezianus
    • Hakim EH, Ulinnuha UZ, Syah YM, and Ghisalberti EL, Artoindonesianins N and O, new prenylated stilbene and prenylated arylbenzofuran derivatives from Atocarpus gomezianus, Fitoterapia 73, 597-603, 2002.
    • (2002) Fitoterapia , vol.73 , pp. 597-603
    • Hakim, E.H.1    Ulinnuha, U.Z.2    Syah, Y.M.3    Ghisalberti, E.L.4
  • 26
    • 0035116497 scopus 로고    scopus 로고
    • Resveratrol analog, 3,4',5,40- tetrahydroxystilbene, differentially induces pro-apoptotic p53/Bax gene expression and inhibits the growth of transformed cells but not their normal counterparts
    • Lu J, Ho CT, Ghai G, and Chen KY, Resveratrol analog, 3,4',5,40- tetrahydroxystilbene, differentially induces pro-apoptotic p53/Bax gene expression and inhibits the growth of transformed cells but not their normal counterparts, Carcinogenesis 22, 321-328, 2001.
    • (2001) Carcinogenesis , vol.22 , pp. 321-328
    • Lu, J.1    Ho, C.T.2    Ghai, G.3    Chen, K.Y.4
  • 27
    • 0003069453 scopus 로고
    • Hydroxystilbene compounds as taxonomic tracers in the genus eucalyptus
    • Hathway DE and Brit L, Hydroxystilbene compounds as taxonomic tracers in the genus eucalyptus, Biochem J 83, 80-84, 1962.
    • (1962) Biochem J , vol.83 , pp. 80-84
    • Hathway, D.E.1    Brit, L.2
  • 28
    • 0344789432 scopus 로고
    • Chemistry of extractives from hardwoods. XXVII. The occurrence of 3,30,4,50-tetrahydroxy and 3,30,4,5,50-pentahydroxystilbene in Vouacapoua species
    • King FE, King TJ, Godson DH, and Manning LC, Chemistry of extractives from hardwoods. XXVII. The occurrence of 3,30,4,50-tetrahydroxy and 3,30,4,5,50-pentahydroxystilbene in Vouacapoua species, J Chem Soc 4477-4480, 1956.
    • (1956) J Chem Soc , pp. 4477-4480
    • King, F.E.1    King, T.J.2    Godson, D.H.3    Manning, L.C.4
  • 29
    • 6944252723 scopus 로고    scopus 로고
    • Stilbenes from Gnetum cleistostachyum
    • Yao CS, Lin M, Liu X, and Wang YH, Stilbenes from Gnetum cleistostachyum, Huaxue Xuebao 61, 1331-1334, 2003.
    • (2003) Huaxue Xuebao , vol.61 , pp. 1331-1334
    • Yao, C.S.1    Lin, M.2    Liu, X.3    Wang, Y.H.4
  • 31
    • 0007651818 scopus 로고    scopus 로고
    • Isolation and characterization of antibacterial constituent from devdaru (lignum of Polyalthia longifolia L.)
    • Ali MA and Debnath DC, Isolation and characterization of antibacterial constituent from devdaru (lignum of Polyalthia longifolia L.), Bang J Sci Ind Res 32, 20-24, 1997.
    • (1997) Bang J Sci Ind Res , vol.32 , pp. 20-24
    • Ali, M.A.1    Debnath, D.C.2
  • 32
    • 0031946505 scopus 로고    scopus 로고
    • Stilbenes, monoterpenes, diarylheptanoids, labdanes and chalcones from Alpinia katsumadai
    • Ngo KS and Brown GD, Stilbenes, monoterpenes, diarylheptanoids, labdanes and chalcones from Alpinia katsumadai, Phytochemistry 47, 1117-1123, 1998.
    • (1998) Phytochemistry , vol.47 , pp. 1117-1123
    • Ngo, K.S.1    Brown, G.D.2
  • 34
    • 5244340570 scopus 로고
    • Biosynthesis of pinosylvin in the sapwood of Pinus resinosa
    • Rudloff E and Jorgensen E, Biosynthesis of pinosylvin in the sapwood of Pinus resinosa, Phytochemistry 2, 297-304, 1963.
    • (1963) Phytochemistry , vol.2 , pp. 297-304
    • Rudloff, E.1    Jorgensen, E.2
  • 36
    • 0036314697 scopus 로고    scopus 로고
    • Efficiency and structure-activity relationship of the antioxidant action of resveratrol and its analogs
    • Lu M, Cai YJ, Fang JG, Zhou YL, Liu ZL, and Wu LM, Efficiency and structure-activity relationship of the antioxidant action of resveratrol and its analogs, Pharmazie 57, 474-478, 2002.
    • (2002) Pharmazie , vol.57 , pp. 474-478
    • Lu, M.1    Cai, Y.J.2    Fang, J.G.3    Zhou, Y.L.4    Liu, Z.L.5    Wu, L.M.6
  • 37
    • 0037454754 scopus 로고    scopus 로고
    • Inhibition of free radicalinduced peroxidation of rat liver microsomes by resveratrol and its analogues
    • Cai YJ, Fang JG, Ma LP, Yang L, and Liu ZL, Inhibition of free radicalinduced peroxidation of rat liver microsomes by resveratrol and its analogues, Biochim Biophys Acta 1637, 31-38, 2003.
    • (2003) Biochim Biophys Acta , vol.1637 , pp. 31-38
    • Cai, Y.J.1    Fang, J.G.2    Ma, L.P.3    Yang, L.4    Liu, Z.L.5
  • 38
    • 0037180317 scopus 로고    scopus 로고
    • The 40-hydroxy group is responsible for the in vitro cytogenetic activity of resveratrol
    • Matsuoka A, Takeshita K, Furuta A, Ozaki M, Fukuhara K, and Miyata N, The 40-hydroxy group is responsible for the in vitro cytogenetic activity of resveratrol, Mutation Res 521, 29-35, 2002.
    • (2002) Mutation Res , vol.521 , pp. 29-35
    • Matsuoka, A.1    Takeshita, K.2    Furuta, A.3    Ozaki, M.4    Fukuhara, K.5    Miyata, N.6
  • 39
    • 0027496717 scopus 로고
    • Synthesis and protein-tyrosine kinase inhibitory activity of polyhydroxylated stilbene analogues of piceatannol
    • Thakkar K, Geahlen RL, and Cushman M, Synthesis and protein-tyrosine kinase inhibitory activity of polyhydroxylated stilbene analogues of piceatannol, J Med Chem 36, 2950-2955, 1993.
    • (1993) J Med Chem , vol.36 , pp. 2950-2955
    • Thakkar, K.1    Geahlen, R.L.2    Cushman, M.3
  • 40
    • 0037120157 scopus 로고    scopus 로고
    • Antioxidant effects of resveratrol and its analogues against the free-radicalinduced peroxidation of linoleic acid in micelles
    • Fang JG, Lu M, Chen ZH, Zhu HH, Li Y, Yang L, Wu LM, and Liu ZL, Antioxidant effects of resveratrol and its analogues against the free-radicalinduced peroxidation of linoleic acid in micelles, Chem Eur J 8, 4191-4198, 2002.
    • (2002) Chem Eur J , vol.8 , pp. 4191-4198
    • Fang, J.G.1    Lu, M.2    Chen, Z.H.3    Zhu, H.H.4    Li, Y.5    Yang, L.6    Wu, L.M.7    Liu, Z.L.8
  • 41
    • 0036401748 scopus 로고    scopus 로고
    • Effects of resveratrol and its analogs on scavenging hydroxyl radicals: Evaluation of EPR spin trapping method
    • Lu M, Fang JG, Liu ZL, and Wu LM, Effects of resveratrol and its analogs on scavenging hydroxyl radicals: evaluation of EPR spin trapping method, Appl Magn Res 22, 475-481, 2002.
    • (2002) Appl Magn Res , vol.22 , pp. 475-481
    • Lu, M.1    Fang, J.G.2    Liu, Z.L.3    Wu, L.M.4
  • 42
    • 0035945001 scopus 로고    scopus 로고
    • Fluorinated resveratrol and pterostilbene
    • Eddarir S, Zouanante A, and Rolando C, Fluorinated resveratrol and pterostilbene, Tetrahedron Lett 42, 9127-9130, 2001.
    • (2001) Tetrahedron Lett , vol.42 , pp. 9127-9130
    • Eddarir, S.1    Zouanante, A.2    Rolando, C.3
  • 43
    • 0346099270 scopus 로고    scopus 로고
    • Synthesis and radical scavenging activities of resveratrol derivatives
    • Lee HJ, Seo JW, Lee BH, Chung KH, and Chi DY, Synthesis and radical scavenging activities of resveratrol derivatives, Bioorg Med Chem Lett 14, 463-466, 2004.
    • (2004) Bioorg Med Chem Lett , vol.14 , pp. 463-466
    • Lee, H.J.1    Seo, J.W.2    Lee, B.H.3    Chung, K.H.4    Chi, D.Y.5
  • 44
    • 0035086905 scopus 로고    scopus 로고
    • Study on anti-oketsu activity of rhubarb: II. Anti-allergic effects of stilbene components from Rhei undulati Rhizoma (dried rhizome of Rheum undulatum cultivated in Korea)
    • Matsuda H, Tomohiro N, Hiraba K, Harima S, Ko S, Matsuo K, Yoshikawa M, and Kubo M, Study on anti-oketsu activity of rhubarb: II. Anti-allergic effects of stilbene components from Rhei undulati Rhizoma (dried rhizome of Rheum undulatum cultivated in Korea). Bio Pharm Bull 24, 264-267, 2001.
    • (2001) Bio Pharm Bull , vol.24 , pp. 264-267
    • Matsuda, H.1    Tomohiro, N.2    Hiraba, K.3    Harima, S.4    Ko, S.5    Matsuo, K.6    Yoshikawa, M.7    Kubo, M.8
  • 45
    • 0032992221 scopus 로고    scopus 로고
    • Homoisoflavanones and stilbenoids from Scilla nervosa
    • Bangani V, Crouch NR, and Mulholland DA, Homoisoflavanones and stilbenoids from Scilla nervosa, Phytochemistry 51, 947-951, 1999.
    • (1999) Phytochemistry , vol.51 , pp. 947-951
    • Bangani, V.1    Crouch, N.R.2    Mulholland, D.A.3
  • 46
    • 0034796857 scopus 로고    scopus 로고
    • Antioxidative activity of natural isorhapontigenin
    • Wang QL, Lin M, and Liu CT, Antioxidative activity of natural isorhapontigenin, Jpn J Pharm 81, 61-66, 2001.
    • (2001) Jpn J Pharm , vol.81 , pp. 61-66
    • Wang, Q.L.1    Lin, M.2    Liu, C.T.3
  • 47
    • 0032252246 scopus 로고    scopus 로고
    • Synthesis of the natural products resveratrol and isorhapotogenin (isorhapontigenin)
    • Feng Y, Bing W, Lin Z, and Zhi ZZ, Synthesis of the natural products resveratrol and isorhapotogenin (isorhapontigenin), Chin Chem Lett 9, 1003-1004, 1998.
    • (1998) Chin Chem Lett , vol.9 , pp. 1003-1004
    • Feng, Y.1    Bing, W.2    Lin, Z.3    Zhi, Z.Z.4
  • 48
    • 0035064593 scopus 로고    scopus 로고
    • Mechanism based inhibition of human cytochrome P450 1A1 by rhapontigenin
    • Chun YJ, Ryu Sy, Jeong TC, and Mie YK, Mechanism based inhibition of human cytochrome P450 1A1 by rhapontigenin, Drug Metab Disposition 29, 389-393, 2001.
    • (2001) Drug Metab Disposition , vol.29 , pp. 389-393
    • Chun, Y.J.1    Sy, R.2    Jeong, T.C.3    Mie, Y.K.4
  • 50
    • 0141566405 scopus 로고    scopus 로고
    • Resveratrol and two monomethylated stilbenes from Israeli Rumex bucephalophorus and their antioxidant potential
    • Kerem Z, Regev-Shoshani G, Flaishman MA, and Sivan L, Resveratrol and two monomethylated stilbenes from Israeli Rumex bucephalophorus and their antioxidant potential, J Nat Prod 66, 1270-1272, 2003.
    • (2003) J Nat Prod , vol.66 , pp. 1270-1272
    • Kerem, Z.1    Regev-Shoshani, G.2    Flaishman, M.A.3    Sivan, L.4
  • 52
    • 0037013315 scopus 로고    scopus 로고
    • Oxyresveratrol and hydroxystilbene compounds: Inhibitory effect on tyrosinase and mechanism of action
    • Kim YM, Yun J, Lee CK, Lee H, Min KR, and Kim Y, Oxyresveratrol and hydroxystilbene compounds: inhibitory effect on tyrosinase and mechanism of action, J Bio Chem 277, 16340-16344, 2002.
    • (2002) J Bio Chem , vol.277 , pp. 16340-16344
    • Kim, Y.M.1    Yun, J.2    Lee, C.K.3    Lee, H.4    Min, K.R.5    Kim, Y.6
  • 53
    • 6944249531 scopus 로고    scopus 로고
    • Determination of pterostilbene in Dragon’s Blood by RP-HPLC
    • Hu Y, Ning Z, and Liu D, Determination of pterostilbene in Dragon’s Blood by RP-HPLC, Yaowu Fenxi Zazhi 22, 428-430, 2002.
    • (2002) Yaowu Fenxi Zazhi , vol.22 , pp. 428-430
    • Hu, Y.1    Ning, Z.2    Liu, D.3
  • 54
    • 0037023981 scopus 로고    scopus 로고
    • Cancer chemopreventive and antioxidant activities of pterostilbene, a naturally occurring analogue of resveratrol
    • Rimando AM, Cuendet M, Desmarchelier C, Mehta RG, Pezzuto JM, and Duke SO, Cancer chemopreventive and antioxidant activities of pterostilbene, a naturally occurring analogue of resveratrol, J Agric Food Chem 50, 3453-3457, 2002.
    • (2002) J Agric Food Chem , vol.50 , pp. 3453-3457
    • Rimando, A.M.1    Cuendet, M.2    Desmarchelier, C.3    Mehta, R.G.4    Pezzuto, J.M.5    Duke, S.O.6
  • 55
    • 0021130576 scopus 로고
    • Chemical constituents of Crotalaria madurensis
    • Bhakuni DS and Chaturvedi R, Chemical constituents of Crotalaria madurensis, J Nat Prod 47, 585-591, 1984.
    • (1984) J Nat Prod , vol.47 , pp. 585-591
    • Bhakuni, D.S.1    Chaturvedi, R.2
  • 57
    • 0038721897 scopus 로고    scopus 로고
    • Inhibition of oxidative stress in blood platelets by different phenolics from Yucca schidigera Roezl. bark
    • Olas B, Wachowicz B, Stochmal A, and Oleszek W, Inhibition of oxidative stress in blood platelets by different phenolics from Yucca schidigera Roezl. bark, Pol Nutr 19, 633-640, 2003.
    • (2003) Pol Nutr , vol.19 , pp. 633-640
    • Olas, B.1    Wachowicz, B.2    Stochmal, A.3    Oleszek, W.4
  • 58
    • 0025937774 scopus 로고
    • An anthraquinone and three naphthopyrone derivatives from Cassia pudibunda
    • Messana I, Ferrari F, Cavalcanti MS, and Morace G, An anthraquinone and three naphthopyrone derivatives from Cassia pudibunda, Phytochemistry 30, 708-710, 1991.
    • (1991) Phytochemistry , vol.30 , pp. 708-710
    • Messana, I.1    Ferrari, F.2    Cavalcanti, M.S.3    Morace, G.4
  • 59
    • 0033653285 scopus 로고    scopus 로고
    • A new type of stilbene-related secondary metabolite, idenburgene, from Cryptocarya idenburgensis
    • Juliawaty LD, Kitajima M, Takayama H, Achmad SA, and Aimi N, A new type of stilbene-related secondary metabolite, idenburgene, from Cryptocarya idenburgensis, Chem Pharm Bull 48, 1726-1728, 2000.
    • (2000) Chem Pharm Bull , vol.48 , pp. 1726-1728
    • Juliawaty, L.D.1    Kitajima, M.2    Takayama, H.3    Achmad, S.A.4    Aimi, N.5
  • 60
    • 0036749125 scopus 로고    scopus 로고
    • Flavonoids and stilbenoids with COX-1 and COX-2 inhibitory activity from Dracaena loureiri
    • Likhitwitayawuid K, Sawasdee K, and Kirtikara K, Flavonoids and stilbenoids with COX-1 and COX-2 inhibitory activity from Dracaena loureiri, Planta Med 68, 841-843, 2002.
    • (2002) Planta Med , vol.68 , pp. 841-843
    • Likhitwitayawuid, K.1    Sawasdee, K.2    Kirtikara, K.3
  • 61
    • 3042589166 scopus 로고    scopus 로고
    • Studies on stilbene derivatives from Dracaena cochinchinensis and their antifungal activities
    • Hu Y, Tu P, Li R, Wan Z, and Wang D, Studies on stilbene derivatives from Dracaena cochinchinensis and their antifungal activities, Zhongcaoyao 32, 104-106, 2001.
    • (2001) Zhongcaoyao , vol.32 , pp. 104-106
    • Hu, Y.1    Tu, P.2    Li, R.3    Wan, Z.4    Wang, D.5
  • 62
    • 0000300676 scopus 로고
    • Stilbene glucosides in the bark of Picea sitchensis
    • Aritomi M and Donnelly DMA, Stilbene glucosides in the bark of Picea sitchensis, Phytochemistry 15, 2006-2008, 1976.
    • (1976) Phytochemistry , vol.15 , pp. 2006-2008
    • Aritomi, M.1    Donnelly, D.M.A.2
  • 63
    • 0346117536 scopus 로고    scopus 로고
    • Phenolic composition of the cotyledon and the seed coat of lentils (Lens culinaris L.)
    • Duenas M, Hernandez T, and Estrella I, Phenolic composition of the cotyledon and the seed coat of lentils (Lens culinaris L.), Eur Food Res Technol 51, 478-483, 2002.
    • (2002) Eur Food Res Technol , vol.51 , pp. 478-483
    • Duenas, M.1    Hernandez, T.2    Estrella, I.3
  • 64
    • 6944228316 scopus 로고    scopus 로고
    • Leukotriene D4 antagonistic activity of a stilbene derivative isolated from the bark of Pinus koraiensis
    • Song HK, Jung J, Park KH, and Lim Y, Leukotriene D4 antagonistic activity of a stilbene derivative isolated from the bark of Pinus koraiensis, Agric Chem Biotech 44, 199-201, 2001.
    • (2001) Agric Chem Biotech , vol.44 , pp. 199-201
    • Song, H.K.1    Jung, J.2    Park, K.H.3    Lim, Y.4
  • 65
    • 0031798517 scopus 로고    scopus 로고
    • Isolation, identification, and antioxidant activity of three stilbene glucosides newly extracted from Vitis vinifera cell cultures
    • Teguo PW, Fauconneau B, Deffieux G, Huguet F, Vercauteren J, and Merillon JM, Isolation, identification, and antioxidant activity of three stilbene glucosides newly extracted from Vitis vinifera cell cultures, J Nat Prod 61, 655-657, 1998.
    • (1998) J Nat Prod , vol.61 , pp. 655-657
    • Teguo, P.W.1    Fauconneau, B.2    Deffieux, G.3    Huguet, F.4    Vercauteren, J.5    Merillon, J.M.6
  • 67
    • 0034932102 scopus 로고    scopus 로고
    • Inhibitors from rhubarb on lipopolysaccharide-induced nitric oxide production in macrophages: Structural requirements of stilbenes for the activity
    • Kageura T, Matsuda H, Morikawa T, Toguchida I, Harima S, Oda M, and Yoshikawa M, Inhibitors from rhubarb on lipopolysaccharide-induced nitric oxide production in macrophages: structural requirements of stilbenes for the activity, Bio Med Chem 9, 1887-1893, 2001.
    • (2001) Bio Med Chem , vol.9 , pp. 1887-1893
    • Kageura, T.1    Matsuda, H.2    Morikawa, T.3    Toguchida, I.4    Harima, S.5    Oda, M.6    Yoshikawa, M.7
  • 68
    • 85008088509 scopus 로고
    • Studies on rhubarb (Rhei rhizoma): XIV. Isolation and characterization of stilbene glucosides from Chinese rhubarb
    • Kashiwada Y, Nonaka G, Nishioka I, Nishizawa M, and Yamagishi T, Studies on rhubarb (Rhei rhizoma): XIV. Isolation and characterization of stilbene glucosides from Chinese rhubarb. Chem Pharm Bull 36, 1545-1549, 1988.
    • (1988) Chem Pharm Bull , vol.36 , pp. 1545-1549
    • Kashiwada, Y.1    Nonaka, G.2    Nishioka, I.3    Nishizawa, M.4    Yamagishi, T.5
  • 70
    • 0030979224 scopus 로고    scopus 로고
    • Synthesis of biologically active polyphenolic glycosides (combretastatin and resveratrol series)
    • Orsini F, Pelizzoni F, Bellini B, and Miglierini G, Synthesis of biologically active polyphenolic glycosides (combretastatin and resveratrol series), Carbohydr Res 301, 95-109, 1997.
    • (1997) Carbohydr Res , vol.301 , pp. 95-109
    • Orsini, F.1    Pelizzoni, F.2    Bellini, B.3    Miglierini, G.4
  • 71
    • 0034865995 scopus 로고    scopus 로고
    • A new stilbene glycoside from Elephantorrhiza goetzei
    • Wanjala CC and Majinda RR, A new stilbene glycoside from Elephantorrhiza goetzei, Fitoterapia 72, 649-655, 2001.
    • (2001) Fitoterapia , vol.72 , pp. 649-655
    • Wanjala, C.C.1    Majinda, R.R.2
  • 72
    • 0030758823 scopus 로고    scopus 로고
    • Sequential glucosylation determined by NMR in the biosynthesis of mulberroside D, a cis-oxyresveratrol diglucoside, in Morus alba cell cultures
    • Hano Y, Goi K, Nomura T, and Ueda S, Sequential glucosylation determined by NMR in the biosynthesis of mulberroside D, a cis-oxyresveratrol diglucoside, in Morus alba cell cultures, Life Sci 53, 237-241, 1997.
    • (1997) Life Sci , vol.53 , pp. 237-241
    • Hano, Y.1    Goi, K.2    Nomura, T.3    Ueda, S.4
  • 73
    • 0022479321 scopus 로고
    • Constituents of the cultivated mulberry tree. Two phenolic glycosides from the root bark of the cultivated mulberry tree (Morus lhou)
    • Hirakura K, Fujimoto Y, Fukai T, and Nomura T, Constituents of the cultivated mulberry tree. Two phenolic glycosides from the root bark of the cultivated mulberry tree (Morus lhou), J Nat Prod 49, 218-224, 1986.
    • (1986) J Nat Prod , vol.49 , pp. 218-224
    • Hirakura, K.1    Fujimoto, Y.2    Fukai, T.3    Nomura, T.4
  • 76
    • 0015311422 scopus 로고
    • Gaylussacin, a new stilbene derivative from species of Gaylussacia
    • Askari A, Worthen LR, and Shimizu Y, Gaylussacin, a new stilbene derivative from species of Gaylussacia, Lloydia 35, 49-54, 1972.
    • (1972) Lloydia , vol.35 , pp. 49-54
    • Askari, A.1    Worthen, L.R.2    Shimizu, Y.3
  • 77
    • 28444465078 scopus 로고    scopus 로고
    • Resveratrol oligomers: Structure, chemistry, and biological activity
    • Cichewicz RH and Kouzi SA, Resveratrol oligomers: structure, chemistry, and biological activity, Stud Nat Prod Chem 26, 507-579, 2002.
    • (2002) Stud Nat Prod Chem , vol.26 , pp. 507-579
    • Cichewicz, R.H.1    Kouzi, S.A.2
  • 79
    • 0001032917 scopus 로고
    • Distribution of resveratrol oligomers in plants
    • Sotheeswaran S and Pasupathy V, Distribution of resveratrol oligomers in plants, Phytochemistry 32, 1083-1092, 1993.
    • (1993) Phytochemistry , vol.32 , pp. 1083-1092
    • Sotheeswaran, S.1    Pasupathy, V.2
  • 80
    • 17944384437 scopus 로고    scopus 로고
    • Spasmolytic effects, mode of action, and structure-activity relationships of stilbenoids from Nidema boothii
    • Hernandez-Romero Y, Rojas JI, Castillo R, Rojas A, and Mata R, Spasmolytic effects, mode of action, and structure-activity relationships of stilbenoids from Nidema boothii, J Nat Prod 67, 160-167, 2004.
    • (2004) J Nat Prod , vol.67 , pp. 160-167
    • Hernandez-Romero, Y.1    Rojas, J.I.2    Castillo, R.3    Rojas, A.4    Mata, R.5
  • 83
    • 0032716519 scopus 로고    scopus 로고
    • Occurrence of resveratrol and pterostilbene in age-old Darakchasava, an Ayurvedic medicine from India
    • Paul B, Masih I, Deopujari J, and Charpentier C, Occurrence of resveratrol and pterostilbene in age-old Darakchasava, an Ayurvedic medicine from India, J. Ethnopharmocol 68, 71-76, 1999.
    • (1999) J. Ethnopharmocol , vol.68 , pp. 71-76
    • Paul, B.1    Masih, I.2    Deopujari, J.3    Charpentier, C.4
  • 84
    • 0001269795 scopus 로고    scopus 로고
    • Resveratrol: Isomeric molar absorptivities and stability
    • Trela B and Waterhouse A, Resveratrol: isomeric molar absorptivities and stability, J Agric Food Chem 44, 1253-1257, 1996.
    • (1996) J Agric Food Chem , vol.44 , pp. 1253-1257
    • Trela, B.1    Waterhouse, A.2
  • 85
    • 0038772355 scopus 로고    scopus 로고
    • On the chemistry of resveratrol diasteromers
    • Deak M and Falk H, On the chemistry of resveratrol diasteromers, Monat fur Chem 134, 883-888, 2003.
    • (2003) Monat fur Chem , vol.134 , pp. 883-888
    • Deak, M.1    Falk, H.2
  • 86
    • 0034645693 scopus 로고    scopus 로고
    • Biological effects of resveratrol
    • Fremont L, Biological effects of resveratrol, Life Sci 66, 663-673, 2000.
    • (2000) Life Sci , vol.66 , pp. 663-673
    • Fremont, L.1
  • 87
    • 0038056144 scopus 로고    scopus 로고
    • Density functional theory calculations for resveratrol
    • Cao H, Pan X, Li Cong, Zhou C, Deng F, and Li T, Density functional theory calculations for resveratrol, Bio Med Chem Lett 13, 1869-1871, 2003.
    • (2003) Bio Med Chem Lett , vol.13 , pp. 1869-1871
    • Cao, H.1    Pan, X.2    Cong, L.3    Zhou, C.4    Deng, F.5    Li, T.6
  • 88
    • 0030963473 scopus 로고    scopus 로고
    • Resveratrol: A molecule whose time has come? And gone?
    • Soleas GJ, Diamandis EP, and Goldberg DM, Resveratrol: a molecule whose time has come? And gone?, Clin Biochem 30, 91-113, 1997.
    • (1997) Clin Biochem , vol.30 , pp. 91-113
    • Soleas, G.J.1    Diamandis, E.P.2    Goldberg, D.M.3
  • 89
    • 46849095716 scopus 로고
    • The production of resveratrol by Vitis vinifera and other members of the Vitaceae as a response to infection or injury
    • Langcake P and Pryce RJ, The production of resveratrol by Vitis vinifera and other members of the Vitaceae as a response to infection or injury, Physiol Plant Pathol 9, 77-86, 1976.
    • (1976) Physiol Plant Pathol , vol.9 , pp. 77-86
    • Langcake, P.1    Pryce, R.J.2
  • 90
    • 9344241819 scopus 로고    scopus 로고
    • Structural basis for antioxidant activity of trans-resveratrol: Ab initio calculations and crystal and molecular structure
    • Caruso F, Tanski J, Villegas-Estrada A, and Rossi M, Structural basis for antioxidant activity of trans-resveratrol: ab initio calculations and crystal and molecular structure, J Agric Food Chem 52, 7304-7310, 2004.
    • (2004) J Agric Food Chem , vol.52 , pp. 7304-7310
    • Caruso, F.1    Tanski, J.2    Villegas-Estrada, A.3    Rossi, M.4
  • 91
    • 4243553342 scopus 로고
    • Phenolic substances of white hellebore (Veratrum grandiflorum Loes. fil.). II. Synthesis of resveratrol and its derivatives
    • Takaoka M, Phenolic substances of white hellebore (Veratrum grandiflorum Loes. fil.). II. Synthesis of resveratrol and its derivatives, Proc Imperial Acad (Tokyo) 16, 405-407, 1940.
    • (1940) Proc Imperial Acad (Tokyo) , vol.16 , pp. 405-407
    • Takaoka, M.1
  • 92
    • 79960378092 scopus 로고
    • Natural stilbenes. III. Synthesis of resveratrol
    • Späth E and Kromp K, Natural stilbenes. III. Synthesis of resveratrol, Ber Dtsch Chem Ges 74B, 867-869, 1941.
    • (1941) Ber Dtsch Chem Ges , vol.74B , pp. 867-869
    • Späth, E.1    Kromp, K.2
  • 93
    • 0031053263 scopus 로고    scopus 로고
    • Simple synthesis of 5-substituted resorcinols: A revisited family of interesting bioactive molecules
    • Alonso E, Ramon DJ, and Yus M, Simple synthesis of 5-substituted resorcinols: a revisited family of interesting bioactive molecules, J Org Chem 62, 417-421, 1997.
    • (1997) J Org Chem , vol.62 , pp. 417-421
    • Alonso, E.1    Ramon, D.J.2    Yus, M.3
  • 94
    • 0037213684 scopus 로고    scopus 로고
    • One-pot palladium-catalyzed highly chemo-, regio-, and stereoselective synthesis of trans-stilbene derivatives. A concise and convenient synthesis of resveratrol
    • Jeffery T and Ferber B, One-pot palladium-catalyzed highly chemo-, regio-, and stereoselective synthesis of trans-stilbene derivatives. A concise and convenient synthesis of resveratrol, Tetrahedron Lett 44, 193-197, 2003.
    • (2003) Tetrahedron Lett , vol.44 , pp. 193-197
    • Jeffery, T.1    Ferber, B.2
  • 96
    • 1842503717 scopus 로고    scopus 로고
    • Regioselective oxidative coupling of 4-hydroxystilbenes: Synthesis of resveratrol and epsilon-viniferin (E)-dehydrodimers
    • Sako M, Hosokawa H, Ito T, and Iinuma M, Regioselective oxidative coupling of 4-hydroxystilbenes: synthesis of resveratrol and epsilon-viniferin (E)-dehydrodimers, J Org Chem 69, 2598-2600, 2004.
    • (2004) J Org Chem , vol.69 , pp. 2598-2600
    • Sako, M.1    Hosokawa, H.2    Ito, T.3    Iinuma, M.4
  • 97
    • 0141904171 scopus 로고    scopus 로고
    • Investigation of the excited states of resveratrol and related molecules
    • Del Nero J and De Melo CP, Investigation of the excited states of resveratrol and related molecules, Int J Quantum Chem 95, 213-218, 2003.
    • (2003) Int J Quantum Chem , vol.95 , pp. 213-218
    • Del Nero, J.1    De Melo, C.P.2
  • 98
    • 0043269199 scopus 로고    scopus 로고
    • Resveratrol and its analogues resveratrol- dihydroxyl isomers: Semi-empirical SCF-MO calculations
    • Erkoc S, Keskin N, and Erkoc F, Resveratrol and its analogues resveratrol- dihydroxyl isomers: semi-empirical SCF-MO calculations, Theor Chem 631, 67-73, 2003.
    • (2003) Theor Chem , vol.631 , pp. 67-73
    • Erkoc, S.1    Keskin, N.2    Erkoc, F.3


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