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Volumn 28, Issue 6, 2013, Pages 1113-1128

Enzymatic biotransformation of terpenes as bioactive agents

Author keywords

Bioactive cyclic terpenoid compounds; Biological significance; Biotransformation

Indexed keywords

15 ALPHA ACETYL DEHYDROSULPHURENIC ACID; 24 METHYLENECYCLOARTANOL; AMBREIN; BETULIC ACID; CARYOPHYLLENE OXIDE; CELASTROL; CUCURBITACIN; CUCURBITACIN B; CUCURBITACIN E; CUCURBITACIN GLYCOSIDE; CUCURBITACIN I; CUCURBITACIN Q; CYCLOARTENOL; DITERPENE; GINSENOSIDE; GLYCYRRHETINIC ACID; LANOSTEROL; LEUCOSCEPTRINE; LIMONOID; MELIANIN B; MELIANIN C; MELIAVOLKININ; MENTHOL; OLEANOLIC ACID; SCLAREOL; SCLAREOLIDE; SESQUITERPENE; TERPENE DERIVATIVE; TRITERPENOID; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 84887456922     PISSN: 14756366     EISSN: 14756374     Source Type: Journal    
DOI: 10.3109/14756366.2012.727411     Document Type: Article
Times cited : (43)

References (141)
  • 1
    • 56449128037 scopus 로고    scopus 로고
    • Oleanolic acid and related derivatives as medicinally important compounds
    • Nighat S, Ather A. Oleanolic acid and related derivatives as medicinally important compounds. J Enzym Inhib Med Chem 2008;23:739-756
    • (2008) J Enzym Inhib Med Chem , vol.23 , pp. 739-756
    • Nighat, S.1    Ather, A.2
  • 2
    • 80052842450 scopus 로고    scopus 로고
    • Clinically useful anticancer, antitumor and antiwrinkle agent, ursolic acid and related derivatives as medicinally important natural product
    • Nighat S. Clinically useful anticancer, antitumor and antiwrinkle agent, ursolic acid and related derivatives as medicinally important natural product. J Enzym Inhib Med Chem 2011;26:616-642
    • (2011) J Enzym Inhib Med Chem , vol.26 , pp. 616-642
    • Nighat, S.1
  • 4
    • 0642368436 scopus 로고    scopus 로고
    • Plant-derived triterpenoids as potential antineoplastic agents
    • Setzer WN, Setzer MC. Plant-derived triterpenoids as potential antineoplastic agents. Mini-Rev Med Chem 2003;3:540-556
    • (2003) Mini-Rev Med Chem , vol.3 , pp. 540-556
    • Setzer, W.N.1    Setzer, M.C.2
  • 6
    • 34247526984 scopus 로고    scopus 로고
    • Triterpenoids and rexinoids as multifunctional agents for the prevention and treatment of cancer
    • Liby KT, Yore MM, Sporn MB. Triterpenoids and rexinoids as multifunctional agents for the prevention and treatment of cancer. Nat Rev Cancer 2007;7:357-369
    • (2007) Nat Rev Cancer , vol.7 , pp. 357-369
    • Liby, K.T.1    Yore, M.M.2    Sporn, M.B.3
  • 7
    • 74049157757 scopus 로고    scopus 로고
    • Pentacyclic triterpenes of the lupane, oleanane and ursane group as tools in cancer therapy
    • Laszczyk MN. Pentacyclic triterpenes of the lupane, oleanane and ursane group as tools in cancer therapy. Planta Med 2009;75:1549-1560
    • (2009) Planta Med , vol.75 , pp. 1549-1560
    • Laszczyk, M.N.1
  • 9
    • 80052674065 scopus 로고    scopus 로고
    • Ursolic acid inhibits, proliferation and induces apoptosis of cancer cells in vitro and in vivo
    • Wang X, Zhang F, Yang L, Mei Y, Long H, Zhang X, et al. Ursolic acid inhibits, proliferation and induces apoptosis of cancer cells in vitro and in vivo. J Biomed Biotechnol 2011
    • (2011) J Biomed Biotechnol
    • Wang, X.1    Zhang, F.2    Yang, L.3    Mei, Y.4    Long, H.5    Zhang, X.6
  • 10
    • 21244470815 scopus 로고    scopus 로고
    • Cucurbitacins and cucurbitane glycosides: Structures and biological activities
    • Chen JC, Chiu MH, Nie RL, Cordell GA, Qiu SX. Cucurbitacins and cucurbitane glycosides: Structures and biological activities. Nat Prod Rep 2005;22:386-399
    • (2005) Nat Prod Rep , vol.22 , pp. 386-399
    • Chen, J.C.1    Chiu, M.H.2    Nie, R.L.3    Cordell, G.A.4    Qiu, S.X.5
  • 11
    • 0037444373 scopus 로고    scopus 로고
    • Discovery of JSI-124 (cucurbitacin I), a selective Janus kinase/ signal transducer and activator of transcription 3 signaling pathway inhibitor with potent antitumor activity against human and murine cancer cells in mice
    • Blaskovich MA, Sun J, Cantor A, Turkson J, Jove R, Sebti SM. Discovery of JSI-124 (cucurbitacin I), a selective Janus kinase/ signal transducer and activator of transcription 3 signaling pathway inhibitor with potent antitumor activity against human and murine cancer cells in mice. Cancer Res 2003;63:1270-1279
    • (2003) Cancer Res , vol.63 , pp. 1270-1279
    • Blaskovich, M.A.1    Sun, J.2    Cantor, A.3    Turkson, J.4    Jove, R.5    Sebti, S.M.6
  • 12
    • 18844370367 scopus 로고    scopus 로고
    • Cucurbitacin Q a selective STAT3 activation inhibitor with potent antitumor activity
    • Sun J, Blaskovich MA, Jove R, Livingston SK, Coppola D, Sebti SM. Cucurbitacin Q: A selective STAT3 activation inhibitor with potent antitumor activity. Oncogene 2005;24:3236-3245
    • (2005) Oncogene , vol.24 , pp. 3236-3245
    • Sun, J.1    Blaskovich, M.A.2    Jove, R.3    Livingston, S.K.4    Coppola, D.5    Sebti, S.M.6
  • 14
    • 0037427563 scopus 로고    scopus 로고
    • Anticancer and antiinflammatory activities of cucurbitacins from Cucurbita andreana
    • Jayaprakasam B, Seeram NP, Nair MG. Anticancer and antiinflammatory activities of cucurbitacins from Cucurbita andreana. Cancer Lett 2003;189:11-16
    • (2003) Cancer Lett , vol.189 , pp. 11-16
    • Jayaprakasam, B.1    Seeram, N.P.2    Nair, M.G.3
  • 16
    • 34548672367 scopus 로고    scopus 로고
    • 23,24-Dihydrocucurbitacin B induces G2/M cell-cycle arrest and mitochondria-dependent apoptosis in human breast cancer cells (Bcap37
    • Yang L, Wu S, Zhang Q, Liu F, Wu P. 23,24-Dihydrocucurbitacin B induces G2/M cell-cycle arrest and mitochondria-dependent apoptosis in human breast cancer cells (Bcap37). Cancer Lett 2007;256:267-278
    • (2007) Cancer Lett , vol.256 , pp. 267-278
    • Yang, L.1    Wu, S.2    Zhang, Q.3    Liu, F.4    Wu, P.5
  • 17
    • 50149105711 scopus 로고    scopus 로고
    • Cucurbitacin B has a potent antiproliferative effect on breast cancer cells in vitro and in vivo
    • Wakimoto N, Yin D, O'Kelly J, Haritunians T, Karlan B, Said J et al. Cucurbitacin B has a potent antiproliferative effect on breast cancer cells in vitro and in vivo. Cancer Sci 2008;99:1793-1797
    • (2008) Cancer Sci , vol.99 , pp. 1793-1797
    • Wakimoto, N.1    Yin, D.2    O'Kelly, J.3    Haritunians, T.4    Karlan, B.5    Said, J.6
  • 19
  • 20
  • 22
    • 70349269114 scopus 로고    scopus 로고
    • Cytotoxic triterpenes from Antrodia camphorate and their mode of action in HT-29 human colon cancer cells
    • Yeh CT, Rao YK, Yao CJ, Yeh CF, Li CH, Chuang SE, et al. Cytotoxic triterpenes from Antrodia camphorate and their mode of action in HT-29 human colon cancer cells. Cancer Lett 2009;285:73-79
    • (2009) Cancer Lett , vol.285 , pp. 73-79
    • Yeh, C.T.1    Rao, Y.K.2    Yao, C.J.3    Yeh, C.F.4    Li, C.H.5    Chuang, S.E.6
  • 23
    • 0035102601 scopus 로고    scopus 로고
    • Isolation and frontier molecular orbital investigation of bioactive quinone-methide triterpenoids from the bark of Salacia petenensis
    • Setzer WN, Holland MT, Bozeman CA, Rozmus GF, Setzer MC, Moriarity DM et al. Isolation and frontier molecular orbital investigation of bioactive quinone-methide triterpenoids from the bark of Salacia petenensis. Planta Med 2001;67:65-69
    • (2001) Planta Med , vol.67 , pp. 65-69
    • Setzer, W.N.1    Holland, M.T.2    Bozeman, C.A.3    Rozmus, G.F.4    Setzer, M.C.5    Moriarity, D.M.6
  • 24
    • 10744220567 scopus 로고    scopus 로고
    • Antitumor agents. 228. Five new agarofurans, Reissantins A-E, and cytotoxic principles from Reissantia buchananii
    • Chang FR, Hayashi K, Chen IH, Liaw CC, Bastow KF, Nakanishi Y et al. Antitumor agents. 228. five new agarofurans, Reissantins A-E, and cytotoxic principles from Reissantia buchananii. J Nat Prod 2003;66:1416-1420
    • (2003) J Nat Prod , vol.66 , pp. 1416-1420
    • Chang, F.R.1    Hayashi, K.2    Chen, I.H.3    Liaw, C.C.4    Bastow, K.F.5    Nakanishi, Y.6
  • 25
    • 23844549870 scopus 로고    scopus 로고
    • Pristimerin induces caspase-dependent apoptosis in MDA-MB-231 cells via direct effects on mitochondria
    • Wu CC, Chan ML, Chen WY, Tsai CY, Chang FR, Wu YC. Pristimerin induces caspase-dependent apoptosis in MDA-MB-231 cells via direct effects on mitochondria. Mol Cancer Ther 2005;4:1277-1285
    • (2005) Mol Cancer Ther , vol.4 , pp. 1277-1285
    • Wu, C.C.1    Chan, M.L.2    Chen, W.Y.3    Tsai, C.Y.4    Chang, F.R.5    Wu, Y.C.6
  • 26
    • 68849116745 scopus 로고    scopus 로고
    • Pharmacologic inhibitors of IkappaB kinase suppress growth and migration of mammary carcinosarcoma cells in vitro and prevent osteolytic bone metastasis in vivo
    • Idris AI, Libouban H, Nyangoga H, Landao-Bassonga E, Chappard D, Ralston SH. Pharmacologic inhibitors of IkappaB kinase suppress growth and migration of mammary carcinosarcoma cells in vitro and prevent osteolytic bone metastasis in vivo. Mol Cancer Ther 2009;8:2339-2347
    • (2009) Mol Cancer Ther , vol.8 , pp. 2339-2347
    • Idris, A.I.1    Libouban, H.2    Nyangoga, H.3    Landao-Bassonga, E.4    Chappard, D.5    Ralston, S.H.6
  • 27
    • 77951215549 scopus 로고    scopus 로고
    • Celastrol, a triterpene, enhances TRAIL-induced apoptosis through the downregulation of cell survival proteins and upregulation of death receptors
    • Sung B, Park B, Yadav VR, Aggarwal BB. Celastrol, a triterpene, enhances TRAIL-induced apoptosis through the downregulation of cell survival proteins and upregulation of death receptors. J Biol Chem 2010;285:11498-11507
    • (2010) J Biol Chem , vol.285 , pp. 11498-11507
    • Sung, B.1    Park, B.2    Yadav, V.R.3    Aggarwal, B.B.4
  • 28
    • 0029044176 scopus 로고
    • Meliavolkenin, a new bioactive triterpenoid from Melia volkensii (Meliaceae
    • Zeng L, Gu ZM, Chang CJ, Wood KV, McLaughlin JL. Meliavolkenin, a new bioactive triterpenoid from Melia volkensii (Meliaceae). Bioorg Med Chem 1995;3:383-390
    • (1995) Bioorg Med Chem , vol.3 , pp. 383-390
    • Zeng, L.1    Gu, Z.M.2    Chang, C.J.3    Wood, K.V.4    McLaughlin, J.L.5
  • 30
    • 0034105345 scopus 로고    scopus 로고
    • Biologically active triterpenoids of Syncarpia glomulifera bark extract from Paluma, north Queensland, Australia
    • Setzer WN, Setzer MC, Bates RB, Jackes BR. Biologically active triterpenoids of Syncarpia glomulifera bark extract from Paluma, north Queensland, Australia. Planta Med 2000;66:176-177
    • (2000) Planta Med , vol.66 , pp. 176-177
    • Setzer, W.N.1    Setzer, M.C.2    Bates, R.B.3    Jackes, B.R.4
  • 31
    • 33244472337 scopus 로고    scopus 로고
    • Antiproliferative terpenoids from almond hulls (Prunus dulcis): Identification and structure-Activity relationships
    • Amico V, Barresi V, Condorelli D, Spatafora C, Tringali C. Antiproliferative terpenoids from almond hulls (Prunus dulcis): Identification and structure-Activity relationships. J Agric Food Chem 2006;54:810-814
    • (2006) J Agric Food Chem , vol.54 , pp. 810-814
    • Amico, V.1    Barresi, V.2    Condorelli, D.3    Spatafora, C.4    Tringali, C.5
  • 32
    • 34249930599 scopus 로고    scopus 로고
    • Betulinic acid decreases expression of bcl-2 and cyclin D1, inhibits proliferation, migration and induces apoptosis in cancer cells
    • Rzeski W, Stepulak A, Szymanski M, Sifringer M, Kaczor J, Wejksza K et al. Betulinic acid decreases expression of bcl-2 and cyclin D1, inhibits proliferation, migration and induces apoptosis in cancer cells. Naunyn Schmiedebergs Arch Pharmacol 2006;374:11-20
    • (2006) Naunyn Schmiedebergs Arch Pharmacol , vol.374 , pp. 11-20
    • Rzeski, W.1    Stepulak, A.2    Szymanski, M.3    Sifringer, M.4    Kaczor, J.5    Wejksza, K.6
  • 33
    • 16644400603 scopus 로고    scopus 로고
    • Apoptosis of human carcinoma cells in the presence of potential anti-cancer drugs: III. Treatment of colo-205 and skbr3 cells with: Cis -platin, tamoxifen, melphalan, betulinic acid, l-pdmp, l-ppmp, and gd3 ganglioside
    • Basu S, Ma R, Boyle PJ, Mikulla B, Bradley M, Smith B et al. Apoptosis of human carcinoma cells in the presence of potential anti-cancer drugs: III. Treatment of Colo-205 and SKBR3 cells with: Cis -platin, Tamoxifen, Melphalan, Betulinic acid, L-PDMP, L-PPMP, and GD3 ganglioside. Glycoconj J 2004;20:563-577
    • (2004) Glycoconj J , vol.20 , pp. 563-577
    • Basu, S.1    Ma, R.2    Boyle, P.J.3    Mikulla, B.4    Bradley, M.5    Smith, B.6
  • 34
    • 34247120086 scopus 로고    scopus 로고
    • Broad in vitro efficacy of plant-derived betulinic acid against cell lines derived from the most prevalent human cancer types
    • Kessler JH, Mullauer FB, De Roo GM, Medema JP. Broad in vitro efficacy of plant-derived betulinic acid against cell lines derived from the most prevalent human cancer types. Cancer Lett 2007;251:132-145
    • (2007) Cancer Lett , vol.251 , pp. 132-145
    • Kessler, J.H.1    Mullauer, F.B.2    De Roo, G.M.3    Medema, J.P.4
  • 36
    • 20444466931 scopus 로고    scopus 로고
    • Expression of estrogen receptor alpha gene in breast cancer cells treated with transcription factor decoy is modulated by Bangladeshi natural plant extracts
    • Lambertini E, Lampronti I, Penolazzi L, Khan MT, Ather A, Giorgi G et al. Expression of estrogen receptor alpha gene in breast cancer cells treated with transcription factor decoy is modulated by Bangladeshi natural plant extracts. Oncol Res 2005;15:69-79
    • (2005) Oncol Res , vol.15 , pp. 69-79
    • Lambertini, E.1    Lampronti, I.2    Penolazzi, L.3    Khan, M.T.4    Ather, A.5    Giorgi, G.6
  • 38
    • 0345161823 scopus 로고    scopus 로고
    • Microbial transformation of sesquiterpene lactones by the fungi cunninghamella echinulata and rhizopus oryzae
    • Barrero AF, Oltra JE, Raslan DS, Saude DA. Microbial transformation of sesquiterpene lactones by the fungi cunninghamella echinulata and rhizopus oryzae. J Nat Prod 1999;62:726-729
    • (1999) J Nat Prod , vol.62 , pp. 726-729
    • Barrero, A.F.1    Oltra, J.E.2    Raslan, D.S.3    Saude, D.A.4
  • 39
    • 85069410569 scopus 로고    scopus 로고
    • Microbial transformation of podocarpic acid and evaluation of transformation products for antioxidant activity
    • EI Syed KA, Hamann MT, Wadling CA, Jansen C, Lee SK, Dunstan CA, et al. Microbial transformation of podocarpic acid and evaluation of transformation products for antioxidant activity. J Org Chem 1998;63:7449-7455
    • (1998) J Org Chem , vol.63 , pp. 7449-7455
    • Ei Syed, K.A.1    Hamann, M.T.2    Wadling, C.A.3    Jansen, C.4    Lee, S.K.5    Dunstan, C.A.6
  • 40
    • 0032776729 scopus 로고    scopus 로고
    • The biocatalytic transformation of furan to amide in the bioactive marine natural product palinurin
    • Khalid A, Syed EI, Mayer AMS, Kelly M, Hamann MT. The biocatalytic transformation of furan to amide in the bioactive marine natural product palinurin. J Org Chem 1999;64:9258-9260
    • (1999) J Org Chem , vol.64 , pp. 9258-9260
    • Khalid, A.1    Syed, E.I.2    Mayer, A.M.S.3    Kelly, M.4    Hamann, M.T.5
  • 42
    • 0032986072 scopus 로고    scopus 로고
    • Isolation from estuarine sediments of a Desulfovibrio strain which can grow on lactate coupled to the reductive dehalogenation of 2 4, 6-Tribromophenol
    • Boyle AW, Phelps CD, Young LY. Isolation from estuarine sediments of a Desulfovibrio strain which can grow on lactate coupled to the reductive dehalogenation of 2,4, 6-Tribromophenol. Appl Environ Microbiol 1999;65:1133-1140
    • (1999) Appl Environ Microbiol , vol.65 , pp. 1133-1140
    • Boyle, A.W.1    Phelps, C.D.2    Young, L.Y.3
  • 45
    • 0007574015 scopus 로고
    • Chemicals, cancer and cytochrome P-4
    • Alexander LS, Goff HM. Chemicals, cancer and cytochrome P-4. J Chem Edu 1982;59:179
    • (1982) J Chem Edu , vol.59 , pp. 179
    • Alexander, L.S.1    Goff, H.M.2
  • 46
    • 0042756233 scopus 로고
    • Peppermint and spearmint tissue culture. II. Dual-carboy culture of spearmint tissues
    • Wang JC, Staba JE. Peppermint and spearmint tissue culture. ii. dual-carboy culture of spearmint tissues. J Pharm Sci 1963;52:1058
    • (1963) J Pharm Sci , vol.52 , pp. 1058
    • Wang, J.C.1    Staba, J.E.2
  • 47
    • 0008032781 scopus 로고
    • Untersuchungen zur frange Der building fluchtiger stoffwechsel produkte in calluskutturen
    • Becker H. Untersuchungen Zur Frange Der Building Fluchtiger stoffwechsel produkte in calluskutturen. Biochem Physiol Pflanz 1970;161:425
    • (1970) Biochem Physiol Pflanz , vol.161 , pp. 425
    • Becker, H.1
  • 48
    • 0042756234 scopus 로고
    • Biotransformation of exogenous substrates by plant cell cultures
    • Suga T, Hirata T, Yamamoto Y. Biotransformation of exogenous substrates by plant cell cultures. Agric Biol Chem 1980;44:325
    • (1980) Agric Biol Chem , vol.44 , pp. 325
    • Suga, T.1    Hirata, T.2    Yamamoto, Y.3
  • 53
    • 44949269802 scopus 로고
    • Biotransformation of exogenous substrates by plant cell cultures
    • Suga T, Hirata T. Biotransformation of exogenous substrates by plant cell cultures. Phytochemistry 1990;29:2393
    • (1990) Phytochemistry , vol.29 , pp. 2393
    • Suga, T.1    Hirata, T.2
  • 55
    • 0034826708 scopus 로고    scopus 로고
    • Assaying the estrogenicity of phytoestrogens in cells of different estrogen sensitive tissues
    • Schmitt E, Dekant W, Stopper H. Assaying the estrogenicity of phytoestrogens in cells of different estrogen sensitive tissues. Toxicol In Vitro 2001;15:433-439
    • (2001) Toxicol In Vitro , vol.15 , pp. 433-439
    • Schmitt, E.1    Dekant, W.2    Stopper, H.3
  • 56
    • 12444285731 scopus 로고    scopus 로고
    • Isolation and characterisation of an equol-producing mixed microbial culture from a human faecal sample and its activity under gastrointestinal conditions
    • Decroos K, Vanhemmens S, Cattoir S, Boon N, Verstraete W. Isolation and characterisation of an equol-producing mixed microbial culture from a human faecal sample and its activity under gastrointestinal conditions. Arch Microbiol 2005;183:45-55
    • (2005) Arch Microbiol , vol.183 , pp. 45-55
    • Decroos, K.1    Vanhemmens, S.2    Cattoir, S.3    Boon, N.4    Verstraete, W.5
  • 58
    • 34248526206 scopus 로고    scopus 로고
    • The biotransformation of sesquiterpenoids by Mucor plumbeus
    • Arantes SF, Hanson JR. The biotransformation of sesquiterpenoids by Mucor plumbeus. Curr Org Chem 2007;11:657-663
    • (2007) Curr Org Chem , vol.11 , pp. 657-663
    • Arantes, S.F.1    Hanson, J.R.2
  • 62
    • 0034518630 scopus 로고    scopus 로고
    • Microbial transformation of the eudesmane sesquiterpene plectranthone
    • Orabi KY. Microbial transformation of the eudesmane sesquiterpene plectranthone. J Nat Prod 2000;63:1709-1711
    • (2000) J Nat Prod , vol.63 , pp. 1709-1711
    • Orabi, K.Y.1
  • 63
    • 0037116403 scopus 로고    scopus 로고
    • Microbial metabolism of partheniol by Mucor circinelloides
    • Maatooq GT. Microbial metabolism of partheniol by Mucor circinelloides. Phytochemistry 2002;59:39-44
    • (2002) Phytochemistry , vol.59 , pp. 39-44
    • Maatooq, G.T.1
  • 65
    • 84887463272 scopus 로고    scopus 로고
    • Novel hydroxylated enantiomers of (-) 3A 6 6,9A-Tetramethylper hydronaphtho [2,1-B] furan as perfuming agents derived from a fungal fermentation process
    • US 2006/0223883 A 1, 5 Oct
    • Atta-Ur-Rahman, Muhammed IC, Syed GM. Novel hydroxylated enantiomers of (-) 3A,6,6,9A-Tetramethylper hydronaphtho [2,1-B] furan as perfuming agents derived from a fungal fermentation process. United states patent application number; US 2006/0223883 A 1, 5 Oct. 2006
    • (2006) United States Patent Application Number
    • Atta-Ur-Rahman1    Muhammed, I.C.2    Syed, G.M.3
  • 67
    • 0035109272 scopus 로고    scopus 로고
    • Biotransformation of terpenoids from the crude drugs and animal origion by micro organisms
    • Hashimoto T, Noma Y, Asakawa Y. Biotransformation of terpenoids from the crude drugs and animal origion by micro organisms. Heterocycles 2001;54:529
    • (2001) Heterocycles , vol.54 , pp. 529
    • Hashimoto, T.1    Noma, Y.2    Asakawa, Y.3
  • 68
    • 33746543517 scopus 로고    scopus 로고
    • Biotransformation of (-)-Ambrox by cell suspension cultures of Actinidia deliciosa
    • Nasib A, Musharraf SG, Hussain S, Khan S, Anjum S, Ali S, et al. Biotransformation of (-)-Ambrox by cell suspension cultures of Actinidia deliciosa. J Nat Prod 2006;69:957-959
    • (2006) J Nat Prod , vol.69 , pp. 957-959
    • Nasib, A.1    Musharraf, S.G.2    Hussain, S.3    Khan, S.4    Anjum, S.5    Ali, S.6
  • 70
    • 0033937786 scopus 로고    scopus 로고
    • Oxidative metabolism of ambrox and sclareolide by Botrytis cinerea
    • Tahara SZ, Farooq A. Oxidative metabolism of ambrox and sclareolide by Botrytis cinerea. Z Naturforsch 2000;55c:341-346
    • (2000) Z Naturforsch , vol.55 C , pp. 341-346
    • Tahara, S.Z.1    Farooq, A.2
  • 72
    • 0032916249 scopus 로고    scopus 로고
    • Biotransformation of the fungistatic sesquiterpenoid patchoulol by botrytis cinerea
    • Aleu J, Hanson JR, Galan RH, Collado IG. Biotransformation of the fungistatic sesquiterpenoid patchoulol by botrytis cinerea. J Nat Prod 1999;62:437-440
    • (1999) J Nat Prod , vol.62 , pp. 437-440
    • Aleu, J.1    Hanson, J.R.2    Galan, R.H.3    Collado, I.G.4
  • 73
    • 13844308927 scopus 로고    scopus 로고
    • Microbial transformation of (-)-isolongifolol and butyrylcholinesterase inhibitory activity of transformed products
    • Muhammed IC, Syed GM, Nawas S, Shazia A, Pervez M, Fun H-K, et al. Microbial transformation of (-)-isolongifolol and butyrylcholinesterase inhibitory activity of transformed products. Bioorg Med Chem 2005;13:1939-1944
    • (2005) Bioorg Med Chem , vol.13 , pp. 1939-1944
    • Muhammed, I.C.1    Syed, G.M.2    Nawas, S.3    Shazia, A.4    Pervez, M.5    Fun, H.-K.6
  • 74
    • 0025011974 scopus 로고
    • Anti-inflammatory constituents of topically applied crude drugs IV Constituents and anti-inflammatory effect of Paraguayan crude drug 'alhucema' (Lavandula latifolia Vill
    • Shimizu M, Shogawa H, Matsuzawa T, Yonezawa S, Hayashi T, Arisawa M et al. Anti-inflammatory constituents of topically applied crude drugs. IV. Constituents and anti-inflammatory effect of Paraguayan crude drug ?alhucema? (Lavandula latifolia Vill.). Chem Pharm Bull 1990;38:2283-2284
    • (1990) Chem Pharm Bull , vol.38 , pp. 2283-2284
    • Shimizu, M.1    Shogawa, H.2    Matsuzawa, T.3    Yonezawa, S.4    Hayashi, T.5    Arisawa, M.6
  • 75
    • 33845431975 scopus 로고    scopus 로고
    • Microbial transformation and butyrylcholinesterase inhibitory activity of (-)-caryophyllene oxide and its derivatives
    • Choudhary MI, Siddiqui ZA, Nawaz SA, Atta-Ur-Rahman. Microbial transformation and butyrylcholinesterase inhibitory activity of (-)-caryophyllene oxide and its derivatives. J Nat Prod 2006;69:1429-1434
    • (2006) J Nat Prod , vol.69 , pp. 1429-1434
    • Choudhary, M.I.1    Siddiqui, Z.A.2    Nawaz, S.A.3    Atta-Ur-Rahman4
  • 77
    • 0033285942 scopus 로고    scopus 로고
    • Use of caryophyllene oxide as an antifungal agent in an in vitro experimental model of onychomycosis
    • Yang D, Michel L, Chaumont JP, Millet-Clerc J. Use of caryophyllene oxide as an antifungal agent in an in vitro experimental model of onychomycosis. Mycopathologia 1999;148:79-82
    • (1999) Mycopathologia , vol.148 , pp. 79-82
    • Yang, D.1    Michel, L.2    Chaumont, J.P.3    Millet-Clerc, J.4
  • 80
    • 14744303540 scopus 로고    scopus 로고
    • Novel biotransformation of pentacyclic triterpenoid acids by Nocardia sp. NRRL 5646
    • Zhang J, Cheng ZH, Yu BY, Cordellb GA, Qiu SQ. Novel biotransformation of pentacyclic triterpenoid acids by Nocardia sp. NRRL 5646. Tetrahedron Lett 2005;46:2337-2340
    • (2005) Tetrahedron Lett , vol.46 , pp. 2337-2340
    • Zhang, J.1    Cheng, Z.H.2    Yu, B.Y.3    Cordellb, G.A.4    Qiu, S.Q.5
  • 81
    • 51349107928 scopus 로고    scopus 로고
    • Microbial metabolism of biologically active secondary metabolites from Nerium oleander L
    • Ibrahim A, Khalifa SI, Khafagi I, Youssef DT, Khan S, Mesbah M et al. Microbial metabolism of biologically active secondary metabolites from Nerium oleander L. Chem Pharm Bull 2008;56:1253-1258
    • (2008) Chem Pharm Bull , vol.56 , pp. 1253-1258
    • Ibrahim, A.1    Khalifa, S.I.2    Khafagi, I.3    Youssef, D.T.4    Khan, S.5    Mesbah, M.6
  • 82
    • 84887422919 scopus 로고    scopus 로고
    • Transformation of ginsenosides Rb1 and Re from Panax ginseng by food microorganisms
    • Oleander L. Transformation of ginsenosides Rb1 and Re from Panax ginseng by food microorganisms. Chem Pharm Bull 2008;56:1253-1258
    • (2008) Chem Pharm Bull , vol.56 , pp. 1253-1258
    • Oleander, L.1
  • 83
    • 23944459284 scopus 로고    scopus 로고
    • Transformation of ginsenosides Rb1and Re from panax ginseng by food micro organisms
    • Chi H, Ji G-E. Transformation of ginsenosides Rb1and Re from panax ginseng by food micro organisms. Biotechnol Lett 2005;27:765-771
    • (2005) Biotechnol Lett , vol.27 , pp. 765-771
    • Chi, H.1    Ji, G.-E.2
  • 84
    • 33644524702 scopus 로고    scopus 로고
    • Microbial transformation of glycyrrhetinic acid by Mucor polymorphosporus
    • Xin X, Liu Y, Ye M, Guo H, Guo D. Microbial transformation of glycyrrhetinic acid by Mucor polymorphosporus. Planta Med 2006;72:156-161
    • (2006) Planta Med , vol.72 , pp. 156-161
    • Xin, X.1    Liu, Y.2    Ye, M.3    Guo, H.4    Guo, D.5
  • 85
    • 0030238940 scopus 로고    scopus 로고
    • Ring-A cleavage of 3-oxo-olean-12-en-28-oic acid by the fungus Chaetomium longirostre
    • Shirane N, Hashimoto Y, Ueda K, Takenaka H, Katoh K. Ring-A cleavage of 3-oxo-olean-12-en-28-oic acid by the fungus Chaetomium longirostre. Phytochemistry 1996;43:99-104
    • (1996) Phytochemistry , vol.43 , pp. 99-104
    • Shirane, N.1    Hashimoto, Y.2    Ueda, K.3    Takenaka, H.4    Katoh, K.5
  • 86
    • 4544224998 scopus 로고    scopus 로고
    • Biotransformation of quinovic acid glycosides by microbes: Direct conversion of the ursane to the oleanane triterpene skeleton by Nocardia sp. NRRL 5646
    • Cheng ZH, Yu BY, Cordell GA, Qiu SX. Biotransformation of quinovic acid glycosides by microbes: Direct conversion of the ursane to the oleanane triterpene skeleton by Nocardia sp. NRRL 5646. Org Lett 2004;6:3163-3165
    • (2004) Org Lett , vol.6 , pp. 3163-3165
    • Cheng, Z.H.1    Yu, B.Y.2    Cordell, G.A.3    Qiu, S.X.4
  • 87
    • 67650700205 scopus 로고    scopus 로고
    • The betulinic acid production from betulin through biotransformation by fungi
    • Chen QH, Liu J, Zhang HF, He GQ, Fu ML. The betulinic acid production from betulin through biotransformation by fungi. Enzyme Microb Tech 2009;45:175-180
    • (2009) Enzyme Microb Tech , vol.45 , pp. 175-180
    • Chen, Q.H.1    Liu, J.2    Zhang, H.F.3    He, G.Q.4    Fu, M.L.5
  • 88
    • 62749096805 scopus 로고    scopus 로고
    • Direct microbial-catalyzed asymmetric [alpha]-hydroxylation of betulonic acid by Nocardia sp NRRL 5646
    • Qian LW, Zhang J, Liu JH, Yu BY. Direct microbial-catalyzed asymmetric [alpha]-hydroxylation of betulonic acid by Nocardia sp., NRRL 5646. Tetrahedron Lett 2009;50:2193-2195
    • (2009) Tetrahedron Lett , vol.50 , pp. 2193-2195
    • Qian, L.W.1    Zhang, J.2    Liu, J.H.3    Yu, B.Y.4
  • 89
    • 0034521516 scopus 로고    scopus 로고
    • Microbial transformations of the antimelanoma agent betulinic acid
    • Kouzi SA, Chatterjee P, Pezzuto JM, Hamann MT. Microbial transformations of the antimelanoma agent betulinic acid. J Nat Prod 2000;63:1653-1657
    • (2000) J Nat Prod , vol.63 , pp. 1653-1657
    • Kouzi, S.A.1    Chatterjee, P.2    Pezzuto, J.M.3    Hamann, M.T.4
  • 90
    • 0033831223 scopus 로고    scopus 로고
    • Biotransformation of the antimelanoma agent betulinic acid by Bacillus megaterium ATCC 13368
    • Chatterjee P, Kouzi SA, Pezzuto JM, Hamann MT. Biotransformation of the antimelanoma agent betulinic acid by Bacillus megaterium ATCC 13368. Appl Environ Microbiol 2000;66:3850-3855
    • (2000) Appl Environ Microbiol , vol.66 , pp. 3850-3855
    • Chatterjee, P.1    Kouzi, S.A.2    Pezzuto, J.M.3    Hamann, M.T.4
  • 91
    • 0036200379 scopus 로고    scopus 로고
    • Microbial transformations of two lupane-Type triterpenes and anti-Tumor-promoting effects of the transformation products
    • Akihisa T, Takamine Y, Yoshizumi K, Tokuda H, Kimura Y, Ukiya M et al. Microbial transformations of two lupane-Type triterpenes and anti-Tumor-promoting effects of the transformation products. J Nat Prod 2002;65:278-282
    • (2002) J Nat Prod , vol.65 , pp. 278-282
    • Akihisa, T.1    Takamine, Y.2    Yoshizumi, K.3    Tokuda, H.4    Kimura, Y.5    Ukiya, M.6
  • 92
    • 33646521514 scopus 로고    scopus 로고
    • Biotransformation of (-)-caryophyllene oxide by cell suspension culture of Catharanthus roseus
    • Muhammed IC, Siddique ZA, Khan SS, Musharraf SG, Atta-Ur-Rahman. Biotransformation of (-)-caryophyllene oxide by cell suspension culture of Catharanthus roseus. Z Naturforsch 2006;59b:197-200
    • (2006) Z Naturforsch , vol.59 B , pp. 197-200
    • Muhammed, I.C.1    Siddique, Z.A.2    Khan, S.S.3    Musharraf, S.G.4    Atta-Ur-Rahman5
  • 94
    • 66249103295 scopus 로고    scopus 로고
    • Anti-AIDS agents. 78. Design, syn thesis, metabolic stability assessment, and antiviral evaluation of novel betulinic acid derivatives as potent anti-human immunodeficiency virus (HIV) agents
    • Qian K, Yu D, Chen CH, Huang L, Morris-Natschke SL, Nitz TJ et al. Anti-AIDS agents. 78. Design, synthesis, metabolic stability assessment, and antiviral evaluation of novel betulinic acid derivatives as potent anti-human immunodeficiency virus (HIV) agents. J Med Chem 2009;52:3248-3258
    • (2009) J Med Chem , vol.52 , pp. 3248-3258
    • Qian, K.1    Yu, D.2    Chen, C.H.3    Huang, L.4    Morris-Natschke, S.L.5    Nitz, T.J.6
  • 96
    • 66349124657 scopus 로고    scopus 로고
    • Cancer preventive agents 9. Betulinic acid derivatives as potent cancer chemopreventive agents
    • Nakagawa-Goto K, Yamada K, Taniguchi M, Tokuda H, Lee KH. Cancer preventive agents 9. Betulinic acid derivatives as potent cancer chemopreventive agents. Bioorg Med Chem Lett 2009;19:3378-3381
    • (2009) Bioorg Med Chem Lett , vol.19 , pp. 3378-3381
    • Nakagawa-Goto, K.1    Yamada, K.2    Taniguchi, M.3    Tokuda, H.4    Lee, K.H.5
  • 97
    • 59049088978 scopus 로고    scopus 로고
    • Anti-oxidative and anti-inflammatory activities of some isolated constituents from the stem bark of Allanblackia monticola Staner L.C (Guttiferae
    • Nguemfo EL, Dimo T, Dongmo AB, Azebaze AG, Alaoui K, Asongalem AE et al. Anti-oxidative and anti-inflammatory activities of some isolated constituents from the stem bark of Allanblackia monticola Staner L.C (Guttiferae). Inflammopharmacology 2009;17:37-41
    • (2009) Inflammopharmacology , vol.17 , pp. 37-41
    • Nguemfo, E.L.1    Dimo, T.2    Dongmo, A.B.3    Azebaze, A.G.4    Alaoui, K.5    Asongalem, A.E.6
  • 98
    • 69749094633 scopus 로고    scopus 로고
    • Targeting mitochondrial apoptosis by betulinic acid in human cancers
    • Fulda S, Kroemer G. Targeting mitochondrial apoptosis by betulinic acid in human cancers. Drug Discov Today 2009;14:885-890
    • (2009) Drug Discov Today , vol.14 , pp. 885-890
    • Fulda, S.1    Kroemer, G.2
  • 99
    • 65449167684 scopus 로고    scopus 로고
    • Lupeol inhibits proliferation of human prostate cancer cells by targeting beta-catenin signaling
    • Saleem M, Murtaza I, Tarapore RS, Suh Y, Adhami VM, Johnson JJ et al. Lupeol inhibits proliferation of human prostate cancer cells by targeting beta-catenin signaling. Carcinogenesis 2009;30:808-817
    • (2009) Carcinogenesis , vol.30 , pp. 808-817
    • Saleem, M.1    Murtaza, I.2    Tarapore, R.S.3    Suh, Y.4    Adhami, V.M.5    Johnson, J.J.6
  • 100
    • 0036066325 scopus 로고    scopus 로고
    • Microbial transformation of a mixture of argentatin A and incanilin
    • Galal TM, Joseph JH. Microbial transformation of a mixture of argentatin A and incanilin. Z Naturforsch C 2002;57:489
    • (2002) Z Naturforsch C , vol.57 , pp. 489
    • Galal, T.M.1    Joseph, J.H.2
  • 104
    • 67049136177 scopus 로고    scopus 로고
    • Microbial transformation of 18beta-glycyrrhetinic acid by Cunninghamella elegans and Fusarium lini, and lipoxygenase inhibitory activity of transformed products
    • Muhammed IC, Siddiqui ZA, Nawaz SA, Atta-Ur-Rahman. Microbial transformation of 18beta-glycyrrhetinic acid by Cunninghamella elegans and Fusarium lini, and lipoxygenase inhibitory activity of transformed products. Nat Prod Res 2009;23:507-513
    • (2009) Nat Prod Res , vol.23 , pp. 507-513
    • Muhammed, I.C.1    Siddiqui, Z.A.2    Nawaz, S.A.3    Atta-Ur-Rahman4
  • 105
    • 0035831359 scopus 로고    scopus 로고
    • Biotransformation of cedrol by Curvularia lunata ATCC 12017
    • Collins DO, Reese PB. Biotransformation of cedrol by Curvularia lunata ATCC 12017. Phytochemistry 2001;56:417-421
    • (2001) Phytochemistry , vol.56 , pp. 417-421
    • Collins, D.O.1    Reese, P.B.2
  • 106
    • 0015986782 scopus 로고
    • Synthesis and biological activities of substituted glycyrrhetic acids
    • Baran JS, Langford DD, Liang C, Pitzele BS. Synthesis and biological activities of substituted glycyrrhetic acids. J Med Chem 1974;17:184-191
    • (1974) J Med Chem , vol.17 , pp. 184-191
    • Baran, J.S.1    Langford, D.D.2    Liang, C.3    Pitzele, B.S.4
  • 107
    • 0000331758 scopus 로고
    • Mechanisms of actions of anti inflammatory drugs
    • Lands MEM. Mechanisms of actions of anti inflammatory drugs. Adv Drug Res 1985;14:147
    • (1985) Adv Drug Res , vol.14 , pp. 147
    • Lands, M.E.M.1
  • 110
    • 0032928637 scopus 로고    scopus 로고
    • 5-Lipoxygenase: A target for antiinflammatory drugs revisited
    • Steinhilber D. 5-Lipoxygenase: A target for antiinflammatory drugs revisited. Curr Med Chem 1999;6:71-85
    • (1999) Curr Med Chem , vol.6 , pp. 71-85
    • Steinhilber, D.1
  • 111
    • 0036283215 scopus 로고    scopus 로고
    • Cyclooxygenase, lipoxygenase and tumor angiogenesis
    • Nie D, Honn KV. Cyclooxygenase, lipoxygenase and tumor angiogenesis. Cell Mol Life Sci 2002;59:799-807
    • (2002) Cell Mol Life Sci , vol.59 , pp. 799-807
    • Nie, D.1    Honn, K.V.2
  • 112
    • 84887487392 scopus 로고    scopus 로고
    • Biotransformation of a bioactive secondary metabolite from Alstonia scholaris
    • Accepted, August
    • Muhammed S, Nighat S, Mustafa K. Biotransformation of a bioactive secondary metabolite from Alstonia scholaris. J Biocatal Biotransfor (Accepted, August 2012
    • (2012) J Biocatal Biotransfor
    • Muhammed, S.1    Nighat, S.2    Mustafa, K.3
  • 113
    • 33744496286 scopus 로고    scopus 로고
    • Biotransformation of cycloartane-Type triterpenes by the fungus Glomerella fusarioides
    • Akihisa TKW, Yoneima R, Suzuki T, Kimura Y. Biotransformation of cycloartane-Type triterpenes by the fungus Glomerella fusarioides. J Nat Prod 2006;69:604-607
    • (2006) J Nat Prod , vol.69 , pp. 604-607
    • Akihisa, T.K.W.1    Yoneima, R.2    Suzuki, T.3    Kimura, Y.4
  • 114
    • 0037296157 scopus 로고    scopus 로고
    • Microbial transformation of ginsenoside Rb1 by Rhizopus stolonifer and Curvularia lunata
    • Dong A, Ye M, Guo H, Zheng J, Guo D. Microbial transformation of ginsenoside Rb1 by Rhizopus stolonifer and Curvularia lunata. Biotechnol Lett 2003;25:339-344
    • (2003) Biotechnol Lett , vol.25 , pp. 339-344
    • Dong, A.1    Ye, M.2    Guo, H.3    Zheng, J.4    Guo, D.5
  • 115
    • 77955815640 scopus 로고    scopus 로고
    • Microbial transformation of ginsenosides Rb1, Rb3 and Rc by Fusarium sacchari
    • Han Y, Sun B, Jiang B, Hu X, Spranger MI, Zhang Y et al. Microbial transformation of ginsenosides Rb1, Rb3 and Rc by Fusarium sacchari. J Appl Microbiol 2010;109:792-798
    • (2010) J Appl Microbiol , vol.109 , pp. 792-798
    • Han, Y.1    Sun, B.2    Jiang, B.3    Hu, X.4    Spranger, M.I.5    Zhang, Y.6
  • 116
    • 0028964260 scopus 로고
    • Microbial transformation of cucurbitacin E 2-O-Î2-d-glucopyranoside
    • Maatooq G, El-Sharkawy S, Afifi MS, Rosazza JPN. Microbial transformation of cucurbitacin E 2-O-Î2-d-glucopyranoside. J Nat Prod 1995;58:165-171
    • (1995) J Nat Prod , vol.58 , pp. 165-171
    • Maatooq, G.1    El-Sharkawy, S.2    Afifi, M.S.3    Rosazza, J.P.N.4
  • 117
    • 27944447292 scopus 로고    scopus 로고
    • Microbial conversion of major ginsenoside rb(1) to pharmaceutically active minor ginsenoside rd
    • Kim MK, Lee JW, Lee KY, Yang DC. Microbial conversion of major ginsenoside rb(1) to pharmaceutically active minor ginsenoside rd. J Microbiol 2005;43:456-462
    • (2005) J Microbiol , vol.43 , pp. 456-462
    • Kim, M.K.1    Lee, J.W.2    Lee, K.Y.3    Yang, D.C.4
  • 118
    • 44949123660 scopus 로고    scopus 로고
    • Biotransformation of β-Amyrin acetate by Rhodobacter sphaeroides
    • Yang GE, Zhang Z, Bai H, Gong J, Wang Y, Li B, et al. Biotransformation of β-Amyrin acetate by Rhodobacter sphaeroides. J Biosci Bioeng 2008;105:558-561
    • (2008) J Biosci Bioeng , vol.105 , pp. 558-561
    • Yang, G.E.1    Zhang, Z.2    Bai, H.3    Gong, J.4    Wang, Y.5    Li, B.6
  • 119
    • 42449106424 scopus 로고    scopus 로고
    • Microbial transformation of oleanolic acid by Fusarium lini and α-glucosidase inhibitory activity of its transformed products
    • Atta-Ur-Rehman, Nighat S, Muhammed IC. Microbial transformation of oleanolic acid by Fusarium lini and α-glucosidase inhibitory activity of its transformed products. Nat Product Research 2008;22:489-494
    • (2008) Nat Product Research , vol.22 , pp. 489-494
    • Atta-Ur-Rehman Nighat, S.1    Muhammed, I.C.2
  • 121
    • 0000327519 scopus 로고
    • Kenntnis des sclareol zur höhere terpenverbindungen L zur kenntnis des sclareols
    • Ruzicka L, Janot MM. Kenntnis des Sclareol, Zur HÖhere Terpenverbindungen L. Zur Kenntnis des Sclareols. Helv Chim Acta 1931;14:645
    • (1931) Helv Chim Acta , vol.14 , pp. 645
    • Ruzicka, L.1    Janot, M.M.2
  • 122
    • 0020455226 scopus 로고
    • Microbial transformations of natural antitumor agents. 21. Conversions of aphidicolin
    • Ipsen J, Fuska J, Foskova, A, Rossaza JP. Microbial transformations of natural antitumor agents. 21. Conversions of aphidicolin. J Org Chem 1982;47:3278
    • (1982) J Org Chem , vol.47 , pp. 3278
    • Ipsen, J.1    Fuska, J.2    Foskova, A.3    Rossaza, J.P.4
  • 123
    • 0036875755 scopus 로고    scopus 로고
    • Antibacterial diterpenoids from Astragalus brachystachys. Z Naturforsch C
    • Jassbi AR, Zamanizadehnajari S, Azar PA, Tahara S. Antibacterial diterpenoids from Astragalus brachystachys. Z Naturforsch, C, J Biosci 2002;57:1016-1021
    • (2002) J Biosci , vol.57 , pp. 1016-1021
    • Jassbi, A.R.1    Zamanizadehnajari, S.2    Azar, P.A.3    Tahara, S.4
  • 128
    • 0037586584 scopus 로고    scopus 로고
    • The biotransformation of the diterpene 2-hydroxy-ent-13-epimanoyl oxide by Gibberella fujikuroi
    • Braulio M, Fragaa P, Gonzá l, Melchor G, Herná N, Sergio S. The biotransformation of the diterpene 2-hydroxy-ent-13-epimanoyl oxide by Gibberella fujikuroi. Phytochemistry 2003;62:67-70
    • (2003) Phytochemistry , vol.62 , pp. 67-70
    • Braulio, M.1    Fragaa, P.2    Gonzá, L.3    Melchor, G.4    Herná, N.5    Sergio, S.6
  • 130
    • 0030061246 scopus 로고    scopus 로고
    • Biotransformation of geraniol and nerol by spores of penicillium italica
    • Demyttenaere RCJ, Pooter De LH. Biotransformation of geraniol and nerol by spores of penicillium italica. Phytochemistry 1996;41:1079
    • (1996) Phytochemistry , vol.41 , pp. 1079
    • Demyttenaere, R.C.J.1    Pooter De, L.H.2
  • 131
    • 0032861743 scopus 로고    scopus 로고
    • Plant products as antimicrobial agents
    • Cowan MM. Plant products as antimicrobial agents. Clin Microbiol Rev 1999;12:564-582
    • (1999) Clin Microbiol Rev , vol.12 , pp. 564-582
    • Cowan, M.M.1
  • 132
    • 0001453179 scopus 로고
    • Charalambous G, ed. Amsterdam, The Netherlands: Elsevier Science BV
    • National N. (1994). Spices, Herbs and Edible Fungi. In: Charalambous G, ed. Amsterdam, The Netherlands: Elsevier Science BV, 251
    • (1994) Spices, Herbs and Edible Fungi , pp. 251
    • National, N.1
  • 134
    • 0023101802 scopus 로고
    • Inhibition of food borne pathogens by thymol, eugenol, menthol and anethol
    • Karapinar M, Aktug SE. Inhibition of food borne pathogens by thymol, eugenol, menthol and anethol. Int J. Food Microbiol 1987;4:161-166
    • (1987) Int J. Food Microbiol , vol.4 , pp. 161-166
    • Karapinar, M.1    Aktug, S.E.2
  • 135
    • 0001075074 scopus 로고
    • Biotransformation of monoterpenenoids, (-)-And (+)-menthols, terpinolene and carvotanacetone by Aspergillus species
    • Asakawa Y, Takahashi H, Toyota M, Noma Y. Biotransformation of monoterpenenoids, (-)-And (+)-menthols, terpinolene and carvotanacetone by Aspergillus species. Phytochemistry 1991;30:3981
    • (1991) Phytochemistry , vol.30 , pp. 3981
    • Asakawa, Y.1    Takahashi, H.2    Toyota, M.3    Noma, Y.4
  • 136
    • 0141718879 scopus 로고    scopus 로고
    • Biopreparation of (1S,3R,4S,6S)-6-hydroxymenthol and (-)-(1S,3R,4S)-1- hydroxymenthol from 1-menthol by Rhizoctonia solani AG-1-IA and I.B
    • Miyazawa M, Kawazoe H, Hyakumachi M. Biopreparation of (1S,3R,4S,6S)-6-hydroxymenthol and (-)-(1S,3R,4S)-1-hydroxymenthol from 1-menthol by Rhizoctonia solani AG-1-IA and IB. Nat Prod Res 2003;17:307-309
    • (2003) Nat Prod Res , vol.17 , pp. 307-309
    • Miyazawa, M.1    Kawazoe, H.2    Hyakumachi, M.3
  • 137
    • 0037421130 scopus 로고    scopus 로고
    • Regioselective free radical phenylsulfenation of nonactivated d-carbon atom by the photolysis of alkyl benzenesulfenates
    • Petrovic G, Saicic NR, Ckovic Z. Regioselective free radical phenylsulfenation of nonactivated d-carbon atom by the photolysis of alkyl benzenesulfenates. Tetrahedron 2003;59:187-191
    • (2003) Tetrahedron , vol.59 , pp. 187-191
    • Petrovic, G.1    Saicic, N.R.2    Ckovic, Z.3
  • 138
    • 8644238019 scopus 로고    scopus 로고
    • Synthesis and absolute configuration at C(8) of 'p-menthane-3 8,9-Triol' derived from (-)-isopulegol
    • Yoshifumi Y, Yoko, Y. Synthesis and absolute configuration at C(8) of ?p-menthane-3,8,9-Triol? derived from (-)-isopulegol. Helv Chim Acta 2004;87:2602-2607
    • (2004) Helv Chim Acta , vol.87 , pp. 2602-2607
    • Yoshifumi, Y.1    Yoko, Y.2


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