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Volumn 68, Issue , 2014, Pages 117-127

Evaluation of the in vitro/in vivo drug interaction potential of BST204, a purified dry extract of ginseng, and its four bioactive ginsenosides through cytochrome P450 inhibition/induction and UDP-glucuronosyltransferase inhibition

Author keywords

A purified dry extract of ginseng; BST204; CYPs inhibition induction; Four bioactive ginsenosides; In vitro drug interaction; UGTs inhibition

Indexed keywords

BST 204; CYTOCHROME P450; CYTOCHROME P450 2B6; CYTOCHROME P450 2C8; CYTOCHROME P450 2C9; CYTOCHROME P450 2D6; GINSENG EXTRACT; GINSENOSIDE RG 3; GINSENOSIDE RH 2; GLUCURONOSYLTRANSFERASE; GLUCURONOSYLTRANSFERASE 1A1; GLUCURONOSYLTRANSFERASE 1A9; GLUCURONOSYLTRANSFERASE 2B7; IRINOTECAN; UNCLASSIFIED DRUG; BST204 GINSENG EXTRACT; CYTOCHROME P450 INHIBITOR; ENZYME INHIBITOR; GINSENOSIDE; PLANT EXTRACT;

EID: 84897951719     PISSN: 02786915     EISSN: 18736351     Source Type: Journal    
DOI: 10.1016/j.fct.2014.03.004     Document Type: Article
Times cited : (30)

References (59)
  • 1
    • 0034945280 scopus 로고    scopus 로고
    • Herbal medicines and perioperative care
    • Ang-Lee M.K., Moss J., Yuan C.S. Herbal medicines and perioperative care. JAMA 2001, 286:208-216.
    • (2001) JAMA , vol.286 , pp. 208-216
    • Ang-Lee, M.K.1    Moss, J.2    Yuan, C.S.3
  • 2
    • 0344549853 scopus 로고    scopus 로고
    • Ginseng pharmacology: multiple constituents and multiple actions
    • Attele A.S., Wu J.A., Yuan C.S. Ginseng pharmacology: multiple constituents and multiple actions. Biochem. Pharmacol. 1999, 58:1685-1693.
    • (1999) Biochem. Pharmacol. , vol.58 , pp. 1685-1693
    • Attele, A.S.1    Wu, J.A.2    Yuan, C.S.3
  • 3
    • 84879228639 scopus 로고    scopus 로고
    • Stereoselective determination of ginsenosides Rg3 and Rh2 epimers in rat plasma by LC-MS/MS: Application to a pharmacokinetic study
    • Bae S.H., Zheng Y.F., Yoo Y.H., Kim J.Y., Kim S.O., Jang M.J., Seo J.H., Bae S.K. Stereoselective determination of ginsenosides Rg3 and Rh2 epimers in rat plasma by LC-MS/MS: Application to a pharmacokinetic study. J. Sep. Sci. 2013, 36:1904-1912.
    • (2013) J. Sep. Sci. , vol.36 , pp. 1904-1912
    • Bae, S.H.1    Zheng, Y.F.2    Yoo, Y.H.3    Kim, J.Y.4    Kim, S.O.5    Jang, M.J.6    Seo, J.H.7    Bae, S.K.8
  • 5
    • 2542460298 scopus 로고    scopus 로고
    • Natural products and adverse drug interactions
    • Bailey D.G., Dresser G.K. Natural products and adverse drug interactions. CMAJ 2004, 170:1531-1532.
    • (2004) CMAJ , vol.170 , pp. 1531-1532
    • Bailey, D.G.1    Dresser, G.K.2
  • 6
    • 70349108450 scopus 로고    scopus 로고
    • Glucuronidation of the antiretroviral drug efavirenz by UGT2B7 and an in vitro investigation of drug-drug interaction with zidovudine
    • Bélanger A.S., Caron P., Harvey M., Zimmerman P.A., Mehlotra R.K. Glucuronidation of the antiretroviral drug efavirenz by UGT2B7 and an in vitro investigation of drug-drug interaction with zidovudine. Drug Metab. Dispos. 2009, 37:1793-1796.
    • (2009) Drug Metab. Dispos. , vol.37 , pp. 1793-1796
    • Bélanger, A.S.1    Caron, P.2    Harvey, M.3    Zimmerman, P.A.4    Mehlotra, R.K.5
  • 8
    • 0036206368 scopus 로고    scopus 로고
    • In vitro effect of standardized ginseng extracts and individual ginsenosides on the catalytic activity of human CYP1A1, CYP1A2, and CYP1B1
    • Chang T.K., Chen J., Benetton S.A. In vitro effect of standardized ginseng extracts and individual ginsenosides on the catalytic activity of human CYP1A1, CYP1A2, and CYP1B1. Drug Metab. Dispos. 2002, 30:378-384.
    • (2002) Drug Metab. Dispos. , vol.30 , pp. 378-384
    • Chang, T.K.1    Chen, J.2    Benetton, S.A.3
  • 9
    • 51349086818 scopus 로고    scopus 로고
    • Comparison of the pharmacological effects of Panax ginseng and Panax quinquefolium
    • Chen C.F., Chiou W.F., Zhang J.T. Comparison of the pharmacological effects of Panax ginseng and Panax quinquefolium. Acta Pharmacol. Sin. 2008, 29:1103-1108.
    • (2008) Acta Pharmacol. Sin. , vol.29 , pp. 1103-1108
    • Chen, C.F.1    Chiou, W.F.2    Zhang, J.T.3
  • 10
    • 50349101675 scopus 로고    scopus 로고
    • Ginsenosides chemistry, biosynthesis, analysis, and potential health effects
    • Christensen L.P. Ginsenosides chemistry, biosynthesis, analysis, and potential health effects. Adv. Food Nutr. Res. 2009, 55:1-99.
    • (2009) Adv. Food Nutr. Res. , vol.55 , pp. 1-99
    • Christensen, L.P.1
  • 11
    • 0036842042 scopus 로고    scopus 로고
    • Stereoselective conjugation of oxazepam by human UDP-glucuronosyltransferases (UGTs): S-oxazepam is glucuronidated by UGT2B15, while R-oxazepam is glucuronidated by UGT2B7 and UGT1A9
    • Court M.H., Duan S.X., Guillemette C., Journault K., Krishnaswamy S., von Moltke L.L., Greenblatt D.J. Stereoselective conjugation of oxazepam by human UDP-glucuronosyltransferases (UGTs): S-oxazepam is glucuronidated by UGT2B15, while R-oxazepam is glucuronidated by UGT2B7 and UGT1A9. Drug Metab. Dispos. 2002, 30:1257-1265.
    • (2002) Drug Metab. Dispos. , vol.30 , pp. 1257-1265
    • Court, M.H.1    Duan, S.X.2    Guillemette, C.3    Journault, K.4    Krishnaswamy, S.5    von Moltke, L.L.6    Greenblatt, D.J.7
  • 15
    • 34547730805 scopus 로고    scopus 로고
    • An in vitro evaluation of cytochrome P450 inhibition and P-glycoprotein interaction with goldenseal, Ginkgo biloba, grape seed, milk thistle, and ginseng extracts and their constituents
    • Etheridge A.S., Black S.R., Patel P.R., So J., Mathews J.M. An in vitro evaluation of cytochrome P450 inhibition and P-glycoprotein interaction with goldenseal, Ginkgo biloba, grape seed, milk thistle, and ginseng extracts and their constituents. Planta Med. 2007, 73:731-741.
    • (2007) Planta Med. , vol.73 , pp. 731-741
    • Etheridge, A.S.1    Black, S.R.2    Patel, P.R.3    So, J.4    Mathews, J.M.5
  • 16
    • 84897940297 scopus 로고    scopus 로고
    • European Medicines Agency, 2010. Guideline on the investigation of drug interactions. Available at:
    • European Medicines Agency, 2010. Guideline on the investigation of drug interactions. Available at: http://www.ema.europa.eu/docs/en_GB/document_library/Scientific_guideline/2010/05/WC500090112.pdf.
  • 17
    • 84872863938 scopus 로고    scopus 로고
    • Structure-inhibition relationship of ginsenosides towards UDP-glucuronosyltransferases (UGTs)
    • Fang Z.Z., Cao Y.F., Hu C.M., Hong M., Sun X.Y. Structure-inhibition relationship of ginsenosides towards UDP-glucuronosyltransferases (UGTs). Toxicol. Appl. Pharmacol. 2013, 267:149-154.
    • (2013) Toxicol. Appl. Pharmacol. , vol.267 , pp. 149-154
    • Fang, Z.Z.1    Cao, Y.F.2    Hu, C.M.3    Hong, M.4    Sun, X.Y.5
  • 18
  • 19
    • 38749138848 scopus 로고    scopus 로고
    • Product inhibition of UDP-glucuronosyltransferase (UGT) enzymes by UDP obfuscates the inhibitory effects of UGT substrates
    • Fujiwara R., Nakajima M., Yamanaka H., Katoh M., Yokoi T. Product inhibition of UDP-glucuronosyltransferase (UGT) enzymes by UDP obfuscates the inhibitory effects of UGT substrates. Drug Metab. Dispos. 2008, 36:361-367.
    • (2008) Drug Metab. Dispos. , vol.36 , pp. 361-367
    • Fujiwara, R.1    Nakajima, M.2    Yamanaka, H.3    Katoh, M.4    Yokoi, T.5
  • 20
    • 3843064658 scopus 로고    scopus 로고
    • The inhibitory effects of herbal components on CYP2C9 and CYP3A4 catalytic activities in human liver microsomes
    • He N., Edeki T. The inhibitory effects of herbal components on CYP2C9 and CYP3A4 catalytic activities in human liver microsomes. Am. J. Ther. 2004, 11:206-212.
    • (2004) Am. J. Ther. , vol.11 , pp. 206-212
    • He, N.1    Edeki, T.2
  • 21
    • 33747066115 scopus 로고    scopus 로고
    • Effects of individual ginsenosides, ginkgolides and flavonoids on CYP2C19 and CYP2D6 activity in human liver microsomes
    • He N., Xie H.G., Collins X., Edeki T., Yan Z. Effects of individual ginsenosides, ginkgolides and flavonoids on CYP2C19 and CYP2D6 activity in human liver microsomes. Clin. Exp. Pharmacol. Physiol. 2006, 33:813-815.
    • (2006) Clin. Exp. Pharmacol. Physiol. , vol.33 , pp. 813-815
    • He, N.1    Xie, H.G.2    Collins, X.3    Edeki, T.4    Yan, Z.5
  • 22
    • 4644356962 scopus 로고    scopus 로고
    • Cancer prevention and therapeutics: Panax ginseng
    • Helms S. Cancer prevention and therapeutics: Panax ginseng. Altern. Med. Rev. 2004, 9:259-274.
    • (2004) Altern. Med. Rev. , vol.9 , pp. 259-274
    • Helms, S.1
  • 23
    • 84866070528 scopus 로고    scopus 로고
    • Clinical evidence of herbal drugs as perpetrators of pharmacokinetic drug interactions
    • Hermann R., von Richter O. Clinical evidence of herbal drugs as perpetrators of pharmacokinetic drug interactions. Planta Med. 2012, 78:1458-1477.
    • (2012) Planta Med. , vol.78 , pp. 1458-1477
    • Hermann, R.1    von Richter, O.2
  • 24
    • 0032519431 scopus 로고    scopus 로고
    • Genetic predisposition to the metabolism of irinotecan (CPT-11). Role of uridine diphosphate glucuronosyltransferase isoform 1A1 in the glucuronidation of its active metabolite (SN38) in human liver microsomes
    • Iyer L., King C.D., Whitington P.F., Green M.D., Roy S.K., Tephly T.R., Coffman B.L., Ratain M.J. Genetic predisposition to the metabolism of irinotecan (CPT-11). Role of uridine diphosphate glucuronosyltransferase isoform 1A1 in the glucuronidation of its active metabolite (SN38) in human liver microsomes. J. Clin. Invest. 1998, 101:847-854.
    • (1998) J. Clin. Invest. , vol.101 , pp. 847-854
    • Iyer, L.1    King, C.D.2    Whitington, P.F.3    Green, M.D.4    Roy, S.K.5    Tephly, T.R.6    Coffman, B.L.7    Ratain, M.J.8
  • 25
    • 70349397280 scopus 로고    scopus 로고
    • Current evaluation of the millennium phytomedicine-ginseng (i): etymology, pharmacognosy, phytochemistry, market and regulations
    • Jia L., Zhao Y.Q. Current evaluation of the millennium phytomedicine-ginseng (i): etymology, pharmacognosy, phytochemistry, market and regulations. Curr. Med. Chem. 2009, 16:2475-2484.
    • (2009) Curr. Med. Chem. , vol.16 , pp. 2475-2484
    • Jia, L.1    Zhao, Y.Q.2
  • 26
    • 0037293063 scopus 로고    scopus 로고
    • Inhibitory effects of the ginsenoside Rg3 on phorbol ester-induced cyclooxygenase-2 expression, NF-kappaB activation and tumor promotion
    • Keum Y.S., Han S.S., Chun K.S., Park K.K., Park J.H., Lee S.K. Inhibitory effects of the ginsenoside Rg3 on phorbol ester-induced cyclooxygenase-2 expression, NF-kappaB activation and tumor promotion. Mutat. Res. 2003, 523-524:75-85.
    • (2003) Mutat. Res. , pp. 75-85
    • Keum, Y.S.1    Han, S.S.2    Chun, K.S.3    Park, K.K.4    Park, J.H.5    Lee, S.K.6
  • 27
    • 15244342411 scopus 로고    scopus 로고
    • UDP-glucuronosyltransferases and clinical drug-drug interactions
    • Kiang T.K., Ensom M.H., Chang T.K. UDP-glucuronosyltransferases and clinical drug-drug interactions. Pharmacol. Ther. 2005, 106:97-132.
    • (2005) Pharmacol. Ther. , vol.106 , pp. 97-132
    • Kiang, T.K.1    Ensom, M.H.2    Chang, T.K.3
  • 29
    • 16544379730 scopus 로고    scopus 로고
    • Effects of ginsenosides Rg3 and Rh2 on the proliferation of prostate cancer cells
    • Kim H.S., Lee E.H., Ko S.R., Choi K.J., Park J.H., Im D.S. Effects of ginsenosides Rg3 and Rh2 on the proliferation of prostate cancer cells. Arch. Pharm. Res. 2004, 27:429-435.
    • (2004) Arch. Pharm. Res. , vol.27 , pp. 429-435
    • Kim, H.S.1    Lee, E.H.2    Ko, S.R.3    Choi, K.J.4    Park, J.H.5    Im, D.S.6
  • 30
    • 0037324354 scopus 로고    scopus 로고
    • Serotonin (5-hydroxytryptamine) glucuronidation in vitro: assay development, human liver microsome activities and species differences
    • Krishnaswamy S., Duan S.X., Von Moltke L.L., Greenblatt D.J., Sudmeier J.L. Serotonin (5-hydroxytryptamine) glucuronidation in vitro: assay development, human liver microsome activities and species differences. Xenobiotica 2003, 33:169-180.
    • (2003) Xenobiotica , vol.33 , pp. 169-180
    • Krishnaswamy, S.1    Duan, S.X.2    Von Moltke, L.L.3    Greenblatt, D.J.4    Sudmeier, J.L.5
  • 31
    • 48649105424 scopus 로고    scopus 로고
    • The chemical and hydroxyl radical scavenging activity changes of ginsenoside-Rb1 by heat processing
    • Lee Y.J., Kim H.Y., Kang K.S., Lee J.G., Yokozawa T., Park J.H. The chemical and hydroxyl radical scavenging activity changes of ginsenoside-Rb1 by heat processing. Bioorg. Med. Chem. Lett. 2008, 18:4515-4520.
    • (2008) Bioorg. Med. Chem. Lett. , vol.18 , pp. 4515-4520
    • Lee, Y.J.1    Kim, H.Y.2    Kang, K.S.3    Lee, J.G.4    Yokozawa, T.5    Park, J.H.6
  • 32
    • 33744799726 scopus 로고    scopus 로고
    • Ginsenoside metabolites, rather than naturally occurring ginsenosides, lead to inhibition of human cytochrome P450 enzymes
    • Liu Y., Zhang J.W., Li W., Ma H., Sun J. Ginsenoside metabolites, rather than naturally occurring ginsenosides, lead to inhibition of human cytochrome P450 enzymes. Toxicol. Sci. 2006, 91:356-364.
    • (2006) Toxicol. Sci. , vol.91 , pp. 356-364
    • Liu, Y.1    Zhang, J.W.2    Li, W.3    Ma, H.4    Sun, J.5
  • 33
    • 65749114119 scopus 로고    scopus 로고
    • 20(R)-ginsenoside Rh2, not 20(S), is a selective osteoclastgenesis inhibitor without any cytotoxicity
    • Liu J., Shiono J., Shimizu K., Yu H., Zhang C. 20(R)-ginsenoside Rh2, not 20(S), is a selective osteoclastgenesis inhibitor without any cytotoxicity. Bioorg. Med. Chem. Lett. 2009, 19:3320-3323.
    • (2009) Bioorg. Med. Chem. Lett. , vol.19 , pp. 3320-3323
    • Liu, J.1    Shiono, J.2    Shimizu, K.3    Yu, H.4    Zhang, C.5
  • 34
    • 77956680962 scopus 로고    scopus 로고
    • Stereospecificity of hydroxyl group at C-20 in antiproliferative action of ginsenoside Rh2 on prostate cancer cells
    • Liu J., Shimizu K., Yu H., Zhang C., Jin F. Stereospecificity of hydroxyl group at C-20 in antiproliferative action of ginsenoside Rh2 on prostate cancer cells. Fitoterapia 2010, 81:902-905.
    • (2010) Fitoterapia , vol.81 , pp. 902-905
    • Liu, J.1    Shimizu, K.2    Yu, H.3    Zhang, C.4    Jin, F.5
  • 35
    • 4344632633 scopus 로고    scopus 로고
    • UGT1A1 gene variations and irinotecan treatment in patients with metastatic colorectal cancer
    • Marcuello E., Altés A., Menoyo A., Del Rio E., Gómez-Pardo M., Baiget M. UGT1A1 gene variations and irinotecan treatment in patients with metastatic colorectal cancer. Br. J. Cancer 2004, 91:678-682.
    • (2004) Br. J. Cancer , vol.91 , pp. 678-682
    • Marcuello, E.1    Altés, A.2    Menoyo, A.3    Del Rio, E.4    Gómez-Pardo, M.5    Baiget, M.6
  • 37
    • 79952819517 scopus 로고    scopus 로고
    • Characterization of niflumic acid as a selective inhibitor of human liver microsomal UDP-glucuronosyltransferase 1A9: application to the reaction phenotyping of acetaminophen glucuronidation
    • Miners J.O., Bowalgaha K., Elliot D.J., Baranczewski P., Knights K.M. Characterization of niflumic acid as a selective inhibitor of human liver microsomal UDP-glucuronosyltransferase 1A9: application to the reaction phenotyping of acetaminophen glucuronidation. Drug Metab. Dispos. 2011, 39:644-652.
    • (2011) Drug Metab. Dispos. , vol.39 , pp. 644-652
    • Miners, J.O.1    Bowalgaha, K.2    Elliot, D.J.3    Baranczewski, P.4    Knights, K.M.5
  • 38
    • 33846449874 scopus 로고    scopus 로고
    • Mechanism-based inactivation of human cytochrome P450 enzymes and the prediction of drug-drug interactions
    • Obach R.S., Walsky R.L., Venkatakrishnan K. Mechanism-based inactivation of human cytochrome P450 enzymes and the prediction of drug-drug interactions. Drug Metab. Dispos. 2007, 35:246-255.
    • (2007) Drug Metab. Dispos. , vol.35 , pp. 246-255
    • Obach, R.S.1    Walsky, R.L.2    Venkatakrishnan, K.3
  • 39
    • 0030777703 scopus 로고    scopus 로고
    • Activation of caspase-3 protease via a Bcl-2-insensitive pathway during the process of ginsenoside Rh2-induced apoptosis
    • Park J.A., Lee K.Y., Oh Y.J., Kim K.W., Lee S.K. Activation of caspase-3 protease via a Bcl-2-insensitive pathway during the process of ginsenoside Rh2-induced apoptosis. Cancer Lett. 1997, 121:73-81.
    • (1997) Cancer Lett. , vol.121 , pp. 73-81
    • Park, J.A.1    Lee, K.Y.2    Oh, Y.J.3    Kim, K.W.4    Lee, S.K.5
  • 40
    • 0036403187 scopus 로고    scopus 로고
    • Structure-function relationship exists for ginsenosides in reducing cell proliferation and inducing apoptosis in the human leukemia (THP-1) cell line
    • Popovich D.G., Kitts D.D. Structure-function relationship exists for ginsenosides in reducing cell proliferation and inducing apoptosis in the human leukemia (THP-1) cell line. Arch. Biochem. Biophys. 2002, 406:1-8.
    • (2002) Arch. Biochem. Biophys. , vol.406 , pp. 1-8
    • Popovich, D.G.1    Kitts, D.D.2
  • 44
    • 21044451729 scopus 로고    scopus 로고
    • Inhibitory effects of a fermented ginseng extract, BST204, on the expression of inducible nitric oxide synthase and nitric oxide production in lipopolysaccharide-activated murine macrophages
    • Seo J.Y., Lee J.H., Kim N.W., Kim Y.J., Chang S.H., Ko N.Y., Her E., Yoo Y.H., Kim J.W., Lee B.Y., Lee H.Y., Kim Y.M., Choi W.S. Inhibitory effects of a fermented ginseng extract, BST204, on the expression of inducible nitric oxide synthase and nitric oxide production in lipopolysaccharide-activated murine macrophages. J. Pharm. Pharmacol. 2005, 57:911-918.
    • (2005) J. Pharm. Pharmacol. , vol.57 , pp. 911-918
    • Seo, J.Y.1    Lee, J.H.2    Kim, N.W.3    Kim, Y.J.4    Chang, S.H.5    Ko, N.Y.6    Her, E.7    Yoo, Y.H.8    Kim, J.W.9    Lee, B.Y.10    Lee, H.Y.11    Kim, Y.M.12    Choi, W.S.13
  • 46
    • 33344473930 scopus 로고    scopus 로고
    • Selectivity of substrate (trifluoperazine) and inhibitor (amitriptyline, androsterone, canrenoic acid, hecogenin, phenylbutazone, quinidine, quinine, and sulfinpyrazone) "probes" for human udp-glucuronosyltransferases
    • Uchaipichat V., Mackenzie P.I., Elliot D.J., Miners J.O. Selectivity of substrate (trifluoperazine) and inhibitor (amitriptyline, androsterone, canrenoic acid, hecogenin, phenylbutazone, quinidine, quinine, and sulfinpyrazone) "probes" for human udp-glucuronosyltransferases. Drug Metab. Dispos. 2006, 34:449-456.
    • (2006) Drug Metab. Dispos. , vol.34 , pp. 449-456
    • Uchaipichat, V.1    Mackenzie, P.I.2    Elliot, D.J.3    Miners, J.O.4
  • 47
    • 84897948460 scopus 로고    scopus 로고
    • U.S. FDA, Center for Drug Evaluation and Research (CDER), 2006. Guidance for industry. Drug interaction studies-study design, data analysis, implication for dosing, and labeling recommendations. Draft guidance.
    • U.S. FDA, Center for Drug Evaluation and Research (CDER), 2006. Guidance for industry. Drug interaction studies-study design, data analysis, implication for dosing, and labeling recommendations. Draft guidance.
  • 48
    • 84897953524 scopus 로고    scopus 로고
    • U.S. FDA, Center for Drug Evaluation and Research (CDER), 2012. Guidance for industry. Drug interaction studies-study design, data analysis, implication for dosing, and labeling recommendations. Draft guidance.
    • U.S. FDA, Center for Drug Evaluation and Research (CDER), 2012. Guidance for industry. Drug interaction studies-study design, data analysis, implication for dosing, and labeling recommendations. Draft guidance.
  • 49
    • 57349164037 scopus 로고    scopus 로고
    • Potential role of ginseng in the treatment of colorectal cancer
    • Wang C.Z., Yuan C.S. Potential role of ginseng in the treatment of colorectal cancer. Am. J. Chin. Med. 2008, 36:1019-1028.
    • (2008) Am. J. Chin. Med. , vol.36 , pp. 1019-1028
    • Wang, C.Z.1    Yuan, C.S.2
  • 51
    • 84864005465 scopus 로고    scopus 로고
    • Stereospecificity of ginsenoside Rg3 in promotion of the immune response to ovalbumin in mice
    • Wei X., Chen J., Su F., Su X., Hu T. Stereospecificity of ginsenoside Rg3 in promotion of the immune response to ovalbumin in mice. Int. Immunol. 2012, 24:465-471.
    • (2012) Int. Immunol. , vol.24 , pp. 465-471
    • Wei, X.1    Chen, J.2    Su, F.3    Su, X.4    Hu, T.5
  • 52
    • 84861680914 scopus 로고    scopus 로고
    • Stereospecific antioxidant effects of ginsenoside Rg3 on oxidative stress induced by cyclophosphamide in mice
    • Wei X., Su F., Su X., Hu T., Hu S. Stereospecific antioxidant effects of ginsenoside Rg3 on oxidative stress induced by cyclophosphamide in mice. Fitoterapia 2012, 83:636-642.
    • (2012) Fitoterapia , vol.83 , pp. 636-642
    • Wei, X.1    Su, F.2    Su, X.3    Hu, T.4    Hu, S.5
  • 53
    • 84870383328 scopus 로고    scopus 로고
    • Implication of the stereoisomers of ginsenoside derivatives in the antiproliferative effect of HSC-T6 cells
    • Yang H., Yoo G., Kim H.S., Kim J.Y., Kim S.O. Implication of the stereoisomers of ginsenoside derivatives in the antiproliferative effect of HSC-T6 cells. J. Agric. Food Chem. 2012, 60:11759-11764.
    • (2012) J. Agric. Food Chem. , vol.60 , pp. 11759-11764
    • Yang, H.1    Yoo, G.2    Kim, H.S.3    Kim, J.Y.4    Kim, S.O.5
  • 54
    • 0036893593 scopus 로고    scopus 로고
    • Evaluation of cytochrom P450 probe substrates commonly used by the pharmaceutical industry to study in vitro drug interactions
    • Yuan R., Madani S., Wei X.X., Reynolds K., Huang S.M. Evaluation of cytochrom P450 probe substrates commonly used by the pharmaceutical industry to study in vitro drug interactions. Drug Metab. Dispos. 2002, 30:1311-1319.
    • (2002) Drug Metab. Dispos. , vol.30 , pp. 1311-1319
    • Yuan, R.1    Madani, S.2    Wei, X.X.3    Reynolds, K.4    Huang, S.M.5
  • 55
    • 0035240033 scopus 로고    scopus 로고
    • Panax ginseng - a non-organ-specific cancer preventive?
    • Yun T.K. Panax ginseng - a non-organ-specific cancer preventive?. Lancet Oncol. 2001, 2:49-55.
    • (2001) Lancet Oncol. , vol.2 , pp. 49-55
    • Yun, T.K.1
  • 56
    • 69749123035 scopus 로고    scopus 로고
    • Quantitation of Irinotecan and its two major metabolites using a liquid chromatography-electrospray ionization tandem mass spectrometric
    • Zhang W., Dutschman G.E., Li X., Ye M., Cheng Y.C. Quantitation of Irinotecan and its two major metabolites using a liquid chromatography-electrospray ionization tandem mass spectrometric. J. Chromatogr. B Analyt. Technol. Biomed. Life Sci. 2009, 877:3038-3044.
    • (2009) J. Chromatogr. B Analyt. Technol. Biomed. Life Sci. , vol.877 , pp. 3038-3044
    • Zhang, W.1    Dutschman, G.E.2    Li, X.3    Ye, M.4    Cheng, Y.C.5
  • 57
    • 77949351406 scopus 로고    scopus 로고
    • Drug interactions evaluation: an integrated part of risk assessment of therapeutics
    • Zhang L., Reynolds K.S., Whao P., Huang S.M. Drug interactions evaluation: an integrated part of risk assessment of therapeutics. Toxicol. Appl. Pharmacol. 2010, 243:134-145.
    • (2010) Toxicol. Appl. Pharmacol. , vol.243 , pp. 134-145
    • Zhang, L.1    Reynolds, K.S.2    Whao, P.3    Huang, S.M.4
  • 58
    • 80052492263 scopus 로고    scopus 로고
    • Effects of 20 (S)-ginsenoside Rh2 and 20 (R)-ginsenoside Rh2 on proliferation and apoptosis of human lung adenocarcinoma A549 cell
    • Zhang C., Yu H., Hou J. Effects of 20 (S)-ginsenoside Rh2 and 20 (R)-ginsenoside Rh2 on proliferation and apoptosis of human lung adenocarcinoma A549 cell. Zhongguo Zhong Yao Za Zhi 2011, 36:1670-1674.
    • (2011) Zhongguo Zhong Yao Za Zhi , vol.36 , pp. 1670-1674
    • Zhang, C.1    Yu, H.2    Hou, J.3
  • 59
    • 84879583960 scopus 로고    scopus 로고
    • Inhibitory effects of astaxanthin, β-cryptoxanthin, canthaxanthin, lutein, and zeaxanthin on cytochrome P450 enzyme activities
    • Zheng Y.F., Bae S.H., Kwon M.J., Park J.B., Choi H.D., Shin W.G., Bae S.K. Inhibitory effects of astaxanthin, β-cryptoxanthin, canthaxanthin, lutein, and zeaxanthin on cytochrome P450 enzyme activities. Food Chem. Toxicol. 2013, 59:78-85.
    • (2013) Food Chem. Toxicol. , vol.59 , pp. 78-85
    • Zheng, Y.F.1    Bae, S.H.2    Kwon, M.J.3    Park, J.B.4    Choi, H.D.5    Shin, W.G.6    Bae, S.K.7


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