메뉴 건너뛰기




Volumn 103, Issue 6, 2014, Pages 1891-1902

Preclinical pharmacokinetics and in vitro metabolism of BMS-605339: A novel HCV NS3 protease inhibitor

Author keywords

ADME; hepatic clearance; in vitro in vivo correlations (IVIVC); metabolism; preclinical pharmacokinetics; oral absorption; protease

Indexed keywords

BMS 605339; CYTOCHROME P450 3A4; ISOQUINOLINE; MULTIDRUG RESISTANCE PROTEIN; NONSTRUCTURAL PROTEIN 3; O DEMETHYLASE; PROTEINASE INHIBITOR; UNCLASSIFIED DRUG; ANTIVIRUS AGENT; BMS-605339; ISOQUINOLINE DERIVATIVE; NS3 PROTEIN, HEPATITIS C VIRUS; SULFONAMIDE; VIRUS PROTEIN;

EID: 84901277262     PISSN: 00223549     EISSN: 15206017     Source Type: Journal    
DOI: 10.1002/jps.23959     Document Type: Article
Times cited : (8)

References (29)
  • 1
    • 23944506014 scopus 로고    scopus 로고
    • Global epidemiology of hepatitis C virus infection
    • Shepard CW, Finelli L, Alter MJ,. 2005. Global epidemiology of hepatitis C virus infection. Lancet Infect Dis 5 (9): 558-567.
    • (2005) Lancet Infect Dis , vol.5 , Issue.9 , pp. 558-567
    • Shepard, C.W.1    Finelli, L.2    Alter, M.J.3
  • 2
    • 0036815962 scopus 로고    scopus 로고
    • Global epidemiology and burden of hepatitis C
    • Kim WR,. 2002. Global epidemiology and burden of hepatitis C. Microbes Infect 4: 1219-1225.
    • (2002) Microbes Infect , vol.4 , pp. 1219-1225
    • Kim, W.R.1
  • 3
    • 7044272621 scopus 로고    scopus 로고
    • Pathogenesis of hepatitis C - Associated hepatocellular carcinoma
    • Liang TJ, Heller T,. 2004. Pathogenesis of hepatitis C-Associated hepatocellular carcinoma. Gastroenterology 127 (5): S62-S71.
    • (2004) Gastroenterology , vol.127 , Issue.5
    • Liang, T.J.1    Heller, T.2
  • 7
    • 34547663275 scopus 로고    scopus 로고
    • Effect of cell differentiation and passage number on the expression of efflux proteins in wild type and vinblastine-induced Caco-2 cell lines
    • Siissalo S, Laitinen L, Koljonen M, Vellonen KS, Kortejarvi H, Urtti A, Hirvonen J, Kaukonen AM,. 2007. Effect of cell differentiation and passage number on the expression of efflux proteins in wild type and vinblastine-induced Caco-2 cell lines. Eur J Pharm Biopharm 67 (2): 548-554.
    • (2007) Eur J Pharm Biopharm , vol.67 , Issue.2 , pp. 548-554
    • Siissalo, S.1    Laitinen, L.2    Koljonen, M.3    Vellonen, K.S.4    Kortejarvi, H.5    Urtti, A.6    Hirvonen, J.7    Kaukonen, A.M.8
  • 8
    • 0041589264 scopus 로고    scopus 로고
    • Utility of Mdr1-gene deficient mice in assessing the impact of P-glycoprotein on pharmacokinetics and pharmacodynamics in drug discovery and development
    • Chen C, Liu X, Smith BJ,. 2003. Utility of Mdr1-gene deficient mice in assessing the impact of P-glycoprotein on pharmacokinetics and pharmacodynamics in drug discovery and development. Curr Drug Metab 4 (4): 272-291.
    • (2003) Curr Drug Metab , vol.4 , Issue.4 , pp. 272-291
    • Chen, C.1    Liu, X.2    Smith, B.J.3
  • 10
    • 4143108324 scopus 로고    scopus 로고
    • Substrate depletion approach for determining in vitro metabolic clearance: Time dependencies in hepatocyte and microsomal incubations
    • Jones HM, Houston JB,. 2004. Substrate depletion approach for determining in vitro metabolic clearance: Time dependencies in hepatocyte and microsomal incubations. Drug Metab Dispos 32 (9): 973-982.
    • (2004) Drug Metab Dispos , vol.32 , Issue.9 , pp. 973-982
    • Jones, H.M.1    Houston, J.B.2
  • 13
    • 0027275566 scopus 로고
    • Physiological parameters in laboratory animals and humans
    • Davies B, Morris T,. 1993. Physiological parameters in laboratory animals and humans. Pharm Res 10 (7): 1093-1095.
    • (1993) Pharm Res , vol.10 , Issue.7 , pp. 1093-1095
    • Davies, B.1    Morris, T.2
  • 16
    • 1442302325 scopus 로고    scopus 로고
    • Intestinal drug transporters: In vivo function and clinical importance
    • Kunta JR, Sinko PJ,. 2004. Intestinal drug transporters: In vivo function and clinical importance. Curr Drug Metab 5 (1): 109-124.
    • (2004) Curr Drug Metab , vol.5 , Issue.1 , pp. 109-124
    • Kunta, J.R.1    Sinko, P.J.2
  • 17
    • 0033730609 scopus 로고    scopus 로고
    • The role of P-glycoprotein in determining the oral absorption and clearance of the NK2 antagonist, UK-224,671
    • Beaumont K, Harper A, Smith DA, Bennett J,. 2000. The role of P-glycoprotein in determining the oral absorption and clearance of the NK2 antagonist, UK-224,671. Eur J Pharm Sci 12 (1): 41-50.
    • (2000) Eur J Pharm Sci , vol.12 , Issue.1 , pp. 41-50
    • Beaumont, K.1    Harper, A.2    Smith, D.A.3    Bennett, J.4
  • 18
    • 43349093221 scopus 로고    scopus 로고
    • Projection of exposure and efficacious dose prior to first-in-human studies: How successful have we been?
    • Huang C, Zheng M, Yang Z, Rodrigues AD, Marathe P,. 2008. Projection of exposure and efficacious dose prior to first-in-human studies: How successful have we been? Pharm Res 25 (4): 713-726.
    • (2008) Pharm Res , vol.25 , Issue.4 , pp. 713-726
    • Huang, C.1    Zheng, M.2    Yang, Z.3    Rodrigues, A.D.4    Marathe, P.5
  • 19
    • 33646640645 scopus 로고    scopus 로고
    • Current industrial practices of assessing permeability and P-glycoprotein interaction
    • Balimane PV, Han YH, Chong S,. 2006. Current industrial practices of assessing permeability and P-glycoprotein interaction. AAPS J 8 (1): E1-E13.
    • (2006) AAPS J , vol.8 , Issue.1
    • Balimane, P.V.1    Han, Y.H.2    Chong, S.3
  • 20
    • 84874944420 scopus 로고    scopus 로고
    • P-glycoprotein and cytochrome P450 3A act together in restricting the oral bioavailability of paclitaxel
    • Hendrikx JJMA, Lagas JS, Rosing H, Schellens JHM, Beijnen JH, Schinkel AH,. 2013. P-glycoprotein and cytochrome P450 3A act together in restricting the oral bioavailability of paclitaxel. Int J Cancer 132 (10): 2439-2447.
    • (2013) Int J Cancer , vol.132 , Issue.10 , pp. 2439-2447
    • Hendrikx, J.1    Lagas, J.S.2    Rosing, H.3    Schellens, J.H.M.4    Beijnen, J.H.5    Schinkel, A.H.6
  • 21
    • 0033798115 scopus 로고    scopus 로고
    • Mdr1 limits CYP3A metabolism in vivo
    • Lan LB, Dalton JT, Schuetz EG,. 2000. Mdr1 limits CYP3A metabolism in vivo. Mol Pharm 58 (4): 863-869.
    • (2000) Mol Pharm , vol.58 , Issue.4 , pp. 863-869
    • Lan, L.B.1    Dalton, J.T.2    Schuetz, E.G.3
  • 22
    • 0033152397 scopus 로고    scopus 로고
    • Unchanged cytochrome P450 3A (CYP3A) expression and metabolism of midazolam, triazolam, and dexamethasone in mdr(-/-) mouse liver microsomes
    • Perloff MD, von Moltke LL, Cotreau MM, Greenblatt DJ,. 1999. Unchanged cytochrome P450 3A (CYP3A) expression and metabolism of midazolam, triazolam, and dexamethasone in mdr(-/-) mouse liver microsomes. Biochem Pharmacol 57 (11): 1227-1232.
    • (1999) Biochem Pharmacol , vol.57 , Issue.11 , pp. 1227-1232
    • Perloff, M.D.1    Von Moltke, L.L.2    Cotreau, M.M.3    Greenblatt, D.J.4
  • 23
    • 80053231859 scopus 로고    scopus 로고
    • The influence of hepatic transport on the distribution volumes and mean residence time of drug in the body and the accuracy of estimating these parameters by the traditional pharmacokinetic calculations
    • Berezhkovskiy LM,. 2011. The influence of hepatic transport on the distribution volumes and mean residence time of drug in the body and the accuracy of estimating these parameters by the traditional pharmacokinetic calculations. J Pharm Sci 100 (11): 5031-5047.
    • (2011) J Pharm Sci , vol.100 , Issue.11 , pp. 5031-5047
    • Berezhkovskiy, L.M.1
  • 24
    • 77954350897 scopus 로고    scopus 로고
    • Animal models for hepatitis C and related liver disease
    • Koike K,. 2010. Animal models for hepatitis C and related liver disease. Hepatol Res 40 (1): 69-82.
    • (2010) Hepatol Res , vol.40 , Issue.1 , pp. 69-82
    • Koike, K.1
  • 26
    • 66349110823 scopus 로고    scopus 로고
    • Use of pre-clinical in vitro and in vivo pharmacokinetics for the selection of a potent hepatitis C virus protease inhibitor, boceprevir, for clinical development
    • Cheng KC,. 2009. Use of pre-clinical in vitro and in vivo pharmacokinetics for the selection of a potent hepatitis C virus protease inhibitor, boceprevir, for clinical development. Lett Drug Design Discov 6 (4): 312-318.
    • (2009) Lett Drug Design Discov , vol.6 , Issue.4 , pp. 312-318
    • Cheng, K.C.1
  • 29
    • 84857395452 scopus 로고    scopus 로고
    • Dual therapy with the nonstructural protein 5A inhibitor, daclatasvir, and the nonstructural protein 3 protease inhibitor, asunaprevir, in hepatitis C virus genotype 1b-infected null responders
    • Chayama K, Takahashi S, Toyota J, Karino Y, Ikeda K, Ishikawa H, Watanabe H, McPhee F, Hughes E, Kumada H,. 2012. Dual therapy with the nonstructural protein 5A inhibitor, daclatasvir, and the nonstructural protein 3 protease inhibitor, asunaprevir, in hepatitis C virus genotype 1b-infected null responders. Hepatology 55 (3): 742-748.
    • (2012) Hepatology , vol.55 , Issue.3 , pp. 742-748
    • Chayama, K.1    Takahashi, S.2    Toyota, J.3    Karino, Y.4    Ikeda, K.5    Ishikawa, H.6    Watanabe, H.7    McPhee, F.8    Hughes, E.9    Kumada, H.10


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.