메뉴 건너뛰기




Volumn 1, Issue 2, 2010, Pages 50-53

Strategic use of plasma and microsome binding to exploit in vitro clearance in early drug discovery

Author keywords

ADME parameters; clearance; dose; fraction unbound; microsome binding; Plasma binding

Indexed keywords

ARTICLE; DRUG CLEARANCE; DRUG DISTRIBUTION; DRUG HALF LIFE; HUMAN; LIVER BLOOD FLOW; LIVER MICROSOME; MICROSOME; PLASMA; PRIORITY JOURNAL;

EID: 77956627250     PISSN: None     EISSN: 19485875     Source Type: Journal    
DOI: 10.1021/ml900012h     Document Type: Article
Times cited : (28)

References (10)
  • 2
    • 60749133620 scopus 로고    scopus 로고
    • Methods for predicting in vivo pharmacokinetics using data from in vitro assays
    • Houston, J. B.; Galetin, A. Methods for predicting in vivo pharmacokinetics using data from in vitro assays Curr. Drug Metab. 2008, 9, 940-951
    • (2008) Curr. Drug Metab. , vol.9 , pp. 940-951
    • Houston, J.B.1    Galetin, A.2
  • 3
    • 1542362349 scopus 로고    scopus 로고
    • Automated high throughput ADME assays for metabolic stability and cytochrome P450 inhibition profiling of combinatorial libraries
    • Jenkins, K. M.; Angeles, R.; Quintos, M. T.; Xu, R.; Kassel, D. B.; Rourick, R. A. Automated high throughput ADME assays for metabolic stability and cytochrome P450 inhibition profiling of combinatorial libraries J. Pharm. Biomed. Anal. 2004, 34, 989-1004
    • (2004) J. Pharm. Biomed. Anal. , vol.34 , pp. 989-1004
    • Jenkins, K.M.1    Angeles, R.2    Quintos, M.T.3    Xu, R.4    Kassel, D.B.5    Rourick, R.A.6
  • 4
    • 0842332512 scopus 로고    scopus 로고
    • High-throughput screening for stability and inhibitory activity of compounds toward cytochrome P450-mediated metabolism
    • Ansede, J. H.; Thakker, D. R. High-throughput screening for stability and inhibitory activity of compounds toward cytochrome P450-mediated metabolism J. Pharm. Sci. 2004, 932, 239-255
    • (2004) J. Pharm. Sci. , vol.932 , pp. 239-255
    • Ansede, J.H.1    Thakker, D.R.2
  • 6
    • 0032733974 scopus 로고    scopus 로고
    • Prediction of human clearance of twenty-nine drugs from hepatic microsomal intrinsic clearance data: An examination of in vitro half-life approach and nonspecific binding to microsomes
    • Obach, R. S. Prediction of human clearance of twenty-nine drugs from hepatic microsomal intrinsic clearance data: An examination of in vitro half-life approach and nonspecific binding to microsomes Drug Metab. Dispos. 1999, 27, 1350-1359
    • (1999) Drug Metab. Dispos. , vol.27 , pp. 1350-1359
    • Obach, R.S.1
  • 9
    • 40849096159 scopus 로고    scopus 로고
    • Drug lipophilicity and microsomal protein concentration as determinants in the prediction of the fraction unbound in microsomal incubations
    • DOI 10.1124/dmd.107.018713
    • Gertz, M.; Kilford, P. J.; Houston, J. B.; Galetin, A. Drug lipophilicity and microsomal protein concentration as determinants in the prediction of the fraction unbound in microsomal incubations Drug Metab. Dispos. 2008, 36, 535-542 (Pubitemid 351397979)
    • (2008) Drug Metabolism and Disposition , vol.36 , Issue.3 , pp. 535-542
    • Gertz, M.1    Kilford, P.J.2    Houston, J.B.3    Galetin, A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.