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Volumn 176, Issue 1-2, 2002, Pages 51-57

Quantitative structure-activity relationships for inducers of cytochromes P450 and nuclear receptor ligands involved in P450 regulation within the CYP1, CYP2, CYP3 and CYP4 families

Author keywords

Cytochromes; Homology modelling studies; Nuclear receptor ligands; Quantitative structure activity relationships

Indexed keywords

CELL NUCLEUS RECEPTOR; CYTOCHROME P450; CYTOCHROME P450 1; CYTOCHROME P450 2; CYTOCHROME P450 3; CYTOCHROME P450 4; ESTROGEN RECEPTOR; LIGAND; PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR; UNCLASSIFIED DRUG;

EID: 0036643983     PISSN: 0300483X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0300-483X(02)00135-X     Document Type: Article
Times cited : (41)

References (29)
  • 10
    • 0030873260 scopus 로고    scopus 로고
    • Quantitative structure-activity relationships (QSARs) in substrates, inhibitors and inducers of cytochrome P4501 (CYP1)
    • (1997) Drug Metabolism Reviews , vol.29 , pp. 589-650
    • Lewis, D.F.V.1
  • 14
    • 0031732405 scopus 로고    scopus 로고
    • Molecular modelling of the rat peroxisome proliferator-activated receptor α (rPPARα) by homology with the human retinoic acid X receptor α (hRXRα) and investigation of peroxisome proliferator binding interactions: QSARs
    • (1998) Toxicology in Vitro , vol.12 , pp. 619-632
    • Lewis, D.F.V.1    Lake, B.G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.