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Volumn 4, Issue 4, 2001, Pages 471-478

The use of bioisosteric groups in lead optimization

Author keywords

Bioisosteres; Bioisosteric replacement; Bioisosteric transformation; Bioisosterism; Lead optimization

Indexed keywords

3 METHYL 5 (1 METHYL 2 PYRROLIDINYL)ISOXAZOLE; 4 [2 (7 HETEROCYCLOMETHOXYNAPHTHALEN 2 YLMETHOXY)ETHYL]BENZOIC ACID; 4 [2 [7 (4 CYCLOBUTYLTHIAZOL 2 YLMETHOXY)NAPHTHALEN 2YLMETHOXY]ETHYL]BENZOIC ACID; AMPA RECEPTOR ANTAGONIST; CLOZAPINE; COUMARIN DERIVATIVE; DOPAMINE 2 RECEPTOR STIMULATING AGENT; EPIBATIDINE; EPIBOXIDINE; LEAD; LEUKOTRIENE RECEPTOR BLOCKING AGENT; NEUROLEPTIC AGENT; NICOTINIC AGENT; PHENYLETHYLTHIAZOLETHIOUREA; RNA DIRECTED DNA POLYMERASE INHIBITOR; SULPIRIDE; THIAZOLE DERIVATIVE; THROMBIN INHIBITOR; UNCLASSIFIED DRUG; UREA DERIVATIVE;

EID: 0034924558     PISSN: 13676733     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (114)

References (33)
  • 4
    • 0030119337 scopus 로고    scopus 로고
    • Similarities in bioanalogous structural transformation patterns among various bioactive compound series
    • (1996) Biosci Biotech Biochem , vol.60 , pp. 557-566
    • Fujita, T.1
  • 24
    • 0038248584 scopus 로고    scopus 로고
    • Conjugated enynes as non-aromatic catechol bioisosteres: Synthesis, binding experiments, and computational studies of novel dopamine receptor agonists recognizing preferentially the D(3) subtype
    • (2000) J Med Chem , vol.43 , pp. 756-762
    • Hubner, H.1    Haubmann, C.2    Utz, W.3    Gmeiner, P.4
  • 33


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.