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Volumn 18, Issue 5, 2008, Pages 1577-1582

Potent, exceptionally selective, orally bioavailable inhibitors of TNF-α Converting Enzyme (TACE): Novel 2-substituted-1H-benzo[d]imidazol-1-yl)methyl)benzamide P1′ substituents

Author keywords

Matrix metalloprotease; MMP; TACE; TNF modulator; TNF Converting Enzyme

Indexed keywords

ADAM PROTEIN; BENZAMIDE DERIVATIVE; HYDROXAMIC ACID DERIVATIVE; INTERSTITIAL COLLAGENASE; LIPOPOLYSACCHARIDE; TUMOR NECROSIS FACTOR ALPHA; TUMOR NECROSIS FACTOR ALPHA CONVERTING ENZYME INHIBITOR;

EID: 39849103710     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2008.01.075     Document Type: Article
Times cited : (38)

References (20)
  • 16
    • 0035945983 scopus 로고    scopus 로고
    • 1H NMR and mass spectral data. 2-(1,1-difluoro-ethyl)-1H-benzo[d]imidazole and 2-(1-fluoro-1-methyl-ethyl)-1H-benzo[d]imidazole used to prepare compounds 28, 30, and 31 were synthesized from o-phenylenediamine and the corresponding carboxylic acids, 2,2-difluoropropanoic acid, and 2-fluoroisobutyric acid, via two-step procedure involving BOP reagent coupling to form the mono-amide and cyclization with AcOH. For a similar benzimidazole cyclization procedure see
    • 1H NMR and mass spectral data. 2-(1,1-difluoro-ethyl)-1H-benzo[d]imidazole and 2-(1-fluoro-1-methyl-ethyl)-1H-benzo[d]imidazole used to prepare compounds 28, 30, and 31 were synthesized from o-phenylenediamine and the corresponding carboxylic acids, 2,2-difluoropropanoic acid, and 2-fluoroisobutyric acid, via two-step procedure involving BOP reagent coupling to form the mono-amide and cyclization with AcOH. For a similar benzimidazole cyclization procedure see. Fonseca T., Gigante B., and Gilchrist T.L. Tetrahedron 57 (2001) 1793
    • (2001) Tetrahedron , vol.57 , pp. 1793
    • Fonseca, T.1    Gigante, B.2    Gilchrist, T.L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.