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Volumn 16, Issue 2, 2006, Pages 457-460

Design and synthesis of 3,4-dihydro-1H-[1]-benzothieno[2,3-c]pyran and 3,4-dihydro-1H-pyrano[3,4-b]benzofuran derivatives as non-nucleoside inhibitors of HCV NS5B RNA dependent RNA polymerase

Author keywords

3,4 Dihydro 1H 1 benzothieno 2,3 c pyran; 3,4 Dihydro 1H pyrano 3,4 b benzofuran; HCV polymerase inhibitors

Indexed keywords

ALKYL GROUP; ANTIVIRUS AGENT; AROMATIC COMPOUND; BENZOFURAN DERIVATIVE; FUNCTIONAL GROUP; NUCLEOTIDYLTRANSFERASE INHIBITOR; PYRAN DERIVATIVE; RNA DIRECTED RNA POLYMERASE;

EID: 27944467051     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2005.08.114     Document Type: Article
Times cited : (46)

References (21)
  • 16
    • 27944503103 scopus 로고    scopus 로고
    • note
    • HPLC Conditions: CHIRAL PACK-AD (250X20 mm) column, 10% isopropyl alcohol in heptane (0.1% TFA) eluant.
  • 17
    • 27944456975 scopus 로고    scopus 로고
    • note
    • The enantiomeric excess (ee) of the separated enantiomers was in the range of 89-100%.
  • 18
    • 27944504869 scopus 로고    scopus 로고
    • (see Ref. 5).
    • Stereochemical assignment for the isomers is tentative based on the earlier work carried out on pyrano[3,4-b]indoles (see Ref. 5).
  • 19
    • 27944454951 scopus 로고    scopus 로고
    • note
    • 50 values reported are mean values for more than two independent measurements. Each assay plate contained at least one proprietary compound that has demonstrated in vitro and in vivo activity as positive inhibitor control.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.