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Volumn 6, Issue 5, 1998, Pages 595-604

Structure-activity relationship of HIV-1 protease inhibitors containing AHPBA. Part III: Modification of P2 site

Author keywords

[No Author keywords available]

Indexed keywords

PROTEINASE INHIBITOR;

EID: 0031746876     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0968-0896(98)00004-2     Document Type: Article
Times cited : (11)

References (29)
  • 26
    • 0344277616 scopus 로고    scopus 로고
    • note
    • Ghosh et al. reported that cyclic urethanes with 3S-configuration were more potent than ones with 3R-configuration (see Ref. 6).
  • 27
    • 0344709638 scopus 로고    scopus 로고
    • The detailed computational studies will be reported elsewhere
    • The detailed computational studies will be reported elsewhere.
  • 29
    • 0344277615 scopus 로고    scopus 로고
    • note
    • The conclusion described by Kempf et al. was that ortho is not a suitable position for interaction with Asp 29 or 30 (see Ref. 7b). But the hydrogen bond interaction between the carbonyls and the ortho hydroxyl groups is presumed to be more important than aforesaid interaction.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.