Inhibition of HIV-1 envelope-mediated fusion by synthetic batzelladine analogues

Journal of Natural Products

Volumn 67, Issue 8, 2004, Pages 1319-1324

  Bewley, Carole A ^a   Ray, Satyajit ^a   Cohen, Frederick ^b   Collins, Shawn K ^b   Overman, Larry E ^b  

^a NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BATZELLADINE DERIVATIVE; BATZELLADINE F; CD4 ANTIGEN; CRAMBESCIDIN; GLYCOPROTEIN GP 120; NATURAL PRODUCT; UNCLASSIFIED DRUG;

ANTIVIRAL ACTIVITY; ARTICLE; BINDING SITE; CHEMICAL MODEL; CHEMICAL STRUCTURE; CRYSTAL STRUCTURE; HERPES SIMPLEX VIRUS; HUMAN IMMUNODEFICIENCY VIRUS; HUMAN IMMUNODEFICIENCY VIRUS 1; IC 50; POLYCYCLIC GUANIDINE MOTIF; PROTEIN MOTIF; STRUCTURE ACTIVITY RELATION; VIRUS ADSORPTION; VIRUS ENVELOPE; VIRUS INHIBITION;

ALKALOIDS; ANTI-HIV AGENTS; ANTIGENS, CD4; GUANIDINE; GUANIDINES; HIV ENVELOPE PROTEIN GP120; HIV-1; MODELS, MOLECULAR; MOLECULAR STRUCTURE; STRUCTURE-ACTIVITY RELATIONSHIP;

HERPES; HUMAN IMMUNODEFICIENCY VIRUS; HUMAN IMMUNODEFICIENCY VIRUS 1; SIMPLEXVIRUS;

EID: 4344665845     PISSN: 01633864     EISSN: None     Source Type: Journal    
DOI: 10.1021/np049958o     Document Type: Article

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