Analogues of N-terminal truncated synthetic peptide fragments derived from RANTES inhibit HIV-1 infectivity

Bioorganic and Medicinal Chemistry Letters

Volumn 16, Issue 1, 2006, Pages 93-95

  Ramnarine, Emabelle J ^a,d   DeVico, Anthony L ^b   Vigil Cruz, Sandra C ^a,c  

^a UNIVERSITY OF CONNECTICUT   (United States)

^b UNIVERSITY OF MARYLAND   (United States)

^c UNIVERSITY OF KANSAS   (United States)

^d BOSTON SCIENTIFIC CORPORATION   (United States)

Author keywords

Chemokine; HIV; Peptide; RANTES; Solid phase synthesis

Indexed keywords

ANTIVIRUS AGENT; RANTES; SYNTHETIC PEPTIDE;

AMINO TERMINAL SEQUENCE; ANTIVIRAL ACTIVITY; ARTICLE; DRUG DESIGN; DRUG DETERMINATION; DRUG EFFECT; DRUG EFFICACY; DRUG INHIBITION; DRUG STRUCTURE; DRUG SYNTHESIS; HUMAN IMMUNODEFICIENCY VIRUS 1; INFECTION PREVENTION; MOLECULAR MIMICRY; STRUCTURE ACTIVITY RELATION; VIRUS INFECTIVITY; VIRUS INHIBITION; VIRUS TRANSMISSION;

ANTI-HIV AGENTS; CELL LINE; CHEMISTRY, PHARMACEUTICAL; DRUG DESIGN; HIV-1; HUMANS; PEPTIDE FRAGMENTS; PEPTIDES; PROTEIN STRUCTURE, TERTIARY; RANTES; STRUCTURE-ACTIVITY RELATIONSHIP;

HUMAN IMMUNODEFICIENCY VIRUS 1;

EID: 27744473682     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2005.09.044     Document Type: Article

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