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Volumn 7, Issue 14, 2009, Pages 2872-2877
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Peptide bond mimicry by (E)-alkene and (Z)-fluoroalkene peptide isosteres: Synthesis and bioevaluation of α-helical anti-HIV peptide analogues
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Author keywords
[No Author keywords available]
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Indexed keywords
AMINO ACID SEQUENCE;
ANTI-HIV;
BIO-EVALUATION;
DIPEPTIDE;
HELIX STABILITY;
HELIX STRUCTURES;
INHIBITORY PEPTIDES;
PEPTIDE BONDS;
AMINO ACIDS;
BINDING SITES;
HYDROGEN;
HYDROGEN BONDS;
OLEFINS;
ORGANIC ACIDS;
AMINES;
ALKENE;
ANTI HUMAN IMMUNODEFICIENCY VIRUS AGENT;
FLUORINE;
PEPTIDE;
AMINO ACID SEQUENCE;
ARTICLE;
BIOMIMETICS;
CHEMISTRY;
DRUG EFFECT;
HUMAN IMMUNODEFICIENCY VIRUS;
HYDROGEN BOND;
MOLECULAR GENETICS;
PROTEIN SECONDARY STRUCTURE;
STEREOISOMERISM;
SYNTHESIS;
ALKENES;
AMINO ACID SEQUENCE;
ANTI-HIV AGENTS;
BIOMIMETICS;
FLUORINE;
HIV;
HYDROGEN BONDING;
MOLECULAR SEQUENCE DATA;
PEPTIDES;
PROTEIN STRUCTURE, SECONDARY;
STEREOISOMERISM;
HUMAN IMMUNODEFICIENCY VIRUS;
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EID: 67650462471
PISSN: 14770520
EISSN: None
Source Type: Journal
DOI: 10.1039/b907983a Document Type: Article |
Times cited : (112)
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References (28)
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