Origin of the inhibitory activity of 4-O-substituted sialic derivatives of human parainfluenza virus

Glycoconjugate Journal

Volumn 29, Issue 4, 2012, Pages 231-237

  Itoh, Yuji ^a   Sando, Ayumi ^a   Ikeda, Kiyoshi ^b   Suzuki, Takashi ^c   Tokiwa, Hiroaki ^a  

^a RIKKYO UNIVERSITY   (Japan)

^b HIROSHIMA INTERNATIONAL UNIVERSITY   (Japan)

^c UNIVERSITY OF SHIZUOKA   (Japan)

Author keywords

Anti hPIV drug; CH interaction; First principles calculation; Fragment molecular orbital; Human parainfluenza; Neu5Ac

Indexed keywords

5 ACETAMIDO 2,6 ANHYDRO 3,5 DIDEOXY DEXTRO GALACTO DEXTRO GLYCERO NON 2 ENONIC ACID; HN PROTEIN; INFLUENZA VIRUS HEMAGGLUTININ; SIALIC ACID DERIVATIVE; UNCLASSIFIED DRUG; ZANAMIVIR;

ANTIVIRAL ACTIVITY; ARTICLE; BINDING AFFINITY; CONTROLLED STUDY; CRYSTAL STRUCTURE; DRUG CONFORMATION; DRUG POTENCY; DRUG STRUCTURE; HYDROGEN BOND; HYDROPHOBICITY; NONHUMAN; PARAINFLUENZA VIRUS; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN BINDING; PROTEIN INTERACTION;

ANTIVIRAL AGENTS; BINDING SITES; HN PROTEIN; HUMANS; MODELS, MOLECULAR; N-ACETYLNEURAMINIC ACID; PARAINFLUENZA VIRUS 1, HUMAN; ZANAMIVIR;

PARAINFLUENZA VIRUS;

EID: 84862532914     PISSN: 02820080     EISSN: 15734986     Source Type: Journal    
DOI: 10.1007/s10719-012-9384-3     Document Type: Article

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