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Volumn 17, Issue 10, 2009, Pages 3671-3679
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On the inhibition of HIV-1 protease by hydrazino-ureas displaying the N→C{double bond, long}O interaction
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Author keywords
Cyclic urea; HIV 1 protease inhibitors; N C double bond, long O interaction; Preorganization; Transition state isostere
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Indexed keywords
1 [1 BENZYL 3 (1 BENZYL 2 OXOETHYL)UREIDO]PYRROLIDINE 2 CARBOXYLIC ACID [1 (1 TERT BUTYLCARBAMOYL 2 METHYLPROPYLCARBAMOYL) 2 METHYL BUTYL]AMIDE;
1 [1 BENZYL 3 (1 BENZYL 2 OXOETHYL)UREIDO]PYRROLIDINE 2 CARBOXYLIC ACID TERT BUTYLAMIDE;
1 BENZYL 3 (1 BENZYL 2 OXOETHYL) 1 PIPERIDIN 1 YLUREA;
ANTI HUMAN IMMUNODEFICIENCY VIRUS AGENT;
HYDRAZINE DERIVATIVE;
MOZENAVIR;
PROTEINASE;
PROTEINASE INHIBITOR;
TIPRANAVIR;
UNCLASSIFIED DRUG;
UREA DERIVATIVE;
ARTICLE;
CARBON NUCLEAR MAGNETIC RESONANCE;
DRUG POTENCY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ENZYME ASSAY;
ENZYME INHIBITION;
FLUORESCENCE RESONANCE ENERGY TRANSFER;
HUMAN IMMUNODEFICIENCY VIRUS 1;
HYDROGEN BOND;
IN VITRO STUDY;
MOLECULAR INTERACTION;
MOLECULAR WEIGHT;
NONHUMAN;
PROTEINASE INHIBITION;
PROTON NUCLEAR MAGNETIC RESONANCE;
VIRUS INHIBITION;
HIV PROTEASE;
HIV PROTEASE INHIBITORS;
HUMANS;
HYDRAZINES;
HYDROGEN BONDING;
KINETICS;
UREA;
HUMAN IMMUNODEFICIENCY VIRUS 1;
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EID: 65349106612
PISSN: 09680896
EISSN: None
Source Type: Journal
DOI: 10.1016/j.bmc.2009.03.059 Document Type: Article |
Times cited : (9)
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References (45)
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