Synthesis and evaluation of trans 3,4-cyclopropyl L-arginine analogues as isoform selective inhibitors of nitric oxide synthase

Bioorganic and Medicinal Chemistry

Volumn 11, Issue 6, 2003, Pages 869-873

  Fishlock, Dan ^a   Perdicakis, Basil ^a   Montgomery, Heather J ^a   Guillemette, J Guy ^a   Jervis, Eric ^a   Lajoie, Gilles A ^a  

^a UNIVERSITY OF WATERLOO   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

3,4 CYCLOPROPYL N (1 IMIOETHYL)ORNITHINE; 3,4 CYCLOPROPYLARGININE; NITRIC OXIDE SYNTHASE; NITRIC OXIDE SYNTHASE INHIBITOR; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHIRALITY; COLUMN CHROMATOGRAPHY; COMPETITIVE INHIBITION; CRYSTALLIZATION; DRUG BINDING; DRUG POTENTIATION; DRUG PURIFICATION; DRUG SCREENING; DRUG SELECTIVITY; DRUG SYNTHESIS; ENZYME INHIBITION; PROTON NUCLEAR MAGNETIC RESONANCE; REDUCTION; STEREOCHEMISTRY; THIN LAYER CHROMATOGRAPHY;

ARGININE; CYCLOPROPANES; ENZYME INHIBITORS; ESCHERICHIA COLI; HUMANS; INDICATORS AND REAGENTS; ISOENZYMES; ISOMERISM; KINETICS; MOLECULAR CONFORMATION; NITRIC OXIDE SYNTHASE; NITRIC OXIDE SYNTHASE TYPE I; NITRIC OXIDE SYNTHASE TYPE II; NITRIC OXIDE SYNTHASE TYPE III;

EID: 0037333459     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0968-0896(02)00554-0     Document Type: Article

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