Synthesis and evaluation of trans 3,4-cyclopropyl l-arginine analogues as isoform selective inhibitors of nitric oxide synthase
- 16 January 2003
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry
- Vol. 11 (6) , 869-873
- https://doi.org/10.1016/s0968-0896(02)00554-0
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Synthesis of Syn and Anti Isomers of trans-Cyclopropyl ArginineThe Journal of Organic Chemistry, 2002
- Asymmetric Synthesis of Conformationally Restricted l-Arginine Analogues as Active Site Probes of Nitric Oxide SynthaseThe Journal of Organic Chemistry, 1999
- INHIBITION OF NITRIC OXIDE SYNTHASE AS A POTENTIAL THERAPEUTIC TARGETAnnual Review of Pharmacology and Toxicology, 1999
- Conformationally constrained no synthase inhibitors: Rigid analogs of L-N-iminoethylornithineBioorganic & Medicinal Chemistry Letters, 1998
- Stereoselective Synthesis of Threo and Erythro β-Hydroxy and β-Disubstituted-β-Hydroxy α-Amino AcidsThe Journal of Organic Chemistry, 1998
- Substituted N-Phenylisothioureas: Potent Inhibitors of Human Nitric Oxide Synthase with Neuronal Isoform SelectivityJournal of Medicinal Chemistry, 1997
- 1400W Is a Slow, Tight Binding, and Highly Selective Inhibitor of Inducible Nitric-oxide Synthase in Vitro and in VivoJournal of Biological Chemistry, 1997
- NO at workCell, 1994
- Nitric oxide synthases: Roles, tolls, and controlsCell, 1994
- The Cyclopropyl Group in Studies of Enzyme Mechanism and InhibitionAngewandte Chemie International Edition in English, 1988