Substituted N-phenylisothioureas: potent inhibitors of human nitric oxide synthase with neuronal isoform selectivity
- J Med Chem. 1997 Jun 6;40(12):1901-5. doi: 10.1021/jm960785c.
- 1. Glaxo Wellcome Research and Development, Research Triangle Park, North Carolina 27709, USA. [email protected]
S-Ethyl N-phenylisothiourea (4) has been found to be a potent inhibitor of both the human constitutive and inducible isoforms of nitric oxide synthase. A series of substituted N-phenylisothiourea analogues was synthesized to investigate the structure-activity relationship of this class of inhibitor. Each analogue was evaluated for human isoform selectivity. One analogue, S-ethyl N-[4-(trifluoromethyl)phenyl]isothiourea (39), exhibited 115-fold and 29-fold selectivity for the neuronal isoform versus the inducible and endothelial derived constitutive isoforms, respectively. Studies have shown the substituted N-phenylisothiourea 39 binds competitively with L-arginine.
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Cat. No.Product NameDescriptionTargetResearch Area
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target: NO SynthaseResearch Areas: Neurological Disease