Journal of Medicinal Chemistry · 2004 · 42 citations · 10 references
Molecular PharmacologyMedicinal Chemistry4-Piperidine CarbamateBioorganic ChemistryInhibitory ActivityBiochemistryNitrogen SubstitutionPyridine RingNatural SciencesMedicineReactive Nitrogen SpecieMechanism Of ActionSimple N-methylationChemical BiologyPharmacologyPharmaceutical ChemistryNitrosative StressDrug Discovery
4-Methylaminopyridine (4-MAP) (5) is a potent but nonselective nitric oxide synthase (NOS) inhibitor. While simple N-methylation in this series results in poor activity, more elaborate N-substitution such as with 4-piperidine carbamate or amide results in potent and selective inducible NOS inhibition. Evidently, a flipping of the pyridine ring between these new inhibitors allows the piperidine to interact with different residues and confer excellent selectivity.
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Species Distributions, Land Values, and Efficient Conservation
Amy W. Ando, Jeffrey D. Camm, Stephen Polasky et al. · Science · 1998 · 816 citations
Conservation Management System, Biodiversity, Engineering +14
Structure of Nitric Oxide Synthase Oxygenase Dimer with Pterin and Substrate
Brian R. Crane, A.S. Arvai, Dipak Ghosh et al. · Science · 1998 · 664 citations