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Reviews on biosynthesis and biological roles of nitric oxide:
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Chemical biology of nitric oxide: Insights into regulatory, cytotoxic and cytoprotective mechanisms of nitric oxide
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(a) Wink, D. A.; Mitchell, J. B. Chemical biology of nitric oxide: insights into regulatory, cytotoxic and cytoprotective mechanisms of nitric oxide. Free Radical Biol. Med. 1998, 25, 434-456.
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(b) Gow, A. J.; Ischiropoulos, H. Nitric oxide chemistry and cellular signaling. J. Cell. Physiol. 2001, 187, 277-282.
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Gow, A.J.1
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The pharmacology of nitric oxide in the peripheral nervous system of blood vessels
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(c) Toda, N.; Okamura, T. The pharmacology of nitric oxide in the peripheral nervous system of blood vessels. Pharmacol. Rev. 2003, 55, 271-324.
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(d) Shapoval, L. N. Nitric oxide: involvement in the nervous control of cardiovascular function. Neurophysiology 2004, 36, 466-478.
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Neurophysiology
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(e) Bruckdorfer, R. The basics about nitric oxide. Mol. Aspects Med. 2005, 26, 3-31.
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Nitric oxide synthase: Models and mechanisms
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(a) Groves, J. T.; Wang, C. C.-Y. Nitric oxide synthase: models and mechanisms. Curr. Opin. Chem. Biol. 2000, 4, 687-695.
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Groves, J.T.1
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(b) Aktan, F. iNOS-mediated nitric oxide production and its regulation. Life Sci. 2004, 75, 639-653.
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Life Sci
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(a) Alderton, W. K.; Cooper, C. E.; Knowles, R. G. Nitric oxide synthases: structure, function and inhibition. Biochem. J. 2001, 357, 593-615.
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Use of nitric oxide synthase inhibitors for the treatment of inflammatory disease and pain
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(b) Cheshire, D. R. Use of nitric oxide synthase inhibitors for the treatment of inflammatory disease and pain. Drugs 2001, 4, 795-803.
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(c) Vallance, P. Nitric oxide: therapeutic opportunities. Fundam. Clin. Pharmacol. 2003, 17, 1-10.
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Current trends in QSAR on NO donors and inhibitors of nitric oxide synthase (NOS)
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(a) Kontogiorgis, C. A.; Hadjipavlou-Litina, D. Current trends in QSAR on NO donors and inhibitors of nitric oxide synthase (NOS). Med. Res. Rev. 2002, 22, 385-418.
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Blocking NO synthesis: How, where and why?
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(b) Vallance, P.; Leiper, J. Blocking NO synthesis: how, where and why? Nat. Rev. Drug Discovery 2002, 1, 939-950.
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Computational studies of competitive inhibitors of nitric oxide synthase (NOS) enzymes: Towards the development of powerful and isoform-selective inhibitors
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(c) Tafi, A.; Angeli, L.; Venturini, G.; Travagli, M.; Corelli, F.; Botta, M. Computational studies of competitive inhibitors of nitric oxide synthase (NOS) enzymes: towards the development of powerful and isoform-selective inhibitors. Curr. Med. Chem. 2007, 13, 1929-1946.
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Tafi, A.1
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Corelli, F.5
Botta, M.6
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Structure and activity of NO synthase inhibitors specific to the L-arginine binding site
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Proskuryakov, S. Ya.; Konoplyannikov, A. G.; Skvortsov, V. G.; Mandrugin, A. A.; Fedoseev, V. M. Structure and activity of NO synthase inhibitors specific to the L-arginine binding site. Biochemistry (Moscow) 2005, 70, 8-23.
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For 1 and amidines: (a) Oplinger, J. A, Garvey, E. P, Furfine, E. S, Shearer, B. G, Collins, J. L.Acetamidine Derivatives and Their Use as Inhibitors for Nitric Oxide Synthase. International patent WO 9619440, 1996
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For 1 and amidines: (a) Oplinger, J. A.; Garvey, E. P.; Furfine, E. S.; Shearer, B. G.; Collins, J. L.Acetamidine Derivatives and Their Use as Inhibitors for Nitric Oxide Synthase. International patent WO 9619440, 1996.
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1400W is a slow, tight binding and highly selective inhibitor of inducible nitric-oxide synthase in vitro and in vivo
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(b) Garvey, E. P.; Oplinger, J. A.; Furfine, E. S.; Kiff, R. J.; Laszlo, F.; Whittle, B. J. R.; Knowles, R. G. 1400W is a slow, tight binding and highly selective inhibitor of inducible nitric-oxide synthase in vitro and in vivo. J. Biol. Chem. 1997, 272, 4959-4963.
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Whittle, B.J.R.6
Knowles, R.G.7
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Young, R. J.; Beams, R. M.; Carter, K.; Clark, H. A. R.; Coe, D. M.; Chambers, C. L.; Davies, P. I.; Dawson, J.; Drysdale, M. J.; Franzman, K. W.; French, C.; Hodgson, S. T.; Hodson, H. F.; Kleanthous, S.; Rider, P.; Sanders, D.; Sawyer, D. A.; Scott, K. J.; Shearer, B. G.; Stocker, R.; Smith, S.; Tackley, M. C.; Knowles, R. G. Inhibition of inducible nitric oxide synthase by acetamidine derivatives of hetero-substituted lysine and homolysine. Bioorg. Med. Chem. Lett. 2000, 10, 597-600.
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(d) Young, R. J.; Beams, R. M.; Carter, K.; Clark, H. A. R.; Coe, D. M.; Chambers, C. L.; Davies, P. I.; Dawson, J.; Drysdale, M. J.; Franzman, K. W.; French, C.; Hodgson, S. T.; Hodson, H. F.; Kleanthous, S.; Rider, P.; Sanders, D.; Sawyer, D. A.; Scott, K. J.; Shearer, B. G.; Stocker, R.; Smith, S.; Tackley, M. C.; Knowles, R. G. Inhibition of inducible nitric oxide synthase by acetamidine derivatives of hetero-substituted lysine and homolysine. Bioorg. Med. Chem. Lett. 2000, 10, 597-600.
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Minimal amidine structure for inhibition of nitric oxide biosynthesis
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(e) Billacka, B.; Hecka, D. E.; Porterfield, D. M.; Malchowc, R. P.; Smithd, P. J. S.; Gardnera, C. R.; Laskina, D. L.; Laskine, J. D. Minimal amidine structure for inhibition of nitric oxide biosynthesis. Biochem. Pharmacol. 2001, 61, 1581-1586.
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Gardnera, C.R.6
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Bicyclic amidine inhibitors of nitric oxide synthase: Discovery of perhydro-iminopyrindine and perhydro-iminoquinoline as potent, orally active inhibitors of inducible nitric oxide synthase
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(f) Guthikonda, R. N.; Shah, S. K.; Pacholok, S. G.; Humes, J. L.; Mumford, R. A.; Grant, S. K.; Chabin, R. M.; Green, B G.; Tsou, N.; Ball, R.; Fletcher, D. S.; Luell, S.; MacIntyred, D. E.; MacCossa, M. Bicyclic amidine inhibitors of nitric oxide synthase: discovery of perhydro-iminopyrindine and perhydro-iminoquinoline as potent, orally active inhibitors of inducible nitric oxide synthase. Bioorg. Med. Chem. Lett. 2005, 15, 1997-2001.
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Bioorg. Med. Chem. Lett
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Chabin, R.M.7
Green, B.G.8
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Fletcher, D.S.11
Luell, S.12
MacIntyred, D.E.13
MacCossa, M.14
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Novel and orally bioavailable inducible nitric oxide synthase inhibitors: Synthesis and evaluation of optically active 4,5- dialkyl-2-iminoselenazolidine derivatives
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(g) Ueda, S.; Terauchi, H.; Suzuki, K.; Yano, A.; Matsumoto, M.; Kubo, T.; Minato, H.; Arai, Y.; Tsujic, J.; Watanabe, N. Novel and orally bioavailable inducible nitric oxide synthase inhibitors: synthesis and evaluation of optically active 4,5- dialkyl-2-iminoselenazolidine derivatives. Bioorg. Med. Chem. Lett. 2005, 15, 1361-1366.
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Zhu, Y.; Nikolic, D.; Van Breemen, R. B.; Silverman, R. B. Mechanism of inactivation of inducible nitric oxide synthase by amidines. Irreversible enzyme inactivation without inactivator modification. J. Am. Chem. Soc. 2005, 127, 858-868.
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S-2-Naphthylmethyl thioace- timidate hydrobromide: A new odorleess reagent for the mild synthesis of substituted acetamidines
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Shearer, B. G.; Oplinger, J. A.; Lee, S. S-2-Naphthylmethyl thioace- timidate hydrobromide: a new odorleess reagent for the mild synthesis of substituted acetamidines. Tetrahedron Lett. 1997, 38, 179-182.
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Chen, G.; Lean, J. T.; Alcala, M.; Mallouk, T. E. Modular synthesis of π-acceptor cyclophanes derived from 1,4,5,8-naphthalenetetracar- boxylic diimide and 1,5-dinitronaphthalene. J. Org. Chem. 2001, 66, 3027-3034.
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Lee, H.; Raman, C. S.; Martàsek, P.; Masters, B. S. S.; Poulos, T. L. Crystallographic studies on endothelial nitric oxide and mechanism based inhibitors. Biochemistry 2001, 40, 5399-5406.
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