-
1
-
-
0028815563
-
Nitric Oxide: A new paradigm for second messengers
-
For reviews, see: (a) Kerwin, J. F., Jr.; Lancaster, J. R.; Feldman, P. L., Jr. Nitric Oxide: A new paradigm for second messengers. J. Med. Chem. 1995, 38, 4343-4362.
-
(1995)
J. Med. Chem.
, vol.38
, pp. 4343-4362
-
-
Kerwin J.F., Jr.1
Lancaster, J.R.2
Feldman P.L., Jr.3
-
2
-
-
0030040255
-
Selective Pharmacological Inhibition of distinct nitric oxide synthase isoforms
-
(b) Southan, G. J.; Szabó, C. Selective Pharmacological Inhibition of distinct nitric oxide synthase isoforms. Biochem. Pharmacol. 1996, 51, 383-394.
-
(1996)
Biochem. Pharmacol.
, vol.51
, pp. 383-394
-
-
Southan, G.J.1
Szabó, C.2
-
3
-
-
0035425503
-
Nitric oxide synthases: Structure, function and inhibition
-
(c) Alderton, W. K.; Cooper, C. E.; Knowles, R. G. Nitric Oxide Synthases: Structure, Function and Inhibition. Biochem. J. 2001, 357, 593-615.
-
(2001)
Biochem. J.
, vol.357
, pp. 593-615
-
-
Alderton, W.K.1
Cooper, C.E.2
Knowles, R.G.3
-
4
-
-
0029913577
-
Insights into the role of nitric oxide in inflammatory arthritis
-
Cochran, F. R.; Selph, J.; Sherman, P. Insights into the role of nitric oxide in inflammatory arthritis. Med. Res. Rev. 1996, 16, 547-563.
-
(1996)
Med. Res. Rev.
, vol.16
, pp. 547-563
-
-
Cochran, F.R.1
Selph, J.2
Sherman, P.3
-
5
-
-
0000255875
-
Inhibitors of nitric oxide synthase in inflammatory arthritis
-
Boughton-Smith, N. K.; Tinker, A. C. Inhibitors of Nitric Oxide Synthase in inflammatory arthritis. IDrugs 1998, 1, 321-334.
-
(1998)
IDrugs
, vol.1
, pp. 321-334
-
-
Boughton-Smith, N.K.1
Tinker, A.C.2
-
8
-
-
0028173010
-
G-(1-iminoethyl)lysine: A selective inhibitor of inducible nitric oxide synthase
-
G-(1-iminoethyl)lysine: A selective inhibitor of inducible nitric oxide synthase. J. Med. Chem. 1994, 37, 3886-3888.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 3886-3888
-
-
Moore, W.M.1
Webber, R.K.2
Jerome, G.M.3
Tjoeng, F.S.4
Misko, T.P.5
Currie, M.G.6
-
9
-
-
0002427551
-
Nitric Oxide and septic shock
-
Ignarro, L. J., Ed.; Academic Press: San Diego
-
Ruetten, H.; Thiemermann, C.; Nitric Oxide and septic shock. In Nitric Oxide; Ignarro, L. J., Ed.; Academic Press: San Diego, 2000; pp 747-757.
-
(2000)
Nitric Oxide
, pp. 747-757
-
-
Ruetten, H.1
Thiemermann, C.2
-
10
-
-
0026641944
-
Aminoguanidine, a novel inhibitor of nitric oxide formation, prevents diabetic vascular dysfunction
-
(a) Corbett, A.; Tilton, R. G.; Chang, K.; Hasan, K. S.; Ido, Y.; Wang, J. L.; Sweetland, M. A.; Lancaster, J. R.; Williamson, J. R.; McDaniel, M. L.: Aminoguanidine, a novel inhibitor of nitric oxide formation, prevents diabetic vascular dysfunction. Diabetes 1992, 41, 552-556.
-
(1992)
Diabetes
, vol.41
, pp. 552-556
-
-
Corbett, A.1
Tilton, R.G.2
Chang, K.3
Hasan, K.S.4
Ido, Y.5
Wang, J.L.6
Sweetland, M.A.7
Lancaster, J.R.8
Williamson, J.R.9
McDaniel, M.L.10
-
11
-
-
0028893884
-
Aminoguanidine is an isoform selective, mechanism based inactivator of nitric oxide synthase
-
(b) Wolff, D. J.; Lubeskie, A. Aminoguanidine is an isoform selective, mechanism based inactivator of nitric oxide synthase. Arch. Biochem. Biophys. 1995, 316, 290-301.
-
(1995)
Arch. Biochem. Biophys.
, vol.316
, pp. 290-301
-
-
Wolff, D.J.1
Lubeskie, A.2
-
12
-
-
0027374229
-
Inhibition of nitric oxide formation by guanidines
-
Hasan, K.; Heesen, B. J.; Corbett, J. A.; McDaniel, M. L.; Chang, K.; Allison, W.; Wolfenbuttel, B. H. R.; Williamson, J. R.; Tilton, R. G. Inhibition of nitric oxide formation by guanidines. Eur. J. Pharmacol. 1993, 249, 101-106.
-
(1993)
Eur. J. Pharmacol.
, vol.249
, pp. 101-106
-
-
Hasan, K.1
Heesen, B.J.2
Corbett, J.A.3
McDaniel, M.L.4
Chang, K.5
Allison, W.6
Wolfenbuttel, B.H.R.7
Williamson, J.R.8
Tilton, R.G.9
-
13
-
-
0028089793
-
Potent and selective inhibition of human nitric oxide synthases: Inhibition by non-amino acid isothioureas
-
(a) Garvey E. P.; Oplinger, J. A.; Tanoury, G. J.; Sherman, P. A.; Fowler, M.; Marshall, S.; Harmon, M. F.; Paith, J. E.; Furfine, E. S. Potent and selective inhibition of human nitric oxide synthases: inhibition by non-amino acid isothioureas. J. Biol. Chem. 1994, 269, 26669-26676.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 26669-26676
-
-
Garvey, E.P.1
Oplinger, J.A.2
Tanoury, G.J.3
Sherman, P.A.4
Fowler, M.5
Marshall, S.6
Harmon, M.F.7
Paith, J.E.8
Furfine, E.S.9
-
14
-
-
0028848015
-
Isothioureas: Potent inhibitors of nitric oxide synthases with variable isoform selectivity
-
(b) Southan, G. J.; Szabó, C.; Thiemermann, C. Isothioureas: potent inhibitors of nitric oxide synthases with variable isoform selectivity. Br. J. Pharmacol. 1995, 114, 510-516.
-
(1995)
Br. J. Pharmacol.
, vol.114
, pp. 510-516
-
-
Southan, G.J.1
Szabó, C.2
Thiemermann, C.3
-
15
-
-
0028847367
-
Amidines are potent inhibitors of nitric oxide synthases: Preferential inhibition of the inducible isoform
-
(a) Southan, G. J.; Szabó, C.; O'Connor, M. P.; Salzman, A. L.; Thiemermann, C. Amidines are potent inhibitors of nitric oxide synthases: Preferential inhibition of the inducible isoform. Eur. J. Pharmacol. 1995, 291, 311-318.
-
(1995)
Eur. J. Pharmacol.
, vol.291
, pp. 311-318
-
-
Southan, G.J.1
Szabó, C.2
O'Connor, M.P.3
Salzman, A.L.4
Thiemermann, C.5
-
16
-
-
0029738974
-
Inhibitors of human nitric oxide synthase with the carbamidine moiety as a common structural element
-
(b) Moore, W. M.; Webber, R. K.; Fok, K. F.; Jerome, G. M.; Kornmeier, C. M.; Tjeong, F. S.; Currie M. G. Inhibitors of human nitric oxide synthase with the carbamidine moiety as a common structural element. Bioorg. Med. Chem. 1996, 4, 1559-1564.
-
(1996)
Bioorg. Med. Chem.
, vol.4
, pp. 1559-1564
-
-
Moore, W.M.1
Webber, R.K.2
Fok, K.F.3
Jerome, G.M.4
Kornmeier, C.M.5
Tjeong, F.S.6
Currie, M.G.7
-
17
-
-
0031040613
-
1400W is a slow, tight binding inhibitor of inducible nitric oxide synthesis in vitro and in vivo
-
(c) 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 inhibitor of inducible nitric oxide synthesis in vitro and in vivo. J. Biol. Chem. 1997, 21, 4959-4963.
-
(1997)
J. Biol. Chem.
, vol.21
, pp. 4959-4963
-
-
Garvey, E.P.1
Oplinger, J.A.2
Furfine, E.S.3
Kiff, R.J.4
Laszlo, F.5
Whittle, B.J.R.6
Knowles, R.G.7
-
18
-
-
0035938426
-
3,4-Dihydro-1-isoquinolinamines: A novel class of Nitric Oxide Synthase Inhibitors with a range of isoform selectivity and potency
-
Beaton, H. G.; Hamley, P.; Nicholls, D. J.; Tinker, A. C.; Wallace, A. V. 3,4-Dihydro-1-isoquinolinamines: A novel class of Nitric Oxide Synthase Inhibitors with a range of isoform selectivity and potency. Bioorg. Med. Chem. Lett. 2001, 11, 1023-1026.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 1023-1026
-
-
Beaton, H.G.1
Hamley, P.2
Nicholls, D.J.3
Tinker, A.C.4
Wallace, A.V.5
-
19
-
-
0035938416
-
Thienopyridines: Nitric oxide synthase inhibitors with potent in vivo activity
-
Beaton, H. G.; Boughton-Smith, N.; Hamley, P.; Ghelani, A.; Nicholls, D. J.; Tinker, A. C.; Wallace, A. V. Thienopyridines: Nitric oxide synthase inhibitors with potent in vivo activity. Bioorg. Med. Chem. Lett. 2001, 11, 1027-1030.
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 1027-1030
-
-
Beaton, H.G.1
Boughton-Smith, N.2
Hamley, P.3
Ghelani, A.4
Nicholls, D.J.5
Tinker, A.C.6
Wallace, A.V.7
-
20
-
-
0001465727
-
Rearrangement of 3-amino-1-benzylindazole to 4-amino-2-phenylquinazoline
-
Finch, N.; Gschwend, H. W. Rearrangement of 3-amino-1-benzylindazole to 4-amino-2-phenylquinazoline. J. Org. Chem. 1971, 36, 1463-1465.
-
(1971)
J. Org. Chem.
, vol.36
, pp. 1463-1465
-
-
Finch, N.1
Gschwend, H.W.2
-
21
-
-
37049052451
-
1,2-Dihydro-2,2-dimethylquinazolines. Condensation of acetone with anthranilamide derivatives
-
Carrington, H. C. 1,2-Dihydro-2,2-dimethylquinazolines. Condensation of acetone with anthranilamide derivatives. J. Chem. Soc. 1955, 2527-2528.
-
(1955)
J. Chem. Soc.
, pp. 2527-2528
-
-
Carrington, H.C.1
-
22
-
-
0026565840
-
Induced RAW264.7 macrophages express soluble and particulate nitric oxide synthase: Inhibition by transforming growth factor-β
-
Förstermann, U.; Schmidt, H. H. H. W.; Kohlhaas, K. L.; Murad, F. Induced RAW264.7 macrophages express soluble and particulate nitric oxide synthase: inhibition by transforming growth factor-β. Eur. J. Pharm. 1992, 225, 161-165.
-
(1992)
Eur. J. Pharm.
, vol.225
, pp. 161-165
-
-
Förstermann, U.1
Schmidt, H.H.H.W.2
Kohlhaas, K.L.3
Murad, F.4
-
23
-
-
0027372580
-
Purification and cDNA sequence of an inducible nitric oxide synthase from a human tumor cell line
-
Sherman, P. A.; Laubach, V. E.; Reep, B. R.; Wood, E. R. Purification and cDNA sequence of an inducible nitric oxide synthase from a human tumor cell line. Biochemistry 1993, 32, 11600-11605.
-
(1993)
Biochemistry
, vol.32
, pp. 11600-11605
-
-
Sherman, P.A.1
Laubach, V.E.2
Reep, B.R.3
Wood, E.R.4
-
24
-
-
0012817554
-
-
Note
-
Neither 9 nor any member of the aldehyde and ketone collection used in this experiment gave a significant inhibition of isolated i-NOS enzyme at the concentrations used in this study. (19) This enantiomer was identified as having the R-configuration from X-ray studies of enzyme inhibitor complexes (unpublished).
-
-
-
-
25
-
-
0012871150
-
-
Note
-
Note that the ring systems are numbered differently, such that C-5 in the quinazoline ring is spatially equivalent to C-8 of the isoquinoline.
-
-
-
|