-
1
-
-
0002302132
-
Adrenocorticotropic hormone; adrenocortical steroids and their synthetic analogues; inhibitors of the synthesis and actions of adrenocortical hormones
-
Gilman, A. G., Goodman, L. S., Rall, T. W., Murad, F., Eds.; Macmillan Publishing Co.: New York
-
Schimmer, B. P.; Parker, K. L. Adrenocorticotropic hormone; adrenocortical steroids and their synthetic analogues; inhibitors of the synthesis and actions of adrenocortical hormones. In The Pharmacological Basis of Therapeutics, 10th ed.; Gilman, A. G., Goodman, L. S., Rall, T. W., Murad, F., Eds.; Macmillan Publishing Co.: New York, 2001; pp 1649-1677.
-
(2001)
The Pharmacological Basis of Therapeutics, 10th Ed.
, pp. 1649-1677
-
-
Schimmer, B.P.1
Parker, K.L.2
-
2
-
-
0036810356
-
Mechanisms involved in the side effects of glucocorticoids
-
Schäcke, H.; Döcke, W. D.; Asadullah, K. Mechanisms involved in the side effects of glucocorticoids. Pharmacol. Ther. 2002, 96, 23-43.
-
(2002)
Pharmacol. Ther.
, vol.96
, pp. 23-43
-
-
Schäcke, H.1
Döcke, W.D.2
Asadullah, K.3
-
3
-
-
0037306208
-
Crystallization of the human glucocorticoid receptor ligand binding domain: A step towards selective glucocorticoids
-
Necela, B. M.; Cidlowski, J. A. Crystallization of the human glucocorticoid receptor ligand binding domain: a step towards selective glucocorticoids. Trends Pharmacol. Sci. 2003, 24, 58-61.
-
(2003)
Trends Pharmacol. Sci.
, vol.24
, pp. 58-61
-
-
Necela, B.M.1
Cidlowski, J.A.2
-
4
-
-
35848945734
-
Selective Glucocorticoid Receptor Modulators
-
Coghlan, M. J.; Elmore, S. W.; Kym P. R.; Kort M. E. Selective Glucocorticoid Receptor Modulators. Annu. Rep. Med. Chem. 2002, 37, 167-176.
-
(2002)
Annu. Rep. Med. Chem.
, vol.37
, pp. 167-176
-
-
Coghlan, M.J.1
Elmore, S.W.2
Kym, P.R.3
Kort, M.E.4
-
6
-
-
0036791714
-
Pharmacology and potential therapeutic applications of nitric oxide-releasing nonsteroidal antiinflammatory and related nitric oxide-donating drugs
-
Keeble, J. E.; Moore, P. K. Pharmacology and potential therapeutic applications of nitric oxide-releasing nonsteroidal antiinflammatory and related nitric oxide-donating drugs. Br. J. Pharmacol. 2002, 137, 295-310.
-
(2002)
Br. J. Pharmacol.
, vol.137
, pp. 295-310
-
-
Keeble, J.E.1
Moore, P.K.2
-
7
-
-
0038393248
-
Nitric oxide-donating nonsteroidal antiinflammatory drugs: The case of nitroderivatives of aspirin
-
Chiroli, V.; Benedini, F.; Ongini, E.; Del Soldato, P. Nitric oxide-donating nonsteroidal antiinflammatory drugs: the case of nitroderivatives of aspirin. Eur. J. Med. Chem. 2003, 38, 441-446.
-
(2003)
Eur. J. Med. Chem.
, vol.38
, pp. 441-446
-
-
Chiroli, V.1
Benedini, F.2
Ongini, E.3
Del Soldato, P.4
-
8
-
-
0025883342
-
Nitric oxide: Physiology, pathophysiology, and pharmacology
-
Moncada, S.; Palmer, R. M.; Higgs, E. A. Nitric oxide: physiology, pathophysiology, and pharmacology. Pharmacol. Rev. 1991, 43, 109-142.
-
(1991)
Pharmacol. Rev.
, vol.43
, pp. 109-142
-
-
Moncada, S.1
Palmer, R.M.2
Higgs, E.A.3
-
9
-
-
0036562261
-
Potential cardioprotective actions of no-releasing aspirin
-
Wallace, J. L.; Ignarro, L. J.; Fiorucci, S. Potential cardioprotective actions of no-releasing aspirin. Nat. Rev. Drug. Discovery 2002, 1, 375-382.
-
(2002)
Nat. Rev. Drug. Discovery
, vol.1
, pp. 375-382
-
-
Wallace, J.L.1
Ignarro, L.J.2
Fiorucci, S.3
-
10
-
-
1642506009
-
Interaction of o-chloromethylphenacyl chloride and primary amines: A novel formation of the isoindoline system
-
Hinton, I. G.; Mann, F. G.; Vanterpool, A. Interaction of o-chloromethylphenacyl chloride and primary amines: a novel formation of the isoindoline system. J. Chem. Soc. 1959, 610-614.
-
(1959)
J. Chem. Soc.
, pp. 610-614
-
-
Hinton, I.G.1
Mann, F.G.2
Vanterpool, A.3
-
11
-
-
0033519252
-
Optimisation of the P2 pharmacophore in a series of thrombin inhibitors: Ion-dipole interactions with lysine 60G
-
Ambler, J.; Brown, L.; Cockcroft, X. L.; Grutter, M.; Hayler, J.; Janus, D.; Jones, D.; Kane, P.; Menear, K.; Priestle, J.; Smith, G.; Talbot, M.; Walker, C. V.; Wathey, B. Optimisation of the P2 pharmacophore in a series of thrombin inhibitors: ion-dipole interactions with lysine 60G. Bioorg. Med. Chem. Lett. 1999, 9, 1317-1322.
-
(1999)
Bioorg. Med. Chem. Lett.
, vol.9
, pp. 1317-1322
-
-
Ambler, J.1
Brown, L.2
Cockcroft, X.L.3
Grutter, M.4
Hayler, J.5
Janus, D.6
Jones, D.7
Kane, P.8
Menear, K.9
Priestle, J.10
Smith, G.11
Talbot, M.12
Walker, C.V.13
Wathey, B.14
-
12
-
-
0027968662
-
Non-peptide fibrinogen receptor antagonists. 2. Optimization of a tyrosine template as a mimic for Arg-Gly-Asp
-
Egbertson, M. S.; Chang, C. T.; Duggan, M. E.; Gould, R. J.; Halczenko, W.; Hartman, G. D.; Laswell, W. L.; Lynch, J. J., Jr.; Lynch, R. J.; Manno, P. D.; Naylor, A. M.; Prugh, J. D.; Ramjit, D. R.; Sitko, G. R.; Smith, R. S.; Turchi, L. M.; Zhang, G. Non-peptide fibrinogen receptor antagonists. 2. Optimization of a tyrosine template as a mimic for Arg-Gly-Asp. J. Med. Chem. 1994, 37, 2537-2551.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 2537-2551
-
-
Egbertson, M.S.1
Chang, C.T.2
Duggan, M.E.3
Gould, R.J.4
Halczenko, W.5
Hartman, G.D.6
Laswell, W.L.7
Lynch Jr., J.J.8
Lynch, R.J.9
Manno, P.D.10
Naylor, A.M.11
Prugh, J.D.12
Ramjit, D.R.13
Sitko, G.R.14
Smith, R.S.15
Turchi, L.M.16
Zhang, G.17
-
13
-
-
0033523897
-
Design and synthesis of thrombin inhibitors: Analogues of MD-805 with reduced stereogenicity and improved potency
-
Brundish, D.; Bull, A.; Donovan, V.; Fullerton, J. D.; Garman, S. M.; Hayler, J. F.; Janus, D.; Kane, P. D.; McDonnell, M.; Smith, G. P.; Wakeford, R.; Walker, C. V.; Howarth, G.; Hoyle, W.; Allen, M. C.; Ambler, J.; Butler, K. ; Talbot, M. D. Design and synthesis of thrombin inhibitors: analogues of MD-805 with reduced stereogenicity and improved potency. J. Med. Chem. 1999, 42, 4584-4603.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 4584-4603
-
-
Brundish, D.1
Bull, A.2
Donovan, V.3
Fullerton, J.D.4
Garman, S.M.5
Hayler, J.F.6
Janus, D.7
Kane, P.D.8
McDonnell, M.9
Smith, G.P.10
Wakeford, R.11
Walker, C.V.12
Howarth, G.13
Hoyle, W.14
Allen, M.C.15
Ambler, J.16
Butler, K.17
Talbot, M.D.18
-
14
-
-
0033600706
-
Rapid parallel synthesis applied to the optimization of a series of potent nonpeptide neuropeptide Y-1 receptor antagonists
-
Siegel, M. G.; Chaney, M. O.; Bruns, R. F.; Clay, M. P.; Schober, D. A.; Van Abbema, A. M.; Johnson, D. W.; Cantrell, B. E.; Hahn, P. J.; Hunden, D. C.; Gehlert, D. R.; Zarrinmayeh, H.; Ornstein, P. L.; Zimmerman, D. M.; Koppel, G. A. Rapid parallel synthesis applied to the optimization of a series of potent nonpeptide neuropeptide Y-1 receptor antagonists. Tetrahedron 1999, 55, 11619-11639.
-
(1999)
Tetrahedron
, vol.55
, pp. 11619-11639
-
-
Siegel, M.G.1
Chaney, M.O.2
Bruns, R.F.3
Clay, M.P.4
Schober, D.A.5
Van Abbema, A.M.6
Johnson, D.W.7
Cantrell, B.E.8
Hahn, P.J.9
Hunden, D.C.10
Gehlert, D.R.11
Zarrinmayeh, H.12
Ornstein, P.L.13
Zimmerman, D.M.14
Koppel, G.A.15
-
15
-
-
1642546832
-
Triethylenediamine (1,4-diazabicyclo-[2.2.2]octane) II
-
Hromatka, O.; Engel, E. Triethylenediamine (1,4-diazabicyclo-[2.2.2]octane) II. Chem. Ber. 1943, 76B, 712-717.
-
(1943)
Chem. Ber.
, vol.76 B
, pp. 712-717
-
-
Hromatka, O.1
Engel, E.2
-
16
-
-
0018850224
-
Studies on the synthesis of some 1-(p-fluorophenyl)-1-pyrid-2′ -ylbutylamines
-
Schliemann, W.; Buege, A.; Reppel, L. Studies on the synthesis of some 1-(p-fluorophenyl)-1-pyrid-2′-ylbutylamines. Pharmazie 1980, 35, 69-72.
-
(1980)
Pharmazie
, vol.35
, pp. 69-72
-
-
Schliemann, W.1
Buege, A.2
Reppel, L.3
-
17
-
-
0030970551
-
Design, synthesis, and in vitro activities of benzamide-core glycoprotein IIb/IIIa antagonists: 2,3-Diaminopropionic acid derivatives as surrogates of aspartic acid
-
Xue, C. B.; Roderick, J.; Jackson, S.; Rafalski, M.; Rockwell, A.; Mousa, S.; Olson, R. E.; DeGrado, W. F. Design, synthesis, and in vitro activities of benzamide-core glycoprotein IIb/IIIa antagonists: 2,3-diaminopropionic acid derivatives as surrogates of aspartic acid. Bioorg. Med. Chem. 1997, 5, 693-705.
-
(1997)
Bioorg. Med. Chem.
, vol.5
, pp. 693-705
-
-
Xue, C.B.1
Roderick, J.2
Jackson, S.3
Rafalski, M.4
Rockwell, A.5
Mousa, S.6
Olson, R.E.7
DeGrado, W.F.8
-
18
-
-
0028090052
-
Alpha 1-adrenoceptor blocking activity of some ring-open analogues of prazosin
-
Boschi, D.; Di Stilo, A.; Fruttero, R.; Medana, C.; Sorba, G.; Gasco, A. Alpha 1-adrenoceptor blocking activity of some ring-open analogues of prazosin. Arch. Pharm. (Weinheim, Germany) 1994, 327, 661-667.
-
(1994)
Arch. Pharm. (Weinheim, Germany)
, vol.327
, pp. 661-667
-
-
Boschi, D.1
Di Stilo, A.2
Fruttero, R.3
Medana, C.4
Sorba, G.5
Gasco, A.6
-
19
-
-
0036883907
-
Blocking NO synthesis: How, where and why?
-
Vallance, P.; Leiper, J.; Blocking NO synthesis: how, where and why? Nat. Rev. Drug Discovery 2002, 1, 939-950.
-
(2002)
Nat. Rev. Drug Discovery
, vol.1
, pp. 939-950
-
-
Vallance, P.1
Leiper, J.2
-
20
-
-
0034886127
-
Nitrosylhemoglobin, an unequivocal index of nitric oxide release from nitroaspirin: In vitro and in vivo studies in the rat by ESR spectroscopy
-
Carini, M.; Aldini, G.; Stefani, R.; Orioli, M.; Facino, R. M. Nitrosylhemoglobin, an unequivocal index of nitric oxide release from nitroaspirin: in vitro and in vivo studies in the rat by ESR spectroscopy. J. Pharm. Biomed. Anal. 2001, 26, 509-518.
-
(2001)
J. Pharm. Biomed. Anal.
, vol.26
, pp. 509-518
-
-
Carini, M.1
Aldini, G.2
Stefani, R.3
Orioli, M.4
Facino, R.M.5
-
21
-
-
0034649604
-
Carbonic anhydrase inhibitors: Water-soluble 4-sulfamoylphenylthioureas as topical intraocular pressure-lowering agents with long-lasting effects
-
Casini, A.; Scozzafava, A.; Mincione, F.; Menabuoni, L.; Ilies, M. A.; Supuran, C. T. Carbonic anhydrase inhibitors: water-soluble 4-sulfamoylphenylthioureas as topical intraocular pressure-lowering agents with long-lasting effects. J. Med. Chem. 2000, 43, 4884-4892.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 4884-4892
-
-
Casini, A.1
Scozzafava, A.2
Mincione, F.3
Menabuoni, L.4
Ilies, M.A.5
Supuran, C.T.6
-
22
-
-
0033639095
-
21-NO-prednisolone is a novel nitric oxide-releasing derivative of prednisolone with enhanced antiinflammatory properties
-
Paul-Clark, M.; Del Soldato, P.; Fiorucci, S.; Flower, R. J.; Perretti, M. 21-NO-prednisolone is a novel nitric oxide-releasing derivative of prednisolone with enhanced antiinflammatory properties. Br. J. Pharmacol. 2000, 131, 1345-1354.
-
(2000)
Br. J. Pharmacol.
, vol.131
, pp. 1345-1354
-
-
Paul-Clark, M.1
Del Soldato, P.2
Fiorucci, S.3
Flower, R.J.4
Perretti, M.5
-
23
-
-
0037180496
-
NCX-1015, a nitric-oxide derivative of prednisolone, enhances regulatory T cells in the lamina propria and protects against 2,4, 6-trinitrobenzenesulfonic acid-induced colitis in mice
-
Fiorucci, S.; Antonelli, E.; Distrutti, E.; Del Soldato, P.; Flower, R. J.; Clark, M. J.; Morelli, A.; Perretti, M.; Ignarro, L. J. NCX-1015, a nitric-oxide derivative of prednisolone, enhances regulatory T cells in the lamina propria and protects against 2,4,6-trinitrobenzenesulfonic acid-induced colitis in mice. Proc. Natl. Acad. Sci. U.S.A. 2002, 99, 15770-15775.
-
(2002)
Proc. Natl. Acad. Sci. U.S.A.
, vol.99
, pp. 15770-15775
-
-
Fiorucci, S.1
Antonelli, E.2
Distrutti, E.3
Del Soldato, P.4
Flower, R.J.5
Clark, M.J.6
Morelli, A.7
Perretti, M.8
Ignarro, L.J.9
-
24
-
-
0037022343
-
Potent antiarthritic properties of a glucocorticoid derivative, NCX-1015, in an experimental model of arthritis
-
Paul-Clark, M.; Mancini, L.; Del Soldato, P.; Flower, R. J.; Perretti, M. Potent antiarthritic properties of a glucocorticoid derivative, NCX-1015, in an experimental model of arthritis. Proc. Natl. Acad. Sci. U.S.A. 2002, 99, 1677-1682.
-
(2002)
Proc. Natl. Acad. Sci. U.S.A.
, vol.99
, pp. 1677-1682
-
-
Paul-Clark, M.1
Mancini, L.2
Del Soldato, P.3
Flower, R.J.4
Perretti, M.5
-
25
-
-
46149152498
-
NCX-1015, a novel nitric oxide-releasing derivative of prednisolone, combines potent antiinflammatory activity and low toxicity in the rat stomach subjected to ischemia-reperfusion
-
abstr
-
Peskar, B.; Maricic, N.; Ehrlich, K.; Swaka, N. NCX-1015, a novel nitric oxide-releasing derivative of prednisolone, combines potent antiinflammatory activity and low toxicity in the rat stomach subjected to ischemia-reperfusion. Gastroenterology 2002, 229 (Suppl. A), M-891 (abstr.)
-
(2002)
Gastroenterology
, vol.229
, Issue.SUPPL. A
-
-
Peskar, B.1
Maricic, N.2
Ehrlich, K.3
Swaka, N.4
-
26
-
-
0028223401
-
ESR spectral transition by arteriovenous cycle in nitric oxide hemoglobin of cytokine-treated rats
-
Kosaka, H.; Sawai, Y.; Sakaguchi, H.; Kumura, E.; Harada, N.; Watanabe, M.; Shiga, T. ESR spectral transition by arteriovenous cycle in nitric oxide hemoglobin of cytokine-treated rats. Am. J. Physiol. 1994, 266, C1400-C1405.
-
(1994)
Am. J. Physiol.
, vol.266
-
-
Kosaka, H.1
Sawai, Y.2
Sakaguchi, H.3
Kumura, E.4
Harada, N.5
Watanabe, M.6
Shiga, T.7
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