Target Validation Information | |||||
---|---|---|---|---|---|
Target ID | T40332 | ||||
Target Name | Leukocyte elastase | ||||
Target Type | Clinical Trial |
||||
Drug Potency against Target | WIN-63395 | Drug Info | Ki = 0.27 nM | ||
ZK-814048 | Drug Info | Ki = 10000 nM | [528872] | ||
(4-bromo-1H-pyrazol-1-yl)(p-tolyl)methanone | Drug Info | Ki = 45 nM | [529037] | ||
1-benzoyl-N-phenyl-1H-pyrazole-3-carboxamide | Drug Info | Ki = 39 nM | [529037] | ||
Sivelestat sodium hydrate | Drug Info | IC50 = 44 nM | [537032] | ||
FR-901451 | Drug Info | Ki = 10 nM | [528807] | ||
FR-901277 | Drug Info | Ki = 12 nM | [528807] | ||
4-Hydroxy-3-nonanoyl-6-octyl-pyran-2-one | Drug Info | Ki = 4600 nM | [533472] | ||
3-Benzyl-3-ethyl-1-phenylazetidine-2,4-dione | Drug Info | Ki = 127 nM | [530511] | ||
Cbz-Val-Pro-Val-(2-benzoxazole) | Drug Info | Ki = 3 nM | [529193] | ||
E-6-O-p-methoxycinnamoyl scandoside methyl ester | Drug Info | IC50 = 18000 nM | [530569] | ||
EPIGALOCATECHIN GALLATE | Drug Info | IC50 = 12800 nM | [530569] | ||
(4-nitro-1H-pyrazol-1-yl)(phenyl)methanone | Drug Info | Ki = 34 nM | [529037] | ||
(3-nitro-1H-pyrazol-1-yl)(p-tolyl)methanone | Drug Info | Ki = 28 nM | [529037] | ||
(4-bromo-1H-pyrazol-1-yl)(m-tolyl)methanone | Drug Info | Ki = 250 nM | [529037] | ||
(4-nitro-1H-pyrazol-1-yl)(o-tolyl)methanone | Drug Info | Ki = 65 nM | [529037] | ||
Ac-Ala-Pro-Val-(2-benzoxazole) | Drug Info | Ki = 73 nM | [529193] | ||
6-Heptyl-4-hydroxy-3-octanoyl-pyran-2-one | Drug Info | Ki = 15000 nM | [533472] | ||
Delanzomib | Drug Info | IC50 = 3550 nM | [529283] | ||
4-methoxy-N'-(2-phenylacetyl)benzohydrazide | Drug Info | Ki = 2500 nM | [529037] | ||
(4-chloro-1H-pyrazol-1-yl)(o-tolyl)methanone | Drug Info | Ki = 230 nM | [529037] | ||
3-butyl-3-ethyl-1-phenylazetidine-2,4-dione | Drug Info | Ki = 0.85 nM | [530511] | ||
3,3-Diethyl-1-o-tolylazetidine-2,4-dione | Drug Info | Ki = 233 nM | [530511] | ||
3-Benzyl-3-methyl-1-phenylazetidine-2,4-dione | Drug Info | Ki = 4450 nM | [530511] | ||
2-methylbut-3-yn-2-yl 4-methoxybenzoate | Drug Info | Ki = 110 nM | [529037] | ||
(1H-pyrazol-1-yl)(o-tolyl)methanone | Drug Info | Ki = 3400 nM | [529037] | ||
3,3-Diethyl-1-(pyridin-3-yl)azetidine-2,4-dione | Drug Info | Ki = 2.2 nM | [530511] | ||
1-benzyl-3,3-diethylazetidine-2,4-dione | Drug Info | Ki = 114 nM | [530511] | ||
1-benzyl-3,3-dimethylazetidine-2,4-dione | Drug Info | Ki = 34.4 nM | [530511] | ||
N,N-bis(cyanomethyl)-3,4-dimethoxybenzamide | Drug Info | Ki = 290 nM | [529037] | ||
(3-nitro-1H-pyrazol-1-yl)(phenyl)methanone | Drug Info | Ki = 46 nM | [529037] | ||
(3,4-dichlorophenyl)(1H-pyrazol-1-yl)methanone | Drug Info | Ki = 104 nM | [529037] | ||
3-Ethyl-3-isobutyl-1-phenylazetidine-2,4-dione | Drug Info | Ki = 3.9 nM | [530511] | ||
3,4-dichloroisocoumarin | Drug Info | IC50 = 3000 nM | [528555] | ||
Bornyl (3,4,5-trihydroxy)-cinnamate | Drug Info | IC50 = 540 nM | [529218] | ||
3,3-diethyl-1-phenylazetidine-2,4-dione | Drug Info | Ki = 1.21 nM | [530511] | ||
3-Decanoyl-4-hydroxy-6-nonyl-pyran-2-one | Drug Info | Ki = 7900 nM | [533472] | ||
(4-bromo-1H-pyrazol-1-yl)(o-tolyl)methanone | Drug Info | Ki = 300 nM | [529037] | ||
References | |||||
Ref 528872 | J Med Chem. 2007 Jun 28;50(13):2967-80. Epub 2007 May 31.Thiophene-anthranilamides as highly potent and orally available factor Xa inhibitors. | ||||
Ref 529037 | J Med Chem. 2007 Oct 4;50(20):4928-38. Epub 2007 Sep 12.N-benzoylpyrazoles are novel small-molecule inhibitors of human neutrophil elastase. | ||||
Ref 529037 | J Med Chem. 2007 Oct 4;50(20):4928-38. Epub 2007 Sep 12.N-benzoylpyrazoles are novel small-molecule inhibitors of human neutrophil elastase. | ||||
Ref 537032 | Neutrophil elastase inhibitor (sivelestat) reduces the levels of inflammatory mediators by inhibiting NF-kB. Inflamm Res. 2009 Apr;58(4):198-203. | ||||
Ref 528807 | Bioorg Med Chem. 2007 Jul 1;15(13):4618-28. Epub 2007 Apr 3.Resisting degradation by human elastase: commonality of design features shared by 'canonical' plant and bacterial macrocyclic protease inhibitor scaffolds. | ||||
Ref 528807 | Bioorg Med Chem. 2007 Jul 1;15(13):4618-28. Epub 2007 Apr 3.Resisting degradation by human elastase: commonality of design features shared by 'canonical' plant and bacterial macrocyclic protease inhibitor scaffolds. | ||||
Ref 533472 | J Med Chem. 1987 Jun;30(6):1017-23.Inhibition of human sputum elastase by substituted 2-pyrones. | ||||
Ref 530511 | J Med Chem. 2010 Jan 14;53(1):241-53.4-Oxo-beta-lactams (azetidine-2,4-diones) are potent and selective inhibitors of human leukocyte elastase. | ||||
Ref 529193 | Bioorg Med Chem. 2008 Feb 15;16(4):1562-95. Epub 2007 Nov 6.Inhibitors of proteases and amide hydrolases that employ an alpha-ketoheterocycle as a key enabling functionality. | ||||
Ref 530569 | Bioorg Med Chem Lett. 2010 Jan 15;20(2):513-5. Epub 2009 Nov 26.Evaluation of human neutrophil elastase inhibitory effect of iridoid glycosides from Hedyotis diffusa. | ||||
Ref 530569 | Bioorg Med Chem Lett. 2010 Jan 15;20(2):513-5. Epub 2009 Nov 26.Evaluation of human neutrophil elastase inhibitory effect of iridoid glycosides from Hedyotis diffusa. | ||||
Ref 529037 | J Med Chem. 2007 Oct 4;50(20):4928-38. Epub 2007 Sep 12.N-benzoylpyrazoles are novel small-molecule inhibitors of human neutrophil elastase. | ||||
Ref 529037 | J Med Chem. 2007 Oct 4;50(20):4928-38. Epub 2007 Sep 12.N-benzoylpyrazoles are novel small-molecule inhibitors of human neutrophil elastase. | ||||
Ref 529037 | J Med Chem. 2007 Oct 4;50(20):4928-38. Epub 2007 Sep 12.N-benzoylpyrazoles are novel small-molecule inhibitors of human neutrophil elastase. | ||||
Ref 529037 | J Med Chem. 2007 Oct 4;50(20):4928-38. Epub 2007 Sep 12.N-benzoylpyrazoles are novel small-molecule inhibitors of human neutrophil elastase. | ||||
Ref 529193 | Bioorg Med Chem. 2008 Feb 15;16(4):1562-95. Epub 2007 Nov 6.Inhibitors of proteases and amide hydrolases that employ an alpha-ketoheterocycle as a key enabling functionality. | ||||
Ref 533472 | J Med Chem. 1987 Jun;30(6):1017-23.Inhibition of human sputum elastase by substituted 2-pyrones. | ||||
Ref 529283 | J Med Chem. 2008 Feb 28;51(4):1068-72. Epub 2008 Feb 5.Discovery of a potent, selective, and orally active proteasome inhibitor for the treatment of cancer. | ||||
Ref 529037 | J Med Chem. 2007 Oct 4;50(20):4928-38. Epub 2007 Sep 12.N-benzoylpyrazoles are novel small-molecule inhibitors of human neutrophil elastase. | ||||
Ref 529037 | J Med Chem. 2007 Oct 4;50(20):4928-38. Epub 2007 Sep 12.N-benzoylpyrazoles are novel small-molecule inhibitors of human neutrophil elastase. | ||||
Ref 530511 | J Med Chem. 2010 Jan 14;53(1):241-53.4-Oxo-beta-lactams (azetidine-2,4-diones) are potent and selective inhibitors of human leukocyte elastase. | ||||
Ref 530511 | J Med Chem. 2010 Jan 14;53(1):241-53.4-Oxo-beta-lactams (azetidine-2,4-diones) are potent and selective inhibitors of human leukocyte elastase. | ||||
Ref 530511 | J Med Chem. 2010 Jan 14;53(1):241-53.4-Oxo-beta-lactams (azetidine-2,4-diones) are potent and selective inhibitors of human leukocyte elastase. | ||||
Ref 529037 | J Med Chem. 2007 Oct 4;50(20):4928-38. Epub 2007 Sep 12.N-benzoylpyrazoles are novel small-molecule inhibitors of human neutrophil elastase. | ||||
Ref 529037 | J Med Chem. 2007 Oct 4;50(20):4928-38. Epub 2007 Sep 12.N-benzoylpyrazoles are novel small-molecule inhibitors of human neutrophil elastase. | ||||
Ref 530511 | J Med Chem. 2010 Jan 14;53(1):241-53.4-Oxo-beta-lactams (azetidine-2,4-diones) are potent and selective inhibitors of human leukocyte elastase. | ||||
Ref 530511 | J Med Chem. 2010 Jan 14;53(1):241-53.4-Oxo-beta-lactams (azetidine-2,4-diones) are potent and selective inhibitors of human leukocyte elastase. | ||||
Ref 530511 | J Med Chem. 2010 Jan 14;53(1):241-53.4-Oxo-beta-lactams (azetidine-2,4-diones) are potent and selective inhibitors of human leukocyte elastase. | ||||
Ref 529037 | J Med Chem. 2007 Oct 4;50(20):4928-38. Epub 2007 Sep 12.N-benzoylpyrazoles are novel small-molecule inhibitors of human neutrophil elastase. | ||||
Ref 529037 | J Med Chem. 2007 Oct 4;50(20):4928-38. Epub 2007 Sep 12.N-benzoylpyrazoles are novel small-molecule inhibitors of human neutrophil elastase. | ||||
Ref 529037 | J Med Chem. 2007 Oct 4;50(20):4928-38. Epub 2007 Sep 12.N-benzoylpyrazoles are novel small-molecule inhibitors of human neutrophil elastase. | ||||
Ref 530511 | J Med Chem. 2010 Jan 14;53(1):241-53.4-Oxo-beta-lactams (azetidine-2,4-diones) are potent and selective inhibitors of human leukocyte elastase. | ||||
Ref 528555 | Antimicrob Agents Chemother. 2007 Feb;51(2):543-50. Epub 2006 Dec 4.Cathepsin A is the major hydrolase catalyzing the intracellular hydrolysis of the antiretroviral nucleotide phosphonoamidate prodrugs GS-7340 and GS-9131. | ||||
Ref 529218 | Bioorg Med Chem. 2008 Mar 1;16(5):2385-90. Epub 2007 Nov 29.Bornyl (3,4,5-trihydroxy)-cinnamate--an optimized human neutrophil elastase inhibitor designed by free energy calculations. | ||||
Ref 530511 | J Med Chem. 2010 Jan 14;53(1):241-53.4-Oxo-beta-lactams (azetidine-2,4-diones) are potent and selective inhibitors of human leukocyte elastase. | ||||
Ref 533472 | J Med Chem. 1987 Jun;30(6):1017-23.Inhibition of human sputum elastase by substituted 2-pyrones. | ||||
Ref 529037 | J Med Chem. 2007 Oct 4;50(20):4928-38. Epub 2007 Sep 12.N-benzoylpyrazoles are novel small-molecule inhibitors of human neutrophil elastase. |
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