Target Validation Information | |||||
---|---|---|---|---|---|
TTD ID | T34296 | ||||
Target Name | Matrix metalloproteinase-13 (MMP-13) | ||||
Type of Target |
Clinical trial |
||||
Drug Potency against Target | Marimastat | Drug Info | IC50 = 2 nM | [19] | |
PG-530742 | Drug Info | Complete Inhibition = 150 ng/mL | [18] | ||
(+/-)5-(biphenyl-4-yl)-3-hydroxypentanoic acid | Drug Info | IC50 = 12000 nM | [15] | ||
1-(4-Methoxy-benzenesulfonyl)-heptane-3-thiol | Drug Info | IC50 = 45 nM | [1] | ||
2-(2-(biphenyl-4-yl)ethylsulfonyl)acetic acid | Drug Info | IC50 = 11300 nM | [15] | ||
2-(4-methoxybenzylthio)-6-methylpyrimidin-4-ol | Drug Info | IC50 = 1600 nM | [13] | ||
2-(biphenyl-4-ylsulfonamido)pentanedioic acid | Drug Info | IC50 = 280 nM | [13] | ||
2-(Biphenyl-4-ylsulfonyl)N-hydroxybenzamide | Drug Info | IC50 = 1400 nM | [16] | ||
3-(4-Methoxy-benzenesulfonyl)-cyclohexanethiol | Drug Info | IC50 = 22 nM | [2] | ||
3-(4-Methoxy-benzenesulfonyl)-cyclopentanethiol | Drug Info | IC50 = 500 nM | [2] | ||
3-(4-Methoxy-benzenesulfonyl)-hexane-1-thiol | Drug Info | IC50 = 6 nM | [1] | ||
3-(4-Methoxy-benzenesulfonyl)-pentane-1-thiol | Drug Info | IC50 = 4 nM | [1] | ||
3-(4-Methoxy-benzenesulfonyl)-propane-1-thiol | Drug Info | IC50 = 50 nM | [1] | ||
3-(4-Phenoxy-benzenesulfonyl)-cyclohexanethiol | Drug Info | IC50 = 1 nM | [2] | ||
3-(4-Phenoxy-benzenesulfonyl)-propane-1-thiol | Drug Info | IC50 = 0.5 nM | [1] | ||
3-Benzenesulfonyl-heptanoic acid hydroxyamide | Drug Info | IC50 = 18 nM | [3] | ||
3-Cyclohexanesulfonyl-heptanoic acid hydroxyamide | Drug Info | IC50 = 100 nM | [3] | ||
4-(2,2'-bithiophen-5-ylmethyleneamino)phenol | Drug Info | IC50 = 1700 nM | [12] | ||
4-(4-Methoxy-benzenesulfonyl)-butane-2-thiol | Drug Info | IC50 = 32 nM | [1] | ||
4-(methyl(4-phenylthiazol-2-yl)amino)phenol | Drug Info | IC50 = 13300 nM | [12] | ||
4-amino-3-(4-(hexyloxy)phenyl)-4-oxobutanoic acid | Drug Info | IC50 = 1300 nM | [13] | ||
5-(4'-cyanobiphenyl-4-yl)-3-hydroxypentanoic acid | Drug Info | IC50 = 2450 nM | [15] | ||
Apratastat | Drug Info | IC50 = 8 nM | [8] | ||
CIPEMASTAT | Drug Info | IC50 = 7 nM | |||
CIPEMASTAT | Drug Info | Ki = 1 nM | [10] | ||
Curcumin | Drug Info | IC50 = 10300 nM | [12] | ||
Ethyl 2-cyano-2-(quinoxalin-2(1H)-ylidene)acetate | Drug Info | IC50 = 3400 nM | [12] | ||
GM6001 | Drug Info | IC50 = 5.2 nM | [11] | ||
IK-862 | Drug Info | Ki = 1417 nM | [5] | ||
MMI270 | Drug Info | IC50 = 4.3 nM | [4] | ||
N-Hydroxy-2-(4-phenoxy-benzenesulfonyl)benzamide | Drug Info | IC50 = 2700 nM | [16] | ||
N1,N3-bis(3-methoxybenzyl)isophthalamide | Drug Info | IC50 = 1350 nM | [17] | ||
N4,N6-dibenzylpyrimidine-4,6-dicarboxamide | Drug Info | IC50 = 400 nM | [14] | ||
PKF-242-484 | Drug Info | Ki = 0.5 nM | [10] | ||
Ro-37-9790 | Drug Info | IC50 = 4.9 nM | |||
RS-130830 | Drug Info | Ki = 0.52 nM | [7] | ||
SR-973 | Drug Info | Ki = 10 nM | [9] | ||
UK-356618 | Drug Info | IC50 = 73 nM | [6] | ||
[2-(Biphenyl-4-sulfonyl)phenyl]acetic Acid | Drug Info | IC50 = 260 nM | [16] | ||
Action against Disease Model | PG-530742 | Drug Info | MMP13 inhibitors have often been tested in explanted bovine nasal cartilage cultures, where the degradation of the cartilage explant is induced by adding the strong stimulus of a combination of interleukin-1a plus Oncostatin M, which induces both MMP1 and MMP13. MMP13 inhibitor could block cartilage degradation in this culture system, but its potency was fairly weak relativeto its in vitro enzyme inhibition potency. MMP13 inhibitors showed significant protection of cartilage as evaluated by examination of the gross structure of the cartilage surface. | [20] | |
References | |||||
REF 1 | Discovery of a novel series of selective MMP inhibitors: identification of the gamma-sulfone-thiols. Bioorg Med Chem Lett. 1999 Apr 5;9(7):943-8. | ||||
REF 2 | Synthesis and identification of conformationally constrained selective MMP inhibitors. Bioorg Med Chem Lett. 1999 Jul 5;9(13):1757-60. | ||||
REF 3 | Hydroxamic acid derivatives as potent peptide deformylase inhibitors and antibacterial agents. J Med Chem. 2000 Jun 15;43(12):2324-31. | ||||
REF 4 | Heterocycle-based MMP inhibitors with P2' substituents. Bioorg Med Chem Lett. 2001 Apr 23;11(8):1009-13. | ||||
REF 5 | Discovery of gamma-lactam hydroxamic acids as selective inhibitors of tumor necrosis factor alpha converting enzyme: design, synthesis, and structu... J Med Chem. 2002 Nov 7;45(23):4954-7. | ||||
REF 6 | A potent, selective inhibitor of matrix metalloproteinase-3 for the topical treatment of chronic dermal ulcers. J Med Chem. 2003 Jul 31;46(16):3514-25. | ||||
REF 7 | Structure-based design of potent and selective inhibitors of collagenase-3 (MMP-13). Bioorg Med Chem Lett. 2005 Feb 15;15(4):1101-6. | ||||
REF 8 | Acetylenic TACE inhibitors. Part 3: Thiomorpholine sulfonamide hydroxamates. Bioorg Med Chem Lett. 2006 Mar 15;16(6):1605-9. | ||||
REF 9 | Synthesis and evaluation of succinoyl-caprolactam gamma-secretase inhibitors. Bioorg Med Chem Lett. 2006 May 1;16(9):2357-63. | ||||
REF 10 | A cassette-dosing approach for improvement of oral bioavailability of dual TACE/MMP inhibitors. Bioorg Med Chem Lett. 2006 May 15;16(10):2632-6. | ||||
REF 11 | Discovery and characterization of a novel inhibitor of matrix metalloprotease-13 that reduces cartilage damage in vivo without joint fibroplasia si... J Biol Chem. 2007 Sep 21;282(38):27781-91. | ||||
REF 12 | High throughput screening of potentially selective MMP-13 exosite inhibitors utilizing a triple-helical FRET substrate. Bioorg Med Chem. 2009 Feb 1;17(3):990-1005. | ||||
REF 13 | Ranking the selectivity of PubChem screening hits by activity-based protein profiling: MMP13 as a case study. Bioorg Med Chem. 2009 Feb 1;17(3):1101-8. | ||||
REF 14 | Calculation of binding free energies for non-zinc chelating pyrimidine dicarboxamide inhibitors with MMP-13. Bioorg Med Chem Lett. 2009 Jan 1;19(1):47-50. | ||||
REF 15 | The identification of beta-hydroxy carboxylic acids as selective MMP-12 inhibitors. Bioorg Med Chem Lett. 2009 Oct 1;19(19):5760-3. | ||||
REF 16 | Design, synthesis, biological evaluation, and NMR studies of a new series of arylsulfones as selective and potent matrix metalloproteinase-12 inhib... J Med Chem. 2009 Oct 22;52(20):6347-61. | ||||
REF 17 | Discovery of (pyridin-4-yl)-2H-tetrazole as a novel scaffold to identify highly selective matrix metalloproteinase-13 inhibitors for the treatment ... Bioorg Med Chem Lett. 2010 Jan 15;20(2):576-80. | ||||
REF 18 | Selective matrix metalloproteinase inhibition attenuates progression of left ventricular dysfunction and remodeling in dogs with chronic heart fail... Am J Physiol Heart Circ Physiol. 2006 Jun;290(6):H2522-7. | ||||
REF 19 | Recent developments in the design of specific Matrix Metalloproteinase inhibitors aided by structural and computational studies. Curr Pharm Des. 2005;11(3):295-322. | ||||
REF 20 | Selective MMP13 inhibitors. Med Res Rev. 2011 Nov;31(6):863-94. | ||||
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