Therapeutic Targets Database
BIDD Pharmainformatics Databases


TTD Target ID: TTDC00042

Target Information
NameMatrix metalloproteinase-14    
Type of targetDiscontinued target    
MT-MMP 1    
Membrane-type matrix metalloproteinase 1    
Membrane-type-1 matrix metalloproteinase    
DiseaseBrain Cancer
[ICD9: 191   ICD10: C71]
Hormone-refractory Prostate cancer
[ICD9: 185   ICD10: C61]
Kaposi's Sarcoma
[ICD9: 176   ICD10: C46]
Lung Cancer
[ICD9: 162   ICD10: C33-C34]
Myocardial infarction (MI)
[ICD9: 410   ICD10: I21, I22]
Non-small Cell Lung Cancer
[ICD9: 162   ICD10: C33, C34]
[ICD9: 715   ICD10: M15-M19, M47]
Pancreatic Cancer
[ICD9: 157   ICD10: C25]
Prostate cancer
[ICD9: 185   ICD10: C61]
EC NumberEC
PathwayGnRH signaling pathway
UniProt IDP50281
PDB Structure1BQQ; 1BUV; 3C7X; 3MA2.    
Target ValidationClick to Find Target Validation Information.    
Inhibitor2- (4-bromophenylsulfonamido)-N-hydroxyacetamide[10]
2- (Biphenyl-4-ylsulfonyl)N-hydroxybenzamide[11]
2- (biphenyl-4-ylsulfonamido)-N-hydroxyacetamide[10]
N-Hydroxy-2- (4-phenoxy-benzenesulfonyl)benzamide[11]
N-hydroxy-2- (4-methoxyphenylsulfonamido)acetamide[10]
[2- (Biphenyl-4-sulfonyl)phenyl]acetic Acid[11]
Cross References 3D Structure
Related Literature
On-Line Medical Dictionary
Ref 1Inhibition of gelatinase activity reduces neural injury in an ex vivo model of hypoxia-ischemia. Neuroscience. 2009 Jun 2;160(4):755-66. Epub 2009 Mar 9. To Reference
Ref 2Delayed administration of a matrix metalloproteinase inhibitor limits progressive brain injury after hypoxia-ischemia in the neonatal rat. J Neuroinflammation. 2008 Aug 11;5:34. To Reference
Ref 3Pharmacoproteomics of a metalloproteinase hydroxamate inhibitor in breast cancer cells: dynamics of membrane type 1 matrix metalloproteinase-mediated membrane protein shedding. Mol Cell Biol. 2008 Aug;28(15):4896-914. Epub 2008 May 27. To Reference
Ref 4Phase 1/2 trial of BMS-275291 in patients with human immunodeficiency virus-related Kaposi sarcoma: a multicenter trial of the AIDS Malignancy Consortium. Cancer. 2008 Mar 1;112(5):1083-8. To Reference
Ref 5Randomized phase II feasibility study of combining the matrix metalloproteinase inhibitor BMS-275291 with paclitaxel plus carboplatin in advanced non-small cell lung cancer. Lung Cancer. 2004 Dec;46(3):361-8. To Reference
Ref 6Novel investigational drugs for gastric cancer. Expert Opin Investig Drugs. 2009 Jul;18(7):945-55. To Reference
Ref 7Matrix metalloproteinase-2 involvement in breast cancer progression: a mini-review. Med Sci Monit. 2009 Feb;15(2):RA32-40. To Reference
Ref 8Matrix metalloproteinase inhibition as a novel anticancer strategy: a review with special focus on batimastat and marimastat. Pharmacol Ther. 1997;75(1):69-75. To Reference
Ref 9Am J Physiol Heart Circ Physiol. 2006 Jun;290(6):H2522-7. Epub 2006 Jan 20.Selective matrix metalloproteinase inhibition attenuates progression of left ventricular dysfunction and remodeling in dogs with chronic heart failure. To Reference
Ref 10J Med Chem. 2010 Mar 25;53(6):2622-35.Potent arylsulfonamide inhibitors of tumor necrosis factor-alpha converting enzyme able to reduce activated leukocyte cell adhesion molecule shedding in cancer cell models. To Reference
Ref 11J Med Chem. 2009 Oct 22;52(20):6347-61.Design, synthesis, biological evaluation, and NMR studies of a new series of arylsulfones as selective and potent matrix metalloproteinase-12 inhibitors. To Reference
Ref 12Bioorg Med Chem. 2007 Feb 1;15(3):1266-74. Epub 2006 Nov 14.Methotrexate gamma-hydroxamate derivatives as potential dual target antitumor drugs. To Reference
Ref 13Bioorg Med Chem Lett. 2009 Aug 1;19(15):4171-4. Epub 2009 Jun 2.Regioselective synthesis of methylated epigallocatechin gallate via nitrobenzenesulfonyl (Ns) protecting group. To Reference
Ref 14J Med Chem. 2002 Nov 7;45(23):4954-7.Discovery of gamma-lactam hydroxamic acids as selective inhibitors of tumor necrosis factor alpha converting enzyme: design, synthesis, and structure-activity relationships. To Reference
Ref 15Bioorg Med Chem. 2008 Sep 15;16(18):8745-59. Epub 2008 Jul 20.Introduction of the 4-(4-bromophenyl)benzenesulfonyl group to hydrazide analogs of Ilomastat leads to potent gelatinase B (MMP-9) inhibitors with improved selectivity. To Reference
Ref 16Bioorg Med Chem Lett. 2006 May 1;16(9):2357-63. Epub 2006 Feb 10.Synthesis and evaluation of succinoyl-caprolactam gamma-secretase inhibitors. To Reference
Ref 17J Med Chem. 2003 Jul 31;46(16):3514-25.A potent, selective inhibitor of matrix metalloproteinase-3 for the topical treatment of chronic dermal ulcers. To Reference


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