General Information of DTT (ID: TTMX39J)

DTT Name Matrix metalloproteinase-1 (MMP-1) DTT Info
Gene Name MMP1

Molecule-Related Drug & Molecule List

Molecule-Related Drug List
Molecule Type:
DTT
DTP
DME
Drug Status:
Discontinued Drug(s)
Approved Drug(s)
Clinical Trial Drug(s)
Patented Agent(s)
Investigative Drug(s)
1 Approved Drug(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
Prinomastat DM9HOKG Lung cancer 2C25.0 Approved [1]
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3 Clinical Trial Drug(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
CIPEMASTAT DM803GL Rheumatoid arthritis FA20 Phase 3 [2]
Marimastat DM6V34C Pancreatic cancer 2C10 Phase 3 [3]
Apratastat DM8W4N9 Rheumatoid arthritis FA20 Phase 2 [4]
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2 Patented Agent(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
PMID29130358-Compound-Figure10(2a) DMFWXPS N. A. N. A. Patented [5]
PMID29130358-Compound-Figure18(14a) DMHIBTZ N. A. N. A. Patented [5]
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10 Discontinued Drug(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
BMS 275291 DMKSFPE Kaposi sarcoma 2B57 Discontinued in Phase 3 [6]
GM6001 DM7V9CT Corneal ulcer 9A76 Discontinued in Phase 2 [7]
RS-130830 DMOTANY Hepatitis C virus infection 1E51.1 Discontinued in Phase 2 [8]
XL784 DMICR39 Diabetic nephropathy GB61.Z Discontinued in Phase 2 [9]
BB-1101 DM7GH5Z Multiple sclerosis 8A40 Terminated [10]
BB-3644 DM7YRFE Solid tumour/cancer 2A00-2F9Z Terminated [11]
L-696418 DMV785R N. A. N. A. Terminated [12]
Ro-31-4724 DM8B9YT Arthritis FA20 Terminated [13]
RO-319790 DML3NEU Rheumatoid arthritis FA20 Terminated [14]
SC-44463 DMBPNKT N. A. N. A. Terminated [15]
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⏷ Show the Full List of 10 Discontinued Drug(s)
22 Investigative Drug(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
3-(4-Methoxy-benzenesulfonyl)-cyclohexanethiol DM206M1 Discovery agent N.A. Investigative [16]
3-(4-Methoxy-benzenesulfonyl)-hexane-1-thiol DMRLAX8 Discovery agent N.A. Investigative [17]
3-(4-Methoxy-benzenesulfonyl)-pentane-1-thiol DM854IG Discovery agent N.A. Investigative [17]
3-(4-Phenoxy-benzenesulfonyl)-cyclohexanethiol DMBKDZ3 Discovery agent N.A. Investigative [16]
3-(4-Phenoxy-benzenesulfonyl)-propane-1-thiol DM2HBGL Discovery agent N.A. Investigative [17]
3-Benzenesulfinyl-heptanoic acid hydroxyamide DMQXD0N Discovery agent N.A. Investigative [18]
3-Benzenesulfonyl-heptanoic acid hydroxyamide DM7XDCF Discovery agent N.A. Investigative [18]
3-Cyclohexanesulfonyl-heptanoic acid hydroxyamide DMJSOTE Discovery agent N.A. Investigative [18]
4-(4-Butoxy-phenyl)-N-hydroxy-4-oxo-butyramide DMNGDOM Discovery agent N.A. Investigative [19]
4-(4-Methoxy-benzenesulfonyl)-butane-2-thiol DM5PTB9 Discovery agent N.A. Investigative [17]
4-Butoxy-N-hydroxycarbamoylmethyl-benzamide DMMGK2B Discovery agent N.A. Investigative [19]
METHYLAMINO-PHENYLALANYL-LEUCYL-HYDROXAMIC ACID DM9JECY Discovery agent N.A. Investigative [20]
MMI270 DM38N2K Discovery agent N.A. Investigative [21]
N-(Ethylphosphoryl)-L-isoleucyl-L-Trp-NHCH3 DMJ6U4H Discovery agent N.A. Investigative [22]
N-Hydroxy-4-(4-methoxy-phenyl)-4-oxo-butyramide DMQN6CL Discovery agent N.A. Investigative [19]
N-Hydroxy-4-oxo-4-(4-phenoxy-phenyl)-butyramide DMQSWO8 Discovery agent N.A. Investigative [19]
N-Hydroxycarbamoylmethyl-4-methoxy-benzamide DM41JIB Discovery agent N.A. Investigative [19]
N-Hydroxycarbamoylmethyl-4-phenoxy-benzamide DMDTX4L Discovery agent N.A. Investigative [19]
PKF-242-484 DMNDLAS Discovery agent N.A. Investigative [23]
Ro-37-9790 DM83QMZ Discovery agent N.A. Investigative [24]
RS-39066 DM2SCM7 Discovery agent N.A. Investigative [25]
SR-973 DMU48OD Discovery agent N.A. Investigative [26]
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⏷ Show the Full List of 22 Investigative Drug(s)
Molecule Interaction Atlas

References

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2 Matrix metalloproteinase inhibition lowers mortality and brain injury in experimental pneumococcal meningitis. Infect Immun. 2014 Apr;82(4):1710-8.
3 Metalloelastase (MMP-12) induced inflammatory response in mice airways: effects of dexamethasone, rolipram and marimastat. Eur J Pharmacol. 2007 Mar 15;559(1):75-81.
4 Acetylenic TACE inhibitors. Part 3: Thiomorpholine sulfonamide hydroxamates. Bioorg Med Chem Lett. 2006 Mar 15;16(6):1605-9.
5 Gelatinase inhibitors: a patent review (2011-2017).Expert Opin Ther Pat. 2018 Jan;28(1):31-46.
6 Phase 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.
7 Introduction of the 4-(4-bromophenyl)benzenesulfonyl group to hydrazide analogs of Ilomastat leads to potent gelatinase B (MMP-9) inhibitors with i... Bioorg Med Chem. 2008 Sep 15;16(18):8745-59.
8 Structure-based design of potent and selective inhibitors of collagenase-3 (MMP-13). Bioorg Med Chem Lett. 2005 Feb 15;15(4):1101-6.
9 Agents in development for the treatment of diabetic nephropathy. Expert Opin Emerg Drugs. 2008 Sep;13(3):447-63.
10 Broad spectrum matrix metalloproteinase inhibitors: an examination of succinamide hydroxamate inhibitors with P1 C alpha gem-disubstitution. Bioorg Med Chem Lett. 1998 Jun 16;8(12):1443-8.
11 Tumour microenvironment - opinion: validating matrix metalloproteinases as drug targets and anti-targets for cancer therapy. Nat Rev Cancer. 2006 Mar;6(3):227-39.
12 Inhibition of matrix metalloproteinases by N-carboxyalkyl peptides containing extended alkyl residues At P1', Bioorg. Med. Chem. Lett. 5(6):539-542 (1995).
13 Receptor flexibility in the in silico screening of reagents in the S1' pocket of human collagenase. J Med Chem. 2004 May 20;47(11):2761-7.
14 The asymmetric synthesis and in vitro characterization of succinyl mercaptoalcohol and mercaptoketone inhibitors of matrix metalloproteinases. Bioorg Med Chem Lett. 1998 May 19;8(10):1163-8.
15 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.
16 Synthesis and identification of conformationally constrained selective MMP inhibitors. Bioorg Med Chem Lett. 1999 Jul 5;9(13):1757-60.
17 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.
18 Hydroxamic acid derivatives as potent peptide deformylase inhibitors and antibacterial agents. J Med Chem. 2000 Jun 15;43(12):2324-31.
19 Receptor flexibility in de novo ligand design and docking. J Med Chem. 2005 Oct 20;48(21):6585-96.
20 The Protein Data Bank. Nucleic Acids Res. 2000 Jan 1;28(1):235-42.
21 The discovery of a potent and selective lethal factor inhibitor for adjunct therapy of anthrax infection. Bioorg Med Chem Lett. 2006 Feb 15;16(4):964-8.
22 Phosphoramidate peptide inhibitors of human skin fibroblast collagenase. J Med Chem. 1990 Jan;33(1):263-73.
23 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.
24 11,21-Bisphenyl-19-norpregnane derivatives are selective antiglucocorticoids, Bioorg. Med. Chem. Lett. 7(17):2299-2302 (1997).
25 Design, synthesis, activity, and structure of a novel class of matrix metalloproteinase inhibitors containing a heterocyclic P2 P3 Bioorg. Med. Chem. Lett. 6(13):1541-1542 (1996).
26 Synthesis and evaluation of succinoyl-caprolactam gamma-secretase inhibitors. Bioorg Med Chem Lett. 2006 May 1;16(9):2357-63.