General Information of DTT (ID: TT6X50U)

DTT Name Matrix metalloproteinase-9 (MMP-9) DTT Info
Gene Name MMP9

Molecule-Related Drug & Molecule List

Molecule-Related Drug List
Molecule Type:
DTT
DTP
DME
Drug Status:
Discontinued Drug(s)
Clinical Trial Drug(s)
Preclinical Drug(s)
Patented Agent(s)
Investigative Drug(s)
6 Clinical Trial Drug(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
Andecaliximab DMLDB1X Gastric adenocarcinoma 2B72 Phase 3 [1]
Curcumin DMQPH29 Solid tumour/cancer 2A00-2F9Z Phase 3 [2]
DP-b99 DM97S10 Stroke 8B20 Phase 3 [3]
GS-5745 DMP8MDW Gastric adenocarcinoma 2B72 Phase 3 [4]
BLZ-100 DMFKA4G Glioma 2A00.0 Phase 1/2 [5]
Neovastat DMXTYWJ Non-small-cell lung cancer 2C25.Y Phase 1 [6]
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⏷ Show the Full List of 6 Clinical Trial Drug(s)
8 Patented Agent(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
PMID29130358-Compound-Figure13(4) DMDFPIO N. A. N. A. Patented [7]
PMID29130358-Compound-Figure17(10) DMVA15O N. A. N. A. Patented [7]
PMID29130358-Compound-Figure17(11) DMSZA9L N. A. N. A. Patented [7]
PMID29130358-Compound-Figure17(12) DMML4PA N. A. N. A. Patented [7]
PMID29130358-Compound-Figure17(13) DM2QRIW N. A. N. A. Patented [7]
PMID29130358-Compound-Figure18(14a) DMHIBTZ N. A. N. A. Patented [7]
PMID29130358-Compound-LonimacranthoideVII DMOGIAU N. A. N. A. Patented [7]
PMID29130358-Compound-SB-3CT DMC64XQ N. A. N. A. Patented [7]
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⏷ Show the Full List of 8 Patented Agent(s)
7 Discontinued Drug(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
Galarubicin DMTNYSF Solid tumour/cancer 2A00-2F9Z Discontinued in Phase 2 [8]
GM6001 DM7V9CT Corneal ulcer 9A76 Discontinued in Phase 2 [9]
RS-130830 DMOTANY Hepatitis C virus infection 1E51.1 Discontinued in Phase 2 [10]
CDP-845 DMGMS2D Solid tumour/cancer 2A00-2F9Z Terminated [12]
CT-1746 DM84KOY Colorectal cancer 2B91.Z 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 7 Discontinued Drug(s)
1 Preclinical Drug(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
DX-2802 DM8YSW7 Solid tumour/cancer 2A00-2F9Z Preclinical [11]
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34 Investigative Drug(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
(+/-)5-(biphenyl-4-yl)-3-hydroxypentanoic acid DMSN7GJ Discovery agent N.A. Investigative [16]
2-(4'-chloro-biphenyl-4-sulfonyl)-pentanoic acid DMQAVM4 Discovery agent N.A. Investigative [17]
2-(biphenyl-4-ylsulfonamido)pentanedioic acid DMH3YBR Discovery agent N.A. Investigative [18]
2-(Biphenyl-4-ylsulfonyl)N-hydroxybenzamide DMCNV5J Discovery agent N.A. Investigative [19]
2-Amino-N,3,3-Trimethylbutanamide DM3YI9P Discovery agent N.A. Investigative [20]
3-(4-(2-phenylethynyl)benzoyl)pentanoic acid DMQDPHT Discovery agent N.A. Investigative [21]
3-(4-Phenylethynylbenzoyl)nonanoic acid DMXL0J5 Discovery agent N.A. Investigative [21]
4-amino-3-(4-(hexyloxy)phenyl)-4-oxobutanoic acid DMGI0YV Discovery agent N.A. Investigative [18]
5-(4-Phenoxy-phenyl)-pyrimidine-2,4,6-trione DM05OMF Discovery agent N.A. Investigative [22]
5-Biphenyl-4-yl-5-ethyl-pyrimidine-2,4,6-trione DMFAITE Discovery agent N.A. Investigative [22]
5-Biphenyl-4-yl-5-hexyl-pyrimidine-2,4,6-trione DMI2PXO Discovery agent N.A. Investigative [22]
5-Hexyl-5-phenyl-pyrimidine-2,4,6-trione DM4S86L Discovery agent N.A. Investigative [22]
5-Methyl-5-phenyl-pyrimidine-2,4,6-trione DMRMKXD Discovery agent N.A. Investigative [22]
ARP100 DM6KQXF Discovery agent N.A. Investigative [23]
Carboxylated glucosamine DM105YR Discovery agent N.A. Investigative [24]
Folate gamma-hydroxamic acid DMJ4F3Q Discovery agent N.A. Investigative [25]
IK-862 DMJA4UE Discovery agent N.A. Investigative [26]
Methotrexate gamma-hydroxamic acid DM8P526 Discovery agent N.A. Investigative [25]
Methotrexate gamma-L-phenylalaninehydroxamic acid DMELK2A Discovery agent N.A. Investigative [25]
Methotrexate gamma-L-proline-hydroxamic acid DMPYJLA Discovery agent N.A. Investigative [25]
MMI270 DM38N2K Discovery agent N.A. Investigative [27]
N-hydroxy-2,3-bis(phenylsulfonamido)propanamide DMZWIVJ Discovery agent N.A. Investigative [28]
N-Hydroxy-2-(4-phenoxy-benzenesulfonyl)benzamide DM4VADN Discovery agent N.A. Investigative [19]
N-hydroxy-3-(2-oxo-2H-chromen-3-yl)propanamide DMWXUCT Discovery agent N.A. Investigative [29]
N-hydroxy-3-(6-methoxy-2-oxo-2H-chromen-3-yl) DMA6EPH Discovery agent N.A. Investigative [29]
PMID15055993C1a DM9V6YK Discovery agent N.A. Investigative [30]
PMID23631440C29e DMM92IB Discovery agent N.A. Investigative [31]
Ro 28-2653 DMDC4HY Discovery agent N.A. Investigative [32]
Ro-37-9790 DM83QMZ Discovery agent N.A. Investigative [33]
Roche 28-2653 DMD4JHK Discovery agent N.A. Investigative [32]
SL422 DM3I2US Discovery agent N.A. Investigative [34]
SR-973 DMU48OD Discovery agent N.A. Investigative [35]
UK-356618 DM02FGH Discovery agent N.A. Investigative [36]
[2-(Biphenyl-4-sulfonyl)phenyl]acetic Acid DM37C25 Discovery agent N.A. Investigative [19]
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⏷ Show the Full List of 34 Investigative Drug(s)
Molecule Interaction Atlas

References

1 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
2 Synthesis and biological evaluation of curcuminoid pyrazoles as new therapeutic agents in inflammatory bowel disease: effect on matrix metalloprote... Bioorg Med Chem. 2009 Feb 1;17(3):1290-6.
3 DP-b99 modulates matrix metalloproteinase activity and neuronal plasticity. PLoS One. 2014 Jun 11;9(6):e99789.
4 National Cancer Institute Drug Dictionary (drug id 747683).
5 Antibodies and venom peptides: new modalities for ion channels. Nat Rev Drug Discov. 2019 May;18(5):339-357.
6 Neovastat, a naturally occurring multifunctional antiangiogenic drug, in phase III clinical trials. Semin Oncol. 2001 Dec;28(6):620-5.
7 Gelatinase inhibitors: a patent review (2011-2017).Expert Opin Ther Pat. 2018 Jan;28(1):31-46.
8 Inhibitory effect of DA-125, a new anthracyclin analog antitumor agent, on the invasion of human fibrosarcoma cells by down-regulating the matrix m... Biochem Pharmacol. 2005 Dec 19;71(1-2):21-31.
9 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.
10 Structure-based design of potent and selective inhibitors of collagenase-3 (MMP-13). Bioorg Med Chem Lett. 2005 Feb 15;15(4):1101-6.
11 Clinical pipeline report, company report or official report of DeepDyve.
12 Clinical potential of matrix metalloprotease inhibitors. Drugs R D. 1999 Feb;1(2):117-29.
13 Conversion of highly malignant colon cancer from an aggressive to a controlled disease by oral administration of a metalloproteinase inhibitor. Clin Exp Metastasis. 1997 Mar;15(2):184-95.
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 Design and synthesis of a series of (2R)-N(4)-hydroxy-2-(3-hydroxybenzyl)-N(1)- [(1S,2R)-2-hydroxy-2,3-dihydro-1H-inden-1-yl]butanediamide derivati... J Med Chem. 2001 Oct 11;44(21):3347-50.
16 The identification of beta-hydroxy carboxylic acids as selective MMP-12 inhibitors. Bioorg Med Chem Lett. 2009 Oct 1;19(19):5760-3.
17 Synthesis and SAR of alpha-sulfonylcarboxylic acids as potent matrix metalloproteinase inhibitors. Bioorg Med Chem Lett. 2006 Jun 15;16(12):3096-100.
18 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.
19 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.
20 How many drug targets are there Nat Rev Drug Discov. 2006 Dec;5(12):993-6.
21 Selective inhibition of matrix metalloproteinase isozymes and in vivo protection against emphysema by substituted gamma-keto carboxylic acids. J Med Chem. 2006 Jan 26;49(2):456-8.
22 Novel 5,5-disubstitutedpyrimidine-2,4,6-triones as selective MMP inhibitors. Bioorg Med Chem Lett. 2001 Apr 23;11(8):969-72.
23 Amber force field implementation, molecular modelling study, synthesis and MMP-1/MMP-2 inhibition profile of (R)- and (S)-N-hydroxy-2-(N-isopropoxy... Bioorg Med Chem. 2006 Jun 15;14(12):4260-76.
24 Carboxy derivatized glucosamine is a potent inhibitor of matrix metalloproteinase-9 in HT1080 cells. Bioorg Med Chem Lett. 2006 Jun 15;16(12):3105-10.
25 Methotrexate gamma-hydroxamate derivatives as potential dual target antitumor drugs. Bioorg Med Chem. 2007 Feb 1;15(3):1266-74.
26 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.
27 Picking the S1, S1' and S2' pockets of matrix metalloproteinases. A niche for potent acyclic sulfonamide inhibitors. Bioorg Med Chem Lett. 1999 Jun 21;9(12):1691-6.
28 Novel bis-(arylsulfonamide) hydroxamate-based selective MMP inhibitors. Bioorg Med Chem Lett. 2008 Jun 1;18(11):3333-7.
29 Chromen-based TNF-alpha converting enzyme (TACE) inhibitors: design, synthesis, and biological evaluation. Bioorg Med Chem. 2008 Jan 1;16(1):530-5.
30 Azasugar-based MMP/ADAM inhibitors as antipsoriatic agents. J Med Chem. 2004 Apr 8;47(8):1930-8.
31 Matrix metalloproteinase inhibitors based on the 3-mercaptopyrrolidine core. J Med Chem. 2013 Jun 13;56(11):4357-73.
32 The new synthetic matrix metalloproteinase inhibitor (Roche 28-2653) reduces tumor growth and prolongs survival in a prostate cancer standard rat model. Oncogene. 2002 Mar 27;21(13):2089-96.
33 11,21-Bisphenyl-19-norpregnane derivatives are selective antiglucocorticoids, Bioorg. Med. Chem. Lett. 7(17):2299-2302 (1997).
34 Design, synthesis, and structure-activity relationships of macrocyclic hydroxamic acids that inhibit tumor necrosis factor alpha release in vitro and in vivo. J Med Chem. 2001 Aug 2;44(16):2636-60.
35 Synthesis and evaluation of succinoyl-caprolactam gamma-secretase inhibitors. Bioorg Med Chem Lett. 2006 May 1;16(9):2357-63.
36 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.