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Cat. No. Product Name Information
PC-61392

Otaplimastat

Otaplimastat is a potent matrix metalloproteinase (MMP) inhibitor.
PC-70316

ND-336

MMP2, 3, 9 inhibitor

ND-336 (ND336) is a potent, selective inhibitor of the gelatinases MMP2 and MMP9 and MMP13 with Ki of 85, 150 and 120 nM, respectively.
PC-61148

PF-152

MMP13 inhibitor

PF-152 is a potent, highly selective and orally bioavailable MMP13 inhibitor with Ki of 1.5 nM, with no activity against MMP3 (Ki>10 uM).
PC-60981

BK-1361

ADAM8 inhibitor

BK-1361 (BK1361, cyclo-RLsKDK) is a cyclic peptide with RLsKDK (s=D-serine) that functions as a potent, selective inhibitor of ADAM8 with IC50 of 120 nM.
PC-60174

ND-378

MMP-2 inhibitor

ND-378 (ND378) is a potent, selective MMP-2 inhibitor with Ki of 230 nM.
PC-42562

CTS-1027

MMP inhibitor

CTS-1027 (RS-130830) is a potent, selective, broad-spectrum MMP inhibitor with Ki of <9 nM for MMP2, 3, 8, 9, 12, 13 and 14, but not MMP1 and 7.
PC-42086

TAPI-2

ADAM17 inhibitor

TAPI-2 is a broad-spectrum inhibitor of TNF-α converting enzyme (TACE, ADAM17), ADAMs, and other MMPs, inhibits ADAM8, 10, 12, and TACE with Ki values of 10, 3, 100, and 0.12 uM, respectively.
PC-42904

Marimastat

MMP inhibitor

Marimastat (BB-2516, TA-2516) is a potent, broad spectrum MMP inhibitor for MMP9/1/2/14/7 with IC50 of 3/5/6/9/13 nM, respectively.
PC-21808

ADAM9i

ADAM9 inhibitor

ADAM9i is a specific small molecule inhibitor of ADAM9 protein with binding KD of 5.9 uM and enzyme IC50 of 5.2 uM, promotes the selective degradation of KRAS and sensitizes pancreatic cancers to chemotherapy.
PC-21754

ADAMTS7 inhibitor 50

ADAMTS7 inhibitor

ADAMTS7 inhibitor 50 is a potent selective ADAMTS7 inhibitor with IC50 of 2 nM, 20-fold selective over ADAMTS12 and highly selective over a range of metalloproteases.
PC-21753

BAY-9835

ADAMTS7 inhibitor

BAY-9835 is the first orally bioavailable, potent and selective inhibitor of dual matrix metalloprotease ADAMTS7/ADAMTS12 with IC50 of 6 nM/30 nM respectively.
PC-21674

TP0628103

MMP-7 inhibitor

TP0628103 is a highly potent, selective matrix metalloproteinase-7 (MMP-7) inhibitor with IC50 of 0.17 nM and 4.1 nM for human and mouse MMP-7, respectively.

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