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Cat. No. Product Name Information
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-45629

NAMI-A

MMP-2/9 inhibitor

A ruthenium anticancer agent that has a selective effect on lung metastases of solid metastasizing tumors.
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-25877

JG26

ADAM17 inhibitor

JG26 is a potent, selective ADAM17 inhibitor with IC50 of IC50 of 1.9 nM, weakly inhibits ADAM-10 and MMP-2 (IC50=150 and 240 nM), does not inhibit MMP-1/9/14.
PC-25875

KP-457

ADAM17 inhibitor

KP-457 is a potent, selective ADAM17 inhibitor with IC50 of 11.1 nM, >50 times more selective for ADAM17 than for other MMPs and ADAM10.
PC-25874

INCB3619

ADAM10/ADAM17 inhibitor

INCB3619 (INCB-3619) is a potent, selective and orally active ADAM inhibitor with IC50 of 22 nM and 14 nM for ADAM10 and ADAM17, respectively.
PC-25431

ADAM17 inhibitor 2155-17

ADAM17 inhibitor

ADAM17 inhibitor 2155-17 is a specific small molecule ADAM17 inhibitor with IC50 of 4.3 uM, with no activity against MMP2, MMP8, MMP9 ,MMP14, and ADAM10 (IC50>100 uM).
PC-24822

FLF-15

ADAM17 inhibitor

FLF-15 is a potent, selective ADAM17 inhibitor with IC50 of 10.43 nM, selectively inhibits its IL-6R cleavage activity, inhibits HCC migration and invasion in vitro and in vivo.

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