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Cat. No. Product Name Information
PC-73195

GI254023X

ADAM10 inhibitor

GI 254023X (GI4023, SRI028594) is a potent, preferential ADAM10 inhibitor with IC50 of 5.3 nM, also inhibits MMP9 (IC50=2.5 nM), preferentially blocking ADAM10 but not TACE.
PC-73156

GW280264X

ADAM10/17 inhibitor

GW280264X is a potent, dual ADAM10/TACE (ADAM17) metalloproteinases inhibitor with IC50 of 8.0 nM and 11.5 nM, respectively.
PC-72743

ADAM17 inhibitor SN-4

ADAM17 inhibitor

ADAM17 inhibitor SN-4 is a novel specific inhibitor of A disintegrin and metalloproteinase 17 (ADAM17), inhibits TNF-α cleavage by SN-4 in cells with IC50 of 3.22 uM.
PC-72450

RF036

MMP-13 inhibitor

RF036 (MMP-13i) is a potent, highly selective MMP-13 inhibitor with IC50 of 2.7 nM, does not inhibit MMP-1, -2, -8, -9, and -14 (IC50 values >5,000 nM).
PC-72040

PG-116800

MMP inhibitor

PG-116800 is a selective, oral matrix metalloproteinase (MMPs) inhibitor with significant antiremodeling effects in animal models of MI and ischemic heart failure.
PC-72039

Rebimastat

MMP inhibitor

Rebimastat (BMS-275291, D2163) is a potent, broad spectrum matrix metalloproteinase (MMPs) inhibitor with potential antineoplastic activity, shows nM potency against MMP-1/2/7/9/14.
PC-72036

SC-78080

MMP inhibitor

SC-78080 (SD-2590) is a potent, selective inhibitor of MMP2/9/13 with IC50 of <0.1/0.18/<0.1 nM, respectively.
PC-72035

IPR-179

MMP-2/9 inhibitor

IPR-179 (ACT-03) is a potent, BBB-permeable, selective gelatinase (MMP2 and MMP9) inhibitor with IC50 of 656 nM and 310 nM, respectively.
PC-35730

ARP101

MMP-2 inhibitor

ARP101 (ARP-101) is a selective MMP-2 inhibitor, induces autophagy-associated cell death in cancer cells.
PC-35659

(R)-ND-336

MMP-9 inhibitor

(R)-ND-336 is a potent and selective small-molecule MMP-9 inhibitor with Ki of 19 nM, weakly inhibits MMP-2 and MMP-14 (Ki=127 and 119 nM), poorly inhibits other MMPs (Ki>10 uM).
PC-35373

ZLDI-8

ADAM17 inhibitor

ZLDI-8 (IAC-8) is a novel Notch signaling pathway inhibitor for Notch activating/cleaving enzyme ADAM-17, significantly decreases the level of NICD and accumulation of NICD in the nucleus.
PC-35111

BAY-7598

MMP-12 inhibitor

BAY-7598 (BAY7598) is a potent, selective MMP12 inhibitor with IC50 of 0.085, 0.67 and 1.1 nM for human, murine, and rat MMP12, respectively.

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