Mmp et Impuretés

ND-322 HCl (ND 322 Hydrochloride) is a selective inhibitor of MT1-MMP and MMP2 and reduces …

DB04760: selective MMP-13 inhibitor, non-zinc-chelating, IC50=8nM, reduces paclitaxel neurotoxicity, anticancer.

MMP13-IN-4 (compound 13) is a potent, selective MMP-13 inhibitor with an IC50 of 14.6 μM, …

TAPI1 (TAPI) , an ADAM17/TACE inhibitor, inhibits shedding of cytokine receptors.

BR351 is a brain penetrant MMP inhibitor (IC50s: 4, 2, 11, 50 nM for MMP2, …

MMP-2/MMP-9-IN-1: oral IV collagenase inhibitor; IC50: 0.24 μM (MMP-9), 0.31 μM (MMP-2); targets cancer.

PG-116800 (PG-530742) is a matrix metalloproteinase (MMP) inhibitor. PG-116800 can be used in studies about …

MMP2-IN-2 is an MMP-2 inhibitor that inhibits MMP-13, MMP-9, and MMP-8, and can be used …

Tanomastat is an orally bioavailable and non-peptidic biphenyl matrix metalloproteinases inhibitor.

Aderamastat (FP-025) is an orally active matrix metalloproteinase 12 (MMP-12) inhibitor indicated for the study …

MMP3 inhibitor 1 is a potent and highly selective inhibitor of MMP-3 (IC50 of 1 …

XL-784 inhibits MMPs; IC50: 1900 nM (MMP-1), 0.81 nM (MMP-2), 120 nM (MMP-3), 10.8 nM …

Ro 31-9790 is a synthetic inhibitor of metalloproteinase (MMP).

TP0556351: potent MMP2 inhibitor with 0.2 nM IC50, reduces collagen in pulmonary fibrosis mice.

Apratastat is an orally active, potent, and reversible dual inhibitor of tumor necrosis factor-α converting …

MMP-7-IN-3 is a potent, selective MMP-7 inhibitor that effectively suppresses the progression of kidney fibrosis …

IK-862 is a selective TACE inhibitor with potential anti-inflammatory and anticancer activity for the study …

MMP13-IN-3 is an oral, selective MMP-13 inhibitor with IC50 of 1 nM, >1000x selective, for …

MMP-7-IN-2 acts as a selective and potent MMP7 inhibitor and can be used to study …

UK-370106 is a potent and highly selective inhibitor of MMP-3 with IC50 of 23 nM …