Free shipping on all orders over $ 500

MMP Matrix metalloproteinase

Cat.No.  Name Information
M2147 Ilomastat Ilomastat (GM6001; Galardin) is a broad spectrum matrix metalloprotease (MMP) inhibitor with Ki values of 0.4 nM, 0.5 nM, 27 nM, 3.7 nM, 0.1 nM, 0.2 nM, 3.6 nM, 13.4 nM and 0.36 nM for MMPs -1, -2, -3, -7, -8, -9, -12, -14 and -26, respectively. Ilomastat (GM6001; Galardin) reduces infarct volume following middle cerebral artery occlusion in an ischemic mouse model.
M4907 Doxycycline Hyclate Doxycycline is a member of the tetracycline antibiotics group, and is commonly used to treat a variety of infections.
M7413 TMI 1 TMI 1 is a adam 17 (TACE) and MMP inhibitor; orally bioavailable.
M9373 T-5224 T-5224 is a transcription factor c-Fos/activator protein (AP)-1 inhibitor with anti-inflammatory effects.
M4779 Cordycepin Cordycepin (3'-Deoxyadenosine) is a nucleoside derivative isolated from Cordyceps, inhibits IL-1β-induced MMP-1 and MMP-3 expression in rheumatoid arthritis synovial fibroblasts.
M11550 3-Aminopropionitrile fumarate 3-amino-propanonitrile (β -amino-propanonitrile (BAPN)) acts as an irreversible inhibitor of lysyl oxidase (LOX), an enzyme involved in collagen cross-linking.
M11508 Isoginkgetin Isoginkgetin is a naturally occurring diflavone with antitumor activity. Isoginkgetin directly inhibits chymotrypsin-like, trypsin-like, and caspase - like activities of the 20S proteasome. Isoginkgetin is an inhibitor of MMP-9 and also an inhibitor of pre-mrna Splicing.
M9640 MMP-9-IN-1 MMP-9-IN-1 is a specific matrix metalloproteinase-9 (MMP-9) inhibitor.
M9466 S-methyl-KE-298 S-methyl-KE-298 is an active metabolite of KE-298. KE-298 inhibits matrix metalloproteinase (MMP-1) production from rheumatoid arthritis (RA) synovial cells.
M8732 T-26c T-26c is a highly potent, selective and cell-permeable matrix metalloproteinases 13 (MMP-13) inhibitor.
M8156 SB-3CT SB-3CT is a potent matrix metalloproteinase MMP-2 and MMP-9 inhibitor, with Ki values of 13.9 and 600 nM, respectively. SB-3CT shows blood-brain barrier permeability and has neuroprotective effects and anticancer activity.
M8041 CP-101537 Cp-101537 is an MMP inhibitor, a candidate compound for the treatment of myocardial infarction, and an antibacterial compound.
M7736 CL-82198 CL-82198 is a selective inhibitor of MMP-13 that displays no activity at MMP-1, MMP-9 or TACE.
M7454 UK 356618 UK 356618 is a potent and selective MMP-3 inhibitor.
M6749 GI 254023X GI 254023X is a selective ADAM10 metalloprotease inhibitor, with IC50 of 5.3 nM.
M6614 CL 82198 hydrochloride CL 82198 hydrochloride is a selective inhibitor of MMP-13.
M6463 ARP 101 ARP 101 is a selective inhibitor of MMP-2 that displays ~ 600-fold selectivity over MMP-1 (IC50 values are 0.81 and 486 nM respectively).
M6216 TAPI-2 TAPI-2 is a broad-spectrum inhibitor of matrix metalloprotease (MMP), tumour necrosis factorα-converting enzyme (TACE) and a disintegrin and metalloproteinase (ADAM), with an IC50 of 20±10 μM for MMP.
M6215 TAPI-0 TAPI-0 is an inhibitor which blocks the maturation of cytokines, soluble cyokine receptors and other proteins that require the action of proteases.
M4612 Arctigenin Arctigenin ((-) -arctigenin) is a bioactive lignan that can be used as an antitumor agent. Arctigenin has effective antioxidant, anti-inflammatory and antiviral activities. Arctigenin can be used to study metabolic disorders and central nervous system dysfunction.
M4473 Morroniside Morroniside plays a neuroprotective role by inhibiting neuronal apoptosis and mMP9/2 expression.
M4463 Abametapir Abametapir (HA-44, BRN 0123183) is an inhibitor of metalloproteinases critical for louse survival and egg development.
M4314 Lucidenic-acid-A Lucideric acid A, A natural product isolated from Ganoderma lucidum, can inhibit THE activity of MMP-9 induced by PMA, and has an anti-invasion effect on liver cancer cells.
M4311 Lucidenic-acid-C Lucidenic acid C, a natural product isolated from Ganoderma lucidum, can inhibit THE activity of MMP-9 induced by PMA, and has an anti-invasion effect on liver cancer cells.
M4210 EGC EGC is a potent inhibitor of amyloidogenic cystatin I66Q amyloid fibril formation in vitro, can bind to unfolded native polypeptides and prevent conversion to amyloid fibrils.




Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2026 AbMole BioScience. All Rights Reserved.