MMPs (Matrix metalloproteinases) are zinc-dependent endopeptidases.The metzincin superfamily of proteases, to which the MMPs belong, is a larger group of enzymes. MMPs can process a variety of bioactive molecules in addition to breaking down various extracellular matrix proteins. They have been linked to the inactivation of chemokines and cytokines as well as the cleavage of cell surface receptors and the release of apoptotic ligands.Additionally, it is believed that MMPs have a significant impact on the proliferation, migration, differentiation, angiogenesis, apoptosis, and host defense of cells. It is believed that MMP-2 and MMP-9 are crucial for metastasis. MMP-1 is regarded as being significant in osteoarthritis and rheumatoid arthritis. Recent research indicates that MMPs are actively involved in the pathogenesis of aortic aneurysms. The structural proteins of the aortic wall are degraded by excess MMPs. Acute and chronic cardiovascular diseases both exhibit dysregulation of the balance between MMPs and TIMPs.
| Structure | Cat No. | Product Name | CAS No. | Product Description |
|---|---|---|---|---|
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V121428 | (2R)-RXP470.1 | (2R)-RXP470.1 is the (2R)-isomer of RXP470.1. | |
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V121775 | (E)-N-(3-Methoxyphenyl)cinnamamide | 127033-74-3 | (E)-N-(3-Methoxyphenyl)cinnamamide is a weakly selective inhibitor of MMP-2 and MMP-9, with weak inhibitory activity against hMMP-2 and hMMP-9, with IC50 values of 1674.81 nM and 1658.63 nM, respectively, and low selectivity for MMP-1. |
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V121945 | (R)-MMP408 | 1258003-93-8 | (R)-MMP408 is an orally effective MMP-12 inhibitor (IC50 for hMMP-12 = 2.0 nM) that effectively interferes with the epithelial-mesenchymal transition (EMT) process. |
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V73230 | (R)-ND-336 | 2252493-33-5 | (R)-ND-336 is a potent and specific MMP-9 inhibitor (antagonist) with Ki of 19 nM. |
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V89019 | (S,S)-TAPI-0 | 143457-40-3 | (S,S)-TAPI-0 is a matrix metalloproteinase (MMP) inhibitor that inhibits the growth of Chlamydia trachomatis by inhibiting PDF enzyme activity. |
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V117198 | 14-3-3-IN-2 | 919751-10-3 | 14-3-3-IN-2 is a 14-3-3 protein inhibitor with an IC50 value of 15 nM. |
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V73262 | 3,3′-Bisdemethylpinoresinol | 340167-81-9 | 3,3′-Bisdemethylpinoresinol, lignin, is a naturally occurring compound with MMP-1 inhibitory activity on UVA-irradiated human dermal fibroblasts. |
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V105509 | 3-Aminobenzene-1,2-diol | 20734-66-1 | 3-Aminobenzene-1,2-diol (Compound C8) is a matrix metalloproteinase (MMP) inhibitor with IC50 values of 20, 26, 16, and 16.3 μM for MMP-2, MMP-8, MMP-9, and MMP-14, respectively. |
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V111850 | 3-Hydroxy-2-pyrone | 496-64-0 | 3-Hydroxy-2-pyranone (compound 12d) is a metalloenzyme inhibitor. |
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V102751 | 4-Epianhydrochlortetracycline hydrochloride | 158018-53-2 | 4-epitope chlortetracycline hydrochloride is an inhibitor of matrix metalloproteinases (MMPs), especially gelatinase B (EC 3.4.24.35), with an inhibition rate of 100% at 500μg/mL, 70% at 125μg/mL, and 40% at 31μg/mL. |
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V127388 | 6-epi Doxycycline | 3219-99-6 | 6-epi Doxycycline is the C-6 epimer of doxycycline and is a degradation impurity resulting from the epimerization of doxycycline under abnormal conditions (such as high temperature, pH changes, or high humidity). |
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V128057 | ABX-MA1 | 561063-60-3 | ABX-MA1 is a humanized IgG2 monoclonal antibody inhibitor that targets MCAM/MUC18. |
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V73256 | Ac-Pro-Leu-Gly-[(S)-2-mercapto-4-methyl-pentanoyl]-Leu-Gly-OEt | 98992-65-5 | Ac-Pro-Leu-Gly-[(S)-2-mercapto-4-methyl-pentanoyl]-Leu-Gly-OEt is a MMP12 substrate and may be utilized to detect MMP12 enzyme activity. |
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V118457 | ADAM17-IN-1 | 1802395-34-1 | ADAM17-IN-1 is a selective ADAM17 inhibitor. |
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V73254 | ADAM8-IN-1 | 2758892-64-5 | ADAM8-IN-1 is a potent ADAM8 inhibitor (antagonist) with IC50 of 73 nM. |
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V73245 | Aderamastat (FP-025) | 877176-23-3 | Aderamastat (FP-025) is an orally bioactive matrix metalloproteinase 12 (MMP-12) inhibitor. |
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V128389 | AG73 | 170655-66-0 | AG73 is a polypeptide derived from the G domain of the laminin α1 chain. |
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V128396 | Ageladine A dihydrochloride | 2757574-06-2 | Ageladine A dihydrochloride is a matrix metalloproteinase (MMP) inhibitor isolated from marine sponges, and it has anti-angiogenic activity. |
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V87609 | Anti-Human/Mouse denatured collagen type-I Antibody (XL313) | Anti-Human/Mouse denatured collagen type-I Antibody (XL313) is a mouse derived IgG1, κ antibody inhibitor against human or mouse denatured collagen type-I. | |
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V128952 | Anticancer agent 204 | Anticancer agent 204 is a fluorinated cinnamamide derivative with anticancer activity. |