MMP
Matrix metalloproteinases
Alle MMP Isoform-spezifische Produkte anzeigen
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MMP-1
(62)
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MMP-2
(136)
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MMP-3
(55)
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MMP-8
(30)
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MMP-9
(175)
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MMP-13
(54)
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MMP-14
(23)
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MMP-17
(3)
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ADAM10
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ADAM17
(10)
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MMP-7
(20)
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MMP-12
(18)
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MMP-10
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MMP
(434)
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ADAM8
(1)
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MMP-19
(1)
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All Product Categories
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MMP Inhibitors
(579)
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MMP Agonists
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MMP Antagonist
(1)
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MMP Activators
(28)
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MMP Modulators
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MMP Chemicals
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MMP Inducers
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MMP Degrader
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MMP Controls
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MMP Substrates
(14)
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MMP Ligands
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Matrix Metalloproteinases Proteins
(43)
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MMP-1 Proteins
(2)
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MMP-2 Proteins
(7)
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MMP-3 Proteins
(2)
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MMP-7 Proteins
(2)
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MMP-10 Proteins
(2)
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MMP-12 Proteins
(3)
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MMP-8 Proteins
(7)
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MMP-9 Proteins
(11)
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MMP-13 Proteins
(1)
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MMP-14 Proteins
(1)
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ADAM8 Proteins
(4)
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ADAM10 Proteins
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ADAM17/TACE Proteins
(3)
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MMP Verwandte Produkte (768)
Verwandte Produkte (768)
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Recombinant Proteins (51)
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Antibodies (15)
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MMP Isoform Comparison
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Mmp12 Rat Pre-designed siRNA Set A
0 ImagesArt. -Nr.: HY-RS08524Mmp12 Rat Pre-designed siRNA Set A contains three designed siRNAs for Mmp12 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.
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Antitumor agent-132
0 ImagesArt. -Nr.: HY-162131Antitumor agent-132 (Compound F9) is an antitumor agent. Antitumor agent-132 induces cell apoptosis and increases intracellular reactive oxygen species and reduces MMP. -
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2-Methoxy-2,4-diphenylfuran-3-one
0 ImagesArt. -Nr.: HY-W277900CAS. Nr.: 50632-57-0 -
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Edaravone sulfate-d5
0 ImagesArt. -Nr.: HY-W801479SEdaravone sulfate-d5 is the deuterium labeled Edaravone sulfate. Edaravone is a strong novel free radical scavenger, and inhibits MMP-9-related brain hemorrhage in rats treated with tissue plasminogen activator. -
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CKD-712
0 ImagesArt. -Nr.: HY-114214CAS. Nr.: 626252-75-3CKD-712 is an orally active multi-target tetrahydroisoquinoline derivatived and a potent inhibitor of the NF-κB pathway. CKD-712 selectively inhibits MMP-9 with no effect on MMP-2, downregulates the expression of TNF-α, IL-6, cyclin A, cyclin B, CDK-1 and other proteins, and activates the PI3K/Akt signaling pathway. CKD-712 blocks the activation and nuclear translocation of NF-κB, downregulates inflammatory factors and pro-tumor metastatic proteins, and induces G2/M phase arrest in tumor cells and thereby inhibits the invasion of cancer cells. CKD-712 can be used for the research of sepsis, myocardial ischemia-reperfusion injury and non-small cell lung cancer. -
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Tianeptine-d6 (hydrochloride)
0 ImagesArt. -Nr.: HY-144224STianeptine-d6 hydrochloride is the deuterium labeled Tianeptine hydrochloride. Tianeptine hydrochloride is an atypical antidepressant. Tianeptine hydrochloride is a moderate-intensity agonist of the μ-opioid receptor (MOR), and to a lesser extent, is an agonist of the δ-opioid receptor (DOR). Tianeptine hydrochloride is a glutamate modulator that can enhance AMPA receptor and antagonize NMDA receptor. Tianeptine hydrochloride increases sensitivity of the α1 adrenergic receptor, which only manifests in chronic treatment. Tianeptine hydrochloride exerts neuroprotective effects under stress/inflammation-induced conditions, exhibiting anti-inflammatory and antioxidant properties. Tianeptine hydrochloride inhibits MMP-9 by suppressing the PI3K/Akt-mediated NF-κB pathway. Tianeptine hydrochloride can be used to alleviate symptoms of depression and anxiety, but does not cause sedative effects. -
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PZ-1657
0 ImagesArt. -Nr.: HY-179724PZ-1657 (Compound 57) is an orally active, blood-brain barrier permeable, highly selective, and metabolically stable 5-HT7 receptor inverse agonist with a Ki value of 5 nM. PZ-1657 inhibits constitutive cyclic adenosine monophosphate (cAMP) production mediated by the Gs signaling pathway (EC50 value of 2.93 nM). PZ-1657 inhibits CYP3A4 P450 (IC50 = 12.2 μM) and hERG channels. PZ-1657 reduces 5-HT7 receptor-mediated MMP-9 activity. PZ-1657 reverses Phencyclidine-induced cognitive impairment. PZ-1657 possesses antidepressant properties. -
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GIP (22-51) human
0 ImagesArt. -Nr.: HY-P10972CAS. Nr.: 957470-49-4Synonyms: Glucose-dependent Insulinotropic Peptide (22-51) (human)GIP (22-51) human (Glucose-dependent Insulinotropic Peptide (22-51) human) is a potent proatherosclerotic peptide hormone consisting of 30 amino acids. GIP (22-51) human can activate the NF-κB signaling pathway, promote the expression of MMP-8, and induce the expression of proinflammatory and proatherosclerotic proteins. GIP (22-51) human can also increase the level of intracellular free Ca2+ in THP-1-induced macrophages. GIP (22-51) human can be used in the research of atherosclerosis. -
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D8P1C1
0 ImagesArt. -Nr.: HY-P992341D8P1C1 is a high-affinity ADAM17 inhibitor (with a Kd of 180 pM targeting ADAM17-ECD) that reduces the shedding and phosphorylation of EGFR ligands. D8P1C1 inhibits cancer cell proliferation in vitro and tumor growth in xenograft models. 89Zr-DFO-D8P1C1 radioimmunological PET imaging shows its substantial accumulation in ovarian tumor xenografts, serving as a platform for generating bispecific T-cell engager derivatives. D8P1C1 can be applied to research on related diseases including triple-negative breast cancer, various types of ovarian cancer, lung adenocarcinoma, glioma, and colon cancer. -
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Colchicine-O-CO-Enyl(Me)-Enyl-Enyl(Me)-Enyl-1,3,3-trimethylcyclohex-1-ene
0 ImagesArt. -Nr.: HY-180765Colchicine-O-CO-Enyl(Me)-Enyl-Enyl(Me)-Enyl-1,3,3-trimethylcyclohex-1-ene (compound L2) is a lipophilic colchicinoid formulation targeting hepatic stellate cells (HSC). Colchicine-O-CO-Enyl(Me)-Enyl-Enyl(Me)-Enyl-1,3,3-trimethylcyclohex-1-ene increases the levels of MMP2, MMP8 and MMP9, demonstrating the protective effect in tissue remodeling. Colchicine-O-CO-Enyl(Me)-Enyl-Enyl(Me)-Enyl-1,3,3-trimethylcyclohex-1-ene exhibits anti-fibrotic activity in CCL4-induced liver fibrosis (LF) mouse model. Colchicine-O-CO-Enyl(Me)-Enyl-Enyl(Me)-Enyl-1,3,3-trimethylcyclohex-1-ene can be used for LF research. -
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MEDI-3622
0 ImagesArt. -Nr.: HY-P992406MEDI-3622 is a human monoclonal antibody against ADAM17. MEDI-3622 blocks the ADAM17-mediated shedding of CD16A and CD62L on NK cells, and binds with high specificity to a surface loop unique to the metalloprotease catalytic domain of ADAM17. MEDI-3622 enhances IFNγ production by NK cells when they bind to antibody-coated tumor cells. MEDI-3622 can be used in the research of ovarian cancer, Burkitt lymphoma, head and neck cancer, and colorectal cancer. -
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Mmp13 Rat Pre-designed siRNA Set A
0 ImagesArt. -Nr.: HY-RS08527Mmp13 Rat Pre-designed siRNA Set A contains three designed siRNAs for Mmp13 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.
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PZ-1657 hydrochloride
0 ImagesArt. -Nr.: HY-179724APZ-1657 hydrochloride (Compound 57) is a potent, selective and orally active 5-HT7 receptor inverse agonist with a Ki of 5 nM. PZ-1657 hydrochloride can inhibit the constitutive cAMP production mediated by the Gs signaling pathway (EC50 = 2.93 nM). PZ-1657 hydrochloride can significantly reduce the MMP-9 activity mediated by 5-HT7 receptors in the hippocampus of mice, and the effect is comparable to that of SB-269970 (HY-15370). PZ-1657 hydrochloride can reverse the cognitive deficits observed in the rat novel object recognition test induced by Phencyclidine without affecting the animals' spontaneous activities. PZ-1657 hydrochloride can be used for the research of emotional disorders, such as depression and bipolar disorder. -
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3-Ethyltoluene
0 ImagesArt. -Nr.: HY-W012856CAS. Nr.: 620-14-4Synonyms: 3-Methylethylbenzene3-Ethyltoluene (3-Methylethylbenzene) is an isomer of Ethyltoluenes. 3-Ethyltoluene inhibits cell survival and proliferation and increases ROS production. 3-Ethyltoluene upregulates cellular inflammatory gene expression. 3-Ethyltoluene induces cell fibrosis with increased level of AST, FGF-23, Cyt-7 p21, TGFβ, TIMP2, and MMP2. 3-Ethyltoluene can be used for liver diseases such as NAFLD research. -
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Mmp10 Mouse Pre-designed siRNA Set A
0 ImagesArt. -Nr.: HY-RS08519Mmp10 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Mmp10 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.
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Anticancer agent 183
0 ImagesArt. -Nr.: HY-162079CAS. Nr.: 3018960-58-9Anticancer agent 183 (compound 4h) inhibits the matrix metalloproteinase-9 (MMP-9) viability than 75% at 100 μg/mL. Anticancer agent 183 has anticancer activity with an IC50 value of <0.14 μM on the A549 cell line. Anticancer agent 183 induces apoptotic. -
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BR351
0 ImagesArt. -Nr.: HY-114396CAS. Nr.: 960113-85-3BR351 is a brain penetrant MMP inhibitor with IC50s of 4, 2, 11, 50 nM for MMP2, MMP8, MMP9 and MMP13, respectively. -
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ST09
0 ImagesArt. -Nr.: HY-15668CAS. Nr.: 1370037-59-4ST09 is an efficient and low toxicity Curcumin (HY-N0005) derivative. ST09 significantly inhibits cell migration and downregulates the expression of MMP1, MMP2, and Vimentin. ST09 has strong cytotoxicity to breast cancer cells, such as MDA-MB-231, MCF7 and T47D cells. ST09 induces cell apoptosis by upregulating Bax and cleaved caspase-3/9. ST09 can be used in the research of cancer such as breast cancer. -
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MMP-9-IN-12
0 ImagesArt. -Nr.: HY-175558MMP-9-IN-12 is a matrix metalloproteinase-9 (MMP-9) inhibitor with an IC50 of 6.57 μM. MMP-9-IN-12 shows an IC50 value of 1.54 μM for HCT-116 cells. MMP-9-IN-12 induces cell apoptosis, ROS production and mitochondrial depolarization. MMP-9-IN-12 inhibits cells migration and disrupts cell cycle progression. MMP-9-IN-12 can be used for the research of colorectal cancer (CRC). -
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Adenosine receptor antagonist 7
0 ImagesArt. -Nr.: HY-179248CAS. Nr.: 2570904-69-5Adenosine receptor antagonist 7 is an orally active triple A1/A2A/A2B adenosine receptor antagonist with Ki values of 1.5, 0.6 and 21 nM. Adenosine receptor antagonist 7 shows potent inhibitory activity (IC50 = 0.8 nM) of cAMP production in A2AR-HEK293 cells. Adenosine receptor antagonist 7 can enhance infiltration of effector T cells and increase the CD8+/Treg ratio companied with Avelumab (HY-108730). Adenosine receptor antagonist 7can be used for the research of cancer, such as colon cancer. -
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Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
try each isoform separately.