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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
35 Results for "
MMP-7
" in MedChemExpress (MCE) Product Catalog:
Products (35)
35 Results for "MMP-7" in MCE Product Catalog:
Cat. No.: HY-161169
CAS No.: 2865102-08-3
TP0628103 is a potent and highly selective MMP-7 inhibitor with an IC50 of 0.17 nM. TP0628103 undergoes structural optimization via molecular isoelectric point shifting, which reduces organic anion transporter (OAT)-mediated clearance, while maintaining potent MMP-7 inhibitory activity and enhancing MMP subtype selectivity. TP0628103 is applicable for research on the regulatory mechanisms of MMP-7-related matrix metalloproteinases .
Cat. No.: HY-P4931A
CAS No.: 1392300-20-7
Target:
Research Areas:
Cat. No.: HY-12169R
CAS No.: 154039-60-8
Synonyms: BB2516 (Standard); TA2516 (Standard)
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Marimastat (Standard) is the analytical standard of Marimastat. This product is intended for research and analytical applications. Marimastat (BB2516) is a broad spectrum and orally bioavailable inhibitor of MMPs, with potent activity against MMP-9 (IC50=3 nM), MMP-1 (IC50=5 nM), MMP-2 (IC50=6 nM), MMP-14 (IC50=9 nM) and MMP-7 (IC50=13 nM), used in the treatment of cancer. Marimastat (BB2516) is an angiogenesis and metastasis inhibitor, which limits the growth and production of blood vessels. As an antimetatstatic agent it prevents malignant cells from breaching the basement membranes .
Synonyms: PG 530742; PGE 530742; PGE 7113313
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PG 116800 (PGE 530742; PGE 7113313) is an orally active, selective and high-affinity inhibitor of MMP. PG 116800 acts as an inhibitor of ventricular remodeling, reduces left ventricular volumes and infarct zone collagen content, and improves ejection fraction. PG 116800 is generally well tolerated, but is associated with higher rates of arthralgia, joint stiffness, and dyspepsia. PG 116800 can be used for the research of myocardial infarction .
Cat. No.: HY-P3123
CAS No.: 172666-82-9
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Cat. No.: HY-13564R
CAS No.: 130370-60-4
Synonyms: BB94 (Standard)
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Batimastat (Standard) is the analytical standard of Batimastat. This product is intended for research and analytical applications. Batimastat is a potent broad spectrum MMP inhibitor with IC50 of 3, 4, 4, 6, and 20 nM for MMP-1, MMP-2, MMP-9, MMP-7 and MMP-3, respectively.
Cat. No.: HY-P3699A
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TNO003 TFA is a selective fluorogenic substrate for stromelysin-1 (MMP-3). TNO003 TFA has higher selectivity for MMP-3 than MMP-1, MMP-2, MMP-7, MMP-8, MMP-9 and MMP-13. TNO003 TFA can be used for the determination of stromelysin activity (Ex/Em = 360/490 nm) .
Cat. No.: HY-N3385
CAS No.: 129314-37-0
Synonyms: 7-O-Methyllicorisoflavan B
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Cat. No.: HY-103444R
CAS No.: 704888-90-4
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ARP-100 (Standard) is the analytical standard of ARP-100. This product is intended for research and analytical applications. ARP-100 is a potent and selective matrix metalloproteinase MMP-2 inhibitor (IC50=12 nM). ARP-100 interacts with S1＇ pocket of MMP-2 and shows anti-invasive properties in an in vitro model of invasion on matrigel. ARP-100 shows the less inhibitory activity towards MMP-1 (>50 μM), MMP-3 (4.5 μM), MMP-7 (>50 μM), and MMP-9 (0.2 μM) .
Cat. No.: HY-P705615
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: MMP7; Pump-1 Protease; Prev. MPSL1; MMP-7; Matrilysin; Matrix Metallopeptidase 7 (Matrilysin, Uterine); PUMP-1; Matrix Metalloproteinase 7; Matrix Metalloproteinase 7 (Matrilysin, Uterine); Uterine Matrilysin; Matrix Metalloproteinase-7; PUMP1; Uterine Me
Species:
Cynomolgus
Source:
CHO
Cat. No.: HY-P703938
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: MMP7; Pump-1 Protease; Prev. MPSL1; MMP-7; Matrilysin; Matrix Metallopeptidase 7 (Matrilysin, Uterine); PUMP-1; Matrix Metalloproteinase 7; Matrix Metalloproteinase 7 (Matrilysin, Uterine); Uterine Matrilysin; Matrix Metalloproteinase-7; PUMP1; Uterine Me
Species:
Human
Source:
HEK293
Cat. No.: HY-181769
CAS No.: 3043892-01-6
Research Areas:
Anticancer agent 306 is a spiro tetramic acid derivative and a inhibitor of MMP1, MMP7 and PLK1. Anticancer agent 306 exerts antiproliferative activity against H1299, RKO and MCF-7 cells with IC50 values of 19.25 μM, 3.29 μM and 102.36 μM, respectively. Anticancer agent 306 can up-regulate p21 protein and down-regulate CCND1 and CCNB1 proteins to induce cell cycle arrest, regulate the expression of Bcl-2 and Bax to induce cell apoptosis. Anticancer agent 306 can down-regulate MMP1 and MMP7 proteins to inhibit tumor invasion and metastasis. Anticancer agent 306 can be used for the research of lung cancer, colorectal cancer, breast cancer .
Cat. No.: HY-184162
CAS No.: 2991567-27-0
HSP110-IN-1 is a HSP110 inhibitor. HSP110-IN-1 binds to HSP110, inhibits the activity of STAT3, and downregulates the expression of downstream genes VEGF, MMP7 and MMP9. HSP110-IN-1 abrogates IL-6-induced epithelial-mesenchymal transition and inhibits the proliferation of colorectal cancer cells. HSP110-IN-1 remodels the tumor microenvironment by inducing a pro-inflammatory phenotype, regulates macrophages, induces PD-L1 expression, and enhances anti-PD-L1 antibody-mediated tumor regression. HSP110-IN-1 can be used in studies related to colorectal cancer .
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
