32 Results for "

MMP7

" in MedChemExpress (MCE) Product Catalog:
Products (32)

32 Results for "MMP7" in MCE Product Catalog:

  • Isoforms Recommended:
  • Targets Recommended:
  • Recombinant Proteins Recommended:
21
21 Publications Verification
Cat. No.: HY-12169
CAS No.: 154039-60-8
Purity:  99.81%
Synonyms: BB2516; TA2516
Target:  

MMP

Research Areas:  

Cancer

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 .
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17
17 Cited Publications
Cat. No.: HY-13564
CAS No.: 130370-60-4
Purity:  98.92%
Synonyms: BB94
Target:  

MMP

Research Areas:  

Cancer

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.
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17
17 Cited Publications
Cat. No.: HY-13564A
CAS No.: 130464-84-5
Purity:  99.04%
Synonyms: BB-94 sodium salt
Target:  

MMP

Research Areas:  

Cancer

Batimastat sodium salt 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.
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4
4 Cited Publications
Cat. No.: HY-N0774
CAS No.: 486-21-5
Isofraxidin, a coumarin component from Acanthopanax senticosus, inhibits MMP-7 expression and cell invasion of human hepatoma cells. Isofraxidin inhibits the phosphorylation of ERK1/2 in hepatoma cells . Isofraxidin attenuates the expression of iNOS and COX-2, Isofraxidinalso inhibits TLR4/myeloid differentiation protein-2 (MD-2) complex formation .
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3
3 Cited Publications
Cat. No.: HY-103444
CAS No.: 704888-90-4
Purity:  98.07%
Target:  

MMP

Research Areas:  

Cancer

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) .
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1
1 Cited Publications
Cat. No.: HY-151540
CAS No.: 2865097-05-6
Purity:  99.64%
Target:  

MMP

Research Areas:  

Cancer

MMP-7-IN-1 is a highly potent and selective MMP-7 inhibitor with an IC50 of 10 nM. MMP-7-IN-1 can be used in the research of diseases such as cancer and fibrosis .
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1
1 Cited Publications
Cat. No.: HY-15606
CAS No.: 304853-42-7
Purity:  99.87%
Synonyms: NSP-989
Target:  

Progesterone Receptor

Research Areas:  

Endocrinology

Tanaproget is an orally effective, selective nonsteroidal progesterone receptor (PR) agonist targeting human PR with an IC50 of 1.7 nM. Tanaproget promotes the interaction between PR receptors and coactivators (such as SRC-1), thereby inhibiting the secretion of matrix metalloproteinases (MMP-3/MMP-7) and reducing endometrial tissue invasion and angiogenesis. Tanaproget can be used for contraception and endometriosis inhibition research .
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1
1 Cited Publications
Cat. No.: HY-P81117
Synonyms: Matrilysin; Matrilysin uterine; Matrin; Matrix Metalloproteinase 7; MMP-7; MMP 7; MMP7; MPSL1; PUMP 1; Pump 1 protease; PUMP1; Uterine Matrilysin; Uterine metalloproteinase; MMP7_HUMAN.

Host:  

Rabbit

Application:  

IHC-P, IHC-F, ICC/IF, ELISA

Reactivity:  

Human, Mouse

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Cat. No.: HY-131498
CAS No.: 140430-53-1
Purity:  99.67%
Synonyms: Mca-Pro-Leu-Gly-Leu-Dpa-Ala-Arg-NH2
Target:  

Fluorescent Dye MMP

Research Areas:  

Cancer

MOCAc-PLGL (Dpa) AR (Mca-Pro-Leu-Gly-Leu-Dpa-Ala-Arg-NH2) is a synthetic fluorescent substrate mainly used for in vitro enzymatic activity assays of MMP-7 (detection at 393 nm after excitation at 328 nm). MOCAc-PLGL (Dpa) AR is specifically cleaved and hydrolyzed by MMP-7 at the Gly-Leu peptide bond, allowing enzymatic activity to be monitored via fluorometry or HPLC (DMSO is usually added to ensure sufficient dissolution when determining kinetic parameters). MOCAc-PLGL (Dpa) AR is used to accurately evaluate the catalytic activity and pH dependence of recombinant mature human MMP-7 in vitro. MOCAc-PLGL (Dpa) AR is suitable for research on the mechanisms of tumor metastasis and invasion, particularly in fields such as prostate cancer, colon cancer, lung cancer and breast cancer .\n
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Cat. No.: HY-153563
CAS No.: 2848717-49-5
Purity:  99.59%
Target:  

MMP

Research Areas:  

Cancer

MMP-7-IN-2 is a potent and selective inhibitor of MMP7 with an IC50 value of 16 nM. MMP-7-IN-2 can be used for the research of diseases such as cancer and fibrosis .
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Cat. No.: HY-156430
CAS No.: 2865097-58-9
Purity:  99.76%
Target:  

MMP

Research Areas:  

Cancer

MMP-7-IN-3 is a potent and selective inhibitor of MMP-7. MMP-7-IN-3 suppresses kidney fibrosis progression in a mouse model with unilateral ureteral obstruction .
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Cat. No.: HY-161169A
CAS No.: 2865106-78-9
Target:  

MMP

Research Areas:  

Cancer

TP0628103 TFA is a potent and highly selective MMP-7 inhibitor with an IC50 of 0.17 nM. TP0628103 TFA 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 TFA is applicable for research on the regulatory mechanisms of MMP-7-related matrix metalloproteinases .
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Cat. No.: HY-119423
CAS No.: 203915-59-7
Purity:  ≥99.0%
Target:  

MMP

Research Areas:  

Cancer

MMP Inhibitor II (compound 4e) is a potent, reversible pan-MMP inhibitor with IC50 values of 24 nM, 18.4 nM, 30 nM, and 2.7 nM for MMP-1,MMP-3, MMP-7, and MMP-9, respectively .
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Cat. No.: HY-RS08552
Research Areas:  

Others

Mmp7 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Mmp7 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS08551
Research Areas:  

Others

MMP7 Human Pre-designed siRNA Set A contains three designed siRNAs for MMP7 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS08553
Research Areas:  

Others

Mmp7 Rat Pre-designed siRNA Set A contains three designed siRNAs for Mmp7 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-P3123A
Target:  

Fluorescent Dye

Research Areas:  

Others

Dnp-RPLALWRS TFA is a fluorescent peptide substrate designed for human matrilysin (MMP-7). After enzymatic cleavage of Dnp-RPLALWRS TFA at the alanine-leucine bond, the release of the Dnp group alleviates fluorescence quenching, thereby enabling real-time quantitative analysis of MMP-7 activity by increasing tryptophan emission. Dnp-RPLALWRS TFA provides a sensitive and efficient detection method for kinetic studies and inhibitor screenin .
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Cat. No.: HY-130076
CAS No.: 869577-51-5
Target:  

MMP

Research Areas:  

Cancer

MMP-2 Inhibitor II (compound 2) is a selective MMP-2 inhibitor. The Kinetic parameters for MMP inhibition are 2.4 μM (MMP-2), 45 μM (MMP-1), and 379 μM (MMP-7), respectively .
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Cat. No.: HY-P3699
CAS No.: 202273-56-1
Target:  

MMP Fluorescent Dye

Research Areas:  

Others

TNO003 is a selective fluorogenic substrate for stromelysin-1 (MMP-3). TNO003 has higher selectivity for MMP-3 than MMP-1, MMP-2, MMP-7, MMP-8, MMP-9 and MMP-13. TNO003 can be used for the determination of stromelysin activity (Ex/Em = 360/490 nm) .
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Cat. No.: HY-161169
CAS No.: 2865102-08-3
Target:  

MMP

Research Areas:  

Cancer

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 .
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