16 Results for "

matrix metalloproteinase-1

" in MedChemExpress (MCE) Product Catalog:
Products (16)

16 Results for "matrix metalloproteinase-1" in MCE Product Catalog:

3
3 Cited Publications
Cat. No.: HY-N5072
CAS No.: 17817-31-1
Synonyms: 4',6,7-Trihydroxyisoflavone
Desmethylglycitein (4',6,7-Trihydroxyisoflavone), a metabolite of daidzein, sourced from Glycine max with antioxidant, and anti-cancer activities. Desmethylglycitein binds directly to CDK1 and CDK2 in vivo, resulting in the suppresses CDK1 and CDK2 activity . Desmethylglycitein is a direct inhibitor of protein kinase C (PKC)α, against solar UV (sUV)-induced matrix matrix metalloproteinase 1 (MMP1) . Desmethylglycitein binds to PI3K in an ATP competitive manner in the cytosol, where it inhibits the activity of PI3K and downstream signaling cascades, leading to the suppression of adipogenesis in 3T3-L1 preadipocytes .
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1
1 Cited Publications
Cat. No.: HY-P70250
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: MMP1; matrix Metallopeptidase 1 (Interstitial Collagenase); Prev. CLG; matrix metalloproteinase 1; Interstitial Collagenase; matrix Metalloprotease 1; Fibroblast Collagenase; Alternative Protein MMP1; matrix metalloproteinase 1 (Interstitial Collagenase); MMP-1; matrix Metallopeptidase 1; matrix metalloproteinase-1
Species:  
Human
Source:  
HEK293
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Cat. No.: HY-126956
CAS No.: 70579-26-9
Porphyra 334 is a carnosine-like amino acid and a natural photoprotective agent and antioxidant. Porphyra-334 exerts its photoprotective effects by scavenging ROS, inhibiting the expression and activity of MMP-1/8, and promoting the synthesis of collagen and elastin. Porphyra 334 effectively inhibits linoleic acid oxidation induced by alkyl radicals (AAPH) and singlet oxygen. Porphyra 334 has anti-obesity potential by inhibiting the expression of PPARγ2 and C/EBPα. Porphyra 334 protects cells against UV-induced DNA damage and apoptosis by inhibiting the activation of caspase-3 .
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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-P10043
CAS No.: 150956-93-7
Target:  

MMP

Research Areas:  

Others

MMP-1 Substrate is a matrix metalloproteinase-1 (MMP-1) selective substrate that can be used for the fluorometric determination of MMP-1 enzymatic activity .
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Cat. No.: HY-P3098
CAS No.: 256394-94-2
Target:  

MMP

Research Areas:  

Others

Mca-P-Cha-G-Nva-HA-Dap(DNP)-NH2 is a fluorogenic substrate for matrix metalloproteinase-1 (MMP-1), MMP-3, and MMP-26. Mca-P-Cha-G-Nva-HA-Dap(DNP)-NH2 can be used to quantify MMP-1, MMP-3 and MMP-26 activity .
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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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Cat. No.: HY-N5072R
CAS No.: 17817-31-1
Synonyms: 4',6,7-Trihydroxyisoflavone (Standard)
Desmethylglycitein (4',6,7-Trihydroxyisoflavone), a metabolite of daidzein, sourced from Glycine max with antioxidant, and anti-cancer activities. Desmethylglycitein binds directly to CDK1 and CDK2 in vivo, resulting in the suppresses CDK1 and CDK2 activity . Desmethylglycitein is a direct inhibitor of protein kinase C (PKC)α, against solar UV (sUV)-induced matrix matrix metalloproteinase 1 (MMP1) . Desmethylglycitein binds to PI3K in an ATP competitive manner in the cytosol, where it inhibits the activity of PI3K and downstream signaling cascades, leading to the suppression of adipogenesis in 3T3-L1 preadipocytes .
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Cat. No.: HY-P70250A
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: MMP1; matrix Metallopeptidase 1 (Interstitial Collagenase); Prev. CLG; matrix metalloproteinase 1; Interstitial Collagenase; matrix Metalloprotease 1; Fibroblast Collagenase; Alternative Protein MMP1; matrix metalloproteinase 1 (Interstitial Collagenase)
Species:  
Human
Source:  
HEK293
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Cat. No.: HY-P80754A
Synonyms: MMP1; CLG; Interstitial collagenase; Fibroblast collagenase; matrix metalloproteinase-1; MMP-1

Host:  

Rabbit

Application:  

WB, FC, ICC/IF, IHC-P

Reactivity:  

Human

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Cat. No.: HY-P85280
Synonyms: MMP1; CLG; Interstitial collagenase; Fibroblast collagenase; matrix metalloproteinase-1; MMP-1

Host:  

Mouse

Application:  

WB

Reactivity:  

Human

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Cat. No.: HY-P80754
Synonyms: MMP1; CLG; Interstitial collagenase; Fibroblast collagenase; matrix metalloproteinase-1; MMP-1

Host:  

Rabbit

Application:  

WB, IP

Reactivity:  

Human

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Cat. No.: HY-N7984
CAS No.: 55481-90-8
Synonyms: Laricitrin 3-O-rutinoside
Laricitrin 3-rutinoside (Laricitrin 3-O-rutinoside) is a flavonol rutin. Laricitrin 3-rutinoside can be isolated from the fruits of Ginkgo biloba. Laricitrin 3-rutinoside inhibits ERK phosphorylation, reactive oxygen species (ROS) production, and matrix metalloproteinase-1 (MMP-1) secretion. Laricitrin 3-rutinoside inhibits Collagen degradation. Laricitrin 3-rutinoside reduces the secretion of proinflammatory cytokines interleukin 6 (IL-6) and interleukin 8 (IL-8). Laricitrin 3-rutinoside is applicable to research related to skin aging .
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Cat. No.: HY-162902
CAS No.: 3001361-04-9
Target:  

TGF-β Receptor

Research Areas:  

Cardiovascular Disease

ALK5-IN-82 is a potent and selective inhibitor against activin receptor-like kinase 5 (ALK5) with an IC50 value of 9.1 nM. ALK5-IN-82 inhibits the protein expression of α-smooth muscle actin (α-SMA), collagen I and tissue inhibitor of metalloproteinase 1 (TIMP-1)/matrix metalloproteinase 13 (MMP-13) in transforming growth factor-β-induced human umbilical vein endothelial cells. ALK5-IN-82 is promising for research of cardiac fibrosis .
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Cat. No.: HY-P87877
Synonyms: CLG, MMP1, Interstitial collagenase, Fibroblast collagenase, matrix metalloproteinase-1, MMP-1

Host:  

Rabbit

Application:  

WB, IHC-P, ICC/IF, IP, ELISA

Reactivity:  

Human

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Cat. No.: HY-119138
CAS No.: 321344-32-5
Target:  

p38 MAPK MMP PGE synthase

Research Areas:  

Inflammation/Immunology

R-130823 is an orally active, highly selective p38α inhibitor with an IC50 of 22 nM against p38α, an IC50 of 820 nM against p38β, and no activity against p38γ or p38δ. R-130823 downregulates downstream cartilage degradation and inflammatory mediators, and inhibits the release of MMP-13, MMP-1 and PGE2. R-130823 reduces hind paw swelling, improves hyperalgesia, and blocks arthritis progression. R-130823 is applicable to research related to osteoarthritis and rheumatoid arthritis .
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