13 Results for "

Caveolin-1

" in MedChemExpress (MCE) Product Catalog:
Products (13)

13 Results for "Caveolin-1" in MCE Product Catalog:

3
3 Cited Publications
Cat. No.: HY-P2288A
Target:  

Peptides

Research Areas:  

Cancer

WL47 TFA, a high-affinity cavolin-1 (CAV1) ligand (Kd=23 nM), is a potent disrupter of CAV1 oligomers. WL47 TFA shows selectivity for CAV1 over BSA, casein and HEWL. WL47 TFA is 80% smaller in length than the original T20 (HY-P0052) parent sequence and can be used for the study of caveolin-1 function [1].
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1
1 Cited Publications
Cat. No.: HY-P80053

Host:  

Rabbit

Application:  

WB, ICC/IF, IHC-P

Reactivity:  

Human, Mouse

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Cat. No.: HY-P5904
CAS No.: 2757108-69-1
Synonyms: Caveolin-1 scaffolding domain peptide
Target:  

c-Met/HGFR

Research Areas:  

Others

Caveolin-1 (82-101) amide (human, mouse, rat) (Caveolin-1 scaffolding domain peptide) is a peptide that reverses aging-associated deleterious changes in multiple organs. Caveolin-1 (82-101) amide (human, mouse, rat) inhibits tyrosine kinases [1].
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Cat. No.: HY-W015820
CAS No.: 87-41-2
Phthalide is a chemical scaffold. Phthalide derivatives act as potent blood-brain barrier modulators. Phthalide exhibits significant anti-inflammatory activity. Some phthalide derivatives possess anti-inflammatory activity. The phthalide derivative Senkyunolide I shows analgesic effects and ameliorates cerebral edema and cerebral infarction volume in rats with focal cerebral ischemia-reperfusion injury. Phthalide can be used in research related to glioma, rheumatoid arthritis, malaria, bacterial infection, fungal infection and ischemic stroke [1] .
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Cat. No.: HY-W011762
CAS No.: 255906-59-3
Target:  

Apoptosis

Research Areas:  

Cancer

VK3-OCH3 is a potent antitumor agent. VK3-OCH3 shows cytotoxicity for neuroblastoma cell lines and low cytotoxicity for normal cell lines. VK3-OCH3 induces apoptosis and cell cycle arrest at G2/M phase in IMR-32 cells. VK3-OCH3 shows antitumor activity [1].
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Cat. No.: HY-P82037
Synonyms: CAV1; CAV; Caveolin-1

Host:  

Rabbit

Application:  

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

Reactivity:  

Human

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Cat. No.: HY-P86337
Synonyms: CAV1; CAV; Caveolin-1

Host:  

Rabbit

Application:  

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

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P82037A
Synonyms: CAV1; CAV; Caveolin-1

Host:  

Rabbit

Application:  

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

Reactivity:  

Human

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Cat. No.: HY-P2288
Target:  

Peptides

Research Areas:  

Cancer

WL47, a high-affinity cavolin-1 (CAV1) ligand (Kd=23 nM), is a potent disrupter of CAV1 oligomers. WL47 shows selectivity for CAV1 over BSA, casein and HEWL. WL47 is 80% smaller in length than the original T20 (HY-P0052) parent sequence and can be used for the study of caveolin-1 function [1].
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Cat. No.: HY-W011762R
CAS No.: 255906-59-3
Research Areas:  

Cancer

Fluoxetine (hydrochloride) (Standard) is the analytical standard of Fluoxetine (hydrochloride). This product is intended for research and analytical applications. Fluoxetine hydrochloride (LY 110140) is an antidepressant and a selective serotonin reuptake inhibitor.
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Cat. No.: HY-W342441
CAS No.: 54827-14-4
Research Areas:  

Metabolic Disease Cancer

Monosialoganglioside GM3 (bovine) is a monosialoganglioside and an inhibitor of VEGFR2 and Akt. At a concentration of 20 μM, Monosialoganglioside GM3 inhibits angiogenesis and reduces the proliferation and migration of human umbilical vein endothelial cells (HUVECs) by inhibiting VEGFR2 and Akt phosphorylation. Ganglioside GM3 also inhibits ferroptosis, providing protective effects during the formation of abdominal aortic aneurysms. Additionally, Monosialoganglioside GM3 (bovine) acts as an inhibitor of insulin signaling, inducing the dissociation of the insulin receptor (IR)-Caveolin-1 complex from lipid microdomains and causing insulin resistance in adipocytes. Monosialoganglioside GM3 (bovine) can be used in cancer and metabolic disease research [1].
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Cat. No.: HY-P10332
Target:  

Peptides

Research Areas:  

Others

WL 47 dimer (ligand 1) is a caveolin-1 (CAV-1) ligand with high affinity, selectivity and oligomer dissociation activity. WL 47 dimer simultaneously occupies two binding sites of CAV-1, inducing the dissociation of oligomers. WL 47 dimer has 7500-fold improved affinity compared to its T20 parent ligand and an 80% decrease in sequence length. WL 47 dimer can be used to permit targeted study of CAV-1 function [1].
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Cat. No.: HY-P790063
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: CAV1; CAV
Species:  
Source:  
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