130 Results for "

vascular permeability

" in MedChemExpress (MCE) Product Catalog:
Products (130)

130 Results for "vascular permeability" in MCE Product Catalog:

43
43 Publications Verification
Cat. No.: HY-108635
CAS No.: 74389-68-7
Purity:  99.85%
Synonyms: PAF (C16)
C16-PAF (PAF (C16)), a phospholipid mediator, is a platelet-activating factor and ligand for PAF G-protein-coupled receptor (PAFR). C16-PAF exhibits anti-apoptotic effect and inhibits caspase-dependent death by activating the PAFR. C16-PAF is a potent MAPK and MEK/ERK activator. C16-PAF induces increased vascular permeability .
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19
19 Cited Publications
Cat. No.: HY-P0206
CAS No.: 58-82-2
Bradykinin is an effective endothelium-dependent vasodilator that can lower blood pressure. Bradykinin can induce contraction of bronchial and intestinal non-vascular smooth muscle, increase vascular permeability, and participate in the mechanism of pain .
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19
19 Cited Publications
Cat. No.: HY-P0206A
CAS No.: 6846-03-3
Bradykinin acetate is an effective endothelium-dependent vasodilator that can lower blood pressure. Bradykinin acetate can induce contraction of bronchial and intestinal non-vascular smooth muscle, increase vascular permeability, and participate in the mechanism of pain .
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19
19 Cited Publications
Cat. No.: HY-P7110A
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: VEGFA; vascular Endothelial Growth Factor A; VEGF; VPF; vascular permeability Factor; vascular Endothelial Growth Factor A, Long Form; VEGF-A; L-VEGF; vascular Endothelial Growth Factor A121; vascular Endothelial Growth Factor A165; vascular Endothelial G
Species:  
Source:  
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18
18 Cited Publications
Cat. No.: HY-B0228
CAS No.: 58-61-7
Synonyms: Adenine riboside; D-Adenosine
Adenosine (Adenine riboside), a ubiquitous and BBB-permeable endogenous autacoid, acts through the enrollment of four G protein-coupled receptors: A1, A2A, A2B, and A3. Adenosine affects almost all aspects of cellular physiology, including neuronal activity, vascular function, platelet aggregation, and blood cell regulation .
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10
10 Cited Publications
Cat. No.: HY-N0570
CAS No.: 10597-60-1
Synonyms: DOPET; 3,4-Dihydroxyphenethyl alcohol; 3-Hydroxytyrosol
Hydroxytyrosol (DOPET; 3,4-Dihydroxyphenethyl alcohol) is an orally active, blood-brain barrier-permeable multi-active compound with multiple effects including antibacterial, antioxidant, anti-platelet aggregation, and neuroprotective activities. Hydroxytyrosol not only inhibits the growth of Vibrio by increasing bacterial membrane permeability, but also interacts with DNA and mediates supercoiled DNA relaxation. Meanwhile, Hydroxytyrosol effectively reduces thrombosis and inhibits lipid oxidation by inhibiting COX activity and promoting vascular nitric oxide production. In terms of neuroprotection, Hydroxytyrosol significantly alleviates neuronal apoptosis and inflammatory responses by up-regulating the expression level of ERβ, thereby improving cognitive function in Alzheimer's disease models. Hydroxytyrosol has been widely used in scientific research related to Vibrio infection, arterial thrombosis, Alzheimer's disease and other related fields .
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10
10 Cited Publications
Cat. No.: HY-10977
CAS No.: 475108-18-0
Purity:  99.80%
Synonyms: AV-951; KRN951
Target:  

VEGFR

Research Areas:  

Cancer

Tivozanib (AV-951; KRN951) is a selective, orally active inhibitor for vascular endothelial growth factor receptor (VEGFR)-1, 2 3, with IC50s of 30, 6.5 and 15 nM, respectively. Tivozanib exhibits antitumor efficacy .
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10
10 Cited Publications
Cat. No.: HY-10977A
CAS No.: 682745-41-1
Purity:  99.77%
Synonyms: AV-951 hydrochloride hydrate; KRN951 hydrochloride hydrate
Target:  

VEGFR

Research Areas:  

Cancer

Tivozanib hydrochloride hydrate is the hydrate hydrochloride form of Tivozanib (HY-10977). Tivozanib hydrochloride hydrate is a selective, orally active inhibitor for vascular endothelial growth factor receptor (VEGFR)-1, 2 3, with IC50s of 30, 6.5 and 15 nM, respectively. Tivozanib hydrochloride hydrate exhibits antitumor efficacy .
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9
9 Cited Publications
Cat. No.: HY-D0799
CAS No.: 191671-46-2
Target:  

Fluorescent Dye

Research Areas:  

Others

Sulfo-NHS-LC-Biotin sodium is an amine-reactive ester derivative of biotin and cannot pass the intact blood-retinal barrier. It can be used to assess vascular permeability of the brain and retinal vasculature.
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9
9 Cited Publications
Cat. No.: HY-P7312
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: VEGFA; vascular Endothelial Growth Factor A; VEGF; VPF; vascular permeability Factor; vascular Endothelial Growth Factor A, Long Form; VEGF-A; L-VEGF; vascular Endothelial Growth Factor A121; vascular Endothelial Growth Factor A165; vascular Endothelial G
Species:  
Source:  
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7
7 Cited Publications
Cat. No.: HY-14668
CAS No.: 202914-84-9
Purity:  99.57%
Synonyms: AEGR-733 mesylate; BMS-201038 mesylate
Lomitapide (AEGR-733; BMS-201038) mesylate is an orally active microsomal triglyceride transfer protein (MTP) inhibitor and a selective mTORC1 inhibitor with lipid-lowering activity and BBB permeability. Lomitapide mesylate significantly reduces plasma LDL levels by blocking the assembly and secretion of very-low-density lipoprotein (VLDL). Lomitapide mesylate inhibits mTORC1 in an ATP-dependent manner, thereby inducing AMPK-independent autophagic cell death and suppressing cancer cell growth and apoptosis. Lomitapide mesylate also enhances tumor infiltration of CD8 + T cells. In addition, Lomitapide mesylate inhibits HDAC, improves endothelial function, effectively alleviates vascular inflammation and oxidative stress, and exerts neuroprotective effects in a cerebral ischemia/reperfusion injury model. Lomitapide mesylate can be used in research on related diseases such as colorectal cancer, breast cancer, melanoma, ischemic stroke, and familial hypercholesterolemia .
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7
7 Cited Publications
Cat. No.: HY-B0377
CAS No.: 76824-35-6
Synonyms: MK-208
Famotidine (MK-208) is an orally active and highly selective histamine H2 receptor antagonist. It inhibits gastric acid secretion by blocking the Gs signaling pathway, and regulates intracellular cAMP and ERK pathways. Famotidine inhibits TLR3-mediated inflammatory pathways, and reduces the expression of various inflammatory mediators and interferon-related genes. Famotidine scavenges DPPH and nitric oxide free radicals, alleviates oxidative stress damage in gastric tissue, inhibits proMMP-9, improves vascular endothelial permeability, and restores the normal physiological functions of neutrophils and eosinophils. Famotidine crosses intestinal epithelial cells via facilitated diffusion and passive diffusion, blocks paracellular cation transport, and increases intestinal transepithelial electrical resistance. Famotidine reduces serum levels of transaminases and alkaline phosphatase, exerts analgesic effects and gastric protective effects simultaneously. Famotidine can be used in studies related to COVID-19, liver injury and acute gastric ulcer .
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6
6 Cited Publications
Cat. No.: HY-P80929
Synonyms: VEGFA; VEGF; vascular endothelial growth factor A; VEGF-A; vascular permeability factor; VPF

Host:  

Rabbit

Application:  

WB

Reactivity:  

Human, Mouse, Rat

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3
3 Cited Publications
Cat. No.: HY-P7311
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: VEGFA; vascular Endothelial Growth Factor A; VEGF; VPF; vascular permeability Factor; vascular Endothelial Growth Factor A, Long Form; VEGF-A; L-VEGF; vascular Endothelial Growth Factor A121; vascular Endothelial Growth Factor A165; vascular Endothelial G
Species:  
Rat
Source:  
CHO
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2
2 Cited Publications
Cat. No.: HY-Y0669
CAS No.: 535-75-1
Pipecolic acid is an orally bioavailable, blood-brain barrier-permeable metabolite of lysine with antioxidant, inhibitor, and inducer activity. Pipecolic acid modulates the YAP-GPX4 signaling pathway, reduces retinal vascular tube formation, and mitigates ferroptosis. Pipecolic acid potentiates voltage-sensitive Ca 2+ channel currents and induces neuronal apoptosis. Pipecolic acid can be used for the research of diabetic retinopathy .
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2
2 Cited Publications
Cat. No.: HY-158082C
Synonyms: Tetramethyl rhodamine isothiocyanate glucan, MW 70000
TRITC-dextran MW 70000 (Tetramethyl rhodamine isothiocyanate glucan, MW 70000) is a fluorescent dye with a molecular weight of 70 kD. The excitation wavelength of TRITC-dextran MW 70000 is 555 nm, and its emission wavelength is 570 nm. TRITC-dextran MW 70000 is used for drug delivery because TRITC maintains stability over a wide pH range (i.e., pH 2-11) and exhibits photobleaching resistance .
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2
2 Cited Publications
Cat. No.: HY-125864B
CAS No.: 9001-32-5
Target:  

MMP Cadherin

Murine Fibrinogen is a native fibrinogen derived from mouse plasma. Murine Fibrinogen acts as a cerebrovascular permeability enhancer. Murine Fibrinogen activates matrix metalloproteinase-9 (MMP-9), downregulates the expression of vascular endothelial cadherin (VE-cadherin), and upregulates the expression of plasmalemmal vesicle-associated protein-1 (PV-1). Murine Fibrinogen increases macromolecular leakage from pial veins, thereby disrupting the microvascular integrity of cerebral blood vessels. Murine Fibrinogen can be used in studies related to cerebrovascular dysfunction .
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2
2 Cited Publications
Cat. No.: HY-P7420
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: VEGFA; vascular Endothelial Growth Factor A; VEGF; VPF; vascular permeability Factor; vascular Endothelial Growth Factor A, Long Form; VEGF-A; L-VEGF; vascular Endothelial Growth Factor A121; vascular Endothelial Growth Factor A165; vascular Endothelial G
Species:  
Source:  
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2
2 Cited Publications
Cat. No.: HY-P70458A
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: VEGFA; vascular Endothelial Growth Factor A; VEGF; VPF; vascular permeability Factor; vascular Endothelial Growth Factor A, Long Form; VEGF-A; L-VEGF; vascular Endothelial Growth Factor A121; vascular Endothelial Growth Factor A165; vascular Endothelial G
Species:  
Source:  
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1
1 Cited Publications
Cat. No.: HY-124379
CAS No.: 402-71-1
Purity:  98.05%
Synonyms: L-1-Tosylamido-2-phenylethyl chloromethyl ketone; L-TPCK
TPCK (L-1-Tosylamido-2-phenylethyl chloromethyl ketone; L-TPCK) is an effective serine protease inhibitor and also a blocker of the PDK1/Akt pathway. TPCK can modify the E7 protein in actively keratinocyte cells. TPCK can induce cellular apoptosis, suppress tumor growth, reduce hypoxic-ischemic brain injury in rat pups, and affect vascular permeability in inflamed rats .
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