EILEVPST CAS 239075-62-8

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EILEVPST CAS 239075-62-8
Details
CAS Number: 239075-62-8
Sequence: EILEVPST
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Related documents
COA/MS/HPLC Report
Peptide Dissolution and Storage Guide
Category
Cell Adhesion Peptides
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Description

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Product name CAS:239075-62-8;EILEVPST
Sequence EILEVPST
Three letter sequence  
Peptide purity (HPLC, %) 95%/99%
Molecular formula C39H66N8O15
Molecular weight (Da) 886.99

 

Product Basic Information Table

 

Product Standard English Name Product Abbreviation / Alias Function Tags (comma-separated) Amino Acid Full Name Sequence Molecular Formula Exact Molecular Weight (Da) Average Molecular Weight (Da) Terminal Modification - N-terminus Terminal Modification - C-terminus Sequence Length (aa)
EILEVPST #EILEVPST #Integrin inhibitory peptide; #Endothelial migration blocking peptide; #Angiogenesis in vitro substrate Integrin signal antagonism, endothelial cell migration inhibition, neovascularization block, anti-tumor metastasis, vascular remodeling research, targeted inhibitor screening Glutamic acid-Isoleucine-Leucine-Glutamic acid-Valine-Proline-Serine-Threonine C₄₃H₇₄N₁₂O₂₀ 1046.527 1047.11 Unmodified Free carboxyl group 8

 

Physicochemical Solubility & Storage Parameters

 

Product Code Appearance Long-term Storage Conditions Short-term Storage Conditions Liquid Stability Solid Powder Stability
PEP-EIL01 White powder -20℃, sealed away from light, aliquoted, avoid repeated freeze-thaw 2-8℃, use within 1 month; prepare fresh before experiment Stable for 24 h at 4℃ 3 years at -20℃, 2 years at 4℃

 

Functional Description

 

Product Code Frontend Short Summary (for search list display) Detailed Biological Function Description Applicable Research Areas (comma-separated) Target / Receptor
PEP-EIL01 Octapeptide EILEVPST competitively antagonizes integrin pathway, inhibits endothelial migration and tube formation for in vitro mechanism study of anti-angiogenesis and tumor metastasis EILEVPST is synthetic functional octapeptide, which specifically binds integrin receptors on endothelial cell membrane and competitively blocks the interaction between extracellular matrix proteins and integrins. It significantly suppresses directional migration, invasion and vascular tube formation of endothelial cells, cutting off neovascular nutrient supply for solid tumors. It serves as standard stimulant/blocking substrate for in vitro angiogenesis models, applied in high-throughput screening of anti-metastatic tumor drugs and integrin pathway antagonists, suitable for vascular biology, tumor pharmacology and tissue engineering vascularization regulation research Vascular biology, anti-tumor angiogenesis, endothelial cell migration, integrin signaling pathway, tumor invasion & metastasis, targeted drug screening Endothelial integrin αvβ3/α5β1, fibronectin, vitronectin, extracellular matrix binding domain

 

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