P11

P11 Suppliers list
Company Name: Shenzhen Nexconn Pharmatechs Ltd
Tel: +86-755-89396905 +86-15013857715
Email: admin@nexconn.com
Products Intro: Product Name:P11
CAS:848644-86-0
Purity:98% Package:1KG;10KG;50KG
Company Name: BOC Sciences
Tel: 16314854226; +16314854226
Email: inquiry@bocsci.com
Products Intro: Product Name:P11
CAS:848644-86-0
Purity:>98% Remarks:BOC Sciences also provides custom synthesis services for P11.
Company Name: Zhejiang Hangyu API Co., Ltd
Tel: +8617531972939
Email: anna@api-made.com
Products Intro: Product Name:P11
CAS:848644-86-0
Purity:99% Package:1g;25g;5KG;25KG
Company Name: Aladdin Scientific
Tel: +1-+1(833)-552-7181
Email: sales@aladdinsci.com
Products Intro: Product Name:P11 ( (trifluoroacetate salt)
CAS:848644-86-0
Purity:98% Package:$39.9/1mg;Bulk package Remarks:98%
Company Name: Creative Peptides   
Tel:
Email: info@creative-peptides.com
Products Intro: Product Name:P11
CAS:848644-86-0
Purity:>98% Package:1g; 10g;100g;1kg Remarks:Peptide Inhibitors
P11 Basic information
Product Name:P11
Synonyms:L-Lysinamide, L-histidyl-L-seryl-L-α-aspartyl-L-valyl-L-histidyl- (9CI);P11 ( (trifluoroacetate salt)
CAS:848644-86-0
MF:C30H48N12O9
MW:720.79
EINECS:
Product Categories:
Mol File:848644-86-0.mol
P11 Structure
P11 Chemical Properties
Boiling point 1380.0±65.0 °C(Predicted)
density 1.381±0.06 g/cm3(Predicted)
storage temp. -20°C, protect from light
solubility Soluble to 1 mg/ml in 20% acetonitrile - 0.1% acetic acid
form Powder
pka4.17±0.10(Predicted)
color White to off-white
SequenceH-His-Ser-Asp-Val-His-Lys-NH2
Safety Information
MSDS Information
P11 Usage And Synthesis
UsesP11 is a useful building block in the synthesis of various pharmaceuticals
Enzyme inhibitorThis potent PDZ motif-containing anti-angiogenic agent (FW = 720.78 g/mol; CAS 848644-86-0; Sequence: HSDVHK-NH2) targets the integrin αvβ3-vitronectin interaction, blocking proliferation and inducing apoptosis in human vascular endothelial cells (HUVECs). Arg-Gly-Asp (or RGD) binding-site recognition by P11 is site-specific, showing a strong antagonism against αvβ3-vitronectin interaction, IC50 = 26 nM. The binding orientation of docked P11 in αvβ3 is similar to that for RGD, suggesting a divalent metal-ion coordination is a common driving force for the formation of both SDV·αvβ3 and RGD·αvβ3 complexes. P11 appears to inhibit b-Fibroblast Growth Factor (or bFGF) -induced HUVEC proliferation via mitogen-activated protein kinase kinase and extracellular- signal regulated kinase inhibition as well as p53-mediated apoptosis related with activation of caspases. (Note: Consisting of 80-90 amino-acids in far-flung signaling proteins and binding to short C-terminal regions in protein interaction partners, “PDZ” is an acronym that includes the first letters of Post-synaptic density protein (PSD95), Drosophila Dlg1 tumor suppressor, and Zonula occludens-1 protein (zo-1), the first proteins discovered to share this domain.)
P11 Preparation Products And Raw materials
Tag:P11(848644-86-0) Related Product Information