ChemicalBook > Product Catalog >API >Antipyretic analgesics >Nonsteroidal Anti-Inflammatory Drugs (NSAIDS) >Asp-Arg-Val-Tyr-Ile-His-Pro

Asp-Arg-Val-Tyr-Ile-His-Pro

Asp-Arg-Val-Tyr-Ile-His-Pro Suppliers list
Company Name: 3B Pharmachem (Wuhan) International Co.,Ltd.  
Tel: 18930552037
Email: 3bsc@sina.com
Company Name: GL Biochem (Shanghai) Ltd  
Tel: 21-61263452 13641803416
Email: ymbetter@glbiochem.com
Company Name: Shanghai Hanhong Scientific Co.,Ltd.  
Tel: 021-54306202 13764082696
Email: info@hanhongsci.com
Company Name: Chemsky(shanghai)International Co.,Ltd.  
Tel: 021-50135380
Email: shchemsky@sina.com
Company Name: ShangHai YuanYe Biotechnology Co., Ltd.  
Tel: 15026964105
Email: shyysw007@163.com

Asp-Arg-Val-Tyr-Ile-His-Pro manufacturers

Asp-Arg-Val-Tyr-Ile-His-Pro Basic information
Product Name:Asp-Arg-Val-Tyr-Ile-His-Pro
Synonyms:angiotensinii(1-7;angiotensin fragment 1-7 human acetate;H2N-DRVYIHP-OH;H-ASP-ARG-VAL-TYR-ILE-HIS-PRO-OH;(DES-PHE8) ANGIOTENSIN II;DRVYIHP;ANGIOTENSIN (HUMAN, 1-7) (CANINE, RAT);ANGIOTENSIN CANINE RAT
CAS:51833-78-4
MF:C41H62N12O11
MW:899.01
EINECS:
Product Categories:API;Cardiovescular;AngiotensinsPeptides for Cell Biology;Angiotensins;Neuropeptides;Peptides for Cell Biology;Angiotensin;Peptide
Mol File:51833-78-4.mol
Asp-Arg-Val-Tyr-Ile-His-Pro Structure
Asp-Arg-Val-Tyr-Ile-His-Pro Chemical Properties
Melting point >202°C (dec.)
density 1.47±0.1 g/cm3(Predicted)
storage temp. −20°C
solubility DMSO (Slightly), Methanol (Slightly), Water (Slightly, Sonicated)
form powder
pka3.29±0.20(Predicted)
color White to Off-White
Water Solubility Soluble to 1 mg/ml in water
InChIKeyPVHLMTREZMEJCG-UHFFFAOYSA-N
SMILESCCC(C)C(NC(=O)C(Cc1ccc(O)cc1)NC(=O)C(NC(=O)C(CCCNC(N)=N)NC(=O)C(N)CC(O)=O)C(C)C)C(=O)NC(Cc2cnc[nH]2)C(=O)N3CCCC3C(O)=O
Safety Information
WGK Germany 3
Storage Class11 - Combustible Solids
MSDS Information
ProviderLanguage
SigmaAldrich English
Asp-Arg-Val-Tyr-Ile-His-Pro Usage And Synthesis
UsesAngiotensin (1-7) can be used in biological study and engineering or chemical process of mechanisms of peptide oxidation by hydroxyl radicals.
DefinitionChEBI: Ile(5)-angiotensin II (1-7) is an angiotensin compound consisting of the linear heptapeptide sequence L-Asp-L-Arg-L-Val-L-Tyr-L-Ile-L-His-L-Pro. It has a role as a vasodilator agent. It is a tautomer of an Ile(5)-angiotensin II (1-7) dizwitterion.
Biological Activityang-(1-7) (h - asp - arg - val - tyr - ile - his - pro - oh) is an endogenous peptide fragment that can be produced from ang i or ang ii via endo- or carboxy-peptidases respectively[1].as described for ang ii, ang-(1-7) also has a broad range of effects in different organs and tissues and goes beyond its initially described cardiovascular and renal actions. those effects are mediated by mas and can counter-regulate most of the deleterious effects of ang ii. the interaction ang-(1-7)/mas regulates different signaling pathways, such as pi3k (phosphoinositide 3-kinase)/akt and erk (extracellular signal-regulated kinase) pathways and involves downstream effectors such as no, foxo1 (forkhead box o1) and cox-2 (cyclo-oxygenase-2). through these mechanisms, ang-(1-7) is able to improve pathological conditions including fibrosis and inflammation in organs such as lungs, liver and kidney. [2]in addition, this heptapeptide has positive effects on metabolism, increasing the glucose uptake and lipolysis while decreasing insulin resistance and dyslipidemia. ang-(1-7) is also able to improve cerebroprotection against ischemic stroke, besides its effects on learning and memory. the reproductive system can also be affected by ang-(1-7) treatment, with enhanced ovulation, spermatogenesis and sexual steroids synthesis. finally, ang-(1-7) is considered a potential anti-cancer treatment since it is able to inhibit cell proliferation and angiogenesis.[2]fig. 1: formula of angiotensin (1-7)fig. 2: cascade of the processing of angiotensin peptides and their interaction with at1 and at1-7 receptor systems.
Biochem/physiol ActionsAngiotensin I metabolite that is an AT2 receptor agonist.
storageStore at -20°C
references1. Santos et al (2000) Angiotensin-(1-7): an update. Regul.Pept. 91 45.2. Danielle G. P., Thiago V., Robson A. S. Angiotensin-(1-7): beyond the cardio-renal actions. Clinical Science (2013) 124, (443–456)
Asp-Arg-Val-Tyr-Ile-His-Pro Preparation Products And Raw materials
Preparation ProductsL-Leucine, L-histidyl-L-prolyl-L-phenylalanyl-L-histidyl-
Tag:Asp-Arg-Val-Tyr-Ile-His-Pro(51833-78-4) Related Product Information
Serum digestion powder NA EC 3.4.15.1 HEMOCYANIN, KEYHOLE LIMPET Blood Agar plate Angiotensin II human acetate ANGIOTENSIN II, HUMAN ANGIOTENSIN I, HUMAN H-ASP-ARG-VAL-TYR-ILE-HIS-PRO-PHE-HIS-LEU-LEU-VAL-TYR-SER-OH,ASP-ARG-VAL-TYR-ILE-HIS-PRO-PHE-HIS-LEU-LEU-VAL-TYR-SER Angiotensin Asp-Arg-Val-Tyr-Ile-His-Pro ASP-ARG-VAL-TYR-ILE-HIS-PRO-PHE-HIS-LEU-LEU-VAL-TYR-SER,H-ASP-ARG-VAL-TYR-ILE-HIS-PRO-PHE-HIS-LEU-LEU-VAL-TYR-SER-OH Asp-Arg-Val-Tyr-Ile-His-Pro-Phe-His-Leu-Val-Ile-His-Asn Angiotensinogen (1-13) (human) Biotinyl-angiotensin I/II (1-7) Asp-Arg-Val-Tyr-Ile-His-Pro-Leu-His-Leu-Leu-Tyr-Tyr-Ser Asp-Arg-Val-Tyr-Ile-His-Pro-Ala Angiotensin I/II (3-7)