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ANGIOTENSIN III, HUMAN

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ANGIOTENSIN III, HUMAN Basic information

Product Name:
ANGIOTENSIN III, HUMAN
Synonyms:
  • ARG-VAL-TYR-ILE-HIS-PRO-PHE
  • ARG-VAL-TYR-ILE-HIS-PRO-PHE 2ACOH 4H2O
  • ARG-VAL-TYR-ILE-HIS-PRO-PHE-OH CH3COOH 4H2O
  • H-ARG-VAL-TYR-ILE-HIS-PRO-PHE-OH
  • [DES-ASP1]-ANGIOTENSIN II
  • DES-ASP-1-ANGIOTENSIN II ACETATE SALT
  • ANGIOTENSIN III ACETATE SALT
  • ANGIOTENSIN III
CAS:
13602-53-4
MF:
C46H66N12O9
MW:
931.09
Product Categories:
  • Cardiovascular
  • Angiotensin
  • peptide
Mol File:
13602-53-4.mol
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ANGIOTENSIN III, HUMAN Chemical Properties

Density 
1.39±0.1 g/cm3(Predicted)
storage temp. 
−20°C
solubility 
H2O: 1.0 mg/mL, clear, colorless
form 
Lyophilized.
pka
3.56±0.10(Predicted)
color 
White to off-white
Sequence
Arg-Val-Tyr-Ile-His-Pro-Phe
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Safety Information

WGK Germany 
3
10

MSDS

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ANGIOTENSIN III, HUMAN Usage And Synthesis

Description

Angiotensin III (Ang III) is a heptapeptide agonist at the angiotensin 1 (AT1) and AT2 receptors, with a 30-fold higher affinity for AT2 compared with AT1 in HEK293 cells. Ang III is the preferred agonist for renal AT2 receptors, which are responsible for sodium excretion into the urine. Ang III induces the same level of aldosterone synthesis as Ang II but has lower vasoconstrictive activity in vivo. In the brain renin-angiotensin system, Ang III increases sympathetic nerve activity and vasopressin release and dampens the baroreflex leading to higher blood pressure.

Uses

Angiotensin III, human, mouse is a heptapeptide, acts as an endogenous angiotensin type 2 receptor (AT2R) agonist, with IC50s of 0.648 nM and 21.1 nM for AT2R and AT1R, respectively.

Definition

ChEBI: Angiotensin III is a peptide.

in vivo

Angiotensin III (7, 14 and 28 nmol/kg/min) increases urine sodium excretion (UNaV), fractional excretion of sodium (FENa), and fractional excretion of lithium (FELi) in SD rat[2]. In RAS (renin-angiotensin system), Angiotensin III increases sympathetic nerve activity and vasopressin release and decreases the baroreflex leading to higher blood pressure in rats[3].

IC 50

AT2 Receptor

References

[1] Bosnyak S, et al. Relative affinity of angiotensin peptides and novel ligands at AT1 and AT2 receptors. Clin Sci (Lond). 2011 Oct;121(7):297-303. DOI:10.1042/CS20110036
[2] Kemp BA, et al. Intrarenal angiotensin III is the predominant agonist for proximal tubule angiotensin type 2 receptors. Hypertension. 2012 Aug;60(2):387-95. DOI:10.1161/HYPERTENSIONAHA.112.191403
[3] Gao J, et al. A new strategy for treating hypertension by blocking the activity of the brain renin-angiotensin system with aminopeptidase A inhibitors. Clin Sci (Lond). 2014 Aug;127(3):135-48. DOI:10.1042/CS20130396

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