Angiotensin (1-7)

Base Information

Chemical Name:Angiotensin (1-7)
CAS No.:51833-78-4
Molecular Formula:C41H62N12O11
Molecular Weight:899.017
Hs Code.:
Nikkaji Number:J285.101F
Wikipedia:Angiotensin_(1-7)
Wikidata:Q27074464
NCI Thesaurus Code:C68962
Metabolomics Workbench ID:58832
ChEMBL ID:CHEMBL3545347
Mol file:51833-78-4.mol

Synonyms:Ang I (1-7);angiotensin (1-7);angiotensin 1-7;angiotensin I (1-7);angiotensin II (1-7);angiotensin II (1-7) heptapeptide;angiotensin II-(1-7);angiotensin-(1-7);angiotensin-I (1-7);TXA-127;TXA127

Suppliers and Price of Angiotensin (1-7)

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Usbiological
Angiotensin 1-7
96Tests
$ 895.00

Usbiological
Ang1-7
96Tests
$ 599.00

Usbiological
Angiotensin 1-7
48Tests
$ 588.00

Usbiological
Angiotensin 1-7
48Tests
$ 588.00

Usbiological
Ang1-7
96Tests
$ 779.00

TRC
Angiotensin(1-7)xTFAsalt
100mg
$ 325.00

TRC
Angiotensin(1-7)xTFAsalt
10mg
$ 65.00

Tocris
A779
5
$ 86.00

Tocris
Angiotensin(1-7)
1
$ 75.00

Sigma-Aldrich
Angiotensin Fragment 1-7 acetate salt hydrate ≥90% (HPLC), powder
5mg
$ 228.00

Total 44 raw suppliers

Chemical Property of Angiotensin (1-7)

Chemical Property:

Appearance/Colour:White lyophilised solid
Refractive Index:1.665
PKA:3.29±0.20(Predicted)
PSA：377.24000
Density:1.47 g/cm³
LogP:1.95110
Storage Temp.:−20°C
Solubility.:DMSO (Slightly), Methanol (Slightly), Water (Slightly, Sonicated)
XLogP3:-3
Hydrogen Bond Donor Count:12
Hydrogen Bond Acceptor Count:14
Rotatable Bond Count:25
Exact Mass:898.46610084
Heavy Atom Count:64
Complexity:1660

Purity/Quality:

99%, ^*data from raw suppliers

Angiotensin 1-7 ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC(C)C(C(=O)NC(CC1=CN=CN1)C(=O)N2CCCC2C(=O)O)NC(=O)C(CC3=CC=C(C=C3)O)NC(=O)C(C(C)C)NC(=O)C(CCCN=C(N)N)NC(=O)C(CC(=O)O)N
Isomeric SMILES:CC[C@H](C)[C@@H](C(=O)N[C@@H](CC1=CN=CN1)C(=O)N2CCC[C@H]2C(=O)O)NC(=O)[C@H](CC3=CC=C(C=C3)O)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(=O)O)N
Uses Angiotensin (1-7) can be used in biological study and engineering or chemical process of mechanisms of peptide oxidation by hydroxyl radicals.

Technology Process of Angiotensin (1-7)

There total 3 articles about Angiotensin (1-7) which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 484-42-4
angiotensin I

: 42014-20-0
His Pro Phe His Leu

: C₄₇H₆₃N₁₁O₉

: 51833-78-4
angiotensin II-(1-7)

: 4474-91-3
angiotensin II

Guidance literature:: With ablated human blood plasma serum; In water; at 37 ℃; for 24h;
DOI:10.1002/anie.201407669

Reference yield:

: 4474-91-3
angiotensin II

: 63-91-2,25191-15-5,658-69-5,67675-33-6
L-phenylalanine

: 51833-78-4
angiotensin II-(1-7)

Guidance literature:: With wheat carboxypeptidase from wheat bran; at 30 ℃; Rate constant; pH 4.0; structure-reactivity relationship;
DOI:10.1016/0031-9422(83)83054-4

Reference yield:

: 51833-78-4
C₄₁H₆₂N₁₂O₁₁

Guidance literature:: Boc-Asp(OCH2Ph)-Arg(NO2)-Val-Tyr(OCH2Ph)-Ile-His(CH2Ph)-Pro (Merrifield Festphasen-Synthese), 1) TFA/HBr(Gas), 2) H2/Pd (Me./Eg./W.);
DOI:10.1139/o74-018