Angiotensin I/II (5-8)

Base Information

Chemical Name:Angiotensin I/II (5-8)
CAS No.:34233-50-6
Molecular Formula:C26H36N6O5
Molecular Weight:512.60100
Hs Code.:
DSSTox Substance ID:DTXSID40430963
Nikkaji Number:J848.769C
Wikidata:Q82244719
Mol file:34233-50-6.mol

Synonyms:Angiotensin I/II (5-8);34233-50-6;Angiotensin II (5-8), human;Angiotensin (5-8);(2S)-2-[[(2S)-1-[(2S)-2-[[(2S,3S)-2-amino-3-methylpentanoyl]amino]-3-(1H-imidazol-5-yl)propanoyl]pyrrolidine-2-carbonyl]amino]-3-phenylpropanoic acid;CTK1B7855;Angiotensin-(5-8);Angiotensin II(5-8);DTXSID40430963;CHEBI:144396;HY-P1769;MFCD00167499;MS-29518;CS-0095581;C20972;Angiotensin I/II (5-8) (H-Ile-His-Pro-Phe-OH)

Suppliers and Price of Angiotensin I/II (5-8)

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

Cayman Chemical
Angiotensin II (5-8) (human, rat, mouse) ≥95%
1mg
$ 79.00

Biosynth Carbosynth
Angiotensin I/II (5-8) H-Ile-His-Pro-Phe-OH
50 mg
$ 236.00

Biosynth Carbosynth
Angiotensin I/II (5-8) H-Ile-His-Pro-Phe-OH
25 mg
$ 136.00

Biosynth Carbosynth
Angiotensin I/II (5-8) H-Ile-His-Pro-Phe-OH
100 mg
$ 410.00

Biosynth Carbosynth
Angiotensin I/II (5-8) H-Ile-His-Pro-Phe-OH
500 mg
$ 1425.00

Biosynth Carbosynth
Angiotensin I/II (5-8) H-Ile-His-Pro-Phe-OH
250 mg
$ 820.00

American Custom Chemicals Corporation
ANGIOTENSIN I/II (5 - 8) 95.00%
5MG
$ 622.55

AK Scientific
AngiotensinI/II(5-8)
50mg
$ 368.00

Total 15 raw suppliers

Chemical Property of Angiotensin I/II (5-8)

Chemical Property:

PSA：177.49000
LogP:2.93230
Storage Temp.:-15°C
XLogP3:-0.8
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:12
Exact Mass:512.27471827
Heavy Atom Count:37
Complexity:804

Purity/Quality:

99%, ^*data from raw suppliers

Angiotensin II (5-8) (human, rat, mouse) ≥95% ^*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)NC(CC3=CC=CC=C3)C(=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)N[C@@H](CC3=CC=CC=C3)C(=O)O)N

Technology Process of Angiotensin I/II (5-8)

There total 1 articles about Angiotensin I/II (5-8) 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: