ANGIOTENSIN II

PubChem Notes:

Angiotensin II The active form of angiotensin. An octapeptide found in blood, it is synthesized from ANGIOTENSIN I and quickly destroyed. Angiotensin II causes profound vasoconstriction with a resulting increase in blood pressure. It differs among species by the amino acid in position 5. The human form has ISOLEUCINE in this position. The clinically and experimentally used bovine form has VALINE in position 5. Medically useful antagonism is obtained with ACE INHIBITORS or with ANGIOTENSIN II TYPE 1 RECEPTOR BLOCKERS.

Molecular Formula: C50H71N13O12


InChI: InChI=1/C50H71N13O12/c1-5-28(4)41(47(72)59-36(23-31-25-54-26-56-31)48(73)63-20-10-14-38(63)45(70)60-37(49(74)75)22-29-11-7-6-8-12-29)62-44(69)35(21-30-15-17-32(64)18-16-30)58-46(71)40(27(2)3)61-43(68)34(13-9-19-55-50(52)53)57-42(67)33(51)24-39(65)66/h6-8,11-12,15-18,25-28,33-38,40-41,64H,5,9-10,13-14,19-24,51H2,1-4H3,(H,54,56)(H,57,67)(H,58,71)(H,59,72)(H,60,70)(H,61,68)(H,62,69)(H,65,66)(H,74,75)(H4,52,53,55)/f/h56-62,65,74H,52-53H2

InChIKey: InChIKey=CZGUSIXMZVURDU-SDCMFMFACQ
SMILES: CCC(C)C(C(=O)NC(CC1=CN=CN1)C(=O)N2CCCC2C(=O)NC(CC3=CC=CC=C3)C(=O)O)NC(=O)C(CC4=CC=C(C=C4)O)NC(=O)C(C(C)C)NC(=O)C(CCCN=C(N)N)NC(=O)C(CC(=O)O)N

Names:
    Angiotensina II [INN-Spanish]
    Angiotensinum II [INN-Latin]
    ANGIOTENSIN II
    1-L-Aspasaginyl-5-L-valyl angiotensin octapeptide
    1-8-Angiotensin I
    11128-99-7
    3-amino-3-[[1-[[1-[[1-[[1-[[1-[2-[(1-carboxy-2-phenyl-ethyl)carbamoyl]pyrrolidin-1-yl]-3-(3H-imidazol-4-yl)-1-oxo-propan-2-yl]carbamoyl]-2-methyl-butyl]carbamoyl]-2-(4-hydroxyphenyl)ethyl]carbamoyl]-2-methyl-propyl]carbamoyl]-4-(diaminomethylideneamino)butyl]carbamoyl]propanoic acid

Registries:
    PubChem CID 25476
    PubChem ID 168235