uteroverdine

Biliverdine 1,3,6,7-Tetramethyl-4,5-dicarboxyethyl-2,8-divinylbilenone. Biosynthesized from hemoglobin as a precursor of bilirubin. Occurs in the bile of amphibia and of birds, but not in normal human bile or serum.

[1. A green bile pigment formed from the oxidation of heme; a bilin with a structure almost identical to that of bilirubin.

Molecular Formula: C₃₃H₃₄N₄O₆

InChI: InChI=1/C33H34N4O6/c1-7-20-19(6)32(42)37-27(20)14-25-18(5)23(10-12-31(40)41)29(35-25)15-28-22(9-11-30(38)39)17(4)24(34-28)13-26-16(3)21(8-2)33(43)36-26/h7-8,13-15,34-35H,1-2,9-12H2,3-6H3,(H,37,42)(H,38,39)(H,40,41)/f/h37-38,40H

InChIKey: InChIKey=RCNSAJSGRJSBKK-XELKVOHMCJ
SMILES: CC1=C(C(=CC2=C(C(=C(N2)C=C3C(=C(C(=O)N3)C)C=C)C)CCC(=O)O)NC1=CC4=NC(=O)C(=C4C)C=C)CCC(=O)O

Names:
    biliverdine
    Biliverdin IX.alpha.
    biliverdin
    dehydrobilirubin
    NSC62793
    Oocyan
    Protobiliverdin IX.alpha.
    uteroverdine
    114-25-0
    21H-Biline-8,12-dipropanoic acid, 3,18-diethenyl-1,19,22, 24-tetrahydro-2,7,13,17-tetramethyl-1,19-dioxo-
    3-[2-[[3-(2-carboxyethyl)-5-[(4-ethenyl-3-methyl-5-oxo-pyrrol-2-yl)methylidene]-4-methyl-pyrrol-2-ylidene]methyl]-5-[(3-ethenyl-4-methyl-5-oxo-pyrrol-2-ylidene)methyl]-4-methyl-1H-pyrrol-3-yl]propanoic acid

Registries:
    PubChem CID 251
    PubChem ID 109792