Identification | Back Directory | [Name]
biliverdin | [CAS]
114-25-0 | [Synonyms]
ocyan biliverdin Biliverdine Uteroverdine Dehydrobilirubin Protobiliverdin IXa BILIVERDINEDIHYDROCHLORIDE 3,18-Diethenyl-1,19,22,24-tetrahydro-2,7,13,17-tetrametyl-1,19-dioxo-21H-biline-8,12-dipropanoic Acid 3-[2-[(E)-[(5E)-3-(2-carboxyethyl)-5-[(4-ethenyl-3-methyl-5-oxo-pyrrol-2-yl)methylidene]-4-methyl-pyrrol-2-ylidene]methyl]-5-[(E)-(3-ethenyl-4-methyl-5-oxo-pyrrol-2-ylidene)methyl]-4-methyl-1H-pyrrol-3-yl]propanoic acid 3-[2-[(Z)-[(5E)-3-(2-carboxyethyl)-5-[(4-ethenyl-3-methyl-5-oxo-pyrrol-2-yl)methylidene]-4-methyl-pyrrol-2-ylidene]methyl]-5-[(Z)-(3-ethenyl-4-methyl-5-oxo-pyrrol-2-ylidene)methyl]-4-methyl-1H-pyrrol-3-yl]propanoic acid | [EINECS(EC#)]
204-042-2 | [Molecular Formula]
C33H34N4O6 | [MOL File]
114-25-0.mol | [Molecular Weight]
582.65 |
Chemical Properties | Back Directory | [Appearance]
Dark Green Crystalline Solid | [Melting point ]
>2000C (dec) | [Boiling point ]
640.55°C (rough estimate) | [density ]
1.2293 (rough estimate) | [refractive index ]
1.6000 (estimate) | [storage temp. ]
-20°C Freezer | [solubility ]
DMSO (Slightly), Methanol (Slightly) | [form ]
Solid | [pka]
4.46±0.10(Predicted) | [color ]
Dark Green | [Stability:]
Light Sensitive | [EPA Substance Registry System]
21H-Biline-8,12-dipropanoic acid, 3,18-diethenyl-1,19,22,24-tetrahydro-2,7,13,17-tetramethyl-1,19-dioxo- (114-25-0) |
Hazard Information | Back Directory | [Chemical Properties]
Dark Green Crystalline Solid | [Uses]
Biliverdine is a precursor of Bilirubin. Biliverdine is formed in the body from hemoglobin. The bile of amphibians and of birds contains Biliverdine only. It is also an inhibitor for hepatitis C virus. | [Uses]
Biliverdineis a precursor of Bilirubin. Biliverdine is formed in the body from hemoglobin. The bile of amphibia and of birds contains Biliverdine only. | [Uses]
Precursor of Bilirubin. Formed in the body from hemoglobin | [Definition]
ChEBI: A linear tetrapyrrole produced in the reticuloendothelial system by the first step of heme degradation, catalysed by heme oxygenase. | [Purification Methods]
This is the precursor of bilirubin (above) and forms dark green plates or prisms, with a violet reflection, from MeOH. The dimethyl ester, when crystallised from MeOH has m 215o(209o), and when crystallised from CHCl3/Pet ether gives blue-green crystals with m 202o. [Gray et al. J Chem Soc 2264 1961, Sheldrick J Chem Soc, Perkin Trans 2 1457 1976, Beilstein 26 III/V 3272.] |
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