biliverdin
biliverdin Basic information
- Product Name:
- biliverdin
- Synonyms:
-
- 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
- BILIVERDINEDIHYDROCHLORIDE
- ocyan
- biliverdin
- Biliverdine
- 3,18-Diethenyl-1,19,22,24-tetrahydro-2,7,13,17-tetrametyl-1,19-dioxo-21H-biline-8,12-dipropanoic Acid
- Dehydrobilirubin
- Uteroverdine
- CAS:
- 114-25-0
- MF:
- C33H34N4O6
- MW:
- 582.65
- EINECS:
- 204-042-2
- Product Categories:
-
- Amines
- Heterocycles
- Intermediates & Fine Chemicals
- Pharmaceuticals
- Amines, Heterocycles, Pharmaceuticals, Intermediates & Fine Chemicals
- Mol File:
- 114-25-0.mol
biliverdin Chemical Properties
- 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)
- pka
- 4.46±0.10(Predicted)
- form
- Solid
- 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)
biliverdin Usage And Synthesis
Chemical Properties
Dark Green Crystalline Solid
Uses
Precursor of Bilirubin. Formed in the body from hemoglobin
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.
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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