Biliverdin
From Wikipedia, the free encyclopedia
Biliverdin | |
---|---|
Identifiers | |
CAS number | [ | ]
PubChem | |
MeSH | |
Properties | |
Molecular formula | C33H34N4O6 |
Molar mass | 582.646 |
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references |
Biliverdin is a green pigment formed as a byproduct of hemoglobin breakdown. It consists of four linearly connected pyrrole rings (a tetrapyrrole). Biliverdin is formed when the heme group in hemoglobin is cleaved at its α-methine bridge. The resulting water-soluble biliverdin (C33H34N4O6) is then reduced to the water-insoluble toxic bilirubin (C33H36N4O6) , a yellow pigment, by the enzyme biliverdin reductase. The changing color of a bruise from deep purple to yellow over time is a graphical indicator of this reaction.
Biliverdin is also present in the bile juice which is secreted by the liver and also imparts colour to the bile juice.
[edit] External links
Biochemicals | Major Families of||
Peptides | Amino acids | Nucleic acids | Carbohydrates | Lipids | Terpenes | Carotenoids | Tetrapyrroles | Enzyme cofactors | Steroids | Flavonoids | Alkaloids | Polyketides | Glycosides | ||
Analogues of nucleic acids: | Types of Tetrapyrroles | Analogues of nucleic acids: |
Bilanes: | Bilirubin | Biliverdin | Urobilinogen | Urobilin | |
---|---|---|
Chlorophylls: | Protochlorophyllide | Chlorophyllide | |
Corrinoids: | Cyanocobalamin | |
Phycobilins: | Phycoerythrobilin | Phycocyanobilin | Phycourobilin | Phycoviolobilin | |
Porphyrins: | Coproporphyrinogen | Protoporphyrin | Uroporphyrinogen |