Prostaglandin G2

Names
IUPAC name (5Z)-7-{(1R,4S,5R,6R)-6-[(1E,3S)-3-Hydroperoxy-1-octen-1-yl]-2,3-dioxabicyclo[2.2.1]hept-5-yl}-5-heptenoic acid
Identifiers
CAS Number	51982-36-6
3D model (JSmol)	Interactive image
ChEBI	CHEBI:27647
ChemSpider	4444406
EC Number	200-662-2
KEGG	C05956
PubChem CID	5280883
InChI InChI=1S/C20H32O6/c1-2-3-6-9-15(24-23)12-13-17-16(18-14-19(17)26-25-18)10-7-4-5-8-11-20(21)22/h4,7,12-13,15-19,23H,2-3,5-6,8-11,14H2,1H3,(H,21,22)/b7-4-,13-12+/t15-,16+,17+,18-,19+/m0/s1 Key: SGUKUZOVHSFKPH-YNNPMVKQSA-N InChI=1/C20H32O6/c1-2-3-6-9-15(24-23)12-13-17-16(18-14-19(17)26-25-18)10-7-4-5-8-11-20(21)22/h4,7,12-13,15-19,23H,2-3,5-6,8-11,14H2,1H3,(H,21,22)/b7-4-,13-12+/t15-,16+,17+,18-,19+/m0/s1 Key: SGUKUZOVHSFKPH-YNNPMVKQBO
SMILES CCCCC[C@@H](/C=C/[C@H]1[C@H]2C[C@@H]([C@@H]1C/C=C\CCCC(=O)O)OO2)OO
Properties
Chemical formula	C20H32O6
Molar mass	368.464
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Prostaglandin G2 is an organic peroxide belonging to the family of prostaglandins.^[1] The compound has been isolated as a solid, although it is usually used in vivo. It quickly converts into prostaglandin H2, a process catalyzed by the enzyme COX.

Prostaglandin G2 is produced from the fatty acid arachidonic acid. The reaction, an oxygenation, requires the enzyme cyclooxygenase, which inserts two molecules of O₂ into the C-H bonds of the substrate acid.^[1][2]

References[edit]