| 词条 | Prostaglandin E3 |
| 释义 |
| Verifiedfields = | Watchedfields = | verifiedrevid = | IUPAC_name = (Z)-7-[(1R,2R,3R)-3-hydroxy-2-[(1E,3S,5Z)-3-hydroxyocta-1,5-dienyl]-5-oxocyclopentyl]hept-5-enoic acid | image = Prostaglandin E3.svg | tradename = | Drugs.com = {{drugs.com|international|prostaglandin-e3}} | MedlinePlus = | CAS_number_Ref = {{cascite|correct|??}} | CAS_number = 802-31-3 | ATC_prefix = | ATC_suffix = | PubChem = 5280937 | IUPHAR_ligand = | DrugBank_Ref = {{drugbankcite|changed|drugbank}} | DrugBank = | ChEBI_Ref = {{ebicite|changed|EBI}} | ChEBI = 28031 | ChEMBL_Ref = {{ebicite|changed|EBI}} | ChEMBL = 2074717 | ChemSpiderID = 4444439 | C=20 | H=30 | O=5 | molecular_weight = 350.5 g/mol | synonyms = | smiles = CC/C=C\\C[C@@H](/C=C/[C@H]1[C@@H](CC(=O)[C@@H]1C/C=C\\CCCC(=O)O)O)O | StdInChI = 1S/C20H30O5/c1-2-3-6-9-15(21)12-13-17-16(18(22)14-19(17)23)10-7-4-5-8-11-20(24)25/h3-4,6-7,12-13,15-17,19,21,23H,2,5,8-11,14H2,1H3,(H,24,25)/b6-3-,7-4-,13-12+/t15-,16+,17+,19+/m0/s1 | StdInChIKey = CBOMORHDRONZRN-QLOYDKTKSA-N }}Prostaglandin E3 (PGE3) is a naturally formed prostaglandin and is formed via the cyclooxygenase (COX) metabolism of eicosapentaenoic acid.[1] See also
References1. ^{{cite journal | author = Kulkarni PS, Srinivasan BD | title = Eicosapentaenoic acid metabolism in human and rabbit anterior uvea | journal = Prostaglandins | volume = 31 | issue = 6 | pages = 1159–64 |date=June 1986 | pmid = 3020617 | doi=10.1016/0090-6980(86)90217-0}} 3 : Prostaglandins|Carboxylic acids|Alcohols |
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