CHEBI:137526 - 20-hydroxyprostaglandin E₁

Main

ChEBI Ontology

Automatic Xrefs

Reactions

Pathways

Models

ChEBI Name 20-hydroxyprostaglandin E1 ChEBI ID CHEBI:137526 ChEBI ASCII Name 20-hydroxyprostaglandin E1 Definition A prostaglandin E derivative that is prostaglandin E1 in which one of the methyl hydrogens at position 20 has been replaced by a hydroxy group. Stars This entity has been manually annotated by the ChEBI Team. Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C20H34O6 Net Charge 0 Average Mass 370.481 Monoisotopic Mass 370.23554 InChI InChI=1S/C20H34O6/c21-13-7-3-4-8-15(22)11-12-17-16(18(23)14-19(17)24)9-5-1-2-6-10-20(25)26/h11-12,15-17,19,21-22,24H,1-10,13-14H2,(H,25,26)/b12-11+/t15-,16+,17+,19+/m0/s1 InChIKey LDUBDFDZFOQXGF-HTGUDJHRSA-N SMILES [C@H]1([C@H]([C@H](O)CC1=O)/C=C/[C@H](CCCCCO)O)CCCCCCC(O)=O Metabolite of Species Details Ovis aries (NCBI:txid9940) See: PubMed Roles Classification Biological Role(s): mammalian metabolite Any animal metabolite produced during a metabolic reaction in mammals. View more via ChEBI Ontology ChEBI Ontology Outgoing 20-hydroxyprostaglandin E1 (CHEBI:137526) has functional parent prostaglandin E1 (CHEBI:15544) 20-hydroxyprostaglandin E1 (CHEBI:137526) has role mammalian metabolite (CHEBI:75768) 20-hydroxyprostaglandin E1 (CHEBI:137526) is a primary alcohol (CHEBI:15734) 20-hydroxyprostaglandin E1 (CHEBI:137526) is a prostaglandins E (CHEBI:26338) 20-hydroxyprostaglandin E1 (CHEBI:137526) is a secondary allylic alcohol (CHEBI:134396) 20-hydroxyprostaglandin E1 (CHEBI:137526) is a triol (CHEBI:27136) 20-hydroxyprostaglandin E1 (CHEBI:137526) is conjugate acid of 20-hydroxyprostaglandin E1(1−) (CHEBI:136661) Incoming 20-hydroxyprostaglandin E1(1−) (CHEBI:136661) is conjugate base of 20-hydroxyprostaglandin E1 (CHEBI:137526) IUPAC Name (13E,15S)-11α,15,20-trihydroxy-9-oxoprost-13-en-1-oic acid Synonyms Sources (11α,13E,15S)-11,15,20-trihydroxy-9-oxoprost-13-en-1-oic acid IUPAC 20-hydroxy prostaglandin E1 ChEBI 20-hydroxy-PGE1 ChEBI 20-hydroxy-prostaglandin E1 ChEBI 20-OH-PGE1 ChEBI Registry Numbers Types Sources 2892253 Reaxys Registry Number Reaxys 57930-99-1 CAS Registry Number ChemIDplus Citations Types Sources 11370662 PubMed citation Europe PMC 3087990 PubMed citation Europe PMC 3196735 PubMed citation Europe PMC 3244833 PubMed citation Europe PMC 3479770 PubMed citation Europe PMC Last Modified 26 June 2017