CHEBI:137370 - 20-hydroxyprostaglandin E₂

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ChEBI Name 20-hydroxyprostaglandin E2 ChEBI ID CHEBI:137370 ChEBI ASCII Name 20-hydroxyprostaglandin E2 Definition A prostaglandin E derivative that is prostaglandin E2 in which one of the methyl hydrogens at position 20 has been replaced by a hydroxy group.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 C20H32O6 Net Charge 0 Average Mass 368.465 Monoisotopic Mass 368.21989 InChI InChI=1S/C20H32O6/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/h1,5,11-12,15-17,19,21-22,24H,2-4,6-10,13-14H2,(H,25,26)/b5-1-,12-11+/t15-,16+,17+,19+/m0/s1 InChIKey AZIGEYVZEVXWAD-NZGURKHLSA-N SMILES C(\[C@H]1[C@@H](CC([C@@H]1C/C=C\CCCC(O)=O)=O)O)=C/[C@H](CCCCCO)O ChEBI Ontology Outgoing 20-hydroxyprostaglandin E2 (CHEBI:137370) has functional parent prostaglandin E2 (CHEBI:15551) 20-hydroxyprostaglandin E2 (CHEBI:137370) is a primary alcohol (CHEBI:15734) 20-hydroxyprostaglandin E2 (CHEBI:137370) is a prostaglandins E (CHEBI:26338) 20-hydroxyprostaglandin E2 (CHEBI:137370) is a secondary allylic alcohol (CHEBI:134396) 20-hydroxyprostaglandin E2 (CHEBI:137370) is a triol (CHEBI:27136) 20-hydroxyprostaglandin E2 (CHEBI:137370) is conjugate acid of 20-hydroxyprostaglandin E2(1−) (CHEBI:136653) Incoming 20-hydroxyprostaglandin E2(1−) (CHEBI:136653) is conjugate base of 20-hydroxyprostaglandin E2 (CHEBI:137370) IUPAC Name (5Z,13E,15S)-11α,15,20-trihydroxy-9-oxoprosta-5,13-dien-1-oic acid Synonyms Sources (5Z,11α,13E,15S)-11,15,20-trihydroxy-9-oxoprosta-5,13-dien-1-oic acid IUPAC 20-hydroxy prostaglandin E2 ChEBI 20-hydroxy-PGE2 ChEBI 20-hydroxy-prostaglandin E2 ChEBI 20-OH-PGE2 ChEBI 9-oxo-11R,15S,20-trihydroxy-5Z,13E-prostadienoic acid LIPID MAPS Manual Xrefs Databases HMDB0003247 HMDB LMFA03010014 LIPID MAPS View more database links Registry Numbers Types Sources 2951905 Reaxys Registry Number Reaxys 57930-95-7 CAS Registry Number ChemIDplus Citation Type Source 11370662 PubMed citation Europe PMC Last Modified 26 June 2017