loading...| Preferred Name | prostaglandin E2 | |
| Synonyms |
(5Z,13E)-(15S)-11alpha,15-Dihydroxy-9-oxoprost-13-enoate Minprostin E2 (Z)-7-((1R,2R,3R)-3-hydroxy-2-((S,E)-3-hydroxyoct-1-enyl)-5-oxocyclopentyl)hept-5-enoic acid Prostarmon E Dinoproston dinoprostona dinoprostone (15S)-prostaglandin E2 dinoprostonum (5Z,13E)-(15S)-11alpha,15-Dihydroxy-9-oxoprosta-5,13-dienoate (E,Z)-(1R,2R,3R)-7-(3-Hydroxy-2-((3S)-(3-hydroxy-1-octenyl))-5-oxocyclopentyl)-5-heptenoic acid Minprositin E2 (5Z,11alpha,13E,15S)-11,15-dihydroxy-9-oxoprosta-5,13-dien-1-oic acid Enzaprost E Cervidil Cerviprime Cerviprost Glandin-E2 PGE2 Prepidil Propess Prostenone Prostin Prostin E2 U 12062 U-12,062 U-12062 Prostaglandin E2 (5Z,13E,15S)-11alpha,15-dihydroxy-9-oxoprosta-5,13-dien-1-oic acid |
|
| Definitions |
Prostaglandin F2alpha in which the hydroxy group at position 9 has been oxidised to the corresponding ketone. Prostaglandin E2 is the most common and most biologically potent of mammalian prostaglandins. |
|
| ID |
http://purl.obolibrary.org/obo/CHEBI_15551 |
|
| alternative term |
(5Z,13E)-(15S)-11alpha,15-Dihydroxy-9-oxoprost-13-enoate Minprostin E2 (Z)-7-((1R,2R,3R)-3-hydroxy-2-((S,E)-3-hydroxyoct-1-enyl)-5-oxocyclopentyl)hept-5-enoic acid Prostarmon E Dinoproston dinoprostona dinoprostone (15S)-prostaglandin E2 dinoprostonum (5Z,13E)-(15S)-11alpha,15-Dihydroxy-9-oxoprosta-5,13-dienoate (E,Z)-(1R,2R,3R)-7-(3-Hydroxy-2-((3S)-(3-hydroxy-1-octenyl))-5-oxocyclopentyl)-5-heptenoic acid Minprositin E2 (5Z,11alpha,13E,15S)-11,15-dihydroxy-9-oxoprosta-5,13-dien-1-oic acid Enzaprost E Cervidil Cerviprime Cerviprost Glandin-E2 PGE2 Prepidil Propess Prostenone Prostin Prostin E2 U 12062 U-12,062 U-12062 Prostaglandin E2 (5Z,13E,15S)-11alpha,15-dihydroxy-9-oxoprosta-5,13-dien-1-oic acid |
|
| bearer_of |
http://purl.obolibrary.org/obo/CHEBI_77746 |
|
| charge |
0 |
|
| database_cross_reference |
KEGG:D00079 PMID:16978535 PMID:9276764 Patent:GB851827 HMDB:HMDB0001220 PMID:32898608 KEGG:C00584 CAS:363-24-6 Beilstein:2224724 PMID:7836930 PMID:34102274 PMID:16405508 LIPID_MAPS_instance:LMFA03010003 Patent:NL6505799 LINCS:LSM-42919 PMID:33715333 PMID:24501112 PMID:14535055 Patent:US3598858 Patent:DE2011969 PMID:33782420 FooDB:FDB022498 PMID:6317292 PMID:15542928 Drug_Central:913 PMID:33559528 PMID:11279302 PMID:20671299 PMID:12746806 PMID:34065827 PMID:14499495 PMID:33271839 PMID:34071686 PMID:33685091 PMID:15661432 Wikipedia:Prostaglandin_E2 PMID:12859290 PDBeChem:P2E PMID:33958485 Reaxys:2224724 PMID:2403792 PMID:7224729 PMID:14703707 PMID:16787416 PMID:33811074 DrugBank:DB00917 PMID:74611 |
|
| formula |
C20H32O5 |
|
| has role |
http://purl.obolibrary.org/obo/CHEBI_77746 |
|
| has_alternative_id |
CHEBI:10910 CHEBI:10911 CHEBI:114125 CHEBI:26323 CHEBI:4625 CHEBI:8512 |
|
| has_exact_synonym |
Prostaglandin E2 (5Z,13E,15S)-11alpha,15-dihydroxy-9-oxoprosta-5,13-dien-1-oic acid |
|
| has_obo_namespace |
chebi_ontology |
|
| has_related_synonym |
(5Z,13E)-(15S)-11alpha,15-Dihydroxy-9-oxoprost-13-enoate Minprostin E2 (Z)-7-((1R,2R,3R)-3-hydroxy-2-((S,E)-3-hydroxyoct-1-enyl)-5-oxocyclopentyl)hept-5-enoic acid Prostarmon E Dinoproston dinoprostona dinoprostone (15S)-prostaglandin E2 dinoprostonum (5Z,13E)-(15S)-11alpha,15-Dihydroxy-9-oxoprosta-5,13-dienoate (E,Z)-(1R,2R,3R)-7-(3-Hydroxy-2-((3S)-(3-hydroxy-1-octenyl))-5-oxocyclopentyl)-5-heptenoic acid Minprositin E2 (5Z,11alpha,13E,15S)-11,15-dihydroxy-9-oxoprosta-5,13-dien-1-oic acid Enzaprost E Cervidil Cerviprime Cerviprost Glandin-E2 PGE2 Prepidil Propess Prostenone Prostin Prostin E2 U 12062 U-12,062 U-12062 |
|
| id |
CHEBI:15551 |
|
| in_subset | ||
| inchi |
InChI=1S/C20H32O5/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/h4,7,12-13,15-17,19,21,23H,2-3,5-6,8-11,14H2,1H3,(H,24,25)/b7-4-,13-12+/t15-,16+,17+,19+/m0/s1 |
|
| inchikey |
XEYBRNLFEZDVAW-ARSRFYASSA-N |
|
| is conjugate acid of | ||
| label |
prostaglandin E2 |
|
| mass |
352.471 |
|
| monoisotopicmass |
352.22497 |
|
| notation |
CHEBI:15551 |
|
| prefLabel |
prostaglandin E2 |
|
| smiles |
CCCCC[C@H](O)\C=C\[C@H]1[C@H](O)CC(=O)[C@@H]1C\C=C/CCCC(O)=O |
|
| textual definition |
Prostaglandin F2alpha in which the hydroxy group at position 9 has been oxidised to the corresponding ketone. Prostaglandin E2 is the most common and most biologically potent of mammalian prostaglandins. |
|
| subClassOf |