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The Drug-Drug Interactions Ontology
Last uploaded:
February 11, 2016
| Id | http://purl.obolibrary.org/obo/CHEBI_63610
http://purl.obolibrary.org/obo/CHEBI_63610
|
|---|---|
| Preferred Name | misoprostol |
| Synonyms |
(11-alpha,13E)-(+-)-11,16-dihydroxy-16-methyl-9-oxoprost-13-en-1-oic acid methyl ester
Methyl (+-)-11-alpha,16-dihydroxy-16-methyl-9-oxoprost-13-en-1-oate
Cytotec
(+-)-methyl (1R,2R,3R)-3-hydroxy-2-((E)-(4RS)-4-hydroxy-4-methyl-1-octenyl)-5-oxocyclopentaneheptanoate
C22H38O5
misoprostolum
misoprostol
methyl 7-[(1R,2R,3R)-3-hydroxy-2-[(1E)-4-hydroxy-4-methyloct-1-en-1-yl]-5-oxocyclopentyl]heptanoate
Arthrotec
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| prefLabel | misoprostol
|
|---|---|
| label | misoprostol
|
| DBSynonym | misoprostolum [inn-latin]
|
| ATCCode | A02BB01
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| Definition | A diastereoisomeric mixture composed of approximately equal amounts of a double racemate of four of the sixteen possible diastereoisomers of methyl (13E)-11,16-dihydroxy-16-methyl-9-oxoprost-13-en-1-oate that is racemic prostaglandin E1 which is lacking the hydroxy group at position 15, but which has an additional hydroxy group at position 16. It is a synthetic prostaglandin E1 analogue, used in the treatment of gastric and duodenal ulcers. A weak abortifacient, it is also used for cervical ripening prior to surgical termination of pregnancy. The (11R,16S)-diastereoisomer is the pharmacologically active form.
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| altId | CHEBI:6952
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| has effect |
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| has pharmacological target | |
| activates | |
| type | |
| has role | |
| InChIKey | InChIKey=OJLOPKGSLYJEMD-URPKTTJQSA-N
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| AHFScode | 56:28.28
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| Synonym | (11-alpha,13E)-(+-)-11,16-dihydroxy-16-methyl-9-oxoprost-13-en-1-oic acid methyl ester
Methyl (+-)-11-alpha,16-dihydroxy-16-methyl-9-oxoprost-13-en-1-oate
Cytotec
(+-)-methyl (1R,2R,3R)-3-hydroxy-2-((E)-(4RS)-4-hydroxy-4-methyl-1-octenyl)-5-oxocyclopentaneheptanoate
C22H38O5
misoprostolum
misoprostol
methyl 7-[(1R,2R,3R)-3-hydroxy-2-[(1E)-4-hydroxy-4-methyloct-1-en-1-yl]-5-oxocyclopentyl]heptanoate
Arthrotec
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| xref |
CiteXplore:19740175
Reaxys:4155643
RxList:http://www.rxlist.com/cgi/generic/misopro.htm
PubChem Compound:5282381
CiteXplore:11136959
Patent:US3965143
Drugs Product Database (DPD):2248846
CiteXplore:1417145
CiteXplore:2109814
PharmGKB:PA450523
National Drug Code Directory:0172-4430-49
CiteXplore:10945193
ChemSpider:4445541
Patent:BE827127
CiteXplore:3080288
KEGG DRUG:D00419
CiteXplore:18690850
DrugBank:DB00929
Wikipedia:Misoprostol
Drugs.com:http://www.drugs.com/cdi/misoprostol.html
PubChem Substance:46505041
CASRN:59122-46-2
Wikipedia:http://en.wikipedia.org/wiki/Misoprostol
CiteXplore:10949752
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| CASRN | 59122-46-2
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| prefixIRI | obo2:CHEBI_63610
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| SMILES | CCCCC(C)(O)C\C=C\[C@H]1[C@H](O)CC(=O)[C@@H]1CCCCCCC(=O)OC
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| DBname | misoprostol
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| InChI | InChI=1S/C22H38O5/c1-4-5-14-22(2,26)15-10-12-18-17(19(23)16-20(18)24)11-8-6-7-9-13-21(25)27-3/h10,12,17-18,20,24,26H,4-9,11,13-16H2,1-3H3/b12-10+/t17-,18-,20-,22?/m1/s1
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| DBBrand |
cytotec
arthrotec
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| subClassOf |
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