InChI=1S/C20H32O5/c1- 2- 3- 4- 7- 14(21) 10- 11- 16- 17- 12- 15(8- 5- 6- 9- 20(23) 24) 25- 19(17) 13- 18(16) 22/h8,10- 11,14,16- 19,21- 22H,2- 7,9,12- 13H2,1H3,(H,23,24) /b11- 10+,15- 8- /t14- ,16+,17+,18+,19- /m0/s1 |
KAQKFAOMNZTLHT-OZUDYXHBSA-N |
[H][C@]12C[C@@H](O)[C@H](\C=C\[C@@H](O)CCCCC)[C@@]1([H])C\C(O2)=C\CCCC(O)=O |
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Mus musculus
(NCBI:txid10090)
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Source: BioModels - MODEL1507180067
See:
PubMed
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mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
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(5Z,13E,15S)-6,9α-epoxy-11α,15-dihydroxyprosta-5,13-dienoic acid
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(5Z,13E)-(15S)-6,9alpha-Epoxy-11alpha,15-dihydroxyprosta-5,13-dienoate
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KEGG COMPOUND
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(5Z,13E)-(15S)-6,9alpha-Epoxy-11alpha,15-dihydroxyprosta-5,13-dienoate
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KEGG COMPOUND
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(5Z,9α,11α,13E,15S)- 6,9- epoxy- 11,15- dihydroxyprosta- 5,13- dien- 1- oic acid
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ChemIDplus
|
Epoprostenol
|
KEGG COMPOUND
|
Flolan
|
ChemIDplus
|
PGI2
|
KEGG COMPOUND
|
PGI2
|
ChEBI
|
PGX
|
ChemIDplus
|
Prostacyclin
|
KEGG COMPOUND
|
Prostaglandin I2
|
KEGG COMPOUND
|
prostaglandin X
|
ChemIDplus
|
Vasocyclin
|
ChemIDplus
|
1690090
|
Beilstein Registry Number
|
ChemIDplus
|
35121-78-9
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CAS Registry Number
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ChemIDplus
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