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Details

Stereochemistry ABSOLUTE
Molecular Formula C24H32O7
Molecular Weight 432.5067
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 2
Charge 0

SHOW SMILES / InChI
Structure of ETIPROSTON

SMILES

O[C@H]1C[C@@H](O)[C@H](\C=C\C3(COC2=CC=CC=C2)OCCO3)[C@H]1C\C=C/CCCC(O)=O

InChI

InChIKey=BPALXSWPHQNCAA-RLJNYRALSA-N
InChI=1S/C24H32O7/c25-21-16-22(26)20(19(21)10-6-1-2-7-11-23(27)28)12-13-24(30-14-15-31-24)17-29-18-8-4-3-5-9-18/h1,3-6,8-9,12-13,19-22,25-26H,2,7,10-11,14-17H2,(H,27,28)/b6-1-,13-12+/t19-,20-,21+,22-/m1/s1

HIDE SMILES / InChI

Molecular Formula C24H32O7
Molecular Weight 432.5067
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 2
Optical Activity UNSPECIFIED

Etiproston is a synthetic analog of prostaglandin F2α. Etiproston induces luteal regression. Etiproston is used in veterinary.

Approval Year

PubMed

PubMed

TitleDatePubMed
Influence of a PGF2alpha-analogue, etiproston tromethamine, on the functional corpus luteum of dogs.
2005-01
Fate of etiproston, a synthetic analogue of PGF2 alpha, in cows.
1994-10
Feed intake and rumen motility in dwarf goats. Effects of some alpha 2-adrenergic agonists, prostaglandins and posterior pituitary hormones.
1991
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:29:03 GMT 2025
Edited
by admin
on Mon Mar 31 18:29:03 GMT 2025
Record UNII
TCU22W0APY
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PROSTAVET
Preferred Name English
ETIPROSTON
INN   MI  
INN  
Official Name English
etiproston [INN]
Common Name English
(Z)-7-((1R,2R,3R,5S)-3,5-DIHYDROXY-2-((E)-2-(2-(PHENOXYMETHYL)-1,3-DIOXOLAN-2-YL)VINYL)CYCLOPENTYL)-5-HEPTENOIC ACID
Systematic Name English
ETIPROSTON [MI]
Common Name English
Classification Tree Code System Code
WHO-VATC QG02AD95
Created by admin on Mon Mar 31 18:29:03 GMT 2025 , Edited by admin on Mon Mar 31 18:29:03 GMT 2025
NCI_THESAURUS C78568
Created by admin on Mon Mar 31 18:29:03 GMT 2025 , Edited by admin on Mon Mar 31 18:29:03 GMT 2025
Code System Code Type Description
NCI_THESAURUS
C65579
Created by admin on Mon Mar 31 18:29:03 GMT 2025 , Edited by admin on Mon Mar 31 18:29:03 GMT 2025
PRIMARY
CAS
59619-81-7
Created by admin on Mon Mar 31 18:29:03 GMT 2025 , Edited by admin on Mon Mar 31 18:29:03 GMT 2025
PRIMARY
PUBCHEM
5311241
Created by admin on Mon Mar 31 18:29:03 GMT 2025 , Edited by admin on Mon Mar 31 18:29:03 GMT 2025
PRIMARY
MERCK INDEX
m5188
Created by admin on Mon Mar 31 18:29:03 GMT 2025 , Edited by admin on Mon Mar 31 18:29:03 GMT 2025
PRIMARY Merck Index
SMS_ID
100000082097
Created by admin on Mon Mar 31 18:29:03 GMT 2025 , Edited by admin on Mon Mar 31 18:29:03 GMT 2025
PRIMARY
MESH
C092017
Created by admin on Mon Mar 31 18:29:03 GMT 2025 , Edited by admin on Mon Mar 31 18:29:03 GMT 2025
PRIMARY
FDA UNII
TCU22W0APY
Created by admin on Mon Mar 31 18:29:03 GMT 2025 , Edited by admin on Mon Mar 31 18:29:03 GMT 2025
PRIMARY
ChEMBL
CHEMBL2104285
Created by admin on Mon Mar 31 18:29:03 GMT 2025 , Edited by admin on Mon Mar 31 18:29:03 GMT 2025
PRIMARY
INN
5113
Created by admin on Mon Mar 31 18:29:03 GMT 2025 , Edited by admin on Mon Mar 31 18:29:03 GMT 2025
PRIMARY
EVMPD
SUB07307MIG
Created by admin on Mon Mar 31 18:29:03 GMT 2025 , Edited by admin on Mon Mar 31 18:29:03 GMT 2025
PRIMARY
EPA CompTox
DTXSID501024232
Created by admin on Mon Mar 31 18:29:03 GMT 2025 , Edited by admin on Mon Mar 31 18:29:03 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY