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Details

Stereochemistry RACEMIC
Molecular Formula C22H36O5
Molecular Weight 380.5182
Optical Activity ( + / - )
Defined Stereocenters 5 / 5
E/Z Centers 3
Charge 0

SHOW SMILES / InChI
Structure of PROSTALENE

SMILES

CCCCC[C@@](C)(O)\C=C\[C@H]1[C@H](O)C[C@H](O)[C@@H]1CC=C=CCCC(=O)OC

InChI

InChIKey=GNIYHUSSKSFYBD-MFZPGRHISA-N
InChI=1S/C22H36O5/c1-4-5-10-14-22(2,26)15-13-18-17(19(23)16-20(18)24)11-8-6-7-9-12-21(25)27-3/h7-8,13,15,17-20,23-24,26H,4-5,9-12,14,16H2,1-3H3/b15-13+/t6?,17-,18-,19+,20-,22-/m1/s1

HIDE SMILES / InChI

Molecular Formula C22H36O5
Molecular Weight 380.5182
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 5 / 5
E/Z Centers 3
Optical Activity UNSPECIFIED

Prostalene is an analogue of prostaglandin PGF-2 alpha. It is used for the control of estrus in mares.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Preventing
Synchrocept B

Approved Use

Indications for use: For the control of estrus in mares.
PubMed

PubMed

TitleDatePubMed
Sources of variation in response intervals after prostaglandin treatment in mares with functional corpora lutea.
1979
Summary of the effect of prostalene, a new synthetic prostaglandin, on the breeding efficiency of mares.
1976-11
Patents

Sample Use Guides

Conditions of use in horses --(1) Amount. Administer 5 micrograms per kilogram of body weight as a single subcutaneous injection.
Route of Administration: Other
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:24:09 GMT 2025
Edited
by admin
on Mon Mar 31 18:24:09 GMT 2025
Record UNII
O02SWY8981
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SYNCHROCEPT
Preferred Name English
PROSTALENE
GREEN BOOK   INN   MART.   MI   USAN  
USAN   INN  
Official Name English
PROSTALENE [MART.]
Common Name English
PROSTALENE [USAN]
Common Name English
(±)-METHYL 7-((1R*,2R*,3R*,5S*)-3,5-DIHYDROXY-2-((E)-3-HYDROXY-3-METHYL-1-OCTENYL)CYCLOPENTYL)-4,5-HEPTADIENOATE
Systematic Name English
prostalene [INN]
Common Name English
RS-9390
Code English
PROSTA-4,5,13-TRIEN-1-OIC ACID, 9,11,15-TRIHYDROXY-15-METHYL-, METHYL ESTER, (9.ALPHA.,11.ALPHA.,13E,15R)-, (±)-
Common Name English
PROSTALENE [GREEN BOOK]
Common Name English
PROSTALENE [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C78568
Created by admin on Mon Mar 31 18:24:09 GMT 2025 , Edited by admin on Mon Mar 31 18:24:09 GMT 2025
CFR 21 CFR 522.2012
Created by admin on Mon Mar 31 18:24:09 GMT 2025 , Edited by admin on Mon Mar 31 18:24:09 GMT 2025
Code System Code Type Description
ChEMBL
CHEMBL2105317
Created by admin on Mon Mar 31 18:24:09 GMT 2025 , Edited by admin on Mon Mar 31 18:24:09 GMT 2025
PRIMARY
NCI_THESAURUS
C76903
Created by admin on Mon Mar 31 18:24:09 GMT 2025 , Edited by admin on Mon Mar 31 18:24:09 GMT 2025
PRIMARY
CAS
54120-61-5
Created by admin on Mon Mar 31 18:24:09 GMT 2025 , Edited by admin on Mon Mar 31 18:24:09 GMT 2025
PRIMARY
FDA UNII
O02SWY8981
Created by admin on Mon Mar 31 18:24:09 GMT 2025 , Edited by admin on Mon Mar 31 18:24:09 GMT 2025
PRIMARY
MERCK INDEX
m9261
Created by admin on Mon Mar 31 18:24:09 GMT 2025 , Edited by admin on Mon Mar 31 18:24:09 GMT 2025
PRIMARY Merck Index
DRUG BANK
DB11454
Created by admin on Mon Mar 31 18:24:09 GMT 2025 , Edited by admin on Mon Mar 31 18:24:09 GMT 2025
PRIMARY
EVMPD
SUB10133MIG
Created by admin on Mon Mar 31 18:24:09 GMT 2025 , Edited by admin on Mon Mar 31 18:24:09 GMT 2025
PRIMARY
EPA CompTox
DTXSID501021602
Created by admin on Mon Mar 31 18:24:09 GMT 2025 , Edited by admin on Mon Mar 31 18:24:09 GMT 2025
PRIMARY
ECHA (EC/EINECS)
258-984-4
Created by admin on Mon Mar 31 18:24:09 GMT 2025 , Edited by admin on Mon Mar 31 18:24:09 GMT 2025
PRIMARY
INN
3873
Created by admin on Mon Mar 31 18:24:09 GMT 2025 , Edited by admin on Mon Mar 31 18:24:09 GMT 2025
PRIMARY
PUBCHEM
6436031
Created by admin on Mon Mar 31 18:24:09 GMT 2025 , Edited by admin on Mon Mar 31 18:24:09 GMT 2025
PRIMARY
SMS_ID
100000080832
Created by admin on Mon Mar 31 18:24:09 GMT 2025 , Edited by admin on Mon Mar 31 18:24:09 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY