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Details

Stereochemistry RACEMIC
Molecular Formula C22H29ClO6
Molecular Weight 424.915
Optical Activity ( + / - )
Defined Stereocenters 5 / 5
E/Z Centers 2
Charge 0

SHOW SMILES / InChI
Structure of CLOPROSTENOL

SMILES

O[C@@H](COC1=CC=CC(Cl)=C1)\C=C\[C@H]2[C@H](O)C[C@H](O)[C@@H]2C\C=C/CCCC(O)=O

InChI

InChIKey=VJGGHXVGBSZVMZ-QIZQQNKQSA-N
InChI=1S/C22H29ClO6/c23-15-6-5-7-17(12-15)29-14-16(24)10-11-19-18(20(25)13-21(19)26)8-3-1-2-4-9-22(27)28/h1,3,5-7,10-12,16,18-21,24-26H,2,4,8-9,13-14H2,(H,27,28)/b3-1-,11-10+/t16-,18-,19-,20+,21-/m1/s1

HIDE SMILES / InChI

Molecular Formula C22H29ClO6
Molecular Weight 424.915
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 5 / 5
E/Z Centers 2
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:32:08 UTC 2023
Edited
by admin
on Fri Dec 15 16:32:08 UTC 2023
Record UNII
4208238832
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CLOPROSTENOL
INN   MI  
INN  
Official Name English
RACEMIC CLOPROSTENOL
Common Name English
cloprostenol [INN]
Common Name English
(±)-(Z)-7-((1R*,2R*,3R*,5S*)-2-((E)-(3R*)-4-(M-CHLOROPHENOXY)-3-HYDROXY-1-BUTENYL)-3,5-DIHYDROXYCYCLOPENTYL)-5-HEPTENOIC ACID
Systematic Name English
CLOPROSTENOL [MI]
Common Name English
REL-(5Z)-7-((1R,2R,3R,5S)-2-((1E,3R)-4-(3-CHLOROPHENOXY)-3-HYDROXY-1-BUTEN-1-YL)-3,5-DIHYDROXYCYCLOPENTYL)-5-HEPTENOIC ACID
Common Name English
(±)-CLOPROSTENOL
Common Name English
CLOPROSTENOL, (±)-
Common Name English
5-HEPTENOIC ACID, 7-((1R,2R,3R,5S)-2-((1E,3S)-4-(3-CHLOROPHENOXY)-3-HYDROXY-1-BUTEN-1-Y))-3,5-DIHYDROXYCYCLOPENTYL)- (5Z)-REL-
Systematic Name English
5-HEPTENOIC ACID, 7-(2-(4-(3-CHLOROPHENOXY)-3-HYDROXY-1-BUTENYL)-3,5-DIHYDROXYCYCLOPENTYL)-, (1A(Z),2B(1E,3R*),3.ALPHA.,5.ALPHA.),- (±)-
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C78568
Created by admin on Fri Dec 15 16:32:08 UTC 2023 , Edited by admin on Fri Dec 15 16:32:08 UTC 2023
WHO-VATC QG02AD90
Created by admin on Fri Dec 15 16:32:08 UTC 2023 , Edited by admin on Fri Dec 15 16:32:08 UTC 2023
Code System Code Type Description
FDA UNII
4208238832
Created by admin on Fri Dec 15 16:32:08 UTC 2023 , Edited by admin on Fri Dec 15 16:32:08 UTC 2023
PRIMARY
CAS
40665-92-7
Created by admin on Fri Dec 15 16:32:08 UTC 2023 , Edited by admin on Fri Dec 15 16:32:08 UTC 2023
PRIMARY
MESH
D003008
Created by admin on Fri Dec 15 16:32:08 UTC 2023 , Edited by admin on Fri Dec 15 16:32:08 UTC 2023
PRIMARY
ChEMBL
CHEMBL2220404
Created by admin on Fri Dec 15 16:32:08 UTC 2023 , Edited by admin on Fri Dec 15 16:32:08 UTC 2023
PRIMARY
MERCK INDEX
m3658
Created by admin on Fri Dec 15 16:32:08 UTC 2023 , Edited by admin on Fri Dec 15 16:32:08 UTC 2023
PRIMARY Merck Index
SMS_ID
100000084020
Created by admin on Fri Dec 15 16:32:08 UTC 2023 , Edited by admin on Fri Dec 15 16:32:08 UTC 2023
PRIMARY
RXCUI
2606
Created by admin on Fri Dec 15 16:32:08 UTC 2023 , Edited by admin on Fri Dec 15 16:32:08 UTC 2023
PRIMARY RxNorm
EPA CompTox
DTXSID7048372
Created by admin on Fri Dec 15 16:32:08 UTC 2023 , Edited by admin on Fri Dec 15 16:32:08 UTC 2023
PRIMARY
ECHA (EC/EINECS)
255-028-8
Created by admin on Fri Dec 15 16:32:08 UTC 2023 , Edited by admin on Fri Dec 15 16:32:08 UTC 2023
PRIMARY
INN
3793
Created by admin on Fri Dec 15 16:32:08 UTC 2023 , Edited by admin on Fri Dec 15 16:32:08 UTC 2023
PRIMARY
DAILYMED
4208238832
Created by admin on Fri Dec 15 16:32:08 UTC 2023 , Edited by admin on Fri Dec 15 16:32:08 UTC 2023
PRIMARY
PUBCHEM
5311053
Created by admin on Fri Dec 15 16:32:08 UTC 2023 , Edited by admin on Fri Dec 15 16:32:08 UTC 2023
PRIMARY
EVMPD
SUB06745MIG
Created by admin on Fri Dec 15 16:32:08 UTC 2023 , Edited by admin on Fri Dec 15 16:32:08 UTC 2023
PRIMARY
NCI_THESAURUS
C79571
Created by admin on Fri Dec 15 16:32:08 UTC 2023 , Edited by admin on Fri Dec 15 16:32:08 UTC 2023
PRIMARY
DRUG BANK
DB11507
Created by admin on Fri Dec 15 16:32:08 UTC 2023 , Edited by admin on Fri Dec 15 16:32:08 UTC 2023
PRIMARY
WIKIPEDIA
Cloprostenol
Created by admin on Fri Dec 15 16:32:08 UTC 2023 , Edited by admin on Fri Dec 15 16:32:08 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> AGONIST
BINDING
Ki
TARGET -> AGONIST
BINDING
Ki
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY