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Details

Stereochemistry RACEMIC
Molecular Formula C23H28F3O6.Na
Molecular Weight 480.4498
Optical Activity ( + / - )
Defined Stereocenters 5 / 5
E/Z Centers 2
Charge 0

SHOW SMILES / InChI
Structure of FLUPROSTENOL SODIUM

SMILES

[Na+].O[C@@H](COC1=CC=CC(=C1)C(F)(F)F)\C=C\[C@H]2[C@H](O)C[C@H](O)[C@@H]2C\C=C/CCCC([O-])=O

InChI

InChIKey=MUVLUMTZYKYXRV-KXXGZHCCSA-M
InChI=1S/C23H29F3O6.Na/c24-23(25,26)15-6-5-7-17(12-15)32-14-16(27)10-11-19-18(20(28)13-21(19)29)8-3-1-2-4-9-22(30)31;/h1,3,5-7,10-12,16,18-21,27-29H,2,4,8-9,13-14H2,(H,30,31);/q;+1/p-1/b3-1-,11-10+;/t16-,18-,19-,20+,21-;/m1./s1

HIDE SMILES / InChI

Molecular Formula C23H28F3O6
Molecular Weight 457.46
Charge -1
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 5 / 5
E/Z Centers 2
Optical Activity UNSPECIFIED

Molecular Formula Na
Molecular Weight 22.9898
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Ligand binding specificities of the eight types and subtypes of the mouse prostanoid receptors expressed in Chinese hamster ovary cells.
1997 Sep
The utilization of recombinant prostanoid receptors to determine the affinities and selectivities of prostaglandins and related analogs.
2000 Jan 17
Niacin promotes adipogenesis by reducing production of anti-adipogenic PGF2α through suppression of C/EBPβ-activated COX-2 expression.
2011 Apr
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:02:59 GMT 2023
Edited
by admin
on Fri Dec 15 15:02:59 GMT 2023
Record UNII
6H4ZY4O7NA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FLUPROSTENOL SODIUM
GREEN BOOK   MART.   USAN  
USAN  
Official Name English
5-HEPTENOIC ACID, 7-(3,5-DIHYDROXY-2-(3-HYDROXY-4-(3-(TRIFLUOROMETHYL)PHENOXY)-1-BUTENYL)CYCLOPENTYL)-, (1.ALPHA.(Z),2.BETA.(1E,3R*),3.ALPHA.,5.ALPHA.)-, SODIUM SALT, (±)-
Common Name English
FLUPROSTENOL SODIUM [GREEN BOOK]
Common Name English
(±)- SODIUM (Z)-7-((1R*,2R*,3R*,5S*)-3,5-DIHYDROXY-2-((E)-(3R*)-3-HYDROXY-4-((.ALPHA.,.ALPHA.,.ALPHA.-TRIFLUORO-M-TOLYL)OXY)-1-BUTENYL)CYCLOPENTYL)-5-HEPTENOATE
Systematic Name English
ICI-80008
Code English
FLUPROSTENOL SODIUM SALT [MI]
Common Name English
FLUPROSTENOL SODIUM [USAN]
Common Name English
ICI 80,008
Code English
SODIUM FLUPROSTENOL
Common Name English
FLUPROSTENOL SODIUM SALT
MI  
Common Name English
FLUPROSTENOL SODIUM [MART.]
Common Name English
EQUIMATE
Brand Name English
Classification Tree Code System Code
NCI_THESAURUS C29705
Created by admin on Fri Dec 15 15:02:59 GMT 2023 , Edited by admin on Fri Dec 15 15:02:59 GMT 2023
CFR 21 CFR 522.995
Created by admin on Fri Dec 15 15:02:59 GMT 2023 , Edited by admin on Fri Dec 15 15:02:59 GMT 2023
Code System Code Type Description
ChEMBL
CHEMBL2220419
Created by admin on Fri Dec 15 15:02:59 GMT 2023 , Edited by admin on Fri Dec 15 15:02:59 GMT 2023
PRIMARY
ECHA (EC/EINECS)
259-438-8
Created by admin on Fri Dec 15 15:02:59 GMT 2023 , Edited by admin on Fri Dec 15 15:02:59 GMT 2023
PRIMARY
PUBCHEM
23695842
Created by admin on Fri Dec 15 15:02:59 GMT 2023 , Edited by admin on Fri Dec 15 15:02:59 GMT 2023
PRIMARY
DRUG BANK
DBSALT001683
Created by admin on Fri Dec 15 15:02:59 GMT 2023 , Edited by admin on Fri Dec 15 15:02:59 GMT 2023
PRIMARY
MERCK INDEX
m5494
Created by admin on Fri Dec 15 15:02:59 GMT 2023 , Edited by admin on Fri Dec 15 15:02:59 GMT 2023
PRIMARY Merck Index
CAS
55028-71-2
Created by admin on Fri Dec 15 15:02:59 GMT 2023 , Edited by admin on Fri Dec 15 15:02:59 GMT 2023
PRIMARY
NCI_THESAURUS
C75209
Created by admin on Fri Dec 15 15:02:59 GMT 2023 , Edited by admin on Fri Dec 15 15:02:59 GMT 2023
PRIMARY
FDA UNII
6H4ZY4O7NA
Created by admin on Fri Dec 15 15:02:59 GMT 2023 , Edited by admin on Fri Dec 15 15:02:59 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY