FLUVASTATIN SODIUM ANTI-ISOMER

Details

Stereochemistry	RACEMIC
Molecular Formula	C24H25FNO4.Na
Molecular Weight	433.4478
Optical Activity	( + / - )
Defined Stereocenters	2 / 2
E/Z Centers	1
Charge	0

SHOW SMILES / InChI

Structure of FLUVASTATIN SODIUM ANTI-ISOMER

Structure Search

SMILES

[Na+].CC(C)N1C(\C=C\[C@H](O)C[C@@H](O)CC([O-])=O)=C(C2=C1C=CC=C2)C3=CC=C(F)C=C3

InChI

InChIKey=ZGGHKIMDNBDHJB-INNGCKGUSA-M

InChI=1S/C24H26FNO4.Na/c1-15(2)26-21-6-4-3-5-20(21)24(16-7-9-17(25)10-8-16)22(26)12-11-18(27)13-19(28)14-23(29)30;/h3-12,15,18-19,27-28H,13-14H2,1-2H3,(H,29,30);/q;+1/p-1/b12-11+;/t18-,19+;/m0./s1

HIDE SMILES / InChI

Molecular Formula	Na
Molecular Weight	22.98976928
Charge	1
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Molecular Formula	C24H25FNO4
Molecular Weight	410.458
Charge	-1
Count

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	2 / 2
E/Z Centers	1
Optical Activity	UNSPECIFIED

Description
Sources: https://www.ncbi.nlm.nih.gov/pubmed/19418962
Curator's Comment: The description was created based on several sources, including https://www.jstage.jst.go.jp/article/dmpk1986/10/6/10_6_779/_pdf

Fluvastatin Anti-Isomer is a metabolite of lipid-lowering agent Fluvastatin. Fluvastatin is very unstable during storage and anti-isomer as well as lactones are the main formed by-products.

Originator

Approval Year

Conditions

Condition	Modality	Targets	Highest Phase	Product
Unknown 2596

PubMed

Title	Date	PubMed
Improvement in chemical and physical stability of fluvastatin drug through hydrogen bonding interactions with different polymer matrices.	2009-01	19418962

Sample Use Guides

In Vivo Use Guide

Unknown

Route of Administration: Unknown

In Vitro Use Guide

Unknown

Substance Class	Chemical Created by `admin` on `Mon Mar 31 21:27:34 GMT 2025` Edited by `admin` on `Mon Mar 31 21:27:34 GMT 2025`
Record UNII	FRP6Z03X99
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

(R*,R*-E)-(±)-7-(3-(4-FLUOROPHENYL)-1-(METHYLETHYL)-1H-INDOL-2-YL)-3,5-DIHYDROXY-6-HEPTENOIC ACID MONOSODIUM SALT

Preferred Name

English

FLUVASTATIN SODIUM ANTI-ISOMER

Common Name

English

6-HEPTENOIC ACID, 7-(3-(4-FLUOROPHENYL)-1-(1-METHYLETHYL)-1H-INDOL-2-YL)-3,5-DIHYDROXY-, SODIUM SALT (1:1), (3R,5R,6E)-REL-

Common Name

English

6-HEPTENOIC ACID, 7-(3-(4-FLUOROPHENYL)-1-(1-METHYLETHYL)-1H-INDOL-2-YL)-3,5-DIHYDROXY-, MONOSODIUM SALT, (R*,R*-(E))-(±)-

Common Name

English

6-HEPTENOIC ACID, 7-(3-(4-FLUOROPHENYL)-1-(1-METHYLETHYL)-1H-INDOL-2-YL)-3,5-DIHYDROXY-, MONOSODIUM SALT, (R*,R*-(E))-

Common Name

English

Code System Code Type Description

EPA CompTox

DTXSID10239940

Created by admin on Mon Mar 31 21:27:34 GMT 2025 , Edited by admin on Mon Mar 31 21:27:34 GMT 2025

PRIMARY

PUBCHEM

71587351

Created by admin on Mon Mar 31 21:27:34 GMT 2025 , Edited by admin on Mon Mar 31 21:27:34 GMT 2025

PRIMARY

FDA UNII

FRP6Z03X99

Created by admin on Mon Mar 31 21:27:34 GMT 2025 , Edited by admin on Mon Mar 31 21:27:34 GMT 2025

PRIMARY

CAS

93957-58-5

Created by admin on Mon Mar 31 21:27:34 GMT 2025 , Edited by admin on Mon Mar 31 21:27:34 GMT 2025

PRIMARY

Related Record Type Details


					PYF7O1FV7F

FLUVASTATIN SODIUM

PARENT -> IMPURITY

Details

SMILES

InChI

DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/19418962Curator's Comment: The description was created based on several sources, including https://www.jstage.jst.go.jp/article/dmpk1986/10/6/10_6_779/_pdf

Originator

Approval Year

Conditions

PubMed

Sample Use Guides

Description
Sources: https://www.ncbi.nlm.nih.gov/pubmed/19418962
Curator's Comment: The description was created based on several sources, including https://www.jstage.jst.go.jp/article/dmpk1986/10/6/10_6_779/_pdf