ENGLITAZONE SODIUM

Details

Stereochemistry	MIXED
Molecular Formula	C20H18NO3S.Na
Molecular Weight	375.417
Optical Activity	UNSPECIFIED
Defined Stereocenters	1 / 2
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

[Na+].O=C1[N-]C(=O)C(CC2=CC3=C(O[C@@H](CC4=CC=CC=C4)CC3)C=C2)S1

InChI

InChIKey=JQWYNJRCVYGLMO-GPPXSFHXSA-M

InChI=1S/C20H19NO3S.Na/c22-19-18(25-20(23)21-19)12-14-6-9-17-15(10-14)7-8-16(24-17)11-13-4-2-1-3-5-13;/h1-6,9-10,16,18H,7-8,11-12H2,(H,21,22,23);/q;+1/p-1/t16-,18?;/m1./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	C20H19NO3S
Molecular Weight	353.435
Charge	0
Count

Stereochemistry	EPIMERIC
Additional Stereochemistry	No
Defined Stereocenters	1 / 2
E/Z Centers	0
Optical Activity	UNSPECIFIED

Description
Sources: https://adisinsight.springer.com/drugs/800000033 | https://www.ncbi.nlm.nih.gov/pubmed/10864893 | https://www.ncbi.nlm.nih.gov/pubmed/9179397 | https://www.ncbi.nlm.nih.gov/pubmed/2210074 | https://www.ncbi.nlm.nih.gov/pubmed/8576907 | https://www.ncbi.nlm.nih.gov/pubmed/8706692

Englitazone is a thiazolidinedione antidiabetic agent. It has insulinomimetic and insulin-enhancing actions in vitro and glucose-, insulin-, triglyceride-, and cholesterol-lowering properties in an animal model of non-insulin-dependent diabetes mellitus. It acts as a peroxisome-proliferator-activated receptor-gamma ligand. Englitazone inhibits ATP-sensitive potassium and calcium-activated non-selective cation channels in a voltage-independent manner.

Originator

Approval Year

PubMed

Title	Date	PubMed
Correlation between activation of PPARγ and resistin downregulation in a mouse adipocyte cell line by a series of thiazolidinediones.	2013-08	23563205
Inhibition of phosphoenolpyruvate carboxykinase (PEPCK) gene expression by troglitazone: a peroxisome proliferator-activated receptor-gamma (PPARgamma)-independent, antioxidant-related mechanism.	2001-10-15	11597575

Patents

Sample Use Guides

In Vitro Use Guide

Application of englitazone to the outside of CRI-G1 cells in the whole-cell recording configuration produced concentration-dependent inhibition of ATP-sensitive potassium currents with an IC50 value of 8 microM.

Substance Class	Chemical Created by `admin` on `Mon Mar 31 18:24:11 GMT 2025` Edited by `admin` on `Mon Mar 31 18:24:11 GMT 2025`
Record UNII	VA5755GIJ8
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

ENGLITAZONE SODIUM

Official Name

English

CP-72,467-2

Preferred Name

English

(-)-5-(((2R)-2-BENZYL-6-CHROMANYL)METHYL)-2,4-THIAZOLIDINEDIONE, SODIUM SALT

Common Name

English

2,4-THIAZOLIDINEDIONE, 5-((3,4-DIHYDRO-2-(PHENYLMETHYL)-2H-1-BENZOPYRAN-6-YL)METHYL)-, SODIUM SALT

Common Name

English

ENGLITAZONE SODIUM [USAN]

Common Name

English

CP-72467-2

Code

English

Classification Tree Code System Code

NCI_THESAURUS

C98241