Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C20H19N3O4S.ClH |
| Molecular Weight | 433.908 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.COC1=CC2=C(C=C1)N=C(COC3=CC=C(CC4SC(=O)NC4=O)C=C3)N2C
InChI
InChIKey=LKKAMJRUPIIUTC-UHFFFAOYSA-N
InChI=1S/C20H19N3O4S.ClH/c1-23-16-10-14(26-2)7-8-15(16)21-18(23)11-27-13-5-3-12(4-6-13)9-17-19(24)22-20(25)28-17;/h3-8,10,17H,9,11H2,1-2H3,(H,22,24,25);1H
| Molecular Formula | ClH |
| Molecular Weight | 36.461 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C20H19N3O4S |
| Molecular Weight | 397.448 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Rivoglitazone hydrochloride (CS-011) is a thiazolidinedione-derivative peroxisome proliferator–activated receptor (PPAR)-γ agonist. It has been developed as potential treatment in type 2 diabetes mellitus and was shown to decrease plasma glucose and triglyceride levels in a dose-dependent manner in animals. Phase II and III clinical studies have assessed the efficacy and safety of rivoglitazone hydrochloride in patients with type 2 diabetes mellitus.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 17 12:57:34 UTC 2022
by
admin
on
Sat Dec 17 12:57:34 UTC 2022
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| Record UNII |
60HQU68H8A
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
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299176-11-7
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SUB107720
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9889104
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admin on Sat Dec 17 12:57:34 UTC 2022 , Edited by admin on Sat Dec 17 12:57:34 UTC 2022
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60HQU68H8A
Created by
admin on Sat Dec 17 12:57:34 UTC 2022 , Edited by admin on Sat Dec 17 12:57:34 UTC 2022
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| Related Record | Type | Details | ||
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PARENT -> SALT/SOLVATE |
