Design and development of novel thiazole-sulfonamide derivatives as a protective agent against diabetic cataract in Wistar rats via inhibition of aldose reductase
In recent years, ALR2 (aldose reductase) inhibitors have attracted attention for their effective ability to reduce the progression of diabetes-associated cataracts. Therefore, in the present article, we intended to develop novel thiazole-sulfonamide hybrids as a potent inhibitor of ALR2. These molec...
Saved in:
Main Authors: | Yin Liang, Zhang Mingxue, He Tiangeng |
---|---|
Format: | article |
Language: | EN |
Published: |
De Gruyter
2021
|
Subjects: | |
Online Access: | https://doaj.org/article/fcbbfce5d0d446fd9f55f238464cbc99 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
AIM2-Like Receptors Positively and Negatively Regulate the Interferon Response Induced by Cytosolic DNA
by: Yuki Nakaya, et al.
Published: (2017) -
SYNTHESIS OF METALLIC AZODERIVATIVES OF 2-AMINO-5-MERCAPTO-1,3,4-THIADIAZOLE
by: ORTEGA-LUONI,PEDRO, et al.
Published: (2007) -
Carbonic Anhydrase Inhibition with Sulfonamides Incorporating Pyrazole- and Pyridazinecarboxamide Moieties Provides Examples of Isoform-Selective Inhibitors
by: Andrea Angeli, et al.
Published: (2021) -
Copolymer Coatings for DNA Biosensors: Effect of Charges and Immobilization Chemistries on Yield, Strength and Kinetics of Hybridization
by: Luka Vanjur, et al.
Published: (2021) -
The use of heterocyclic-based azo compounds bearing pyrrolidine, imidazole, triazole, and thiazole moieties for the treatment of neglected tropical disease caused by Schistosoma mansoni
by: Cauê Benito Scarim, et al.
Published: (2021)