66117-23-5

Upstream product

• 854006-82-9 5-(5-methyl-4-nitro-2-thienyl)-1,3,4-oxathiazol-2-one 
• 64-17-5 ethanol 
• 1918-79-2 2-methylthiophene-5-carboxylic acid 
• 36050-35-8 5-methyl-4-nitro-thiophene-2-carboxylic acid 
• 98-03-3 thiophene-2-carbaldehyde 
• 554-14-3 2-Methylthiophene 

Relevant academic research and scientific papers

THIENOPYRROLE COMPOUNDS AS S-NITROSOGLUTATHIONE REDUCTASE INHIBITORS

The present disclosure is directed to compounds of formula (Ib) and pharmaceutically acceptable salts thereof, wherein A, Q, R1, R3, R5 and m are as defined herein, which are active as inhibitors of S-Nitrosoglutathione re

Synthesis and biological evaluation of thiophene [3,2-b] pyrrole derivatives as potential anti-inflammatory agents

A series of thiophene [3,2-b] pyrrole derivatives were synthesized and evaluated their abilities to inhibit anti-inflammatory activity. In this series, substituent effects at the N-1, 2 and 5 positions of thiophene [3,2-b] pyrrole were examined. The results obtained are compared to those previously reported anti-inflammatory drugs like Tenidap sodium, Diclofenac sodium and Piroxicam. The results indicated the critical role of the group linked in the N-1 position and 2, 5 positions of thiophene [3,2-b] pyrrole with different functional groups.