70318-85-3

Upstream product

• 98-10-2 benzenesulfonamide 
• 1424-53-9 benzenesulfonyl isothiocyanate 
• 90-04-0 2-methoxy-phenylamine 

Downstream Products

• 98-10-2 benzenesulfonamide 
• 86379-76-2 N-[3-(2-Methoxy-phenyl)-4-(4-nitro-phenyl)-3H-thiazol-(2E)-ylidene]-benzenesulfonamide 
• 86379-74-0 N-[3-(2-Methoxy-phenyl)-4-phenyl-3H-thiazol-(2E)-ylidene]-benzenesulfonamide 
• 79752-34-4 C₁₅H₁₆N₂O₃S₂ 
• 247031-61-4 N-[4-hydroxy-3-(2-methoxyphenyl)-2-thiazolidinylidene]phenylsulfonamide 
• 247031-63-6 N-[2,3-dihydro-3-(2-methoxyphenyl)-2-thiazolylidene]phenylsulfonamide 
• 247031-75-0 N-[2,3-dihydro-3-(2-hydroxyphenyl)-2-thiazolylidene]phenylsulfonamide 
• 247031-76-1 2-[2,3-dihydro-2-[(phenylsulfonyl)imino]thiazol-3-yl]phenoxyacetic acid ethyl ester 

Relevant academic research and scientific papers

Synthesis, structural characterization and thromboxane A2 receptor antagonistic activity of 3-substituted 2-[(arylsulfonyl)imino]-2,3- dihydrothiazolyl derivatives

A series of new 2-[(arylsulfonyl)imino]-2,3-dihydrothiazolyl derivatives substituted on the heterocyclic N by a phenoxyacetic moiety was prepared according to a Hantzsch's synthesis between N, N'-disubstituted thioureas and chloroacetaldehyde. The regiochemistry of the cyclocondensation reaction was established by high resolution NMR methods. Potential thromboxane A2/prostaglandin H2 (TxA2/PGH2) receptor antagonism was evaluated using human platelet aggregation assays and radioligand binding studies. The results showed that the affinity for the TxA2/PGH2 receptor was strongly dependent on the position of the oxyacetic acid side chain. On the basis of the X-ray crystal analysis of compound 9f, a molecular modelling was undertaken on compounds 3d, 3e, and 3f. Comparison with the 3D structure of sulotroban was discussed.