690959-20-7

Upstream product

• 690959-19-4 (2-methylsulfanyl-thiazolo[5,4-b]quinolin-9-yl)-phenyl-amine 
• 120933-01-9 4-(ethoxycarbonyl)-2-(methylthio)-5-(phenylamino)thiazole 
• 690959-18-3 4-(phenylcarbamoyl)-2-(methylthio)-5-(phenylamino)thiazole 
• 1027549-72-9 2-Methylsulfanyl-5-phenylamino-thiazole-4-carbonyl chloride 
• 186545-61-9 4-carboxy-2-(methylthio)-5-(phenylamino)thiazole 

Downstream Products

• 1160636-54-3 9-phenylamino-2-(1-piperidinyl)thiazolo[5,4-b]quinoline 
• 1160636-56-5 9-phenylamino-2-(morpholin-4-yl)thiazolo[5,4-b]quinoline 
• 1160636-55-4 9-phenylamino-2-(4-methylpiperazin-1-yl)thiazolo[5,4-b]quinoline 
• 1160636-63-4 9-(phenylamino)-2-[3-(N,N-diethylamino)]propylaminothiazolo[5,4-b]quinoline 

Relevant academic research and scientific papers

Synthesis, cytotoxic activity, DNA binding and molecular docking studies of novel 9-anilinothiazolo[5,4-b]quinoline derivatives

Novel thiazolo[5,4-b]quinoline derivatives were prepared with or without a (2-(azacycloalkyl)ethyl)amino substituent at the 2-position. The effect of the substituent at 2-position on cytotoxic activity, DNA-intercalation and cytotoxic properties were evaluated. Substituents at 2-position bearing an aliphatic amine favored cytotoxicity, while removal of these substituents resulted in low or negligible cytotoxic properties. Additionally, the in silico predicted binding mode of the novel compounds into DNA correlated with the experimental intercalation data. These results suggest a strong influence of the substituent at 2-position on the DNA intercalation properties.

Synthesis and evaluation of 9-anilinothiazolo[5,4-b]quinoline derivatives as potential antitumorals

Five new 9-anilinothiazolo[5,4-b]quinoline derivatives (compounds 5, 7, 9, 10, 11) have been prepared. Some of the compounds were prepared by coupling properly substituted anilines to the novel compound 9-chloro-2-(methylthio) thiazolo[5,4-b]quinoline. Of