54648-92-9

Usage

Molecular structure

Consists of an indole ring, a methyl group, and a hydrazinecarbothioamide moiety.

Chemical classification

Hydrazinecarbothioamide derivative.

Potential pharmaceutical applications

Has shown promising anti-cancer and anti-inflammatory properties in preclinical studies.

Potential as a drug candidate

Due to its unique structure and biological activities.

Interesting molecule to study

For its potential therapeutic applications.

Upstream product

• 59-88-1 phenylhydrazine hydrochloride 
• 123-76-2 levulinic acid 
• 21909-49-9 ethyl (2-methylindol-3-yl)acetate 
• 78564-10-0 2-methylindole-3-acetic acid methyl ester 
• 1912-43-2 2-methyl-3-indoleacetic acid 
• 21909-51-3 2-(2-methyl-1H-indol-3-yl)acetohydrazide 
• 622-59-3 1-isothiocyanato-4-methylbenzene 

Downstream Products

• 110109-49-4 5-<3-(2-methylindolyl)methyl>-4-p-tolyl-1,2,4-triazol-3-ylthioglycolic acid 
• 54649-00-2 3-mercapto-4-p-tolyl-5-<3-(2-methylindoly)methyl>-1,2,4-triazole 

Relevant academic research and scientific papers

Synthesis, lipophilicity and biological evaluation of indole-containing derivatives of 1,3,4-thiadiazole and 1,2,4-triazole

3-[(2-Methyl-1H-3-indolyl)methyl]-4-aryl-4,5-dihydro-1H-1,2,4-triazole- 5-thiones 6a-c and their respective N-{5-[(2-methyl-1H-3-indolyl) methyl] - 1,3,4-thiadiazol-2-yl }-N-arylamines 7a,b have been prepared. The antidepressant profile of 6a,c and 7a was

Synthesis of Some Indole Derivatives as Potential Antibacterial Agents

Thiosemicarbazides (III), ureas (V), triazoles (VI) and organotin compounds (VII) having 2-alkylindole as a common structural feature have been synthesized and their antibacterial activity has been evaluated against Bacillus subtilis, Bacillus pumilus, St