99590-22-4

Upstream product

• 99590-19-9 ethyl 1-(4-nitrobenzyl)-1H-1,2,3-triazole-4-carboxylate 
• 99590-18-8 dimethyl 1-(4-nitrobenzyl)-1H-1,2,3-triazole-4,5-dicarboxylate 
• 17271-88-4 p-nitrobenzyl azide 
• 471-25-0 Propiolic acid 
• 99590-21-3 1-(p-nitrobenzyl)-1H-1,2,3-triazole-4,5-dicarboxylic acid, monopotassium salt 

Downstream Products

• 99590-25-7 1-(1,2,3-traizol-1-ylmethyl)-4-nitrobenzene 
• 99590-42-8 1--benzyl>-1H-1,2,3-triazole 
• 99590-41-7 1--1H-1,2,3-triazole 
• 99590-30-4 1--1H-1,2,3-triazole 
• 99590-40-6 1--benzyl>-1H-1,2,3-triazole 
• 99590-38-2 1-(p-N-benzoylaminobenzyl)-1H-1,2,3-triazole 
• 99590-39-3 1--1H-1,2,3-triazole 
• 99590-31-5 1--1H-1,2,3-triazole 
• 99590-36-0 1--1H-1,2,3-triazole 
• 99590-28-0 1-(p-acetyloxybenzyl)-1H-1,2,3-triazole 
• 99590-33-7 1--1H-1,2,3-triazole 
• 99590-34-8 1--1H-1,2,3-triazole 
• 99590-29-1 1-(p-benzoyloxybenzyl)-1H-1,2,3-triazole 
• 99590-37-1 1-(p-N,N-diacetylaminobenzyl)-1H-1,2,3-triazole 

Relevant academic research and scientific papers

TRIAZOLE MODIFIED COUMARIN AND BIPHENYL AMIDE-BASED HSP90 INHIBITORS

Provided herein are compounds of the formulas:. which are 90-kDa heat shock protein inhibitors. Pharmaceutical compositions of the compounds are also provided. In some aspects, these compounds may be used for the treatment of diseases, including cancer, e

Triazole containing novobiocin and biphenyl amides as Hsp90 C-terminal inhibitors

Hsp90 C-terminal inhibitors are advantageous for the development of new cancer chemotherapeutics due to their ability to segregate client protein degradation from induction of the prosurvival heat shock response, which is a major detriment associated with

1-(4-Substituted-benzyl)-1,2,3-triazoles, in vitro inhibitors of prostaglandin synthesis

This paper describes the preparation of some 1-(4-substituted-benzyl)-1,2,3-triazole derivatives from 4-nitrobenzyl azide by 1,3-dipolar cycloaddition, functional group conversion and nucleophilic substitution reactions. Evaluation of these compounds as i