136343-83-4

Upstream product

• 6270-17-3 ethyl 3-benzoylpropanoate 
• 68-12-2 N,N-dimethyl-formamide 

Downstream Products

• 875271-86-6 (2-phenylthiophen-3-yl)acetic acid ethyl ester 
• 62404-09-5 2-Phenyl-3-thienylacetic acid 
• 1021171-88-9 (6-{2-phenyl-6-[5-phenyl-4-(trityloxycarbamoyl-methyl)-thiophene-2-carbonyl]-indol-1-yl}-hexyl)-carbamic acid tert-butyl ester 
• 875271-95-7 2-{5-[1-(5-N-Boc-aminopentyl)-2-phenyl-1H-indol-6-carbonyl]-2-phenylthiophen-3-yl}-O-tritylhydroxy-acetamide 
• 875272-00-7 (4-{2-phenyl-6-[5-phenyl-4-(trityloxycarbamoyl-methyl)-thiophene-2-carbonyl]-indol-1-yl}-butyl)-carbamic acid tert-butyl ester 
• 1021171-86-7 2-{5-[1-(5-N-Boc-aminopentyl)-2-phenyl-1H-indol-6-carbonyl]-2-phenylthiophen-3-yl}-N-hydroxyacetamide 
• 917079-03-9 {4-[6-(4-hydrazinocarbonylmethyl-5-phenyl-thiophene-2-carbonyl)-2-phenyl-indol-1-yl]-butyl}-carbamic acid tert-butyl ester 
• 875271-89-9 2-[2-phenyl-5-(2-phenyl-1H-indole-6-carbonyl)-thiophen-3-yl]-N-trityloxy-acetamide 
• 875271-92-4 2-{5-[1-(4-N-Boc-aminobutyl)-2-phenyl-1H-indol-6-carbonyl]-2-phenylthiophen-3-yl}-N-hydroxyacetamide 
• 875271-93-5 2-{5-[1-(5-N-Boc-aminopentyl)-2-phenyl-1H-indol-6-carbonyl]-2-phenylthiophen-3-yl}acetic acid methyl ester 
• 875271-94-6 2-{5-[1-(5-N-Boc-aminopentyl)-2-phenyl-1H-indol-6-carbonyl]-2-phenylthiophen-3-yl}acetic acid 
• 875271-91-3 [5-(1-{4-[(tert-butoxycarbonyl)amino]butyl}-2-phenyl-1H-indole-6-carbonyl)-2-phenylthiophene-3-yl]acetic acid 
• 875271-90-2 {5-[1-(4-N-boc-aminobutyl)-2-phenyl-1H-indol-6-carbonyl]-2-phenylthiophen-3-yl}acetic acid methyl ester 
• 875271-82-2 (5-{3-[(tert-butoxycarbonyl)amino]-4-iodobenzoyl}-2-phenylthiophene-3-yl)acetic acid 

Relevant academic research and scientific papers

SMALL-MOLECULE BOTULINUM TOXIN INHIBITORS

Small-molecule inhibitors of Botulinum toxin, including BoNTA, BoNTD and BoNTE are provided, as well as methods of using the inhibitors.

Serotype-selective, small-molecule inhibitors of the zinc endopeptidase of botulinum neurotoxin serotype A

Botulinum neurotoxin serotype A (BoNTA) is one of the most toxic substances known. Currently, there is no antidote to BoNTA. Small molecules identified from high-throughput screening reportedly inhibit the endopeptidase-the zinc-bound, catalytic domain of

The Vilsmeier Reaction In The Series Of Esters Of Alkyl, Aryl, And Heteryl Keto Acids

In the reaction of the esters of aliphatic, aromatic, and heterocyclic keto acids with the Vilsmeier reagent the alkoxycarbonyl group is not affected, while the ketone carbonyl is transformed with the formation of a chloroacrolein containing the alkanoic