492464-47-8

Upstream product

• 91425-31-9 2-(triphenylmethylthio)ethanoic acid-N-hydroxysuccinimido ester 
• 76-83-5 trityl chloride 
• 34914-36-8 2-(triphenylmethylthio)ethanoic acid 
• 492464-46-7 N-[[(triphenylmethyl)thio]acetyl]-L-valine 
• 6066-82-6 1-hydroxy-pyrrolidine-2,5-dione 

Downstream Products

• 886439-43-6 N-[[(triphenylmethyl)thio]acetyl]-L-valylglycyl-L-glutamine 
• 586351-17-9 N-[(cyclohexylcarbamoylmethyl-carbamoyl)-methyl]-3-methyl-2-(2-tritylsulfanyl-acetylamino)-butyramide 
• 586351-16-8 N-[(butylcarbamoylmethyl-carbamoyl)-methyl]-3-methyl-2-(2-tritylsulfanyl-acetylamino)-butyramide 
• 492464-48-9 N-(2-dimethylamino-ethyl)-3-methyl-2-(2-tritylsulfanyl-acetylamino)-butyramide 
• 548485-18-3 {2-[(S)-3-Methyl-2-(2-tritylsulfanyl-acetylamino)-butyrylamino]-acetylamino}-acetic acid 

Relevant academic research and scientific papers

Synthesis, biodistribution and qsar studies of five Tc-99M labeled novel N3S pseudo-peptide complexes

Five novel N3S pseudo-peptide chelators derived from mercaptoacetic acid have been synthesized and characterized based on the spectroscopic data. All the chelators were labeled with Technicium-99m to evaluate their biological activities. Invest

Synthesis and characterization of novel N3S chelators and biodistribution of their 99Tcm labeled complexes as potential kidney imaging agents

Two new target chelators were synthesized through five steps with mercaptoacetic acid as the primary material, and identified by spectroscopy data including IR, 1HNMR, 13CNMR, Ms as new kidney imaging agents. The chelators were label

Synthesis of novel N3S pseudo-peptide and biodistribution of 99Tcm-pseudo-peptide complexes in mice

An excellent reaction condition of active ester with amine acid was developed, and a series of novel N3S pseudo-peptide chelators starting from mercaptoacetic acid were synthesized and characterized based on the spectroscopic data, such as IR,