168050-48-4

Basic information

• Product Name: 4-({(S)-1-[(S)-3-Benzyloxy-2-(naphthalene-2-sulfonylamino)-propionyl]-pyrrolidin-2-ylmethyl}-carbamoyl)-piperidine-1-carboxylic acid benzyl ester
• CAS NO: 168050-48-4
• Molecular Weight: 712.867
• Mol File: 168050-48-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-({(S)-1-[(S)-3-Benzyloxy-2-(naphthalene-2-sulfonylamino)-propionyl]-pyrrolidin-2-ylmethyl}-carbamoyl)-piperidine-1-carboxylic acid benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 4-({(S)-1-[(S)-3-Benzyloxy-2-(naphthalene-2-sulfonylamino)-propionyl]-pyrrolidin-2-ylmethyl}-carbamoyl)-piperidine-1-carboxylic acid benzyl ester(168050-48-4)
• EPA Substance Registry System: 4-({(S)-1-[(S)-3-Benzyloxy-2-(naphthalene-2-sulfonylamino)-propionyl]-pyrrolidin-2-ylmethyl}-carbamoyl)-piperidine-1-carboxylic acid benzyl ester(168050-48-4)

Safety Data

• Hazardous Substances Data: 168050-48-4(Hazardous Substances Data)

Upstream product

• 10314-98-4 1-benzyloxycarbonylpiperidine-4-carboxylic acid 
• 168050-46-2 Naphthalene-2-sulfonic acid [(S)-2-((S)-2-aminomethyl-pyrrolidin-1-yl)-1-benzyloxymethyl-2-oxo-ethyl]-amide 
• 23680-31-1 BOC-O-benzyl-L-serine 
• 86661-32-7 (S)-tert-butyl 2-((tosyloxy)methyl)pyrrolidine-1-carboxylate 
• 168049-26-1 tert-butyl (2S)-2-(azidomethyl)-1-pyrrolidinecarboxylate 
• 174698-95-4 (2S)-2-azidomethyl-pyrrolidine 
• 168050-40-6 (S)-2-Amino-1-((S)-2-azidomethyl-pyrrolidin-1-yl)-3-benzyloxy-propan-1-one 
• 168050-38-2 [(S)-2-((S)-2-Azidomethyl-pyrrolidin-1-yl)-1-benzyloxymethyl-2-oxo-ethyl]-carbamic acid tert-butyl ester 
• 168050-45-1 Naphthalene-2-sulfonic acid [(S)-2-((S)-2-azidomethyl-pyrrolidin-1-yl)-1-benzyloxymethyl-2-oxo-ethyl]-amide 

Relevant articles and documents

Thrombin active site inhibitors: Chemical synthesis, in vitro and in vivo pharmacological profile of a novel and selective agent BMS-189090 and analogues

A series of structurally novel small molecule inhibitors of human α-thrombin was prepared to elucidate their structure- activity relationships (SAR), selectivity and activity in vivo. BMS-189090 (5) is identified as a potent, selective, and reversible inh