1583283-24-2

Basic information

• Product Name: (S)-2-((N-(benzyloxycarbonyl)aminomethylphosphonyl)amino)-N-isopentyl-4-methylpentanamide lithium
• Synonyms: (S)-2-((N-(benzyloxycarbonyl)aminomethylphosphonyl)amino)-N-isopentyl-4-methylpentanamide lithium
• CAS NO: 1583283-24-2
• Molecular Weight: 433.414
• Mol File: 1583283-24-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (S)-2-((N-(benzyloxycarbonyl)aminomethylphosphonyl)amino)-N-isopentyl-4-methylpentanamide lithium(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-((N-(benzyloxycarbonyl)aminomethylphosphonyl)amino)-N-isopentyl-4-methylpentanamide lithium(1583283-24-2)
• EPA Substance Registry System: (S)-2-((N-(benzyloxycarbonyl)aminomethylphosphonyl)amino)-N-isopentyl-4-methylpentanamide lithium(1583283-24-2)

Safety Data

• Hazardous Substances Data: 1583283-24-2(Hazardous Substances Data)

Upstream product

• 76203-93-5 methyl <(N-carbobenzoxyamino)methyl>phosphonic acid 
• 84851-37-6 (S)-1-(isopentylamino)-2-amino-4-methyl-1-oxopentan hydrochloride 
• 84863-67-2 (S)-t-butyl 1-(isopentylamino)-4-methyl-1-oxopentan-2-ylcarbamate 
• 541-23-1 isoamylamine hydrochloride 
• 13139-15-6 N-tert-butoxycarbonyl-L-leucine 
• 1583283-69-5 C₂₁H₃₆N₃O₅P 
• 59191-35-4 dimethyl N-(benzyloxycarbonyl)aminomethylphosphonate 
• 67799-92-2 benzyloxycarbonylaminomethyl acetate 
• 31037-42-0 hydroxymethyl carbamic acid benzyl ester 
• 621-84-1 O-benzyl carbamate 

Relevant articles and documents

Additivity or cooperativity: Which model can predict the influence of simultaneous incorporation of two or more functionalities in a ligand molecule?

Predicting how binding affinity responds to ligand structural modifications in structure-activity relationship studies (SAR) is a major challenge in medicinal chemistry. This is particularly true when two or more of these modifications are carried out simultaneously. In this study, we present binding affinity data from several series of thermolysin inhibitors in which simultaneous structural modifications were investigated to determine whether they are cooperative or additive. Data revealed that, while additivity is at work in some cases, cooperativity is more commonly demonstrated. Cooperativity and additivity were then correlated with ligand descriptors, such as the spacing and the topological features of the modified groups, in a manner that may provide guidance as to when each model should be utilized. Cooperativity was particularly associated with contiguous groups and small unbranched hydrophobic side chain. Additivity, on the other hand, was associated with moderately distant hydrophobic group combinations and side chain branching. Such correlations can improve the predictability of SAR studies and can provide a starting point for additional investigations that may lead to further significant enhancements in the current scoring functions.