84851-37-6

Basic information

• Product Name: N1-isoamylleucinamide
• Synonyms: (2S)-2-amino-4-methyl-N-(3-methylbutyl)pentanamide;S-2-Amino-4-methylpentanoic acid (3-methylbutyl)amide;(2S)-2-Amino-4-Methyl-N-(3-Methylbutyl)Pentanamide(WX665178)
• CAS NO: 84851-37-6
• Molecular Formula: C₁₁H₂₄N₂O
• Molecular Weight: 200.33
• Mol File: 84851-37-6.mol
• Article Data: 16

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N1-isoamylleucinamide(CAS DataBase Reference)
• NIST Chemistry Reference: N1-isoamylleucinamide(84851-37-6)
• EPA Substance Registry System: N1-isoamylleucinamide(84851-37-6)

Safety Data

• Hazardous Substances Data: 84851-37-6(Hazardous Substances Data)

Upstream product

• 107-85-7 1-amino-3-methylbutane 
• 13139-15-6 N-tert-butoxycarbonyl-L-leucine 
• 102123-80-8 C₁₉H₂₇NO₆ 
• 2018-66-8 Z-Leu-OH 
• 3392-09-4 Boc-Leu-ONSu 
• 76411-85-3 N-carbobenzyloxy-L-leucine isopentylamide 
• 84863-67-2 (S)-t-butyl 1-(isopentylamino)-4-methyl-1-oxopentan-2-ylcarbamate 
• 541-23-1 isoamylamine hydrochloride 
• 66866-44-2 Boc-Leu-O-COO-isoBu 

Downstream Products

• 76684-89-4 loxistatin acid 
• 179082-53-2 (2S,3S)-Oxirane-2,3-dicarboxylic acid 2-(benzyloxy-amide) 3-{[(S)-3-methyl-1-(3-methyl-butylcarbamoyl)-butyl]-amide} 
• 1583283-69-5 C₂₁H₃₆N₃O₅P 
• 88321-09-9 aloxistatin 
• 1583283-24-2 (S)-2-((N-(benzyloxycarbonyl)aminomethylphosphonyl)amino)-N-isopentyl-4-methylpentanamide lithium 
• 1000072-67-2 (2S)-4-methyl-N-(2-methylbutyl)-2-((3-phenylaziridin-2-yl)methylamino)pentanamide 

Relevant articles and documents

COMPOSITIONS AND METHODS FOR SYNTHESIZING (2S,3S)-TRANS-EPOXYSUCCINYL-L-LEUCYL-AMIDO-3-METHYLBUTANE ETHYL ESTER

In alternative embodiments the invention provides methods for synthesizing AB-007 (also called loxistatin, E64d, EST or ((2S,3S)-trans-epoxysuccinyl-L-leucyl-amido-3-methylbutane ethyl ester) and its acid form E64c (loxistatin acid), and various synthetic

Influence of neighboring groups on the thermodynamics of hydrophobic binding: An added complex facet to the hydrophobic effect

The thermodynamic consequences of systematic modifications in a ligand side chain that binds in a shallow hydrophobic pocket, in the presence and absence of a neighboring ligand carboxylate group, were evaluated using isothermal titration calorimetry (ITC

Design, synthesis and evaluation of 3-methylene-substituted indolinones as antimalarials

The design, synthesis and evaluation of 3-methylene-substituted indolinones as falcipain inhibitors and antiplasmodial agents are described. These compounds react readily with thiols via an addition-elimination mechanism, indicating their potential as cys