H-Ala-Obzl.HCl
H-Ala-Obzl.HCl structure
|
Common Name | H-Ala-Obzl.HCl | ||
|---|---|---|---|---|
| CAS Number | 5557-83-5 | Molecular Weight | 215.677 | |
| Density | 1.1g/cm3 | Boiling Point | 293ºC at 760 mmHg | |
| Molecular Formula | C10H14ClNO2 | Melting Point | 135 to 145ºC | |
| MSDS | Chinese USA | Flash Point | 131ºC | |
|
The Benzyl Ester Group of Amino Acid Monomers Enhances Substrate Affinity and Broadens the Substrate Specificity of the Enzyme Catalyst in Chemoenzymatic Copolymerization.
Biomacromolecules 17 , 314-23, (2016) The chemoenzymatic polymerization of amino acid monomers by proteases involves a two-step reaction: the formation of a covalent acyl-intermediate complex between the protease and the carboxyl ester group of the monomer and the subsequent deacylation of the co... |
|
|
Positively charged microemulsions for topical application.
Int. J. Pharm. 346 , 119-123, (2008) The study reports pig-skin permeation and skin accumulation of miconazole nitrate (MCZ) from positively charged microemulsions containing water, 1-decanol/1-dodecanol (2:1, w/w), lecithin and/or decyl polyglucoside at different weight ratios, propylene glycol... |
|
|
Synthesis, QSAR and anti-HIV activity of new 5-benzylthio-1,3,4-oxadiazoles derived from α-amino acids.
J. Enzyme Inhib. Med. Chem. 26 , 668-680, (2011) 2-(1-[(4-Chloro/methylphenylsulfonylamino)alkyl]-5-thioxo-4,5-dihydro-1,3,4-oxadiazoles (4a-e) were synthesized, in four steps, via the sulfonyl derivatives of l-amino acids (l-alanine, l-methionine and l-phenylalanine) 1a-e, the esters 2a-e, the hydrazides 3... |
|
|
Novel lipidic enaminones from a C18 keto-allenic ester.
Lipids 35 , 1135-1145, (2000) Primary amines (ammonia, methyl, propyl, octyl, octadecyl, phenyl, benzyl, phenethyl) including methyl esters of amino acids (glycine, DL-alanine, L-valine, L-leucine, L-tyrosine, and L-methionine), and secondary amines (dimethyl, diethyl, dipropyl, diisoprop... |