The synthesis of an α-azaornithine derivative and its reaction with trypsin
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
1. The reaction of an α-aza-amino acid derivative with chymotrypsin and its use as a ligand for covalent affinity purification
2. N- [2-Isopropyl-3-(L-aspartyl-L-arginyl)-carbazoyl]-L- tyrosyl-L-valyl-L-histidyl-L-prolyl-L-phenylalanine,1 an Isostere of Bovine Angiotensin II
3. Synthesis and Properties of Ethyl 1-Acetyl-2-benzyl Carbazate, an Analog of Acetyl-D- and L-Phenylalanine Ethyl Ester1
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1. Asymmetric Total Synthesis of Novel Pentacyclic Indole Alkaloid, Kopsiyunnanine E, Isolated from Kopsia arborea;Organic Letters;2014-09-24
2. Azaproline as a β-turn-inducer residue opposed to proline;The Journal of Peptide Research;2009-01-12
3. X-ray structures of aza-proline-containing peptides;The Journal of Peptide Research;2009-01-12
4. Incorporation of azaglutamine residues into peptides synthesised by the ultra-high load solid (gel)-phase technique;International Journal of Peptide and Protein Research;2009-01-12
5. Inhibition of trypsin by t-Butyloxycarbonyl-α-aza-(4-aminophenyl)alanine phenyl ester;Journal of Chemical Technology & Biotechnology;2007-04-24
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