Aziridine‐2‐carboxylic acid A reactive amino acid unit for a new class of cysteine proteinase inhibitors

[1]  T. Rao,et al.  Synthesis of a new class of Tc chelating agents: N2S2 monoaminemonoamide (mama) ligands , 1991 .

[2]  K. Nakajima,et al.  Chemistry of 2-Aziridinecarboxylic Acid , 1984 .

[3]  K. Nakajima,et al.  Studies on 2‐aziridinecarboxylic acid peptides: Their reaction and uses , 1981 .

[4]  K. Nakajima,et al.  Studies on Aziridine-2-carboxylic Acid. I. Synthesis of the Optically Active L-Aziridine-2-carboxylic Acid and Its Derivatives , 1978 .

[5]  W. Scouten,et al.  N-dansylaziridine: A new fluorescent modification for cysteine thiols , 1974 .

[6]  I. Chaiken,et al.  Reaction of chloroacetamide with the sulfhydryl group of papain. , 1969, The Journal of biological chemistry.

[7]  R. Kitz,et al.  Esters of methanesulfonic acid as irreversible inhibitors of acetylcholinesterase. , 1962, The Journal of biological chemistry.

[8]  R. Rosenthal,et al.  Use of γ-(4-Nitrobenzyl)pyridine as Analytical Reagent for Ethylenimines and Alkylating Agents , 1955 .

[9]  W N ALDRIDGE,et al.  Some properties of specific cholinesterase with particular reference to the mechanism of inhibition by diethyl p-nitrophenyl thiophosphate (E 605) and analogues. , 1950, The Biochemical journal.

[10]  Masamichi Watanabe,et al.  Reaction of aziridinecar☐ylic acids with thiols in aqueous solution. the formation of β-amino acid , 1987 .

[11]  A. Barrett,et al.  L-trans-Epoxysuccinyl-leucylamido(4-guanidino)butane (E-64) and its analogues as inhibitors of cysteine proteinases including cathepsins B, H and L. , 1982, The Biochemical journal.

[12]  B. Eisele,et al.  Stereospecific alkylation with asymmetric reagents. , 1968, European journal of biochemistry.