Non-classical antimetabolites. IX. The bridge principle of specificity with exo-alkylating irreversible inhibitors. III. Detection of differences in specificity of enzymic nucleophilic sites by the carbophenoxy group
- 30 September 1962
- journal article
- research article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 9 (3) , 199-203
- https://doi.org/10.1016/0006-291x(62)90057-8
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Modification of a Methionine Residue Near the Active Site of ChymotrypsinJournal of the American Chemical Society, 1962
- Non-classical Antimetabolites. VII.1,2 The Bridge Principle of Specificity with Exo-alkylating Irreversible InhibitorsJournal of Medicinal Chemistry, 1962
- POTENTIAL ANTICANCER AGENTS.1 LXVI. NON-CLASSICAL ANTIMETABOLITES. III.2 4-(IODOACETAMIDO)-SALICYLIC ACID, AN EXO-ALKYLATING IRREVERSIBLE INHIBITOR OF GLUTAMIC DEHYDROGENASEJournal of the American Chemical Society, 1961
- Potential Anticancer Agents --L. Non-Classical Antimetabolites--II. Some Factors in the Design of Exo-Alkylating Enzyme Inhibitors, partcularly of Lactic DehydrogenaseJournal of Medicinal Chemistry, 1960
- N‐Trifluoracetyl‐aminosäuren, XIV. N‐Trifluoracetylierungen von Aminosäuren und Peptiden mit Trifluoressigsäure‐phenylesterEuropean Journal of Inorganic Chemistry, 1959