DESIGN OF ALKYLATING AGENTS FOR SELECTIVITY OF ACTION
- 1 April 1958
- journal article
- Published by Wiley in Annals of the New York Academy of Sciences
- Vol. 68 (3) , 1238-1245
- https://doi.org/10.1111/j.1749-6632.1958.tb42686.x
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- 151. Synthesis of new sugar derivatives of potential antitumour activity. Part I. Ethyleneimino- and 2-chloroethylamino-derivativesJournal of the Chemical Society, 1957
- 341. Cyto-active amino-acids and peptides. Part III. Synthesis of para-substituted phenyl and alkoxymethyl ethers of tyrosineJournal of the Chemical Society, 1957
- Tumour Growth-inhibitory Alkyl SulphonatesNature, 1956
- 276. Aryl-2-halogenoalkylamines. Part XVI. The preparation of derivatives of 4-[di-(2-chloroalkyl)amino]azobenzenesJournal of the Chemical Society, 1956
- Aryl-2-halogenoalkylamines. Part XV. Some cationic and basically substituted aryl compoundsJournal of the Chemical Society, 1955
- Aryl-2-halogenoalkylamines. Part XIV. Some compounds possessing latent cytotoxic activityJournal of the Chemical Society, 1955
- Preparation of N-Phosphorylated Derivatives of Bis-β-chloroethylamine1aJournal of the American Chemical Society, 1954
- The Effect of 1:3‐Bis (Ethyleneimino Sulphonyl) Propane in Animal Tumours and Human LeukæmiaPublished by Wiley ,1954
- Chemical constitution and pharmacological actionTransactions of the Faraday Society, 1943
- V.—On the Connection between Chemical Constitution and Physiological Action. Part. I.—On the Physiological Action of the Salts of the Ammonium Bases, derived from Strychnia, Brucia, Thebaia, Codeia, Morphia, and NicotiaTransactions of the Royal Society of Edinburgh, 1868