July, 1964. ACRIDINE AXD QUINOLINE NITROGEN MUSTARDS. 48 1. 9. N. '9. N. ". ?y? N. N. 3. L? I. 0 n. 2. 0 m m b: 00. '9. 2. 'L u. L? E-. 9. El m. 09. 3...
molar and biological activities of the nitrogen mustard moiety. Although not strictly comparable in struc- ture, E-l was inactive. The quinazoline monofunc-.
Acridine and Quinoline Analogs of Nitrogen Mustard with Amide Side Chains1. Richard M. Peck, Evelyn R. Breuninger, Ann J. Miller, and Hugh J. Creech.
Acridine and Quinoline Analogs of Nitrogen Mustard with Amide Side Chains1. Richard M. Peck, Evelyn R. Breuninger, Ann J. Miller, Hugh J. Creech. J. Med.
\vas prepared hy dilut>ion of a mixture of 200 nil. of a 0.2J1 sodium carhnate solution and 800 ml. of :t 0.2.11 sodiuni bicarbonate soliition to 4 liters with water.
Mono- and Difunctional Analogs of Some Quinoline and Acridine Nitrogen Mustards1. RICHARD M. PECK, ROBERT K. PRESTON, and HUGH J. CREECH.
Mono- and Difunctional Analogs of Some Quinoline and Acridine Nitrogen Mustards1. RICHARD M. PECK, ROBERT K. PRESTON, HUGH J. CREECH.
reported 2-chloroethyl-S-sulfinylamine.2 It would be expected that the presence of a phenyl group on C-2, as in S',S '-bis(2-chlorophenethyl)-S-sulfinylhydrazine,.
Note: In lieu of an abstract, this is the article's first page. ... Fatima Marankan, Debbie C. Mulhearn, Linda Wanna, Andrew D. Mesecar, Bernard D. Santarsiero, ...
The salts of acridine, pyridine and quinoline are universally classified as ammonium salts, i. e., as salts in which the acid radical is held in the molecule by one of ...
Potent Antitumor 9-Anilinoacridines and Acridines Bearing an Alkylating N-Mustard Residue on the Acridine Chromophore: Synthesis and Biological Activity.
