Anticancer anilinoacridines. A process synthesis of the disubstituted amsacrine analog CI??921
ST Brennan, NL Colbry, RL Leeds…
Index: Journal of Heterocyclic Chemistry, , vol. 26, # 5 p. 1469 - 1476
Full Text: HTML
Citation Number: 13
Abstract
... 1469 /. Heterocyclic Chem., 26, 1469 (1989). ... Solutions of the isethionic acid salt were found to be stable in sterile water and 5% dextrose over a one day period. The overall yield of CI-921 isethionate utilizing the chemistry shown in Scheme 1 was 62%. ... С Baguley, J. Med. ...
Related Articles:
[Journal of Medicinal Chemistry, , vol. 30, # 4 p. 652 - 658]
Anticancer anilinoacridines. A process synthesis of the disubstituted amsacrine analog CI??921
[Brennan; Colbry; Leeds; Leja; Priebe; Reily; Showalter; Uhlendorf; Atwell; Denny Journal of Heterocyclic Chemistry, 1989 , vol. 26, # 5 p. 1469 - 1476]
[Ferlin, Maria Grazia; Marzano, Cristina; Chiarelotto, Gianfranco; Baccichetti, Francarosa; Bordin, Franco European Journal of Medicinal Chemistry, 2000 , vol. 35, # 9 p. 827 - 837]
[European Journal of Medicinal Chemistry, , vol. 35, # 9 p. 827 - 837]
[Journal of Medicinal Chemistry, , vol. 30, # 4 p. 652 - 658]