Journal of Medicinal Chemistry p. 1619 - 1625 (1983)
Update date:2022-08-03
Topics:
Denny
Atwell
Baguley
The synthesis and biological evaluation of a series of 3-substituted 5-carboxamido derivatives of amsacrine (m-AMSA) are described. This series was developed as the result of previous quantitative structure-activity relationship (QSAR) studies of the antitumor activity of 9-anilinoacridine derivatives. In agreement with these studies, this class of compounds, possessing a variety of small nonpolar groups at the 3-position, together with very hydrophilic carboxamido groups at the 5-position, have high in vivo activity against animal leukemia models.
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Doi:10.1021/jo00230a011
(1987)Doi:10.1021/acs.orglett.0c03108
(2020)Doi:10.1016/0223-5234(87)90060-2
(1987)Doi:10.1016/S0040-4039(00)85288-0
(1986)Doi:10.1016/0022-328X(86)80443-0
(1986)Doi:10.1016/0040-4020(58)88006-0
(1958)