2-(Aminoalkyl)-5-nitropyrazolo[3,4,5-kl]acridines, a new class of anticancer agents
摘要:
2-(Aminoalkyl)-5-nitropyrazolo[3,4,5-kl]acridines were prepared from substituted anilines via the 1-chloro-4-nitroacridones followed by condensation with [(alkylamino)alkyl]hydrazines. Impressive activity was demonstrated for the 9-hydroxy, 9-alkoxy, and 9-acyloxy analogs in vitro on a L1210 leukemia line and in vivo against the P388 leukemia. Advanced studies led to the selection of 3bbb for clinical trial.
Pyrazolo[3,4,5-kl]acridine compositions and methods for their production
申请人:Warner-Lambert Company
公开号:US04555572A1
公开(公告)日:1985-11-26
Pyrazolo[3,4,5-kl]acridines are described as antibacterial agents and antitumor agents as well as pharmaceutical compositions and methods for their preparation.
吡唑并[3,4,5-kl]蒽啉被描述为抗菌剂和抗肿瘤剂,以及它们的制备方法和药物组合物。
1,8-NAPHTHALIMIDE IMIDAZO{4,5,1-DE}ACRIDONES WITH ANTI-TUMOR ACTIVITY
申请人:——
公开号:US20030203916A1
公开(公告)日:2003-10-30
The invention provides imidazoacridone compounds of general formula (1) which have cytotoxic and anti-tumor activity. The invention also provides methods of preparing the compounds, and methods of using the compounds for the treatment of cancer or other mammalian diseases characterized by undesirably high levels of cell proliferation. The compounds of the invention are also expected to have utility as research tools.
1
Pyrazolo[3,4,5-k1]acridine compositions and methods for their use as
申请人:Warner-Lambert Company
公开号:US04588730A1
公开(公告)日:1986-05-13
Pyrazolo[3,4,5-k1]acridines are described as antibacterial agents and antitumor agents as well as pharmaceutical compositions and methods for their preparation.
Method of treating leukemia with pyrazolo[3,4,5-kl]acridines
申请人:Warner-Lambert Company
公开号:US04621086A1
公开(公告)日:1986-11-04
Pyrazolo[3,4,5-kl]acridines are described as antibacterial agents and antitumor agents as well as pharmaceutical compositions and methods for their preparation.
Imidazoacridine Compounds for Treating FLT3-Mediated Disorders
申请人:Ajami Alfred M.
公开号:US20100016300A1
公开(公告)日:2010-01-21
A method of treating a FLT3-mediated condition in a patient in need thereof, comprising administering to the patient a therapeutically effective amount of a compound of formula (I) or a pharmaceutically acceptable salt thereof: (I), The conditions that can be treated by the compounds of the present invention and the definitions for the variables in formula (I) are provided herein.