Cotargeting of Bcl-2 and Mcl-1 Shows Promising Antileukemic Activity against AML Cells Including those with Acquired Cytarabine Resistance

Author(s):  
Fangbing Liu ◽  
Qiushi Zhao ◽  
Yongwei Su ◽  
Jing Lv ◽  
Yuqing Gai ◽  
...  
2004 ◽  
Vol 38 (3) ◽  
pp. 120-122
Author(s):  
A. V. Osintsev ◽  
G. L. Levit ◽  
V. P. Krasnov ◽  
G. D. Miles ◽  
S. Yu. Solodnikov ◽  
...  

Synthesis ◽  
2021 ◽  
Author(s):  
Muhammad Syafiq Bin Shahari ◽  
Ahmad Junaid ◽  
Edward R. T. Tiekink ◽  
Anton V. Dolzhenko

A new method for the fast synthesis of diverse 4-aryl-6-cycloamino-1,3,5-triazin-2-amines was developed. The synthesis is performed under microwave irradiation in a one-pot manner from cyanoguanidine, aromatic aldehydes, and cyclic amines. Their three-component reaction in the presence of hydrochloric acid produced dihydrotriazines, which were then converted (without isolation) to the targeted compounds via aromatic dehydrogenation in the presence of alkali. The reaction tolerated various aromatic aldehydes (including heterocyclic) and cyclic amines. Crystal structures of two representative 4-aryl-6-morpholino-1,3,5-triazin-2-amines were established by X-ray crystallography. The results of preliminary biological screening identified potent antileukemic activity for 6-(3,4-dihydroisoquinolin-2(1<i>H</i>)-yl)-4-phenyl-1,3,5-triazin-2-amine.


ChemInform ◽  
2010 ◽  
Vol 31 (28) ◽  
pp. no-no
Author(s):  
David A. Perrey ◽  
Rama Krishna Narla ◽  
Fatih M. Uckun

2018 ◽  
Vol 148 ◽  
pp. 13-26 ◽  
Author(s):  
Yongwei Su ◽  
Xinyu Li ◽  
Jun Ma ◽  
Jianyun Zhao ◽  
Shuang Liu ◽  
...  

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