由于三唑并喹唑啉与某些具有抗炎活性的5元环中离子杂环之间的结构相似,我们制备了一些新的1,2,4-三唑并[4,3- c ]喹唑啉环系统用于他们的治疗潜力。这些化合物可以通过用光气环合适当取代的4-肼基喹唑啉来制备。当中离子产物在5位(即喹唑啉2位)未被取代时,只能以其盐酸盐形式分离,而不能以其不稳定的游离碱形式分离。没有任何一种中离子产物在溶液中足够稳定,无法评估其抗炎活性。
由于三唑并喹唑啉与某些具有抗炎活性的5元环中离子杂环之间的结构相似,我们制备了一些新的1,2,4-三唑并[4,3- c ]喹唑啉环系统用于他们的治疗潜力。这些化合物可以通过用光气环合适当取代的4-肼基喹唑啉来制备。当中离子产物在5位(即喹唑啉2位)未被取代时,只能以其盐酸盐形式分离,而不能以其不稳定的游离碱形式分离。没有任何一种中离子产物在溶液中足够稳定,无法评估其抗炎活性。
Disclosed are 4-arylamino-quinazolines and analogs thereof effective as activators of caspases and inducers of apoptosis. The compounds of this invention are useful in the treatment of a variety of clinical conditions in which uncontrolled growth and spread of abnormal cells occurs.
Disclosed are 4-arylamino-quinazolines and analogs thereof that are effective as activators of caspases and inducers of apoptosis. The compounds of this invention are useful in the treatment of a variety of clinical conditions in which uncontrolled growth and spread of abnormal cells occurs.