激酶
计算生物学
医学
药理学
计算机科学
化学
生物
生物化学
作者
Anushka Sharma,Rahul Dubey,Shankar Gupta,Vivek Asati,Vipul Kumar,Dileep Kumar,Debarshi Kar Mahapatra,Meenakshi Jaiswal,Sanmati Kumar Jain,Sanjay Kumar Bharti
标识
DOI:10.1080/13543776.2024.2365411
摘要
Recently, PIM kinases viz. PIM-1, PIM-2, and PIM-3 (members of the serine/threonine protein kinase family) as therapeutic targets have attracted considerable interest in oncology especially in hematological malignancies. The patented PIM kinase inhibitors comprised of heterocyclic (fused)ring structure(s) like indole, pyridine, pyrazine, pyrazole, pyridazine, piperazine, thiazole, oxadiazole, quinoline, triazolo-pyridine, pyrazolo-pyridine, imidazo-pyridazine, oxadiazole-thione, pyrazolo-pyrimidine, triazolo-pyridazine, imidazo-pyridazine, pyrazolo-quinazoline and pyrazolo-pyridine etc. showed promising results in cancer chemotherapy.
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