Pujala Brahmam, Agarwal Anil K, Middya Sandip, Banerjee Monali, Surya Arjun, Nayak Anjan K, Gupta Ashu, Khare Sweta, Guguloth Rambabu, Randive Nitin A, Shinde Bharat U, Thakur Anamika, Patel Dhananjay I, Raja Mohd, Green Michael J, Alfaro Jennifer, Avila Patricio, Pérez de Arce Felipe, Almirez Ramona G, Kanno Stacy, Bernales Sebastián, Hung David T, Chakravarty Sarvajit, McCullagh Emma, Quinn Kevin P, Rai Roopa, Pham Son M
Integral BioSciences, Pvt. Ltd. , C-64, Hosiery Complex Phase II Extension, Noida, Uttar Pradesh 201306, India.
Curadev, Pvt. Ltd. , B-87, Sector 83, Noida, Uttar Pradesh 201305, India.
ACS Med Chem Lett. 2016 Oct 28;7(12):1161-1166. doi: 10.1021/acsmedchemlett.6b00356. eCollection 2016 Dec 8.
The aberrant activation of B-cells has been implicated in several types of cancers and hematological disorders. BTK and PI3Kδ are kinases responsible for B-cell signal transduction, and inhibitors of these enzymes have demonstrated clinical benefit in certain types of lymphoma. Simultaneous inhibition of these pathways could result in more robust responses or overcome resistance as observed in single agent use. We report a series of novel compounds that have low nanomolar potency against both BTK and PI3Kδ as well as acceptable PK properties that could be useful in the development of treatments against B-cell related diseases.
B细胞的异常激活与多种类型的癌症和血液系统疾病有关。BTK和PI3Kδ是负责B细胞信号转导的激酶,这些酶的抑制剂已在某些类型的淋巴瘤中显示出临床疗效。同时抑制这些信号通路可能会产生更强的反应或克服单药使用时出现的耐药性。我们报道了一系列新型化合物,它们对BTK和PI3Kδ均具有低纳摩尔效力,并且具有可接受的药代动力学特性,这可能有助于开发针对B细胞相关疾病的治疗方法。