Design and synthesis of phosphoryl-substituted diphenylpyrimidines (Pho-DPPYs) as potent Bruton’s tyrosine kinase (BTK) inhibitors: Targeted treatment of B lymphoblastic leukemia cell lines-Reference-Cited by-同舟云学术

Design and synthesis of phosphoryl-substituted diphenylpyrimidines (Pho-DPPYs) as potent Bruton’s tyrosine kinase (BTK) inhibitors: Targeted treatment of B lymphoblastic leukemia cell lines

Published:2017-01 Issue:2 Volume:25 Page:765-772
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Ge Yang,Yang Haijun,Wang Changyuan,Meng Qiang,Li Lei,Sun Huijun,Zhen Yuhong,Liu Kexin,Li Yanxia,Ma Xiaodong

Funder

National Natural Science Foundation of China

Natural Science Foundation of Liaoning Province

Cultivation Project of Youth Techstars

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference35 articles.

1. Signaling the end of chronic lymphocytic leukemia: new frontline treatment strategies

2. Prognostic factors in chronic lymphocytic leukemia—what do we need to know?

3. The Role of Tec Family Kinases in Myeloid Cells

4. TEC FAMILY KINASES IN T LYMPHOCYTE DEVELOPMENT AND FUNCTION

5. Structural Bioinformatics-Based Design of Selective, Irreversible Kinase Inhibitors

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