Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Chai Ping Lee"'
Autor:
Chang Kai Soh, Kay Lin Goh, Meredith Williams, Kantharaj Ethirajulu, Haishan Wang, Zahid Bonday, Jeanette Marjorie Wood, Miah Kiat Goh, Kee Chuan Goh, Brian Dymock, Anders Poulsen, Stéphanie Blanchard, Mohammed Khalid Pasha, Chai Ping Lee
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 22:2880-2884
A series of 2-anilino substituted 4-aryl-8H-purines were prepared as potent inhibitors of PDK1, a serine-threonine kinase thought to play a role in the PI3K/Akt signaling pathway, a key mediator of cancer cell growth, survival and tumorigenesis. The
Autor:
Ramesh Jayaraman, Anders Poulsen, Angeline C.-H. Lee, Jeanette Marjorie Wood, Haishan Wang, Kantharaj Ethirajulu, Stefan Hart, Babita Madan, Evelyn Tan, Chai Ping Lee, Eric T. Sun, Anthony D. William, Dizhong Chen, Harish Kumar Mysore Nagaraj, Mohammad Khalid Pasha, Brian Dymock, Kee Chuan Goh
Publikováno v:
Journal of Medicinal Chemistry. 55:2623-2640
Herein, we describe the synthesis and SAR of a series of small molecule macrocycles that selectively inhibit JAK2 kinase within the JAK family and FLT3 kinase. Following a multiparameter optimization of a key aryl ring of the previously described SB1
Autor:
Stéphanie Blanchard, Mohammed Khalid Pasha, Harish Kumar Mysore Nagaraj, Eric T. Sun, Changyong Hu, Anthony D. William, Chai Ping Lee, Anders Poulsen, Ramesh Jayaraman, Meredith Williams, Jeanette Marjorie Wood, Kee Chuan Goh, Kantharaj Ethirajulu, Angeline C.-H. Lee, Haishan Wang, Ee Ling Teo, Brian Dymock
Publikováno v:
Journal of Medicinal Chemistry. 55:169-196
Herein, we describe the design, synthesis, and SAR of a series of unique small molecule macrocycles that show spectrum selective kinase inhibition of CDKs, JAK2, and FLT3. The most promising leads were assessed in vitro for their inhibition of cancer
Autor:
Anthony D, William, Angeline C-H, Lee, Anders, Poulsen, Kee Chuan, Goh, Babita, Madan, Stefan, Hart, Evelyn, Tan, Haishan, Wang, Harish, Nagaraj, Dizhong, Chen, Chai Ping, Lee, Eric T, Sun, Ramesh, Jayaraman, Mohammad Khalid, Pasha, Kantharaj, Ethirajulu, Jeanette M, Wood, Brian W, Dymock
Publikováno v:
Journal of medicinal chemistry. 55(6)
Herein, we describe the synthesis and SAR of a series of small molecule macrocycles that selectively inhibit JAK2 kinase within the JAK family and FLT3 kinase. Following a multiparameter optimization of a key aryl ring of the previously described SB1