Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Cbp p300"'
Autor:
Isaac W Vock, Allison J L Huldin, Matthew S. Beyersdorf, Anna K. Mapp, Stephen T. Joy, Matthew J. Henley, Samantha N. De Salle
Publikováno v:
Journal of the American Chemical Society. 143:15056-15062
The protein-protein interaction between the KIX motif of the transcriptional coactivator CBP/p300 and the transcriptional activator Myb is a high-value target due to its established role in certain acute myeloid leukemias (AML) and potential contribu
Autor:
Gagan Dhawan, Jon Erickson, Wei Zhang, Tingjian Wang, Zied Gaieb, Deyao Li, Jun Qi, Shuai Liu, Logan H. Sigua, Hailemichael O. Yosief, Ernst Schönbrunn, Virangika K. Wimalasena, Alex Muthengi, M.J. Bikowitz, Rommie E. Amaro
Publikováno v:
Journal of Medicinal Chemistry. 64:5787-5801
The use of epigenetic bromodomain inhibitors as anticancer therapeutics has transitioned from targeting bromodomain extraterminal domain (BET) proteins into targeting non-BET bromodomains. The two most relevant non-BET bromodomain oncology targets ar
Publikováno v:
Klinische Pädiatrie.
Publikováno v:
Frontiers in Biology. 13:168-179
CREB binding protein (CBP) and its close paralogue p300 are transcriptional coactivators with intrinsic acetyltransferase activity. Both CBP/p300 play critical roles in development and diseases. The enzymatic and biological functions of CBP/p300 are
Autor:
Yuwei Wang, Xiaojun Yao, Elaine Lai-Han Leung, Qianqian Wang, Liang Liu, Jiahui Xu, Xiaoli An
Publikováno v:
Organic & Biomolecular Chemistry. 16:6521-6530
The selective modulation of individual bromodomains (BDs) by small molecules represents an important strategy for the treatment of various cancers, considering that the BD-containing proteins share common BD structures and distinct pharmacological fu
Autor:
Maureen Beresini, Vickie Tsui, John S. Wai, F. Anthony Romero, Gladys de Leon Boenig, Patrick Cyr, Xiaoyu Zhu, Kevin X. Chen, Jiangpeng Liao, Edna F. Choo, Susan Kaufman, Fei Wang, Kwong Wah Lai, Caicai Zhu, Zhongguo Chen, Terry Crawford, Weichao Shen, Wenfeng Liu, Jeremy Murray, Yingjie Li, Sarah M. Bronner, Steven Magnuson, Justin Ly
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 28:15-23
A novel, potent, and orally bioavailable inhibitor of the bromodomain of CBP, compound 35 (GNE-207), has been identified through SAR investigations focused on optimizing al bicyclic heteroarene to replace the aniline present in the published GNE-272
Autor:
Alex Sedkov, Michael S. Gordon, Sylvie Guichard, Sonia Kumar, Melissa A. Reimers, Juliana Snavely-Merhaut, Kate Lipford, Neal D. Shore, Andrew J. Armstrong
Publikováno v:
Journal of Clinical Oncology. 39:TPS5085-TPS5085
TPS5085 Background: Prostate cancer is the second leading cause of cancer-related death among men in the U.S., largely due to metastatic disease that progresses despite hormonal therapy (tx). The role for androgen receptor (AR) signaling in prostate
Autor:
Andy Conery, Jann N. Sarkaria, Danielle M. Burgenske, Archana Bommi-Reddy, Jonathan E. Wilson, Katrina K. Bakken, Lihong He, Zeng Hu, Gaspar J. Kitange, Brett L. Carlson
Publikováno v:
Neuro Oncol
There is an unmet need to identify novel targets that can sensitize temozolomide (TMZ) or prevent resistance in GBM. We have demonstrated that retinoblastoma binding protein 4 (RBBP4) interacts with p300 to modulate expression of genes involved in ho