These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
180 related articles for article (PubMed ID: 28892380)
1. GNE-781, A Highly Advanced Potent and Selective Bromodomain Inhibitor of Cyclic Adenosine Monophosphate Response Element Binding Protein, Binding Protein (CBP). Romero FA; Murray J; Lai KW; Tsui V; Albrecht BK; An L; Beresini MH; de Leon Boenig G; Bronner SM; Chan EW; Chen KX; Chen Z; Choo EF; Clagg K; Clark K; Crawford TD; Cyr P; de Almeida Nagata D; Gascoigne KE; Grogan JL; Hatzivassiliou G; Huang W; Hunsaker TL; Kaufman S; Koenig SG; Li R; Li Y; Liang X; Liao J; Liu W; Ly J; Maher J; Masui C; Merchant M; Ran Y; Taylor AM; Wai J; Wang F; Wei X; Yu D; Zhu BY; Zhu X; Magnuson S J Med Chem; 2017 Nov; 60(22):9162-9183. PubMed ID: 28892380 [TBL] [Abstract][Full Text] [Related]
2. Discovery of a Potent and Selective in Vivo Probe (GNE-272) for the Bromodomains of CBP/EP300. Crawford TD; Romero FA; Lai KW; Tsui V; Taylor AM; de Leon Boenig G; Noland CL; Murray J; Ly J; Choo EF; Hunsaker TL; Chan EW; Merchant M; Kharbanda S; Gascoigne KE; Kaufman S; Beresini MH; Liao J; Liu W; Chen KX; Chen Z; Conery AR; Côté A; Jayaram H; Jiang Y; Kiefer JR; Kleinheinz T; Li Y; Maher J; Pardo E; Poy F; Spillane KL; Wang F; Wang J; Wei X; Xu Z; Xu Z; Yen I; Zawadzke L; Zhu X; Bellon S; Cummings R; Cochran AG; Albrecht BK; Magnuson S J Med Chem; 2016 Dec; 59(23):10549-10563. PubMed ID: 27682507 [TBL] [Abstract][Full Text] [Related]
3. A Unique Approach to Design Potent and Selective Cyclic Adenosine Monophosphate Response Element Binding Protein, Binding Protein (CBP) Inhibitors. Bronner SM; Murray J; Romero FA; Lai KW; Tsui V; Cyr P; Beresini MH; de Leon Boenig G; Chen Z; Choo EF; Clark KR; Crawford TD; Jayaram H; Kaufman S; Li R; Li Y; Liao J; Liang X; Liu W; Ly J; Maher J; Wai J; Wang F; Zheng A; Zhu X; Magnuson S J Med Chem; 2017 Dec; 60(24):10151-10171. PubMed ID: 29155580 [TBL] [Abstract][Full Text] [Related]
4. Structure-based drug optimization and biological evaluation of tetrahydroquinolin derivatives as selective and potent CBP bromodomain inhibitors. Bi X; Chen Y; Sun Z; Lu W; Xu P; Lu T; Ding H; Zhang N; Jiang H; Chen K; Zhou B; Luo C Bioorg Med Chem Lett; 2020 Nov; 30(22):127480. PubMed ID: 32882416 [TBL] [Abstract][Full Text] [Related]
5. Preclinical Safety Assessment of a Highly Selective and Potent Dual Small-Molecule Inhibitor of CBP/P300 in Rats and Dogs. Katavolos P; Cain G; Farman C; Romero FA; Magnuson S; Ly JQ; Choo EF; Katakam AK; Andaya R; Maher J Toxicol Pathol; 2020 Apr; 48(3):465-480. PubMed ID: 32124659 [TBL] [Abstract][Full Text] [Related]
6. Discovery of novel CBP bromodomain inhibitors through TR-FRET-based high-throughput screening. Zhang FC; Sun ZY; Liao LP; Zuo Y; Zhang D; Wang J; Chen YT; Xiao SH; Jiang H; Lu T; Xu P; Yue LY; Du DH; Zhang H; Liu CP; Luo C Acta Pharmacol Sin; 2020 Feb; 41(2):286-292. PubMed ID: 31253937 [TBL] [Abstract][Full Text] [Related]
7. Design, synthesis, and biological evaluation of tetrahydroquinolin derivatives as potent inhibitors of CBP bromodomain. Chen Y; Bi X; Zhang F; Sun Z; Xu P; Jiang H; Lu W; Lu T; Ding H; Zhang N; Jiang H; Chen K; Zhou B; Luo C Bioorg Chem; 2020 Aug; 101():103991. PubMed ID: 32559581 [TBL] [Abstract][Full Text] [Related]
8. Y08197 is a novel and selective CBP/EP300 bromodomain inhibitor for the treatment of prostate cancer. Zou LJ; Xiang QP; Xue XQ; Zhang C; Li CC; Wang C; Li Q; Wang R; Wu S; Zhou YL; Zhang Y; Xu Y Acta Pharmacol Sin; 2019 Nov; 40(11):1436-1447. PubMed ID: 31097763 [TBL] [Abstract][Full Text] [Related]
9. Discovery of Highly Potent and Efficient CBP/p300 Degraders with Strong Hu J; Xu H; Wu T; Zhang C; Shen H; Dong R; Hu Q; Xiang Q; Chai S; Luo G; Chen X; Huang Y; Zhao X; Peng C; Wu X; Lin B; Zhang Y; Xu Y J Med Chem; 2024 May; 67(9):6952-6986. PubMed ID: 38649304 [TBL] [Abstract][Full Text] [Related]
10. Discovery of a potent and selective CBP bromodomain inhibitor (Y08262) for treating acute myeloid leukemia. Xiang Q; Wu T; Zhang C; Wang C; Xu H; Hu Q; Hu J; Luo G; Zhuang X; Wu X; Zhang Y; Xu Y Bioorg Chem; 2024 Jan; 142():106950. PubMed ID: 37924753 [TBL] [Abstract][Full Text] [Related]
11. Discovery of a Promising CBP/p300 Degrader XYD129 for the Treatment of Acute Myeloid Leukemia. Wu T; Hu J; Zhao X; Zhang C; Dong R; Hu Q; Xu H; Shen H; Zhang X; Zhang Y; Lin B; Wu X; Xiang Q; Xu Y J Med Chem; 2024 Jun; 67(11):9194-9213. PubMed ID: 38829718 [TBL] [Abstract][Full Text] [Related]
12. Design, Synthesis, and Biological Evaluation of 1-(Indolizin-3-yl)ethan-1-ones as CBP Bromodomain Inhibitors for the Treatment of Prostate Cancer. Xiang Q; Wang C; Wu T; Zhang C; Hu Q; Luo G; Hu J; Zhuang X; Zou L; Shen H; Wu X; Zhang Y; Kong X; Liu J; Xu Y J Med Chem; 2022 Jan; 65(1):785-810. PubMed ID: 34962793 [TBL] [Abstract][Full Text] [Related]
13. Development of Dimethylisoxazole-Attached Imidazo[1,2- Muthengi A; Wimalasena VK; Yosief HO; Bikowitz MJ; Sigua LH; Wang T; Li D; Gaieb Z; Dhawan G; Liu S; Erickson J; Amaro RE; Schönbrunn E; Qi J; Zhang W J Med Chem; 2021 May; 64(9):5787-5801. PubMed ID: 33872011 [TBL] [Abstract][Full Text] [Related]
14. Discovery of Highly Potent, Selective, and Orally Efficacious p300/CBP Histone Acetyltransferases Inhibitors. Yang Y; Zhang R; Li Z; Mei L; Wan S; Ding H; Chen Z; Xing J; Feng H; Han J; Jiang H; Zheng M; Luo C; Zhou B J Med Chem; 2020 Feb; 63(3):1337-1360. PubMed ID: 31910017 [TBL] [Abstract][Full Text] [Related]
15. Discovery and optimization of 1-(1H-indol-1-yl)ethanone derivatives as CBP/EP300 bromodomain inhibitors for the treatment of castration-resistant prostate cancer. Xiang Q; Wang C; Zhang Y; Xue X; Song M; Zhang C; Li C; Wu C; Li K; Hui X; Zhou Y; Smaill JB; Patterson AV; Wu D; Ding K; Xu Y Eur J Med Chem; 2018 Mar; 147():238-252. PubMed ID: 29448139 [TBL] [Abstract][Full Text] [Related]
16. Discovery of a series of dihydroquinoxalin-2(1H)-ones as selective BET inhibitors from a dual PLK1-BRD4 inhibitor. Hu J; Wang Y; Li Y; Xu L; Cao D; Song S; Damaneh MS; Wang X; Meng T; Chen YL; Shen J; Miao Z; Xiong B Eur J Med Chem; 2017 Sep; 137():176-195. PubMed ID: 28586718 [TBL] [Abstract][Full Text] [Related]
17. Design and synthesis of a biaryl series as inhibitors for the bromodomains of CBP/P300. Lai KW; Romero FA; Tsui V; Beresini MH; de Leon Boenig G; Bronner SM; Chen K; Chen Z; Choo EF; Crawford TD; Cyr P; Kaufman S; Li Y; Liao J; Liu W; Ly J; Murray J; Shen W; Wai J; Wang F; Zhu C; Zhu X; Magnuson S Bioorg Med Chem Lett; 2018 Jan; 28(1):15-23. PubMed ID: 29169673 [TBL] [Abstract][Full Text] [Related]
18. Structural insights revealed by the cocrystal structure of CCS1477 in complex with CBP bromodomain. Xu H; Luo G; Wu T; Hu J; Wang C; Wu X; Zhang Y; Xu Y; Xiang Q Biochem Biophys Res Commun; 2022 Oct; 623():17-22. PubMed ID: 35868068 [TBL] [Abstract][Full Text] [Related]
19. Synthesis and anti-tumor activities of some new pyridines and pyrazolo[1,5-a]pyrimidines. Ahmed OM; Mohamed MA; Ahmed RR; Ahmed SA Eur J Med Chem; 2009 Sep; 44(9):3519-23. PubMed ID: 19398146 [TBL] [Abstract][Full Text] [Related]
20. Discovery of 3,5-substituted 6-azaindazoles as potent pan-Pim inhibitors. Hu H; Wang X; Chan GK; Chang JH; Do S; Drummond J; Ebens A; Lee W; Ly J; Lyssikatos JP; Murray J; Moffat JG; Chao Q; Tsui V; Wallweber H; Kolesnikov A Bioorg Med Chem Lett; 2015 Nov; 25(22):5258-64. PubMed ID: 26459208 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]