日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Design and synthesis of biphenyl and biphenyl ether inhibitors of sulfatases

联苯和联苯醚类硫酸酯酶抑制剂的设计与合成

Reuillon, Tristan; Alhasan, Sari F; Beale, Gary S; Bertoli, Annalisa; Brennan, Alfie; Cano, Celine; Reeves, Helen L; Newell, David R; Golding, Bernard T; Miller, Duncan C; Griffin, Roger J

Pharmacologic biomarkers in the development of stratified cancer medicine

分层癌症治疗中的药理学生物标志物

Figg, William Douglas; Newell, David R

Preclinical evaluation of a novel ATM inhibitor, KU59403, in vitro and in vivo in p53 functional and dysfunctional models of human cancer.

在人类癌症的 p53 功能和功能障碍模型中,对新型 ATM 抑制剂 KU59403 进行体外和体内临床前评估

Batey Michael A, Zhao Yan, Kyle Suzanne, Richardson Caroline, Slade Andrew, Martin Niall M B, Lau Alan, Newell David R, Curtin Nicola J

Diaryl- and triaryl-pyrrole derivatives: inhibitors of the MDM2-p53 and MDMX-p53 protein-protein interactions†Electronic supplementary information (ESI) available: Experimental details for compound synthesis, analytical data for all compounds and intermediates. Details for the biological evaluation. Further details for the modeling. Table of combustion analysis data. See DOI: 10.1039/c3md00161jClick here for additional data file

二芳基和三芳基吡咯衍生物:MDM2-p53 和 MDMX-p53 蛋白-蛋白相互作用的抑制剂†电子补充信息 (ESI) 提供:化合物合成的实验细节、所有化合物和中间体的分析数据、生物学评价详情、建模详情以及燃烧分析数据表。参见 DOI:10.1039/c3md00161j。点击此处获取其他数据文件。

Blackburn, Tim J; Ahmed, Shafiq; Coxon, Christopher R; Liu, Junfeng; Lu, Xiaohong; Golding, Bernard T; Griffin, Roger J; Hutton, Claire; Newell, David R; Ojo, Stephen; Watson, Anna F; Zaytzev, Andrey; Zhao, Yan; Lunec, John; Hardcastle, Ian R

Compromised CDK1 activity sensitizes BRCA-proficient cancers to PARP inhibition

CDK1活性受损会使具有BRCA功能的癌症对PARP抑制剂更加敏感

Johnson, Neil; Li, Yu-Chen; Walton, Zandra E; Cheng, Katherine A; Li, Danan; Rodig, Scott J; Moreau, Lisa A; Unitt, Christine; Bronson, Roderick T; Thomas, Huw D; Newell, David R; D'Andrea, Alan D; Curtin, Nicola J; Wong, Kwok-Kin; Shapiro, Geoffrey I