Results
1 -
10 of
319
(Click
here to explore results)
- Synthesis and biological evaluation of 5-substituted O
4-alkylpyrimidines as CDK2 inhibitors. Francesco Marchetti, Céline Cano, Nicola J. Curtin, Bernard T. Golding, Roger J. Griffin, Karen Haggerty, David R. Newell, Rachel J. Parsons, Sara L. Payne, Lan Z. Wang, Ian R. Hardcastle
, Org. Biomol. Chem.
, 2010
, 8
, 2397
- Design, synthesis and biological evaluation of indazole–pyrimidine based derivatives as anticancer agents with anti-angiogenic and antiproliferative activities. Nevine M. Y. Elsayed, Dalal A. Abou El Ella, Rabah A. T. Serya, Mai F. Tolba, Raed Shalaby, Khaled A. M. Abouzid
, Med. Chem. Commun.
, 2016
, 7
, 881
- Structural evolution of toll-like receptor 7/8 agonists from imidazoquinolines to imidazoles. Deepender Kaushik, Arshpreet Kaur, Nikolai Petrovsky, Deepak B. Salunke
, RSC Med. Chem.
, 2021
, 12
, 1065
- Effect of substituents on the excited-state dynamics of the modified DNA bases 2,4-diaminopyrimidine and 2,6-diaminopurine. Zsolt Gengeliczki, Michael P. Callahan, Nathan Svadlenak, Csaba István Pongor, Bálint Sztáray, Leo Meerts, Dana Nachtigallová, Pavel Hobza, Mario Barbatti, Hans Lischka, Mattanjah S. de Vries
, Phys. Chem. Chem. Phys.
, 2010
, 12
, 5375
- Preparation, biological evaluation and QSAR analysis of urea substituted 2,4-diamino-pyrimidine anti-malarials. Borvornwat Toviwek, Jennifer Riley, Nicole Mutter, Mark Anderson, Lauren Webster, Irene Hallyburton, Duangkamol Gleeson, Kevin D. Read, M. Paul Gleeson
, RSC Med. Chem.
, 2022
, 13
, 1587
- Tunable iridium catalyst designs with bidentate N-heterocyclic carbene ligands for SABRE hyperpolarization of sterically hindered substrates. Pierce Pham, Christian Hilty
, Chem. Commun.
, 2020
, 56
, 15466
- Synthesis and structure–activity relationship of N
4-benzylamine-N
2-isopropyl-quinazoline-2,4-diamines derivatives as potential antibacterial agents. Zhengyun Jiang, W. David Hong, Xiping Cui, Hongcan Gao, Panpan Wu, Yingshan Chen, Ding Shen, Yang Yang, Bingjie Zhang, Mark J. Taylor, Stephen A. Ward, Paul M. O'Neill, Suqing Zhao, Kun Zhang
, RSC Adv.
, 2017
, 7
, 52227
- Discovery of rigid biphenyl Plasmodium falciparum DHFR inhibitors using a fragment linking strategy. Marie Hoarau, Patpanat Sermmai, Thaveechai Varatthan, Ratthiya Thiabma, Tararat Jantra, Roonglawan Rattanajak, Danoo Vitsupakorn, Jarunee Vanichtanankul, Siriporn Saepua, Yongyuth Yuthavong, Chawanee Thongpanchang, Sumalee Kamchonwongpaisan
, RSC Med. Chem.
, 2023
, 14
, 1755
- Structure-based discovery of potent inhibitors of Axl: design, synthesis, and biological evaluation. Shuang Wu, Min Liao, Minxiong Li, Mingming Sun, Ning Xi, Youlin Zeng
, RSC Med. Chem.
, 2022
, 13
, 1246
- Structure-based design of 2,4-diaminopyrimidine derivatives bearing a pyrrolyl group as ALK and ROS1 inhibitors. Jie Wang, Shangfei Wei, Tong Li, Lingyun Xing, Meng Cao, Nan Jiang, Ming Guo, Daiying Zuo, Xin Zhai
, New J. Chem.
, 2020
, 44
, 5850