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- The synthesis of Bcr-Abl inhibiting anticancer pharmaceutical agents imatinib, nilotinib and dasatinib. Benjamin J. Deadman, Mark D. Hopkin, Ian R. Baxendale, Steven V. Ley
, Org. Biomol. Chem.
, 2013
, 11
, 1766
- Effects of nilotinib on leukaemia cells using vibrational microspectroscopy and cell cloning. M. R. Siddique, A. V. Rutter, K. Wehbe, G. Cinque, G. Bellisola, J. Sulé-Suso
, Analyst
, 2017
, 142
, 1299
- Novel design of dual-action Pt(iv) anticancer pro-drugs based on cisplatin and derivatives of the tyrosine kinase inhibitors imatinib and nilotinib. Darren Fergal Beirne, Barbara Farkaš, Chiara Donati, Valentina Gandin, Isabel Rozas, Trinidad Velasco-Torrijos, Diego Montagner
, Dalton Trans.
, 2023
, 52
, 14110
- An efficient d-glucosamine-based copper catalyst for C–X couplings and its application in the synthesis of nilotinib intermediate. Ming Wen, Chao Shen, Linfang Wang, Pengfei Zhang, Jianzhong Jin
, RSC Adv.
, 2015
, 5
, 1522
- Ferrocene modified analogues of imatinib and nilotinib as potent anti-cancer agents. Irena Philipova, Rositsa Mihaylova, Georgi Momekov, Rostislava Angelova, Georgi Stavrakov
, RSC Med. Chem.
, 2023
, 14
, 880
- In silico identification of novel kinase inhibitors targeting wild-type and T315I mutant ABL1 from FDA-approved drugs. Huai-long Xu, Zi-jie Wang, Xiao-meng Liang, Xin Li, Zheng Shi, Nan Zhou, Jin-ku Bao
, Mol. BioSyst.
, 2014
, 10
, 1524
- The medicinal chemistry of mitochondrial dysfunction: a critical overview of efforts to modulate mitochondrial health. Maximillian Taro William Lee, William Mahy, Mark David Rackham
, RSC Med. Chem.
, 2021
, 12
, 1281
- Expanding the scope of native chemical ligation – templated small molecule drug synthesis via benzanilide formation. Richard Houska, Marvin Björn Stutz, Oliver Seitz
, Chem. Sci.
, 2021
, 12
, 13450
- Simultaneous identification and determination of eleven tyrosine kinase inhibitors by supercritical fluid chromatography-mass spectrometry. Shaomin Zhang, Wei Jin, Yongjian Yang
, Anal. Methods
, 2019
, 11
, 2211
- Inhibitory effects of UDP-glucuronosyltransferase (UGT) typical ligands against E. coli beta-glucuronidase (GUS). Ling Xiao, Dehui Chi, Guiju Sheng, Wenjuan Li, Penghui Lin, Sicheng Liang, Liangliang Zhu, Peipei Dong
, RSC Adv.
, 2020
, 10
, 22966