Liu F - Search Results

1

Exploration of (S)-3-aminopyrrolidine as a potentially interesting scaffold for discovery of novel Abl and PI3K dual inhibitors.

Zhang C, Tan C, Zu X, Zhai X, Liu F, Chu B, Ma X, Chen Y, Gong P, Jiang Y. Zhang C, et al. Among authors: liu f. Eur J Med Chem. 2011 Apr;46(4):1404-14. doi: 10.1016/j.ejmech.2011.01.020. Epub 2011 Jan 21. Eur J Med Chem. 2011. PMID: 21295380

2

Exploration of 1-(3-chloro-4-(4-oxo-4H-chromen-2-yl)phenyl)-3-phenylurea derivatives as selective dual inhibitors of Raf1 and JNK1 kinases for anti-tumor treatment.

Jin F, Gao D, Zhang C, Liu F, Chu B, Chen Y, Chen YZ, Tan C, Jiang Y. Jin F, et al. Among authors: liu f. Bioorg Med Chem. 2013 Feb 1;21(3):824-31. doi: 10.1016/j.bmc.2012.04.006. Epub 2012 Apr 11. Bioorg Med Chem. 2013. PMID: 23260578

3

Exploration of N-(2-aminoethyl)piperidine-4-carboxamide as a potential scaffold for development of VEGFR-2, ERK-2 and Abl-1 multikinase inhibitor.

Jin F, Gao D, Wu Q, Liu F, Chen Y, Tan C, Jiang Y. Jin F, et al. Among authors: liu f. Bioorg Med Chem. 2013 Sep 15;21(18):5694-706. doi: 10.1016/j.bmc.2013.07.026. Epub 2013 Jul 20. Bioorg Med Chem. 2013. PMID: 23932071

4

Novel multi-substituted benzyl acridone derivatives as survivin inhibitors for hepatocellular carcinoma treatment.

Zhang B, Wang N, Zhang C, Gao C, Zhang W, Chen K, Wu W, Chen Y, Tan C, Liu F, Jiang Y. Zhang B, et al. Among authors: liu f. Eur J Med Chem. 2017 Mar 31;129:337-348. doi: 10.1016/j.ejmech.2017.02.027. Epub 2017 Feb 17. Eur J Med Chem. 2017. PMID: 28237663

5

Discovery of 1-(3-aryl-4-chlorophenyl)-3-(p-aryl)urea derivatives against breast cancer by inhibiting PI3K/Akt/mTOR and Hedgehog signalings.

Li W, Sun Q, Song L, Gao C, Liu F, Chen Y, Jiang Y. Li W, et al. Among authors: liu f. Eur J Med Chem. 2017 Dec 1;141:721-733. doi: 10.1016/j.ejmech.2017.09.002. Epub 2017 Oct 6. Eur J Med Chem. 2017. PMID: 29107429

6

Novel synthetic 2-amino-10-(3,5-dimethoxy)benzyl-9(10H)-acridinone derivatives as potent DNA-binding antiproliferative agents.

Gao C, Liu F, Luan X, Tan C, Liu H, Xie Y, Jin Y, Jiang Y. Gao C, et al. Among authors: liu h, liu f. Bioorg Med Chem. 2010 Nov 1;18(21):7507-14. doi: 10.1016/j.bmc.2010.08.058. Epub 2010 Sep 20. Bioorg Med Chem. 2010. PMID: 20863710

7

Novel synthetic acridine derivatives as potent DNA-binding and apoptosis-inducing antitumor agents.

Lang X, Li L, Chen Y, Sun Q, Wu Q, Liu F, Tan C, Liu H, Gao C, Jiang Y. Lang X, et al. Among authors: liu h, liu f. Bioorg Med Chem. 2013 Jul 15;21(14):4170-7. doi: 10.1016/j.bmc.2013.05.008. Epub 2013 May 16. Bioorg Med Chem. 2013. PMID: 23735826

8

Design, synthesis and anticancer evaluation of acridine hydroxamic acid derivatives as dual Topo and HDAC inhibitors.

Chen J, Li D, Li W, Yin J, Zhang Y, Yuan Z, Gao C, Liu F, Jiang Y. Chen J, et al. Among authors: liu f. Bioorg Med Chem. 2018 Aug 7;26(14):3958-3966. doi: 10.1016/j.bmc.2018.06.016. Epub 2018 Jun 20. Bioorg Med Chem. 2018. PMID: 29954683

9

Survivin transcription is associated with P-glycoprotein/MDR1 overexpression in the multidrug resistance of MCF-7 breast cancer cells.

Liu F, Liu S, He S, Xie Z, Zu X, Jiang Y. Liu F, et al. Among authors: liu s. Oncol Rep. 2010 May;23(5):1469-75. doi: 10.3892/or_00000786. Oncol Rep. 2010. PMID: 20372866

10

2'-chloro-4'-aminoflavone derivatives selectively targeting hepatocarcinoma cells: convenient synthetic process, G(2)/M cell cycle arrest and apoptosis triggers.

Jin F, Zhang N, Tan C, Gao D, Zhang C, Liu F, Chen Z, Gao C, Liu H, Li S, Jiang Y. Jin F, et al. Among authors: liu h, liu f. Arch Pharm (Weinheim). 2012 Jul;345(7):525-34. doi: 10.1002/ardp.201100383. Epub 2012 Mar 30. Arch Pharm (Weinheim). 2012. PMID: 22467491

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