Yao CF - Search Results

1

Using gene expression database to uncover biology functions of 1,4-disubstituted 1,2,3-triazole analogues synthesized via a copper (I)-catalyzed reaction.

Su CL, Tseng CL, Ramesh C, Liu HS, Huang CF, Yao CF. Su CL, et al. Among authors: yao cf. Eur J Med Chem. 2017 May 26;132:90-107. doi: 10.1016/j.ejmech.2017.03.034. Epub 2017 Mar 18. Eur J Med Chem. 2017. PMID: 28342400

2

Synthesis and evaluation of the cytotoxicities of tetraindoles: observation that the 5-hydroxy tetraindole (SK228) induces G₂ arrest and apoptosis in human breast cancer cells.

Li WS, Wang CH, Ko S, Chang TT, Jen YC, Yao CF, More SV, Jao SC. Li WS, et al. Among authors: yao cf. J Med Chem. 2012 Feb 23;55(4):1583-92. doi: 10.1021/jm2013425. Epub 2012 Feb 9. J Med Chem. 2012. PMID: 22277074

3

A convenient one-pot preparation of 2-methyl-3-(phenylthio- methyl)quinolines from Morita-Baylis-Hillman adducts and their oxidation to the corresponding sulfones.

Ramesh C, Lei PM, Kavala V, Kuo CW, Yao CF. Ramesh C, et al. Among authors: yao cf. Molecules. 2012 May 3;17(5):5081-94. doi: 10.3390/molecules17055081. Molecules. 2012. PMID: 22555297 Free PMC article.

4

Synthesis of indolylquinolines, indolylacridines, and indolylcyclopenta[b]quinolines from the Baylis-Hillman adducts: an in situ [1,3]-sigmatropic rearrangement of an indole nucleus to access indolylacridines and indolylcyclopenta[b]quinolines.

Ramesh C, Lei PM, Janreddy D, Kavala V, Kuo CW, Yao CF. Ramesh C, et al. Among authors: yao cf. J Org Chem. 2012 Oct 5;77(19):8451-64. doi: 10.1021/jo301313m. Epub 2012 Sep 25. J Org Chem. 2012. PMID: 22967265

5

An indolylquinoline derivative promotes apoptosis in human lung cancer cells by impairing mitochondrial functions.

Liu CY, Wu PT, Wang JP, Fan PW, Hsieh CH, Su CL, Chiu CC, Yao CF, Fang K. Liu CY, et al. Among authors: yao cf. Apoptosis. 2015 Nov;20(11):1471-82. doi: 10.1007/s10495-015-1165-6. Apoptosis. 2015. PMID: 26349782

6

The potential of synthetic indolylquinoline derivatives for Aβ aggregation reduction by chemical chaperone activity.

Chang KH, Chiu YJ, Chen SL, Huang CH, Lin CH, Lin TH, Lee CM, Ramesh C, Wu CH, Huang CC, Fung HC, Chen YC, Lin JY, Yao CF, Huang HJ, Lee-Chen GJ, Lee MC, Hsieh-Li HM. Chang KH, et al. Among authors: yao cf. Neuropharmacology. 2016 Feb;101:309-19. doi: 10.1016/j.neuropharm.2015.09.005. Epub 2015 Sep 8. Neuropharmacology. 2016. PMID: 26362358

7

The Potential of Indole/Indolylquinoline Compounds in Tau Misfolding Reduction by Enhancement of HSPB1.

Chang KH, Lin CH, Chen HC, Huang HY, Chen SL, Lin TH, Ramesh C, Huang CC, Fung HC, Wu YR, Huang HJ, Lee-Chen GJ, Hsieh-Li HM, Yao CF. Chang KH, et al. Among authors: yao cf. CNS Neurosci Ther. 2017 Jan;23(1):45-56. doi: 10.1111/cns.12592. Epub 2016 Jul 18. CNS Neurosci Ther. 2017. PMID: 27424519 Free PMC article.

8

An indolylquinoline derivative activates DNA damage response and apoptosis in human hepatocellular carcinoma cells.

Liu CY, Hsieh CH, Kim SH, Wang JP, Ni YL, Su CL, Yao CF, Fang K. Liu CY, et al. Among authors: yao cf. Int J Oncol. 2016 Dec;49(6):2431-2441. doi: 10.3892/ijo.2016.3717. Epub 2016 Oct 5. Int J Oncol. 2016. PMID: 27748837

9

Synthesis of Biologically Active Indenoisoquinoline Derivatives via a One-Pot Copper(II)-Catalyzed Tandem Reaction.

Huang CY, Kavala V, Kuo CW, Konala A, Yang TH, Yao CF. Huang CY, et al. Among authors: yao cf. J Org Chem. 2017 Feb 17;82(4):1961-1968. doi: 10.1021/acs.joc.6b02814. Epub 2017 Feb 8. J Org Chem. 2017. PMID: 28177250

10

A potent indolylquinoline alleviates growth of human lung cancer cell tumorspheres.

Ni YL, Hsieh CH, Kim SH, Wang JP, Su CL, Yao CF, Fang K. Ni YL, et al. Among authors: yao cf. Apoptosis. 2017 Oct;22(10):1235-1245. doi: 10.1007/s10495-017-1401-3. Apoptosis. 2017. PMID: 28741092

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