Cao Y - Search Results

1

Discovery of the selective sphingomyelin synthase 2 inhibitors with the novel structure of oxazolopyridine.

Qi XY, Cao Y, Li YL, Mo MG, Zhou L, Ye DY. Qi XY, et al. Among authors: cao y. Bioorg Med Chem Lett. 2017 Aug 1;27(15):3511-3515. doi: 10.1016/j.bmcl.2017.05.074. Epub 2017 May 25. Bioorg Med Chem Lett. 2017. PMID: 28619536

2

Discovery of Metal Ions Chelator Quercetin Derivatives with Potent Anti-HCV Activities.

Zhong D, Liu M, Cao Y, Zhu Y, Bian S, Zhou J, Wu F, Ryu KC, Zhou L, Ye D. Zhong D, et al. Among authors: cao y. Molecules. 2015 Apr 16;20(4):6978-99. doi: 10.3390/molecules20046978. Molecules. 2015. PMID: 25913935 Free PMC article.

3

Xanthone derivatives as phosphoglycerate mutase 1 inhibitors: Design, synthesis, and biological evaluation.

Wang P, Jiang L, Cao Y, Zhang X, Chen B, Zhang S, Huang K, Ye D, Zhou L. Wang P, et al. Among authors: cao y. Bioorg Med Chem. 2018 May 1;26(8):1961-1970. doi: 10.1016/j.bmc.2018.02.044. Epub 2018 Feb 24. Bioorg Med Chem. 2018. PMID: 29530347

4

The Design and Synthesis of N-Xanthone Benzenesulfonamides as Novel Phosphoglycerate Mutase 1 (PGAM1) Inhibitors.

Wang P, Jiang L, Cao Y, Ye D, Zhou L. Wang P, et al. Among authors: cao y. Molecules. 2018 Jun 8;23(6):1396. doi: 10.3390/molecules23061396. Molecules. 2018. PMID: 29890679 Free PMC article.

5

Discovery, synthesis and anti-atherosclerotic activities of a novel selective sphingomyelin synthase 2 inhibitor.

Li Y, Huang T, Lou B, Ye D, Qi X, Li X, Hu S, Ding T, Chen Y, Cao Y, Mo M, Dong J, Wei M, Chu Y, Li H, Jiang XC, Cheng N, Zhou L. Li Y, et al. Among authors: cao y. Eur J Med Chem. 2019 Feb 1;163:864-882. doi: 10.1016/j.ejmech.2018.12.028. Epub 2018 Dec 13. Eur J Med Chem. 2019. PMID: 30580239

6

Discovery of Novel 3-Hydroxyquinazoline-2,4(1H,3H)-Dione Derivatives: A Series of Metal Ion Chelators with Potent Anti-HCV Activities.

Cao Y, Aimaiti A, Zhu Z, Zhou L, Ye D. Cao Y, et al. Int J Mol Sci. 2022 May 25;23(11):5930. doi: 10.3390/ijms23115930. Int J Mol Sci. 2022. PMID: 35682608 Free PMC article.

7

Synthesis and biological characterization of 1-methyl-1,2,5,6-tetrahydropyridyl-1,2,5-thiadiazole derivatives as muscarinic agonists for the treatment of neurological disorders.

Cao Y, Zhang M, Wu C, Lee S, Wroblewski ME, Whipple T, Nagy PI, Takács-Novák K, Balázs A, Torös S, Messer WS Jr. Cao Y, et al. J Med Chem. 2003 Sep 25;46(20):4273-86. doi: 10.1021/jm0301235. J Med Chem. 2003. PMID: 13678406

8

Structure-activity relationship (SAR) studies on substituted N-(pyridin-3-yl)-2-amino-isonicotinamides as highly potent and selective glycogen synthase kinase-3 (GSK-3) inhibitors.

Luo G, Chen L, Jacutin-Porte S, Han Y, Burton CR, Xiao H, Krause CM, Cao Y, Liu N, Kish K, Lewis HA, Macor JE, Dubowchik GM. Luo G, et al. Among authors: cao y. Bioorg Med Chem Lett. 2023 Feb 1;81:129143. doi: 10.1016/j.bmcl.2023.129143. Epub 2023 Jan 18. Bioorg Med Chem Lett. 2023. PMID: 36669575

9

Design, synthesis, and molecular docking of 4‑Thiol‑N‑acetylhexosamine uridine diphosphate donors for glycan synthesis.

Zheng J, Cao Y, Tao Q, Bi J, Zhang X, Chang M, Ji Y, He P, Zhang X. Zheng J, et al. Among authors: cao y. Bioorg Chem. 2025 Jan;154:108069. doi: 10.1016/j.bioorg.2024.108069. Epub 2024 Dec 16. Bioorg Chem. 2025. PMID: 39709736

10

The discovery of N-((2H-tetrazol-5-yl)methyl)-4-((R)-1-((5r,8R)-8-(tert-butyl)-3-(3,5-dichlorophenyl)-2-oxo-1,4-diazaspiro[4.5]dec-3-en-1-yl)-4,4-dimethylpentyl)benzamide (SCH 900822): a potent and selective glucagon receptor antagonist.

DeMong D, Dai X, Hwa J, Miller M, Lin SI, Kang L, Stamford A, Greenlee W, Yu W, Wong M, Lavey B, Kozlowski J, Zhou G, Yang DY, Patel B, Soriano A, Zhai Y, Sondey C, Zhang H, Lachowicz J, Grotz D, Cox K, Morrison R, Andreani T, Cao Y, Liang M, Meng T, McNamara P, Wong J, Bradley P, Feng KI, Belani J, Chen P, Dai P, Gauuan J, Lin P, Zhao H. DeMong D, et al. Among authors: cao y. J Med Chem. 2014 Mar 27;57(6):2601-10. doi: 10.1021/jm401858f. Epub 2014 Feb 26. J Med Chem. 2014. PMID: 24527772

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