Wang K - Search Results

1

Design, synthesis and biological evaluation of triaryl compounds as novel 20S proteasome inhibitors.

Yang Y, Wang K, Wu B, Yang Y, Lai F, Chen X, Xiao Z. Yang Y, et al. Among authors: wang k. Bioorg Med Chem Lett. 2020 Nov 1;30(21):127508. doi: 10.1016/j.bmcl.2020.127508. Epub 2020 Aug 24. Bioorg Med Chem Lett. 2020. PMID: 32853683

2

Design, synthesis and biological evaluation of dipeptides as novel non-covalent 20S proteasome inhibitors.

Yang YJ, Wang K, Yang Y, Lai FF, Chen XG, Xiao ZY. Yang YJ, et al. Among authors: wang k. J Asian Nat Prod Res. 2021 May;23(5):436-451. doi: 10.1080/10286020.2021.1910241. Epub 2021 Apr 12. J Asian Nat Prod Res. 2021. PMID: 33844614

3

Discovery of novel non-covalent inhibitors selective to the β5-subunit of the human 20S proteasome.

Xu K, Wang K, Yang Y, Yan DA, Huang L, Chen CH, Xiao Z. Xu K, et al. Among authors: wang k. Eur J Med Chem. 2015 Jun 15;98:61-8. doi: 10.1016/j.ejmech.2015.05.023. Epub 2015 May 16. Eur J Med Chem. 2015. PMID: 26005024

4

Design, synthesis, and biological evaluation of 1-methyl-1H-pyrazolo[4,3-b]pyridine derivatives as novel small-molecule inhibitors targeting the PD-1/PD-L1 interaction.

Dai X, Wang K, Chen H, Huang X, Feng Z. Dai X, et al. Among authors: wang k. Bioorg Chem. 2021 Sep;114:105034. doi: 10.1016/j.bioorg.2021.105034. Epub 2021 May 30. Bioorg Chem. 2021. PMID: 34116264

5

Design, synthesis, and structure-activity relationship of PD-1/PD-L1 inhibitors with a benzo[d]isoxazole scaffold.

Huang X, Chen H, Dai X, Xu M, Wang K, Feng Z. Huang X, et al. Among authors: wang k. Bioorg Med Chem Lett. 2021 Nov 15;52:128403. doi: 10.1016/j.bmcl.2021.128403. Epub 2021 Oct 2. Bioorg Med Chem Lett. 2021. PMID: 34610423

6

Synthesis and antitumor activity of bisindolylmaleimide and amino acid ester conjugates.

Wang K, Li XY, Chen XG, Liu ZZ. Wang K, et al. J Asian Nat Prod Res. 2010 Jan;12(1):36-42. doi: 10.1080/10286020903413385. J Asian Nat Prod Res. 2010. PMID: 20390741

7

Design, synthesis, evaluation, and SAR of 4-phenylindoline derivatives, a novel class of small-molecule inhibitors of the programmed cell death-1/ programmed cell death-ligand 1 (PD-1/PD-L1) interaction.

Yang Y, Wang K, Chen H, Feng Z. Yang Y, et al. Among authors: wang k. Eur J Med Chem. 2021 Feb 5;211:113001. doi: 10.1016/j.ejmech.2020.113001. Epub 2020 Nov 10. Eur J Med Chem. 2021. PMID: 33272783

8

Design, synthesis, and structure-activity relationship of programmed cell death-1/programmed cell death-ligand 1 interaction inhibitors bearing a benzo[d]isothiazole scaffold.

Chen H, Wang K, Yang Y, Huang X, Dai X, Feng Z. Chen H, et al. Among authors: wang k. Eur J Med Chem. 2021 May 5;217:113377. doi: 10.1016/j.ejmech.2021.113377. Epub 2021 Mar 15. Eur J Med Chem. 2021. PMID: 33770574

9

Synthesis of new ent-labdane diterpene derivatives from andrographolide and evaluation on cytotoxic activities.

Luo Y, Wang K, Zhang MH, Zhang DY, Wu YC, Wu XM, Hua WY. Luo Y, et al. Among authors: wang k. Bioorg Med Chem Lett. 2015 Jun 1;25(11):2421-4. doi: 10.1016/j.bmcl.2015.03.086. Epub 2015 Apr 4. Bioorg Med Chem Lett. 2015. PMID: 25913115

10

[Synthesis and in vitro cytotoxic activities of sorafenib derivatives].

Wang K, Li Y, Zhang LJ, Yang HZ, Chen XG, Feng ZQ. Wang K, et al. Yao Xue Xue Bao. 2014 May;49(5):639-43. Yao Xue Xue Bao. 2014. PMID: 25151734 Chinese.

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