Wang K - Search Results

1

Synthesis and cytotoxic activities of a series of novel N-methyl-bisindolylmaleimide amide derivatives.

Wang K, Liu ZZ. Wang K, et al. J Asian Nat Prod Res. 2014;16(3):296-303. doi: 10.1080/10286020.2013.877452. J Asian Nat Prod Res. 2014. PMID: 24456252

2

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

3

Synthesis of N-methyl-bisindolylmaleimide amino acid methyl ester conjugates and cytotoxicity study.

Wang K, Liu ZZ. Wang K, et al. Eur J Med Chem. 2010 Sep;45(9):4175-9. doi: 10.1016/j.ejmech.2010.06.009. Epub 2010 Jun 12. Eur J Med Chem. 2010. PMID: 20598779

4

A novel bisindolymaleimide derivative (WK234) inhibits proliferation and induces apoptosis through the protein kinase Cβ pathway, in chronic myelogenous leukemia K562 cells.

Li XY, Li Y, Zhang Y, Wang K, Yuan X, Jin J, Zhang Y, Liu ZZ, Chen XG. Li XY, et al. Among authors: wang k. Leuk Lymphoma. 2011 Jul;52(7):1312-20. doi: 10.3109/10428194.2011.565393. Epub 2011 May 3. Leuk Lymphoma. 2011. PMID: 21534868

5

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

6

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

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

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

9

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

10

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

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