These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
290 related articles for article (PubMed ID: 33770574)
1. 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 Eur J Med Chem; 2021 May; 217():113377. PubMed ID: 33770574 [TBL] [Abstract][Full Text] [Related]
2. 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 Bioorg Med Chem Lett; 2021 Nov; 52():128403. PubMed ID: 34610423 [TBL] [Abstract][Full Text] [Related]
3. Design, synthesis, pharmacological evaluation, and computational study of benzo[d] isothiazol-based small molecule inhibitors targeting PD-1/PD-l1 interaction. Wang H; Shen L; Chen L; Gao Y; Ma L; Lian W; Zhang Z; Liu H; Yang H; Wang J; Zhao D; Cheng M Eur J Med Chem; 2024 Sep; 275():116622. PubMed ID: 38959727 [TBL] [Abstract][Full Text] [Related]
4. 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 Eur J Med Chem; 2021 Feb; 211():113001. PubMed ID: 33272783 [TBL] [Abstract][Full Text] [Related]
5. Design, synthesis, and evaluation of antitumor activity of 2-arylmethoxy-4-(2-fluoromethyl-biphenyl-3-ylmethoxy) benzylamine derivatives as PD-1/PD-l1 inhibitors. Zhang F; Zhang H; Zhou S; Plewka J; Wang M; Sun S; Wu C; Yu Q; Zhu M; Awadasseid A; Wu Y; Magiera-Mularz K; Zhang W Eur J Med Chem; 2024 Oct; 276():116683. PubMed ID: 39032403 [TBL] [Abstract][Full Text] [Related]
6. Molecular hybridization used to design and synthesize neo-tanshinlactone derivatives as PD-1/PD-L1 inhibitors. Zhang M; Liu J; Wang Y; Wang P; Morris-Natschke S; Lee KH Bioorg Med Chem; 2022 Jan; 54():116579. PubMed ID: 34954618 [TBL] [Abstract][Full Text] [Related]
7. Design, synthesis and evaluation of PD-L1 peptide antagonists as new anticancer agents for immunotherapy. Orafaie A; Sadeghian H; Bahrami AR; Rafatpanah H; Matin MM Bioorg Med Chem; 2021 Jan; 30():115951. PubMed ID: 33360579 [TBL] [Abstract][Full Text] [Related]
8. Discovery of benzo[d]isothiazole derivatives as novel scaffold inhibitors targeting the programmed cell death-1/programmed cell death-ligand 1 (PD-1/PD-L1) interaction through "ring fusion" strategy. Gao Y; Wang H; Shen L; Xu H; Deng M; Cheng M; Wang J Bioorg Chem; 2022 Jun; 123():105769. PubMed ID: 35405572 [TBL] [Abstract][Full Text] [Related]
9. Improving tumor sensitivity by the introduction of an ester chain to triaryl derivatives targeting PD-1/PD-L1. Zhang Y; Yin F; Luo Z; Li S; Li X; Wan S; Chen Y; Kong L; Wang X Eur J Med Chem; 2024 May; 271():116433. PubMed ID: 38678826 [TBL] [Abstract][Full Text] [Related]
10. Discovery of phenyl-linked symmetric small molecules as inhibitors of the programmed cell death-1/programmed cell death-ligand 1 interaction. Wu Y; Zhang Y; Guo Y; Pan Z; Zhong S; Jin X; Zhuang W; Chen S; Gao J; Huang W; Dong X; Che J Eur J Med Chem; 2021 Nov; 223():113637. PubMed ID: 34147746 [TBL] [Abstract][Full Text] [Related]
11. Discovery of the programmed cell death-1/programmed cell death-ligand 1 interaction inhibitors bearing an indoline scaffold. Qin M; Cao Q; Wu X; Liu C; Zheng S; Xie H; Tian Y; Xie J; Zhao Y; Hou Y; Zhang X; Xu B; Zhang H; Wang X Eur J Med Chem; 2020 Jan; 186():111856. PubMed ID: 31734021 [TBL] [Abstract][Full Text] [Related]
12. Insights into non-peptide small-molecule inhibitors of the PD-1/PD-L1 interaction: Development and perspective. Wu X; Meng Y; Liu L; Gong G; Zhang H; Hou Y; Liu C; Wu D; Qin M Bioorg Med Chem; 2021 Mar; 33():116038. PubMed ID: 33517226 [TBL] [Abstract][Full Text] [Related]
13. 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 Bioorg Chem; 2021 Sep; 114():105034. PubMed ID: 34116264 [TBL] [Abstract][Full Text] [Related]
14. Design, Synthesis, and Pharmacological Evaluation of Biaryl-Containing PD-1/PD-L1 Interaction Inhibitors Bearing a Unique Difluoromethyleneoxy Linkage. Song Z; Liu B; Peng X; Gu W; Sun Y; Xing L; Xu Y; Geng M; Ai J; Zhang A J Med Chem; 2021 Nov; 64(22):16687-16702. PubMed ID: 34761679 [TBL] [Abstract][Full Text] [Related]
15. Preparation of Biphenyl-Conjugated Bromotyrosine for Inhibition of PD-1/PD-L1 Immune Checkpoint Interactions. Kim EH; Kawamoto M; Dharmatti R; Kobatake E; Ito Y; Miyatake H Int J Mol Sci; 2020 May; 21(10):. PubMed ID: 32455628 [TBL] [Abstract][Full Text] [Related]
16. Anti-PD-L1 DNA aptamer antagonizes the interaction of PD-1/PD-L1 with antitumor effect. Gao T; Mao Z; Li W; Pei R J Mater Chem B; 2021 Jan; 9(3):746-756. PubMed ID: 33319876 [TBL] [Abstract][Full Text] [Related]
17. Design, Synthesis, and Evaluation of OuYang Y; Gao J; Zhao L; Lu J; Zhong H; Tang H; Jin S; Yue L; Li Y; Guo W; Xu Q; Lai Y J Med Chem; 2021 Jun; 64(11):7646-7666. PubMed ID: 34037385 [TBL] [Abstract][Full Text] [Related]
18. Discovery of novel CA-4 analogs as dual inhibitors of tubulin polymerization and PD-1/PD-L1 interaction for cancer treatment. Yang X; Cheng B; Xiao Y; Xue M; Liu T; Cao H; Chen J Eur J Med Chem; 2021 Mar; 213():113058. PubMed ID: 33280898 [TBL] [Abstract][Full Text] [Related]
19. Syntheses, Biological Evaluations, and Mechanistic Studies of Benzo[ Liu L; Yao Z; Wang S; Xie T; Wu G; Zhang H; Zhang P; Wu Y; Yuan H; Sun H J Med Chem; 2021 Jun; 64(12):8391-8409. PubMed ID: 34115499 [TBL] [Abstract][Full Text] [Related]
20. Discovery of 4-phenyl-1H-indazole derivatives as novel small-molecule inhibitors targeting the PD-1/PD-L1 interaction. Xu C; Sun Z; Zhang X; Zang Q; Yang Z; Li L; Yang X; He Y; Ma Z; Chen J Bioorg Chem; 2024 Jun; 147():107376. PubMed ID: 38640722 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]