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.
4. Spiro-oxindole derivative 5-chloro-4',5'-diphenyl-3'-(4-(2-(piperidin-1-yl) ethoxy) benzoyl) spiro[indoline-3,2'-pyrrolidin]-2-one triggers apoptosis in breast cancer cells via restoration of p53 function. Saxena R; Gupta G; Manohar M; Debnath U; Popli P; Prabhakar YS; Konwar R; Kumar S; Kumar A; Dwivedi A Int J Biochem Cell Biol; 2016 Jan; 70():105-17. PubMed ID: 26556313 [TBL] [Abstract][Full Text] [Related]
5. Computational analysis of spiro-oxindole inhibitors of the MDM2-p53 interaction: insights and selection of novel inhibitors. Huang W; Cai L; Chen C; Xie X; Zhao Q; Zhao X; Zhou HY; Han B; Peng C J Biomol Struct Dyn; 2016; 34(2):341-51. PubMed ID: 25808617 [TBL] [Abstract][Full Text] [Related]
6. MDM2 non-genotoxic inhibitors as innovative therapeutic approaches for the treatment of pediatric malignancies. Tisato V; Norcio A; Voltan R; Celeghini C; Zella D; Secchiero P Curr Med Chem; 2013; 20(17):2226-36. PubMed ID: 23458617 [TBL] [Abstract][Full Text] [Related]
7. p53-Mdm2 Interaction Inhibitors as Novel Nongenotoxic Anticancer Agents. Nayak SK; Khatik GL; Narang R; Monga V; Chopra HK Curr Cancer Drug Targets; 2018; 18(8):749-772. PubMed ID: 28669344 [TBL] [Abstract][Full Text] [Related]
8. In vivo activation of the p53 pathway by small-molecule antagonists of MDM2. Vassilev LT; Vu BT; Graves B; Carvajal D; Podlaski F; Filipovic Z; Kong N; Kammlott U; Lukacs C; Klein C; Fotouhi N; Liu EA Science; 2004 Feb; 303(5659):844-8. PubMed ID: 14704432 [TBL] [Abstract][Full Text] [Related]
9. Spiro-oxindoles as a Promising Class of Small Molecule Inhibitors of p53-MDM2 Interaction Useful in Targeted Cancer Therapy. Gupta AK; Bharadwaj M; Kumar A; Mehrotra R Top Curr Chem (Cham); 2017 Feb; 375(1):3. PubMed ID: 27943171 [TBL] [Abstract][Full Text] [Related]
11. Structure-based design of spiro-oxindoles as potent, specific small-molecule inhibitors of the MDM2-p53 interaction. Ding K; Lu Y; Nikolovska-Coleska Z; Wang G; Qiu S; Shangary S; Gao W; Qin D; Stuckey J; Krajewski K; Roller PP; Wang S J Med Chem; 2006 Jun; 49(12):3432-5. PubMed ID: 16759082 [TBL] [Abstract][Full Text] [Related]
12. Targeted Degradation of MDM2 as a New Approach to Improve the Efficacy of MDM2-p53 Inhibitors. Wurz RP; Cee VJ J Med Chem; 2019 Jan; 62(2):445-447. PubMed ID: 30575392 [TBL] [Abstract][Full Text] [Related]
13. Identification of antipsychotic drug fluspirilene as a potential p53-MDM2 inhibitor: a combined computational and experimental study. Patil SP; Pacitti MF; Gilroy KS; Ruggiero JC; Griffin JD; Butera JJ; Notarfrancesco JM; Tran S; Stoddart JW J Comput Aided Mol Des; 2015 Feb; 29(2):155-63. PubMed ID: 25377899 [TBL] [Abstract][Full Text] [Related]
15. Inhibitors of MDM2 and MDMX: a structural perspective. Riedinger C; McDonnell JM Future Med Chem; 2009 Sep; 1(6):1075-94. PubMed ID: 21425995 [TBL] [Abstract][Full Text] [Related]
16. Molecular basis for the inhibition of p53 by Mdmx. Popowicz GM; Czarna A; Rothweiler U; Szwagierczak A; Krajewski M; Weber L; Holak TA Cell Cycle; 2007 Oct; 6(19):2386-92. PubMed ID: 17938582 [TBL] [Abstract][Full Text] [Related]
17. MDM2/X inhibitors under clinical evaluation: perspectives for the management of hematological malignancies and pediatric cancer. Tisato V; Voltan R; Gonelli A; Secchiero P; Zauli G J Hematol Oncol; 2017 Jul; 10(1):133. PubMed ID: 28673313 [TBL] [Abstract][Full Text] [Related]
18. Small-molecule inhibitors of the MDM2-p53 protein-protein interaction to reactivate p53 function: a novel approach for cancer therapy. Shangary S; Wang S Annu Rev Pharmacol Toxicol; 2009; 49():223-41. PubMed ID: 18834305 [TBL] [Abstract][Full Text] [Related]
19. Small-molecule inhibitors of the p53-MDM2 interaction. Vu BT; Vassilev L Curr Top Microbiol Immunol; 2011; 348():151-72. PubMed ID: 21046355 [TBL] [Abstract][Full Text] [Related]
20. Discovery of potent and selective spiroindolinone MDM2 inhibitor, RO8994, for cancer therapy. Zhang Z; Ding Q; Liu JJ; Zhang J; Jiang N; Chu XJ; Bartkovitz D; Luk KC; Janson C; Tovar C; Filipovic ZM; Higgins B; Glenn K; Packman K; Vassilev LT; Graves B Bioorg Med Chem; 2014 Aug; 22(15):4001-9. PubMed ID: 24997575 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]