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.
201 related articles for article (PubMed ID: 33725632)
1. Design, synthesis, and biological evaluation of nitroisoxazole-containing spiro[pyrrolidin-oxindole] derivatives as novel glutathione peroxidase 4/mouse double minute 2 dual inhibitors that inhibit breast adenocarcinoma cell proliferation. Liu SJ; Zhao Q; Peng C; Mao Q; Wu F; Zhang FH; Feng QS; He G; Han B Eur J Med Chem; 2021 May; 217():113359. PubMed ID: 33725632 [TBL] [Abstract][Full Text] [Related]
2. Molecular hybridization design and synthesis of novel spirooxindole-based MDM2 inhibitors endowed with BCL2 signaling attenuation; a step towards the next generation p53 activators. Lotfy G; Abdel Aziz YM; Said MM; El Ashry ESH; El Tamany ESH; Abu-Serie MM; Teleb M; Dömling A; Barakat A Bioorg Chem; 2021 Dec; 117():105427. PubMed ID: 34794098 [TBL] [Abstract][Full Text] [Related]
3. Synthesis of new thiazolo-pyrrolidine-(spirooxindole) tethered to 3-acylindole as anticancer agents. Islam MS; Ghawas HM; El-Senduny FF; Al-Majid AM; Elshaier YAMM; Badria FA; Barakat A Bioorg Chem; 2019 Feb; 82():423-430. PubMed ID: 30508794 [TBL] [Abstract][Full Text] [Related]
4. Design, synthesis and biological evaluation of novel antitumor spirotetrahydrothiopyran-oxindole derivatives as potent p53-MDM2 inhibitors. Ji C; Wang S; Chen S; He S; Jiang Y; Miao Z; Li J; Sheng C Bioorg Med Chem; 2017 Oct; 25(20):5268-5277. PubMed ID: 28797774 [TBL] [Abstract][Full Text] [Related]
5. Design, Synthesis and Antitumor Activity of Novel Dispiro[oxindole-cyclohexanone]- pyrrolidines. Gouda M; Bawazeer M; Hegazy L; Azab M; Elagawany M; Rateb M; Yaseen M; Elgendy B Curr Pharm Des; 2022; 28(3):198-207. PubMed ID: 34176458 [TBL] [Abstract][Full Text] [Related]
6. Inhibition of p53-Murine Double Minute 2 (MDM2) Interactions with 3,3'-Spirocyclopentene Oxindole Derivatives. Gicquel M; Gomez C; Garcia Alvarez MC; Pamlard O; Guérineau V; Jacquet E; Bignon J; Voituriez A; Marinetti A J Med Chem; 2018 Oct; 61(20):9386-9392. PubMed ID: 30221935 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. One-pot synthesis of spiro(indoline-3,4'-pyrazolo[3,4-b]pyridine)-5'-carbonitriles as p53-MDM2 interaction inhibitors. Ibrahim HS; Eldehna WM; Fallacara AL; Ahmed ER; Ghabbour HA; Elaasser MM; Botta M; Abou-Seri SM; Abdel-Aziz HA Future Med Chem; 2018 Dec; 10(24):2771-2789. PubMed ID: 30526032 [TBL] [Abstract][Full Text] [Related]
10. Synthesis of Spiro[indole-3,5'-isoxazoles] with Anticancer Activity via a Formal [4 + 1]-Spirocyclization of Nitroalkenes to Indoles. Aksenov AV; Aksenov DA; Arutiunov NA; Aksenov NA; Aleksandrova EV; Zhao Z; Du L; Kornienko A; Rubin M J Org Chem; 2019 Jun; 84(11):7123-7137. PubMed ID: 31070030 [TBL] [Abstract][Full Text] [Related]
11. Synthesis of spiro-tetrahydrothiopyran-oxindoles by Michael-aldol cascade reactions: discovery of potential P53-MDM2 inhibitors with good antitumor activity. Wang S; Chen S; Guo Z; He S; Zhang F; Liu X; Chen W; Zhang S; Sheng C Org Biomol Chem; 2018 Jan; 16(4):625-634. PubMed ID: 29302672 [TBL] [Abstract][Full Text] [Related]
12. Organocatalytic Asymmetric Synthesis of Spiro-oxindole Piperidine Derivatives That Reduce Cancer Cell Proliferation by Inhibiting MDM2-p53 Interaction. Yang MC; Peng C; Huang H; Yang L; He XH; Huang W; Cui HL; He G; Han B Org Lett; 2017 Dec; 19(24):6752-6755. PubMed ID: 29210587 [TBL] [Abstract][Full Text] [Related]
13. Stereoselective Synthesis of the Di-Spirooxindole Analogs Based Oxindole and Cyclohexanone Moieties as Potential Anticancer Agents. Al-Majid AM; Ali M; Islam MS; Alshahrani S; Alamary AS; Yousuf S; Choudhary MI; Barakat A Molecules; 2021 Oct; 26(20):. PubMed ID: 34684885 [TBL] [Abstract][Full Text] [Related]
14. Design, synthesis and biological evaluation of artesunate-Se derivatives as anticancer agents by inducing GPX4-mediated ferroptosis. Ren M; Liang S; Lin S; Huang R; Chen Y; Zhang Y; Xu Y Bioorg Chem; 2024 Nov; 152():107733. PubMed ID: 39180865 [TBL] [Abstract][Full Text] [Related]
15. Design, synthesis and biological evaluation of novel indanone containing spiroisoxazoline derivatives with selective COX-2 inhibition as anticancer agents. Abolhasani H; Zarghi A; Komeili Movahhed T; Abolhasani A; Daraei B; Dastmalchi S Bioorg Med Chem; 2021 Feb; 32():115960. PubMed ID: 33477020 [TBL] [Abstract][Full Text] [Related]
16. Design of chemically stable, potent, and efficacious MDM2 inhibitors that exploit the retro-mannich ring-opening-cyclization reaction mechanism in spiro-oxindoles. Aguilar A; Sun W; Liu L; Lu J; McEachern D; Bernard D; Deschamps JR; Wang S J Med Chem; 2014 Dec; 57(24):10486-98. PubMed ID: 25496041 [TBL] [Abstract][Full Text] [Related]
17. Synthesis of some novel methyl β-orsellinate based 3, 5-disubstituted isoxazoles and their anti-proliferative activity: Identification of potent leads active against MCF-7 breast cancer cell. Reddy ST; Mendonza JJ; Makani VKK; Bhadra MP; Uppuluri VM Bioorg Chem; 2020 Dec; 105():104374. PubMed ID: 33130349 [TBL] [Abstract][Full Text] [Related]
18. Discovery of new LXRβ agonists as glioblastoma inhibitors. Chen H; Chen Z; Zhang Z; Li Y; Zhang S; Jiang F; Wei J; Ding P; Zhou H; Gu Q; Xu J Eur J Med Chem; 2020 May; 194():112240. PubMed ID: 32248003 [TBL] [Abstract][Full Text] [Related]
19. Design, synthesis, and biological evaluation of RSL3-based GPX4 degraders with hydrophobic tags. Ning Y; Zhu Z; Wang Y; Fan X; Wang J; Qian H; Qiu X; Wang Y Eur J Med Chem; 2024 Nov; 277():116719. PubMed ID: 39094276 [TBL] [Abstract][Full Text] [Related]
20. Spiro[pyrrolidine-3, 3´-oxindole] as potent anti-breast cancer compounds: Their design, synthesis, biological evaluation and cellular target identification. Hati S; Tripathy S; Dutta PK; Agarwal R; Srinivasan R; Singh A; Singh S; Sen S Sci Rep; 2016 Aug; 6():32213. PubMed ID: 27573798 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]