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.
157 related articles for article (PubMed ID: 35164276)
1. Design, Synthesis and Cytotoxicity of Thiazole-Based Stilbene Analogs as Novel DNA Topoisomerase IB Inhibitors. Liu JC; Chen B; Yang JL; Weng JQ; Yu Q; Hu DX Molecules; 2022 Feb; 27(3):. PubMed ID: 35164276 [TBL] [Abstract][Full Text] [Related]
2. Synthesis, Biological Evaluation and Molecular Docking Study of Cyclic Diarylheptanoids as Potential Anticancer Therapeutics. Lu Y; Yin W; Alam MS; Kadi AA; Jahng Y; Kwon Y; Rahman AFMM Anticancer Agents Med Chem; 2020; 20(4):464-475. PubMed ID: 31763968 [TBL] [Abstract][Full Text] [Related]
3. Facile synthesis of novel substituted aryl-thiazole (SAT) analogs via one-pot multi-component reaction as potent cytotoxic agents against cancer cell lines. Mirza S; Asma Naqvi S; Mohammed Khan K; Salar U; Choudhary MI Bioorg Chem; 2017 Feb; 70():133-143. PubMed ID: 28038777 [TBL] [Abstract][Full Text] [Related]
4. Design, synthesis, topoisomerase I & II inhibitory activity, antiproliferative activity, and structure-activity relationship study of pyrazoline derivatives: An ATP-competitive human topoisomerase IIα catalytic inhibitor. Ahmad P; Woo H; Jun KY; Kadi AA; Abdel-Aziz HA; Kwon Y; Rahman AF Bioorg Med Chem; 2016 Apr; 24(8):1898-908. PubMed ID: 26988802 [TBL] [Abstract][Full Text] [Related]
5. Synthesis, anticancer evaluation and molecular docking studies of new heterocycles linked to sulfonamide moiety as novel human topoisomerase types I and II poisons. Halawa AH; Elgammal WE; Hassan SM; Hassan AH; Nassar HS; Ebrahim HY; Mehany ABM; El-Agrody AM Bioorg Chem; 2020 May; 98():103725. PubMed ID: 32199303 [TBL] [Abstract][Full Text] [Related]
6. Molecular modelling design, synthesis and cytotoxic evaluation of certain substituted 2-(3,4,5-triacetoxybenzoylamino)benzo[d]thiazole and 2-(galloylamino)benzo[d]thiazole derivatives having potential topoisomerase-I inhibitory activity. Ismail MA; Tratrat C; Haroun MG J Enzyme Inhib Med Chem; 2013 Dec; 28(6):1331-45. PubMed ID: 22957723 [TBL] [Abstract][Full Text] [Related]
7. Design, Synthesis, In Vitro Anti-cancer Activity, ADMET Profile and Molecular Docking of Novel Triazolo[3,4-a]phthalazine Derivatives Targeting VEGFR-2 Enzyme. El-Helby AA; Sakr H; Ayyad RRA; El-Adl K; Ali MM; Khedr F Anticancer Agents Med Chem; 2018; 18(8):1184-1196. PubMed ID: 29651967 [TBL] [Abstract][Full Text] [Related]
8. Design, synthesis and antibreast cancer MCF-7 cells biological evaluation of heterocyclic analogs of resveratrol. Du C; Dong MH; Ren YJ; Jin L; Xu C J Asian Nat Prod Res; 2017 Sep; 19(9):890-902. PubMed ID: 27809606 [TBL] [Abstract][Full Text] [Related]
9. Novel 2-indolinone thiazole hybrids as sunitinib analogues: Design, synthesis, and potent VEGFR-2 inhibition with potential anti-renal cancer activity. Mahmoud HK; Farghaly TA; Abdulwahab HG; Al-Qurashi NT; Shaaban MR Eur J Med Chem; 2020 Dec; 208():112752. PubMed ID: 32947227 [TBL] [Abstract][Full Text] [Related]
10. Synthesis and Evaluation of 2-Naphthaleno trans-Stilbenes and Cyanostilbenes as Anticancer Agents. Madadi NR; Penthala NR; Ketkar A; Eoff RL; Trujullo-Alonso V; Guzman ML; Crooks PA Anticancer Agents Med Chem; 2018; 18(4):556-564. PubMed ID: 28403783 [TBL] [Abstract][Full Text] [Related]
11. Development of 13H-benzo[f]chromeno[4,3-b][1,7]naphthyridines and their salts as potent cytotoxic agents and topoisomerase I/IIα inhibitors. Arepalli SK; Lee C; Sim S; Lee K; Jo H; Jun KY; Kwon Y; Kang JS; Jung JK; Lee H Bioorg Med Chem; 2018 Oct; 26(18):5181-5193. PubMed ID: 30253887 [TBL] [Abstract][Full Text] [Related]
12. Design, synthesis and biological evaluation of indeno[1,2-d]thiazole derivatives as potent histone deacetylase inhibitors. Zhou M; Ning C; Liu R; He Y; Yu N Bioorg Med Chem Lett; 2013 Jun; 23(11):3200-3. PubMed ID: 23639537 [TBL] [Abstract][Full Text] [Related]
13. New thiazole-2(3H)-thiones containing 4-(3,4,5-trimethoxyphenyl) moiety as anticancer agents. Ansari M; Shokrzadeh M; Karima S; Rajaei S; Fallah M; Ghassemi-Barghi N; Ghasemian M; Emami S Eur J Med Chem; 2020 Jan; 185():111784. PubMed ID: 31669850 [TBL] [Abstract][Full Text] [Related]
14. Synthesis and biological evaluation of thiazole derivatives as novel USP7 inhibitors. Chen C; Song J; Wang J; Xu C; Chen C; Gu W; Sun H; Wen X Bioorg Med Chem Lett; 2017 Feb; 27(4):845-849. PubMed ID: 28108249 [TBL] [Abstract][Full Text] [Related]
15. Design, synthesis and anticancer evaluation of acridine hydroxamic acid derivatives as dual Topo and HDAC inhibitors. Chen J; Li D; Li W; Yin J; Zhang Y; Yuan Z; Gao C; Liu F; Jiang Y Bioorg Med Chem; 2018 Aug; 26(14):3958-3966. PubMed ID: 29954683 [TBL] [Abstract][Full Text] [Related]
16. A New Series of Antileukemic Agents: Design, Synthesis, In Vitro and In Silico Evaluation of Thiazole-Based ABL1 Kinase Inhibitors. Zeytün E; Altıntop MD; Sever B; Özdemir A; Ellakwa DE; Ocak Z; Ciftci HI; Otsuka M; Fujita M; Radwan MO Anticancer Agents Med Chem; 2021; 21(9):1099-1109. PubMed ID: 32838725 [TBL] [Abstract][Full Text] [Related]
17. Dihydroxylated 2,4,6-triphenyl pyridines: synthesis, topoisomerase I and II inhibitory activity, cytotoxicity, and structure-activity relationship study. Karki R; Thapa P; Yoo HY; Kadayat TM; Park PH; Na Y; Lee E; Jeon KH; Cho WJ; Choi H; Kwon Y; Lee ES Eur J Med Chem; 2012 Mar; 49():219-28. PubMed ID: 22318164 [TBL] [Abstract][Full Text] [Related]
18. Nanomolar potency of imidazo[2,1-b]thiazole analogs as indoleamine 2,3-dioxygenase inhibitors. Ewida MA; Ewida HA; Ahmed MS; Allam HA; ElBagary RI; George RF; Georgey HH; El-Subbagh HI Arch Pharm (Weinheim); 2021 Nov; 354(11):e2100202. PubMed ID: 34313342 [TBL] [Abstract][Full Text] [Related]
19. Design, synthesis, molecular docking and anti-proliferative evaluations of [1,2,4]triazolo[4,3-a]quinoxaline derivatives as DNA intercalators and Topoisomerase II inhibitors. El-Adl K; El-Helby AA; Sakr H; Elwan A Bioorg Chem; 2020 Dec; 105():104399. PubMed ID: 33113414 [TBL] [Abstract][Full Text] [Related]
20. Discovery of 4-alkoxy-2-aryl-6,7-dimethoxyquinolines as a new class of topoisomerase I inhibitors endowed with potent in vitro anticancer activity. Elbadawi MM; Eldehna WM; Wang W; Agama KK; Pommier Y; Abe M Eur J Med Chem; 2021 Apr; 215():113261. PubMed ID: 33631697 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]