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Journal Abstract Search

288 related items for PubMed ID: 30961509

  • 1. Novel Curcumin Inspired Antineoplastic 1-Sulfonyl-4-Piperidones: Design, Synthesis and Molecular Modeling Studies.
    Fawzy NG, Panda SS, Fayad W, El-Manawaty MA, Srour AM, Girgis AS.
    Anticancer Agents Med Chem; 2019; 19(8):1069-1078. PubMed ID: 30961509
    [Abstract] [Full Text] [Related]

  • 2. Synthesis, human topoisomerase IIα inhibitory properties and molecular modeling studies of anti-proliferative curcumin mimics.
    Fawzy NG, Panda SS, Fayad W, Shalaby EM, Srour AM, Girgis AS.
    RSC Adv; 2019 Oct 18; 9(58):33761-33774. PubMed ID: 35528906
    [Abstract] [Full Text] [Related]

  • 3. Synthesis of aspirin-curcumin mimic conjugates of potential antitumor and anti-SARS-CoV-2 properties.
    Srour AM, Panda SS, Mostafa A, Fayad W, El-Manawaty MA, A F Soliman A, Moatasim Y, El Taweel A, Abdelhameed MF, Bekheit MS, Ali MA, Girgis AS.
    Bioorg Chem; 2021 Dec 18; 117():105466. PubMed ID: 34775204
    [Abstract] [Full Text] [Related]

  • 4. Synthesis and evaluation of anticancer and antiobesity activity of 1-ethoxy carbonyl-3,5-bis (3'-indolyl methylene)-4-pyperidone analogs.
    Buduma K, Chinde S, Dommati AK, Sharma P, Shukla A, Srinivas KVNS, Arigari NK, Khan F, Tiwari AK, Grover P, Jonnala KK.
    Bioorg Med Chem Lett; 2016 Mar 15; 26(6):1633-1638. PubMed ID: 26873414
    [Abstract] [Full Text] [Related]

  • 5. Novel 3,5-bis(arylidene)-4-piperidone dimers: potent cytotoxins against colon cancer cells.
    Das S, Das U, Michel D, Gorecki DK, Dimmock JR.
    Eur J Med Chem; 2013 Jun 15; 64():321-8. PubMed ID: 23644215
    [Abstract] [Full Text] [Related]

  • 6. Design, synthesis and bioevaluation of novel N-substituted-3,5-bis(arylidene)-4-piperidone derivatives as cytotoxic and antitumor agents with fluorescent properties.
    Sun J, Zhang S, Yu C, Hou G, Zhang X, Li K, Zhao F.
    Chem Biol Drug Des; 2014 Apr 15; 83(4):392-400. PubMed ID: 24148151
    [Abstract] [Full Text] [Related]

  • 7. Curcumin-inspired cytotoxic 3,5-bis(arylmethylene)-1-(N-(ortho-substituted aryl)maleamoyl)-4-piperidones: A novel group of topoisomerase II alpha inhibitors.
    Jha A, Duffield KM, Ness MR, Ravoori S, Andrews G, Bhullar KS, Rupasinghe HP, Balzarini J.
    Bioorg Med Chem; 2015 Oct 01; 23(19):6404-17. PubMed ID: 26456623
    [Abstract] [Full Text] [Related]

  • 8. Novel thiazolidines: Synthesis, antiproliferative properties and 2D-QSAR studies.
    Singh RP, Aziz MN, Gout D, Fayad W, El-Manawaty MA, Lovely CJ.
    Bioorg Med Chem; 2019 Oct 15; 27(20):115047. PubMed ID: 31471102
    [Abstract] [Full Text] [Related]

  • 9. Halogenated Bis(methoxybenzylidene)-4-piperidone Curcuminoids with Improved Anticancer Activity.
    Schmitt F, Subramaniam D, Anant S, Padhye S, Begemann G, Schobert R, Biersack B.
    ChemMedChem; 2018 Jun 06; 13(11):1115-1123. PubMed ID: 29570947
    [Abstract] [Full Text] [Related]

  • 10. All trans 1-(3-arylacryloyl)-3,5-bis(pyridin-4-ylmethylene)piperidin-4-ones as curcumin-inspired antineoplastics.
    Paul NK, Jha M, Bhullar KS, Rupasinghe HP, Balzarini J, Jha A.
    Eur J Med Chem; 2014 Nov 24; 87():461-70. PubMed ID: 25282269
    [Abstract] [Full Text] [Related]

  • 11. Design, synthesis and cytotoxic properties of novel 1-[4-(2-alkylaminoethoxy)phenylcarbonyl]-3,5-bis(arylidene)-4-piperidones and related compounds.
    Das U, Alcorn J, Shrivastav A, Sharma RK, De Clercq E, Balzarini J, Dimmock JR.
    Eur J Med Chem; 2007 Jan 24; 42(1):71-80. PubMed ID: 16996657
    [Abstract] [Full Text] [Related]

  • 12. Synthesis and anticancer evaluation of furfurylidene 4-piperidone analogs.
    Jadhav RL, Magdum CS, Patil MV.
    Arch Pharm (Weinheim); 2014 Jun 24; 347(6):407-14. PubMed ID: 24623392
    [Abstract] [Full Text] [Related]

  • 13. Synthesis, antitumor activity evaluation of some new N-aroyl-α,β-unsaturated piperidones with fluorescence.
    Sun J, Wang S, Li H, Jiang W, Hou G, Zhao F, Cong W.
    J Enzyme Inhib Med Chem; 2016 Jun 24; 31(3):495-502. PubMed ID: 26382011
    [Abstract] [Full Text] [Related]

  • 14. Molecular Hybrid Design, Synthesis, In Vitro Cytotoxicity, In Silico ADME and Molecular Docking Studies of New Benzoate Ester-Linked Arylsulfonyl Hydrazones.
    Ergan E, Çakmak R, Başaran E, Mali SN, Akkoc S, Annadurai S.
    Molecules; 2024 Jul 25; 29(15):. PubMed ID: 39124882
    [Abstract] [Full Text] [Related]

  • 15. Synthesis and Biological Evaluations of Monocarbonyl Curcumin Inspired Pyrazole Analogues as Potential Anti-Colon Cancer Agent.
    Min Z, Zhu Y, Hong X, Yu Z, Ye M, Yuan Q, Hu X.
    Drug Des Devel Ther; 2020 Jul 25; 14():2517-2534. PubMed ID: 32636614
    [Abstract] [Full Text] [Related]

  • 16. Synthesis and biological evaluation of curcumin inspired imidazo[1,2-a]pyridine analogues as tubulin polymerization inhibitors.
    Ramya PVS, Guntuku L, Angapelly S, Digwal CS, Lakshmi UJ, Sigalapalli DK, Babu BN, Naidu VGM, Kamal A.
    Eur J Med Chem; 2018 Jan 01; 143():216-231. PubMed ID: 29174816
    [Abstract] [Full Text] [Related]

  • 17. Tumour-specific cytotoxicity and structure-activity relationships of novel 1-[3-(2-methoxyethylthio)propionyl]-3,5-bis(benzylidene)-4-piperidones.
    Hossain M, Das U, Umemura N, Sakagami H, Balzarini J, De Clercq E, Kawase M, Dimmock JR.
    Bioorg Med Chem; 2016 May 15; 24(10):2206-14. PubMed ID: 27073056
    [Abstract] [Full Text] [Related]

  • 18. Design, Synthesis and Antiproliferative Activities of Oxidative Stress Inducers Based on 2-Styryl-3,5-dihydro-4H-imidazol-4-one Scaffold.
    Omar AM, Abdelghany TM, Abdel-Bakky MS, Alahdal AM, Radwan MF, El-Araby ME.
    Chem Pharm Bull (Tokyo); 2018 Oct 01; 66(10):967-975. PubMed ID: 30047515
    [Abstract] [Full Text] [Related]

  • 19. Synthesis and biological evaluation of allylated mono-carbonyl analogues of curcumin (MACs) as anti-cancer agents for cholangiocarcinoma.
    Qiu C, Hu Y, Wu K, Yang K, Wang N, Ma Y, Zhu H, Zhang Y, Zhou Y, Chen C, Li S, Fu L, Zhang X, Liu Z.
    Bioorg Med Chem Lett; 2016 Dec 15; 26(24):5971-5976. PubMed ID: 27825763
    [Abstract] [Full Text] [Related]

  • 20. Synthesis and biological evaluation of curcumin derivatives modified with α-amino boronic acid as proteasome inhibitors.
    Zhang W, Bai H, Han L, Zhang H, Xu B, Cui J, Wang X, Ge Z, Li R.
    Bioorg Med Chem Lett; 2018 Aug 01; 28(14):2459-2464. PubMed ID: 29886021
    [Abstract] [Full Text] [Related]

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