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Journal Abstract Search

281 related items for PubMed ID: 30472605

  • 1. Synthesis and evaluation of chalcone analogues containing a 4-oxoquinazolin-2-yl group as potential anti-tumor agents.
    Han X, Peng B, Xiao BB, Sheng-Li Cao, Yang CR, Wang WZ, Wang FC, Li HY, Yuan XL, Shi R, Liao J, Wang H, Li J, Xu X.
    Eur J Med Chem; 2019 Jan 15; 162():586-601. PubMed ID: 30472605
    [Abstract] [Full Text] [Related]

  • 2. Synthesis and cytotoxic activity of chalcone analogues containing a thieno[2,3-d]pyrimidin-2-yl group as the A-ring or B-ring.
    Wang FC, Peng B, Cao SL, Li HY, Yuan XL, Zhang TT, Shi R, Li Z, Liao J, Wang H, Li J, Xu X.
    Bioorg Chem; 2020 Jan 15; 94():103346. PubMed ID: 31645277
    [Abstract] [Full Text] [Related]

  • 3. Design, synthesis and QSAR study of 2'-hydroxy-4'-alkoxy chalcone derivatives that exert cytotoxic activity by the mitochondrial apoptotic pathway.
    Marquina S, Maldonado-Santiago M, Sánchez-Carranza JN, Antúnez-Mojica M, González-Maya L, Razo-Hernández RS, Alvarez L.
    Bioorg Med Chem; 2019 Jan 01; 27(1):43-54. PubMed ID: 30482548
    [Abstract] [Full Text] [Related]

  • 4. Design and Synthesis of DNA-Interactive β-Carboline-Oxindole Hybrids as Cytotoxic and Apoptosis-Inducing Agents.
    Tokala R, Thatikonda S, Vanteddu US, Sana S, Godugu C, Shankaraiah N.
    ChemMedChem; 2018 Sep 19; 13(18):1909-1922. PubMed ID: 30010248
    [Abstract] [Full Text] [Related]

  • 5. Synthesis of novel β-carboline based chalcones with high cytotoxic activity against breast cancer cells.
    Chauhan SS, Singh AK, Meena S, Lohani M, Singh A, Arya RK, Cheruvu SH, Sarkar J, Gayen JR, Datta D, Chauhan PM.
    Bioorg Med Chem Lett; 2014 Jul 01; 24(13):2820-4. PubMed ID: 24844196
    [Abstract] [Full Text] [Related]

  • 6. Design, Synthesis, and Antiproliferative Activity of Quinazolin-4-One/Chalcone Hybrids via the EGFR Inhibition Pathway.
    Hisham M, Hassan HA, Gomaa HAM, Youssif BGM, Hayalah AM, Abdel-Aziz M.
    Anticancer Agents Med Chem; 2023 Jul 01; 23(17):1932-1943. PubMed ID: 37497685
    [Abstract] [Full Text] [Related]

  • 7. 3-Aminomethyl pyridine chalcone derivatives: Design, synthesis, DNA binding and cytotoxic studies.
    Durgapal SD, Soni R, Umar S, Suresh B, Soman SS.
    Chem Biol Drug Des; 2018 Jul 01; 92(1):1279-1287. PubMed ID: 29575807
    [Abstract] [Full Text] [Related]

  • 8. Novel 1-(7-ethoxy-1-benzofuran-2-yl) substituted chalcone derivatives: Synthesis, characterization and anticancer activity.
    Coskun D, Erkisa M, Ulukaya E, Coskun MF, Ari F.
    Eur J Med Chem; 2017 Aug 18; 136():212-222. PubMed ID: 28494257
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  • 11. Synthesis and biological evaluation of benzo[d][1,3]dioxol-5-yl chalcones as antiproliferating agents.
    Kamal A, Balakrishna M, Loka Reddy V, Riyaz S, Bagul C, Satyanarayana BM, Venkateswar Rao J.
    Chem Biol Drug Des; 2015 Nov 18; 86(5):1267-84. PubMed ID: 26032623
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  • 14. The synthetic flavanone 6-methoxy-2-(naphthalen-1-yl)chroman-4-one induces apoptosis and activation of the MAPK pathway in human U-937 leukaemia cells.
    Saavedra E, Del Rosario H, Brouard I, Hernández-Garcés J, García C, Quintana J, Estévez F.
    Bioorg Chem; 2020 Jan 18; 94():103450. PubMed ID: 31785856
    [Abstract] [Full Text] [Related]

  • 15. (E)-N'-Arylidene-2-(4-oxoquinazolin-4(3H)-yl) acetohydrazides: Synthesis and evaluation of antitumor cytotoxicity and caspase activation activity.
    Huan LC, Phuong CV, Truc LC, Thanh VN, Pham-The H, Huong LT, Thuan NT, Park EJ, Ji AY, Kang JS, Han SB, Tran PT, Nam NH.
    J Enzyme Inhib Med Chem; 2019 Dec 18; 34(1):465-478. PubMed ID: 30734614
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  • 16. Chalcones with electron-withdrawing and electron-donating substituents: anticancer activity against TRAIL resistant cancer cells, structure-activity relationship analysis and regulation of apoptotic proteins.
    Mai CW, Yaeghoobi M, Abd-Rahman N, Kang YB, Pichika MR.
    Eur J Med Chem; 2014 Apr 22; 77():378-87. PubMed ID: 24675137
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  • 18. Synthesis of carbazole derivatives containing chalcone analogs as non-intercalative topoisomerase II catalytic inhibitors and apoptosis inducers.
    Li PH, Jiang H, Zhang WJ, Li YL, Zhao MC, Zhou W, Zhang LY, Tang YD, Dong CZ, Huang ZS, Chen HX, Du ZY.
    Eur J Med Chem; 2018 Feb 10; 145():498-510. PubMed ID: 29335211
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  • 19. Novel ciprofloxacin hybrids using biology oriented drug synthesis (BIODS) approach: Anticancer activity, effects on cell cycle profile, caspase-3 mediated apoptosis, topoisomerase II inhibition, and antibacterial activity.
    Kassab AE, Gedawy EM.
    Eur J Med Chem; 2018 Apr 25; 150():403-418. PubMed ID: 29547830
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  • 20. Synthesis of phenstatin/isocombretastatin-chalcone conjugates as potent tubulin polymerization inhibitors and mitochondrial apoptotic inducers.
    Kamal A, Kumar GB, Vishnuvardhan MV, Shaik AB, Reddy VS, Mahesh R, Sayeeda IB, Kapure JS.
    Org Biomol Chem; 2015 Apr 07; 13(13):3963-81. PubMed ID: 25721862
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