BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

253 related articles for article (PubMed ID: 28743509)

  • 1. Synthesis and evaluation of modified chalcone based p53 stabilizing agents.
    Iftikhar S; Khan S; Bilal A; Manzoor S; Abdullah M; Emwas AH; Sioud S; Gao X; Chotana GA; Faisal A; Saleem RSZ
    Bioorg Med Chem Lett; 2017 Sep; 27(17):4101-4106. PubMed ID: 28743509
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Synthesis and anti-proliferative activity of fluoro-substituted chalcones.
    Burmaoglu S; Algul O; Anıl DA; Gobek A; Duran GG; Ersan RH; Duran N
    Bioorg Med Chem Lett; 2016 Jul; 26(13):3172-3176. PubMed ID: 27217001
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Anti-breast cancer activity of heteroaryl chalcone derivatives.
    Solomon VR; Lee H
    Biomed Pharmacother; 2012 Apr; 66(3):213-20. PubMed ID: 22440895
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Synthesis, biological evaluation and molecular docking studies of aminochalcone derivatives as potential anticancer agents by targeting tubulin colchicine binding site.
    Wang G; Peng Z; Zhang J; Qiu J; Xie Z; Gong Z
    Bioorg Chem; 2018 Aug; 78():332-340. PubMed ID: 29627654
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Design and multi-step synthesis of chalcone-polyamine conjugates as potent antiproliferative agents.
    Rioux B; Pouget C; Fidanzi-Dugas C; Gamond A; Laurent A; Semaan J; Pinon A; Champavier Y; Léger DY; Liagre B; Duroux JL; Fagnère C; Sol V
    Bioorg Med Chem Lett; 2017 Sep; 27(18):4354-4357. PubMed ID: 28838697
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Synthesis and evaluation of novel α-substituted chalcones with potent anti-cancer activities and ability to overcome multidrug resistance.
    Riaz S; Iqbal M; Ullah R; Zahra R; Chotana GA; Faisal A; Saleem RSZ
    Bioorg Chem; 2019 Jun; 87():123-135. PubMed ID: 30884306
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Design, synthesis, characterization, and anticancer activity of a novel series of O-substituted chalcone derivatives.
    Ngameni B; Cedric K; Mbaveng AT; Erdoğan M; Simo I; Kuete V; Daştan A
    Bioorg Med Chem Lett; 2021 Mar; 35():127827. PubMed ID: 33508467
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Synthesis and biological evaluation of novel synthetic chalcone derivatives as anti-tumor agents targeting Cat L and Cat K.
    Wang Y; Xue S; Li R; Zheng Z; Yi H; Li Z
    Bioorg Med Chem; 2018 Jan; 26(1):8-16. PubMed ID: 29223717
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Anti-proliferative effect of chalcone derivatives through inactivation of NF-κB in human cancer cells.
    Venkateswararao E; Sharma VK; Yun J; Kim Y; Jung SH
    Bioorg Med Chem; 2014 Jul; 22(13):3386-92. PubMed ID: 24835787
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Synthesis and anti-cancer activity evaluation of novel prenylated and geranylated chalcone natural products and their analogs.
    Wang HM; Zhang L; Liu J; Yang ZL; Zhao HY; Yang Y; Shen D; Lu K; Fan ZC; Yao QW; Zhang YM; Teng YO; Peng Y
    Eur J Med Chem; 2015 Mar; 92():439-48. PubMed ID: 25590864
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Targeting the MDM2-p53 protein-protein interaction with prenylchalcones: Synthesis of a small library and evaluation of potential antitumor activity.
    Brandão P; Loureiro JB; Carvalho S; Hamadou MH; Cravo S; Moreira J; Pereira D; Palmeira A; Pinto M; Saraiva L; Cidade H
    Eur J Med Chem; 2018 Aug; 156():711-721. PubMed ID: 30041135
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Synthetic chalcone derivatives as inhibitors of cathepsins K and B, and their cytotoxic evaluation.
    Ramalho SD; Bernades A; Demetrius G; Noda-Perez C; Vieira PC; Dos Santos CY; da Silva JA; de Moraes MO; Mousinho KC
    Chem Biodivers; 2013 Nov; 10(11):1999-2006. PubMed ID: 24243608
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Design, Synthesis, and Biological Evaluation of Aromatic Amide-Substituted Benzimidazole-Derived Chalcones. The Effect of Upregulating
    Wu L; Yang Y; Wang Z; Wu X; Su F; Li M; Jing X; Han C
    Molecules; 2020 Mar; 25(5):. PubMed ID: 32150865
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Discovery of thiazole-based-chalcones and 4-hetarylthiazoles as potent anticancer agents: Synthesis, docking study and anticancer activity.
    Farghaly TA; Masaret GS; Muhammad ZA; Harras MF
    Bioorg Chem; 2020 May; 98():103761. PubMed ID: 32200332
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Chalcone derivatives targeting mitosis: synthesis, evaluation of antitumor activity and lipophilicity.
    Pinto P; Machado CM; Moreira J; Almeida JDP; Silva PMA; Henriques AC; Soares JX; Salvador JAR; Afonso C; Pinto M; Bousbaa H; Cidade H
    Eur J Med Chem; 2019 Dec; 184():111752. PubMed ID: 31610374
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Synthesis, Characterization, and Biological Study of 3-Trifluoromethylpyrazole Tethered Chalcone-Pyrrole and Pyrazoline-Pyrrole Derivatives.
    Kisan Rasal N; Bhaskar Sonawane R; Vijay Jagtap S
    Chem Biodivers; 2021 Oct; 18(10):e2100504. PubMed ID: 34409724
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 136():212-222. PubMed ID: 28494257
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A new chalcone derivative (E)-3-(4-methoxyphenyl)-2-methyl-1-(3,4,5-trimethoxyphenyl)prop-2-en-1-one suppresses prostate cancer involving p53-mediated cell cycle arrests and apoptosis.
    Zhang Y; Srinivasan B; Xing C; Lü J
    Anticancer Res; 2012 Sep; 32(9):3689-98. PubMed ID: 22993307
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Design, synthesis, and biological evaluation of imidazoline derivatives as p53-MDM2 binding inhibitors.
    Hu C; Li X; Wang W; Zhang L; Tao L; Dong X; Sheng R; Yang B; Hu Y
    Bioorg Med Chem; 2011 Sep; 19(18):5454-61. PubMed ID: 21855354
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cytotoxicity, molecular modeling, cell cycle arrest, and apoptotic induction induced by novel tetrahydro-[1,2,4]triazolo[3,4-a]isoquinoline chalcones.
    Mohamed MF; Hassaneen HM; Abdelhamid IA
    Eur J Med Chem; 2018 Jan; 143():532-541. PubMed ID: 29207336
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.