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.
232 related articles for article (PubMed ID: 19155103)
1. DNA-targeting pyrroloquinoline-linked butenone and chalcones: synthesis and biological evaluation. Dalla Via L; Gia O; Chiarelotto G; Ferlin MG Eur J Med Chem; 2009 Jul; 44(7):2854-61. PubMed ID: 19155103 [TBL] [Abstract][Full Text] [Related]
2. DNA binding ellipticine analogues: synthesis, biological evaluation, and structure-activity relationships. Ferlin MG; Marzano C; Gandin V; Dall'Acqua S; Dalla Via L ChemMedChem; 2009 Mar; 4(3):363-77. PubMed ID: 19197924 [TBL] [Abstract][Full Text] [Related]
3. Synthesis and biological evaluation of indolyl chalcones as antitumor agents. Kumar D; Kumar NM; Akamatsu K; Kusaka E; Harada H; Ito T Bioorg Med Chem Lett; 2010 Jul; 20(13):3916-9. PubMed ID: 20627724 [TBL] [Abstract][Full Text] [Related]
4. Synthesis and antitumor characterization of pyrazolic analogues of the marine pyrroloquinoline alkaloids: wakayin and tsitsikammamines. Legentil L; Benel L; Bertrand V; Lesur B; Delfourne E J Med Chem; 2006 May; 49(10):2979-88. PubMed ID: 16686539 [TBL] [Abstract][Full Text] [Related]
5. Cytotoxic activity of 4'-hydroxychalcone derivatives against Jurkat cells and their effects on mammalian DNA topoisomerase I. Gul HI; Cizmecioglu M; Zencir S; Gul M; Canturk P; Atalay M; Topcu Z J Enzyme Inhib Med Chem; 2009 Jun; 24(3):804-7. PubMed ID: 18830876 [TBL] [Abstract][Full Text] [Related]
6. Synthesis and topoisomerase II inhibitory and cytotoxic activity of oxiranylmethoxy- and thiiranylmethoxy-chalcone derivatives. Na Y; Nam JM Bioorg Med Chem Lett; 2011 Jan; 21(1):211-4. PubMed ID: 21115246 [TBL] [Abstract][Full Text] [Related]
7. Quinolinyl and quinolinyl N-oxide chalcones: synthesis, antifungal and cytotoxic activities. de Carvalho Tavares L; Johann S; Maria de Almeida Alves T; Guerra JC; Maria de Souza-Fagundes E; Cisalpino PS; Bortoluzzi AJ; Caramori GF; de Mattos Piccoli R; Braibante HT; Braibante ME; Pizzolatti MG Eur J Med Chem; 2011 Sep; 46(9):4448-56. PubMed ID: 21816519 [TBL] [Abstract][Full Text] [Related]
8. New water soluble pyrroloquinoline derivatives as new potential anticancer agents. Ferlin MG; Marzano C; Dalla Via L; Chilin A; Zagotto G; Guiotto A; Moro S Bioorg Med Chem; 2005 Aug; 13(15):4733-9. PubMed ID: 15936202 [TBL] [Abstract][Full Text] [Related]
9. Novel antitumor indenoindole derivatives targeting DNA and topoisomerase II. Bal C; Baldeyrou B; Moz F; Lansiaux A; Colson P; Kraus-Berthier L; Léonce S; Pierré A; Boussard MF; Rousseau A; Wierzbicki M; Bailly C Biochem Pharmacol; 2004 Nov; 68(10):1911-22. PubMed ID: 15476662 [TBL] [Abstract][Full Text] [Related]
10. Synthesis and in vitro and in vivo antitumor activity of 2-phenylpyrroloquinolin-4-ones. Ferlin MG; Chiarelotto G; Gasparotto V; Dalla Via L; Pezzi V; Barzon L; Palù G; Castagliuolo I J Med Chem; 2005 May; 48(9):3417-27. PubMed ID: 15857148 [TBL] [Abstract][Full Text] [Related]
11. Novel tetra-acridine derivatives as dual inhibitors of topoisomerase II and the human proteasome. Vispé S; Vandenberghe I; Robin M; Annereau JP; Créancier L; Pique V; Galy JP; Kruczynski A; Barret JM; Bailly C Biochem Pharmacol; 2007 Jun; 73(12):1863-72. PubMed ID: 17391647 [TBL] [Abstract][Full Text] [Related]
12. Synthesis and biological evaluation of 3',4',5'-trimethoxychalcone analogues as inhibitors of nitric oxide production and tumor cell proliferation. Rao YK; Fang SH; Tzeng YM Bioorg Med Chem; 2009 Dec; 17(23):7909-14. PubMed ID: 19875299 [TBL] [Abstract][Full Text] [Related]
13. Synthesis and biological evaluation of simple methoxylated chalcones as anticancer, anti-inflammatory and antioxidant agents. Bandgar BP; Gawande SS; Bodade RG; Totre JV; Khobragade CN Bioorg Med Chem; 2010 Feb; 18(3):1364-70. PubMed ID: 20064725 [TBL] [Abstract][Full Text] [Related]
14. Differential effects of synthesized 2'-oxygenated chalcone derivatives: modulation of human cell cycle phase distribution. Rao YK; Fang SH; Tzeng YM Bioorg Med Chem; 2004 May; 12(10):2679-86. PubMed ID: 15110849 [TBL] [Abstract][Full Text] [Related]
15. Synthesis and biological evaluation of pyrroloiminoquinone derivatives. Passarella D; Belinghieri F; Scarpellini M; Pratesi G; Zunino F; Gia OM; Via LD; Santoro G; Danieli B Bioorg Med Chem; 2008 Mar; 16(5):2431-8. PubMed ID: 18077173 [TBL] [Abstract][Full Text] [Related]
16. Synthesis and antitumoral activity of novel thiazolobenzotriazole, thiazoloindolo[3,2-c]quinoline and quinolinoquinoline derivatives. Beauchard A; Jaunet A; Murillo L; Baldeyrou B; Lansiaux A; Chérouvrier JR; Domon L; Picot L; Bailly C; Besson T; Thiéry V Eur J Med Chem; 2009 Oct; 44(10):3858-65. PubMed ID: 19427714 [TBL] [Abstract][Full Text] [Related]
17. Structure-activity studies of novel amidine analogues of chlorambucil: correlation of cytotoxic activity with DNA-binding affinity and topoisomerase II inhibition. Bielawska A; Bielawski K; Wołczyński S; Anchim T Arch Pharm (Weinheim); 2003 Aug; 336(6-7):293-9. PubMed ID: 12953217 [TBL] [Abstract][Full Text] [Related]
18. Synthesis and biological screening of a combinatorial library of beta-chlorovinyl chalcones as anticancer, anti-inflammatory and antimicrobial agents. Bandgar BP; Gawande SS Bioorg Med Chem; 2010 Mar; 18(5):2060-5. PubMed ID: 20138527 [TBL] [Abstract][Full Text] [Related]
19. Design, synthesis, and biological evaluation of Mannich bases of heterocyclic chalcone analogs as cytotoxic agents. Reddy MV; Su CR; Chiou WF; Liu YN; Chen RY; Bastow KF; Lee KH; Wu TS Bioorg Med Chem; 2008 Aug; 16(15):7358-70. PubMed ID: 18602831 [TBL] [Abstract][Full Text] [Related]
20. Synthesis, cytotoxicity, DNA interaction, and topoisomerase II inhibition properties of novel indeno[2,1-c]quinolin-7-one and indeno[1,2-c]isoquinolin-5,11-dione derivatives. Ryckebusch A; Garcin D; Lansiaux A; Goossens JF; Baldeyrou B; Houssin R; Bailly C; Hénichart JP J Med Chem; 2008 Jun; 51(12):3617-29. PubMed ID: 18507368 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]