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.
46. Quadruplex-interactive agents as telomerase inhibitors: synthesis of porphyrins and structure-activity relationship for the inhibition of telomerase. Shi DF; Wheelhouse RT; Sun D; Hurley LH J Med Chem; 2001 Dec; 44(26):4509-23. PubMed ID: 11741471 [TBL] [Abstract][Full Text] [Related]
47. The number and distances of positive charges of polyamine side chains in a series of perylene diimides significantly influence their ability to induce G-quadruplex structures and inhibit human telomerase. Franceschin M; Lombardo CM; Pascucci E; D'Ambrosio D; Micheli E; Bianco A; Ortaggi G; Savino M Bioorg Med Chem; 2008 Mar; 16(5):2292-304. PubMed ID: 18165014 [TBL] [Abstract][Full Text] [Related]
48. Cyclic ferrocenylnaphthalene diimide derivative as a new class of G-quadruplex DNA binding ligand. Islam MM; Sato S; Shinozaki S; Takenaka S Bioorg Med Chem Lett; 2017 Jan; 27(2):329-335. PubMed ID: 27899264 [TBL] [Abstract][Full Text] [Related]
49. Structure-activity relationships among guanine-quadruplex telomerase inhibitors. Neidle S; Harrison RJ; Reszka AP; Read MA Pharmacol Ther; 2000 Mar; 85(3):133-9. PubMed ID: 10739868 [TBL] [Abstract][Full Text] [Related]
51. Rational design of acridine-based ligands with selectivity for human telomeric quadruplexes. Sparapani S; Haider SM; Doria F; Gunaratnam M; Neidle S J Am Chem Soc; 2010 Sep; 132(35):12263-72. PubMed ID: 20718414 [TBL] [Abstract][Full Text] [Related]
52. Selective recognition and stabilization of new ligands targeting the potassium form of the human telomeric G-quadruplex DNA. Lin YH; Chuang SM; Wu PC; Chen CL; Jeyachandran S; Lo SC; Huang HS; Hou MH Sci Rep; 2016 Aug; 6():31019. PubMed ID: 27511133 [TBL] [Abstract][Full Text] [Related]
53. Selective interaction of ethidium derivatives with quadruplexes: an equilibrium dialysis and electrospray ionization mass spectrometry analysis. Rosu F; De Pauw E; Guittat L; Alberti P; Lacroix L; Mailliet P; Riou JF; Mergny JL Biochemistry; 2003 Sep; 42(35):10361-71. PubMed ID: 12950163 [TBL] [Abstract][Full Text] [Related]
54. Human telomerase inhibition by substituted acridine derivatives. Harrison RJ; Gowan SM; Kelland LR; Neidle S Bioorg Med Chem Lett; 1999 Sep; 9(17):2463-8. PubMed ID: 10498189 [TBL] [Abstract][Full Text] [Related]
55. Platinum squares with high selectivity and affinity for human telomeric G-quadruplexes. Zheng XH; Chen HY; Tong ML; Ji LN; Mao ZW Chem Commun (Camb); 2012 Aug; 48(61):7607-9. PubMed ID: 22728887 [TBL] [Abstract][Full Text] [Related]
56. G-quadruplex DNA: a target for drug design. Mergny JL; Hélène C Nat Med; 1998 Dec; 4(12):1366-7. PubMed ID: 9846570 [No Abstract] [Full Text] [Related]
57. Stabilization of G-quadruplex DNA, inhibition of telomerase activity and live cell imaging studies of chiral ruthenium(II) complexes. Sun D; Liu Y; Liu D; Zhang R; Yang X; Liu J Chemistry; 2012 Apr; 18(14):4285-95. PubMed ID: 22367788 [TBL] [Abstract][Full Text] [Related]
58. Trisubstituted acridine derivatives as potent and selective telomerase inhibitors. Harrison RJ; Cuesta J; Chessari G; Read MA; Basra SK; Reszka AP; Morrell J; Gowan SM; Incles CM; Tanious FA; Wilson WD; Kelland LR; Neidle S J Med Chem; 2003 Oct; 46(21):4463-76. PubMed ID: 14521409 [TBL] [Abstract][Full Text] [Related]
59. Synthetic 2'-O-methyl-modified hammerhead ribozymes targeted to the RNA component of telomerase as sequence-specific inhibitors of telomerase activity. Wan MS; Fell PL; Akhtar S Antisense Nucleic Acid Drug Dev; 1998 Aug; 8(4):309-17. PubMed ID: 9743468 [TBL] [Abstract][Full Text] [Related]
60. Cyclic perylene diimide: Selective ligand for tetraplex DNA binding over double stranded DNA. Vasimalla S; Sato S; Takenaka F; Kurose Y; Takenaka S Bioorg Med Chem; 2017 Dec; 25(24):6404-6411. PubMed ID: 29089258 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]