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Journal of Natural Products
|
December 20, 2008
Bioactive pyridine-N-oxide disulfides from Allium stipitatum
Gemma O'Donnell, Rosemarie Poeschl, Oren Zimhony, et al.
Scientific Reports
|
April 9, 2015
KRAS oncogene repression in colon cancer cell lines by G-quadruplex binding indolo[3,2-c]quinolines
João Lavrado, Hugo Brito, Pedro M Borralho, et al.
Chemmedchem
|
June 5, 2019
Combining 1,3-Ditriazolylbenzene and Quinoline to Discover a New G-Quadruplex-Interactive Small Molecule Active against Cancer Stem-Like Cells
Eduarda Mendes, Enrico Cadoni, Filipa Carneiro, et al.
Nucleic Acids Research
|
February 19, 2025
The G-quadruplex experimental drug QN-302 impairs liposarcoma cell growth by inhibiting MDM2 expression and restoring p53 levels
Beatrice Tosoni, Eisa Naghshineh, Irene Zanin, et al.
Journal of Medicinal Chemistry
|
May 26, 2016
Toward the Development of Specific G-Quadruplex Binders: Synthesis, Biophysical, and Biological Studies of New Hydrazone Derivatives
Jussara Amato, Rita Morigi, Bruno Pagano, et al.
Nucleic Acids Research
|
February 13, 2025
The G-quadruplex experimental drug QN-302 impairs liposarcoma cell growth by inhibiting MDM2 expression and restoring p53 levels
Beatrice Tosoni, Eisa Naghshineh, Irene Zanin, et al.
FEBS Letters
|
February 26, 2013
Observation of unphosphorylated STAT3 core protein binding to target dsDNA by PEMSA and X-ray crystallography
Edwin Nkansah, Rahi Shah, Gavin W Collie, et al.
Journal of Medicinal Chemistry
|
February 2, 2011
N-cyclic bay-substituted perylene G-quadruplex ligands have selective antiproliferative effects on cancer cells and induce telomere damage
Valentina Casagrande, Erica Salvati, Antonello Alvino, et al.
Plos One
|
May 30, 2015
Targeting KRAS Oncogene in Colon Cancer Cells with 7-Carboxylate Indolo[3,2-b]quinoline Tri-Alkylamine Derivatives
Hugo Brito, Ana Cláudia Martins, João Lavrado, et al.
Journal of Medicinal Chemistry
|
October 3, 2003
Trisubstituted acridine derivatives as potent and selective telomerase inhibitors
R John Harrison, Javier Cuesta, Gianni Chessari, et al.
Page
of 21
Search research articles
Search
Showing results (191-200 of 210) with videos related to
Sort By:
Page
of 21
Journal of Natural Products
|
December 20, 2008
Bioactive pyridine-N-oxide disulfides from Allium stipitatum
Gemma O'Donnell, Rosemarie Poeschl, Oren Zimhony, et al.
Scientific Reports
|
April 9, 2015
KRAS oncogene repression in colon cancer cell lines by G-quadruplex binding indolo[3,2-c]quinolines
João Lavrado, Hugo Brito, Pedro M Borralho, et al.
Chemmedchem
|
June 5, 2019
Combining 1,3-Ditriazolylbenzene and Quinoline to Discover a New G-Quadruplex-Interactive Small Molecule Active against Cancer Stem-Like Cells
Eduarda Mendes, Enrico Cadoni, Filipa Carneiro, et al.
Nucleic Acids Research
|
February 19, 2025
The G-quadruplex experimental drug QN-302 impairs liposarcoma cell growth by inhibiting MDM2 expression and restoring p53 levels
Beatrice Tosoni, Eisa Naghshineh, Irene Zanin, et al.
Journal of Medicinal Chemistry
|
May 26, 2016
Toward the Development of Specific G-Quadruplex Binders: Synthesis, Biophysical, and Biological Studies of New Hydrazone Derivatives
Jussara Amato, Rita Morigi, Bruno Pagano, et al.
Nucleic Acids Research
|
February 13, 2025
The G-quadruplex experimental drug QN-302 impairs liposarcoma cell growth by inhibiting MDM2 expression and restoring p53 levels
Beatrice Tosoni, Eisa Naghshineh, Irene Zanin, et al.
FEBS Letters
|
February 26, 2013
Observation of unphosphorylated STAT3 core protein binding to target dsDNA by PEMSA and X-ray crystallography
Edwin Nkansah, Rahi Shah, Gavin W Collie, et al.
Journal of Medicinal Chemistry
|
February 2, 2011
N-cyclic bay-substituted perylene G-quadruplex ligands have selective antiproliferative effects on cancer cells and induce telomere damage
Valentina Casagrande, Erica Salvati, Antonello Alvino, et al.
Plos One
|
May 30, 2015
Targeting KRAS Oncogene in Colon Cancer Cells with 7-Carboxylate Indolo[3,2-b]quinoline Tri-Alkylamine Derivatives
Hugo Brito, Ana Cláudia Martins, João Lavrado, et al.
Journal of Medicinal Chemistry
|
October 3, 2003
Trisubstituted acridine derivatives as potent and selective telomerase inhibitors
R John Harrison, Javier Cuesta, Gianni Chessari, et al.
Page
of 21