Herrera-Vazquez, FS; Matadamas-Martinez, F; Aguayo-Ortiz, R; Dominguez, L; Ramirez-Apan, T; Yepez-Mulia, L; Hernandez-Luis, F in [Herrera-Vazquez, Frida S.; Matadamas-Martinez, Felix; Hernandez-Luis, Francisco] Univ Nacl Autonoma Mexico, Dept Farm, Mexico City 04510, DF, Mexico; [Matadamas-Martinez, Felix; Yepez-Mulia, Lilian] Inst Mexicano Seguro Social, Ctr Med Nacl Siglo XXI, Unidad Med Alta Especialidad, Hosp Pediat, Mexico City 06720, DF, Mexico; [Aguayo-Ortiz, Rodrigo; Dominguez, Laura] Univ Nacl Autonoma Mexico, Dept Fisicoquim, Mexico City 04510, DF, Mexico; [Aguayo-Ortiz, Rodrigo] Univ Michigan, Dept Internal Med, Div Cardiovasc Med, Ann Arbor, MI 48109 USA; [Ramirez-Apan, Teresa] Univ Nacl Autonoma Mexico, Inst Quim, Mexico City 04510, DF, Mexico published Design, Synthesis and Evaluation of 2,4-Diaminoquinazoline Derivatives as Potential Tubulin Polymerization Inhibitors in 2020, Cited 56. Computed Properties of C7H8O2. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6.
Microtubules are highly dynamic polymers composed of alpha- and beta-tubulin proteins that have been shown to be potential therapeutic targets for the development of anticancer drugs. Currently, a wide variety of chemically diverse agents that bind to beta-tubulin have been reported. Nocodazole (NZ) and colchicine (COL) are well-known tubulin-depolymerizing agents that have close binding sites in the beta-tubulin. In this study, we designed and synthesized a set of nine 2,4-diaminoquinazoline derivatives that could occupy both NZ and COL binding sites. The synthesized compounds were evaluated for their antiproliferative activities against five cancer cell lines (PC-3, HCT-15, MCF-7, MDA-MB-231, and SK-LU-1), a noncancerous one (COS-7), and peripheral blood mononuclear cells (PBMC). The effect of compounds4 eand4 ion tubulin organization and polymerization was analyzed on the SK-LU-1 cell line by indirect immunofluorescence, western blotting, and tubulin polymerization assays. Our results demonstrated that both compounds exert their antiproliferative activity by inhibiting tubulin polymerization. Finally, a possible binding pose of4 iin the NZ/COL binding site was determined by using molecular docking and molecular dynamics (MD) approaches. To our knowledge, this is the first report of non-N-substituted 2,4-diaminoquinazoline derivatives with the ability to inhibit tubulin polymerization.
Computed Properties of C7H8O2. About m-Methoxyphenol, If you have any questions, you can contact Herrera-Vazquez, FS; Matadamas-Martinez, F; Aguayo-Ortiz, R; Dominguez, L; Ramirez-Apan, T; Yepez-Mulia, L; Hernandez-Luis, F or concate me.
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,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles