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RSS FeedsMolecules, Vol. 24, Pages 267: Synthesis, Anticancer Activity, and Apoptosis Induction of Novel 3,6-Diazaphenothiazines (Molecules)


12 january 2019 12:01:21

Molecules, Vol. 24, Pages 267: Synthesis, Anticancer Activity, and Apoptosis Induction of Novel 3,6-Diazaphenothiazines (Molecules)

New 10-substituted derivatives of 3,6-diazaphenothiazine, containing the triple bond linker terminated with tertiary cyclic and acyclic amine groups, were synthesized and screened for their anticancer action. The compounds exhibited varied anticancer activities against human glioblastoma SNB-19, melanoma C-32, and breast cancer MDA-MB231 cell lines, depending on the nature of the substituents. The most active 3,6-diazaphenothiazine, 4, was the derivative with the N,N-diethylamino-2-butynyl substituent against glioblastoma SNB-19, and was ten times more potent than cisplatin. For this compound, the expression of H3, TP53, CDKN1A, BCL-2, and BAX genes was detected by the RT-qPCR method. The gene expression ratio BAX/BCL-2 indicated the induction of mitochondrial apoptosis in cancer cell lines. The transformation of the propynyl substituent into amino-2-butynyl can be a method applicable to the search for more anticancer-active azaphenothiazines. Digg Facebook Google StumbleUpon Twitter
16 viewsCategory: Biochemistry, Chemistry, Molecular Biology
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