1451739-70-0Relevant articles and documents
Microwave-assisted synthesis of novel bis-flavone dimers as new anticancer agents
McGown, Andrew,Ragazzon-Smith, Abby,Hadfield, John A.,Potgetier, Herman,Ragazzon, Patricia A.
, p. 66 - 75 (2019/05/04)
In this study, we describe a microwave-based click chemistry method used to prepare a family of novel bis-flavone dimers. The substituted 7-hydroxy and 4’-hydroxy flavonoids were linked through a triazole ring. The compounds were easily synthesized and purified in high yields. The bis-flavonoids were tested on different cell lines including HCT116, HepG2, MCF7 and MOLT-4. Several analogues showed to have anticancer activity with IC50 values in the range of 20-60 μM. Flavonoids are known for their anticancer properties and this method provides the basis for new medicinal structures.
Five-membered heterocycle (or amide)-flavonoid compound-matrine ternary conjugate and application thereof
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Paragraph 0045; 0046, (2016/10/08)
The invention discloses a five-membered heterocycle (or amide)-flavonoid compound-matrine ternary conjugate and application thereof. The five-membered heterocycle (or amide)-flavonoid compound-matrine ternary conjugate has a structure as shown in the specification, has an effective antibacterial activity, and has a potential application value in the aspect of antibacterial drug development. The five-membered heterocycle (or amide)-flavonoid compound-matrine ternary conjugate has a remarkable effect on the antibacterial aspect, and can be applied to prevention and treatment of MRSA, P.aeru, E.coli, Ab and other clinical common pathogens.