The first synthesis of the antiangiogenic homoisoflavanone, cremastranone.

Autor: Lee B; College of Pharmacy and Gachon Institute of Pharmaceutical Sciences, Gachon University, Incheon, South Korea. syseo@gachon.ac.kr., Basavarajappa HD, Sulaiman RS, Fei X, Seo SY, Corson TW
Jazyk: angličtina
Zdroj: Organic & biomolecular chemistry [Org Biomol Chem] 2014 Oct 21; Vol. 12 (39), pp. 7673-7. Date of Electronic Publication: 2014 Aug 28.
DOI: 10.1039/c4ob01604a
Abstrakt: An antiangiogenic homoisoflavanone, cremastranone, was synthesized for the first time. This scalable synthesis, which includes selective demethylation, could be used to develop lead molecules to treat angiogenesis-induced eye diseases. Synthetic cremastranone inhibited the proliferation, migration and tube formation ability of human retinal microvascular endothelial cells, important steps in pathological angiogenesis.
Databáze: MEDLINE