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Synthesis and Biological Evaluation of the Salicylamide and Salicylic Acid Derivatives as Anti-Estrogen Agents

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dc.creator Ergin, Volkan
dc.creator Ozatik, Orhan
dc.creator DÜNDAR, YASEMİN
dc.creator ÖNKOL, TİJEN
dc.creator Ozatik, Yasemin
dc.creator Sahin, M. Fethi
dc.creator EROL, Kevser
dc.creator Menevse, Adnan
dc.date 2012-05-01T00:00:00Z
dc.date.accessioned 2021-12-03T11:15:24Z
dc.date.available 2021-12-03T11:15:24Z
dc.identifier 13c79a7a-4ab7-4253-9581-77de7329a989
dc.identifier 10.2174/1573406411208030481
dc.identifier https://avesis.sdu.edu.tr/publication/details/13c79a7a-4ab7-4253-9581-77de7329a989/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/90056
dc.description Alkylphenols have xenoestrogenic activity, which mimic the action of physiological estrogens and these mim-icking activities are mainly mediated by nongenomic pathway. Nongenomic pathway plays a pivotal role in breast, endometrial and ovarian cancers' growth and development. In this study, various alkylphenol derivatives were prepared and screened for their anti-uterotrophic and uterotrophic activity. Among these compounds, 2-hydroxy-5-nonanoylbenzamide (compound 1b) showed 93.99% inhibitory activity in the anti-uterotrophic test performed, and was found inactive in the uterotrophic activity test. Moreover, all test compounds were examined for the effect on uterine histopathological changes, and plasma 17 beta-estradiol (E-2) level. Compound 1b was also tested for in vitro anti-cancer activity against ER+, human breast cancer cell line MCF-7, and it reduced cell viability to 74.01% at 50 nM concentration.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title Synthesis and Biological Evaluation of the Salicylamide and Salicylic Acid Derivatives as Anti-Estrogen Agents
dc.type info:eu-repo/semantics/article


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