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Synthesis and biological evaluation of thiophosphate tricyclic coumarin derivatives as steroid sulfatase inhibitors

Abstract

Steroid sulfatase (STS) enzyme inhibition is an important approach to the management of hormone-dependent breast cancer. In this paper, we report convenient methods for the synthesis and biological evaluation of thiophosphate tricyclic coumarin analogs exhibiting STS activity. The described methods are based on the straightforward preparation of 7-hydroxy-2,3-dihydro-1H-cyclopenta[c]chromen-2-one, 3-hydroxy- 7,8,9,10-tetrahydro-6H-benzo[c]chromen-6-one, and 3-hydroxy-8,9,10,11-tetrahydro- 7H-cyclohepta[c]chromen-6-one and their further modification by the introduction of various thiophosphate moieties. The inhibition properties of the synthesized compounds were tested toward STS isolated from human placenta. Most of the new STS inhibitors possessed good to moderate activity toward STS. During the course of our investigation, the largest inhibitory effects in the STS enzyme assays were observed for the two compounds 3f and 4r, with IC50 values of 13.3 and 30.3mM, respectively (the IC50 value of 1mM for the 665-COUMATE was used as a reference). The structure–activity relationships of the synthesized coumarin derivatives toward STS enzymes are discussed.

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Category:
Articles
Type:
artykuł w czasopiśmie wyróżnionym w JCR
Published in:
JOURNAL OF ASIAN NATURAL PRODUCTS RESEARCH no. 17, edition 11, pages 1091 - 1096,
ISSN: 1028-6020
Language:
English
Publication year:
2015
Bibliographic description:
Kozak W., Daśko M., Masłyk M., Gielniewski B., Rachoń J., Demkowicz S.: Synthesis and biological evaluation of thiophosphate tricyclic coumarin derivatives as steroid sulfatase inhibitors// JOURNAL OF ASIAN NATURAL PRODUCTS RESEARCH. -Vol. 17, iss. 11 (2015), s.1091-1096
DOI:
Digital Object Identifier (open in new tab) 10.1080/10286020.2015.1054815
Verified by:
Gdańsk University of Technology

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