@ARTICLE{Morozkina2015411,
author={Morozkina, S.N. and Gluzdikov, I.A. and Drozdov, A.S. and Selivanov, S.I. and Kovalev, R.A. and Filatov, M.V. and Shavva, A.G.},
title={Synthesis and some biological properties of sulfamates derived from 8α-analogs of steroidal estrogens},
journal={Russian Journal of Organic Chemistry},
year={2015},
volume={51},
number={3},
pages={411-416},
doi={10.1134/S1070428015030215},
note={cited By 0},
url={https://www.scopus.com/inward/record.uri?eid=2-s2.0-84928333727&doi=10.1134%2fS1070428015030215&partnerID=40&md5=911c9d5ff7da174e600a9815e94f60e9},
affiliation={St. Petersburg State University, Universitetskii pr. 26, St. Petersburg, 198504, Russian Federation; Petersburg Nuclear Physics Institute, Kurchatov Institute National Research Center, Orlova Roshcha, Gatchina, Leningrad oblast, 188300, Russian Federation; Peter the Great St. Petersburg Polytechnic University, Politekhnicheskaya ul. 29, St. Petersburg, 195251, Russian Federation},
abstract={Sulfamates derived from estrogens of the 8α-series have been synthesized, and their effect on the growth of MCF-7 breast cancer cells has been studied. The best anticancer effect has been found for 7β-methyl-D-homo-6-oxa-8α-estrone sulfamate and 3-methoxy-2,17β-sulfamoyloxy-8α-estra-1,3,5(10)-triene which almost completely inhibit the growth of cancer cells. © 2015 Pleiades Publishing, Ltd.},
correspondence_address1={Shavva, A.G.; St. Petersburg State University, Universitetskii pr. 26, Russian Federation},
publisher={Maik Nauka Publishing / Springer SBM},
issn={10704280},
coden={RJOCE},
language={English},
abbrev_source_title={Russ. J. Org. Chem.},
document_type={Article},
source={Scopus},
}

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