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Synthesis and studies of structure and biological properties of D-homoanalogs of steroid estrogens. / Morozkina, S.N.; Fidarov, A.F.; Mushtukov, A.S.; Selivanov, S.I.; Starova, G.L.; Shawa, A.G.

In: Russian Journal of General Chemistry, No. 10, 2013, p. 1869-1873.

Research output: Contribution to journalArticlepeer-review

Harvard

Morozkina, SN, Fidarov, AF, Mushtukov, AS, Selivanov, SI, Starova, GL & Shawa, AG 2013, 'Synthesis and studies of structure and biological properties of D-homoanalogs of steroid estrogens', Russian Journal of General Chemistry, no. 10, pp. 1869-1873. https://doi.org/10.1134/S1070363213100125

APA

Morozkina, S. N., Fidarov, A. F., Mushtukov, A. S., Selivanov, S. I., Starova, G. L., & Shawa, A. G. (2013). Synthesis and studies of structure and biological properties of D-homoanalogs of steroid estrogens. Russian Journal of General Chemistry, (10), 1869-1873. https://doi.org/10.1134/S1070363213100125

Vancouver

Morozkina SN, Fidarov AF, Mushtukov AS, Selivanov SI, Starova GL, Shawa AG. Synthesis and studies of structure and biological properties of D-homoanalogs of steroid estrogens. Russian Journal of General Chemistry. 2013;(10):1869-1873. https://doi.org/10.1134/S1070363213100125

Author

Morozkina, S.N. ; Fidarov, A.F. ; Mushtukov, A.S. ; Selivanov, S.I. ; Starova, G.L. ; Shawa, A.G. / Synthesis and studies of structure and biological properties of D-homoanalogs of steroid estrogens. In: Russian Journal of General Chemistry. 2013 ; No. 10. pp. 1869-1873.

BibTeX

@article{6e582cc837ea4d91ab58bb047ebae90d,
title = "Synthesis and studies of structure and biological properties of D-homoanalogs of steroid estrogens",
abstract = "In order to estimate the potential of steroid estrogens modification, three D-homoanalogs of estrogens have been prepared; their structures and biological properties have been studied. The expansion of D-ring in such compounds has lead to strong decrease if the uterotropic action, however, the unfavorable hypertriglyceridemic effect has been retained. The latter has been eliminated by combined action of the studied steroids and ursolic acid; therewith the hypocholesterolemic activity has been retained. {\textcopyright} 2013 Pleiades Publishing, Ltd.",
author = "S.N. Morozkina and A.F. Fidarov and A.S. Mushtukov and S.I. Selivanov and G.L. Starova and A.G. Shawa",
year = "2013",
doi = "10.1134/S1070363213100125",
language = "English",
pages = "1869--1873",
journal = "Russian Journal of General Chemistry",
issn = "1070-3632",
publisher = "МАИК {"}Наука/Интерпериодика{"}",
number = "10",

}

RIS

TY - JOUR

T1 - Synthesis and studies of structure and biological properties of D-homoanalogs of steroid estrogens

AU - Morozkina, S.N.

AU - Fidarov, A.F.

AU - Mushtukov, A.S.

AU - Selivanov, S.I.

AU - Starova, G.L.

AU - Shawa, A.G.

PY - 2013

Y1 - 2013

N2 - In order to estimate the potential of steroid estrogens modification, three D-homoanalogs of estrogens have been prepared; their structures and biological properties have been studied. The expansion of D-ring in such compounds has lead to strong decrease if the uterotropic action, however, the unfavorable hypertriglyceridemic effect has been retained. The latter has been eliminated by combined action of the studied steroids and ursolic acid; therewith the hypocholesterolemic activity has been retained. © 2013 Pleiades Publishing, Ltd.

AB - In order to estimate the potential of steroid estrogens modification, three D-homoanalogs of estrogens have been prepared; their structures and biological properties have been studied. The expansion of D-ring in such compounds has lead to strong decrease if the uterotropic action, however, the unfavorable hypertriglyceridemic effect has been retained. The latter has been eliminated by combined action of the studied steroids and ursolic acid; therewith the hypocholesterolemic activity has been retained. © 2013 Pleiades Publishing, Ltd.

U2 - 10.1134/S1070363213100125

DO - 10.1134/S1070363213100125

M3 - Article

SP - 1869

EP - 1873

JO - Russian Journal of General Chemistry

JF - Russian Journal of General Chemistry

SN - 1070-3632

IS - 10

ER -

ID: 7521925