Zobrazeno 1 - 4
of 4
pro vyhledávání: '"I A, Gluzdikov"'
Publikováno v:
Russian Journal of Organic Chemistry. 42:1675-1682
Stereoselectivity of reaction with Raney nickel of D-homoestra-1,3,5(10),8,14-pentaenes containing one or two methyl groups in position 16 was investigated. The reaction direction is governed by the orientation of the substituent at C17a. The signals
Autor:
E. A. Urusova, Stanislav I. Selivanov, Galina L. Starova, S. V. Nikolaev, A. G. Shavva, I. A. Gluzdikov
Publikováno v:
Russian Journal of Organic Chemistry. 40:506-512
Modified equilenin analogs were synthesized with a view to examine the relation between the structure and biological properties of steroid estrogens. The 1H and 13C NMR signals of six estra-1,3,5,7,9-pentaenes were completely assigned using homo- and
Autor:
T. R. Boronoeva, A. G. Shavva, V. G. Isaeva, B. P. Surinov, Galina L. Starova, A. N. Sharetskii, I. A. Gluzdikov, I. V. Ishchenko, Stanislav I. Selivanov
Publikováno v:
Russian Journal of Bioorganic Chemistry. 28:215-223
The study of the binding of estradiol B-nor-8-isonalogues to estrogen receptors from the rat uterus helped create the proposed model of the corresponding ligand–receptor complexes. The use of this model ensured the choice of such micromodifications
Autor:
A G, Shavva, S I, Selivanov, G L, Starova, T R, Boronoeva, I V, Ishchenko, I A, Gluzdikov, A N, Sharetskiĭ, V G, Isaeva, B P, Surinov
Publikováno v:
Bioorganicheskaia khimiia. 28(3)
The study of the binding of estradiol B-nor-8-isonalogues to estrogen receptors from the rat uterus helped create the proposed model of the corresponding ligand-receptor complexes. The use of this model ensured the choice of such micromodifications i