Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Dihydroequilin"'
Publikováno v:
Crystals, Vol 7, Iss 7, p 218 (2017)
The crystal structure of 17α-dihydroequilin has been solved and refined using synchrotron X-ray powder diffraction data, and optimized using density functional techniques. 17α-dihydroequilin crystallizes in space group P212121 (#19) with a = 6.7684
Externí odkaz:
https://doaj.org/article/28fedb33d2c44619ad69dda1c7eea6b3
Publikováno v:
Crystals; Volume 7; Issue 7; Pages: 218
Crystals, Vol 7, Iss 7, p 218 (2017)
Crystals, Vol 7, Iss 7, p 218 (2017)
The crystal structure of 17α-dihydroequilin has been solved and refined using synchrotron X-ray powder diffraction data, and optimized using density functional techniques. 17α-dihydroequilin crystallizes in space group P212121 (#19) with a = 6.7684
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abf16bde092ce93098a5f853a50cbb5b
Akademický článek
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Publikováno v:
Atherosclerosis. 109:102-103
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::651d43f4070cc2f8854fa71a91b26c34
https://doi.org/10.1016/0021-9150(94)93422-3
https://doi.org/10.1016/0021-9150(94)93422-3
Publikováno v:
Journal of Biological Chemistry. 185:267-270
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1472a907d455ca5cda9146515eb631f
https://doi.org/10.1016/s0021-9258(18)56415-2
https://doi.org/10.1016/s0021-9258(18)56415-2
Autor:
Clara Revesz, Yvon Lefebvre
Publikováno v:
Journal of Medicinal Chemistry. 18:217-219
A series of 17alpha-furylestradiol and dihydroequilin derivatives was synthesized by reacting the appropriate 3-substituted estrone and equilin with 2- or 3-furyllithium. The oral estrogenic activity of the compounds was compared with that of mestran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fc8bc5ee9d665e355963b3e654baf97
https://doi.org/10.1021/jm00236a027
https://doi.org/10.1021/jm00236a027
Autor:
Rudi Ansbacher
Publikováno v:
JAMA. 259(2)
To the Editor. —In the SPECIAL COMMUNICATION by Nightingale and Morrison 1 concerning generic drugs, the subject of bioequivalence was discussed. However, no mention was made of bioavailability. In the past year, I have personally seen six patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c14a3ee2c5e562f2179888ff63c829e
https://pubmed.ncbi.nlm.nih.gov/2826829
https://pubmed.ncbi.nlm.nih.gov/2826829
Autor:
Y. Lefebvre, C. Revesz
Publikováno v:
Chemischer Informationsdienst. 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3097ffc861ac57ee291c3b77777d0787
https://doi.org/10.1002/chin.197525433
https://doi.org/10.1002/chin.197525433
Publikováno v:
Journal of chromatography. 135(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9560d2ea4f369a2a8cf0fbb486bfbc91
https://pubmed.ncbi.nlm.nih.gov/874036
https://pubmed.ncbi.nlm.nih.gov/874036
Publikováno v:
Journal of the American Pharmaceutical Association. American Pharmaceutical Association. 42(3)
The use of iron-Kober reagent for the determination of α-estradiol in estrogen preparations has been limited by the interfering reactions of some other phenolic estrogens. A simple partition chromatographic procedure is now described for separating
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6acd80bc2cd5f5f6de3fca673347818
https://pubmed.ncbi.nlm.nih.gov/13034657
https://pubmed.ncbi.nlm.nih.gov/13034657