Zobrazeno 1 - 6
of 6
pro vyhledávání: '"M. M. Cruz Silva"'
Publikováno v:
Acta Crystallographica Section E, Vol 68, Iss 1, Pp o237-o237 (2012)
The title cholestan, C28H46O3, was prepared by epoxidation of 7-norcholest-5-en-3β-yl acetate and crystallized by slow evaporation from an ethanolic solution. All rings are trans fused. The 3β-acetate and the 17β-cholestane side chain are in equat
Externí odkaz:
https://doaj.org/article/aa5d5c1afb3d493c8960bd57e06fe675
Autor:
José A. Paixão, M. M. Cruz Silva, M. J. M. de Almeida, M. J. S. M. Moreno, M. L. Sa E Melo, A. S. Campos Neves, L. C. R. Andrade
Publikováno v:
Acta Crystallographica Section E Structure Reports Online. 58:o898-o900
The title compound, C25H36O5, has two independent molecules in the asymmetric unit with similar geometry. The main difference between the two molecules relates to the conformation of the 17β-methyl ketone and 3β-acetoxy groups, the latter being
Publikováno v:
Acta Crystallographica Section E: Structure Reports
The title cholestan, C(28)H(46)O(3), was prepared by epoxidation of 7-norcholest-5-en-3β-yl acetate and crystallized by slow evaporation from an ethano-lic solution. All rings are trans fused. The 3β-acetate and the 17β-cholestane side chain are i
Publikováno v:
Medicinal Chemistry in the 21st Century, Lisbon (Portogallo), 2006
info:cnr-pdr/source/autori:M. M. Cruz Silva, S. RIVA, S. Simões, J. N. Moreira, A. Marques, M. L. Sá e Melo/congresso_nome:Medicinal Chemistry in the 21st Century/congresso_luogo:Lisbon (Portogallo)/congresso_data:2006/anno:2006/pagina_da:/pagina_a:/intervallo_pagine
info:cnr-pdr/source/autori:M. M. Cruz Silva, S. RIVA, S. Simões, J. N. Moreira, A. Marques, M. L. Sá e Melo/congresso_nome:Medicinal Chemistry in the 21st Century/congresso_luogo:Lisbon (Portogallo)/congresso_data:2006/anno:2006/pagina_da:/pagina_a:/intervallo_pagine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::834327dc48d6537320c9bb7d9e10a556
http://www.cnr.it/prodotto/i/105706
http://www.cnr.it/prodotto/i/105706
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
4-Hydroxytamoxifen (OHTAM) is the most active metabolite of the widely prescribed anticancer drug tamoxifen (TAM) used in breast cancer therapy. This work describes the effects of OHTAM on isolated human erythrocytes, using standardized test conditio
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Tamoxifen (TAM), the antiestrogenic drug most widely prescribed in the chemotherapy of breast cancer, induces changes in normal discoid shape of erythrocytes and hemolytic anemia. This work evaluates the effects of TAM on isolated human erythrocytes,