Selective manipulation of steroid hydroxyl groups with boronate esters: efficient access to antigenic C-3 linked steroid–protein conjugates and steroid sulfate standards for drug detection
N.L. Hungerford A.R. McKinney A.M. Stenhouse M.D. McLeod Selective manipulation of steroid hydroxyl groups with boronate esters: efficient access to antigenic C-3 linked steroid–protein conjugates and steroid sulfate standards for drug detection Org Biomol Chem 4 21 2006 3951 3959
A direct antigen heterologous enzyme immunoassay for measuring progesterone in serum without using displacer
A. Basu T.G. Shrivastav S.K. Maitra A direct antigen heterologous enzyme immunoassay for measuring progesterone in serum without using displacer Steroids 71 2006 222 230
A novel radioimmunoassay of 7-oxo-HDEA and its physiological levels
H. Kazhnitková L. Zamrazilová M. Hill O. Lapčík V. Pouzar R. Hampl A novel radioimmunoassay of 7-oxo-HDEA and its physiological levels Steroids 72 2007 342 350
2-Substituted estradiol bis-sulfamates, multitargeted antitumor agents: synthesis, in vitro SAR, protein crystallography, and in vivo activity
M.P. Leese B. Leblond A. Smith S.P. Newman A.D. Fiore G.D. Simone 2-Substituted estradiol bis-sulfamates, multitargeted antitumor agents: synthesis, in vitro SAR, protein crystallography, and in vivo activity J Med Chem 49 26 2006 7683 7696
Structural identification of methyl protodioscin metabolites in rats’ urine and their antiproliferative activities against human tumor cell lines
X. He A. Qiao X. Wang B. Liu M. Jiang L. Su Structural identification of methyl protodioscin metabolites in rats’ urine and their antiproliferative activities against human tumor cell lines Steroids 71 2006 828 833
Synthesis of unique 17β-estradiol homo-dimers, estrogen receptors binding affinity evaluation and cytocidal activity on breast, intestinal and skin cancer cell lines
G. Bérubé D. Rabouin V. Perron B. N’Zemba R.-C. Gaudreault S. Parent Synthesis of unique 17β-estradiol homo-dimers, estrogen receptors binding affinity evaluation and cytocidal activity on breast, intestinal and skin cancer cell lines Steroids 71 2006 911 921
Type 2 11β-hydroxysteroid dehydrogenase activity in human ovarian cancer
S. Temkin V.L. Nacharaju M. Hellman Y.-C. Lee O. Abulafia Type 2 11β-hydroxysteroid dehydrogenase activity in human ovarian cancer Steroids 71 2006 1019 1023
Antitumor steroids. 1. Synthesis and biological activity of 11α-hydroxyestra-1,3,5(10)-triene derivatives with bis-(2-chloroethyl)amino-containing substituent at position 3
V.M. Rzheznikov L.E. Golubovskaya O.N. Minailova B.I. Keda T.I. Ivanenko V.P. Fedotov Antitumor steroids. 1. Synthesis and biological activity of 11α-hydroxyestra-1,3,5(10)-triene derivatives with bis-(2-chloroethyl)amino-containing substituent at position 3 Pharm Chem J 41 4 2007 183 187
Development and evolution of therapies targeted to the estrogen receptor for the treatment and prevention of breast cancer
V.C. Jordan A.M.H. Brodie Development and evolution of therapies targeted to the estrogen receptor for the treatment and prevention of breast cancer Steroids 72 2007 7 25
Synthesis of chalcone derivatives on steroidal framework and their anticancer activities
H.O. Saxena U. Faridi J.K. Kumar S. Luqman M.P. Darokar K. Shanker Synthesis of chalcone derivatives on steroidal framework and their anticancer activities Steroids 72 2007 892 900
Norethindrone acetate (NA) and ethinyl estrodiol (EE) related oxidative transformation products in stability samples of formulated drug product: synthesis of authentic references
I.V. Ekhato T. Hurley M. Lovdahl T.J. Revitte L. Guo Y. Huang Norethindrone acetate (NA) and ethinyl estrodiol (EE) related oxidative transformation products in stability samples of formulated drug product: synthesis of authentic references Steroids 67 2002 165 174
Synthèse stéréosélective de 12α-amino et 12α-aminométhyl 19-nor-stéroïdes
J. Doussot R. Garreau L. Dallery J.-P. Guetté A. Guy Synthèse stéréosélective de 12α-amino et 12α-aminométhyl 19-nor-stéroïdes Bull Soc Chim Fr 132 1995 59 66
