Revisiting the 7,8-cis-vitamin D3 derivatives: synthesis, evaluating the biological activity, and study of the binding configuration

Tetrahedron ◽  
2016 ◽  
Vol 72 (22) ◽  
pp. 2838-2848 ◽  
Author(s):  
Daisuke Sawada ◽  
Shinji Kakuda ◽  
Midori Kamimura-Takimoto ◽  
Akiko Takeuchi ◽  
Yotaro Matsumoto ◽  
...  
1974 ◽  
Vol 46 (4) ◽  
pp. 433-448 ◽  
Author(s):  
J. Silver ◽  
G. Neale ◽  
G. R. Thompson

1. The metabolism of radioactive cholecalciferol was studied in control and phenobarbitone-treated rats and pigs. 2. Treatment with phenobarbitone enhanced the appearance in plasma of 25-hydroxycholecalciferol (peak IV on silicic acid chromatography), and of more-polar metabolites (peak V), but not of the most-polar metabolites (peak VI). Peak IV had the chromatographic properties of authentic 25-hydroxycholecalciferol (25-HCC) and had biological activity. 3. There was no effect on the appearance of peaks V and VI in plasma after an injection of radioactive 25-HCC. 4. Treatment with phenobarbitone enhanced the excretion of metabolites of radioactive vitamin D3 in bile. These metabolites were largely water-soluble conjugates of peaks IV, V and VI, which included glucuronides. Peak IV in bile was not identical with 25-HCC. 5. Prolonged treatment with phenobarbitone depleted the tissue radioactivity of rats given radioactive vitamin D3.


1986 ◽  
Vol 20 (3) ◽  
pp. 149-153
Author(s):  
M. Yu. Valinietse ◽  
V. K. Bauman ◽  
D. A. Babarykin ◽  
N. A. Bogoslovskii ◽  
T. A. Kisel'nikova

1987 ◽  
Vol 27 (6) ◽  
pp. 979-997 ◽  
Author(s):  
Leonor CANCELA ◽  
P. J. MARIE ◽  
Noélie LE BOULCH ◽  
Livia MIRAVET

1980 ◽  
Vol 11 (17) ◽  
Author(s):  
R. I. YAKHIMOVICH ◽  
L. K. KURCHENKO ◽  
V. K. BAUMAN ◽  
V. N. MIRONOVA ◽  
R. K. ZHUK

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