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A New Look at the Most Successful Prodrugs for Active Vitamin D (D Hormone): Alfacalcidol and Doxercalciferol

Alfacalcidol (1α-hydroxyvitamin D(3)) has been widely used since 1981 as a prodrug for calcitriol (1α,25-dihydroxyvitamin D(3)) in the treatment of hypocalcemia, chronic renal failure, hypoparathyroidism and osteoporosis. More recently, doxercalciferol (1α-hydroxyvitamin D(2)) has been used since 19...

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Autor principal: Kubodera, Noboru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254965/
https://www.ncbi.nlm.nih.gov/pubmed/19924035
http://dx.doi.org/10.3390/molecules14103869
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author Kubodera, Noboru
author_facet Kubodera, Noboru
author_sort Kubodera, Noboru
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description Alfacalcidol (1α-hydroxyvitamin D(3)) has been widely used since 1981 as a prodrug for calcitriol (1α,25-dihydroxyvitamin D(3)) in the treatment of hypocalcemia, chronic renal failure, hypoparathyroidism and osteoporosis. More recently, doxercalciferol (1α-hydroxyvitamin D(2)) has been used since 1999 as a prodrug for 1α,25-dihydroxyvitamin D(2) for the treatment of secondary hyperparathyroidism. Currently, six forms of vitamin D are known. They range from vitamin D(2) to vitamin D(7) and are distinguished by their differing side chains. Only vitamin D(2) and vitamin D(3) have been found to be biologically active based on the elucidation of activation pathways. Alfacalcidol and osteoporosis/doxercalciferol and secondary hyperparathyroidism are discussed, with a new look at old compounds including their practical syntheses.
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spelling pubmed-62549652018-11-30 A New Look at the Most Successful Prodrugs for Active Vitamin D (D Hormone): Alfacalcidol and Doxercalciferol Kubodera, Noboru Molecules Review Alfacalcidol (1α-hydroxyvitamin D(3)) has been widely used since 1981 as a prodrug for calcitriol (1α,25-dihydroxyvitamin D(3)) in the treatment of hypocalcemia, chronic renal failure, hypoparathyroidism and osteoporosis. More recently, doxercalciferol (1α-hydroxyvitamin D(2)) has been used since 1999 as a prodrug for 1α,25-dihydroxyvitamin D(2) for the treatment of secondary hyperparathyroidism. Currently, six forms of vitamin D are known. They range from vitamin D(2) to vitamin D(7) and are distinguished by their differing side chains. Only vitamin D(2) and vitamin D(3) have been found to be biologically active based on the elucidation of activation pathways. Alfacalcidol and osteoporosis/doxercalciferol and secondary hyperparathyroidism are discussed, with a new look at old compounds including their practical syntheses. Molecular Diversity Preservation International 2009-09-29 /pmc/articles/PMC6254965/ /pubmed/19924035 http://dx.doi.org/10.3390/molecules14103869 Text en © 2009 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Kubodera, Noboru
A New Look at the Most Successful Prodrugs for Active Vitamin D (D Hormone): Alfacalcidol and Doxercalciferol
title A New Look at the Most Successful Prodrugs for Active Vitamin D (D Hormone): Alfacalcidol and Doxercalciferol
title_full A New Look at the Most Successful Prodrugs for Active Vitamin D (D Hormone): Alfacalcidol and Doxercalciferol
title_fullStr A New Look at the Most Successful Prodrugs for Active Vitamin D (D Hormone): Alfacalcidol and Doxercalciferol
title_full_unstemmed A New Look at the Most Successful Prodrugs for Active Vitamin D (D Hormone): Alfacalcidol and Doxercalciferol
title_short A New Look at the Most Successful Prodrugs for Active Vitamin D (D Hormone): Alfacalcidol and Doxercalciferol
title_sort new look at the most successful prodrugs for active vitamin d (d hormone): alfacalcidol and doxercalciferol
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254965/
https://www.ncbi.nlm.nih.gov/pubmed/19924035
http://dx.doi.org/10.3390/molecules14103869
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