Dihydrotachysterol: Difference between revisions
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{{drugbox | {{drugbox | ||
| IUPAC_name = 3-[2-[7a-methyl-1- (1,4,5-trimethylhex-2-enyl)- 1,2,3,3a,5,6,7,7a- octahydroinden-4-ylidene] ethylidene]- 4-methyl-cyclohexan-1-ol | | IUPAC_name = 3-[2-[7a-methyl-1- (1,4,5-trimethylhex-2-enyl)- 1,2,3,3a,5,6,7,7a- octahydroinden-4-ylidene] ethylidene]- 4-methyl-cyclohexan-1-ol | ||
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__NOTOC__ | __NOTOC__ | ||
{{SI}} | {{SI}} | ||
{{CMG}} | {{CMG}} | ||
==Overview== | ==Overview== | ||
'''Dihydrotachysterol''' (DHT) is a synthetic [[vitamin D]] analog activated in the [[liver]] that does not require [[renal]] hydroxylation like vitamin D2 ([[ergocalciferol]]) and vitamin D3 ([[cholecalciferol]]). DHT has a rapid onset of action (2 hours), a shorter half-life, and a greater effect on [[mineralization]] of bone salts than does vitamin | |||
D. | |||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
Revision as of 18:05, 10 April 2015
Clinical data | |
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ATC code | |
Pharmacokinetic data | |
Protein binding | >99% |
Identifiers | |
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CAS Number | |
PubChem CID | |
DrugBank | |
E number | {{#property:P628}} |
ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value). |
Chemical and physical data | |
Formula | C28H46O |
Molar mass | 398.664 g/mol |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Dihydrotachysterol (DHT) is a synthetic vitamin D analog activated in the liver that does not require renal hydroxylation like vitamin D2 (ergocalciferol) and vitamin D3 (cholecalciferol). DHT has a rapid onset of action (2 hours), a shorter half-life, and a greater effect on mineralization of bone salts than does vitamin D.
References
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