Dihydrotachysterol
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| Systematic (IUPAC) name | |
|---|---|
| (1S,3E,4S)-3-[(2E)-2-[(1R,3aS,7aR)-1-[(E,2R,5R)-5,6-Dimethylhept-3-en-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylcyclohexan-1-ol | |
| Clinical data | |
| AHFS/Drugs.com | Micromedex Detailed Consumer Information |
| MedlinePlus | a682335 |
| Pregnancy cat. | ? |
| Legal status | ? |
| Identifiers | |
| CAS number | 67-96-9 |
| ATC code | A11CC02 |
| PubChem | CID 5311071 |
| DrugBank | APRD00143 |
| ChemSpider | 4470607 |
| UNII | R5LM3H112R |
| KEGG | D00299 |
| ChEBI | CHEBI:4591 |
| Chemical data | |
| Formula | C28H46O |
| Mol. mass | 398.664 g/mol |
| SMILES | eMolecules & PubChem |
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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.
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