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Calcitriol

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Calcitriol
Systematic (IUPAC) name
(1R,3S)- 5-[2-[(1R,3aR,7aS)-1- [(2R)-6-hydroxy-6-methyl-heptan-2-yl]-
7a-methyl-2,3,3a,5,6,7-hexahydro-1H- inden-4-ylidene]ethylidene]-
4-methylidene-cyclohexane-1,3-diol
Identifiers
CAS number 32222-06-3
ATC code A11CC04 D05AX03
PubChem 134070
DrugBank APRD00246
Chemical data
Formula C27H44O3 
Mol. weight 416.64 g.mol-1
Pharmacokinetic data
Bioavailability  ?
Metabolism Renal
Half life 5–8 hours
Excretion Renal
Therapeutic considerations
Pregnancy cat.

B3 (Au), C (U.S.)

Legal status

S4 (Au), POM (UK)

Routes Oral, IV, topical

Calcitriol (INN) (IPA: [kælsɪˈtraɪɒl, kælˈsɪtrɪɒl]) or 1,25-dihydroxycholecalciferol (abbreviated 1,25-(OH)2D3) is the active form of vitamin D found in the body (vitamin D3). It is produced in the kidneys by conversion from 25-hydroxycholecalciferol (calcidiol) and regulates calcium levels by increasing the absorption of calcium from the gastrointestinal tract. Calcitriol is also commonly used as a medication in the treatment of hypocalcaemia and osteoporosis. Calcitriol is marketed under various trade names including Rocaltrol (Roche) and Calcijex (Abbott).

[edit] Indications

Calcitriol is indicated for:<ref name="AMH2006">Rossi S, editor. Australian Medicines Handbook 2006. Adelaide: Australian Medicines Handbook; 2006. ISBN 0-9757919-2-3</ref>

Calcitriol is also sometimes used topically in the treatment of psoriasis, however the evidence to support its efficacy is inconclusive.<ref name="MicromedexDrugdex">Calcitriol. In: Klasco RK, editor. Drugdex system. vol 128. Greenwood Village (CO): Thomson Micromedex; 2006.</ref> The vitamin D analogue calcipotriol is more commonly used for psoriasis.

[edit] Adverse effects

The main adverse drug reaction associated with calcitriol therapy is hypercalcaemia – early symptoms include: nausea, vomiting, constipation, anorexia, apathy, headache, thirst, sweating, and/or polyuria). Compared to other vitamin D compounds in clinical use (cholecalciferol, ergocalciferol), calcitriol has a higher risk of inducing hypercalcaemia. However, such episodes may be shorter and easier to treat due to its relatively short half-life.<ref name="AMH2006" />

[edit] References

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