Langbahn Team – Weltmeisterschaft

Falecalcitriol

Falecalcitriol
Clinical data
AHFS/Drugs.comInternational Drug Names
Routes of
administration		Oral
ATC code
  • none
Legal status
Legal status
  • In general: ℞ (Prescription only)
Identifiers
  • (1R,3S,5Z)-5-[(2E)-2-[(1R,3aS,7aR)-7a-Methyl-1-[(2R)-7,7,7-trifluoro-6-hydroxy-6-(trifluoromethyl)heptan-2-yl]-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexane-1,3-diol
CAS Number
PubChem CID
IUPHAR/BPS
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC27H38F6O3
Molar mass524.588 g·mol−1
3D model (JSmol)
  • C[C@H](CCCC(C(F)(F)F)(C(F)(F)F)O)[C@H]1CC[C@@H]\2[C@@]1(CCC/C2=C\C=C/3\C[C@H](C[C@@H](C3=C)O)O)C
  • InChI=1S/C27H38F6O3/c1-16(6-4-13-25(36,26(28,29)30)27(31,32)33)21-10-11-22-18(7-5-12-24(21,22)3)8-9-19-14-20(34)15-23(35)17(19)2/h8-9,16,20-23,34-36H,2,4-7,10-15H2,1,3H3/b18-8+,19-9-/t16-,20-,21-,22+,23+,24-/m1/s1 ☒N
  • Key:XPYGGHVSFMUHLH-UUSULHAXSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Falecalcitriol (INN) is an analog of calcitriol. It has a higher potency both in vivo and in vitro systems, and longer duration of action in vivo.[1]

References

  1. ^ Okamoto S, Ejima E, Kiriyama T, et al. (1991). "Mechanism of action of newly developed vitamin D analogue". Contrib Nephrol. Contributions to Nephrology. 91: 146–8. doi:10.1159/000420171. ISBN 978-3-8055-5372-8. PMID 1666031.


Quelle: http://en.wikipedia.org/wiki/Falecalcitriol