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Clofibride

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Chemical compound
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This articleis missing information about everything. Please expand the article to include this information. Further details may exist on thetalk page.(January 2017)
Pharmaceutical compound
Clofibride
Clinical data
ATC code
Pharmacokinetic data
MetabolismHydrolyzed toclofibric acid;hepaticglucuronidation
Eliminationhalf-life12 hours (clofibric acid)
ExcretionRenal (mostly) and fecal
Identifiers
  • 3-(dimethylcarbamoyl)propyl 2-(4-chlorophenoxy)-2-methylpropanoate
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.043.542Edit this at Wikidata
Chemical and physical data
FormulaC16H22ClNO4
Molar mass327.81 g·mol−1
3D model (JSmol)
  • Clc1ccc(OC(C(=O)OCCCC(=O)N(C)C)(C)C)cc1
  • InChI=1S/C16H22ClNO4/c1-16(2,22-13-9-7-12(17)8-10-13)15(20)21-11-5-6-14(19)18(3)4/h7-10H,5-6,11H2,1-4H3 checkY
  • Key:CXQGFLBVUNUQIA-UHFFFAOYSA-N checkY
  (verify)

Clofibride is afibrate. Clofibride is a derivative ofclofibrate. In the body it is converted into 4-chlorophenoxyisobutyric acid (clofibric acid),[1] which is the truehypolipidemic agent.[2] So clofibride, just like clofibrate is aprodrug of clofibric acid.

References

[edit]
  1. ^"Clofibride".
  2. ^Entry onClofibrat. at:Römpp Online. Georg Thieme Verlag, retrieved 06. Mai 2020.
GI tract
Cholesterol absorption inhibitors,NPC1L1
Bile acid sequestrants/resins (LDL)
Liver
Statins (HMG-CoA reductase,LDL)
Niacin and derivatives (HDL andLDL)
MTTP inhibitors (VLDL)
ATP citrate lyase inhibitors (LDL)
Thyromimetics (VLDL)
Blood vessels
PPAR agonists (LDL)
Fibrates
Others
CETP inhibitors (HDL)
PCSK9 inhibitors (LDL)
ANGPTL3 inhibitors (LDL/HDL)
Combinations
Other
PPARTooltip Peroxisome proliferator-activated receptormodulators
PPARαTooltip Peroxisome proliferator-activated receptor alpha
PPARδTooltip Peroxisome proliferator-activated receptor delta
PPARγTooltip Peroxisome proliferator-activated receptor gamma
Non-selective


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