Details
Stereochemistry | ACHIRAL |
Molecular Formula | C16H22ClNO4 |
Molecular Weight | 327.803 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CN(C)C(=O)CCCOC(=O)C(C)(C)OC1=CC=C(Cl)C=C1
InChI
InChIKey=CXQGFLBVUNUQIA-UHFFFAOYSA-N
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
Molecular Formula | C16H22ClNO4 |
Molecular Weight | 327.803 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Clofibride is a hypolipaemic drug of p-chlorophenoxyisobutyric type. Clofibride hypolipaemic effects could be due, partially, to a reduction of hormono-dependent lipolysis. Clofibride decreased blood cholesterol and total lipids, increased liver weight and liver catalase content, and decreased biliary excretion of cholesterol in normolipidemic rats after a 7 day treatment.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/576423
Healthy volunteers received therapeutic doses of clofibrate as 2x500 mg capsules, clofibride as 2x450 mg capsules, twice daily for ten days.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/7040821
One dose of clofibride (Cf) is administered, after sacrifice of normal fasting rat, in vitro: 2 mg/100 mg adipocytes in 2 ml medium.
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 16:21:17 GMT 2023
by
admin
on
Sat Dec 16 16:21:17 GMT 2023
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Record UNII |
0S9SLS3L93
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Record Status |
Validated (UNII)
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Record Version |
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WHO-ATC |
C10AB10
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NCI_THESAURUS |
C98150
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WHO-VATC |
QC10AB10
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0S9SLS3L93
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DTXSID1022841
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C007089
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100000084335
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C78055
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DB13849
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CHEMBL1697831
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3245
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160134
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696
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CLOFIBRIDE
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SUB06708MIG
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247-912-7
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26717-47-5
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Related Record | Type | Details | ||
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ACTIVE MOIETY |