Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C20H23ClO3 |
| Molecular Weight | 346.848 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCOC(=O)C(C)(CC)OC1=CC=C(CC2=CC=C(Cl)C=C2)C=C1
InChI
InChIKey=YWQGBCXVCXMSLJ-UHFFFAOYSA-N
InChI=1S/C20H23ClO3/c1-4-20(3,19(22)23-5-2)24-18-12-8-16(9-13-18)14-15-6-10-17(21)11-7-15/h6-13H,4-5,14H2,1-3H3
| Molecular Formula | C20H23ClO3 |
| Molecular Weight | 346.848 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Beclobrate is a fibric acid derivative with potent cholesterol- and triglyceride-lowering effects. The effectiveness of the drug has been investigated in a variety of studies including patients with hyperlipidemia types IIa, IIb and IV and patients suffering from secondary hyperlipidemia attributable to diabetes mellitus, liver disease, end-stage renal failure requiring hemodialysis, and kidney transplantation. In general, side-effects of beclobrate therapy are comparable with those of other fibric acid derivatives. Gastrointestinal disturbances, nausea were the major side-effects. Beclobrate has now been withdrawn from the market since the risk of hepatic damage is believed to outweigh the potential benefits of the drug.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2044651
Once-daily - 100 mg
Route of Administration:
Oral
| Substance Class |
Chemical
Created
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Wed Apr 02 08:44:43 GMT 2025
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C98150
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| Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |
| Related Record | Type | Details | ||
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ACTIVE MOIETY |