Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C15H11ClO2 |
| Molecular Weight | 258.7 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(C1=CC2=C(O1)C=CC=C2)C3=CC=C(Cl)C=C3
InChI
InChIKey=KBFBRIPYVVGWRS-UHFFFAOYSA-N
InChI=1S/C15H11ClO2/c16-12-7-5-10(6-8-12)15(17)14-9-11-3-1-2-4-13(11)18-14/h1-9,15,17H
| Molecular Formula | C15H11ClO2 |
| Molecular Weight | 258.7 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Cloridarol is a vasodilator that was studied for the treatment of coronary insufficiency in Italy in the 1970s. In normolipidemic rats, cloridarol decreased plasma triglycerides without affecting cholesterolemia and fast- or norepinephrine-induced lipolysis. The drug proved effective in reducing fructose-induced hypertriglyceridemia and dietary hypercholesterolemia in rats.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:12:40 UTC 2023
by
admin
on
Fri Dec 15 16:12:40 UTC 2023
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| Record UNII |
2L2063955H
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
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Official Name | English | ||
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Common Name | English | ||
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| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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WHO-VATC |
QC01DX15
Created by
admin on Fri Dec 15 16:12:40 UTC 2023 , Edited by admin on Fri Dec 15 16:12:40 UTC 2023
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WHO-ATC |
C01DX15
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admin on Fri Dec 15 16:12:40 UTC 2023 , Edited by admin on Fri Dec 15 16:12:40 UTC 2023
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NCI_THESAURUS |
C29707
Created by
admin on Fri Dec 15 16:12:40 UTC 2023 , Edited by admin on Fri Dec 15 16:12:40 UTC 2023
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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71132
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CHEMBL2104094
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3348
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C002971
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SUB06757MIG
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m1076
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PRIMARY | Merck Index | ||
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DTXSID70863220
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2L2063955H
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CLORIDAROL
Created by
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DB13291
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C80876
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3106
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3611-72-1
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100000084006
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222-780-3
Created by
admin on Fri Dec 15 16:12:40 UTC 2023 , Edited by admin on Fri Dec 15 16:12:40 UTC 2023
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PRIMARY |
| Related Record | Type | Details | ||
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ACTIVE MOIETY |
