Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C22H23ClFNO2.ClH |
| Molecular Weight | 424.336 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.FC1=CC=C(C=C1)C(=O)CCCN2CCC(CC2)C(=O)C3=CC=C(Cl)C=C3
InChI
InChIKey=ZIJIVCQJKDRJOL-UHFFFAOYSA-N
InChI=1S/C22H23ClFNO2.ClH/c23-19-7-3-17(4-8-19)22(27)18-11-14-25(15-12-18)13-1-2-21(26)16-5-9-20(24)10-6-16;/h3-10,18H,1-2,11-15H2;1H
| Molecular Formula | ClH |
| Molecular Weight | 36.461 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C22H23ClFNO2 |
| Molecular Weight | 387.875 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Cloroperone (AHR 6134) is a derivative of butyrophenone with anxiolytic properties. In animals, cloroperone causes slight CNS depression in mice, prevents the lethal effects of d-amphetamine under crowded conditions in mice, suppresses emesis in dogs. The drug was investigated in the clinic for the treatment of psychotic patients. It was shown to be effective anxiolytic at low dosages without sedation, listlessness, drowsiness or neurologic reactions. Cloroperone is a selective binder to 5-HT2 receptors (Ki 4.5 nM).
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL2095200 Sources: https://www.ncbi.nlm.nih.gov/pubmed/1407003 |
4.5 nM [Ki] |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 17:52:42 GMT 2025
by
admin
on
Mon Mar 31 17:52:42 GMT 2025
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| Record UNII |
95U4NV3X82
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| Record Status |
Validated (UNII)
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| Record Version |
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NCI_THESAURUS |
C28197
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admin on Mon Mar 31 17:52:42 GMT 2025 , Edited by admin on Mon Mar 31 17:52:42 GMT 2025
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55695-56-2
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C72728
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41535
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309709
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DTXSID40204227
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300000055289
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95U4NV3X82
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CHEMBL2110929
Created by
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |