Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C23H27ClN2O2.2ClH |
| Molecular Weight | 471.848 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.Cl.OCCN1CCN(CC\C=C2\C3=CC=CC=C3COC4=CC=C(Cl)C=C24)CC1
InChI
InChIKey=URBVIISFALGUAB-LZWUXPCZSA-N
InChI=1S/C23H27ClN2O2.2ClH/c24-19-7-8-23-22(16-19)21(20-5-2-1-4-18(20)17-28-23)6-3-9-25-10-12-26(13-11-25)14-15-27;;/h1-2,4-8,16,27H,3,9-15,17H2;2*1H/b21-6-;;
| 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 | C23H27ClN2O2 |
| Molecular Weight | 398.926 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Optical Activity | NONE |
Pinoxepin belongs to the dibenzoxepine series of drugs which are characterized by a 6-7-6 tricyclic nuclear structure. Clinical studies indicated that pinoxepin was a potent antipsychotic-sedative equally effective to chlorpromazine and thioridazine. Pinoxepin in studies with chronic schizophrenic patients displayed useful effects on behavior without unduly prominent side effects. In doses above 300 mg seizures are reported and more frequent changes in liver-function tests were noted than with standard drug, but below 300 mg pinoxepin was found to have side effects similar to chlorpromazine and marked sedative effects.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Comparison of perphenazine and P-5227 in chronic schizophrenics: clinical and EEG effects. | 1969-05-01 |
|
| Comparison of P-5227 and thioridazine in chronic schizophrenic patients. | 1967-09-01 |
|
| Pinoxepin vs. chlorpromazine: a double-blind comparison. | 1967-08 |
|
| Effects of pinoxepin and imipramine on the mesencephalic reticular formation and amygdaloid complex in the cat: neurophysiological and clinical correlations in human subjects. | 1967-07 |
|
| A PRELIMINARY STUDY OF P-5227, a new active tricyclic antipsychotic agent. | 1966-10 |
|
| P-5227: an active dibenzoxepine antipsychotic. | 1966-05 |
|
| P-5227: a 6-7-6 tricyclic antipsychotic compound. | 1966-05 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/5237376
Daily dosage: 50 mg - 1st week, 100mg - 2nd week, 150 mg - 3rd week, 200 mg - 4th week, 250 mg - 5th week, 250-400 mg - 6-10th weeks.
Route of Administration:
Oral
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 17:55:57 GMT 2025
by
admin
on
Mon Mar 31 17:55:57 GMT 2025
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| Record UNII |
7KE5R66TSY
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| Record Status |
Validated (UNII)
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| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C66883
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CHEMBL2110968
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C76653
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6433591
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14008-46-9
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300000055523
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DTXSID301337302
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7KE5R66TSY
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