Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C28H38N4O |
| Molecular Weight | 446.6275 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC(=O)C1(CCN(CCCN2C3=CC=CC=C3CCC4=CC=CC=C24)CC1)N5CCCCC5
InChI
InChIKey=NWPJLRSCSQHPJV-UHFFFAOYSA-N
InChI=1S/C28H38N4O/c29-27(33)28(31-18-6-1-7-19-31)15-21-30(22-16-28)17-8-20-32-25-11-4-2-9-23(25)13-14-24-10-3-5-12-26(24)32/h2-5,9-12H,1,6-8,13-22H2,(H2,29,33)
| Molecular Formula | C28H38N4O |
| Molecular Weight | 446.6275 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Carpipramine (Prazinil, Defekton) is an atypical antipsychotic used for the treatment of schizophrenia and anxiety in France and Japan. In addition to its neuroleptic and anxiolytic effects, carpipramine also has hypnotic properties. In september 2014 L'ANSM decided to withdraw the marketing of Prazinil (carpipramine).
Originator
Sources: http://www.ncbi.nlm.nih.gov/pubmed/2808634
Curator's Comment: 1970
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| [Hebephrenic schizophrenia]. | 2005-10 |
|
| Atypical properties of several classes of antipsychotic drugs on the basis of differential induction of Fos-like immunoreactivity in the rat brain. | 2004-11-26 |
|
| Simultaneous determination of four antipsychotic drugs in plasma by high-performance liquid chromatography. Application to management of acute intoxications. | 2003-10-05 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/19231
Doses varied from 50 to 400 mg per day
Route of Administration:
Oral
| Substance Class |
Chemical
Created
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8AFK6F91EQ
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Validated (UNII)
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C265
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DTXSID40208149
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C006922
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1989
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20342
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m1058
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517
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8AFK6F91EQ
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Carpipramine
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100000081326
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227-700-0
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ACTIVE MOIETY |