Details
Stereochemistry | ACHIRAL |
Molecular Formula | C18H13ClN2O |
Molecular Weight | 308.762 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
ClC1=CC2=C(C=C1)N(CC#C)C(=O)CN=C2C3=CC=CC=C3
InChI
InChIKey=MFZOSKPPVCIFMT-UHFFFAOYSA-N
InChI=1S/C18H13ClN2O/c1-2-10-21-16-9-8-14(19)11-15(16)18(20-12-17(21)22)13-6-4-3-5-7-13/h1,3-9,11H,10,12H2
Pinazepam, a benzodiazepine derivative, differs from other drugs of its class by the presence of an unsaturated bond, the propargyl group, at the N-1 position. In animals, pinazepam controls anxiety and aggressiveness and exerts anticonvulsant activity. In clinical trials with open or controlled design, pinazepam, compared with diazepam, showed significant and purely anxiolytic action in patients suffering from anxiety with or without somatic manifestations, particularly in gastrointestinal disorders. Even though it is not a specific hypnotic drug, it seems to help patients in whom the physiological course of the sleep is disturbed. Pinazepam is used in the treatment of anxiety and insomnia associated with anxiety.
CNS Activity
Approval Year
PubMed
Title | Date | PubMed |
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Determination of midazolam in human plasma by solid-phase microextraction and gas chromatography/mass spectrometry. | 2001 |
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Structural requirements of benzodiazepines for the inhibition of pig brain nitric oxide synthase. | 2001 Nov 30 |
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Development of a list of potentially inappropriate drugs for the korean elderly using the delphi method. | 2010 Dec |
Patents
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Classification Tree | Code System | Code | ||
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WHO-ATC |
N05BA14
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NCI_THESAURUS |
C1012
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DEA NO. |
2883
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WHO-VATC |
QN05BA14
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DTXSID3023475
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m8823
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2175
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CHEMBL1213352
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257-934-9
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PINAZEPAM
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52463-83-9
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C66388
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SUB09852MIG
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40391
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ACTIVE MOIETY