Details
Stereochemistry | RACEMIC |
Molecular Formula | C11H8ClNO2 |
Molecular Weight | 221.64 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@]12C[C@]1(C(=O)NC2=O)C3=CC=C(Cl)C=C3
InChI
InChIKey=YYGANUVABKDFDW-KCJUWKMLSA-N
InChI=1S/C11H8ClNO2/c12-7-3-1-6(2-4-7)11-5-8(11)9(14)13-10(11)15/h1-4,8H,5H2,(H,13,14,15)/t8-,11+/m1/s1
Molecular Formula | C11H8ClNO2 |
Molecular Weight | 221.64 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Cyproximide is a psychoactive drug discovered by American Cyanamid company. The drug exhibited activity as a central nervous system depressant and was claimed to be useful as a tranquilizing agent, hypnotic agent or muscle relaxant. The phenobarbital-like activity of cyproximide after intraperitoneal administration was demonstrated in rod traversal, clinging and righting reflex tests in mice. In addition to CNS depressant activity, cyproximide had a mild stimulant and antidepressant effects, which were shown by the restoration of exploratory behavior and an increase in locomotor activity in mice. Chronic administration of the drug led to a greater incidence of proliferative lesions in the liver of treated rats; however, the incidence of hepatocellular neoplasms was the same in treated and control rats.
CNS Activity
Originator
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://patents.google.com/patent/GB1187796A/en
CNS depressant activity was demonstrated after acute i.p. administration of 150-300 mg/kg to mice.
Route of Administration:
Intraperitoneal
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 17:55:14 GMT 2023
by
admin
on
Sat Dec 16 17:55:14 GMT 2023
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Record UNII |
KE6K6JP8FP
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Record Status |
Validated (UNII)
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Record Version |
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C175759
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Related Record | Type | Details | ||
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ACTIVE MOIETY |