Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C20H20ClN5O3S2 |
| Molecular Weight | 477.988 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CN1CCN(CC1)C(=O)OC2N(C(=O)C3=C2SCCS3)C4=CC=C5C=CC(Cl)=NC5=N4
InChI
InChIKey=RMXOUBDDDQUBKD-UHFFFAOYSA-N
InChI=1S/C20H20ClN5O3S2/c1-24-6-8-25(9-7-24)20(28)29-19-16-15(30-10-11-31-16)18(27)26(19)14-5-3-12-2-4-13(21)22-17(12)23-14/h2-5,19H,6-11H2,1H3
| Molecular Formula | C20H20ClN5O3S2 |
| Molecular Weight | 477.988 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Suriclone is a dithiinopyrrole derivative patented by Rhone-Poulenc S. A. as a sedative and anxiolytic drug. The mechanism of action by which suriclone produces it's sedative and anxiolytic effects is by modulating GABAA receptors, although suriclone is more subtype-selective than most benzodiazepines. In clinical trials, Suriclone shows a significant anxiolytic effect. The most common adverse reaction was dizziness.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Effects of etizolam and ethyl loflazepate on the P300 event-related potential in healthy subjects. | 2010-11-03 |
|
| Objective markers of drug effects on brain function from recordings of scalp potential in healthy volunteers. | 2002-12 |
|
| Pharmacokinetic and -dynamic studies with a new anxiolytic, suriclone, utilizing EEG mapping and psychometry. | 1994-02 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/7910470
0.1, 0.2 and 0.4 mg
Route of Administration:
Oral
| Substance Class |
Chemical
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| Record UNII |
LNC9G689VR
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Validated (UNII)
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NCI_THESAURUS |
C28197
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C29710
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53813-83-5
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SUB10782MIG
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C037283
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SURICLONE
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C96876
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258-794-1
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104355-41-1
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SUPERSEDED |
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ACTIVE MOIETY |