Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C17H17ClN2O |
| Molecular Weight | 300.783 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCNC1=NC2=C(C=C(Cl)C=C2)[C@](C)(O1)C3=CC=CC=C3
InChI
InChIKey=IBYCYJFUEJQSMK-QGZVFWFLSA-N
InChI=1S/C17H17ClN2O/c1-3-19-16-20-15-10-9-13(18)11-14(15)17(2,21-16)12-7-5-4-6-8-12/h4-11H,3H2,1-2H3,(H,19,20)/t17-/m1/s1
| Molecular Formula | C17H17ClN2O |
| Molecular Weight | 300.783 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
DescriptionSources: https://www.google.ch/patents/WO2007109288A3
Sources: https://www.google.ch/patents/WO2007109288A3
(R)-Etifoxine is an isomer, chemically isolated from Etifoxine (Stresam), an approved racemic drug (off patent) prescribed in Europe. (R)-Etifoxine was developed by Xytis Inc for treatment pain, mental disease, and central nervous system disorders. However future development has been discontinued.
CNS Activity
Sources: https://www.ncbi.nlm.nih.gov/pubmed/25589941
Curator's Comment: Data for R/S-Etifoxine
Originator
Approval Year
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | Unknown Approved UseUnknown |
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| Primary | Unknown Approved UseUnknown |
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Sources: https://www.google.ch/patents/WO2007109288A3 |
Primary | Unknown Approved UseUnknown |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.google.ch/patents/WO2007109288A3
50 mg up to about 150 mg/day.
Route of Administration:
Oral
| Substance Class |
Chemical
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RACEMATE -> ENANTIOMER |