Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C17H17ClN2O |
| Molecular Weight | 300.783 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCNC1=NC2=CC=C(Cl)C=C2C(C)(O1)C3=CC=CC=C3
InChI
InChIKey=IBYCYJFUEJQSMK-UHFFFAOYSA-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)
| Molecular Formula | C17H17ClN2O |
| Molecular Weight | 300.783 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:17:34 UTC 2023
by
admin
on
Fri Dec 15 16:17:34 UTC 2023
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| Record UNII |
X24X82MX4X
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| Record Status |
Validated (UNII)
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| Record Version |
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-
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Official Name | English | ||
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Common Name | English | ||
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Code | English | ||
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Code | English | ||
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Code | English | ||
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Systematic Name | English |
| Classification Tree | Code System | Code | ||
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WHO-ATC |
N05BX03
Created by
admin on Fri Dec 15 16:17:34 UTC 2023 , Edited by admin on Fri Dec 15 16:17:34 UTC 2023
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WHO-VATC |
QN05BX03
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admin on Fri Dec 15 16:17:34 UTC 2023 , Edited by admin on Fri Dec 15 16:17:34 UTC 2023
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NCI_THESAURUS |
C28197
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| Code System | Code | Type | Description | ||
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C81619
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24441
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X24X82MX4X
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DTXSID00865010
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21715-46-8
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135413553
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CHEMBL2106227
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100000082075
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2846
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SUB07302MIG
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DB08986
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ETIFOXINE
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m5183
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PRIMARY | Merck Index | ||
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1099
Created by
admin on Fri Dec 15 16:17:34 UTC 2023 , Edited by admin on Fri Dec 15 16:17:34 UTC 2023
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ENANTIOMER -> RACEMATE |
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TARGET->LIGAND |
Enhances cholesterol transport into mitochondria leading to increase level of neurosteroid synthesis.
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ENANTIOMER -> RACEMATE |
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |
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