Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C16H23NO2 |
| Molecular Weight | 261.3593 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC[C@@]1(OC[C@@H](O1)[C@@H]2CCCCN2)C3=CC=CC=C3
InChI
InChIKey=INOYCBNLWYEPSB-XHSDSOJGSA-N
InChI=1S/C16H23NO2/c1-2-16(13-8-4-3-5-9-13)18-12-15(19-16)14-10-6-7-11-17-14/h3-5,8-9,14-15,17H,2,6-7,10-12H2,1H3/t14-,15+,16-/m0/s1
| Molecular Formula | C16H23NO2 |
| Molecular Weight | 261.3593 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
CNS Activity
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Synthesis, absolute configuration, and molecular modeling study of etoxadrol, a potent phencyclidine-like agonist. | 1988-12 |
|
| Discriminative stimulus and reinforcing properties of etoxadrol and dexoxadrol in monkeys. | 1982-01 |
|
| Clinical investigation of a new intravenous anesthetic--etoxadrol hydrochloride (CL-1848; U-37862A). | 1976-05-01 |
|
| Effects of intravenous anesthetics on continuous avoidance behavior in the rat. | 1976-02 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 01:22:09 GMT 2025
by
admin
on
Wed Apr 02 01:22:09 GMT 2025
|
| Record UNII |
RO44G6QT80
|
| Record Status |
Validated (UNII)
|
| Record Version |
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-
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Preferred Name | English | ||
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Common Name | English |
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DTXSID00865419
Created by
admin on Wed Apr 02 01:22:09 GMT 2025 , Edited by admin on Wed Apr 02 01:22:09 GMT 2025
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30163-01-0
Created by
admin on Wed Apr 02 01:22:09 GMT 2025 , Edited by admin on Wed Apr 02 01:22:09 GMT 2025
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RO44G6QT80
Created by
admin on Wed Apr 02 01:22:09 GMT 2025 , Edited by admin on Wed Apr 02 01:22:09 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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SALT/SOLVATE -> PARENT |
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