Details
Stereochemistry | ACHIRAL |
Molecular Formula | C11H10N2O |
Molecular Weight | 186.2099 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1=CC=CC(=C1)N2C=CC=CC2=O
InChI
InChIKey=ZVSGUZQJNXHNIL-UHFFFAOYSA-N
InChI=1S/C11H10N2O/c12-9-4-3-5-10(8-9)13-7-2-1-6-11(13)14/h1-8H,12H2
Molecular Formula | C11H10N2O |
Molecular Weight | 186.2099 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Amphenidone is a sedative and hypnotic drug. Aminophenidone was launched as Dornwal in April 1960 through a retail division of Wallace & Tiernan called Maltbie Laboratories. Amphenidone was a mild to moderate and safe antianxiety and antitension substance and suited
mainly for neurotic anxiety reaction. Amphenidone has also been shown to have antithyroid activity.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/13685432
Curator's Comment: Rats: The amphenidone was suspended in 0.5 per cent gelatin and administered every twelve hours by stomach tube in
a total daily dose of 0.6 or 1.0 mg per g of body weight. https://www.ncbi.nlm.nih.gov/pubmed/14038388
Anxiety and tension: Ampheidone was administered orally to 40 patients, with an
average daily dose of 3700 mg (maximum
6400 mg, minimum 1600 mg) for an average period of 3 weeks. T
Route of Administration:
Oral
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:21:02 GMT 2023
by
admin
on
Fri Dec 15 15:21:02 GMT 2023
|
Record UNII |
M61FM2VCSV
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NCI_THESAURUS |
C29756
Created by
admin on Fri Dec 15 15:21:02 GMT 2023 , Edited by admin on Fri Dec 15 15:21:02 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
CHEMBL2104057
Created by
admin on Fri Dec 15 15:21:02 GMT 2023 , Edited by admin on Fri Dec 15 15:21:02 GMT 2023
|
PRIMARY | |||
|
134-37-2
Created by
admin on Fri Dec 15 15:21:02 GMT 2023 , Edited by admin on Fri Dec 15 15:21:02 GMT 2023
|
PRIMARY | |||
|
M61FM2VCSV
Created by
admin on Fri Dec 15 15:21:02 GMT 2023 , Edited by admin on Fri Dec 15 15:21:02 GMT 2023
|
PRIMARY | |||
|
8641
Created by
admin on Fri Dec 15 15:21:02 GMT 2023 , Edited by admin on Fri Dec 15 15:21:02 GMT 2023
|
PRIMARY | |||
|
DTXSID50158449
Created by
admin on Fri Dec 15 15:21:02 GMT 2023 , Edited by admin on Fri Dec 15 15:21:02 GMT 2023
|
PRIMARY | |||
|
SUB05484MIG
Created by
admin on Fri Dec 15 15:21:02 GMT 2023 , Edited by admin on Fri Dec 15 15:21:02 GMT 2023
|
PRIMARY | |||
|
194
Created by
admin on Fri Dec 15 15:21:02 GMT 2023 , Edited by admin on Fri Dec 15 15:21:02 GMT 2023
|
PRIMARY | |||
|
100000086933
Created by
admin on Fri Dec 15 15:21:02 GMT 2023 , Edited by admin on Fri Dec 15 15:21:02 GMT 2023
|
PRIMARY | |||
|
m48
Created by
admin on Fri Dec 15 15:21:02 GMT 2023 , Edited by admin on Fri Dec 15 15:21:02 GMT 2023
|
PRIMARY | Merck Index | ||
|
928
Created by
admin on Fri Dec 15 15:21:02 GMT 2023 , Edited by admin on Fri Dec 15 15:21:02 GMT 2023
|
PRIMARY | |||
|
C76934
Created by
admin on Fri Dec 15 15:21:02 GMT 2023 , Edited by admin on Fri Dec 15 15:21:02 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
ACTIVE MOIETY |