Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C18H21N |
| Molecular Weight | 251.366 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C=C(C1=CC=CC=C1)C2=CC=CC=C2)N(C)C
InChI
InChIKey=QZWMYBWMOFESDA-UHFFFAOYSA-N
InChI=1S/C18H21N/c1-15(19(2)3)14-18(16-10-6-4-7-11-16)17-12-8-5-9-13-17/h4-15H,1-3H3
| Molecular Formula | C18H21N |
| Molecular Weight | 251.366 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Analgesic effect and bioavailability of oral ketogan given as tablets or mixture to patients with chronic pain of malignant origin. | 1988 |
|
| Premedication for day-case surgery: double-blind comparison of ketobemidone + dimethylaminodiphenylbuten (A-29) and morphine + scopolamine. | 1986-10 |
|
| 5-HT-uptake inhibition potentiates antinociception induced by morphine, pethidine, methadone and ketobemidone in rats. | 1985-09 |
|
| Histamine release from human basophils and isolated rat mast cells induced by ketobemidone, pethidine and the spasmolytic A29. | 1982-01 |
|
| Clinical pharmacokinetics of ketobemidone. Its bioavailability after rectal administration. | 1981-02 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:25:41 GMT 2025
by
admin
on
Mon Mar 31 23:25:41 GMT 2025
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| Record UNII |
A6FGC19UYP
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| Record Status |
Validated (UNII)
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| Record Version |
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100000138721
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A6FGC19UYP
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122535
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29869-90-7
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249-909-6
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SUB78417
Created by
admin on Mon Mar 31 23:25:41 GMT 2025 , Edited by admin on Mon Mar 31 23:25:41 GMT 2025
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| Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT |
| Related Record | Type | Details | ||
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ACTIVE MOIETY |