Details
Stereochemistry | RACEMIC |
Molecular Formula | C19H22N2 |
Molecular Weight | 278.3914 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(CC(C#N)(C1=CC=CC=C1)C2=CC=CC=C2)N(C)C
InChI
InChIKey=GJJQIGFCGLPOQK-UHFFFAOYSA-N
InChI=1S/C19H22N2/c1-16(21(2)3)14-19(15-20,17-10-6-4-7-11-17)18-12-8-5-9-13-18/h4-13,16H,14H2,1-3H3
Molecular Formula | C19H22N2 |
Molecular Weight | 278.3914 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
CNS Activity
Sources: https://www.ncbi.nlm.nih.gov/pubmed/20239733
Curator's Comment: CNS active in rats
Originator
Approval Year
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Sources: https://www.ncbi.nlm.nih.gov/pubmed/20239733 |
Primary | Unknown Approved UseUnknown |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/20239733
To study the analgetic effect of didiavalo the drug was administered to rats intravenously. Didiavalo was 30 times less potent than morphine, with effects of dose 60 mg/kg similar to the effect of 2.0 mg/kg morphine.
Route of Administration:
Intravenous
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:14:49 GMT 2023
by
admin
on
Fri Dec 15 15:14:49 GMT 2023
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Record UNII |
0GYB2HJA89
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Record Status |
Validated (UNII)
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Record Version |
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Classification Tree | Code System | Code | ||
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DEA NO. |
9254
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admin on Fri Dec 15 15:14:49 GMT 2023 , Edited by admin on Fri Dec 15 15:14:49 GMT 2023
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50382
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204-755-9
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0GYB2HJA89
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admin on Fri Dec 15 15:14:49 GMT 2023 , Edited by admin on Fri Dec 15 15:14:49 GMT 2023
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DTXSID1048912
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1398020
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31331
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125-79-1
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Methadone intermediate
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2089
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admin on Fri Dec 15 15:14:49 GMT 2023 , Edited by admin on Fri Dec 15 15:14:49 GMT 2023
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