Details
Stereochemistry | UNKNOWN |
Molecular Formula | C16H21N |
Molecular Weight | 227.3446 |
Optical Activity | ( - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 1 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
C1CN(C1)C2CCCC\C2=C/C3=CC=CC=C3
InChI
InChIKey=DOWWDQZIFWLREB-FYWRMAATSA-N
InChI=1S/C16H21N/c1-2-7-14(8-3-1)13-15-9-4-5-10-16(15)17-11-6-12-17/h1-3,7-8,13,16H,4-6,9-12H2/b15-13+
Molecular Formula | C16H21N |
Molecular Weight | 227.3446 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 1 |
Optical Activity | ( + / - ) |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/2855569
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2855569
Tazadolene was developed as a novel non-opioid analgesic with antidepressant properties. Experiments on rodents have revealed that unique analgesia properties of tazadolene was due to the ability of this compound to activate both serotonergic and alpha 2 adrenergic antinociceptive systems. Information about the current use of this drug is not available.
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Reversed-phase high-performance liquid chromatographic assay for the determination of potency and impurities in tazadolene succinate bulk drug and capsules. | 1986 Feb 26 |
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Tazadolene succinate: a structurally novel non-opioid analgesic with antidepressant properties. | 1986 Nov |
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Evidence for the combined involvement of serotonergic and alpha 2 adrenergic mechanisms in the analgesic activity of tazadolene succinate. | 1987 Dec |
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Isolation, identification and synthesis of a metabolite of tazadolene succinate. | 1987 Feb |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 04:17:46 GMT 2023
by
admin
on
Sat Dec 16 04:17:46 GMT 2023
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Record UNII |
P3G7HF4MQR
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Record Status |
Validated (UNII)
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Record Version |
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-
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P3G7HF4MQR
Created by
admin on Sat Dec 16 04:17:46 GMT 2023 , Edited by admin on Sat Dec 16 04:17:46 GMT 2023
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87936-76-3
Created by
admin on Sat Dec 16 04:17:46 GMT 2023 , Edited by admin on Sat Dec 16 04:17:46 GMT 2023
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PRIMARY |
Related Record | Type | Details | ||
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ENANTIOMER -> ENANTIOMER |
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RACEMATE -> ENANTIOMER |