Details
Stereochemistry | RACEMIC |
Molecular Formula | C16H21N.C4H6O4 |
Molecular Weight | 345.4327 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 1 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)CCC(O)=O.C1CN(C1)C2CCCC\C2=C/C3=CC=CC=C3
InChI
InChIKey=IEXXCIWKNWOEKZ-GVYCEHEKSA-N
InChI=1S/C16H21N.C4H6O4/c1-2-7-14(8-3-1)13-15-9-4-5-10-16(15)17-11-6-12-17;5-3(6)1-2-4(7)8/h1-3,7-8,13,16H,4-6,9-12H2;1-2H2,(H,5,6)(H,7,8)/b15-13+;
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 |
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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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Evidence for the combined involvement of serotonergic and alpha 2 adrenergic mechanisms in the analgesic activity of tazadolene succinate. | 1987 Dec |
Patents
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NCI_THESAURUS |
C2198
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CHEMBL2111124
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20L521S4UL
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U-66
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100000088913
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C048351
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87936-82-1
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C152521
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SUB22021
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6536916
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ACTIVE MOIETY
SUBSTANCE RECORD