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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
Structure of TAZADOLENE, (-)-

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+

HIDE SMILES / InChI

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 ( + / - )

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

PubMed

TitleDatePubMed
Reversed-phase high-performance liquid chromatographic assay for the determination of potency and impurities in tazadolene succinate bulk drug and capsules.
1986 Feb 26
Tazadolene succinate: a structurally novel non-opioid analgesic with antidepressant properties.
1986 Nov
Evidence for the combined involvement of serotonergic and alpha 2 adrenergic mechanisms in the analgesic activity of tazadolene succinate.
1987 Dec
Isolation, identification and synthesis of a metabolite of tazadolene succinate.
1987 Feb
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 04:17:46 GMT 2023
Edited
by admin
on Sat Dec 16 04:17:46 GMT 2023
Record UNII
P3G7HF4MQR
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TAZADOLENE, (-)-
Common Name English
AZETIDINE, 1-(2-(PHENYLMETHYLENE)CYCLOHEXYL)-, (E)-(-)-
Systematic Name English
Code System Code Type Description
FDA UNII
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
PRIMARY
CAS
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
PRIMARY
Related Record Type Details
ENANTIOMER -> ENANTIOMER
RACEMATE -> ENANTIOMER