U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C23H35NO2.CH4O3S
Molecular Weight 453.635
Optical Activity ( + / - )
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TONAZOCINE MESYLATE

SMILES

CS(O)(=O)=O.CCCCCC(=O)CC[C@]1(C)[C@H]2CC3=CC=C(O)C=C3[C@]1(C)CCN2C

InChI

InChIKey=CQSTVPYARYSBNS-HZLAGBECSA-N
InChI=1S/C23H35NO2.CH4O3S/c1-5-6-7-8-18(25)11-12-23(3)21-15-17-9-10-19(26)16-20(17)22(23,2)13-14-24(21)4;1-5(2,3)4/h9-10,16,21,26H,5-8,11-15H2,1-4H3;1H3,(H,2,3,4)/t21-,22+,23-;/m1./s1

HIDE SMILES / InChI

Molecular Formula CH4O3S
Molecular Weight 96.106
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C23H35NO2
Molecular Weight 357.5295
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Tonazocine is a nonpeptide, partial delta-opioid agonist with mu antagonist properties and weak k agonist activity. Tonazocine augmented the efficacy of L-DOPA in the reserpine model. Tonazocine evoked a dose-related, ipsilateral rotation, consistent with augmentation of dopaminergic function on the unlesioned side. Tonazocine has a narcotic antagonist activity which is 90 times that of pentazocine and 5 times less than that of naloxone as measured by the antagonism of morphine analgesia in the rat tail-flick test. Total pain relief scores for tonazocine 4 mg were nearly identical with that of morphine sulfate 10 mg while 8 mg of tonazocine were superior to 10 mg of morphine. Drowsiness was the main adverse reaction of tonazocine. Tonazocine has undergone phase II clinical trials for postoperative pain and appeared to possess reasonable efficacy.

Approval Year

PubMed

PubMed

TitleDatePubMed
Pharmacological profiles of tonazocine (Win 42156) and zenazocine (Win 42964).
1985 Feb
Tonazocine mesylate in postoperative pain patients: a double-blind placebo controlled analgesic study.
1989 Apr
Antiparkinson potential of delta-opioid receptor agonists.
2000 May 19

Sample Use Guides

Single dose - 2, 4, 8 mg
Route of Administration: Intramuscular
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:07:09 UTC 2023
Edited
by admin
on Fri Dec 15 16:07:09 UTC 2023
Record UNII
2F5K551CB4
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TONAZOCINE MESYLATE
USAN  
USAN  
Official Name English
WIN-42156-2
Code English
TONAZOCINE MESYLATE [USAN]
Common Name English
TONAZOCINE MESILATE
MART.  
Common Name English
WIN 42156-2
Code English
(±)-1-((2R*,6S*,11S*)-1,2,3,4,5,6-HEXAHYDRO-8-HYDROXY-3,6,11-TRIMETHYL-2,6-METHANO-3-BENZAZOCIN-11-YL)-3-OCTANONE METHANESULPHONATE (SALT)
Common Name English
3-OCTANONE, 1-(1,2,3,4,5,6-HEXAHYDRO-8-HYDROXY-3,6,11-TRIMETHYL-2,6-METHANO-3-BENZAZOCIN-11-YL)-, METHANESULFONATE (SALT), (2.ALPHA.,6.ALPHA.,11S*)-(±)-
Common Name English
3-OCTANONE, 1-(1,2,3,4,5,6-HEXAHYDRO-8-HYDROXY-3,6,11-TRIMETHYL-2,6-METHANO-3-BENZAZOCIN-11-YL)-, METHANESULPHONATE (SALT), (2.ALPHA.,6.ALPHA.,11S*)-(±)-
Common Name English
(±)-1-((2R*,6S*,11S*)-1,2,3,4,5,6-HEXAHYDRO-8-HYDROXY-3,6,11-TRIMETHYL-2,6-METHANO-3-BENZAZOCIN-11-YL)-3-OCTANONE METHANESULFONATE (SALT)
Common Name English
TONAZOCINE MESILATE [MART.]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C67413
Created by admin on Fri Dec 15 16:07:10 UTC 2023 , Edited by admin on Fri Dec 15 16:07:10 UTC 2023
Code System Code Type Description
EPA CompTox
DTXSID90994722
Created by admin on Fri Dec 15 16:07:10 UTC 2023 , Edited by admin on Fri Dec 15 16:07:10 UTC 2023
PRIMARY
NCI_THESAURUS
C81379
Created by admin on Fri Dec 15 16:07:10 UTC 2023 , Edited by admin on Fri Dec 15 16:07:10 UTC 2023
PRIMARY
ChEMBL
CHEMBL2111044
Created by admin on Fri Dec 15 16:07:10 UTC 2023 , Edited by admin on Fri Dec 15 16:07:10 UTC 2023
PRIMARY
PUBCHEM
76965006
Created by admin on Fri Dec 15 16:07:10 UTC 2023 , Edited by admin on Fri Dec 15 16:07:10 UTC 2023
PRIMARY
CAS
73789-00-1
Created by admin on Fri Dec 15 16:07:10 UTC 2023 , Edited by admin on Fri Dec 15 16:07:10 UTC 2023
PRIMARY
FDA UNII
2F5K551CB4
Created by admin on Fri Dec 15 16:07:10 UTC 2023 , Edited by admin on Fri Dec 15 16:07:10 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY