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

Details

Stereochemistry RACEMIC
Molecular Formula C16H19NO2S
Molecular Weight 289.393
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TENILOXAZINE

SMILES

C(OC1=CC=CC=C1CC2=CC=CS2)C3CNCCO3

InChI

InChIKey=OILWWIVKIDXCIB-UHFFFAOYSA-N
InChI=1S/C16H19NO2S/c1-2-6-16(19-12-14-11-17-7-8-18-14)13(4-1)10-15-5-3-9-20-15/h1-6,9,14,17H,7-8,10-12H2

HIDE SMILES / InChI

Molecular Formula C16H19NO2S
Molecular Weight 289.393
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Teniloxazine (also known as sulfoxazine or sufoxazine or Y 8894) was developed as an antidepressant. Teniloxazine belongs to the selective norepinephrine reuptake inhibitors (NRIs) and was studied for the treatment of the major depressive disorder. Clinical trials have shown that 50 mg of the drug lacked the anticholinergic, sedative and cardiovascular effects. In the elderly, some effects were recognized, in part, due to pharmacokinetic alteration. In addition, teniloxazine was studied for patients with Alzheimer's disease, however, doesn’t exist any development report for this study.

Approval Year

PubMed

PubMed

TitleDatePubMed
The emergence of new antidepressants for clinical use: Agomelatine paradox versus other novel agents.
2019-06
[Pharmacological studies on Y-8894. (IV). Ameliorative effect on a cerebral energy metabolism disorder induced by KCN].
1986-11
[Pharmacological studies on Y-8894. (III). Its effect on the abnormal electrocorticogram induced by destruction of the internal capsule].
1986-10
[Pharmacological studies on sufoxazine (Y-8894). (II). Anti-anoxic effect].
1985-10
[Pharmacological studies on sufoxazine (Y-8894). (I) Effects on experimental amnesia in mice].
1985-02

Sample Use Guides

Y-8894 (TENILOXAZINE) 50 mg
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:35:27 GMT 2025
Edited
by admin
on Mon Mar 31 18:35:27 GMT 2025
Record UNII
95Q6WNP25P
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TENILOXAZINE
INN   MART.  
INN  
Official Name English
TENILOXAZINE [MART.]
Preferred Name English
teniloxazine [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C265
Created by admin on Mon Mar 31 18:35:27 GMT 2025 , Edited by admin on Mon Mar 31 18:35:27 GMT 2025
Code System Code Type Description
PUBCHEM
119114
Created by admin on Mon Mar 31 18:35:27 GMT 2025 , Edited by admin on Mon Mar 31 18:35:27 GMT 2025
PRIMARY
MESH
C045330
Created by admin on Mon Mar 31 18:35:27 GMT 2025 , Edited by admin on Mon Mar 31 18:35:27 GMT 2025
PRIMARY
ChEMBL
CHEMBL2105438
Created by admin on Mon Mar 31 18:35:27 GMT 2025 , Edited by admin on Mon Mar 31 18:35:27 GMT 2025
PRIMARY
WIKIPEDIA
TENILOXAZINE
Created by admin on Mon Mar 31 18:35:27 GMT 2025 , Edited by admin on Mon Mar 31 18:35:27 GMT 2025
PRIMARY
INN
5897
Created by admin on Mon Mar 31 18:35:27 GMT 2025 , Edited by admin on Mon Mar 31 18:35:27 GMT 2025
PRIMARY
CAS
62473-79-4
Created by admin on Mon Mar 31 18:35:27 GMT 2025 , Edited by admin on Mon Mar 31 18:35:27 GMT 2025
PRIMARY
FDA UNII
95Q6WNP25P
Created by admin on Mon Mar 31 18:35:27 GMT 2025 , Edited by admin on Mon Mar 31 18:35:27 GMT 2025
PRIMARY
SMS_ID
100000082948
Created by admin on Mon Mar 31 18:35:27 GMT 2025 , Edited by admin on Mon Mar 31 18:35:27 GMT 2025
PRIMARY
EPA CompTox
DTXSID10866932
Created by admin on Mon Mar 31 18:35:27 GMT 2025 , Edited by admin on Mon Mar 31 18:35:27 GMT 2025
PRIMARY
EVMPD
SUB10893MIG
Created by admin on Mon Mar 31 18:35:27 GMT 2025 , Edited by admin on Mon Mar 31 18:35:27 GMT 2025
PRIMARY
NCI_THESAURUS
C75182
Created by admin on Mon Mar 31 18:35:27 GMT 2025 , Edited by admin on Mon Mar 31 18:35:27 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY