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Details

Stereochemistry RACEMIC
Molecular Formula C11H12N2O2
Molecular Weight 204.2252
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of IDAZOXAN

SMILES

C1CN=C(N1)C2COC3=CC=CC=C3O2

InChI

InChIKey=HPMRFMKYPGXPEP-UHFFFAOYSA-N
InChI=1S/C11H12N2O2/c1-2-4-9-8(3-1)14-7-10(15-9)11-12-5-6-13-11/h1-4,10H,5-7H2,(H,12,13)

HIDE SMILES / InChI

Molecular Formula C11H12N2O2
Molecular Weight 204.2252
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:50:15 UTC 2023
Edited
by admin
on Fri Dec 15 16:50:15 UTC 2023
Record UNII
Y310PA316B
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
IDAZOXAN
INN   MI  
INN  
Official Name English
IDAZOXAN [MI]
Common Name English
DL-IDAZOXAN
Common Name English
NSC-759867
Code English
RACEMIC IDAZOXAN
Common Name English
2-(2,3-DIHYDRO-1,4-BENZODIOXIN-2-YL)-4,5-DIHYDRO-1H-IMIDAZOLE
Systematic Name English
idazoxan [INN]
Common Name English
1H-IMIDAZOLE, 2-(2,3-DIHYDRO-1,4-BENZODIOXIN-2-YL)-4,5-DIHYDRO-
Systematic Name English
2-IMIDAZOLINE, 2-(1,4-BENZODIOXAN-2-YL)-
Systematic Name English
(±)-2-(1,4-BENZODIOXAN-2-YL)-2-IMIDAZOLINE
Systematic Name English
(±)-IDAZOXAN
Common Name English
Code System Code Type Description
INN
5337
Created by admin on Fri Dec 15 16:50:15 UTC 2023 , Edited by admin on Fri Dec 15 16:50:15 UTC 2023
PRIMARY
CAS
84720-37-6
Created by admin on Fri Dec 15 16:50:15 UTC 2023 , Edited by admin on Fri Dec 15 16:50:15 UTC 2023
SUPERSEDED
CAS
79944-58-4
Created by admin on Fri Dec 15 16:50:15 UTC 2023 , Edited by admin on Fri Dec 15 16:50:15 UTC 2023
PRIMARY
NSC
759867
Created by admin on Fri Dec 15 16:50:15 UTC 2023 , Edited by admin on Fri Dec 15 16:50:15 UTC 2023
PRIMARY
CHEBI
5862
Created by admin on Fri Dec 15 16:50:15 UTC 2023 , Edited by admin on Fri Dec 15 16:50:15 UTC 2023
PRIMARY
MERCK INDEX
m6198
Created by admin on Fri Dec 15 16:50:15 UTC 2023 , Edited by admin on Fri Dec 15 16:50:15 UTC 2023
PRIMARY Merck Index
MESH
D019329
Created by admin on Fri Dec 15 16:50:15 UTC 2023 , Edited by admin on Fri Dec 15 16:50:15 UTC 2023
PRIMARY
FDA UNII
Y310PA316B
Created by admin on Fri Dec 15 16:50:15 UTC 2023 , Edited by admin on Fri Dec 15 16:50:15 UTC 2023
PRIMARY
DRUG BANK
DB12551
Created by admin on Fri Dec 15 16:50:15 UTC 2023 , Edited by admin on Fri Dec 15 16:50:15 UTC 2023
PRIMARY
EVMPD
SUB08113MIG
Created by admin on Fri Dec 15 16:50:15 UTC 2023 , Edited by admin on Fri Dec 15 16:50:15 UTC 2023
PRIMARY
EPA CompTox
DTXSID6045161
Created by admin on Fri Dec 15 16:50:15 UTC 2023 , Edited by admin on Fri Dec 15 16:50:15 UTC 2023
PRIMARY
SMS_ID
100000083695
Created by admin on Fri Dec 15 16:50:15 UTC 2023 , Edited by admin on Fri Dec 15 16:50:15 UTC 2023
PRIMARY
ChEMBL
CHEMBL10316
Created by admin on Fri Dec 15 16:50:15 UTC 2023 , Edited by admin on Fri Dec 15 16:50:15 UTC 2023
PRIMARY
WIKIPEDIA
IDAZOXAN
Created by admin on Fri Dec 15 16:50:15 UTC 2023 , Edited by admin on Fri Dec 15 16:50:15 UTC 2023
PRIMARY
NCI_THESAURUS
C170049
Created by admin on Fri Dec 15 16:50:15 UTC 2023 , Edited by admin on Fri Dec 15 16:50:15 UTC 2023
PRIMARY
PUBCHEM
54459
Created by admin on Fri Dec 15 16:50:15 UTC 2023 , Edited by admin on Fri Dec 15 16:50:15 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
TARGET -> AGONIST
SHORT-ACTING
Related Record Type Details
ACTIVE MOIETY