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

Details

Stereochemistry ACHIRAL
Molecular Formula C7H10N4O4
Molecular Weight 214.1787
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETANIDAZOLE

SMILES

OCCNC(=O)CN1C=CN=C1[N+]([O-])=O

InChI

InChIKey=WCDWBPCFGJXFJZ-UHFFFAOYSA-N
InChI=1S/C7H10N4O4/c12-4-2-8-6(13)5-10-3-1-9-7(10)11(14)15/h1,3,12H,2,4-5H2,(H,8,13)

HIDE SMILES / InChI

Molecular Formula C7H10N4O4
Molecular Weight 214.1787
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 18:54:42 UTC 2023
Edited
by admin
on Sat Dec 16 18:54:42 UTC 2023
Record UNII
30DKA3Q1HL
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ETANIDAZOLE
INN   MART.   MI   USAN  
INN   USAN  
Official Name English
ETANIDAZOLE [MART.]
Common Name English
N-(2-Hydroxyethyl)-2-nitroimidazole-1-acetamide
Systematic Name English
NSC-301467
Code English
etanidazole [INN]
Common Name English
RADINYL
Brand Name English
SR 2508
Code English
SR-2508
Code English
ETANIDAZOLE [USAN]
Common Name English
ETANIDAZOLE [MI]
Common Name English
1H-IMIDAZOLE-1-ACETAMIDE, N-(2-HYDROXYETHYL)-2-NITRO-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C798
Created by admin on Sat Dec 16 18:54:43 UTC 2023 , Edited by admin on Sat Dec 16 18:54:43 UTC 2023
Code System Code Type Description
WIKIPEDIA
ETANIDAZOLE
Created by admin on Sat Dec 16 18:54:43 UTC 2023 , Edited by admin on Sat Dec 16 18:54:43 UTC 2023
PRIMARY
CAS
22668-01-5
Created by admin on Sat Dec 16 18:54:43 UTC 2023 , Edited by admin on Sat Dec 16 18:54:43 UTC 2023
PRIMARY
FDA UNII
30DKA3Q1HL
Created by admin on Sat Dec 16 18:54:43 UTC 2023 , Edited by admin on Sat Dec 16 18:54:43 UTC 2023
PRIMARY
EPA CompTox
DTXSID8045434
Created by admin on Sat Dec 16 18:54:43 UTC 2023 , Edited by admin on Sat Dec 16 18:54:43 UTC 2023
PRIMARY
ChEMBL
CHEMBL47405
Created by admin on Sat Dec 16 18:54:43 UTC 2023 , Edited by admin on Sat Dec 16 18:54:43 UTC 2023
PRIMARY
CHEBI
75473
Created by admin on Sat Dec 16 18:54:43 UTC 2023 , Edited by admin on Sat Dec 16 18:54:43 UTC 2023
PRIMARY
INN
6142
Created by admin on Sat Dec 16 18:54:43 UTC 2023 , Edited by admin on Sat Dec 16 18:54:43 UTC 2023
PRIMARY
MESH
D017341
Created by admin on Sat Dec 16 18:54:43 UTC 2023 , Edited by admin on Sat Dec 16 18:54:43 UTC 2023
PRIMARY
USAN
Y-21
Created by admin on Sat Dec 16 18:54:43 UTC 2023 , Edited by admin on Sat Dec 16 18:54:43 UTC 2023
PRIMARY
NSC
301467
Created by admin on Sat Dec 16 18:54:43 UTC 2023 , Edited by admin on Sat Dec 16 18:54:43 UTC 2023
PRIMARY
PUBCHEM
3276
Created by admin on Sat Dec 16 18:54:43 UTC 2023 , Edited by admin on Sat Dec 16 18:54:43 UTC 2023
PRIMARY
MERCK INDEX
m5038
Created by admin on Sat Dec 16 18:54:43 UTC 2023 , Edited by admin on Sat Dec 16 18:54:43 UTC 2023
PRIMARY Merck Index
DRUG BANK
DB12736
Created by admin on Sat Dec 16 18:54:43 UTC 2023 , Edited by admin on Sat Dec 16 18:54:43 UTC 2023
PRIMARY
NCI_THESAURUS
C1092
Created by admin on Sat Dec 16 18:54:43 UTC 2023 , Edited by admin on Sat Dec 16 18:54:43 UTC 2023
PRIMARY
EVMPD
SUB07261MIG
Created by admin on Sat Dec 16 18:54:43 UTC 2023 , Edited by admin on Sat Dec 16 18:54:43 UTC 2023
PRIMARY
SMS_ID
100000082369
Created by admin on Sat Dec 16 18:54:43 UTC 2023 , Edited by admin on Sat Dec 16 18:54:43 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SOLVATE->ANHYDROUS
Related Record Type Details
ACTIVE MOIETY