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

Details

Stereochemistry ABSOLUTE
Molecular Formula C9H8N3O3S.C4H5O6
Molecular Weight 387.322
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FURAZOLIUM TARTRATE

SMILES

O[C@H]([C@@H](O)C([O-])=O)C(O)=O.[O-][N+](=O)C1=CC=C(O1)C2=CSC3=[N+]2CCN3

InChI

InChIKey=UAGFATMWHGHRCP-LREBCSMRSA-N
InChI=1S/C9H7N3O3S.C4H6O6/c13-12(14)8-2-1-7(15-8)6-5-16-9-10-3-4-11(6)9;5-1(3(7)8)2(6)4(9)10/h1-2,5H,3-4H2;1-2,5-6H,(H,7,8)(H,9,10)/t;1-,2-/m.1/s1

HIDE SMILES / InChI

Molecular Formula C9H7N3O3S
Molecular Weight 237.235
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C4H6O6
Molecular Weight 150.0868
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Furazolium, an antibacterial agent, was studied for the management of skin infections. However, information about the current use of this drug is not available.

Approval Year

PubMed

PubMed

TitleDatePubMed
Induction of delayed hypersensitivity in guinea pigs by aflatoxins, other coumarins and furazolium.
1970 Dec

Sample Use Guides

Unknown
Route of Administration: Topical
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:03:22 GMT 2023
Edited
by admin
on Fri Dec 15 15:03:22 GMT 2023
Record UNII
ITG80WU2KB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FURAZOLIUM TARTRATE
USAN  
USAN  
Official Name English
5H-IMIDAZO(2,1-B)THIAZOL-4-IUM, 6,7-DIHYDRO-3-(5-NITRO-2-FURANYL)-, (R-(R*,R*))-2,3-DIHYDROXYBUTANEDIOATE (1:1)
Common Name English
6,7-Dihydro-3-(5-nitro-2-furyl)-5H-imidazo[2,1-b]thiazolium hydrogen tartrate
Systematic Name English
FURAZOLIUM TARTRATE [USAN]
Common Name English
NF-1425
Code English
Code System Code Type Description
PUBCHEM
5360550
Created by admin on Fri Dec 15 15:03:22 GMT 2023 , Edited by admin on Fri Dec 15 15:03:22 GMT 2023
PRIMARY
CAS
17692-15-8
Created by admin on Fri Dec 15 15:03:22 GMT 2023 , Edited by admin on Fri Dec 15 15:03:22 GMT 2023
PRIMARY
EPA CompTox
DTXSID40938873
Created by admin on Fri Dec 15 15:03:22 GMT 2023 , Edited by admin on Fri Dec 15 15:03:22 GMT 2023
PRIMARY
ChEMBL
CHEMBL2110940
Created by admin on Fri Dec 15 15:03:22 GMT 2023 , Edited by admin on Fri Dec 15 15:03:22 GMT 2023
PRIMARY
NCI_THESAURUS
C170015
Created by admin on Fri Dec 15 15:03:22 GMT 2023 , Edited by admin on Fri Dec 15 15:03:22 GMT 2023
PRIMARY
FDA UNII
ITG80WU2KB
Created by admin on Fri Dec 15 15:03:22 GMT 2023 , Edited by admin on Fri Dec 15 15:03:22 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY