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Details

Stereochemistry ACHIRAL
Molecular Formula C7H8N2O5
Molecular Weight 200.1488
Optical Activity UNSPECIFIED
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of NIFURATRONE

SMILES

OCC\[N+]([O-])=C\C1=CC=C(O1)[N+]([O-])=O

InChI

InChIKey=QSWZUVFMUIEHAG-YVMONPNESA-N
InChI=1S/C7H8N2O5/c10-4-3-8(11)5-6-1-2-7(14-6)9(12)13/h1-2,5,10H,3-4H2/b8-5-

HIDE SMILES / InChI

Molecular Formula C7H8N2O5
Molecular Weight 200.1488
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Description

Nifuratrone is a nitrofuran which was used for the control of Salmonella choleraesuis in swine. It was also used for the treatment of gonorrhea.

Approval Year

PubMed

PubMed

TitleDatePubMed

Sample Use Guides

In Vivo Use Guide
Gilts were given single oral doses of nifuratrone at a level of 6 or 12 mg/kg body weight.
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Tue Oct 22 19:50:14 UTC 2019
Edited
by admin
on Tue Oct 22 19:50:14 UTC 2019
Record UNII
4V8564T36O
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NIFURATRONE
INN   USAN  
INN   USAN  
Official Name English
NIFURATRONE [INN]
Common Name English
N-(2-HYDROXYETHYL)-.ALPHA.-(5-NITRO-2-FURYL)NITRONE
Common Name English
NSC-303603
Code English
NIFURATRONE [USAN]
Common Name English
ETHANOL, 2-(((5-NITRO-2-FURANYL)METHYLENE)AMINO)-, N-OXIDE
Common Name English
Code System Code Type Description
CAS
19561-70-7
Created by admin on Tue Oct 22 19:50:14 UTC 2019 , Edited by admin on Tue Oct 22 19:50:14 UTC 2019
PRIMARY
ChEMBL
CHEMBL2106512
Created by admin on Tue Oct 22 19:50:14 UTC 2019 , Edited by admin on Tue Oct 22 19:50:14 UTC 2019
PRIMARY
INN
2911
Created by admin on Tue Oct 22 19:50:14 UTC 2019 , Edited by admin on Tue Oct 22 19:50:14 UTC 2019
PRIMARY
PUBCHEM
5910161
Created by admin on Tue Oct 22 19:50:14 UTC 2019 , Edited by admin on Tue Oct 22 19:50:14 UTC 2019
PRIMARY
MESH
C001391
Created by admin on Tue Oct 22 19:50:14 UTC 2019 , Edited by admin on Tue Oct 22 19:50:14 UTC 2019
PRIMARY
EVMPD
SUB09262MIG
Created by admin on Tue Oct 22 19:50:14 UTC 2019 , Edited by admin on Tue Oct 22 19:50:14 UTC 2019
PRIMARY
Related Record Type Details
ACTIVE MOIETY