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

Details

Stereochemistry ACHIRAL
Molecular Formula C8H10N4O5
Molecular Weight 242.1888
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of NIDROXYZONE

SMILES

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

InChI

InChIKey=FJVAAURIDNIYAE-BJMVGYQFSA-N
InChI=1S/C8H10N4O5/c9-8(14)11(3-4-13)10-5-6-1-2-7(17-6)12(15)16/h1-2,5,13H,3-4H2,(H2,9,14)/b10-5+

HIDE SMILES / InChI

Molecular Formula C8H10N4O5
Molecular Weight 242.1888
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Nidroxyzone (Furadroxyl) is an antibacterial agent. It was used for the treatment of experimental trypanosomiasis in laboratory animals.

Approval Year

PubMed

PubMed

TitleDatePubMed
The effect of furadroxyl treatment and x-irradiation on the hyaluronidase concentration of rat testes.
1957-01
Pyruvate oxidation in testicular tissues during furadroxyl-induced spermatogenic arrest.
1955-06
The use of 5-nitro-2-furaldehyde-2(2-hydroxyethyl) semicarbazone (furadroxyl) in the treatment of experimental trypanosomiasis in laboratory animals.
1953-04
[Antibacterial action of neomycin and furadroxyl in vitro and in vivo].
1950-06-26
Patents
Substance Class Chemical
Created
by admin
on Wed Apr 02 08:29:45 GMT 2025
Edited
by admin
on Wed Apr 02 08:29:45 GMT 2025
Record UNII
YN9DMN3CVQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-6474
Preferred Name English
NIDROXYZONE
INN   MI  
INN  
Official Name English
nidroxyzone [INN]
Common Name English
5-NITRO-2-FURALDEHYDE 2-(2-HYDROXYETHYL)SEMICARBAZONE
Systematic Name English
NIDROXYZONE [MI]
Common Name English
NITROFUROXIZONE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C28394
Created by admin on Wed Apr 02 08:29:45 GMT 2025 , Edited by admin on Wed Apr 02 08:29:45 GMT 2025
Code System Code Type Description
ECHA (EC/EINECS)
206-970-3
Created by admin on Wed Apr 02 08:29:45 GMT 2025 , Edited by admin on Wed Apr 02 08:29:45 GMT 2025
PRIMARY
NSC
6474
Created by admin on Wed Apr 02 08:29:45 GMT 2025 , Edited by admin on Wed Apr 02 08:29:45 GMT 2025
PRIMARY
SMS_ID
100000084401
Created by admin on Wed Apr 02 08:29:45 GMT 2025 , Edited by admin on Wed Apr 02 08:29:45 GMT 2025
PRIMARY
NCI_THESAURUS
C84014
Created by admin on Wed Apr 02 08:29:45 GMT 2025 , Edited by admin on Wed Apr 02 08:29:45 GMT 2025
PRIMARY
INN
693
Created by admin on Wed Apr 02 08:29:45 GMT 2025 , Edited by admin on Wed Apr 02 08:29:45 GMT 2025
PRIMARY
EVMPD
SUB09252MIG
Created by admin on Wed Apr 02 08:29:45 GMT 2025 , Edited by admin on Wed Apr 02 08:29:45 GMT 2025
PRIMARY
CAS
405-22-1
Created by admin on Wed Apr 02 08:29:45 GMT 2025 , Edited by admin on Wed Apr 02 08:29:45 GMT 2025
PRIMARY
DRUG CENTRAL
3794
Created by admin on Wed Apr 02 08:29:45 GMT 2025 , Edited by admin on Wed Apr 02 08:29:45 GMT 2025
PRIMARY
FDA UNII
YN9DMN3CVQ
Created by admin on Wed Apr 02 08:29:45 GMT 2025 , Edited by admin on Wed Apr 02 08:29:45 GMT 2025
PRIMARY
EPA CompTox
DTXSID701015578
Created by admin on Wed Apr 02 08:29:45 GMT 2025 , Edited by admin on Wed Apr 02 08:29:45 GMT 2025
PRIMARY
PUBCHEM
9570072
Created by admin on Wed Apr 02 08:29:45 GMT 2025 , Edited by admin on Wed Apr 02 08:29:45 GMT 2025
PRIMARY
ChEMBL
CHEMBL92444
Created by admin on Wed Apr 02 08:29:45 GMT 2025 , Edited by admin on Wed Apr 02 08:29:45 GMT 2025
PRIMARY
MERCK INDEX
m366
Created by admin on Wed Apr 02 08:29:45 GMT 2025 , Edited by admin on Wed Apr 02 08:29:45 GMT 2025
PRIMARY Merck Index
Related Record Type Details
ACTIVE MOIETY