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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
[Antibacterial action of neomycin and furadroxyl in vitro and in vivo].
1950 Jun 26
The use of 5-nitro-2-furaldehyde-2(2-hydroxyethyl) semicarbazone (furadroxyl) in the treatment of experimental trypanosomiasis in laboratory animals.
1953 Apr
The effect of furadroxyl treatment and x-irradiation on the hyaluronidase concentration of rat testes.
1957 Jan
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:53:38 GMT 2023
Edited
by admin
on Sat Dec 16 16:53:38 GMT 2023
Record UNII
YN9DMN3CVQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NIDROXYZONE
INN   MI  
INN  
Official Name English
nidroxyzone [INN]
Common Name English
NSC-6474
Code 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 Sat Dec 16 16:53:38 GMT 2023 , Edited by admin on Sat Dec 16 16:53:38 GMT 2023
Code System Code Type Description
ECHA (EC/EINECS)
206-970-3
Created by admin on Sat Dec 16 16:53:38 GMT 2023 , Edited by admin on Sat Dec 16 16:53:38 GMT 2023
PRIMARY
NSC
6474
Created by admin on Sat Dec 16 16:53:38 GMT 2023 , Edited by admin on Sat Dec 16 16:53:38 GMT 2023
PRIMARY
SMS_ID
100000084401
Created by admin on Sat Dec 16 16:53:38 GMT 2023 , Edited by admin on Sat Dec 16 16:53:38 GMT 2023
PRIMARY
NCI_THESAURUS
C84014
Created by admin on Sat Dec 16 16:53:38 GMT 2023 , Edited by admin on Sat Dec 16 16:53:38 GMT 2023
PRIMARY
INN
693
Created by admin on Sat Dec 16 16:53:38 GMT 2023 , Edited by admin on Sat Dec 16 16:53:38 GMT 2023
PRIMARY
EVMPD
SUB09252MIG
Created by admin on Sat Dec 16 16:53:38 GMT 2023 , Edited by admin on Sat Dec 16 16:53:38 GMT 2023
PRIMARY
CAS
405-22-1
Created by admin on Sat Dec 16 16:53:38 GMT 2023 , Edited by admin on Sat Dec 16 16:53:38 GMT 2023
PRIMARY
DRUG CENTRAL
3794
Created by admin on Sat Dec 16 16:53:38 GMT 2023 , Edited by admin on Sat Dec 16 16:53:38 GMT 2023
PRIMARY
FDA UNII
YN9DMN3CVQ
Created by admin on Sat Dec 16 16:53:38 GMT 2023 , Edited by admin on Sat Dec 16 16:53:38 GMT 2023
PRIMARY
EPA CompTox
DTXSID701015578
Created by admin on Sat Dec 16 16:53:38 GMT 2023 , Edited by admin on Sat Dec 16 16:53:38 GMT 2023
PRIMARY
PUBCHEM
9570072
Created by admin on Sat Dec 16 16:53:38 GMT 2023 , Edited by admin on Sat Dec 16 16:53:38 GMT 2023
PRIMARY
ChEMBL
CHEMBL92444
Created by admin on Sat Dec 16 16:53:38 GMT 2023 , Edited by admin on Sat Dec 16 16:53:38 GMT 2023
PRIMARY
MERCK INDEX
m366
Created by admin on Sat Dec 16 16:53:38 GMT 2023 , Edited by admin on Sat Dec 16 16:53:38 GMT 2023
PRIMARY Merck Index
Related Record Type Details
ACTIVE MOIETY