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Details

Stereochemistry RACEMIC
Molecular Formula C13H16N4O6
Molecular Weight 324.2893
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of FURALTADONE

SMILES

[O-][N+](=O)C1=CC=C(O1)\C=N\N2CC(CN3CCOCC3)OC2=O

InChI

InChIKey=YVQVOQKFMFRVGR-VGOFMYFVSA-N
InChI=1S/C13H16N4O6/c18-13-16(14-7-10-1-2-12(22-10)17(19)20)9-11(23-13)8-15-3-5-21-6-4-15/h1-2,7,11H,3-6,8-9H2/b14-7+

HIDE SMILES / InChI

Molecular Formula C13H16N4O6
Molecular Weight 324.2893
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 1
Optical Activity ( + / - )

Furaltadone is a veterinary product, which is marketed for the treatment and control of salmonella infection of poultry. In 1960th was investigated the antibacterial properties of this drug against human Rhodesian sleeping sickness. In three cases treated, two were apparently curated and the third relapsed. No toxic effects attributable to the product had been observed. However, the further investigation of the furaltadone in human was not provided.

Approval Year

Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
Patents

Patents

Sample Use Guides

oral: 250 mg every 6 hour intravenous: 500 mg
Route of Administration: Other
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:23:15 UTC 2023
Edited
by admin
on Fri Dec 15 15:23:15 UTC 2023
Record UNII
5X4V82ZN30
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FURALTADONE
INN   MI   WHO-DD  
INN  
Official Name English
(±)-5-(MORPHOLINOMETHYL)-3-((5-NITROFURFURYLIDENE)AMINO)-2-OXAZOLIDINONE
Systematic Name English
Furaltadone [WHO-DD]
Common Name English
ALTAFUR
Brand Name English
NSC-42388
Code English
FURALTADONE [MI]
Common Name English
furaltadone [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C52588
Created by admin on Fri Dec 15 15:23:15 UTC 2023 , Edited by admin on Fri Dec 15 15:23:15 UTC 2023
WHO-VATC QJ01XX93
Created by admin on Fri Dec 15 15:23:15 UTC 2023 , Edited by admin on Fri Dec 15 15:23:15 UTC 2023
Code System Code Type Description
CAS
8059-21-0
Created by admin on Fri Dec 15 15:23:15 UTC 2023 , Edited by admin on Fri Dec 15 15:23:15 UTC 2023
SUPERSEDED
CAS
59302-14-6
Created by admin on Fri Dec 15 15:23:15 UTC 2023 , Edited by admin on Fri Dec 15 15:23:15 UTC 2023
SUPERSEDED
FDA UNII
5X4V82ZN30
Created by admin on Fri Dec 15 15:23:15 UTC 2023 , Edited by admin on Fri Dec 15 15:23:15 UTC 2023
PRIMARY
ECHA (EC/EINECS)
205-384-5
Created by admin on Fri Dec 15 15:23:15 UTC 2023 , Edited by admin on Fri Dec 15 15:23:15 UTC 2023
PRIMARY
CAS
83454-29-9
Created by admin on Fri Dec 15 15:23:15 UTC 2023 , Edited by admin on Fri Dec 15 15:23:15 UTC 2023
SUPERSEDED
CHEBI
74803
Created by admin on Fri Dec 15 15:23:15 UTC 2023 , Edited by admin on Fri Dec 15 15:23:15 UTC 2023
PRIMARY
DRUG CENTRAL
1256
Created by admin on Fri Dec 15 15:23:15 UTC 2023 , Edited by admin on Fri Dec 15 15:23:15 UTC 2023
PRIMARY
NCI_THESAURUS
C75249
Created by admin on Fri Dec 15 15:23:15 UTC 2023 , Edited by admin on Fri Dec 15 15:23:15 UTC 2023
PRIMARY
ChEMBL
CHEMBL1189513
Created by admin on Fri Dec 15 15:23:15 UTC 2023 , Edited by admin on Fri Dec 15 15:23:15 UTC 2023
PRIMARY
INN
811
Created by admin on Fri Dec 15 15:23:15 UTC 2023 , Edited by admin on Fri Dec 15 15:23:15 UTC 2023
PRIMARY
PUBCHEM
9553856
Created by admin on Fri Dec 15 15:23:15 UTC 2023 , Edited by admin on Fri Dec 15 15:23:15 UTC 2023
PRIMARY
MERCK INDEX
m5593
Created by admin on Fri Dec 15 15:23:15 UTC 2023 , Edited by admin on Fri Dec 15 15:23:15 UTC 2023
PRIMARY Merck Index
CAS
94107-51-4
Created by admin on Fri Dec 15 15:23:15 UTC 2023 , Edited by admin on Fri Dec 15 15:23:15 UTC 2023
SUPERSEDED
SMS_ID
100000080675
Created by admin on Fri Dec 15 15:23:15 UTC 2023 , Edited by admin on Fri Dec 15 15:23:15 UTC 2023
PRIMARY
NSC
42388
Created by admin on Fri Dec 15 15:23:15 UTC 2023 , Edited by admin on Fri Dec 15 15:23:15 UTC 2023
PRIMARY
CAS
51728-00-8
Created by admin on Fri Dec 15 15:23:15 UTC 2023 , Edited by admin on Fri Dec 15 15:23:15 UTC 2023
SUPERSEDED
CAS
139-91-3
Created by admin on Fri Dec 15 15:23:15 UTC 2023 , Edited by admin on Fri Dec 15 15:23:15 UTC 2023
PRIMARY
CAS
8048-02-0
Created by admin on Fri Dec 15 15:23:15 UTC 2023 , Edited by admin on Fri Dec 15 15:23:15 UTC 2023
SUPERSEDED
CAS
71-05-6
Created by admin on Fri Dec 15 15:23:15 UTC 2023 , Edited by admin on Fri Dec 15 15:23:15 UTC 2023
SUPERSEDED
EPA CompTox
DTXSID4048016
Created by admin on Fri Dec 15 15:23:15 UTC 2023 , Edited by admin on Fri Dec 15 15:23:15 UTC 2023
PRIMARY
EVMPD
SUB07831MIG
Created by admin on Fri Dec 15 15:23:15 UTC 2023 , Edited by admin on Fri Dec 15 15:23:15 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
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ACTIVE MOIETY