Details
Stereochemistry | EPIMERIC |
Molecular Formula | C13H16N4O6.C4H6O6 |
Molecular Weight | 474.3762 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 2 / 3 |
E/Z Centers | 1 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
O[C@H]([C@@H](O)C(O)=O)C(O)=O.[O-][N+](=O)C1=CC=C(O1)\C=N\N2CC(CN3CCOCC3)OC2=O
InChI
InChIKey=NUQMJOZPYRELIB-FPEFUVJDSA-N
InChI=1S/C13H16N4O6.C4H6O6/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;5-1(3(7)8)2(6)4(9)10/h1-2,7,11H,3-6,8-9H2;1-2,5-6H,(H,7,8)(H,9,10)/b14-7+;/t;1-,2-/m.1/s1
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
PubMed
Title | Date | PubMed |
---|---|---|
The therapeutic effect of 16 antimicrobial agents on Cryptosporidium infection in mice. | 1982 Apr |
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Bactericidal activity of nitrofurans against growing and dormant Mycobacterium bovis BCG. | 2000 Dec |
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Antiprotozoals effective in vitro against the scuticociliate fish pathogen Philasterides dicentrarchi. | 2002 Jun 3 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/13681531
oral: 250 mg every 6 hour
intravenous: 500 mg
Route of Administration:
Other
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DTXSID60931881
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14343-71-6
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71586978
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7J526T0OZJ
Created by
admin on Sat Dec 16 05:39:33 GMT 2023 , Edited by admin on Sat Dec 16 05:39:33 GMT 2023
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ACTIVE MOIETY
SUBSTANCE RECORD