Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C13H16N4O6.ClH |
| Molecular Weight | 360.75 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.[O-][N+](=O)C1=CC=C(O1)\C=N\N2CC(CN3CCOCC3)OC2=O
InChI
InChIKey=PPSVFZXMDMUIGB-FJUODKGNSA-N
InChI=1S/C13H16N4O6.ClH/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;1H/b14-7+;
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
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9576185
Created by
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37Q02H7JT2
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223-169-4
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SUB02285MIG
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DTXSID5045380
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100000087020
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3759-92-0
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53270
Created by
admin on Fri Dec 15 16:39:31 GMT 2023 , Edited by admin on Fri Dec 15 16:39:31 GMT 2023
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ACTIVE MOIETY
SUBSTANCE RECORD
