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
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 | ( + / - ) |
Molecular Formula | C4H6O6 |
Molecular Weight | 150.0868 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
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
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
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 05:39:33 UTC 2023
by
admin
on
Sat Dec 16 05:39:33 UTC 2023
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Record UNII |
7J526T0OZJ
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Record Status |
Validated (UNII)
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Record Version |
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-
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DTXSID60931881
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14343-71-6
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71586978
Created by
admin on Sat Dec 16 05:39:33 UTC 2023 , Edited by admin on Sat Dec 16 05:39:33 UTC 2023
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7J526T0OZJ
Created by
admin on Sat Dec 16 05:39:33 UTC 2023 , Edited by admin on Sat Dec 16 05:39:33 UTC 2023
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PRIMARY |
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ACTIVE MOIETY |