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
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+
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 |
Originator
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
[Antibacterial action of neomycin and furadroxyl in vitro and in vivo]. | 1950 Jun 26 |
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The use of 5-nitro-2-furaldehyde-2(2-hydroxyethyl) semicarbazone (furadroxyl) in the treatment of experimental trypanosomiasis in laboratory animals. | 1953 Apr |
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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
Edited
Sat Dec 16 16:53:38 GMT 2023
by
admin
on
Sat Dec 16 16:53:38 GMT 2023
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Record UNII |
YN9DMN3CVQ
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Record Status |
Validated (UNII)
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Record Version |
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Classification Tree | Code System | Code | ||
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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
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Code System | Code | Type | Description | ||
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206-970-3
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6474
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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
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C84014
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admin on Sat Dec 16 16:53:38 GMT 2023 , Edited by admin on Sat Dec 16 16:53:38 GMT 2023
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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
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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
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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
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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
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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
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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
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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
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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
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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
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PRIMARY | Merck Index |
Related Record | Type | Details | ||
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ACTIVE MOIETY |