Details
Stereochemistry | RACEMIC |
Molecular Formula | C10H13N3O5S |
Molecular Weight | 287.292 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 1 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1CS(=O)(=O)CCN1\N=C\C2=CC=C(O2)[N+]([O-])=O
InChI
InChIKey=ARFHIAQFJWUCFH-IZZDOVSWSA-N
InChI=1S/C10H13N3O5S/c1-8-7-19(16,17)5-4-12(8)11-6-9-2-3-10(18-9)13(14)15/h2-3,6,8H,4-5,7H2,1H3/b11-6+
Approval Year
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Classification Tree | Code System | Code | ||
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WHO-ESSENTIAL MEDICINES LIST |
6.5.5.1
Created by
admin on Sat Dec 16 05:43:39 UTC 2023 , Edited by admin on Sat Dec 16 05:43:39 UTC 2023
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WHO-VATC |
QP51AC01
Created by
admin on Sat Dec 16 05:43:39 UTC 2023 , Edited by admin on Sat Dec 16 05:43:39 UTC 2023
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FDA ORPHAN DRUG |
310110
Created by
admin on Sat Dec 16 05:43:39 UTC 2023 , Edited by admin on Sat Dec 16 05:43:39 UTC 2023
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WHO-ESSENTIAL MEDICINES LIST |
6.5.5.2
Created by
admin on Sat Dec 16 05:43:39 UTC 2023 , Edited by admin on Sat Dec 16 05:43:39 UTC 2023
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NCI_THESAURUS |
C277
Created by
admin on Sat Dec 16 05:43:39 UTC 2023 , Edited by admin on Sat Dec 16 05:43:39 UTC 2023
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FDA ORPHAN DRUG |
419213
Created by
admin on Sat Dec 16 05:43:39 UTC 2023 , Edited by admin on Sat Dec 16 05:43:39 UTC 2023
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WHO-ATC |
P01CC01
Created by
admin on Sat Dec 16 05:43:39 UTC 2023 , Edited by admin on Sat Dec 16 05:43:39 UTC 2023
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Code System | Code | Type | Description | ||
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m7892
Created by
admin on Sat Dec 16 05:43:39 UTC 2023 , Edited by admin on Sat Dec 16 05:43:39 UTC 2023
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PRIMARY | Merck Index | ||
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DB11820
Created by
admin on Sat Dec 16 05:43:39 UTC 2023 , Edited by admin on Sat Dec 16 05:43:39 UTC 2023
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PRIMARY | |||
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Nifurtimox
Created by
admin on Sat Dec 16 05:43:39 UTC 2023 , Edited by admin on Sat Dec 16 05:43:39 UTC 2023
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PRIMARY | |||
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245-531-0
Created by
admin on Sat Dec 16 05:43:39 UTC 2023 , Edited by admin on Sat Dec 16 05:43:39 UTC 2023
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PRIMARY | |||
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100000083878
Created by
admin on Sat Dec 16 05:43:39 UTC 2023 , Edited by admin on Sat Dec 16 05:43:39 UTC 2023
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PRIMARY | |||
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CHEMBL290960
Created by
admin on Sat Dec 16 05:43:39 UTC 2023 , Edited by admin on Sat Dec 16 05:43:39 UTC 2023
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PRIMARY | |||
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7421
Created by
admin on Sat Dec 16 05:43:39 UTC 2023 , Edited by admin on Sat Dec 16 05:43:39 UTC 2023
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PRIMARY | RxNorm | ||
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M84I3K7C2O
Created by
admin on Sat Dec 16 05:43:39 UTC 2023 , Edited by admin on Sat Dec 16 05:43:39 UTC 2023
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PRIMARY | |||
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DTXSID3045439
Created by
admin on Sat Dec 16 05:43:39 UTC 2023 , Edited by admin on Sat Dec 16 05:43:39 UTC 2023
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PRIMARY | |||
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D009547
Created by
admin on Sat Dec 16 05:43:39 UTC 2023 , Edited by admin on Sat Dec 16 05:43:39 UTC 2023
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PRIMARY | |||
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23256-30-6
Created by
admin on Sat Dec 16 05:43:39 UTC 2023 , Edited by admin on Sat Dec 16 05:43:39 UTC 2023
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PRIMARY | |||
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Nifurtimox
Created by
admin on Sat Dec 16 05:43:39 UTC 2023 , Edited by admin on Sat Dec 16 05:43:39 UTC 2023
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PRIMARY | |||
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SUB09280MIG
Created by
admin on Sat Dec 16 05:43:39 UTC 2023 , Edited by admin on Sat Dec 16 05:43:39 UTC 2023
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PRIMARY | |||
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CD-134
Created by
admin on Sat Dec 16 05:43:39 UTC 2023 , Edited by admin on Sat Dec 16 05:43:39 UTC 2023
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PRIMARY | |||
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2615
Created by
admin on Sat Dec 16 05:43:39 UTC 2023 , Edited by admin on Sat Dec 16 05:43:39 UTC 2023
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PRIMARY | |||
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1929
Created by
admin on Sat Dec 16 05:43:39 UTC 2023 , Edited by admin on Sat Dec 16 05:43:39 UTC 2023
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PRIMARY | |||
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M84I3K7C2O
Created by
admin on Sat Dec 16 05:43:39 UTC 2023 , Edited by admin on Sat Dec 16 05:43:39 UTC 2023
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PRIMARY | |||
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NIFURTIMOX
Created by
admin on Sat Dec 16 05:43:39 UTC 2023 , Edited by admin on Sat Dec 16 05:43:39 UTC 2023
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PRIMARY | Description: A yellow to orange-yellow, crystalline powder; odourless. Solubility: Practically insoluble in water and ether R; freely soluble in dimethylformamide R; sparingly soluble in dioxan R. Category: Antitrypanosomal drug. Storage: Nifurtimox should be kept in a well-closed container. Definition: Nifurtimox contains not less than 98.0% and not more than 102.0% of C10H13N3O5S, calculated with reference to thedried substance. | ||
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6842999
Created by
admin on Sat Dec 16 05:43:39 UTC 2023 , Edited by admin on Sat Dec 16 05:43:39 UTC 2023
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PRIMARY | |||
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C71734
Created by
admin on Sat Dec 16 05:43:39 UTC 2023 , Edited by admin on Sat Dec 16 05:43:39 UTC 2023
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PRIMARY |
ACTIVE MOIETY
METABOLITE (PARENT)
METABOLITE (PARENT)
METABOLITE INACTIVE (PARENT)