Details
Stereochemistry | ACHIRAL |
Molecular Formula | C14H11N3O4 |
Molecular Weight | 285.2548 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C1=CC=C(\C=C\C2=NC=C(N2C=C)[N+]([O-])=O)C=C1
InChI
InChIKey=RBNZISNWCHORNF-VMPITWQZSA-N
InChI=1S/C14H11N3O4/c1-2-16-12(15-9-13(16)17(20)21)8-5-10-3-6-11(7-4-10)14(18)19/h2-9H,1H2,(H,18,19)/b8-5+
Molecular Formula | C14H11N3O4 |
Molecular Weight | 285.2548 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Optical Activity | NONE |
Stirimazole is an imidazole derivative patented by Lilly Industries Ltd. as an antiparasitic agent effective against Trypanosoma congolense, T. gambiense, T. rhodesiense, and T. cruzi. Stirimazole inhibited Trichomonas vaginalis in vitro at 0.225 μg/ml and eliminated infected lesions in mice at 20 mg/kg orally. Stirimazole eliminated intestinal amebiasis in rats at 50 mg/kg orally and hepatic amebiasis in hamsters at 100 mg/kg i.p. Stirimazole was curative against Trypanosoma rhodesiense, Trypanosoma cruzi, Trypanosoma gambiense, and Trypanosoma congolense in mice at 25, 100, 12.5, and 25 mg/kg (4 times, i.p.), respectively, and against Trypanosoma vivax in calves at 25 mg/kg i.v.
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:51:06 GMT 2023
by
admin
on
Fri Dec 15 15:51:06 GMT 2023
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Record UNII |
AX8T791ON0
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Record Status |
Validated (UNII)
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Record Version |
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-
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Common Name | English | ||
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Code | English |
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NCI_THESAURUS |
C277
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271231
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3068
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100000083502
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CHEMBL2104913
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5476886
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AX8T791ON0
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30529-16-9
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SUB10653MIG
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DTXSID901009868
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C90759
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Related Record | Type | Details | ||
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ACTIVE MOIETY |