Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C17H12Cl3N3O |
| Molecular Weight | 380.656 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
ClC1=CC=C(C=C1)[C@@]3(CN2C=NC=N2)O[C@@H]3C4=CC=C(Cl)C=C4Cl
InChI
InChIKey=HUSJLAKLJPOCEL-IAGOWNOFSA-N
InChI=1S/C17H12Cl3N3O/c18-12-3-1-11(2-4-12)17(8-23-10-21-9-22-23)16(24-17)14-6-5-13(19)7-15(14)20/h1-7,9-10,16H,8H2/t16-,17-/m1/s1
| Molecular Formula | C17H12Cl3N3O |
| Molecular Weight | 380.656 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Alteconazole is a triazole that was under development by Knoll Pharmaceuticals as both an orally and topically active antifungal drug. MICs were reported against Microsporum ferruginium, C. albicans, and Mucor pusilis. In mice, alteconazole administered orally produced greater antifungal activity than the reference compounds assayed. In a rat model of experimental vaginal candidiasis, alteconazole was active following both oral and topical administration. Alteconazole developed for the treatment of superficial mycoses, dermatomycoses, and systemic mycoses.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/3069196
Curator's Comment: Mice data
Administered for 4 days at 100 mg/kg
Route of Administration:
Oral
| Substance Class |
Chemical
Created
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admin
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Edited
Mon Mar 31 18:31:45 GMT 2025
by
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Mon Mar 31 18:31:45 GMT 2025
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| Record UNII |
EA590X615B
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| Record Status |
Validated (UNII)
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C514
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DTXSID301024767
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CHEMBL2104617
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C78031
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5725
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EA590X615B
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172289
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |