Details
| Stereochemistry | MIXED |
| Molecular Formula | C35H38F2N8O4 |
| Molecular Weight | 672.7242 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 2 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC(C)N1N=CN(C1=O)C2=CC=C(C=C2)N3CCN(CC3)C4=CC=C(OC[C@@H]5CO[C@](CN6C=NC=N6)(O5)C7=CC=C(F)C=C7F)C=C4
InChI
InChIKey=HUADITLKOCMHSB-AVQIMAJZSA-N
InChI=1S/C35H38F2N8O4/c1-3-25(2)45-34(46)44(24-40-45)29-7-5-27(6-8-29)41-14-16-42(17-15-41)28-9-11-30(12-10-28)47-19-31-20-48-35(49-31,21-43-23-38-22-39-43)32-13-4-26(36)18-33(32)37/h4-13,18,22-25,31H,3,14-17,19-21H2,1-2H3/t25?,31-,35-/m1/s1
| Molecular Formula | C35H38F2N8O4 |
| Molecular Weight | 672.7242 |
| Charge | 0 |
| Count |
|
| Stereochemistry | EPIMERIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 3 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Saperconazole, a N-1-substituted triazole antifungal that is a selective inhibitor of the cytochrome P-450-dependent ergosterol synthesis in Candida albicans, Aspergillus fumigatus, and Trichophyton mentagrophytes. Saperconazole participated in a clinical trial for the treatment of mycoses. However, further, development was discontinued because of concerns about the possibility of drug-induced carcinogenesis.
Originator
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Saperconazole therapy of murine disseminated candidiasis: efficacy and interactions with amphotericin B. | 1994-02 |
|
| Saperconazole therapy in a rabbit model of invasive aspergillosis. | 1992-12 |
|
| Saperconazole in the treatment of systemic and subcutaneous mycoses. | 1992-10 |
|
| Saperconazole: in vitro and in vivo anticandidal activity. | 1992 |
|
| Saperconazole: a selective inhibitor of the cytochrome P-450-dependent ergosterol synthesis in Candida albicans, Aspergillus fumigatus and Trichophyton mentagrophytes. | 1990-07-01 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/1399205
In a 2-year period, 30 patients with culture-proven mycoses (chromoblastomycosis, sporotrichosis, and paracoccidioidomycosis) were treated with the new orally administered triazole, saperconazole (SPZ) (R66905). The daily dose varied from 100 to 200 mg
Route of Administration:
Oral
| Substance Class |
Chemical
Created
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Edited
Mon Mar 31 17:59:16 GMT 2025
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| Record UNII |
R2I5PI29CA
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Validated (UNII)
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NCI_THESAURUS |
C514
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110588-57-3
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DTXSID10891401
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6236
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C1221
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100000084073
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m9769
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C060571
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R2I5PI29CA
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DD-36
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SUB10443MIG
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CHEMBL2105770
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60456
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