Details
Stereochemistry | ACHIRAL |
Molecular Formula | C18H15ClN2O.ClH |
Molecular Weight | 347.238 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.ClC1=CC=CC(COC2=C(C=CC=C2)C(=C)N3C=CN=C3)=C1
InChI
InChIKey=LWJUIYYIILPRRI-UHFFFAOYSA-N
InChI=1S/C18H15ClN2O.ClH/c1-14(21-10-9-20-13-21)17-7-2-3-8-18(17)22-12-15-5-4-6-16(19)11-15;/h2-11,13H,1,12H2;1H
DescriptionSources: http://www.ncbi.nlm.nih.gov/pubmed/3069196
Sources: http://www.ncbi.nlm.nih.gov/pubmed/3069196
Croconazole is a antifungal drug developed for the treatment of dermatomycoses and candidiasis. It has a broad spectrum activity against many microorganisms such as T. mentagrophytes, T. rubrum, M. canis, Microsporum gypseum, and Epidermophyton floccosum. The drug was used as a topical 1% cream under the name Pilzcin. According to the information on the manufacturer (Merz pharma) website, Pilzcin is no longer marketed.
Originator
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/7607787
One topical application per day (1% cream formulation).
Route of Administration:
Topical
In Vitro Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/3069196
The range of MICs against isolates of T. mentagrophytes, T. rubrum, M. canis, Microsporum gypseum, and Epidermophyton floccosum were 0.16 to 1.25 ug/ml. Five isolates of Aspergillus species and two isolates of Penicillium species were susceptible, with MICs of 0.63 to 5.0 ug/ml. However, this compound was less active (MICs, 10 to 80 ug/ml) against yeast-like fungi, including isolates of C. albicans, Candida species, Torulopsis glabrata, and Cryptococcus neoformans.
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NCI_THESAURUS |
C514
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C038008
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m3850
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CHEMBL27289
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C97991
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I0WFH323HZ
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77174-66-4
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ACTIVE MOIETY
SUBSTANCE RECORD