|   Isavuconazole structure | Common Name | Isavuconazole | ||
|---|---|---|---|---|
| CAS Number | 241479-67-4 | Molecular Weight | 437.46500 | |
| Density | 1.38 | Boiling Point | 678ºC at 760 mmHg | |
| Molecular Formula | C22H17F2N5OS | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 363.8ºC | |
| Use of IsavuconazoleIsavuconazole is a moderate inhibitor of CYP3A4 and a water-soluble triazole with broad-spectrum antifungal activity. | 
| Name | isavuconazole | 
|---|---|
| Synonym | More Synonyms | 
| Description | Isavuconazole is a moderate inhibitor of CYP3A4 and a water-soluble triazole with broad-spectrum antifungal activity. | 
|---|---|
| Related Catalog | |
| In Vitro | Isavuconazole shows good activity against all Candida spp., with active MIC50 of 0.004 mg/L. The MIC50s/MIC90s range from 0.002/0.004 mg/L for C. albicans to 0.25/0.5 mg/L for C. glabrata[1]. Isavuconazole has potent in vitro activity against most common Aspergillus species, Purpureocillium lilacinum, and Scedosporium apiospermum[2]. Isavuconazole shows potent activity against molds, yeasts, and dimorphic fungi. Rhizopus isolates have MIC values to isavuconazole as low as 0.12 µg/mL with others as high as 32 µg/mL[3]. In the study of pharmacokinetics and pharmacodynamics of isavuconazole against the GFP transformant, F/11628, NIH 4215, and F/16216, the modal MICs of isavuconazole are 1, 8, 1, 4 mg/L, respectively[4]. | 
| References | 
| Density | 1.38 | 
|---|---|
| Boiling Point | 678ºC at 760 mmHg | 
| Molecular Formula | C22H17F2N5OS | 
| Molecular Weight | 437.46500 | 
| Flash Point | 363.8ºC | 
| Exact Mass | 437.11200 | 
| PSA | 115.86000 | 
| LogP | 4.24298 | 
| Precursor 1 | |
|---|---|
| DownStream 0 | |
| 4-{2-[(2R,3R)-3-(2,5-difluorophenyl)-3-hydroxy-4-(1H-1,2,4-triazol-1-yl)butan-2-yl]-1,3-thiazol-4-yl}benzonitrile | 
| BAL 4815 | 
| UNII-60UTO373KE | 
| 4-[2-[(2R,3R)-3-(2,5-difluorophenyl)-3-hydroxy-4-(1,2,4-triazol-1-yl)butan-2-yl]-1,3-thiazol-4-yl]benzonitrile | 
| Isavuconazole | 
| Bal4815 | 
| 4-{2-[(2R,3R)-3-(2,5-Difluorophenyl)-3-hydroxy-4-(1H-1,2,4-triazol-1-yl)-2-butanyl]-1,3-thiazol-4-yl}benzonitrile | 
| Benzonitrile, 4-[2-[(1R,2R)-2-(2,5-difluorophenyl)-2-hydroxy-1-methyl-3-(1H-1,2,4-triazol-1-yl)propyl]-4-thiazolyl]- |