Fungal infection, also known as a mycosis, refers to the invasion of a host's tissue by specific types of fungi. Mycoses often start in the lungs following inhalation of fungal spores or on the skin due to localized colonization.
Cat. No. | Product Name | CAS No. | Information |
---|---|---|---|
H1232 |
VT-1161 |
1340593-59-0 | VT-1161 is a potent, highly-selective, and oral fungal CYP51 inhibitor with Kd of ≤ 39 nM; demonstrates >2,000-fold selectivit over human CYP51, weakly inhibits human CYP2C9, CYP2C19, and CYP3A4; exhibits excellent potency against key yeast and dermatophyte strains. |
H1231 |
Voriconazole |
137234-62-9 | Voriconazole is a a triazole antifungal agent that acts as a 14α-demethylase inhibitor; used to treat and prevent invasive fungal infections including aspergillosis andcandidiasis and fungal infections caused by Scedosporium and Fusarium species. |
H1230 |
Terbinafine hydrochloride |
78628-80-5 | Terbinafine hydrochloride is a synthetic antifungal agent that inhibits the synthesis of ergosterol by inhibiting squalene epoxidase; used to treat ringworm, pityriasis versicolor, and fungal nail infections. |
H1229 |
Terbinafine |
91161-71-6 | Terbinafine is a synthetic antifungal agent that inhibits the synthesis of ergosterol by inhibiting squalene epoxidase; used to treat ringworm, pityriasis versicolor, and fungal nail infections. |
H1228 |
SCY-078 |
1207753-03-4 | SCY-078 is a novel orally bioavailable fungal beta-1,3-D glucan synthetase inhibitor against Candida species C. glabrata (MIC 0.03 to 0.25 ug/ml), C. parapsilosis (MIC 0.06 to 0.25 ug/ml); shows actvity in an in vivo neutropenic murine model. |
H1226 |
Posaconazole hydrate |
1198769-38-8 | Posaconazole hydrate is a triazole antifungal agent that blocks the synthesis of ergosterol by inhibiting of the enzyme lanosterol 14α-demethylase and accumulation of methylated sterol precursors, more potent at inhibiting 14α-demethylase than itraconazole. |
H1225 |
Posaconazole |
171228-49-2 | Posaconazole is a triazole antifungal agent that blocks the synthesis of ergosterol by inhibiting of the enzyme lanosterol 14α-demethylase and accumulation of methylated sterol precursors, more potent at inhibiting 14α-demethylase than itraconazole. |
H1222 |
PC945 |
1931946-73-4 | PC945(Opelconazole) is a novel broad spectrum antifungal agent that potently inhibits Aspergillus fumigatus sterol 14α-demethylase (CYP51A and CYP51B) with IC50 of 0.23 and 0.22 uM, respectively; shows MIC values 0.032 to >8 ug/ml against 96 clinically isolated A. fumigatus strains, demonstrates activity against itraconazole-susceptible and -resistant A. fumigatus growth with IC50 of 0.0012 to 0.034 ug/ml; PC945 is a broad spectrum of pathogenic fungi with MIC 0.0078 to 2 ug/ml, and exhibits activity in vivo. |
H1220 |
Nystatin |
1400-61-9 | Nystatin is a polyene antifungal antibiotic that works by disrupting the cell membrane of the fungal cells. |
H1218 |
Micafungin |
235114-32-6 | Micafungin is an echinocandin antifungal drug which can inhibit 1,3-beta-D-glucan synthase. |
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