Fluconazole
Fluconazole is an antifungal medication used to treat a variety of fungal infections. It is a triazole antifungal agent that works by inhibiting the biosynthesis of ergosterol, a vital component of the fungal cell membrane.
Lab products found in correlation
2 protocols using fluconazole
Synthesis and Characterization of Novel Antifungal Compounds
Synthesis and Characterization of Azole Antifungals
voriconazole, ravuconazole, clotrimazole, miconazole, letrozole, and
anastrozole were purchased from Santa Cruz Biotechnology (Dallas,
TX), and fluconazole was from ICN Biomedicals. VNI and VFV were synthesized
by the Chemical Synthesis Core Facility (Vanderbilt Institute of Chemical
Biology).70 (link) The synthesis of their analogue
LFV was described previously.68 (link) The purity
of the compounds was >95%. The pyridine derivatives UDO and UDD
were
from DNDi;46 (link) the tetrazole-based compounds
VT116147 (link) and VT159848 (link) were from Mycovia Pharmaceuticals (Durham, NC). Hydroxypropyl-β-cyclodextrin
(HPCD) was purchased from Cyclodextrin Technology Development (Gainesville,
FL). Q- and CM-Sepharose resins were from GE Healthcare, and Ni2+-nitrilotriacetate (NTA) agarose was from Qiagen. The synthesis
of the CYP51 reaction product (3β,5α)-4,4-dimethyl-cholesta-8,14,24-trien-3-ol
(dihydro-FF-MAS) was reported elsewhere.71 (link) All compounds were >95% pure by high-performance liquid chromatography
(HPLC).
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