An antifungal agent and hedgehog pathway inhibitor
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Active Metabolite(s)
22576Hydroxy Itraconazole
Labeled Version(s)
25219Itraconazole-d5
Technical Support & Resources

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Itraconazole

Item No. 13288

Technical Information
Formal Name
4-[4-[4-[4-[[2-(2,4-dichlorophenyl)-2-(1H-1,2,4-triazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy]phenyl]-1-piperazinyl]phenyl]-2,4-dihydro-2-(1-methylpropyl)-3H-1,2,4-triazol-3-one
CAS Number
84625-61-6
Molecular Formula
C35H38Cl2N8O4
Formula Weight
Purity
≥95%
A crystalline solid
DMF: 0.5 mg/mlDMSO: 0.5 mg/ml
λmax
263 nm
SMILES
O=C(N(C(C)CC)N=C1)N1C(C=C2)=CC=C2N3CCN(C4=CC=C(OC[C@]5([H])O[C@](C6=C(Cl)C=C(Cl)C=C6)(CN7N=CN=C7)OC5)C=C4)CC3
InChi Code
InChI=1S/C35H38Cl2N8O4/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-/m0/s1
InChi Key
VHVPQPYKVGDNFY-ZPGVKDDISA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Itraconazole is an antifungal agent and inhibitor of hedgehog signaling (IC50 = 800 nM).1,2 It binds to 14-α sterol demethylase/CYP51 isoform B (AF51B; Kd = 31 nM for A. fumigatus enzyme expressed in E. coli) and inhibits ergosterol biosynthesis in C. neoformans (IC50 = 6 nM after a 16-hour incubation).1,3 It inhibits the growth of C. neoformans by 50% when used at a concentration of 3.2 nM. Itraconazole inhibits hedgehog signaling, reducing accumulation of Smoothened induced by sonic hedgehog (Shh) in primary cilia of NIHT-3T3 cells.2 It suppresses growth of medulloblastomas in a Ptch+/-p53-/- mouse allograft model when administered at a dose of 100 mg/kg twice daily. Itraconazole (1.25-100 µM) also reduces viral titers of several enteroviruses, including human rhinovirus 17, in infected cells, effects that can be reversed by overexpression of OSBP, the gene encoding oxysterol-binding protein (OSBP).4

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Vanden Bossche, H., Marichal, P., Le Jeune, L., et alEffects of itraconazole on cytochrome P-450-dependent sterol 14α-demethylation and reduction of 3-ketosteroids in Cryptococcus neoformans. Antimicrob. Agents Chemother. 37(10), 2101-2105 (1993).

    2. Kim, J., Tang, J.Y., Gong, R., et alItraconazole, a commonly used antifungal that inhibits Hedgehog pathway activity and cancer growth. Cancer Cell 17(4), 388-399 (2010).

    3. Warrilow, A.G., Melo, N., Martel, C.M., et alExpression, purification, and characterization of Aspergillus fumigatus sterol 14-a demethylase (CYP51) isoenzymes A and B. Antimicrob. Agents Chemother. 54(10), 4225-4234 (2010).

    4. Strating, J.R.P.M., van der Linden, L., Albulescu, L., et alItraconazole inhibits enterovirus replication by targeting the oxysterol-binding protein. Cell Rep. 10(4), 600-615 (2015).