Quilseconazole

  Cat. No.:  DC11527   Featured
Chemical Structure
1340593-70-5
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More than 5000 active chemicals with high quality for research!
Field of application
A novel selective, orally available fungal CYP51 (lanosterol 14-α-demethylase) inhibitor.
Cas No.: 1340593-70-5
Chemical Name: Quilseconazole
Synonyms: Quilseconazole
SMILES: FC(C1C([H])=C([H])C(C2C([H])=C([H])C(=C([H])C=2[H])OC(F)(F)F)=C([H])N=1)([C@](C1C([H])=C([H])C(=C([H])C=1F)F)(C([H])([H])N1C([H])=NN=N1)O[H])F
Formula: C22H14F7N5O2
M.Wt: 513.3677
Purity: >98%
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: A novel selective, orally available fungal CYP51 (lanosterol 14-α-demethylase) inhibitor; displays greater selectivity for fungal enzyme than for mammalian CYP450 compared to the approved azole class of antifungal drugs; inhibits C. albicans and T. rubrum with MIC of <0.001 ug/mL, also demonstrated potent activities against Cryptococcusspecies as demonstrated by low MIC50 and MIC90 values.
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
Cat. No. Product name Field of application
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DCAPI1497 Cancidas Caspofungin is a semi-synthetic analogue of pneumocandin B0 with improved water solubility, a significant limitation in the development of the echinocandin class as pharmaceuticals. Caspofungin acts by inhibition of the synthesis of β (1,3)-D-glucan, an e
DC11527 Quilseconazole A novel selective, orally available fungal CYP51 (lanosterol 14-α-demethylase) inhibitor.
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