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CYP51-IN-22

CYP51-IN-22, the non-deuterated analog of CYP51-IN-23-d3 , is a potent and broad-spectrum CYP51 inhibitor.CYP51-IN-22 inhibits Aspergillus fumigatum with a MIC80 of 1 μg/mL. CYP51-IN-22 can prevent fungal phase transformation and biofilm formation. CYP51-IN-22 exhibits anti-drug resistance activity and fungal activity, and shows excellent safety for cells and significant pharmacological activity in mice. CYP51-IN-22 can be used for the study of invasive fungal infections (IFIs).

Product Specifications

UNSPSC

12352005

Target

Cytochrome P450; Fungal

Related Pathways

Anti-infection; Metabolic Enzyme/Protease

Applications

COVID-19-immunoregulation

Field of Research

Infection

Smiles

FC1=CC(F)=CC=C1C(CN(C)CC2=CC=C(N3CCN(C(C4=CC(Br)=CC=C4)=O)CC3)C=C2)(O)CN5C=NN=N5

Molecular Formula

C29H30BrF2N7O2

Molecular Weight

626.50

References & Citations

[1]Luo Z et al. Discovery of a potent, broad-spectrum and in vivo effective deuterated tetrazole CYP51 inhibitor. Eur J Med Chem. 2025 May 28;296:117817.

Shipping Conditions

Room temperature

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Isoform

CYP51

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