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Cat. No.: HY-181159

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Antifungal agent-164

Antifungal agent-164 is an exo-β-(1,3)-glucanase inhibitor that binds to the enzyme’s binding site. Antifungal agent-164 inhibits the growth of fungal. Antifungal agent-164 can be used for the research of candida infection.

For research use only. We do not sell to patients.

Formula: C₁₂H₁₄N₆O₆S₂
Molecular Weight:402.41

Storage:

Please store the product under the recommended conditions in the Certificate of Analysis.

Data Sheet (267 KB)

Antifungal agent-164 Chemical Structure

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Use of MCE Products

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Biological Activity
- Description
- In Vitro
Chemical Information
Purity & Documentation
References
Calculators
Help & FAQs
Classifications
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Biological Activity

Description

In Vitro

Antifungal agent-164 (compound 9) (0.031-5000 μg/mL; 24 h) exhibits fungicidal activity against C. albicans ATCC 10231 (MIC = 39.06 μg/mL), C. tropicalis ATCC 750 (MIC = 78.125 μg/mL), and C. parapsilosis ATCC 22019 (MIC = 312.5 μg/mL) with MFC/MIC ratios of 1^[1].
Antifungal agent-164 (compound 9) (500 ns) forms a stable complex with exo-β-(1,3)-glucanase from Candida albicans over 500 ns, with RMSD below 2 Å and key stabilizing interactions^[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Chemical Information

Molecular Weight 402.41
Formula C₁₂H₁₄N₆O₆S₂
SMILES

S=C(NNC(N1CCN(S(=O)(C)=O)C1=O)=O)NC2=CC=C([N+]([O-])=O)C=C2
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation

Select Batch:

Purity: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (267 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

References

[1]. Başoğlu F, et al. Exploring New Thiosemicarbazide Derivatives Bearing Imidazolidine Ring as Potential Antimicrobial Agents: Design, Synthesis, and Molecular Dynamics Studies. Chem Biodivers. 2026;23(1):e03059. [Content Brief]

Calculators

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Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

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100 mg

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