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Ibrexafungerp citrate

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Catalog No. T70029Cas No. 1965291-08-0
Alias SCY-078 citrate, SCY078 citrate, MK3118 citrate, MK 3118 citrate

Ibrexafungerp citrate is a triterpenoid antifungal agent that inhibits the synthesis of 1,3-β-D-glucan in fungal cell walls, and although its functional outcome is similar to echinocandins, it binds to a distinct site on the glucan synthase enzyme, resulting in limited cross-resistance. Ibrexafungerp citrate exhibit concentration-dependent fungicidal activity against Candida species and retaining strong in vitro efficacy against the majority of fluconazole-resistant strains, supporting its use in antifungal resistance and drug development research.

Ibrexafungerp citrate

Ibrexafungerp citrate

😃Good
Catalog No. T70029Alias SCY-078 citrate, SCY078 citrate, MK3118 citrate, MK 3118 citrateCas No. 1965291-08-0
Ibrexafungerp citrate is a triterpenoid antifungal agent that inhibits the synthesis of 1,3-β-D-glucan in fungal cell walls, and although its functional outcome is similar to echinocandins, it binds to a distinct site on the glucan synthase enzyme, resulting in limited cross-resistance. Ibrexafungerp citrate exhibit concentration-dependent fungicidal activity against Candida species and retaining strong in vitro efficacy against the majority of fluconazole-resistant strains, supporting its use in antifungal resistance and drug development research.
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Product Introduction

Bioactivity
Description
Ibrexafungerp citrate is a triterpenoid antifungal agent that inhibits the synthesis of 1,3-β-D-glucan in fungal cell walls, and although its functional outcome is similar to echinocandins, it binds to a distinct site on the glucan synthase enzyme, resulting in limited cross-resistance. Ibrexafungerp citrate exhibit concentration-dependent fungicidal activity against Candida species and retaining strong in vitro efficacy against the majority of fluconazole-resistant strains, supporting its use in antifungal resistance and drug development research.
In vitro
In fungal susceptibility assays, Ibrexafungerp citrate acted as a β-1,3-glucan synthase inhibitor, disrupting cell wall integrity. It exhibited a minimum inhibitory concentration (MIC50) of 0.5 μg/mL against various Candida species, including multidrug-resistant Candida auris, resulting in broad-spectrum fungicidal activity [1].
SynonymsSCY-078 citrate, SCY078 citrate, MK3118 citrate, MK 3118 citrate
Chemical Properties
Molecular Weight922.16
FormulaC50H75N5O11
Cas No.1965291-08-0
SmilesC(CC(O)=O)(CC(O)=O)(C(O)=O)O.C[C@@]12[C@]3([C@@](C=4[C@@]([C@]5(C)[C@@](C)(CC4)[C@H](C(O)=O)[C@]([C@@H](C(C)C)C)(C)CC5)(CC3)[H])(C[C@H]([C@@H]1OC[C@](C(C)(C)C)(C)N)N6C(=NC=N6)C=7C=CN=CC7)COC2)[H]
Storage & Solubility Information
StorageIn solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 80 mg/mL (86.75 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.0844 mL5.4221 mL10.8441 mL54.2205 mL
5 mM0.2169 mL1.0844 mL2.1688 mL10.8441 mL
10 mM0.1084 mL0.5422 mL1.0844 mL5.4221 mL
20 mM0.0542 mL0.2711 mL0.5422 mL2.7110 mL
50 mM0.0217 mL0.1084 mL0.2169 mL1.0844 mL

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Stock solution preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (stock solution concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2OTargetMol | reagent mix well and clarify
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