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Pneumocandin C0

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Catalog No. TN8324Cas No. 144074-96-4

Pneumocandin C0, an isomer of Pneumocandin B0, exhibits antifungal activity. It was identified during fermentation by the filamentous fungus Glarea lozoyensis under conditions of high residual fructose concentration.

Pneumocandin C0

Pneumocandin C0

😃Good
Catalog No. TN8324Cas No. 144074-96-4
Pneumocandin C0, an isomer of Pneumocandin B0, exhibits antifungal activity. It was identified during fermentation by the filamentous fungus Glarea lozoyensis under conditions of high residual fructose concentration.
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Product Introduction

Bioactivity
Description
Pneumocandin C0, an isomer of Pneumocandin B0, exhibits antifungal activity. It was identified during fermentation by the filamentous fungus Glarea lozoyensis under conditions of high residual fructose concentration.
Chemical Properties
Molecular Weight1065.21
FormulaC50H80N8O17
Cas No.144074-96-4
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor 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 μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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