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Kojic acid

Kojic acid
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Purity:98%
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Kojic acid

Catalog No. T5889Cas No. 501-30-4
Kojic acid is a fungal metabolite that inhibits tyrosinase, an enzyme involved in melanin synthesis, with an IC50 value of 30.6 μM for mushroom tyrosinase.
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Pack SizePriceAvailabilityQuantity
5 g$39In Stock
10 g$55In Stock
1 mL x 10 mM (in DMSO)$43In Stock
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Product Introduction

Bioactivity
Description
Kojic acid is a fungal metabolite that inhibits tyrosinase, an enzyme involved in melanin synthesis, with an IC50 value of 30.6 μM for mushroom tyrosinase.
In vitro
Kojic acid(KA) (50 μg/mL) was found to decrease the growth by 62% (IC50 34 μg/mL) and 79% (IC50 27.84 μg/mL) of promastigotes and amastigotes in vitro, respectively. KA-treated amastigotes showed the presence of vesicles bodies into the flagellar pocket, and an intense intracellular vacuolization and swelling of the mitochondrion. During the in vitro interaction of parasites and the host cell, KA reverses the superoxide anions (O2-) inhibitory mechanism promoted by parasite[1].
In vivo
4 weeks after KA-topical formulation treatment of infected animals, a healing process was observed with a high production of collagen fibers and a decrease in parasite burden. The great potential of KA as an anti-leishmanial compound[1].
Cell Research
Amazonensis promastigotes (10^6 parasites/mL) were inoculated in a 24-well plate containing RPMI medium supplemented with 10% inactivated fetal bovine serum treated with different concentrations of KA and incubated at 25 °C for 5 days without medium replacement. Every 24 h after treatment, aliquots were harvested and the effect of Kojic acid on promastigotes growth was evaluated using a Neubauer chamber and compared with untreated parasites culture. The cultures were performed in triplicate[1].
Animal Research
Animals (eight-week-old female Golden hamsters) were infected with 10^6 of L. amazonensis promastigotes/mL during the stationary growth phase with a maximum volume of 0.2 mL on both hind paws.?Animals were separated in 3 groups: untreated (n?=?5);?KA-treated 100 mg/kg/day (n?=?5) and KA vehicle (n?=?5).?KA topical formulation treatment was initiated after 5 weeks of infection.?The KA formulation and vehicle was applied topically to all lesions once daily for 4 weeks.?Control groups were also maintained in parallel.?During the treatment period, the lesion size was measured weekly using a caliper.?Width and height of both hind paws were used to calculate the lesion area (mm^2)[1].
Chemical Properties
Molecular Weight142.11
FormulaC6H6O4
Cas No.501-30-4
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 55 mg/mL (387.02 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM7.0368 mL35.1840 mL70.3680 mL351.8401 mL
5 mM1.4074 mL7.0368 mL14.0736 mL70.3680 mL
10 mM0.7037 mL3.5184 mL7.0368 mL35.1840 mL
20 mM0.3518 mL1.7592 mL3.5184 mL17.5920 mL
50 mM0.1407 mL0.7037 mL1.4074 mL7.0368 mL
100 mM0.0704 mL0.3518 mL0.7037 mL3.5184 mL

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