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3-Isomangostin

3-Isomangostin
3-Isomangostin is an acetylcholinesterase selective inhibitor and a potent human aldose reductase inhibitor with an IC50 of 3.48 uM. 3-Isomangostin has free radical scavenging activity and inhibits MutT homolog 1 (MTH1) with an IC50 of 52 nM. It shows antiplasmodial activity with an IC50 values in the range of 4.71-11.40 uM. 3-Isomangostin can be used to develop anticancer agents as well.
Catalog No. T2S1635Cas No. 19275-46-8
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3-Isomangostin

Catalog No. T2S1635Cas No. 19275-46-8

3-Isomangostin is an acetylcholinesterase selective inhibitor and a potent human aldose reductase inhibitor with an IC50 of 3.48 uM. 3-Isomangostin has free radical scavenging activity and inhibits MutT homolog 1 (MTH1) with an IC50 of 52 nM. It shows antiplasmodial activity with an IC50 values in the range of 4.71-11.40 uM. 3-Isomangostin can be used to develop anticancer agents as well.
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Pack SizePriceAvailabilityQuantity
1 mg$35In Stock
5 mg$106In Stock
10 mg$179In Stock
25 mg$297In Stock
50 mg$453In Stock
1 mL x 10 mM (in DMSO)$128In Stock
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Product Introduction

Bioactivity
Description
3-Isomangostin is a potent human aldose reductase inhibitor with an IC50 of 3.48 uM; it is also an acetylcholinesterase selective inhibitor. 3-Isomangostin has free radical scavenging activity; it shows antiplasmodial activity with IC50 values in the rang
Targets&IC50
MTH1:52 nM
In vitro
Species of Garcinia have been used to combat malaria in traditional African and Asian medicines, including Ayurveda. In the current study, we have identified antiplasmodial benzophenone and xanthone compounds from edible Garcinia species by testing for in vitro inhibitory activity against Plasmodium falciparum. Whole fruits of Garcinia xanthochymus, G. mangostana, G. spicata, and G. livingstonei were extracted and tested for antiplasmodial activity. Garcinia xanthochymus was subjected to bioactivity-guided fractionation to identify active partitions. Purified benzophenones (1-9) and xanthones (10-18) were then screened in the plasmodial lactate dehydrogenase assay and tested for cytotoxicity against mammalian (Vero) cells. The benzophenones guttiferone E (4), isoxanthochymol (5), and guttiferone H (6), isolated from G. xanthochymus, and the xanthones α-mangostin (15), β-mangostin (16), and 3-Isomangostin (17), known from G. mangostana, showed antiplasmodial activity with an IC50 values in the range of 4.71-11.40 μM. Artemisinin and chloroquine were used as positive controls and exhibited an IC50 values in the range of 0.01-0.24 μM.
Chemical Properties
Molecular Weight410.46
FormulaC24H26O6
Cas No.19275-46-8
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
Ethanol: 40 mg/mL (97.45 mM)
DMSO: 40 mg/mL (97.45 mM)
Solution Preparation Table
Ethanol/DMSO
1mg5mg10mg50mg
1 mM2.4363 mL12.1815 mL24.3629 mL121.8145 mL
5 mM0.4873 mL2.4363 mL4.8726 mL24.3629 mL
10 mM0.2436 mL1.2181 mL2.4363 mL12.1815 mL
20 mM0.1218 mL0.6091 mL1.2181 mL6.0907 mL
50 mM0.0487 mL0.2436 mL0.4873 mL2.4363 mL

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