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Dehydroglyasperin D

Cat. No. M42282
Dehydroglyasperin D Structure
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Biological Activity

Dehydroglyasperin D inhibits rat and human Aldose Reductase (AR) (IC50: 62.4 μM and 176.2 μM respectively).

Chemical Information
Molecular Weight 368.42
Formula C22H24O5
CAS Number 517885-72-2
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Eun Ji Baek et al. J Microbiol Biotechnol. Dehydroglyasperin D Suppresses Melanin Synthesis through MITF Degradation in Melanocytes

[2] Sung Keun Jung et al. J Cancer Prev. Dehydroglyasperin D Inhibits the Proliferation of HT-29 Human Colorectal Cancer Cells Through Direct Interaction With Phosphatidylinositol 3-kinase

[3] Sung Keun Jung et al. J Cell Mol Med. MLK3 is a novel target of dehydroglyasperin D for the reduction in UVB-induced COX-2 expression in vitro and in vivo

[4] Hyo Jung Kim et al. Nutr Res Pract. Antioxidant activities of licorice-derived prenylflavonoids

[5] Yeon Sil Lee et al. Biol Pharm Bull. Aldose reductase inhibitory compounds from Glycyrrhiza uralensis

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Keywords: Dehydroglyasperin D supplier, Aldose Reductase, inhibitors, activators


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