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Dehydroglyasperin D

Catalog No. TMA0291 CAS 517885-72-2

Dehydroglyasperin D exhibits anticancer, anti-inflammatory, anti-obesity, Antioxidant and anti-aldose Reductase effects, it inhibits the proliferation of HT-29 human colorectal cancer cells through direct interaction with phosphatidylinositol 3-kinase; it also mediates suppression of both COX-2 expression and the MLK3 signalling pathway through direct binding and inhibition of MLK3. Dehydroglyasperin D shows strong ferric reducing activities and effectively scavenged DPPH, ABTS(+), and singlet oxygen radicals.

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Dehydroglyasperin D, CAS 517885-72-2

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Purity: 98%

Biological Description

Chemical Properties

Storage & Solubility Information

Description

Dehydroglyasperin D exhibits anticancer, anti-inflammatory, anti-obesity, antioxidant and anti-aldose reductase effects, it inhibits the proliferation of HT-29 human colorectal cancer cells through direct interaction with phosphatidylinositol 3-kinase; it also mediates suppression of both COX-2 expression and the MLK3 signalling pathway through direct binding and inhibition of MLK3. Dehydroglyasperin D shows strong ferric reducing activities and effectively scavenged DPPH, ABTS(+), and singlet oxygen radicals.

Molecular Weight	368.42
Formula	C22H24O5
CAS No.	517885-72-2

Storage

Powder: -20°C for 3 years

In solvent: -80°C for 2 years

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( < 1 mg/ml refers to the product slightly soluble or insoluble )

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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc.

Keywords

Dehydroglyasperin D 517885-72-2 Cell Cycle/Checkpoint Cytoskeletal Signaling DNA Damage/DNA Repair GPCR/G Protein Immunology/Inflammation MAPK Neuroscience PI3K/Akt/mTOR signaling Stem Cells ROS PI3K DNA/RNA Synthesis COX Akt Prostaglandin Receptor JNK GSK-3 p38 MAPK Inhibitor inhibitor inhibit

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