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Quercetin dihydrate

Quercetin dihydrate CAS: 6151-25-3 | MF: C15H10O7 · 2H2O | MW: 338.27, Part Number S10161, Buy Histological Stains & Dyes for Histology, Cytology, Microbiology, Hematology & Biology Lab from TriStains at Chemical World.

Quercetin dihydrate is a naturally occurring flavonoid compound that is derived from various plant sources. It is commonly found in fruits, vegetables, and grains, and it is known for its antioxidant and anti-inflammatory properties at Dawnscientific.com.

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Alternate Names 2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-4H-1-benzopyran-4-one dihydrate,  3,3,4,5,7-Pentahydroxyflavone dihydrate
Application Quercetin Dihydrate is a natural flavonoid antiproliferative kinase inhibitor
CAS Number 6151-25-3
Molecular Weight 338.27
Molecular Formula C15H10O7 · 2H2O
Supplemental Information This is classified as a Dangerous Good for transport and may be subject to additional shipping charges
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use. * Refer to Certificate of Analysis for lot specific data (including water content).

Quercetin Dihydrate is the dihydrate preparation of Quercetin, a ubiquitous natural flavonoid with antiproliferative properties. Quercetin is described to inhibit PLA2 and PI 3-kinase (IC50 = 3.8 microM), blocking the ATP binding site of this kinase and interrupting the role of this enzyme in propagating cellular responses to growth factors. Quercetin is further described to inhibit nucleotide-dependent kinase enzymes through competition with ATP and GTP, demonstrating inhibition of pp60src phosphotransferase, tyrosine protein kinase, calcium- and phospholipid-dependent protein kinase, and cyclic GMP phosphodiesterases. Inhibition of PI 4-kinase (1-phosphatidylinositol 4-kinase) and PI-4-phosphate 5-kinase (1-phosphatidylinositol 4-phosphate 5-kinase) by Quercetin blocks the participation of these enzymes in signal transduction pathways and reduces cellular levels of the second messenger IP3 (inositol 1,4,5-trisphosphate), decreasing the release of intracellular Ca2+ stores. The antiproliferative and cytotoxic effects of Quercetin on cultured breast cancer cells are attributed to inhibition of PI 4-kinase and PI-4-phosphate 5-kinase, reduction of IP3 levels, and blockade of oncogenic growth signaling. Quercetin was shown to induce apoptosis in tumor cell lines at the G1 and S phases. Potential fatty acid synthase, PKC, and ATP5 (mitochondrial ATPase) inhibitor as well as an SIRT1 activator. SIRT1 deacetylates histones. Quercetin Dihydrate is an inhibitor of Pim-1 and an activator of GPR30.

Physical State Solid
Solubility Soluble in DMSO (68 mg/ml at 25° C), Acetic Acid (1 mg/ml), Aqueous Alkali (1 mg/ml), water (<1 at 25° C), and ethanol (21 mg/ml at 25° C).
Storage Store at room temperature
Melting Point 310-315° C
Refractive Index n20D 1.82 (Predicted)
IC50 Monoamine oxidase A: IC50 = 10 nM (bovine); CYP19: IC50 = 12 nM (human); Aldose Reductase: IC50 = 14.8 nM (human); Pim-1: IC50 = 43 nM (human); CYP1B1: IC50 = 77 nM (human)
Ki Data D4DR: Ki= 7.8 nM (human); Enoyl-acyl-carrier protein reductase: Ki= 22 nM (plasmodium falciparum); CYP1B1: Ki= 23 nM (human); 5'-nucleotidase: Ki= 45.3 nM (rat); CYP1A1: Ki= 660 nM (human)

SAFETY INFORMATION

WGK Germany 3
RTECS LK8950000
PubChem CID 5284452
Merck Index 14: 8034
MDL Number MFCD00149487
EC Number 204-187-1
Beilstein Registry 317313
SMILES C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O.O.O

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