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5'-Geranyl-5,7,2',4'-tetrahydroxyflavone

CAS# 1221762-70-4

5'-Geranyl-5,7,2',4'-tetrahydroxyflavone

Catalog No. BCN1601----Order now to get a substantial discount!

Product Name & Size Price Stock
5'-Geranyl-5,7,2',4'-tetrahydroxyflavone: 5mg Please Inquire In Stock
5'-Geranyl-5,7,2',4'-tetrahydroxyflavone: 10mg Please Inquire In Stock
5'-Geranyl-5,7,2',4'-tetrahydroxyflavone: 20mg Please Inquire Please Inquire
5'-Geranyl-5,7,2',4'-tetrahydroxyflavone: 50mg Please Inquire Please Inquire
5'-Geranyl-5,7,2',4'-tetrahydroxyflavone: 100mg Please Inquire Please Inquire
5'-Geranyl-5,7,2',4'-tetrahydroxyflavone: 200mg Please Inquire Please Inquire
5'-Geranyl-5,7,2',4'-tetrahydroxyflavone: 500mg Please Inquire Please Inquire
5'-Geranyl-5,7,2',4'-tetrahydroxyflavone: 1000mg Please Inquire Please Inquire

Quality Control of 5'-Geranyl-5,7,2',4'-tetrahydroxyflavone

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Chemical structure

5'-Geranyl-5,7,2',4'-tetrahydroxyflavone

3D structure

Chemical Properties of 5'-Geranyl-5,7,2',4'-tetrahydroxyflavone

Cas No. 1221762-70-4 SDF Download SDF
PubChem ID 46211767 Appearance Yellow powder
Formula C25H26O6 M.Wt 422.5
Type of Compound Flavonoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 2-[5-[(2E)-3,7-dimethylocta-2,6-dienyl]-2,4-dihydroxyphenyl]-5,7-dihydroxychromen-4-one
SMILES CC(=CCCC(=CCC1=C(C=C(C(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O)C)C
Standard InChIKey CGAAHNXTXSLXAJ-VIZOYTHASA-N
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Source of 5'-Geranyl-5,7,2',4'-tetrahydroxyflavone

The root bark of Morus alba L.

Biological Activity of 5'-Geranyl-5,7,2',4'-tetrahydroxyflavone

Description1. 5'-Geranyl-5,7,2',4'-tetrahydroxyflavone inhibits cholinesterase enzyme in a dose-dependent manner against acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) enzymes. 2. 5′-Geranyl-5,7,2′,4′-tetrahydroxyflavone shows better tyrosinase inhibitory activities than kojic acid.
TargetsTyrosinase | AChR

5'-Geranyl-5,7,2',4'-tetrahydroxyflavone Dilution Calculator

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5'-Geranyl-5,7,2',4'-tetrahydroxyflavone Molarity Calculator

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Preparing Stock Solutions of 5'-Geranyl-5,7,2',4'-tetrahydroxyflavone

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.3669 mL 11.8343 mL 23.6686 mL 47.3373 mL 59.1716 mL
5 mM 0.4734 mL 2.3669 mL 4.7337 mL 9.4675 mL 11.8343 mL
10 mM 0.2367 mL 1.1834 mL 2.3669 mL 4.7337 mL 5.9172 mL
50 mM 0.0473 mL 0.2367 mL 0.4734 mL 0.9467 mL 1.1834 mL
100 mM 0.0237 mL 0.1183 mL 0.2367 mL 0.4734 mL 0.5917 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on 5'-Geranyl-5,7,2',4'-tetrahydroxyflavone

Isolation of cholinesterase-inhibiting flavonoids from Morus lhou.[Pubmed:21434689]

J Agric Food Chem. 2011 May 11;59(9):4589-96.

Cholinesterases are key enzymes that play important roles in cholinergic transmission. Nine flavonoids displaying cholinesterase inhibitory activity were isolated from the root bark of Morus lhou L., a cultivated edible plant. The isolated compounds were identified as a new flavone (1), 5'-geranyl-5,7,2',4'-tetrahydroxyflavone (2), kuwanon U (3), kuwanon E (4), morusin (5), morusinol (6), cyclomorusin (7), neocyclomorusin (8), and kuwanon C (9). All compounds apart from compound 6 inhibited cholinesterase enzyme in a dose-dependent manner with K(i) values ranging between 3.1 and 37.5 muM and between 1.7 and 19.1 muM against acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) enzymes, respectively. The new compound was charactierized as 5'-geranyl-4'-methoxy-5,7,2'-trihydroxyflavone (1). It showed the most potent inhibitory activity (K(i) = 3.1 muM for AChE, K(i) = 1.74 muM for BChE). Lineweaver-Burk and Dixon plots and their secondary replots indicated that flavones (5-9) with prenyl substitution on C-3 were noncompetitive inhibitors, whereas those unsubstituted (1-4) at C-3 were mixed inhibitors of both AChE and BChE. In conclusion, this is the first study to demonstrate that alkylated flavonoids of M. lhou have potent inhibitory activities against AChE and BChE.

Tyrosinase inhibitory constituents from the roots of Morus nigra: a structure-activity relationship study.[Pubmed:20297841]

J Agric Food Chem. 2010 May 12;58(9):5368-73.

The phytochemical profiles of Morus nigra roots and twigs were compared by HPLC with those of the old and young twigs of Morus alba which are known to contain oxyresveratrol and mulberroside A as major components. It was found that M. nigra root extract contains some unknown natural products with potential tyrosinase inhibitory activity. The extract (95% ethanol) of the roots of M. nigra was further investigated in this study. One new compound, 5'-geranyl-5,7,2',4'-tetrahydroxyflavone, and twenty-eight known phenolic compounds were isolated. Their structures were identified by mass spectrometry and NMR spectroscopy. Nine compounds, 5'-geranyl-5,7,2',4'-tetrahydroxyflavone, steppogenin-7-O-beta-D-glucoside, 2,4,2',4'-tetrahydroxychalcone, moracin N, kuwanon H, mulberrofuran G, morachalcone A, oxyresveratrol-3'-O-beta-D-glucopyranoside and oxyresveratrol-2-O-beta-D-glucopyranoside, showed better tyrosinase inhibitory activities than kojic acid. It was noteworthy that the IC(50) values of 2,4,2',4'-tetrahydroxychalcone and morachalcone A were 757-fold and 328-fold lower than that of kojic acid, respectively, suggesting a great potential for their development as effective natural tyrosinase inhibitors.

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