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7,4'-Dihydroxy-8-methylflavan

CAS# 82925-55-1

7,4'-Dihydroxy-8-methylflavan

Catalog No. BCN6841----Order now to get a substantial discount!

Product Name & Size Price Stock
7,4'-Dihydroxy-8-methylflavan: 5mg $828 In Stock
7,4'-Dihydroxy-8-methylflavan: 10mg Please Inquire In Stock
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7,4'-Dihydroxy-8-methylflavan: 500mg Please Inquire Please Inquire
7,4'-Dihydroxy-8-methylflavan: 1000mg Please Inquire Please Inquire

Quality Control of 7,4'-Dihydroxy-8-methylflavan

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Chemical structure

7,4'-Dihydroxy-8-methylflavan

3D structure

Chemical Properties of 7,4'-Dihydroxy-8-methylflavan

Cas No. 82925-55-1 SDF Download SDF
PubChem ID 442361 Appearance Powder
Formula C16H16O3 M.Wt 256.30
Type of Compound Flavonoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (2S)-2-(4-hydroxyphenyl)-8-methyl-3,4-dihydro-2H-chromen-7-ol
SMILES CC1=C(C=CC2=C1OC(CC2)C3=CC=C(C=C3)O)O
Standard InChIKey GDHZZZRERDPSTA-HNNXBMFYSA-N
Standard InChI InChI=1S/C16H16O3/c1-10-14(18)8-4-12-5-9-15(19-16(10)12)11-2-6-13(17)7-3-11/h2-4,6-8,15,17-18H,5,9H2,1H3/t15-/m0/s1
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 7,4'-Dihydroxy-8-methylflavan

The red resin of Dracaena cochinchinensis.

Biological Activity of 7,4'-Dihydroxy-8-methylflavan

Description1. 7,4'-Dihydroxy-8-methylflavan can significantly promote mesenchymal stem cells (MSCs) osteogenic differentiation by increasing the levels of alkaline phosphatase (ALP) activity. 2. 7,4'-Dihydroxy-8-methylflavan has free radical scavenging properties.

7,4'-Dihydroxy-8-methylflavan Dilution Calculator

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7,4'-Dihydroxy-8-methylflavan Molarity Calculator

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Preparing Stock Solutions of 7,4'-Dihydroxy-8-methylflavan

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.9017 mL 19.5084 mL 39.0168 mL 78.0336 mL 97.5419 mL
5 mM 0.7803 mL 3.9017 mL 7.8034 mL 15.6067 mL 19.5084 mL
10 mM 0.3902 mL 1.9508 mL 3.9017 mL 7.8034 mL 9.7542 mL
50 mM 0.078 mL 0.3902 mL 0.7803 mL 1.5607 mL 1.9508 mL
100 mM 0.039 mL 0.1951 mL 0.3902 mL 0.7803 mL 0.9754 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 7,4'-Dihydroxy-8-methylflavan

Three new flavanoids from artificially induced dragon's blood of Dracaena cambodiana.[Pubmed:28597686]

J Asian Nat Prod Res. 2018 Jan;20(1):55-61.

Three new flavanoids, (2R)-7,4'-dihydroxy-8-methylflavan (1), (2R)-7,4'-dihydroxy-6-methylflavan (2), and (3R)-7,3',4'-trihydroxyhomoisoflavan (3), together with seven known compounds (4-10), were isolated from artificially induced dragon's blood of Dracaena cambodiana, and their structures were determined based on HR-ESI-MS and extensive spectroscopic techniques (UV, IR, 1D-, and 2D-NMR). Compound 2 exhibited weak cytotoxicity against BEL-7402 cells line with the IC50 value of 39.2 muM. In addition, compound 3 showed significant acetylcholinesterase (AChE) inhibitory activity.

Isolation and chatacterization of homoisoflavonoids from Dracaena cochinchinensis and their osteogenic activities in mouse mesenchymal stem cells.[Pubmed:27497307]

J Pharm Biomed Anal. 2016 Sep 10;129:466-472.

Two new homoisoflavonoids, dracaeconolide A (1) and dracaeconolide B (2), together with ten known compounds, namely (3R)-7,4'-dihydroxy-8-methoxyhomoisoflavane (3), (3R)-7-hydroxy-3-(4-hydroxybenzyl)chromane (4), (3R)-7,4'-dihydroxy-5-methoxy-homoisoflavane (5), (3R)-6,4'-dihydroxy-8-methoxyhomoisoflavan (6), 7,4'-dihydroxy-8-methylflavan (7), (2R)-7,4'-dihydroxy-5-methoxy-8-methylflavan (8), 5,4'-dihydroxy-7-methoxy-6-methylflavane (9), 7,4'-dihydroxy-3'-methoxyflavan (10), 7,4'-dihydroxyflavan (11), 4,4'-dihydroxy-2,6-dimethoxydihydrochlcone (12), were isolated from the red resin of Dracaena cochinchinensis (dragon's blood, DB). All the compounds were then evaluated for their effects on mouse bone marrow-derived mesenchymal stem cells (MSCs) proliferation using CCK8 assay and their abilities in promoting MSCs differentiating into osteoblast through the assay of alkaline phosphatase (ALP) activity in vitro. Compounds 2, 3, 4, 7, 9, and 11, at a concentration of 10muM with no cytotoxicity, significantly promoted MSC osteogenic differentiation by increasing the levels of ALP activity to percents of 159.6+/-5.9, 167.6+/-10.9, 162.0+/-1.4, 151.3+/-4.0, 171.0+/-8.2, and 169.9+/-7.3 in relative to the control, respectively. The results of ALP staining were in accordance to that of ALP activity.

A methylflavan with free radical scavenging properties from Pancratium littorale.[Pubmed:11163938]

Fitoterapia. 2001 Jan;72(1):35-9.

The isolation of 7,4'-dihydroxy-8-methylflavan (1) from the dichloromethane extract of Pancratium littorale stem was guided by an assay for free radical scavenging activity towards the 2,2-diphenyl-1-picryl-hydrazyl radical (DPPH). The structure of 1 was established by spectrometric methods including UV, EI mass spectrometry, 1H and 13C-NMR. The free radical scavenging properties of 1 were quantified in solution using spectrophotometry.

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