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7-Hydroxy-3-(4-hydroxybenzyl)chroman

CAS# 1180504-64-6

7-Hydroxy-3-(4-hydroxybenzyl)chroman

Catalog No. BCN3578----Order now to get a substantial discount!

Product Name & Size Price Stock
7-Hydroxy-3-(4-hydroxybenzyl)chroman: 5mg Please Inquire In Stock
7-Hydroxy-3-(4-hydroxybenzyl)chroman: 10mg Please Inquire In Stock
7-Hydroxy-3-(4-hydroxybenzyl)chroman: 20mg Please Inquire Please Inquire
7-Hydroxy-3-(4-hydroxybenzyl)chroman: 50mg Please Inquire Please Inquire
7-Hydroxy-3-(4-hydroxybenzyl)chroman: 100mg Please Inquire Please Inquire
7-Hydroxy-3-(4-hydroxybenzyl)chroman: 200mg Please Inquire Please Inquire
7-Hydroxy-3-(4-hydroxybenzyl)chroman: 500mg Please Inquire Please Inquire
7-Hydroxy-3-(4-hydroxybenzyl)chroman: 1000mg Please Inquire Please Inquire

Quality Control of 7-Hydroxy-3-(4-hydroxybenzyl)chroman

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Chemical structure

7-Hydroxy-3-(4-hydroxybenzyl)chroman

3D structure

Chemical Properties of 7-Hydroxy-3-(4-hydroxybenzyl)chroman

Cas No. 1180504-64-6 SDF Download SDF
PubChem ID 11708657 Appearance Powder
Formula C16H16O3 M.Wt 256.3
Type of Compound Flavonoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 3-[(4-hydroxyphenyl)methyl]-3,4-dihydro-2H-chromen-7-ol
SMILES C1C(COC2=C1C=CC(=C2)O)CC3=CC=C(C=C3)O
Standard InChIKey GXMQROMLTBPBKV-UHFFFAOYSA-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 7-Hydroxy-3-(4-hydroxybenzyl)chroman

The herbs of Dracaena cochinchinensis

Biological Activity of 7-Hydroxy-3-(4-hydroxybenzyl)chroman

Description1. 7-Hydroxy-3-(4-hydroxybenzyl)chroman shows moderate inhibitory activity against a chymotrypsin-like activity of the proteasome.

7-Hydroxy-3-(4-hydroxybenzyl)chroman Dilution Calculator

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7-Hydroxy-3-(4-hydroxybenzyl)chroman Molarity Calculator

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Preparing Stock Solutions of 7-Hydroxy-3-(4-hydroxybenzyl)chroman

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-Hydroxy-3-(4-hydroxybenzyl)chroman

7-hydroxy-3-(4-hydroxybenzyl)chroman and broussonin b: neurotrophic compounds, isolated from Anemarrhena asphodeloides BUNGE, function as proteasome inhibitors.[Pubmed:16141565]

Biol Pharm Bull. 2005 Sep;28(9):1798-800.

The extract of Anemarrhenae Rhizoma (rhizomes of Anemarrhena asphodeloides BUNGE) showed neurotrophic activity toward rat pheochromocytoma (PC-12) cells. Bioassay-guided purification afforded four compounds, 2,6,4'-trihydroxy-4-methoxybenzophenone (1), 7-Hydroxy-3-(4-hydroxybenzyl)chroman (2), broussonin B (3), and cis-hinokiresinol (4). Compounds 1-3 induced neurite outgrowth in PC-12 cells at concentration of 50 microg/ml, while 4 was less active. In addition, compounds 2-4 showed moderate inhibitory activities against a chymotrypsin-like activity of the proteasome.

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