Sanggenon B

CAS# 81381-67-1

Sanggenon B

Catalog No. BCX0252----Order now to get a substantial discount!

Product Name & Size Price Stock
Sanggenon B: 5mg $989 In Stock
Sanggenon B: 10mg Please Inquire In Stock
Sanggenon B: 20mg Please Inquire Please Inquire
Sanggenon B: 50mg Please Inquire Please Inquire
Sanggenon B: 100mg Please Inquire Please Inquire
Sanggenon B: 200mg Please Inquire Please Inquire
Sanggenon B: 500mg Please Inquire Please Inquire
Sanggenon B: 1000mg Please Inquire Please Inquire

Quality Control of Sanggenon B

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Chemical structure

Sanggenon B

3D structure

Chemical Properties of Sanggenon B

Cas No. 81381-67-1 SDF Download SDF
PubChem ID 157791 Appearance Powder
Formula C33H30O9 M.Wt 570.6
Type of Compound Phenols Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 1,3,5a,8-tetrahydroxy-2-(5-hydroxy-9-methyl-8-oxatricyclo[7.3.1.02,7]trideca-2(7),3,5,10-tetraen-11-yl)-10a-(3-methylbut-2-enyl)-[1]benzofuro[3,2-b]chromen-11-one
SMILES CC(=CCC12C(=O)C3=C(C=C(C(=C3O)C4=CC5(CC(C4)C6=C(O5)C=C(C=C6)O)C)O)OC1(C7=C(O2)C=C(C=C7)O)O)C
Standard InChIKey UIIUFSXWGFBRFW-UHFFFAOYSA-N
Standard InChI InChI=1S/C33H30O9/c1-16(2)8-9-32-30(38)28-26(42-33(32,39)22-7-5-20(35)12-25(22)41-32)13-23(36)27(29(28)37)18-10-17-14-31(3,15-18)40-24-11-19(34)4-6-21(17)24/h4-8,11-13,15,17,34-37,39H,9-10,14H2,1-3H3
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.

Sanggenon B Dilution Calculator

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Sanggenon B Molarity Calculator

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Preparing Stock Solutions of Sanggenon B

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.7525 mL 8.7627 mL 17.5254 mL 35.0508 mL 43.8135 mL
5 mM 0.3505 mL 1.7525 mL 3.5051 mL 7.0102 mL 8.7627 mL
10 mM 0.1753 mL 0.8763 mL 1.7525 mL 3.5051 mL 4.3814 mL
50 mM 0.0351 mL 0.1753 mL 0.3505 mL 0.701 mL 0.8763 mL
100 mM 0.0175 mL 0.0876 mL 0.1753 mL 0.3505 mL 0.4381 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 Sanggenon B

Anti-inflammatory effects of mulberry (Morus alba L.) root bark and its active compounds.[Pubmed:30470128]

Nat Prod Res. 2020 Jun;34(12):1786-1790.

Mulberry (Morus alba L.) root bark (MRB) was extracted using methanol and the extracts were subjected to tests of anti-inflammatory effects. The ethyl acetate fraction demonstrated the best anti-inflammatory effects. Purified compounds, Sanggenon B, albanol B and sanggenon D, showed inhibitory effects on NO production in LPS-stimulated RAW264.7 cells and albanol B demonstrated the best anti-inflammatory effects. Regarding the underlying molecular mechanisms, further investigations showed that treatments with Albanol B reduced production of pro-inflammatory cytokines and decreased expression of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2). These results would contribute to development of novel anti-inflammatory drugs from MRB.

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