|Source:||The herbs of Symphonia globulifera L.|
|Biological Activity or Inhibitors:|
|Solvent:||Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.|
|Storage:||Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.
Need more advice on solubility, usage and handling? Please email to: email@example.com
|After receiving:||The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.|
|1 mg||5 mg||10 mg||20 mg||25 mg|
|1 mM||3.0458 mL||15.229 mL||30.4581 mL||60.9162 mL||76.1452 mL|
|5 mM||0.6092 mL||3.0458 mL||6.0916 mL||12.1832 mL||15.229 mL|
|10 mM||0.3046 mL||1.5229 mL||3.0458 mL||6.0916 mL||7.6145 mL|
|50 mM||0.0609 mL||0.3046 mL||0.6092 mL||1.2183 mL||1.5229 mL|
|100 mM||0.0305 mL||0.1523 mL||0.3046 mL||0.6092 mL||0.7615 mL|
Nat Prod Commun. 2009 Jun;4(6):803-8.
|Globulixanthone F, a new polyoxygenated xanthone with an isoprenoid group and two antimicrobial biflavonoids from the stem bark of Symphonia globulifera.[Pubmed: 19634326]|
|Bioassay-guided fractionation of the stem bark of Symphonia globulifera has yielded three known xanthones, Ugaxanthone (1), mbarraxanthone (2) and gentisein (3), two biflavonoid derivatives named GB2 (4) and manniflavanone GB3 (5), and one new polyoxygenated xanthone with an isoprenoid group, named globulixanthone F (6). The structures of these compounds were elucidated by means of spectroscopic methods. The spectral data of 1 and 2 are reported here for the first time, as well as the antimicrobial activity of globulixanthone F against a range of microorganisms. We also report the total synthesis of the xanthone skeleton.|