|Source:||The barks of Calophyllum lanigerum|
|Biological Activity or Inhibitors:|| 1. Calanolide E2 has anti-HIV activity.
|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: firstname.lastname@example.org
|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||2.574 mL||12.87 mL||25.74 mL||51.4801 mL||64.3501 mL|
|5 mM||0.5148 mL||2.574 mL||5.148 mL||10.296 mL||12.87 mL|
|10 mM||0.2574 mL||1.287 mL||2.574 mL||5.148 mL||6.435 mL|
|50 mM||0.0515 mL||0.2574 mL||0.5148 mL||1.0296 mL||1.287 mL|
|100 mM||0.0257 mL||0.1287 mL||0.2574 mL||0.5148 mL||0.6435 mL|
J Nat Prod. 1996 Aug;59(8):754-8.
|New pyranocoumarins isolated from Calophyllum lanigerum and Calophyllum teysmannii.[Pubmed: 8792623 ]|
|During a chemotaxonomic survey of Calophyllum extracts present in the National Cancer Institute's natural product repository, four new pyranocoumarins were isolated from extracts of C. lanigerum var. austrocoriaceum and C. teysmannii var. inophylloide (King.) P. F. Stevens (Clusiaceae). The structure elucidation and anti-HIV activity of Calanolide E2 (4), cordatolide E (5), pseudocordatolide C (6), and calanolide F (9), along with a simple prenylated coumarin precursor (11), are described here.|