Arborine
Arborine has a growth inhibitory effect on the larvae of Drosophila melanogaster.
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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: service@chemfaces.com
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.
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Universiti Putra Malaysia Press,1994.
Arborine, a Larval Growth Inhibitor from Glycoslnis pentaphylla.[Reference:
WebLink]
Arborine (I), a quinazolone alkaloid was isolated from the leaves of Glycosmis pentaphylla (Rutaceae) and was found to have a growth inhibitory effect on the larvae of Drosophila melanogaster.
Phytochemistry, 1993, 34(1):175-179.
Sulphur-containing amides from Glycosmis species with different antifungal activity.[Reference:
WebLink]
METHODS AND RESULTS:
Leaf extracts from different Sri Lankan provenances of Glycosmis mauritiana and G. pentaphylla have been compared by HPLC analyses and tested for antifungal activity. All collections of G. pentaphylla are uniformly characterized by the known alkaloids Arborine, skimmianine and arborinine, whereas the different provenances of G. mauritiana differ by displaying chemical polymorphism of different sulphur-containing amides. Three new amides, named illukumbin B, methylillukumbin B and methylillukumbin A, have been isolated and their structures are described on the basis of spectroscopic evidence.
CONCLUSIONS:
They show different antifungal activities in bioautographic tests and appear to be accumulated mainly in individuals collected from more humid and elevated habitats.
