R(+)-Gomisin M1
(+/-)-Gomisin M1 exhibits potent anti-HIV activity, with EC50 and therapeutic index (TI) values of <0.65 microM and >68, respectively.
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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.
Chemistry of Plant Raw Materials2022, 20220210569.
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Biochem Pharmacol.2020, 178:114083
Appl. Sci.2020, 10,1304
Front Plant Sci.2022, 12:811166.
Curr Med Sci.2024, 44(2):355-368.
Pharmaceuticals (Basel).2024, 17(3):341.
Phytomedicine.2019, 58:152893
Food Funct.2022, D1FO03838A.
Related and Featured Products
J Nat Prod. 2006 Dec;69(12):1697-701.
Rubrisandrins A and B, lignans and related anti-HIV compounds from Schisandra rubriflora.[Pubmed:
17190445 ]
METHODS AND RESULTS:
Bioactivity-directed fractionation of an ethanolic extract of the fruits of Schisandra rubriflora led to the isolation and identification of dibenzocyclooctadiene lignans including the new lignans rubrisandrins A (1a + 1b) and B (2) and the known lignans gomisin J (3), (+/-)-gomisin M1 (R(+)-Gomisin M1,4), (+)-gomisin M2 (5), schisanhenol (6), deoxyschisandrin, schisantherin B, schisandrin, tigloylgomisin P, gomisin O, angeloylgomisin P, and epigomisin O. Their structure and stereochemistry were determined by spectroscopic methods, including 2D-NMR techniques. Compounds 1 and 3-6 were active as anti-HIV agents.
CONCLUSIONS:
(+/-)-Gomisin M1 (R(+)-Gomisin M1,4) exhibited the most potent anti-HIV activity, with EC50 and therapeutic index (TI) values of <0.65 microM and >68, respectively.
Planta Med 1984; 50(5): 414-417
Studies on the Chemical Constituents of Kadsura longipedunculata: Isolation and Structure Elucidation of Five New Lignans[Reference:
WebLink]
METHODS AND RESULTS:
Five new dibenzocyclooctadiene lignans, R(+)-wuweizisu C (1), kadsuranin (2), R(+)-Gomisin M1 (3), R(+)-angeloylgomisin M1 (4) and angeloylgomisin R (5) were isolated from the ethereal extract of roots and stems of Kadsura longipedunculata Finet et Gagnep.
CONCLUSIONS:
Their structures were elucidated on the basis of chemical and spectral analysis.
