Caboxine A
Standard reference
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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.
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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.
Nanjing University of Chinese Medicine2022, 345930.
J Nat Prod.2023, 86(2):264-275.
Molecules2022, 27(12):3824.
Front Endocrinol (Lausanne).2020, 11:568436.
Eur J Pharmacol.2021, 899:174010.
Front Pharmacol.2021, 12:690113.
Nat Commun.2021, 12(1):681.
J of App. Res. on Med&Aromatic Plants2020, 100291.
Virol J.2024, 21(1):95.
Green Chemistry2021, ISSUE 2.
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Phytochemistry Letters,2011,4(4):399–403.
Two new indole alkaloids from Vinca herbacea L.[Reference:
WebLink]
Six indole alkaloids were isolated from the aerial parts of Vinca herbacea Waldst. et Kit.
METHODS AND RESULTS:
Structures of the isolated compounds were elucidated as two new alkaloids, 10-methoxyraucaffrinoline (1) and 11-methoxyburnamine (2), and four known alkaloids, picrinine (3), burnamine (4), Caboxine A (5) and elegantine (6) by intensive 1D- and 2D-NMR spectroscopic techniques.
Phytochemistry,1975,14(2):565-568.
Structure des caboxines: Alcaloïdes oxindoliques du Cabucala fasciculata[Reference:
WebLink]
METHODS AND RESULTS:
The structures of three new 11-monomethoxy pentacyclic oxindole alkaloids have been elucidated by chemical correlations with reserpinine: Caboxine A was assigned to the allo C19-méthyl α series: 3S, 4R, 7S, 19S; isocaboxine-A and B to the epi-allo C19-methyl α series and have, respectively, the following configurations 3R, 4S, 7S, 19S and 3R, 4S, 7R, 19S.
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