7-Hydroxy-beta-carboline-1-propionic acid
7-Hydroxy-beta-carboline-1-propionic acid shows cytotoxic activity.
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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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Molecules.2023, 28(8):3376.
Universitat Stuttgart2022, opus-12200.
Evid Based Complement Alternat Med.2022, 9767292,2.
Cell J.2024, 26(8):496-504.
Separations2023, 10(11), 567;
Food Science and Biotechnology2022, 10.1007.
Molecules.2023, 28(9):3685.
Pharmacognosy Magazine2024, 20(2):632-645.
Plant Cell Physiol.2018, 59(1):128-141
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Phytochemistry, 2001, 56(4):383-6.
Canthin-6-one and beta-carboline alkaloids from Eurycoma harmandiana.[Pubmed:
11249106]
METHODS AND RESULTS:
Two alkaloids, canthin-6-one 9-O-beta-glucopyranoside and 7-Hydroxy-beta-carboline-1-propionic acid, were isolated from the roots of Eurcoma harmandiana together with the five known canthin-6-one alkaloids, 9-hydroxycanthin-6-one, 9-methoxycanthin-6-one, 9,10-dimethoxycanthin-6-one, canthin-6-one and canthin-6-one N-oxide, and the two known beta-carboline alkaloids, beta-carboline 1-propionic acid and 7-methoxy-beta-carboline 1-propionic acid. Their structures were based on analyses of spectroscopic data.
