Griffithinam
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.
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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Phytomedicine.2018, 41:62-66
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Integr Med Res.2021, 10(3):100723.
Sci Rep.2023, 13(1):13610.
Oxid Med Cell Longev.2020, 2020:8887251.
Chemistry of Plant Raw Materials2019, 4:135-147
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Fitoterapia. 2011 Oct;82(7):964-8.
Cytotoxic alkaloids from stems, leaves and twigs of Dasymaschalon blumei.[Pubmed:
21641972]
METHODS AND RESULTS:
Bioassay-guided fractionation of the cytotoxic ethyl acetate extract from the stems of Dasymaschalon blumei (Annonaceae) led to the isolation of four aristololactam alkaloids, including the hitherto unknown 3,5-dihydroxy-2,4-dimethoxyaristolactam (1), as well as the three known compounds, aristolactam BI, goniopedaline, and Griffithinam. Additionally, the cytotoxic extract from the combined leaves and twigs of the same plant yielded three known oxoaporphine alkaloids, oxodiscoguattine, dicentrinone, and duguevalline. The structures of aristolactams and oxoaporphine alkaloids were elucidated on the basis of spectroscopic methods. All isolates were evaluated for cytotoxicity against a panel of mammalian cancer cell lines and a noncancerous human embryonic kidney cell Hek 293.
J Nat Prod. 1999 Jul;62(7):1050-2.
Alkaloids from the roots of goniothalamus griffithii.[Pubmed:
10425141]
METHODS AND RESULTS:
Three new alkaloids-griffithazanone A (1), griffithdione (2), and Griffithinam (3)-were isolated from the roots of Goniothalamus griffithii, along with six known compounds, 4-methyl-2,9, 10-(2H)-1-azaanthracenetrione (4), velutinam, aristololactam BI, aristololactam BII, aristololactam AII, and norcepharanone B. Their structures were elucidated on the basis of spectral and chemical methods.
CONCLUSIONS:
The absolute configuration of griffithazanone A (1) was determined by the preparation of Mosher's esters.
