Neocryptomerin
Reference standards.
Inquire / Order:
manager@chemfaces.com
Technical Inquiries:
service@chemfaces.com
Tel:
+86-27-84237783
Fax:
+86-27-84254680
Address:
1 Building, No. 83, CheCheng Rd., Wuhan Economic and Technological Development Zone, Wuhan, Hubei 430056, PRC
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.
Adaptive Medicine 2020, 12(1): 4-10
J Agric Food Chem.2021, 69(11):3496-3510.
Sci Rep.2021, 11(1):21038.
Phytomedicine Plus2022, 2(1):100207.
Anal Bioanal Chem.2016, 408(1):177-90.
International J of Green Pharmacy2019, 13(3)
Srinakharinwirot University2023, 2669.
J Agric Food Chem.2023, 71(47):18510-18523.
Korean J. Crop Sci.2018, 63(2):131-139
Enzyme Microb Technol.2022, 161:110111.
Related and Featured Products
Planta Med. 2012 Mar;78(4):390-2.
Isolation and cytotoxic activity of selaginellin derivatives and biflavonoids from Selaginella tamariscina.[Pubmed:
22271084 ]
METHODS AND RESULTS:
Five selaginellin derivatives, including two new selaginellins termed selaginellins M (1) and N (2), and three previously identified compounds, selaginellin (3), selaginellin A (4), and selaginellin C (5), were isolated from the Selaginella tamariscina (Beauv.) Spring plant. In addition, four known biflavonoids, namely Neocryptomerin ( 6), hinokiflavone (7), pulvinatabiflavone (8), and 7''- O-methylamentoflavone (9), were also isolated. The structures of new compounds 1 and 2 were elucidated by spectroscopic analysis. The cytotoxic activity of compounds 1- 9 was evaluated against a small panel of human cancer cell lines, including U251 (human glioma cells), HeLa (human cervical carcinoma cells), and MCF-7 (human breast cancer cells).
CONCLUSIONS:
The two new selaginellins, selaginellins M (1) and N (2), showed medium activity against the human cancer cell lines.
