1,7-Diphenyl-5-hydroxy-4,6-hepten-3-one
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.
J Ginseng Res.2023, 47(4):572-582.
Food Bioscience2023, 59:103903
J.Korean Soci. Food Sci. Nutri.2024, 53(11):1166-1177
Chin J Appl. Physiol.2019, 35(3):283-288
Herbal Formula Science2024, 32(3):203-221
Foods2023, 12(23), 4342.
SSRN2024, 4937625.
Chinese Journal of Tissue Engineering Research2024, 28(8):1149-1154.
Eur J Pharmacol.2024, 981:176883.
World J Microbiol Biotechnol.2024, 40(9):265.
Related and Featured Products
Chinese Journal of Natural Medicines, 2010:81 - 91.
Chemical Constituents from the Seeds of Alpinia katsumadai Hayata[Reference:
WebLink]
To investigate the chemical constituents from the seeds of Alpinia katsumadai Hayata.
METHODS AND RESULTS:
Compounds were isolated and purified by column chromatography with silica gel and Sephadex LH-20, and their structures were identified on the basis of physiochemical properties and spectroscopic data. Ten compounds are isolated and elucidated as trans, trans-1,7-Diphenyl-5-hydroxy-4,6-hepten-3-one (1), pinocembrin (2), alpinetin (3), 7, 4′-dihydroxy-5-methoxy flavanone (4), helichrysetin (5), uvangoletin (6), (1E, 4Z)-5-hydroxy-1-phenyl-hexa-1, 4-dien-3-one (7), katsumadain B (8), rhodomollein I (9), and aurantiamide acetate (10).
CONCLUSIONS:
Compound 7 was a new natural product. Compounds 9 and 10 were isolated from the genus for the first time.
