14-Deoxy-epsilon-caesalpin
14-Deoxy-epsilon-caesalpin is a natural product from Caesalpinia minax HANCE.
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 Nat Prod.2019, 82(4):1002-1008
BMC Complement Altern Med.2014, 14:352
Toxins (Basel).2022, 14(12):824.
ACS Pharmacol. Transl. Sci.2022, 5,7,479-490
Antioxidants (Basel).2019, 8(8):E307
Journal of functional foods2018, 171-182
Antioxidants (Basel).2023, 13(1):12.
Molecules.2015, 20(11):20014-30
Phytomedicine.2018, 38:12-23
Food Res Int.2020, 128:108778
Related and Featured Products
Chem Biodivers. 2006 Nov;3(11):1260-5.
Cassane diterpene-lactones from the seed of Caesalpinia minax HANCE.[Pubmed:
17193240 ]
METHODS AND RESULTS:
Five new neocaesalpins, named neocaesalpin J-N (1-5, resp.), along with the known neocaesalpin A and eight known furanditerpenoids, namely epsilon-caesalpin, 7-acetoxy-epsilon-caesalpin, 14-Deoxy-epsilon-caesalpin, caesalmins D-F, and bonducellins C and D, were isolated from the seeds of Caesalpinia minax HANCE.
CONCLUSIONS:
Their structures were determined on the basis of spectroscopic analyses.
