Myrrhone
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 Biol Chem.2021, 297(6):101362.
Anticancer Res.2022, 42(9):4403-4410.
Pak J Pharm Sci.2019, 32(6)
Auburn University2015, 1-58
Anal Bioanal Chem.2020, 412(12):3005-3015.
Phytochemistry Letters2015, 243-247
Front Microbiol.2023, 14:921653.
GENENCELL2023, 25:4356740
Mol Neurobiol.2021, 58(8):3665-3676.
Antioxidants (Basel).2020, 9(6):526.
Related and Featured Products
J Nat Prod. 2013 Jul 26;76(7):1254-9.
Agarsenone, a Cadinane Sesquiterpenoid from Commiphora erythraea.[Pubmed:
23844767 ]
METHODS AND RESULTS:
Agarsenone (1), a new cadinane sesquiterpenoid, was isolated from the resin of Commiphora erythraea. The structures of 1 and its decomposition products agarsenolides (2a and 2b) and Myrrhone (3) were established by extensive NMR spectroscopic analysis.
CONCLUSIONS:
The absolute configuration of 3 and the relative and absolute configurations of 1 were assigned by comparison of experimental and calculated optical rotatory dispersion and electronic circular dichroism spectra.
