Evonine
Evonine shows insecticidal activity against Mythimna separata, the LC50 value of 23.23 mg /mL.
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.
PLoS One.2018, 13(11):e0208055
J Clin Med.2022, 11(13):3662.
Food Chem.2024, 436:137768.
Heliyon.2024, 10(23):e40758.
Proc. Sci. Math.2024, V25:108-123
Biochem Pharmacol.2017, 130:10-20
Malaysian J of Fundamental and Applied Sciences 2018, 14(3):368-373
Appl Microbiol Biotechnol.2018, 102(12):5105-5120
Hum Exp Toxicol.2017, 36(11):1169-1176
Int J Mol Sci.2023, 24(8):7442.
Related and Featured Products
Acta Botanica Boreali-Occidentalia Sinica, 2007 , 27 (5) :983-988.
Sesquiterpene pyridine alkaloids from Euonymus japonicus and their insecticidal activity[Reference:
WebLink]
Four β-dihydroagarofuran sesquiterpene pyridine alkaloids were isolated from ethyl acetate extracts of the root bark of Euonymus japonicus by column chromatography and HPLC preparation with Bioaasy-guided fractionation.
METHODS AND RESULTS:
Their chemical structures were elucidated as Evonine(A),1-deacetyl-1-benzoylEvonine(B),ebenifoline E-IV(C) and mayteine(D) by mp,1H and 13C NMR.Their LC50 values against Mythimna separata were 23.23,5.44,5.25 and 4.66 mg·mL-1,respectively.
