Picropodophyllotoxin
Picropodophyllotoxin shows highly antifeeding and toxic activities against the 3rd-instar larve of Mythimna separate W.and the 4th-instar larvae of Pieris rapae L.and the 3rd-instar larve of Plutella xylostella L.
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.
International Food Research Journal2018, 25(6):2560-2571
Cell Physiol Biochem.2017, 44(4):1381-1395
J Food Drug Anal.2023, 31(2):254-277.
Int J Mol Sci.2024, 25(1):616.
J Pharmacol Sci.2021, 147(2):184-191.
Anal Bioanal Chem. 2016, 408(15)
Plant Physiol.2024, 194(4):2580-2599.
RSC Adv.2023, 13(9):6317-6326.
Int J Mol Sci.2018, 19(9):E2601
Neurochem Int.2020, 133:104629
Related and Featured Products
《Journal of Northwest A & F University(Natural Science Edition)》 2007-09
Study on 6 insecticidal podophyllotoxin compounds from the berries of Sabina vulgaris Ant.[Reference:
WebLink]
In order to isolate other insecticidal podophyllotoxin compounds from the berries of Sabina vulgaris Ant.,six podophyllotoxin compounds were isolated by tracing with insecticidal activity.They were identified as acetyl Picropodophyllotoxin,deoxyPicropodophyllotoxin,acetyl epipodophyllotoxin,podophyllotoxin,deoxypodophyllotoxin and Picropodophyllotoxin.
METHODS AND RESULTS:
The antifeeding activities against the 3rd-instar larve of Mythimna separate W.and the toxic activities against the 4th-instar larvae of Pieris rapae L.and the 3rd-instar larve of Plutella xylostella L.were tested by leaf-disk method and leaf-dipping method,respectively.The bioassay results indicated that all these compounds showed highly antifeeding and toxic activities against the 3 tested insects.Podophyllotoxin and deoxypodophyllotoxin were the two with the highest insecticidal activities among the six,while Picropodophyllotoxin was the lowest.Besides,acetyl Picropodophyllotoxin,deoxyPicropodophyllotoxin,acetyl epipodophyllotoxin and Picropodophyllotoxin were insecticidal compounds firstly reported from S.vulgaris.
Bioprocess Biosyst Eng. 2009 Aug;32(5):663-71.
Novel biotransformation process of podophyllotoxin to produce podophyllic acid and picropodophyllotoxin by Pseudomonas aeruginosa CCTCC AB93066. Part I: process development.[Pubmed:
19115065]
A novel biotransformation process of podophyllotoxin (1) to produce Picropodophyllotoxin (2) and podophyllic acid (3) was developed in this work.
METHODS AND RESULTS:
Eight bacteria which could modify the structure of podophyllotoxin were screened out from the tested fourteen bacteria. The highest conversion of podophyllotoxin (i.e., 70.2 +/- 8.0%) was obtained when Pseudomonas aeruginosa CCTCC AB93066 was used as biocatalyst, so P. aeruginosa was selected as a typical biocatalyst in the following study. Product (2) and (3) were separated through D312 macroporous resin and sephadex LH-20 gel column chromatograph. On the basis of (1)H NMR, (13)C NMR, ESI-MS and Elemental Analysis, product (2) and (3) were identified as Picropodophyllotoxin (2) and podophyllic acid (3), respectively.
CONCLUSIONS:
This suggested the site-specific isomerization and hydrolization of podophyllotoxin occurred during its biotransformation process by P. aeruginosa. For the first time, podophyllotoxin was biotransformed into its hydrolytic derivate (i.e., podophyllic acid).
