Matairesinoside
Matairesinoside is a natural product from Styrax japonica.
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.
Int J Mol Sci.2023, 24(4):3682.
Metabolites.2020, 10(11):440.
Thorac Cancer.2023, 14(21):2007-2017.
J of the Society of Cosmetic Scientists of Korea2018, 44(4):407-417
J Nat Med.2017, 71(2):380-388
Cell Death Differ.2021, 1-8.
ARPN Journal of Eng.& Applied Sci.2016, 2199-2204
Pharmaceutics.2021, 13(2):187.
Pharmaceuticals (Basel).2024 Feb 24;17(3):292.
Biomol Ther (Seoul).2020, 28(6):542-548.
Related and Featured Products
Arch Pharm Res. 2010 Jun;33(6):863-6.
Isolation of virus-cell fusion inhibitory components from the stem bark of Styrax japonica S. et Z.[Pubmed:
20607490 ]
METHODS AND RESULTS:
Five compounds, styraxjaponoside A (1), Matairesinoside (2), egonol glucoside (3), dihydrodehydrodiconiferyl alcohol 9'-O-glucoside (4), and styraxjaponoside B (5) were isolated from the stem bark of Styrax japonica. Among them, compounds 1 and 5 showed significantly high virus-cell fusion inhibitory activity. In addition, compound 5 exhibited almost equivalent virus-cell fusion inhibitory activity to that of dextran sulfate, which is used as a positive control.
Buddlenoid A
Catalog No: CFN95025
CAS No: 142750-32-1
Price: $368/5mg
2''-O-Galloylquercitrin
Catalog No: CFN95041
CAS No: 80229-08-9
Price: $418/5mg
[(1(10)E,2R,4R)]-2-Methoxy-8,12-epoxygemacra-1(10),7,11-trien-6-one
Catalog No: CFN95198
CAS No: 75412-95-2
Price: $318/10mg
2-Methoxyfuranoguaia-9-ene-8-one
Catalog No: CFN95220
CAS No: 88010-62-2
Price: $318/10mg
3-Acetyl-ginsenoside F1
Catalog No: CFN95238
CAS No: 1881225-08-6
Price: $318/5mg
(-)-Cadin-4,10(15)-dien-11-oic acid
Catalog No: CFN95246
CAS No: 1124353-23-6
Price: $318/5mg
Benzyl beta-D-glucopyranoside
Catalog No: CFN95427
CAS No: 4304-12-5
Price: $318/10mg
12beta-Acetoxy-3,7,11,15,23-pentaoxo-lanost-8,20-dien-26-oic acid
Catalog No: CFN95505
CAS No: 1309931-91-6
Price: $318/5mg
Methyl lucidenate C
Catalog No: CFN95541
CAS No: N/A
Price: $413/5mg
Oxyphyllol B
Catalog No: CFN95575
CAS No: 226546-99-2
Price: Inquiry(manager@chemfaces.com)