Isoarundinin II

Isoarundinin II
Product Name Isoarundinin II
CAS No.: 151538-56-6
Catalog No.: CFN91181
Molecular Formula: C22H22O4
Molecular Weight: 350.4 g/mol
Purity: >=98%
Type of Compound: Phenols
Physical Desc.: Powder
Source: The herbs of Cremastra appendiculata
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price: $388/5mg
Reference standards.
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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.
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  • Molecules.2021, 26(16):4722.
  • Horticulturae2023, 9(2), 213.
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  • Chem Biol Interact.2024, 394:110995.
  • Sci Rep. 2018, 1-9
  • The Japan Society for Analytical Chemistry2018, 67(4):201-206
  • Phytomedicine.2022, 99:154025.
  • Plant Physiol Biochem.2023, 203:108073.
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    Phytochemistry, 1993, 35(32):439-444.
    Two stilbenoids from the orchid arundina bambusifolia.[Reference: WebLink]

    METHODS AND RESULTS:
    Isoarundinin I and Isoarundinin II, two new stilbenoids, were isolated from the orchid Arundina bambusifolia which earlier afforded, besides arundinin [3,3′-dihydroxy-4-(p-hydroxybenzyl)-5-methoxybibenzyl], a number of other stilbenoids and a triterpenoid.
    CONCLUSIONS:
    The structures of isoarundinin I and Isoarundinin II were established as 3′,5-dihydroxy-2-(p-hydroxybenzyl)-3-methoxybibenzyl and 3,3′-dihydroxy-2-(p-hydroxy-benzyl)-5-methoxy-bibenzyl, respectively, mainly from spectroscopic evidence.
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