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DESMETHYLXANTHOHUMOL

Product Name: DESMETHYLXANTHOHUMOL
CAS No.: 115063-39-3
Chemical Name: DESMETHYLXANTHOHUMOL
Synonyms: Mentholatum;DESMETHYLXANTHOHUMOL;(E)-3-(4-hydroxyphenyl)-1-[2,4,6-trihydroxy-3-(3-methylbut-2-enyl)phenyl]prop-2-en-1-one;(E)-3-(4-Hydroxyphenyl)-1-(2,4,6-trihydroxy-3-(3-methylbut-2-en-1-yl)phenyl)prop-2-en-1-one;2-Propen-1-one,3-(4-hydroxyphenyl)-1-[2,4,6-trihydroxy-3-(3-methyl-2-buten-1-yl)phenyl]-,(2E)-
CBNumber: CB8371854
Molecular Formula: C20H20O5
Formula Weight: 340.37
MOL File: 115063-39-3.mol

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DESMETHYLXANTHOHUMOL Property

Melting point:: 154-155 °C
Boiling point:: 570.7±50.0 °C(Predicted)
Density: 1.312±0.06 g/cm3(Predicted)
solubility: Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form: powder
pka: 7.35±0.50(Predicted)
color: Yellow

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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Arctom

Product number: CFN92015
Product name: Desmethylxanthohumol
Packaging: 5mg
Price: $498
Updated: 2021/12/16

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DESMETHYLXANTHOHUMOL Chemical Properties,Usage,Production

Uses

Desmethylxanthohumol is a prenylated hydroxychalcone isolated from hop cones (Humulus lupulus L.). Desmethylxanthohumol is a powerful apoptosis inducing agent. Desmethylxanthohumol has antiplasmodial, antiproliferative, and antioxidant bioactivities[1][2].

Definition

ChEBI: A member of the class of chalcones that is trans-chalcone substituted by hydroxy groups at positions 4, 2', 4', and 6' and a 3-methylbut-2-en-1-yl group at position 3' respectively.

References

[1] Yuou Teng, et al. Synthesis and Antioxidant Evaluation of Desmethylxanthohumol Analogs and Their Dimers. Eur J Med Chem. 2017 Jan 5;125:335-345. DOI:10.1016/j.ejmech.2016.09.024
[2] Reinhard A.Diller, et al. 71-Desmethylxanthohumol from Hops, Chemistry and Biological Effects. Beer in Health and Disease Prevention, 2009, Pages 703-709.

DESMETHYLXANTHOHUMOL Preparation Products And Raw materials

Raw materials

Preparation Products

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2-Propen-1-one,3-(4-hydroxyphenyl)-1-[2,4,6-trihydroxy-3-(3-methyl-2-buten-1-yl)phenyl]-,(2E)-

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