IsobavachroMene CAS 56083-03-5

Introduction:Basic information about IsobavachroMene CAS 56083-03-5, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

IsobavachroMene Basic information

Product Name:IsobavachroMene
Synonyms:IsobavachroMene;(2E)-1-(5-Hydroxy-2,2-dimethyl-2H-1-benzopyran-6-yl)-3-(4-hydroxyphenyl)-2-propen-1-one;4-Hydroxylonchocarpin;2-Propen-1-one,1-(5-hydroxy-2,2-dimethyl-2H-1-benzopyran-6-yl)-3-(4-hydroxyphenyl)-,(E)-;2-Propen-1-one, 1-(5-hydroxy-2,2-dimethyl-2H-1-benzopyran-6-yl)-3-(4-hydroxyphenyl)-, (2E)-;4-Hydroxylonchocarpin/Isobavachromene;(E)-1-(5-hydroxy-2,2-dimethylchromen-6-yl)-3-(4-hydroxyphenyl)prop-2-en-1-one;4Hydroxylonchocarpin,4 Hydroxylonchocarpin
CAS:56083-03-5
MF:C20H18O4
MW:322.35
EINECS:
Product Categories:
Mol File:56083-03-5.mol

IsobavachroMene Chemical Properties

Melting point 203-204℃
Boiling point 535.1±50.0 °C(Predicted)
density 1.257±0.06 g/cm3(Predicted)
storage temp. 4°C, protect from light
solubility Soluble in DMSO
form Solid
pka7.25±0.40(Predicted)
color Yellow to orange

Safety Information

IsobavachroMene Usage And Synthesis

Uses4-Hydroxylonchocarpin is a chalcone compound from an extract of Psoralea corylifolia. 4-Hydroxylonchocarpin increases phosphorylation of p38 MAPK, JNK and ERK. 4-Hydroxylonchocarpin has diverse pharmacological activities, including antibacterial, antifungal, anticancer, antireverse transcriptase, antitubercular, antimalarial, anti-inflammatory and antioxidant activities[1].
References[1] Lim J, et al. Antimelanogenic effect of 4-hydroxylonchocarpin through the inhibition of tyrosinase-related proteins and MAPK phosphatase. Exp Dermatol. 2016 Jul;25(7):574-6. DOI:10.1111/exd.13004

IsobavachroMene Preparation Products And Raw materials

ISOBAVACHALCONE CAS 20784-50-3
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