Skip to Content
Merck
All Photos(2)

Documents

SML3713

Sigma-Aldrich

HM-chromanone

≥98% (HPLC)

Synonym(s):

(3E)-2,3-Dihydro-5-hydroxy-3-[(2-hydroxyphenyl)methylene]-7-methoxy-4H-1-benzopyran-4-one, (E)-5-hydroxy-7-methoxy-3-(20-hydroxybenzyl)-4-chromanone, Portulacanone D

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C17H14O5
CAS Number:
Molecular Weight:
298.29
UNSPSC Code:
12352200
NACRES:
NA.77

Quality Level

Assay

≥98% (HPLC)

form

powder

color

white to beige

solubility

DMSO: 2 mg/mL, clear

storage temp.

2-8°C

Biochem/physiol Actions

Sappanine-type homoisoflavonoid, isolated from Portulaca oleracea (purslane) that exhibits anti-diabetic effects.

HM-chromanone is a sappanine-type homoisoflavonoid, isolated from Portulaca oleracea (purslane). HM-chromanone exhibits anti-diabetic effects and inhibits adipogenesis by regulating AMPK activity in adipocytes. HM-chromanone potently activates AMPK in hepatocytes, thus suppressing hepatic glucose production. HM-chromanone does not display significant toxicity.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

HM-chromanone suppresses hepatic glucose production via activation of AMP-activated protein kinase in HepG2 cell
European Journal of Pharmacology, 928, 175108-175108 (2022)
HM-Chromanone Isolated from Portulaca oleracea L. Protects INS-1 Pancreatic ? Cells against Glucotoxicity-Induced Apoptosis
Nutrients, 11(2), 404-404 (2019)
HM-Chromanone Ameliorates Hyperglycemia and Dyslipidemia in Type 2 Diabetic Mice
Nutrients, 14(9), 1951-1951 (2022)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service