700125P
Avanti
DMHCA
Avanti Research™ - A Croda Brand 700125P, powder
Synonym(s):
N,N-dimethyl-3β-hydroxycholenamide
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About This Item
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Assay
>99% (TLC)
form
powder
packaging
pkg of 1 × 5 mg (700125P-5mg)
manufacturer/tradename
Avanti Research™ - A Croda Brand 700125P
shipped in
dry ice
storage temp.
−20°C
General description
N,N-dimethyl-3β-hydroxy-cholenamide (DMHCA) is a potent steroidal liver X receptor (LXR) ligand in vitro and in vivo. It is used to treat atherosclerosis.
N,N-dimethyl-3β-hydroxycholenamide (DHMCA) is a synthetic ligand for liver X receptor (LXR).
Application
DMHCA has been used as LXR activator to treat retinal endothelial cells in order to activate the sirtuin 1- liver X receptors (SIRT1-LXR) pathway.
It may be used as 3β-hydroxysterol-Δ24-reductase (DHCR24) inhibitor.
Biochem/physiol Actions
N,N-dimethyl-3β-hydroxycholenamide (DHMCA) halts cholesterol biosynthesis by inhibiting 3β-hydroxysterol-Δ24-reductase (DHCR24) enzyme. It may serve as a therapeutic agent for treating atherosclerosis, age-related macular degeneration and diabetic retinopathy.
DMHCA (N,N-dimethyl-3β-hydroxycholenamide) is a synthetic oxysterol and is an agonist for liver X receptors (LXR). It promotes cholesterol transport, expression of adenosine triphosphate (ATP) binding cassette transporters. DMHCA suppresses the proinflammatory cytokines stimulation, induced by oxysterol.
Packaging
5 mL Amber Glass Screw Cap Vial (700125P-5mg)
Legal Information
Avanti Research is a trademark of Avanti Polar Lipids, LLC
Storage Class Code
11 - Combustible Solids
Certificates of Analysis (COA)
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Synthetic LXR agonist attenuates plaque formation in apoE-/-mice without inducing liver steatosis and hypertriglyceridemia
Journal of Lipid Research, 50(2), 312-326 (2009)
Liver X receptor agonist inhibits proliferation of ovarian carcinoma cells stimulated by oxidized low density lipoprotein
Gynecologic Oncology, 116(1), 109-116 (2010)
The mechanism of diabetic retinopathy pathogenesis unifying key lipid regulators, sirtuin 1 and liver X receptor
EBioMedicine, 22, 181-190 (2017)
Gene-selective modulation by a synthetic oxysterol ligand of the liver X receptor.
Journal of Lipid Research, 45(10), 1929-1942 (2004)
Current pharmaceutical biotechnology, 12(2), 285-292 (2010-12-31)
The liver X receptors (LXRs) are key regulators of genes involved in cholesterol homeostasis. Natural ligands and activators of LXRs are oxysterols. Numerous steroidal and non-steroidal synthetic LXR ligands are under development as potential drugs for individuals suffering from lipid
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