30 Results for "

hypolipidemic agent

" in MedChemExpress (MCE) Product Catalog:
Products (30)

30 Results for "hypolipidemic agent" in MCE Product Catalog:

15
15 Publications Verification
Cat. No.: HY-B0637
CAS No.: 41859-67-0
Synonyms: BM15075
Target:  

PPAR

Bezafibrate is an agonist of PPAR, with EC50s of 50 μM, 60 μM, 20 μM for human PPARα, PPARγ and PPARδ, and 90 μM, 55 μM, 110 μM for murine PPARα, PPARγ and PPARδ, respectively; Bezafibrate is used as an hypolipidemic agent.
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1
1 Cited Publications
Cat. No.: HY-147246
CAS No.: 1868138-66-2
Purity:  99.34%
Synonyms: HTD1801; BUDCA
Research Areas:  

Metabolic Disease

Berberine ursodeoxycholate (HTD1801), an ionic salt of Berberine and Ursodeoxycholic acid, is an orally active and potent hypolipidemic agent. Berberine ursodeoxycholate shows significantly great reduction in liver fat content. Berberine ursodeoxycholate has a broad spectrum of metabolic activity. Berberine ursodeoxycholate can be used for the research of hyperlipidemia, non-alcoholic steatohepatitis (NASH) and diabetes .
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1
1 Cited Publications
Cat. No.: HY-107579
CAS No.: 72420-38-3
Purity:  99.25%
Synonyms: AY 25712
Target:  

GPR109A ERK

Acifran (AY 25712) is an orally active, full GPR109A and GPR109B agonist and hypolipidemic agent. Acifran reduces Forskolin (HY-15371)-induced cAMP elevation, triggers ERK1/ERK2 phosphorylation, and inhibits lipolysis in adipose tissue through Gi-coupled GPCR activation. Acifran is used for research on atherosclerosis, hyperlipidemia, and type 2 diabetes .
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Cat. No.: HY-34781
CAS No.: 84392-17-6
Target:  

Drug Derivative

4'-Trifluoromethyl-2-biphenyl carboxylic acid is an orally active hypolipidemic agent .
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Cat. No.: HY-117549
CAS No.: 133208-93-2
Purity:  99.48%
Synonyms: NO-1886
Target:  

Lipase

Research Areas:  

Cardiovascular Disease

Ibrolipim (NO-1886) is an orally active lipoprotein lipase (LPL)-promoting agent. Ibrolipim decreases plasma triglycerides, increases high-density lipoprotein cholesterol levels. Ibrolipim has renoprotective and hypolipidemic effects .
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Cat. No.: HY-W009410
CAS No.: 932710-63-9
Target:  

Fungal

Research Areas:  

Infection

Amphos is a monophosphazene hypolipidemic agent and yeast growth inducer. Amphos reduces intracellular lipid levels and promotes the growth of yeast cells. Amphos exhibits no antibacterial activity against bacterial and yeast cells .
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Cat. No.: HY-119964
CAS No.: 55986-43-1
Purity:  ≥99.0%
Target:  

PPAR

Research Areas:  

Cardiovascular Disease

Cetaben is a PPARα-independent peroxisome proliferator. Cetaben is a non-fibrate hypolipidemic agent and potently reduces the concentration of cholesterol and triglycerides .
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Cat. No.: HY-137318
CAS No.: 86621-94-5
Purity:  98.20%
Target:  

Drug Derivative

Research Areas:  

Metabolic Disease

BM 15766 sulfate is an inhibitor of 7-dehydrocholesterol δ7-reductase and reduces plasma cholesterol levels. BM 15766 sulfate is a hypolipidemic agent .
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Cat. No.: HY-A0127
CAS No.: 31637-97-5
Target:  

LDLR

Research Areas:  

Metabolic Disease

Etofibrate is the ethandiol-1,2 diester of the nicotinic and clofibric acids. Etofibrate has been shown to be a potent hypolipidemic agent in animal and human.
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Cat. No.: HY-B0637S
CAS No.: 1219802-74-0
Bezafibrate-d6 is the deuterium labeled Bezafibrate. Bezafibrate is an agonist of PPAR, with EC50s of 50 μM, 60 μM, 20 μM for human PPARα, PPARγ and PPARδ, and 90 μM, 55 μM, 110 μM for murine PPARα, PPARγ and PPARδ, respectively; Bezafibrate is used as an hypolipidemic agent.
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Cat. No.: HY-100144
CAS No.: 54110-25-7
Purity:  98.31%
Target:  

LDLR

Research Areas:  

Metabolic Disease

Pirozadil is a hypolipidemic agent.
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Cat. No.: HY-100334
CAS No.: 65089-17-0
Synonyms: BR-931
Target:  

Drug Derivative

Research Areas:  

Metabolic Disease

Pirinixil is a hypolipidemic agent of low toxicity.
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Cat. No.: HY-175005
CF-Carvacrol is an orally active lipid-lowering agent synthesized by merging the pharmacophores of Carvacrol (HY-N0711) and Clofibric acid (HY-B1415). CF-Carvacrol has a good affinity for PPAR-α. CF-Carvacrol has significant hypolipidemic activity and may exert antioxidant and anti-inflammatory activity by activating the Nrf2/HO-1 signaling pathway to reduce liver injury. CF-Carvacrol can be used for the study of CF-induced liver damage .
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Cat. No.: HY-100258
CAS No.: 59399-41-6
Target:  

Others

Research Areas:  

Cardiovascular Disease

Y-9738 is a hypolipidemic agent.
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Cat. No.: HY-19030
CAS No.: 88352-44-7
Target:  

Others

Research Areas:  

Metabolic Disease

TA-1801 is a hypolipidemic agent.
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Cat. No.: HY-100144R
CAS No.: 54110-25-7
Research Areas:  

Metabolic Disease

Pirozadil (Standard) is the analytical standard of Pirozadil. This product is intended for research and analytical applications. Pirozadil is a hypolipidemic agent.
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Cat. No.: HY-124560
CAS No.: 96609-16-4
Target:  

LDLR

Research Areas:  

Metabolic Disease

Lifibrol is a potent and oral activity hypolipidemic agent. Lifibrol decreases the plasma total cholesterol. Lifibrol has the potential for the research of hypercholesterolemia .
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Cat. No.: HY-121755
CAS No.: 37087-94-8
Synonyms: CP 18524
Target:  

PPAR

Research Areas:  

Metabolic Disease

Tibric acid (CP 18524) has similar effects to those of hypolipidemic agents. Tibric acid has orally active triglyceride-lowering effects. Tibric acid can be used for research of hypertriglyceridemia .
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Cat. No.: HY-115914
CAS No.: 2304859-34-3
Target:  

LDLR

Research Areas:  

Others

Lipid-lowering agent-1 is a potent lipid-lowering agent. Lipid-lowering agent-1 has significant pharmacological effects on the inhibition of low-density lipoprotein cholesterol (LDLC) and promotion of high-density lipoprotein cholesterol (HDLC) production. Lipid-lowering agent-1 shows potent hypolipidemic effect in high-fat diet rats .
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Cat. No.: HY-121776
CAS No.: 27959-26-8
Purity:  98.40%
Target:  

Drug Derivative

Research Areas:  

Cardiovascular Disease

Nicomol is an orally active hypolipidemic agent that can increase the high density lipoprotein cholesterol (HDL-C) level. Nicomol inhibits the rapid rise of plasma free fatty acids .
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