228 Results for "

LDL

" in MedChemExpress (MCE) Product Catalog:
Products (228)

228 Results for "LDL" in MCE Product Catalog:

Cat. No.: HY-158827
CAS No.: 2604215-74-7
Target:  

PCSK9

Research Areas:  

Metabolic Disease

AZD8233, a liver-targeting antisense oligonucleotide (ASO), inhibits proprotein convertase subtilisin/kexin type 9 (PCSK9) protein synthesis. AZD8233 increases the available LDL receptors by reducing PCSK9 levels, thereby clearing LDL from the blood and decreasing LDL-C levels.
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Cat. No.: HY-W791754
CAS No.: 827610-11-7
Target:  

NF-κB

Research Areas:  

Cardiovascular Disease

Paeonolsilate (sodium) can inhibit ox-LDL-induced macrophage foam cell formation and inflammation in atherosclerosis. Paeonolsilate (sodium) inhibits NF-κB activation and oxidative stress response induced by ox-LDL. Paeonolsilate (sodium) can be studied in anti-atherosclerosis research .
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Cat. No.: HY-125554
CAS No.: 439904-34-4
Research Areas:  

Cardiovascular Disease

KDdiA-PC is one of the most potent CD36 ligands in oxidized LDL (oxLDL) .
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Cat. No.: HY-108922
CAS No.: 216168-45-5
Purity:  99.14%
Target:  

Drug Derivative

Research Areas:  

Metabolic Disease

Probucol Disuccinate is a derivative of Probucol (HY-B0388), a lipid-regulating agent and can reduce LDL-cholesterol levels .
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Cat. No.: HY-161435
Target:  

PCSK9

Research Areas:  

Metabolic Disease

PCSK9-IN-27 (Compound 108) is a PCSK9 inhibitor (IC50: 3.4 nM). PCSK9-IN-27 reduces LDLR degradation and increases LDL-C uptake .
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Cat. No.: HY-128334
CAS No.: 2365416-53-9
Target:  

PCSK9

Research Areas:  

Metabolic Disease

PCSK9 modulator-2 (Compound 1) is a potent modulator of PCSK9 with an EC50 value of 202 nM. PCSK9 is a recently validated target for lowering low-density lipoprotein cholesterol (LDL-C). PCSK9 modulator-2 has the potential for the research of hyperlipidemia .
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Cat. No.: HY-19251
CAS No.: 107376-72-7
Target:  

Acyltransferase

CL-283796 is a potent and orally active acyl-CoA:cholesterol acyltransferase (ACAT) inhibitor. CL-283796 reduces low-density lipoprotein (LDL) cholesterol without affecting cholesterol absorption in African green monkeys. CL-283796 can be used for hypercholesterolemia research .
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Cat. No.: HY-119265
CAS No.: 615264-62-5
Target:  

Acyltransferase

Research Areas:  

Metabolic Disease

LDL-IN-4 (Compound 2) inhibits human acyl-CoA:cholesterol acyltransferase-1 and -2 activities. LDL-IN-4 inhibits copper-mediated low density lipoprotein (LDL) oxidation, with an IC50 of 3 μM. LDL-IN-4 has anti-atherosclerotic biological activity .
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Cat. No.: HY-118486
CAS No.: 615264-52-3
Purity:  ≥99.0%
Target:  

Acyltransferase

Research Areas:  

Metabolic Disease

LDL-IN-1 (Compound 1) is an antioxidant, and is active against copper mediated LDL oxidation (IC50 = 52 μM). LDL-IN-1 is also an Acyl-CoA:cholesterol acyltransferase-1 and -2 (ACAT-1/2) inhibitor, with IC50s of 60 μM. LDL-IN-1 can be used for anti-atherosclerotic research .
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Cat. No.: HY-U00054
CAS No.: 180908-67-2
Target:  

LDLR

LDL-IN-3 is an anti-atherosclerotic compound extracted from patent WO/2005/039596A1, example C25 and patent US 6133467, example 3.
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Cat. No.: HY-123016A
CAS No.: 33783-76-5
Target:  

Endogenous Metabolite

Research Areas:  

Metabolic Disease

(±)9-HODE cholesteryl ester is originally extracted from atherosclerotic lesions1 and shown to be produced by Cu2+-catalyzed oxidation of LDL.2 Later studies determined that 15-LO from rabbit reticulocytes and human monocytes were able to metabolize cholesteryl linoleate, a major component of LDL, to 9-HODE cholesteryl ester.
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Cat. No.: HY-W747575
CAS No.: 167354-91-8
Target:  

Endogenous Metabolite

Research Areas:  

Metabolic Disease

(±)13-HODE cholesteryl ester is originally extracted from atherosclerotic lesions1 and shown to be produced by Cu2+-catalyzed oxidation of LDL. Later studies determined that 15-LO from rabbit reticulocytes and human monocytes were able to metabolize cholesteryl linoleate, a major component of LDL, to 13-HODE cholesteryl ester.
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Cat. No.: HY-165512
CAS No.: 150443-71-3
Target:  

LDLR

Research Areas:  

Cardiovascular Disease

Nicanartine, an orally active antioxidant and lipid-lowering compound, is an antiatherogenic drug. Nicanartine inhibits the oxidation of low-density lipoprotein (LDL).
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Cat. No.: HY-147279
CAS No.: 2643306-81-2
Target:  

LDLR

Research Areas:  

Others

Milpocitide is a low-density lipoprotein receptor (human LDL receptor, LDLR), (293-333)-peptide fragment (EGF-like domain 1) .
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Cat. No.: HY-N0339S
CAS No.: 84759-06-8
Syringic acid-d6 is the deuterium labeled Syringic acid . Syringic acid is correlated with high antioxidant activity and inhibition of LDL oxidation .
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Cat. No.: HY-B0388S1
Synonyms: DH-581-d6
Probucol-d6 is deuterium labeled Probucol. Probucol (DH-581) is an anti-hyperlipidemic agent by lowering the level of cholesterol in the bloodstream by increasing the rate of LDL catabolism.
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Cat. No.: HY-P3731
CAS No.: 237392-85-7
Target:  

CDK

Research Areas:  

Cancer

Cdk2/Cyclin Inhibitory Peptide II (Tat-LDL), a CDK2 inhibitor, kills U2OS osteosarcoma cells in a dose-dependent manner .
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Cat. No.: HY-B0388S
CAS No.: 1173019-29-8
Probucol- 13C3 is the 13C-labeled Probucol. Probucol (DH-581) is an anti-hyperlipidemic agent by lowering the level of cholesterol in the bloodstream by increasing the rate of LDL catabolism.
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Cat. No.: HY-118518
CAS No.: 85247-77-4
Target:  

Calcium Channel

Research Areas:  

Cardiovascular Disease Cancer

Ronipamil is a calcium ion antagonist. Ronipamil increases the specific binding and internalization of human 125I-LDL in human skin fibroblasts (HSF) and the human hepatoma cell line Hep G2 .
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Cat. No.: HY-155006
Target:  

PCSK9

Research Areas:  

Metabolic Disease

PCSK9-IN-19 (Compound 1) is a PCSK9 inhibitor. PCSK9-IN-19 can be used for research of high LDL-cholesterol levels and prevention of coronary artery disease .
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