9 Results for "

LDL-IN-1

" in MedChemExpress (MCE) Product Catalog:
Products (9)

9 Results for "LDL-IN-1" in MCE Product Catalog:

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 [1].
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2
2 Cited Publications
Cat. No.: HY-125039
CAS No.: 1287585-40-3
Purity:  99.57%
N-Acetyl lysyltyrosylcysteine amide is a potent, reversible, specific, and non-toxic tripeptide inhibitor of myeloperoxidase (MPO). N-Acetyl lysyltyrosylcysteine amide effectively inhibits MPO generation of toxic oxidants in vivo. N-Acetyl lysyltyrosylcysteine amide reduces neuronal damage and preserves brain tissue and neurological function in the stroked brain. N-Acetyl lysyltyrosylcysteine amide inhibits MPO-dependent hypochlorous acid (HOCl) generation, protein nitration, and LDL oxidation .
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1
1 Cited Publications
Cat. No.: HY-W778608
CAS No.: 38934-20-2
Synonyms: QuercetIN 7-O-β-glucuronide
Quercetin 7-glucuronide (Quercetin 7-O-β-glucuronide), a metabolite of Quercetin (HY-18085), can be isolated from Madagascarian Uncarina species. Quercetin 7-glucuronide can inhibit LDL oxidation .
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Cat. No.: HY-114294A
CAS No.: 103476-21-7
Purity:  ≥99.0%
Synonyms: HMG-CoA disodium hydrate
DL-3-Hydroxy-3-methylglutaryl coenzyme A disodium hydrate is a disodium salt compound of HMG-CoA, is a intermediate of terpenes and ketone bodies. DL-3-Hydroxy-3-methylglutaryl coenzyme A disodium also involves in ester metabolism in vivo, as a precursor for cholesterol synthesis, and regulates cholesterol synthesis by coupling LDL receptor .
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Cat. No.: HY-130245
Purity:  98.33%
Target:  

PCSK9

Research Areas:  

Metabolic Disease

PCSK9 degrader 1 (Compound 16) is a small molecule ligand for proprotein convertase substilisin-like/kexin type 9 (PCSK9) and shows high affinity to PCSK9 with a Ki of 107 nM. PCSK9 degrader 1 can involve in a protein-protein interaction with the low-density lipoprotein (LDL) receptor .
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Cat. No.: HY-120651
CAS No.: 778624-05-8
Purity:  ≥99.0%
Target:  

LDLR

Research Areas:  

Metabolic Disease

LDL-IN-2 (compound 3) is an antioxidant against copper mediated low-density lipoproteins (LDL) oxidation .
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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-132303
CAS No.: 1432054-03-9
Target:  

CETP

MK-8262 is an orally active and potent cholesteryl ester transfer protein (CETP) inhibitor with an IC50 of 53 nM and a log D of 5.3. MK-8262, a bistrifluoromethyl analogue, has the potential for coronary heart disease (CHD) correlated high-density lipoprotein (HDL) and low-density lipoprotein (LDL) research .
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Cat. No.: HY-130245A
CAS No.: 2216703-12-5
Target:  

PCSK9

Research Areas:  

Metabolic Disease

(R,R)-PCSK9 degrader 1 is the isomer of PCSK9 degrader 1 (HY-130245). PCSK9 degrader 1 (Compound 16) is a small molecule ligand for proprotein convertase substilisin-like/kexin type 9 (PCSK9) and shows high affinity to PCSK9 with a Ki of 107 nM. PCSK9 degrader 1 can involve in a protein-protein interaction with the low-density lipoprotein (LDL) receptor .
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