121 Results for "

ACAT

" in MedChemExpress (MCE) Product Catalog:
Products (121)

121 Results for "ACAT" in MCE Product Catalog:

  • Isoforms Recommended:
Cat. No.: HY-P78986A
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: ACAT1; Acetyl-Coenzyme A Acetyltransferase 1; Prev. ACAT; MAT; Acetyl-CoA Acetyltransferase, Mitochondrial; T2; Acetoacetyl-CoA Thiolase; Mitochondrial Acetoacetyl-CoA Thiolase; THIL; Testicular Tissue Protein Li 198; Acetyl-CoA Acetyltransferase 1; Aceto
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-P82226
Synonyms: T2; MAT; ACAT; THIL

Host:  

Rabbit

Application:  

WB, IHC-P, IP

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-105445R
CAS No.: 135025-12-6
Research Areas:  

Neurological Disease

CP-113818 (Standard) is the analytical standard of CP-113818 (HY-105445). This product is intended for research and analytical applications. CP-113818 is a potent cholesterol acyltransferase (ACAT) inhibitor. CP-113818 can be used for the research of Alzheimer's disease .
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Cat. No.: HY-P82226A
Synonyms: T2; MAT; ACAT; THIL

Host:  

Rabbit

Application:  

WB, IP

Reactivity:  

Human

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Cat. No.: HY-138198
CAS No.: 214265-97-1
Target:  

Drug Isomer

Research Areas:  

Others

(E)-YIC-C8-434 is the E double-bond configuration of YIC-C8-434. YIC-C8-434 is an orally active ACAT inhibitor with anti-hypercholesterolemic activity .
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Cat. No.: HY-P87995
Synonyms: ACAT, MAT, ACAT1, Acetoacetyl-CoA thiolase, T2

Host:  

Rabbit

Application:  

WB, IHC-P, IHC-F, IF-Tissue, IP

Reactivity:  

Human

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Cat. No.: HY-P7730
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: CES1; Cocaine Carboxylesterase; Carboxylesterase 1; Retinyl Ester Hydrolase; HMSE; Serine Esterase 1; CES2; CES1A1; SES1; CES1A2; CEH; Egasyn; HMSE1; HCE-1; Carboxylesterase 1 (Monocyte/Macrophage Serine Esterase 1); ACAT; Human Monocyte/Macrophage Serine
Species:  
Human
Source:  
HEK293
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Cat. No.: HY-P11865
CAS No.: 2379342-67-1
Target:  

Caspase Apoptosis

Research Areas:  

Cancer

Ac-ATS010-KE is a selective polypeptide inhibitor of caspase-3. Ac-ATS010-KE protects cells from FasL-induced apoptosis. The unmethylated form of Ac-ATS010-KE exhibits better cell viability than the fully methylated form. Ac-ATS010-KE can be used in research on cancers such as colorectal cancer and the development of caspase-3-targeted molecular probes .
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Cat. No.: HY-101576R
CAS No.: 136609-26-2
Research Areas:  

Metabolic Disease

RP 70676 (Standard) is the analytical standard of RP 70676 (HY-101576). This product is intended for research and analytical applications. RP 70676 is a potent inhibitor of ACAT, with IC50 of 25 and 44 nM for rat and rabbit ACAT.
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Cat. No.: HY-138198A
Target:  

Acyltransferase

Research Areas:  

Infection

YIC-C8-434 is an orally active ACAT inhibitor. YIC-C8-434 selectively blocks cholesterol esterification in intestinal epithelial cells and hepatocytes without affecting the production of triglycerides or phospholipids. YIC-C8-434 effectively reduces intracellular cholesteryl ester levels and induces an increase in lipid droplet volume, exhibiting excellent cholesterol-lowering activity and safety. YIC-C8-434 disrupts the assembly of hepatitis C virus (HCV) virions, reduces HCV RNA synthesis and viral particle release. YIC-C8-434 can be used in studies related to hepatitis C virus infection .
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Cat. No.: HY-N17326
CAS No.: 242794-72-5
Ilekudinol B is an inhibitor of ACAT and PTP1B, with an IC50 of 5.3 μM and a Ki of 11.6 μM against human PTP1B. Ilekudinol B inhibits the classical pathway of the complement system, with an IC50 of 51 μM. Ilekudinol B inhibits TNF-α-induced cellular IL-8 secretion, promotes glucose uptake in skeletal muscle myotubes, and acts as an insulin mimetic and insulin sensitizer. Ilekudinol B can be used in research related to type 2 diabetes, obesity, and inflammatory diseases .
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Cat. No.: HY-N18066
CAS No.: 854381-37-6
Esculeogenin A is the sapogenol of tomato saponin Esculeoside A (HY-N18067). Esculeogenin A is an orally active hepatoprotective, hypolipidemic, and antioxidant agent. Esculeogenin A regulates molecular targets like PPARα, SREBP1, Nrf2, NF-κB, ACAT1/ACAT2 to promote hepatic fatty acid oxidation, suppress de novo lipogenesis, enhance antioxidant defense, and inhibit inflammation. Esculeogenin A improves liver function, alleviates hyperlipidemia, and inhibits hepatic steatosis and foam cell formation, preventing nonalcoholic fatty liver disease in high-fat-diet-fed rats and reducing atherosclerotic lesions in apoE-deficient mice. Esculeogenin A can be used for the research of nonalcoholic fatty liver disease, atherosclerosis, and hyperlipidemia .
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Cat. No.: HY-P88953
Synonyms: ACACT2; ACAT2; ARGP2

Host:  

Mouse

Application:  

IHC-P

Reactivity:  

Human

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Cat. No.: HY-107396R
CAS No.: 138046-43-2
YM-750 (Standard) is the analytical standard of YM-750 (HY-107396). This product is intended for research and analytical applications. YM-750 is a potent acyl-CoA:cholesterol acyltransferase (ACAT) inhibitor (IC50=0.18 μM). ACAT catalyzes the formation of cholesteryl esters from cholesterol and long-chain fatty-acyl-coenzyme A .
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Cat. No.: HY-P88953A
Synonyms: ACACT2; ACAT2; ARGP2

Host:  

Mouse

Application:  

IHC-P

Reactivity:  

Human

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Cat. No.: HY-19140
CAS No.: 124884-99-7
Target:  

Acyltransferase

Research Areas:  

Metabolic Disease

YM17E hydrochloride is an acyl CoA:cholesterol acyltransferase (ACAT) inhibitor, with IC50 of 44 nM. YM17E hydrochloride has hypocholesterolemic effect .
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Cat. No.: HY-100401AR
CAS No.: 608510-47-0
Synonyms: CS-505 (Standard)
Pactimibe (sulfate) (Standard) is the analytical standard of Pactimibe (sulfate) (HY-100401A). This product is intended for research and analytical applications. Pactimibe sulfate (CS-505) is a dual ACAT1/2 inhibitor with IC50s of 4.9 μM and 3.0 μM, respectively. Pactimibe sulfate (CS-505) inhibits ACAT with IC50s of 2.0 μM, 2.7 μM, 4.7 μM in the liver, macrophages and THP-1 cells, respectively . Pactimibe sulfate (CS-505) noncompetitively inhibits oleoyl-CoA with a Ki value of 5.6 μM. Moreover, Pactimibe sulfate (CS-505) obviously inhibits cholesteryl ester formation with an IC50 of 6.7 μM. Pactimibe sulfate (CS-505) possesses anti-atherosclerotic potential with lowering plasma cholesterol activity .
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Cat. No.: HY-167717
CAS No.: 191791-65-8
Synonyms: (Rac)-F 12511
Target:  

Endogenous Metabolite

Research Areas:  

Metabolic Disease

(Rac)-Eflucimibe ((Rac)-F 12511) is an ACAT inhibitor with endogenous hypercholesterolemia modulating activity. (Rac)-Eflucimibe has shown high potency and efficacy as an anti-hypercholesterol compound in different hypercholesterolemia animal models .
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Cat. No.: HY-P82583
Synonyms: ACAT; CE 1; CEH; CES1; CES2; CESDD1; Egasyn; ES-HTEL; ES-x; Es22; Esterase 22; hCE 1; HMSE; HMSE1; REH; SES1; TGH; Triacylglycerol hydrolase

Host:  

Rabbit

Application:  

WB, IP, FC

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P75543
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: ACAT2; Acetoacetyl Coenzyme A Thiolase; Acetyl-CoA Acetyltransferase 2; Acetyl-Coenzyme A Acetyltransferase 2 (Acetoacetyl Coenzyme A Thiolase); Acetyl-CoA Acetyltransferase, Cytosolic; Acetyl-Coenzyme A Acetyltransferase 2; Acetyl-CoA Transferase-Like Pr
Species:  
Rat
Source:  
E. coli
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