119 Results for "

ACAT

" in MedChemExpress (MCE) Product Catalog:
Products (119)

119 Results for "ACAT" in MCE Product Catalog:

  • Isoforms Recommended:
20
20 Publications Verification
Cat. No.: HY-13215
CAS No.: 166518-60-1
Purity:  99.77%
Synonyms: CI-1011; PD-148515
Target:  

Acyltransferase

Research Areas:  

Cancer

Avasimibe (CI-1011; PD-148515) is an orally active acyl coenzyme A-cholesterol acyltransferase (ACAT; also called SOAT)) inhibitor with IC50s of 24 and 9.2 µM for ACAT1 and ACAT2, respectively . Avasimibe can be used for the research of prostate cancer .
7
7 Cited Publications
Cat. No.: HY-100400A
CAS No.: 217094-32-1
Purity:  99.42%
Target:  

Acyltransferase

Research Areas:  

Cardiovascular Disease

K-604 dihydrochloride is a potent and selective acyl-CoA:cholesterol acyltransferase 1 (ACAT-1) inhibitor with an IC50 of 0.45±0.06 μM.
4
4 Cited Publications
Cat. No.: HY-100399
CAS No.: 133825-80-6
Synonyms: PD-132301; ATR-101
Research Areas:  

Cancer

Nevanimibe (PD-132301) is an orally active and selective acyl-coenzyme A:cholesterol O-acyltransferase 1 (ACAT1) inhibitor with an EC50 of 9 nM. Nevanimibe inhibits ACAT2 with an EC50 of 368 nM. Nevanimibe induces cell apoptosis and has the potential for adrenocortical cancer .
4
4 Cited Publications
Cat. No.: HY-100399A
CAS No.: 133825-81-7
Purity:  99.49%
Synonyms: PD-132301 hydrochloride; ATR101 hydrochloride
Research Areas:  

Cancer

Nevanimibe hydrochloride (PD-132301 hydrochloride) is an orally active and selective acyl-coenzyme A:cholesterol O-acyltransferase 1 (ACAT1) inhibitor with an EC50 of 9 nM. Nevanimibe hydrochloride inhibits ACAT2 with an EC50 of 368 nM. Nevanimibe hydrochloride induces cell apoptosis and has the potential for adrenocortical cancer .
3
3 Cited Publications
Cat. No.: HY-N4193
CAS No.: 59870-65-4
Glabrol (Compound 1), One isoprenyl flavonoid was isolated from ethanol extract of licorice roots, is a potent and non-competitive Acyl-coenzyme A: cholesterol acyltransferase (ACAT) inhibitor with an IC50 value of 24.6 μM for rat liver microsomal ACAT activity .
2
2 Cited Publications
Cat. No.: HY-105445
CAS No.: 135025-12-6
Purity:  99.13%
Target:  

Acyltransferase

Research Areas:  

Neurological Disease

CP-113818 is a potent cholesterol acyltransferase (ACAT) inhibitor. CP-113818 can be used for the research of Alzheimer's disease .
2
2 Cited Publications
Cat. No.: HY-133968
CAS No.: 474-63-5
Purity:  99.48%
Synonyms: Ostreasterol
24-Methylenecholesterol (Ostreasterol) is a regulator targeting acyl-CoA cholesterol acyltransferase (ACAT) with anti-aging and neuroprotective effects. 24-Methylenecholesterol mimics the effects of nerve growth factor (NGF), can extend yeast lifespan through an anti-oxidative stress mechanism, and exhibits neuroprotective activity in PC12 cells. 24-Methylenecholesterol can reduce intracellular reactive oxygen species (ROS) and malondialdehyde (MDA) levels, activate anti-oxidative stress pathways (such as UTH1, SOD-related genes), and promote synaptic growth .
1
1 Cited Publications
Cat. No.: HY-107572
CAS No.: 114289-47-3
Purity:  99.97%
Synonyms: CI 976
Target:  

Acyltransferase

Research Areas:  

Metabolic Disease

PD 128042 (CI 976) is a potent, orally active, and selective inhibitor of ACAT (acyl coenzyme A:cholesterol acyltransferase) with an IC50s of 73 nM. PD 128042 is also a potent LPAT (lysophospholipid acyltransferase) inhibitor. PD 128042 inhibits Golgi-associated LPAT activity (IC50=15 μM). PD 128042 inhibits multiple membrane trafficking steps, including ones found in the endocytic and secretory pathway .
1
1 Cited Publications
Cat. No.: HY-117832
CAS No.: 147444-03-9
Purity:  99.71%
Pyripyropene A is an orally active, potent and selective sterol O-acyltransferase 2 (SOAT2)/acyl-coenzyme A:cholesterol acyltransferase 2 (ACAT2) inhibitor, with an IC50 of 0.07 µM. Pyripyropene A attenuates hypercholesterolemia and atherosclerosis in vivo .
1
1 Cited Publications
Cat. No.: HY-N3807
CAS No.: 19914-20-6
Enniatin B1 is a Fusarium mycotoxin. Enniatin B1 inhibits acyl-CoA: cholesterol acyltransferase (ACAT) activity with an IC50 of 73 μM in an enzyme assay using rat liver microsomes . Enniatin B1 crosss the blood-brain barrier . Enniatin B1 decreases the activation of ERK (p44/p42). Enniatin B1 inhibits moderately TNF-α-induced NF-κB activation .
Cat. No.: HY-111880
CAS No.: 78886-65-4
Purity:  99.23%
γ-Sanshool can be isolated from Zanthoxylum piperitum. γ-Sanshool inhibits human ACAT-1 and ACAT-2 activities with IC50s of 12.0 and 82.6 μM .
Cat. No.: HY-100401
CAS No.: 189198-30-9
Purity:  99.98%
Synonyms: CS-505 free base
Target:  

Acyltransferase

Research Areas:  

Cardiovascular Disease

Pactimibe (CS-505 free base) is a dual ACAT1/2 inhibitor with IC50s of 4.9 μM and 3.0 μM, respectively. Pactimibe (CS-505 free base) inhibits ACAT with IC50s of 2.0 μM, 2.7 μM, 4.7 μM in the liver, macrophages and THP-1 cells, respectively . Pactimibe (CS-505 free base) noncompetitively inhibits oleoyl-CoA with a Ki value of 5.6 μM. Moreover, Pactimibe (CS-505 free base) obviously inhibits cholesteryl ester formation with an IC50 of 6.7 μM. Pactimibe (CS-505 free base) possesses anti-atherosclerotic potential with lowering plasma cholesterol activity .
Cat. No.: HY-107396
CAS No.: 138046-43-2
Purity:  99.95%
Target:  

Acyltransferase

Research Areas:  

Cardiovascular Disease

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 .
Cat. No.: HY-16437
CAS No.: 135239-65-5
Target:  

Acyltransferase

Research Areas:  

Cardiovascular Disease

RP-64477 is a potent inhibitor of the cholesterol esterifying enzyme Acyl-coenzyme A:cholesterol O-acyltransferase (ACAT).
Cat. No.: HY-100401A
CAS No.: 608510-47-0
Purity:  ≥98.0%
Synonyms: CS-505
Target:  

Acyltransferase

Research Areas:  

Cardiovascular Disease

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 .
Cat. No.: HY-121254
CAS No.: 119-47-1
Purity:  99.77%
GERI-BP002-A is an inhibitor of acyl-CoA:cholesterol acyltransferase (ACAT) produced by Aspergillus fumigatus F93, which can be used in cancer research .
Cat. No.: HY-19286
CAS No.: 202340-45-2
Synonyms: F 12511
Target:  

Acyltransferase

Research Areas:  

Cancer

Eflucimibe (F 12511) is a new acyl-coenzyme A cholesterol O-acyltransferase (ACAT) inhibitor. Eflucimibe can be used in the research of atherosclerosis .
Cat. No.: HY-RS00136
Research Areas:  

Others

ACAT1 Human Pre-designed siRNA Set A contains three designed siRNAs for ACAT1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

Cat. No.: HY-169813
CAS No.: 81840-57-5
Yakuchinone B is an Acyl-CoA: cholesterol O-acyltransferase (ACAT) inhibitor with hypocholesterolemic activity, which is found in the seeds of Zingiberaceae. Yakuchinone B inhibits rat hepatic ACAT with an IC50 value of 20.6 μM. Yakuchinone B is promising for research of hypercholesterolemia and atherosclerosis .
Cat. No.: HY-N10224
CAS No.: 156967-65-6
Terpendole C, produced by Albophoma yamanashiensis, shows potent inhibitory activity against acyl-CoA: cholesterol acyltransferase (ACAT) .