atorvastatin,

Atorvastatin, (3S,5R)- is an Atorvastatin impurity.

Atorvastatin Hemicalcium Trihydrate, an orally active HMG-CoA reductase inhibitor, effectively reduces blood lipids. It also inhibits human SV-SMC proliferation and invasion, showing IC50 values of 0.39 μM and 2.39 μM, respectively.

3-Oxo Atorvastatin, an impurity of Atorvastatin, acts as an HMG-CoA reductase inhibitor and effectively decreases blood lipids.

Atorvastatin 3-Deoxyhept-2E-Enoic Acid is an impurity of Atorvastatin, an HMG-CoA reductase inhibitor that effectively decreases blood lipids.

Atorvastatin acetonide tert-butyl ester, a valuable pharmaceutical intermediate, is used in preparing Atorvastatin salts, an HMG-CoA reductase inhibitor.

Atorvastatin acetonide [Atorvastatin Impurity B] is an impurity of Atorvastatin, an HMG-CoA reductase inhibitor known for its efficacy in lowering blood lipids.

Atorvastatin ethyl ester, a derivative of Atorvastatin, exhibits potent inhibition of 9-cis-RA-induced Gal4 reporter activity.

O-Methyl Atorvastatin is an impurity of Atorvastatin that is an orally active inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase, has the ability to effectively decrease blood lipids.

Atorvastatin methyl ester is a derivative of Atorvastatin. It inhibits the 9-cis-RA-induced Gal4 reporter activity more strongly than Atorvastatin.

Desfluoro-atorvastatin is an Atorvastatin impurity. Atorvastatin is an orally active inhibitor of HMG-CoA reductase. It has the ability to effectively decrease blood lipids.

Difluoro atorvastatin is an Atorvastatin impurity. Atorvastatin is an orally active HMG-CoA reductase inhibitor and it has the ability to effectively decrease blood lipids. Atorvastatin inhibits human SV-SMC proliferation and invasion (IC50s: 0.39 μM and

2-Hydroxy atorvastatin lactone, a metabolite of Atorvastatin, is an orally active HMG-CoA reductase inhibitor that efficiently reduces blood lipids [1][2].

Atorvastatin magnesium is an HMG-CoA inhibitor.

Atorvastatin lysine is a selective and competitive HMGCR (HMG-CoA reductase) inhibitor.

Atorvastatin strontium is used primarily for lowering blood cholesterol and for prevention of events associated with cardiovascular disease. Like all statins, atorvastatin works by inhibiting HMG-CoA reductase, an enzyme found in liver tissue that plays a key role in production of cholesterol in the body.Atorvastatin is also used for the treatment of dyslipidemia.

Atorvastatin magnesium trihydrate is used primarily for lowering blood cholesterol and for prevention of events associated with cardiovascular disease. Like all statins, atorvastatin works by inhibiting HMG-CoA reductase, an enzyme found in liver tissue that plays a key role in production of cholesterol in the body.Atorvastatin is also used for the treatment of dyslipidemia.

2-Hydroxy atorvastatin-d5 (Atorvastatin impurity K-d5) is a deuterium-labeled form of 2-Hydroxy atorvastatin. The calcium salt of 2-Hydroxy atorvastatin is a hydroxylated metabolite of Atorvastatin calcium salt. Atorvastatin is a potent inhibitor of HMG-CoA reductase, with an IC50 value of 8 nM.

Atorvastatin calcium trihydrate (Standard) is a reference standard for research and analysis in studies involving Atorvastatin calcium trihydrate. Atorvastatin is used to inhibits HMG-CoA reductase for lowering blood cholesterol and for prevention of events associated with cardiovascular disease.

Atorvastatin hemicalcium salt (Atorvastatin Calcium) is an HMG-CoA reductase inhibitor with oral activity. Atorvastatin hemicalcium salt is used to lower cholesterol.

Atorvastatin lactone is a prodrug form of atorvastatin. Which is an orally active 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitor.

Atorvastatin, an orally active HMG-CoA reductase inhibitor, effectively lowers blood lipids by activating liver cytochrome p450 to accelerate metabolism. Atorvastatin inhibits the proliferation and invasion of human SV-SMC cells with IC50 values of 0.39 μM and 2.39 μM, respectively. [Atorvastatin] combined with clopidogrel may lead to increased thrombotic events in patients.

(3S,5S)-Atorvastatin is the inactive enantiomer of atorvastatin that has no inhibitory activity against HMG-CoA reductase but can activate the pregnane X receptor (PXR). Atorvastatin is an orally active HMG-CoA reductase inhibitor with the ability to effectively lower blood lipid levels.

Atorvastatin calcium hydrate is an oral lipid-lowering compound belonging to the class of HMG-CoA reductase inhibitors. Atorvastatin calcium hydrate significantly reduces serum LDL cholesterol levels by inhibiting a key enzyme involved in cholesterol biosynthesis. Atorvastatin calcium hydrate is used in in vitro experiments to study cholesterol metabolism, lipid accumulation, and the regulation of related signaling pathways, and is commonly employed in high-fat diet animal models to validate its lipid-lowering effects.

Atorvastatin Sodium (Lipitor) is a competitive inhibitor of HMG-CoA reductase and increases the expression of low density lipoprotein (LDL) receptors on hepatocytes. Atorvastatin Sodium treatment inhibits aquaporin 4 to reduce ischaemic brain oedema.