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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.

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

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

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.

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.

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.

(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-D5 Calcium Salt is a deuterated compound of Atorvastatin Calcium Salt. Atorvastatin Calcium Salt (T3116) has a CAS number of 134523-00-5.

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 (Standard) is the standard substance of Atorvastatin hemicalcium salt, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Atorvastatin hemicalcium salt (Atorvastatin Calcium) is an HMG-CoA reductase inhibitor with oral activity. Atorvastatin hemicalcium salt is used to lower cholesterol.

Atorvastatin-D is the deuterated form of Atorvastatin (T20765) sodium. Atorvastatin (T20765) sodium acts as an orally active HMG-CoA reductase inhibitor, effectively reducing blood lipid levels. It inhibits the proliferation and invasion of human SV-SMC cells with IC50 values of 0.39 μM and 2.39 μM, respectively.

Atorvastatin Calcium Salt-[D5] (Standard) is a reference standard of Atorvastatin Calcium Salt-[D5] intended for quantitative analysis, quality control, and related biochemical research applications.

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