About: Atorvastatin Calcium     Goto   Sponge   NotDistinct   Permalink

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AttributesValues
rdf:type
rdfs:label
  • Atorvastatin Calcium
rdfs:subClassOf
Has_Free_Acid_Or_Base_Form
Concept_In_Subset
Semantic_Type
  • Organic Chemical
  • Pharmacologic Substance
Preferred_Name
  • Atorvastatin Calcium
UMLS_CUI
  • C0286650
CAS_Registry
  • 134523-03-8
  • 344423-98-9
FDA_UNII_Code
  • 48A5M73Z4Q
Contributing_Source
  • FDA
ALT_DEFINITION
  • A drug used to lower the amount of cholesterol in the blood and to prevent stroke, heart attack, and angina (chest pain). It is also being studied in the prevention and treatment of some types of cancer and other conditions. Atorvastatin calcium blocks an enzyme that helps make cholesterol in the body. It also causes an increase in the breakdown of cholesterol. It is a type of HMG-CoA reductase inhibitor and a type of statin.NCI-GLOSS
PDQ_Open_Trial_Search_ID
  • 460239
PDQ_Closed_Trial_Search_ID
  • 460239
Chemical_Formula
  • 2C33H34FN2O5.Ca.3H2O
Legacy_Concept_Name
  • Atorvastatin
CHEBI_ID
  • CHEBI:2911
FULL_SYN
  • ATORVASTATIN CALCIUMPTFDA48A5M73Z4Q
  • atorvastatin calciumPTNCI-GLOSSCDR0000535469
  • Atorvastatin CalciumPTDCP09486
  • CI-981CNNCI
  • LipitorPTNCI-GLOSSCDR0000535468
  • LipitorBRNCI
  • Atorvastatin CalciumPTNCI
DEFINITION
  • The calcium salt of atorvastatin, a synthetic lipid-lowering agent. Atorvastatin competitively inhibits hepatic hydroxymethyl-glutaryl coenzyme A (HMG-CoA) reductase, the enzyme which catalyzes the conversion of HMG-CoA to mevalonate, a key step in cholesterol synthesis. This agent increases the number of LDL receptors on hepatic cell surfaces, enhancing the uptake and catabolism of LDL and reducing LDL production and the number of LDL particles, and lowers plasma cholesterol and lipoprotein levels. Like other statins, atorvastatin may also display direct antineoplastic activity, possibly by inhibiting farnesylation and geranylgeranylation of proteins such as small GTP-binding proteins, which may result in the arrest of cells in the G1 phase of the cell cycle. This agent may also sensitize tumor cells to cyctostatic drugs, possibly through the mTOR-dependent inhibition of Akt phosphorylation.NCI
code
  • C28837
is Has_Salt_Form of
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