Title : ATP-citrate lyase (ACLY) in lipid metabolism and atherosclerosis: An updated review.

Pub. Date : 2020 Jan

PMID : 31499095






4 Functional Relationships(s)
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1 Among current ACLY inhibitors, Bempedoic acid (ETC-1002) is a first-in-class, prodrug-based direct competitive inhibitor of ACLY which regulates lipid metabolism by upregulating hepatic LDL receptor (LDLr) expression and activity. 8-hydroxy-2,2,14,14-tetramethylpentadecanedioic acid ATP citrate lyase Homo sapiens
2 Among current ACLY inhibitors, Bempedoic acid (ETC-1002) is a first-in-class, prodrug-based direct competitive inhibitor of ACLY which regulates lipid metabolism by upregulating hepatic LDL receptor (LDLr) expression and activity. 8-hydroxy-2,2,14,14-tetramethylpentadecanedioic acid ATP citrate lyase Homo sapiens
3 Among current ACLY inhibitors, Bempedoic acid (ETC-1002) is a first-in-class, prodrug-based direct competitive inhibitor of ACLY which regulates lipid metabolism by upregulating hepatic LDL receptor (LDLr) expression and activity. 8-hydroxy-2,2,14,14-tetramethylpentadecanedioic acid ATP citrate lyase Homo sapiens
4 Among current ACLY inhibitors, Bempedoic acid (ETC-1002) is a first-in-class, prodrug-based direct competitive inhibitor of ACLY which regulates lipid metabolism by upregulating hepatic LDL receptor (LDLr) expression and activity. 8-hydroxy-2,2,14,14-tetramethylpentadecanedioic acid ATP citrate lyase Homo sapiens