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Bempedoic acid (ETC-1002)

Name: Bempedoic acid (ETC-1002)
Brand: Selleck Chemicals
SKU: S7953
Rating: 5 (4 reviews)

Synonyms: ESP-55016

Catalog No.S7953 Purity: 99.13%

Bempedoic acid (ETC-1002),also known as Bempedoic acid, is an orally available, once-daily LDL-C lowering small molecule designed to lower elevated levels of LDL-C and to avoid side effects associated with existing LDL-C lowering therapies.ETC-1002 is an activator of hepatic AMP-activated protein kinase (AMPK). It has potent inhibitory activity against hepatic ATP-citrate lyase(IC50=29 uM).

Bempedoic acid (ETC-1002) Chemical Structure

CAS: 738606-46-7

Selleck's Bempedoic acid (ETC-1002) has been cited by 4 publications

Purity & Quality Control

Batch: S795301 DMSO] 68 mg/mL] false] Water] Insoluble] false] Ethanol] Insoluble] false Purity: 99.13%

99.13

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Biological Activity

Description

Targets

AMPK ^[1]

In vitro
In vitro	ETC-1002 is a new investigational low density lipoprotein cholesterol (LDL-C)-lowering agent which is a dicarboxylic acid derivative with a novel mechanism of action targeting two hepatic enzymes--adenosine triphosphate-citrate lyase (ACL) and adenosine monophosphate-activated protein kinase (AMPK), inhibiting sterol and fatty acid synthesis and promoting mitochondrial long-chain fatty acid oxidation^[1]. It increases levels of AMP-activated protein kinase (AMPK) phosphorylation, reduces activity of MAP kinases and decreases production of proinflammatory cytokines and chemokines. These effects on soluble mediators of inflammation can be significantly abrogated by LKB1 siRNAs, indicating that ETC-1002 activates AMPK and exerts its anti-inflammatory effects via an LKB1-dependent mechanism^[2].
Cell Research	Cell lines	Primary rat hepatocytes and differentiated human monocyte-derived macrophages
	Concentrations	30 μM or 100 μM
	Incubation Time	12 h
	Method	Primary rat hepatocytes and differentiated human MDMs are treated with indicated concentrations of ETC-1002 for 12 h. Working solutions of ETC-1002 are prepared in serum-free RPMI 1640 containing 12 mM HEPES, 10,000 U/ml penicillin, and 100 μg/ml streptomycin.
Experimental Result Images	Methods	Biomarkers	Images	PMID
Experimental Result Images	Western blot	p-ACC / ACC / p-AMPK / AMPK / p-HMGR		23118444

In Vivo
In vivo	In vivo, ETC-1002 suppresses thioglycollate-induced homing of leukocytes into mouse peritoneal cavity. Similarly, in a mouse model of diet-induced obesity, ETC-1002 restores adipose AMPK activity, reduces JNK phosphorylation, and diminishes expression of macrophage-specific marker 4F/80^[2]. ETC-1002 is an inactive prodrug and converted to an active ACL inhibitor(ECT-1002-CoA) by endogenous liver ACS activity in vivo^[3].
Animal Research	Animal Models	C57BL/6 male mice
	Dosages	10 ml/kg
	Administration	i.p.

NCT Number	Recruitment	Conditions	Sponsor/Collaborators	Start Date	Phases
Clinical Trial Information (data from https://clinicaltrials.gov, updated on 2024-01-11)
NCT05694260	Recruiting	Hypercholesterolemia	Esperion Therapeutics Inc.	January 12 2023	Phase 2
NCT04929249	Completed	Atherosclerotic Cardiovascular Disease	Novartis Pharmaceuticals\|Novartis	June 25 2021	Phase 3
NCT02659397	Completed	Hyperlipidemia	Esperion Therapeutics Inc.	December 2015	Phase 2
NCT02178098	Completed	Hypercholesterolemia\|Hypertension	Esperion Therapeutics Inc.\|Medpace Inc.	June 16 2014	Phase 2

References

Chemical lnformation & Solubility

Molecular Weight	344.49	Formula	C₁₉H₃₆O₅
CAS No.	738606-46-7	SDF	Download Bempedoic acid (ETC-1002) SDF
Smiles	CC(C)(CCCCCC(CCCCCC(C)(C)C(=O)O)O)C(=O)O
Storage (From the date of receipt)	3 years-20°Cpowder	Storage of Stock Solutions Aliquot the stock solutions to avoid repeated freeze-thaw cycles	1 year-80°Cin solvent
Storage (From the date of receipt)	3 years-20°Cpowder		1 month-20°Cin solvent

In vitro
Batch:

DMSO : 68 mg/mL ( (197.39 mM)； Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Water : Insoluble

Ethanol : Insoluble

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In vivo
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