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Cat. No.: HY-107054

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ESP-31015

(Synonyms: ETC-1001)

ESP-31015 (ETC-1001) is an orally active and non-fibrate based PPARα agonists. ESP-31015 demonstrates significant lipid-regulating effects in the obese Zucker rat model. ESP-31015 can be used in cardiovascular disease research.

For research use only. We do not sell to patients.

CAS No.: 413624-55-2
Formula: C₁₇H₃₄O₃
Molecular Weight:286.45

Storage:

Please store the product under the recommended conditions in the Certificate of Analysis.

Data Sheet (263 KB)

ESP-31015 Chemical Structure

CAS No.: 413624-55-2

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Top Publications Citing

Use of MCE Products

Fluorescent Dye

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Biological Activity
- Description
- IC₅₀ & Target
- Cellular Effect
- In Vivo
Chemical Information
Purity & Documentation
References
Calculators
Help & FAQs
Classifications
Bioz

Biological Activity

Description

IC₅₀ & Target^[1]

PPARα

All PPAR Isoforms :

Cellular Effect

Cell Line	Type	Value	Description	References
Hepatocyte	IC₅₀	1.5 μM Compound: 39	Inhibition of lipid synthesis in primary rat hepatocytes by incorporation radiolabeled acetate into cellular lipids Inhibition of lipid synthesis in primary rat hepatocytes by incorporation radiolabeled acetate into cellular lipids	[PMID: 16392818]
Hepatocyte	IC₅₀	4 μM Compound: 14c	Concentration required for inhibition of lipid synthesis in primary cultures of rat hepatocytes Concentration required for inhibition of lipid synthesis in primary cultures of rat hepatocytes	[PMID: 15537362]

In Vivo

ESP-31015 (100 mg/kg, p.o., once daily for 2 weeks) shows a 34.6% increase in serum HDL-cholesterol and a 71% reduction in serum triglycerides in female obese Zucker fatty rats^[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model:

Female obese Zucker fatty rats model^[1]
Dosage:

100 mg/kg
Administration:

Oral administration (p.o.), once daily for 2 weeks
Result:

Showed a 34.6% increase in serum HDL-cholesterol and a 71% reduction in serum triglycerides.

Chemical Information

CAS No. 413624-55-2
Molecular Weight 286.45
Formula C₁₇H₃₄O₃
SMILES

OCC(C)(C)CCCCC(CCCCC(C)(C)CO)=O
Synonyms

ETC-1001
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation

Select Batch:

Purity: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (263 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

References

[1]. Pal M, et al. HDL elevators and mimetics--emerging therapies for atherosclerosis. Cardiovasc Hematol Agents Med Chem. 2007 Jan;5(1):55-66. [Content Brief]

Calculators

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Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

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MOQ

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100 mg

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Biological Activity
- Description
- IC₅₀ & Target
- In Vivo
Chemical Information
Purity & Documentation
References

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ESP-31015

All PPAR Isoforms

Biological Activity

Chemical Information

Purity & Documentation

References

Calculators

Help & FAQs

ESP-31015 Related Classifications

HY-107054 Related Classifications