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AZD7687

Cat. No. M2722

All AbMole products are for research use only, cannot be used for human consumption.

AZD7687 Structure
Size Price Availability
5mg USD 220 Out of stock
10mg USD 390 Out of stock
Free Delivery on orders over USD 500 Bulk Inquiry?

Quality Control & Documentation
Biological Activity

AZD7687 is a reversible and selective DGAT1 inhibitor with IC50 value of 80 nM. AZD7687 markedly reduced postprandial TAG excursion with a steep concentration-effect relationship. AZD7687 shows inhibition of acyl-CoA:cholesterol acetyltransferase (79% at 10 μM), fatty acid amide hydrolase (IC50 = 3.7 μM), muscarinic M2 receptor (IC50 = 80.5 μM), and phosphodiesterase PDE10A1 (IC50 = 5.5 μM).

Chemical Information
Molecular Weight 367.44
Formula C21H25N3O3
CAS Number 1166827-44-6
Solubility (25°C) DMSO 40 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Pablo Morentin Gutierrez, et al. Evolving data analysis of an Oral Lipid Tolerance Test toward the standard for the Oral Glucose Tolerance Test: Cross species modeling effects of AZD7687 on plasma triacylglycerol

[2] Eike Floettmann, et al. Pharmacological inhibition of DGAT1 induces sebaceous gland atrophy in mouse and dog skin while overt alopecia is restricted to the mouse

[3] H Denison, et al. Proof of mechanism for the DGAT1 inhibitor AZD7687: results from a first-time-in-human single-dose study

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Keywords: AZD7687 supplier, DGAT, inhibitors, activators

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