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GPR40 agonist 4 

Cat. No. M29237
GPR40 agonist 4  Structure
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Biological Activity

GPR40 agonist 4 is a potent free fatty acid receptor 1 (FFA1/ GPR40) agonist with a pEC50 of 7.54.

Chemical Information
Molecular Weight 416.87
Formula C21H17ClO5S
CAS Number 2102196-57-4
Form Solid
Solubility (25°C) DMSO 160 mg/mL (Need ultrasonic and warming)
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Ryokichi Koyama, et al. Mol Pharmacol. Chronic Exposure to SCO-267, an Allosteric GPR40 Full Agonist, Is Effective in Improving Glycemic Control in Rats

[2] Hideki Furukawa, et al. J Med Chem. Design and Identification of a GPR40 Full Agonist ( SCO-267) Possessing a 2-Carbamoylphenyl Piperidine Moiety

[3] M J Nanjan, et al. Bioorg Chem. Thiazolidinediones as antidiabetic agents: A critical review

[4] Sanath K Meegalla, et al. Bioorg Med Chem Lett. Discovery of a novel potent GPR40 full agonist

[5] Vasundhara Kain, et al. Sci Rep. Resolution Agonist 15-epi-Lipoxin A4 Programs Early Activation of Resolving Phase in Post-Myocardial Infarction Healing

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