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Firuglipel

Names

[ CAS No. ]:
1371591-51-3

[ Name ]:
Firuglipel

[Synonym ]:
4-(5-{(1R)-1-[4-(Cyclopropylcarbonyl)phenoxy]propyl}-1,2,4-oxadiazol-3-yl)-2-fluoro-N-[(2R)-1-hydroxy-2-propanyl]benzamide

Biological Activity

[Description]:

Firuglipel (DS-8500a) is an orally available, potent and selective GPR119 agonist.

[Related Catalog]:

Signaling Pathways >> GPCR/G Protein >> GPR119
Research Areas >> Metabolic Disease

[Target]

GPR119[1]


[In Vitro]

Firuglipel (DS-8500a) increases intracellular cAMP in a concentration-dependent manner in human, rat, and mouse GPR119-expressing Chinese hamster ovary (CHO)-K1 cells, with EC50 values of 51.5, 98.4, and 108.1 nM, respectively. DS-8500a has no effect on intracellular cAMP in pcDNA3.1/CHO-K1 cells[1].

[In Vivo]

Firuglipel (DS-8500a) (1-30 mg/kg) upregulates glucagon-like peptide-1 and enhances glucose-dependent insulin secretion and improves glucose homeostasis in type 2 diabetic rats[1].

[Animal admin]

Rats[1] Male SD rats (8 weeks) are fasted overnight and orally given vehicle (0.5% MC), DS-8500a (0.1, 1, 3 and 10 mg/kg), or glimepiride (10 mg/kg). Thirty minutes later, all animals received a 50% glucose solution intravenously (glucose load: 0.5 g/kg). Blood collection is performed from the tail vein 35 minutes before, 5 minutes before, and 5 minutes after the glucose load. The plasma insulin concentration is measured using ELISA kits.

[References]

[1]. Matsumoto K, et al. DS-8500a, an Orally Available G Protein-Coupled Receptor 119 Agonist, Upregulates Glucagon-Like Peptide-1 and Enhances Glucose-Dependent Insulin Secretion and Improves Glucose Homeostasis in Type 2 Diabetic Rats. J Pharmacol Exp Ther. 2018 Dec;367(3):509-517.


[Related Small Molecules]

AR 231453 | MBX-2982 | JNJ-38431055 | PSN632408 | GSK1292263 | APD 668

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Molecular Formula ]:
C25H26FN3O5

[ Molecular Weight ]:
467.489

[ Exact Mass ]:
467.185638

[ LogP ]:
3.51

[ Index of Refraction ]:
1.592


Related Compounds

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