| Identification | Back Directory | [Name]
APD668 | [CAS]
832714-46-2 | [Synonyms]
APD668
CS-1179
APD 668, >=98%
APD 668; APD-668
4-[[1-(2-Fluoro-4-methylsulfonylphenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl]oxy]piperidine-1-carboxylic acid isopropyl ester
1-Piperidinecarboxylic acid,4-[[1-[2-fluoro-4-(methylsulfonyl)phenyl]-1H-pyrazolo[3,4-d]pyrimidin-4-yl]oxy]-, 1-methylethyl ester
isopropyl 4-((1-(2-fluoro-4-(methylsulfonyl)phenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl)oxy)piperidine-1-carboxylate APD668
APD668 ISOPROPYL 4-(1-(2-FLUORO-4-(METHYLSULFONYL)PHENYL)-1H-PYRAZOLO[3,4-D]PYRIMIDIN-4-YLOXY)PIPERIDINE-1-CARBOXYLATE | [Molecular Formula]
C21H24FN5O5S | [MDL Number]
MFCD12032117 | [MOL File]
832714-46-2.mol | [Molecular Weight]
477.51 |
| Chemical Properties | Back Directory | [Boiling point ]
611.6±55.0 °C(Predicted) | [density ]
1.47±0.1 g/cm3(Predicted) | [storage temp. ]
Store at -20°C | [solubility ]
insoluble in H2O; ≥17.4 mg/mL in DMSO; ≥2.61 mg/mL in EtOH with gentle warming and ultrasonic | [form ]
solid | [pka]
2.13±0.30(Predicted) | [color ]
White to off-white |
| Hazard Information | Back Directory | [Uses]
APD 668 is a potent agonist of GPR119, a glucose-dependant insulinotropic receptor expressed in pancreatic β-cells and intestinal L-cells. | [Biological Activity]
apd688 is a selective and potent g protein-coupled receptor 119 (gpr119) agonist with an ec50 value of 2.7 nm for hgpr119 and 33 nm for rgpr119, and showed a moderate inhibition of the herg channel (ic50 = 3 ?m), exhibiting an in vivo activity of glucose regulation in rodent models [1].gpr199, which is predominantly expressed in human and rodent pancreas, is a membrane receptor that plays a role in the production of insulin as a response to high glucose concentration in male wistar rats, and is a probable target for the treatment of diabetes [2]. gpr199 is also localized in the gastrointestinal track, providing a potential target for obesity therapy and other related metabolic disorders through reduced food intake [3].in hek293 cells transfected with human gpr119, application of apd688 displayed an increase in adenylatecyclase activation subsequently leading to enhanced release of insulin in a glucose-dependent manner [1].oral administration of apd688 in zucker diabetic fatty (zdf) rats for over 8 weeks resulted in the significant decrease in blood glucose and glycated hemoglobin (hba1c) levels. in addition, the compound is mostly non-genotoxic, and shows no significant inhibition of cyp isoforms except for cyp2c9 (ki = 0.1 ?m) in human hepatic microsomes [1]. | [in vivo]
APD668 (10-30 mg/kg; p.o. once daily for 8 weeks) significantly reduces blood glucose and glycated hemoglobin (HbA1c) levels, with no desensitization of the acute drug response[1].
APD668 (1-10 mg/kg; a single p.o.) markedly reduces blood glucose levels during oral glucose tolerance test in a dose-dependent manner in mice[1].
APD668 (0.08 mg/kg/min; i.v.) shows no effect during euglycemic condition, but significantly stimulates insulin release when blood glucose levels are raised to approximately 300 mg/dl in a hyperglycemic clamp model in the Sprague-Dawley rat[1].
APD668 (p.o.) exhibits rapid to moderate absorption (tmax≤2 h) in mice, rats, and monkeys, but slower in dogs (tmax=6 h), and moderate to good absolute oral bioavailability (44-79%) in mice, rats, and monkeys, but lower in dogs (22%)[1]. | Animal Model: | Male Zucker Diabetic Fatty (ZDF) rats (6 weeks old, 200-250 g)[1] | | Dosage: | 10, 30 mg/kg | | Administration: | P.o. once daily for 8 weeks | | Result: | Decreased the blood glucose and HbA1c levels at 30 mg/kg/day.
Did not develop diabetes, whereas the vehicle treated rats did.
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| [IC 50]
hGPR119: 2.7 nM (IC50); rGPR119: 33 nM (IC50); CYP2C9: 0.1 μM (Ki); hERG channel: 3 μM (IC50) | [References]
[1]. semple g, ren a, fioravanti b, et al. discovery of fused bicyclic agonists of the orphan g-protein coupled receptor gpr119 with in vivo activity in rodent models of glucose control. bioorg med chem lett, 2011, 21(10):3134-41.
[2]. soga t, ohishi t, matsui t, et al. lysophosphatidylcholine enhances glucose-dependent insulin secretion via an orphan g-protein-coupled receptor. biochem biophys res commun, 2005, 326(4):744-51.
[3]. overton ha, babbs aj, doel sm, et al. deorphanization of a g protein coupled receptor for oleoylethanolamide and its use in the discovery of small molecule hypophagic agents. cell metab, 2006, 3(3):167-75. |
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| Company Name: |
SPIRO PHARMA
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| Telephone: |
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| Website: |
www.spiropharma.com.cn |
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