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APD668 (Synonyms: JNJ-28630368)

Katalog-Nr.GC12738

APD668 ist ein potenter, selektiver und oral aktiver Agonist des G-Protein-gekoppelten Rezeptors GPR119 mit EC50-Werten von 2,7 nM und 33 nM fÜr hGPR119 bzw. rGPR119.

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APD668 Chemische Struktur

Cas No.: 832714-46-2

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10mM (in 1mL DMSO)
116,00 $
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5mg
77,00 $
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10mg
163,00 $
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50mg
515,00 $
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100mg
904,00 $
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Sample solution is provided at 25 µL, 10mM.

Description of APD668

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].

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.

Chemical Properties of APD668

Cas No. 832714-46-2 SDF
Überlieferungen JNJ-28630368
Formula C21H24FN5O5S M.Wt 477.51
Löslichkeit ≥ 17.4mg/mL in DMSO Storage Store at -20°C
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of APD668

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1 mg 5 mg 10 mg
1 mM 2.0942 mL 10.471 mL 20.942 mL
5 mM 0.4188 mL 2.0942 mL 4.1884 mL
10 mM 0.2094 mL 1.0471 mL 2.0942 mL
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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
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