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LY3104607
本半岛bd体育手机客户端 不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
LY3104607图片
CAS NO: 1795232-22-2
规格: ≥98%
包装与价格:
包装 价格(元)
10mg 电议
25mg 电议
50mg 电议
100mg 电议
250mg 电议

半岛bd体育手机客户端 介绍
理化性质和储存条件
Molecular Weight (MW) 439.52
Formula C27H25N3O3
CAS No. 1795232-22-2
Storage -20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility(In vitro) DMSO: 10 mM
Water: <1mg/mL
Ethanol: <1mg/mL
Chemical Name (S)-3-(4-((2-(2,6-dimethylphenyl)-[1,2,4]triazolo[1,5-a]pyridin-6-yl)methoxy)phenyl)hex-4-ynoic acid
Synonyms LY3104607; LY-3104607; LY 3104607
实验参考方法
In Vitro

In vitroactivity: LY3104607 is a potent, selective and orally available G Protein-Coupled Receptor 40 (GPR40) agonist with potential antidiabetic application. It has optimized pharmacokinetic properties to support once daily oral treatment in patients with Type 2 Diabetes Mellitus. LY3104607 demonstrated functional potency and glucose-dependent insulin secretion (GDIS) in primary islets from rats. Potent, efficacious, and durable dose-dependent reductions in glucose levels were seen during glucose tolerance test (GTT) studies. Low clearance, volume of distribution, and high oral bioavailability were observed in all species. The combination of enhanced pharmacology and pharmacokinetic properties supported further development of this compound as a potential glucose-lowering drug candidate.


Kinase Assay: All in vitro assays including binding, calcium flux, β-arrestin agonist, and peroxisome proliferator-activated receptor (PPAR) α, δ, and γ assays were described previously in detail. The use of animals was in accordance with international guidelines (NIH 85-23) and was approved by the local animal ethics committee at Lilly Research Laboratories.


Cell Assay: Glucose-Dependent Insulin Secretion (GDIS) in Rat Islet. GDIS assays were performed in primary islets. Pancreatic islets of Langerhans were isolated from male SD (Sprague–Dawley) rats by collagenasedigestion and Histopaque density gradient separation. The islets were cultured overnight in RPMI-1640 medium with GlutaMAXn to facilitate recovery from the isolation process. Insulin secretion was determined using 90 min incubation in EBSS (Earle’s Balances Salt Solution) buffer in a 48-well plate. Islets were first preincubated in EBSS with 2.8 mM glucose for 60 min, then transferred to a 48-well plate (four islets/well) containing 150 μL of 2.8 mM glucose, and incubated with 150 μL of EBSS with 2.8 or 11.2 mM glucose in the presence or absence of test compounds for 90 min. The buffer was removed from the wells at the end of the incubation period and assayed for insulin levels using a rat insulin ELISA kit (Mercodia).

In Vivo Oral Glucose Tolerance Test (OGTT) in Zucker ( fa/fa) Rats. OGTTs were performed in male Zucker ( fa/fa) rats (10 weeks of age), a rodent model of insulin resistance, after 1 and 21 days of oral administration. Compounds were administered orally at various doses to provide a dose–response efficacy curve. Compound 1 served as the positive control and reference standard for the study. OGTTs were performed 1 h after compound administration with blood samples taken for determination of glucose and insulin levels at 0, 10, 20, 40, and 60 min post glucose administration (2g/kg).
Animal model Zucker ( fa/fa) Rats
Formulation & Dosage 1,3,10mg/kg; Oral
References J Med Chem. 2018 Feb 8;61(3):934-945.
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