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LY2119620 Sale

(Synonyms: 3-氨基-5-氯-N-环丙基-4-甲基-6-[2-(4-甲基-1-哌嗪基)-2-氧代乙氧基]-噻吩并[2,3-B]吡啶-2-甲酰胺) 目录号 : GC13445

A positive allosteric modulator of M2 and M4 mAChRs

LY2119620 Chemical Structure

Cas No.:886047-22-9

规格 价格 库存 购买数量
10mM (in 1mL DMSO)
¥1,188.00
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5mg
¥1,080.00
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10mg
¥1,755.00
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25mg
¥3,510.00
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50mg
¥6,300.00
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100mg
¥10,800.00
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Sample solution is provided at 25 µL, 10mM.

Description

LY2119620 is a selective positive allosteric modulator of M2/M4 receptor [1].

Muscarinic acetylcholine receptors (M1-M5) are G-protein coupled receptors regulating the action of the neurotransmitter ACh and play an important role in smooth muscle control, exocrine gland function, mood and cognition [1].

LY2119620 is a selective positive allosteric modulator of M2/M4 receptor. In [35S]GTPγS-binding experiments, LY2119620 exhibited a modest allosteric agonism of 23.2% and 16.8% at the M2 and M4 receptors, respectively. LY2119620 and ACh binding caused cooperativity factor α of 79.4 and 19.5 for the M4 receptor and the M2 receptor, respectively. The cooperativity between LY2119620 and orthosteric agonists (Iperoxo or Oxo-M) was also observed [1]. M2 receptor simultaneously bound to LY2119620 and iperoxo. LY2119620 exhibited mild negative cooperativity with the inverse agonist NMS and strong positive cooperativity with iperoxo [2]. LY2119620 significantly increased Bmax values without changes in Kd when cooperativity binding of [3H]LY2119620 with mAChR, suggesting a G protein-dependent process [3].

References:
[1].  Croy CH, Schober DA, Xiao H, et al. Characterization of the novel positive allosteric modulator, LY2119620, at the muscarinic M(2) and M(4) receptors. Mol Pharmacol, 2014, 86(1): 106-115.
Kruse AC, Ring AM, Manglik A, et al.  Activation and allosteric modulation of a muscarinic acetylcholine receptor. Nature, 2013, 504(7478): 101-106.
Schober DA, Croy CH, Xiao H, et al.  Development of a radioligand, [(3)H]LY2119620, to probe the human M(2) and M(4) muscarinic receptor allosteric binding sites. Mol Pharmacol, 2014, 86(1): 116-123.

实验参考方法

Kinase experiment:

[3H]LY2119620 equilibrium binding is achieved by incubating 15 µg membranes, orthosteric ligand (100 µM), and various concentrations of [3H]LY2119620 (0.2 to 60 nM) for 1 hour at 25°C. The specific binding versus time data are fit to a one-site specific binding model, and the Bmax and Kd for the allosteric molecule are calculated for each orthosteric ligand[1].

References:

[1]. Croy CH, et al. Characterization of the novel positive allosteric modulator, LY2119620, at the muscarinic M(2) and M(4) receptors. Mol Pharmacol. 2014 Jul;86(1):106-15.

化学性质

Cas No. 886047-22-9 SDF
别名 3-氨基-5-氯-N-环丙基-4-甲基-6-[2-(4-甲基-1-哌嗪基)-2-氧代乙氧基]-噻吩并[2,3-B]吡啶-2-甲酰胺
化学名 3-amino-5-chloro-N-cyclopropyl-4-methyl-6-[2-(4-methylpiperazin-1-yl)-2-oxoethoxy]thieno[2,3-b]pyridine-2-carboxamide
Canonical SMILES CC1=C2C(=C(SC2=NC(=C1Cl)OCC(=O)N3CCN(CC3)C)C(=O)NC4CC4)N
分子式 C19H24ClN5O3S 分子量 437.94
溶解度 ≥ 21.897mg/mL in DMSO 储存条件 Store at -20°C
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1 mM 2.2834 mL 11.4171 mL 22.8342 mL
5 mM 0.4567 mL 2.2834 mL 4.5668 mL
10 mM 0.2283 mL 1.1417 mL 2.2834 mL
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