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首页-小分子抑制剂&激动剂-GPCR-mAChR-VU0152100
VU0152100

Chemical Structure : VU0152100

CAS No.: 409351-28-6

VU0152100 (VU152100;VU 0152100;VU-0152100)

货号: PC-43505Not For Human Use, Lab Use Only.

VU0152100 (VU152100) is a potent, selective positive allosteric modulator of M4 mAChR with EC50 of 0.38 uM for rat M4.

规格 价格 库存 数量
10 mg ¥1180 In stock
25 mg ¥1980 In stock
50 mg ¥3280 In stock
100 mg Get quote

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

VU0152100 (VU152100) is a potent, selective positive allosteric modulator of M4 mAChR with EC50 of 0.38 uM for rat M4.
VU0152100 potentiates the M4-mediated calcium response calcium response with maximal shifts of 70-fold with 10 uM in vitro assays.
VU0152100 inhibits behavioral and neurochemical effects of cocaine in vivo, also dose-dependently reverses amphetamine-induced hyperlocomotion in rats and wild-type mice, blocks amphetamine-induced disruption of the acquisition of contextual fear conditioning.

物理化学性质&存储条件

分子量
分子式 C18H19N3O2S
外观性状 Solid
CAS No.
储存条件
固体粉末
-20 °C 12 个月; 4°C 6 个月
配置液
-80 °C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

Thieno[2,3-b]pyridine-2-carboxamide, 3-amino-N-[(4-methoxyphenyl)methyl]-4,6-dimethyl-

参考文献

1. Byun NE, et al. Neuropsychopharmacology. 2014 Jun;39(7):1578-93.

2. Brady AE, et al. J Pharmacol Exp Ther. 2008 Dec;327(3):941-53.

3. Dencker D, et al. Psychopharmacology (Berl). 2012 Nov;224(2):277-87.

4. Huynh T, et al. J Med Chem. 2013 Oct 24;56(20):8196-200.

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