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首页-小分子抑制剂&激动剂-GPCR-mGluR-PHCCC
PHCCC

Chemical Structure : PHCCC

CAS No.: 179068-02-1

PHCCC

货号: PC-42140Not For Human Use, Lab Use Only.

PHCCC is a potent, selective allosteric potentiator of mGluR4 with EC50 of 4.1 uM, also is a selective antagonist of group mGlu1 receptors.

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

生物&药学活性

PHCCC is a potent, selective allosteric potentiator of mGluR4 with EC50 of 4.1 uM, also is a selective antagonist of group mGlu1 receptors.
PHCCC potentiates the response to glutamate (2 uM) 5.6-fold compared with glutamate alone in FLIPR assay.
PHCCC shows significant, dose-dependent anticonflict effects without affecting the threshold current or water intake in rats.
PHCCC also reduces proliferation and promotes differentiation of cerebellar granule cell neuroprecursors in rats.

物理化学性质&存储条件

分子量 294.3047
分子式 C17H14N2O3
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

DMSO: ≥ 32 mg/mL

Chemical Name/SMILES

Benzo[b]cyclopropa[e]pyran-1a(1H)-carboxamide, 7,7a-dihydro-7-(hydroxyimino)-N-phenyl-

参考文献

1. Stachowicz K, et al. Eur J Pharmacol. 2004 Sep 13;498(1-3):153-6.

2. Canudas AM, et al. J Neurosci. 2004 Nov 17;24(46):10343-52.

3. Marino MJ, et al. Proc Natl Acad Sci U S A. 2003 Nov 11;100(23):13668-73.

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