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NS6740

有货

库存信息

关闭

库存信息

关闭
货号 (SKU) 包装规格 是否现货 价格 数量
N612406-5mg
5mg 期货 Stock Image
N612406-25mg
25mg 期货 Stock Image

基本描述

英文名称 NS6740
别名 A-793394;A793394;NS-6740
英文别名 A-793394;A793394;NS-6740

名称和标识符

IUPAC Name 1,4-diazabicyclo[3.2.2]nonan-4-yl-[5-[3-(trifluoromethyl)phenyl]furan-2-yl]methanone
INCHI InChI=1S/C19H19F3N2O2/c20-19(21,22)14-3-1-2-13(12-14)16-4-5-17(26-16)18(25)24-11-10-23-8-6-15(24)7-9-23/h1-5,12,15H,6-11H2
InChi Key VSOWCIMCDKXVRC-UHFFFAOYSA-N
Canonical SMILES O=C(N1CCN2CCC1CC2)c1ccc(o1)c1cccc(c1)C(F)(F)F
PubChem CID 10021664

关联配体

Ligand ID 11383
名称 NS6740
别名 A-793394
类别 Synthetic organic
学名 1,4-diazabicyclo[3.2.2]nonan-4-yl-[5-[3-(trifluoromethyl)phenyl]furan-2-yl]methanone
生物活性评价 The sulfonamide class of antibacterial compounds are primarily bacteriostatic agents and have a broad spectrum of activity against both Gram-positive and Gram-negative species of bacteria (reviewed in ).
评价 NS6740 (A-582941) is described as a silent agonist (or metagonist) of α7 nicotinic acetylcholine receptors (CHRNA7; nAChR, a ligand-gated ion channel) . This means that it binds to the receptor but has no intrinsic agonist activity (and may induce conformational change to a non-conducting state), but it does increase receptor sensitivity to positive allosteric modulators (PAMs). The α7 nAChR; is a promising drug target inflammatory diseases and neurological disorders (e.g. chronic and neuropathic) pain. NS6740 can be used to explore the most suitable mechanistic approach by which to achive clinical benefit from modulating the α7 nAChR .

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参考文献

1. Briggs CA, Gr?nlien JH, Curzon P, Timmermann DB, Ween H, Thorin-Hagene K, Kerr P, Anderson DJ, Malysz J, Dyhring T et al..  (2009)  Role of channel activation in cognitive enhancement mediated by alpha7 nicotinic acetylcholine receptors..  Br J Pharmacol,  158  (6):  (1486-94).  [PMID:19845675]
2. Papke RL, Bagdas D, Kulkarni AR, Gould T, AlSharari SD, Thakur GA, Damaj MI.  (2015)  The analgesic-like properties of the alpha7 nAChR silent agonist NS6740 is associated with non-conducting conformations of the receptor..  Neuropharmacology,  91  (13):  (34-42).  [PMID:25497451]

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品牌简介

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