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LOE 908 HYDROCHLORIDE

更新时间:2025-08-24 10:32:32

LOE 908 HYDROCHLORIDE结构式
LOE 908 HYDROCHLORIDE结构式
品牌特惠专场
常用名 LOE 908 HYDROCHLORIDE 英文名 LOE 908 HYDROCHLORIDE
CAS号 149759-26-2 分子量 749.28900
密度 1.17g/cm3 沸点 803.7ºC at 760mmHg
分子式 C41H49ClN2O9 熔点 N/A
MSDS N/A 闪点 439.9ºC

 LOE 908 HYDROCHLORIDE用途


匹诺卡兰是一种广谱非选择性通道抑制剂。匹诺卡兰显著减少皮层梗死体积。匹诺卡兰o改善缺血半暗带的代谢和电生理状态。匹诺卡兰在大鼠大脑中动脉阻塞后的急性期减少磁共振图像上的病灶大小。皮诺卡兰具有研究中风的潜力。匹诺卡兰还显示出抗SARS-CoV-2活性[1]。

 LOE 908 HYDROCHLORIDE名称

英文名 2-(6,7-dimethoxy-3,4-dihydroisoquinolin-1-yl)-2-phenyl-N,N-bis[2-(2,3,4-trimethoxyphenyl)ethyl]acetamide
英文别名 更多

 LOE 908 HYDROCHLORIDE生物活性

描述 匹诺卡兰是一种广谱非选择性通道抑制剂。匹诺卡兰显著减少皮层梗死体积。匹诺卡兰o改善缺血半暗带的代谢和电生理状态。匹诺卡兰在大鼠大脑中动脉阻塞后的急性期减少磁共振图像上的病灶大小。皮诺卡兰具有研究中风的潜力。匹诺卡兰还显示出抗SARS-CoV-2活性[1]。
相关类别
体内研究 匹诺卡兰显著减少皮质梗死体积,从33.8 mm3减少到24.5 mm3[1]。
参考文献

[1]. Christensen T, et al. The broad-spectrum cation channel blocker pinokalant (LOE 908 MS) reduces brain infarct volume in rats: a temperature-controlled histological study. Basic Clin Pharmacol Toxicol. 2005 Apr;96(4):316-24.

[2]. Simard JM, et al. Non-selective cation channels, transient receptor potential channels and ischemic stroke. Biochim Biophys Acta. 2007 Aug;1772(8):947-57.

[3]. Serdar Durdagi, et al. Screening of Clinically Approved and Investigation Drugs as Potential Inhibitors of SARS-CoV-2 Main Protease and Spike Receptor-Binding Domain Bound with ACE2 COVID19 Target Proteins: A Virtual Drug Repurposing Study. 2020.

 LOE 908 HYDROCHLORIDE物理化学性质

密度 1.17g/cm3
沸点 803.7ºC at 760mmHg
分子式 C41H49ClN2O9
分子量 749.28900
闪点 439.9ºC
精确质量 748.31300
PSA 106.51000
LogP 6.43600
InChIKey PYWYBTRACMRUQV-UHFFFAOYSA-N
SMILES COc1cc2c(cc1OC)C(C(C(=O)N(CCc1ccc(OC)c(OC)c1OC)CCc1ccc(OC)c(OC)c1OC)c1ccccc1)=NCC2
蒸汽压 7.33E-26mmHg at 25°C
折射率 1.561

 LOE 908 HYDROCHLORIDE靶点实验

查看更多实验

实验名称:qHTS Assay for Substrates of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1):...
来源:NCGC
靶标:thioredoxin reductase [Rattus norvegicus]
External Id:TRXR101
实验名称:qHTS for Inhibitors of Polymerase Iota
来源:NCGC
靶标:DNA polymerase iota [Homo sapiens]
External Id:PolI100
实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1100
实验名称:qHTS for Stage-Specific Inhibitors of Vaccinia Orthopoxvirus: mCherry Reporter Primar...
来源:NCGC
靶标:67.9K protein [Vaccinia virus]
External Id:Vaccinia-p2mCherry
实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1101
实验名称:S16 Schwann cell PMP22 intronic element firefly luciferase assay
来源:NCGC
靶标:peripheral myelin protein 22 [Rattus norvegicus]
External Id:cmt-p4-fluc-fda_regid
实验名称:qHTS for Inhibitors of Polymerase Kappa
来源:NCGC
靶标:DNA polymerase kappa [Homo sapiens]
External Id:PolK100
实验名称:qHTS Assay for Inhibitors of Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1):...
来源:NCGC
靶标:thioredoxin reductase [Rattus norvegicus]
External Id:TRXR100
实验名称:qHTS for Stage-Specific Inhibitors of Vaccinia Orthopoxvirus: Venus Reporter Primary ...
来源:NCGC
靶标:67.9K protein [Vaccinia virus]
External Id:Vaccinia-p2Venus
实验名称:qHTS for Inhibitors of TGF-b: Cytotox Counterscreen
来源:NCGC
靶标:N/A
External Id:SMAD3201
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 LOE 908 HYDROCHLORIDE英文别名

unii-7j9zz971ao
pinokalant
loe 908
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