Anticonvulsant agent 2结构式
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常用名 | Anticonvulsant agent 2 | 英文名 | Anticonvulsant agent 2 |
|---|---|---|---|---|
| CAS号 | 75220-84-7 | 分子量 | 332.83 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C21H17ClN2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
Anticonvulsant agent 2用途抗惊厥剂2是一种强效口服活性抗惊厥剂。抗惊厥剂2具有抗癫痫活性[1]。 |
| 英文名 | 4-(4-chlorophenyl)-2-phenyl-2,3-dihydro-1H-1,5-benzodiazepine |
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| 描述 | 抗惊厥剂2是一种强效口服活性抗惊厥剂。抗惊厥剂2具有抗癫痫活性[1]。 |
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| 相关类别 | |
| 体内研究 | 抗惊厥剂2(化合物10 a;50 mg/kg,p.o.)降低大鼠运动活性,抑制率为 21.01%[1]抗惊厥剂2(50 mg/kg;口服)显示出抗癫痫活性,对大鼠的抑制率为24.45%[1]动物模型:180-250g,雄性Wistar大鼠[1]剂量:50mg/kg给药:口服。结果:具有抗癫痫活性,抑制率为24.45%。 |
| 参考文献 |
| 分子式 | C21H17ClN2 |
|---|---|
| 分子量 | 332.83 |
| 精确质量 | 332.10800 |
| PSA | 24.39000 |
| LogP | 5.59130 |
| InChIKey | HGXLBVMEBUESSS-UHFFFAOYSA-N |
| SMILES | Clc1ccc(C2=Nc3ccccc3NC(c3ccccc3)C2)cc1 |
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~90%
Anticonvulsant ... 75220-84-7 |
| 文献:Du, Yuying; Tian, Fuli Journal of Chemical Research, 2006 , # 8 p. 486 - 489 |
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~59%
Anticonvulsant ... 75220-84-7 |
| 文献:Orlov, V. D.; Kolos, N. N.; Yaremenko, F. G.; Lavrushin, V. F. Chemistry of Heterocyclic Compounds (New York, NY, United States), 1980 , vol. 16, # 5 p. 547 - 550 Khimiya Geterotsiklicheskikh Soedinenii, 1980 , # 5 p. 697 - 700 |
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~%
Anticonvulsant ... 75220-84-7 |
| 文献:Verma, Anil K.; Koul, Summon; Razdan, Tej K.; Kapoor, Kamal K. Canadian Journal of Chemistry, 2006 , vol. 84, # 8 p. 1064 - 1073 |
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~%
Anticonvulsant ... 75220-84-7 |
| 文献:Verma, Anil K.; Koul, Summon; Razdan, Tej K.; Kapoor, Kamal K. Canadian Journal of Chemistry, 2006 , vol. 84, # 8 p. 1064 - 1073 |
| Anticonvulsant agent 2上游产品 5 | |
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| Anticonvulsant agent 2下游产品 1 | |
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实验名称:Cell-based high throughput primary assay to identify activators of GPR151
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=G-protein coupled receptor 151; AltName: Full=G-protein coupled receptor PGR7; AltName: Full=GPCR-2037; AltName: Full=Galanin receptor 4; AltName: Full=Galanin-receptor-like protein; Short=GalRL
External Id:GPR151_PHUNTER_AG_LUMI_1536_1X%ACT
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实验名称:AlphaScreen-based biochemical high throughput primary assay to identify activators of...
来源:The Scripps Research Institute Molecular Screening Center
靶标:N/A
External Id:FBW7_ACT_ALPHA_1536_1X%ACT PRUN
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实验名称:AlphaScreen-based biochemical high throughput primary assay to identify inhibitors of...
来源:The Scripps Research Institute Molecular Screening Center
External Id:MITF_INH_Alpha_1536_1X%INH PRUN
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