N-Phenyl-1H-indazole-3-carboxamide结构式
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常用名 | N-Phenyl-1H-indazole-3-carboxamide | 英文名 | N-Phenyl-1H-indazole-3-carboxamide |
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| CAS号 | 23706-99-2 | 分子量 | 237.25700 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C14H11N3O | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 英文名 | N-Phenyl-1H-indazole-3-carboxamide |
|---|---|
| 英文别名 | 更多 |
| 分子式 | C14H11N3O |
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| 分子量 | 237.25700 |
| 精确质量 | 237.09000 |
| PSA | 57.78000 |
| LogP | 2.88820 |
| InChIKey | XQJXNILPLUCHQG-UHFFFAOYSA-N |
| SMILES | O=C(Nc1ccccc1)c1n[nH]c2ccccc12 |
| 海关编码 | 2933990090 |
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~64%
N-Phenyl-1H-ind... 23706-99-2 |
| 文献:Wyatt, Paul G.; Woodhead, Andrew J.; Berdini, Valerio; Boulstridge, John A.; Carr, Maria G.; Cross, David M.; Davis, Deborah J.; Devine, Lindsay A.; Early, Theresa R.; Feltell, Ruth E.; Lewis, E. Jonathan; McMenamin, Rachel L.; Navarro, Eva F.; O'Brien, Michael A.; O'Reilly, Marc; Reule, Matthias; Saxty, Gordon; Seavers, Lisa C. A.; Smith, Donna-Michelle; Squires, Matt S.; Trewartha, Gary; Walker, Margaret T.; Woolford, Alison J.-A. Journal of Medicinal Chemistry, 2008 , vol. 51, # 16 p. 4986 - 4999 |
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~52%
N-Phenyl-1H-ind... 23706-99-2 |
| 文献:Shi, Jing-Jing; Ji, Fei-Hong; He, Pei-Lan; Yang, Ya-Xi; Tang, Wei; Zuo, Jian-Ping; Li, Yuan-Chao ChemMedChem, 2013 , vol. 8, # 5 p. 722 - 725 |
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~%
N-Phenyl-1H-ind... 23706-99-2 |
| 文献:Shi, Jing-Jing; Ji, Fei-Hong; He, Pei-Lan; Yang, Ya-Xi; Tang, Wei; Zuo, Jian-Ping; Li, Yuan-Chao ChemMedChem, 2013 , vol. 8, # 5 p. 722 - 725 |
| N-Phenyl-1H-indazole-3-carboxamide上游产品 2 | |
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| N-Phenyl-1H-indazole-3-carboxamide下游产品 0 | |
| 海关编码 | 2933990090 |
|---|---|
| 中文概述 | 2933990090. 其他仅含氮杂原子的杂环化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0% |
| 申报要素 | 品名, 成分含量, 用途, 乌洛托品请注明外观, 6-己内酰胺请注明外观, 签约日期 |
| Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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实验名称:Inhibition of full length human N-terminal GST-tagged PAK2 (1 to 524 residues) expres...
来源:ChEMBL
靶标:Serine/threonine-protein kinase PAK 2
External Id:CHEMBL3794943
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实验名称:Inhibition of human N-terminal GST-tagged p70S6K catalytic domain (1 to 421 residues)...
来源:ChEMBL
靶标:Ribosomal protein S6 kinase beta-1
External Id:CHEMBL3794942
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实验名称:Inhibition of human N-terminal GST-tagged p38alpha (9 to 352 residues) expressed in E...
来源:ChEMBL
靶标:Mitogen-activated protein kinase 14
External Id:CHEMBL3794941
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实验名称:Inhibition of full length human N-terminal His-tagged NEK2 (1 to 445 residues) expres...
来源:ChEMBL
靶标:Serine/threonine-protein kinase Nek2
External Id:CHEMBL3794940
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实验名称:Inhibition of full length human N-terminal GST-tagged PKACalpha (1 to 351 residues) e...
来源:ChEMBL
靶标:cAMP-dependent protein kinase catalytic subunit alpha
External Id:CHEMBL3794947
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实验名称:Inhibition of full length human N-terminal His-tagged PIM1 (1 to 313 residues) expres...
来源:ChEMBL
靶标:Serine/threonine-protein kinase pim-1
External Id:CHEMBL3794946
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实验名称:Inhibition of full length human N-terminal GST-tagged PDK1 (1 to 436 residues) expres...
来源:ChEMBL
靶标:[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial
External Id:CHEMBL3794945
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实验名称:Inhibition of full length human N-terminal GST-tagged PBK (1 to 322 residues) express...
来源:ChEMBL
靶标:Lymphokine-activated killer T-cell-originated protein kinase
External Id:CHEMBL3794944
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实验名称:Inhibition of human N-terminal GST-tagged SGK (61 to 431 residues) expressed in bacul...
来源:ChEMBL
靶标:Serine/threonine-protein kinase Sgk1
External Id:CHEMBL3794951
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实验名称:Inhibition of human N-terminal GST-tagged ROCK1 catalytic domain (1 to 477 residues) ...
来源:ChEMBL
靶标:Rho-associated protein kinase 1
External Id:CHEMBL3794950
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| Indazol-carbonsaeure-(3)-anilid |
| 1H-Indazole-3-carboxamide,N-phenyl |
| 1(2)H-indazole-3-carboxylic acid anilide |
| N-phenyl-2H-indazole-3-carboxamide |
| 1H-indazole-3-carboxylic acid phenyl-amide |
| indazole amide,13 |