N-Phenyl-1H-indazole-3-carboxamide structure
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Common Name | N-Phenyl-1H-indazole-3-carboxamide | ||
|---|---|---|---|---|
| CAS Number | 23706-99-2 | Molecular Weight | 237.25700 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C14H11N3O | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
| Name | N-Phenyl-1H-indazole-3-carboxamide |
|---|---|
| Synonym | More Synonyms |
| Molecular Formula | C14H11N3O |
|---|---|
| Molecular Weight | 237.25700 |
| Exact Mass | 237.09000 |
| PSA | 57.78000 |
| LogP | 2.88820 |
| InChIKey | XQJXNILPLUCHQG-UHFFFAOYSA-N |
| SMILES | O=C(Nc1ccccc1)c1n[nH]c2ccccc12 |
| HS Code | 2933990090 |
|---|
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~64%
N-Phenyl-1H-ind... CAS#:23706-99-2 |
| Literature: 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 |
|
~52%
N-Phenyl-1H-ind... CAS#:23706-99-2 |
| Literature: 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... CAS#:23706-99-2 |
| Literature: 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 |
| Precursor 2 | |
|---|---|
| DownStream 0 | |
| HS Code | 2933990090 |
|---|---|
| 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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Name: Inhibition of full length human N-terminal GST-tagged PAK2 (1 to 524 residues) expres...
Source: ChEMBL
Target: Serine/threonine-protein kinase PAK 2
External Id: CHEMBL3794943
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Name: Inhibition of human N-terminal GST-tagged p70S6K catalytic domain (1 to 421 residues)...
Source: ChEMBL
Target: Ribosomal protein S6 kinase beta-1
External Id: CHEMBL3794942
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Name: Inhibition of human N-terminal GST-tagged p38alpha (9 to 352 residues) expressed in E...
Source: ChEMBL
Target: Mitogen-activated protein kinase 14
External Id: CHEMBL3794941
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Name: Inhibition of full length human N-terminal His-tagged NEK2 (1 to 445 residues) expres...
Source: ChEMBL
Target: Serine/threonine-protein kinase Nek2
External Id: CHEMBL3794940
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Name: Inhibition of full length human N-terminal GST-tagged PKACalpha (1 to 351 residues) e...
Source: ChEMBL
Target: cAMP-dependent protein kinase catalytic subunit alpha
External Id: CHEMBL3794947
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Name: Inhibition of full length human N-terminal His-tagged PIM1 (1 to 313 residues) expres...
Source: ChEMBL
Target: Serine/threonine-protein kinase pim-1
External Id: CHEMBL3794946
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Name: Inhibition of full length human N-terminal GST-tagged PDK1 (1 to 436 residues) expres...
Source: ChEMBL
Target: [Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial
External Id: CHEMBL3794945
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Name: Inhibition of full length human N-terminal GST-tagged PBK (1 to 322 residues) express...
Source: ChEMBL
Target: Lymphokine-activated killer T-cell-originated protein kinase
External Id: CHEMBL3794944
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Name: Inhibition of human N-terminal GST-tagged SGK (61 to 431 residues) expressed in bacul...
Source: ChEMBL
Target: Serine/threonine-protein kinase Sgk1
External Id: CHEMBL3794951
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Name: Inhibition of human N-terminal GST-tagged ROCK1 catalytic domain (1 to 477 residues) ...
Source: ChEMBL
Target: 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 |