Reaction Details |
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Target | Tyrosine-protein kinase ITK/TSK |
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Ligand | BDBM50320986 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_639388 (CHEMBL1167768) |
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IC50 | >100000±n/a nM |
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Citation | Velankar, AD; Quintini, G; Prabhu, A; Weber, A; Hunaeus, G; Voland, B; Wuest, M; Orjeda, C; Harel, D; Varghese, S; Gore, V; Patil, M; Gayke, D; Herdemann, M; Heit, I; Zaliani, A Synthesis and biological evaluation of novel (4 or 5-aryl)pyrazolyl-indoles as inhibitors of interleukin-2 inducible T-cell kinase (ITK). Bioorg Med Chem18:4547-59 (2010) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Tyrosine-protein kinase ITK/TSK |
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Name: | Tyrosine-protein kinase ITK/TSK |
Synonyms: | EMT | ITK | ITK_HUMAN | Kinase EMT | LYK | T-cell-specific kinase | Tyrosine-protein kinase ITK | Tyrosine-protein kinase ITK (ITK) | Tyrosine-protein kinase Lyk |
Type: | Protein |
Mol. Mass.: | 71839.20 |
Organism: | Homo sapiens (Human) |
Description: | Q08881 |
Residue: | 620 |
Sequence: | MNNFILLEEQLIKKSQQKRRTSPSNFKVRFFVLTKASLAYFEDRHGKKRTLKGSIELSRI
KCVEIVKSDISIPCHYKYPFQVVHDNYLLYVFAPDRESRQRWVLALKEETRNNNSLVPKY
HPNFWMDGKWRCCSQLEKLATGCAQYDPTKNASKKPLPPTPEDNRRPLWEPEETVVIALY
DYQTNDPQELALRRNEEYCLLDSSEIHWWRVQDRNGHEGYVPSSYLVEKSPNNLETYEWY
NKSISRDKAEKLLLDTGKEGAFMVRDSRTAGTYTVSVFTKAVVSENNPCIKHYHIKETND
NPKRYYVAEKYVFDSIPLLINYHQHNGGGLVTRLRYPVCFGRQKAPVTAGLRYGKWVIDP
SELTFVQEIGSGQFGLVHLGYWLNKDKVAIKTIREGAMSEEDFIEEAEVMMKLSHPKLVQ
LYGVCLEQAPICLVFEFMEHGCLSDYLRTQRGLFAAETLLGMCLDVCEGMAYLEEACVIH
RDLAARNCLVGENQVIKVSDFGMTRFVLDDQYTSSTGTKFPVKWASPEVFSFSRYSSKSD
VWSFGVLMWEVFSEGKIPYENRSNSEVVEDISTGFRLYKPRLASTHVYQIMNHCWKERPE
DRPAFSRLLRQLAEIAESGL
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BDBM50320986 |
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n/a |
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Name | BDBM50320986 |
Synonyms: | 3-[(3-Hydroxy-propylamino)-methyl]-2-(4-phenyl-1Hpyrazol-3-yl)-1H-indole-6-carboxylic acid isobutyl-methylamide | CHEMBL1165616 |
Type | Small organic molecule |
Emp. Form. | C27H33N5O2 |
Mol. Mass. | 459.5832 |
SMILES | CC(C)CN(C)C(=O)c1ccc2c(CNCCCO)c([nH]c2c1)-c1n[nH]cc1-c1ccccc1 |
Structure |
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