Reaction Details |
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Target | Tyrosine-protein kinase Tec |
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Ligand | BDBM50176316 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_327882 (CHEMBL864602) |
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Kd | 292000±n/a nM |
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Citation | Inglis, SR; Jones, RK; Booker, GW; Pyke, SM Synthesis of N-benzylated-2-aminoquinolines as ligands for the Tec SH3 domain. Bioorg Med Chem Lett16:387-90 (2005) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Tyrosine-protein kinase Tec |
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Name: | Tyrosine-protein kinase Tec |
Synonyms: | PSCTK4 | TEC | TEC_HUMAN | Tyrosine-protein kinase TEC (TEC) |
Type: | Protein |
Mol. Mass.: | 73597.00 |
Organism: | Homo sapiens (Human) |
Description: | n/a |
Residue: | 631 |
Sequence: | MNFNTILEEILIKRSQQKKKTSPLNYKERLFVLTKSMLTYYEGRAEKKYRKGFIDVSKIK
CVEIVKNDDGVIPCQNKYPFQVVHDANTLYIFAPSPQSRDLWVKKLKEEIKNNNNIMIKY
HPKFWTDGSYQCCRQTEKLAPGCEKYNLFESSIRKALPPAPETKKRRPPPPIPLEEEDNS
EEIVVAMYDFQAAEGHDLRLERGQEYLILEKNDVHWWRARDKYGNEGYIPSNYVTGKKSN
NLDQYEWYCRNMNRSKAEQLLRSEDKEGGFMVRDSSQPGLYTVSLYTKFGGEGSSGFRHY
HIKETTTSPKKYYLAEKHAFGSIPEIIEYHKHNAAGLVTRLRYPVSVKGKNAPTTAGFSY
EKWEINPSELTFMRELGSGLFGVVRLGKWRAQYKVAIKAIREGAMCEEDFIEEAKVMMKL
THPKLVQLYGVCTQQKPIYIVTEFMERGCLLNFLRQRQGHFSRDVLLSMCQDVCEGMEYL
ERNSFIHRDLAARNCLVSEAGVVKVSDFGMARYVLDDQYTSSSGAKFPVKWCPPEVFNYS
RFSSKSDVWSFGVLMWEVFTEGRMPFEKYTNYEVVTMVTRGHRLYQPKLASNYVYEVMLR
CWQEKPEGRPSFEDLLRTIDELVECEETFGR
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BDBM50176316 |
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n/a |
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Name | BDBM50176316 |
Synonyms: | 4-((quinolin-2-ylamino)methyl)phenol | CHEMBL202984 |
Type | Small organic molecule |
Emp. Form. | C16H14N2O |
Mol. Mass. | 250.2952 |
SMILES | Oc1ccc(CNc2ccc3ccccc3n2)cc1 |
Structure |
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