Reaction Details |
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Target | Tyrosine-protein kinase Lck |
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Ligand | BDBM50029221 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_221642 |
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IC50 | 40000±n/a nM |
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Citation | BurkeJr., TR; Ford, H; Osherov, N; Levitzki, A; Stefanova, I; Horak, ID; Marquez, VE Arylamides of hydroxylated isoquinolines as protein-tyrosine kinase inhibitors Bioorg Med Chem Lett2:1771-1774 (1992) Article |
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More Info.: | Get all data from this article, Assay Method |
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Tyrosine-protein kinase Lck |
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Name: | Tyrosine-protein kinase Lck |
Synonyms: | 2.7.10.2 | LCK | LCK_HUMAN | LSK | Leukocyte C-terminal Src kinase | Lymphocyte cell-specific protein-tyrosine kinase | Lymphocyte-specific protein tyrosine kinase | P56-LCK | Protein YT16 | Proto-oncogene Lck | Proto-oncogene tyrosine-protein kinase LCK | Src/Lck kinase | T cell-specific protein-tyrosine kinase |
Type: | n/a |
Mol. Mass.: | 57987.83 |
Organism: | Homo sapiens (Human) |
Description: | P06239 |
Residue: | 509 |
Sequence: | MGCGCSSHPEDDWMENIDVCENCHYPIVPLDGKGTLLIRNGSEVRDPLVTYEGSNPPASP
LQDNLVIALHSYEPSHDGDLGFEKGEQLRILEQSGEWWKAQSLTTGQEGFIPFNFVAKAN
SLEPEPWFFKNLSRKDAERQLLAPGNTHGSFLIRESESTAGSFSLSVRDFDQNQGEVVKH
YKIRNLDNGGFYISPRITFPGLHELVRHYTNASDGLCTRLSRPCQTQKPQKPWWEDEWEV
PRETLKLVERLGAGQFGEVWMGYYNGHTKVAVKSLKQGSMSPDAFLAEANLMKQLQHQRL
VRLYAVVTQEPIYIITEYMENGSLVDFLKTPSGIKLTINKLLDMAAQIAEGMAFIEERNY
IHRDLRAANILVSDTLSCKIADFGLARLIEDNEYTAREGAKFPIKWTAPEAINYGTFTIK
SDVWSFGILLTEIVTHGRIPYPGMTNPEVIQNLERGYRMVRPDNCPEELYQLMRLCWKER
PEDRPTFDYLRSVLEDFFTATEGQYQPQP
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BDBM50029221 |
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n/a |
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Name | BDBM50029221 |
Synonyms: | 7,8-Dihydroxy-isoquinoline-3-carboxylic acid phenethyl-amide | CHEMBL49350 |
Type | Small organic molecule |
Emp. Form. | C18H16N2O3 |
Mol. Mass. | 308.3312 |
SMILES | Oc1ccc2cc(ncc2c1O)C(=O)NCCc1ccccc1 |
Structure |
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