Reaction Details |
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Target | Tyrosine-protein kinase Lck |
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Ligand | BDBM50083643 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_221647 |
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IC50 | 1100±n/a nM |
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Citation | Moffat, D; Davis, P; Hutchings, M; Davis, J; Berg, D; Batchelor, M; Johnson, J; O'Connell, J; Martin, R; Crabbe, T; Delgado, J; Perry, M 4-Pyridin-5-yl-2-(3,4,5-trimethoxyphenylamino)pyrimidines: potent and selective inhibitors of ZAP 70. Bioorg Med Chem Lett9:3351-6 (2000) [PubMed] |
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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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BDBM50083643 |
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n/a |
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Name | BDBM50083643 |
Synonyms: | (4-Pyridin-3-yl-pyrimidin-2-yl)-(3,4,5-trimethoxy-phenyl)-amine | CHEMBL112263 |
Type | Small organic molecule |
Emp. Form. | C18H18N4O3 |
Mol. Mass. | 338.3605 |
SMILES | COc1cc(Nc2nccc(n2)-c2cccnc2)cc(OC)c1OC |
Structure |
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