Reaction Details |
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Target | Proto-oncogene tyrosine-protein kinase LCK |
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Ligand | BDBM13222 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_221476 |
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IC50 | 720±n/a nM |
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Citation | Wityak, J; Das, J; Moquin, RV; Shen, Z; Lin, J; Chen, P; Doweyko, AM; Pitt, S; Pang, S; Shen, DR; Fang, Q; de Fex, HF; Schieven, GL; Kanner, SB; Barrish, JC Discovery and initial SAR of 2-amino-5-carboxamidothiazoles as inhibitors of the Src-family kinase p56(Lck). Bioorg Med Chem Lett13:4007-10 (2003) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Proto-oncogene tyrosine-protein kinase LCK |
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Name: | Proto-oncogene tyrosine-protein kinase LCK |
Synonyms: | LCK_MOUSE | LSK | Lck | Lsk-t | Lymphocyte cell-specific protein-tyrosine kinase | Proto-oncogene tyrosine-protein kinase LCK | Tyrosine-protein kinase LCK | p56-LCK |
Type: | PROTEIN |
Mol. Mass.: | 57927.84 |
Organism: | Mus musculus |
Description: | ChEMBL_806408 |
Residue: | 509 |
Sequence: | MGCVCSSNPEDDWMENIDVCENCHYPIVPLDSKISLPIRNGSEVRDPLVTYEGSLPPASP
LQDNLVIALHSYEPSHDGDLGFEKGEQLRILEQSGEWWKAQSLTTGQEGFIPFNFVAKAN
SLEPEPWFFKNLSRKDAERQLLAPGNTHGSFLIRESESTAGSFSLSVRDFDQNQGEVVKH
YKIRNLDNGGFYISPRITFPGLHDLVRHYTNASDGLCTKLSRPCQTQKPQKPWWEDEWEV
PRETLKLVERLGAGQFGEVWMGYYNGHTKVAVKSLKQGSMSPDAFLAEANLMKQLQHPRL
VRLYAVVTQEPIYIITEYMENGSLVDFLKTPSGIKLNVNKLLDMAAQIAEGMAFIEEQNY
IHRDLRAANILVSDTLSCKIADFGLARLIEDNEYTAREGAKFPIKWTAPEAINYGTFTIK
SDVWSFGILLTEIVTHGRIPYPGMTNPEVIQNLERGYRMVRPDNCPEELYHLMMLCWKER
PEDRPTFDYLRSVLDDFFTATEGQYQPQP
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BDBM13222 |
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n/a |
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Name | BDBM13222 |
Synonyms: | 2-[[(Methoxy)carbonyl]-amino]-4-methyl-N-(2,4,6-trimethylphenyl)-1,3-thiazole-5-carboxamide | BMS-354825 2-Amino-4-methyl-thiazole Analog 7a | CHEMBL128589 | methyl N-{4-methyl-5-[(2,4,6-trimethylphenyl)carbamoyl]-1,3-thiazol-2-yl}carbamate |
Type | Small organic molecule |
Emp. Form. | C16H19N3O3S |
Mol. Mass. | 333.405 |
SMILES | COC(=O)Nc1nc(C)c(s1)C(=O)Nc1c(C)cc(C)cc1C |
Structure |
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