Reaction Details |
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Target | Tyrosine-protein kinase Lck |
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Ligand | BDBM50120090 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_96910 |
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IC50 | 2±n/a nM |
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Citation | Chen, P; Iwanowicz, EJ; Norris, D; Gu, HH; Lin, J; Moquin, RV; Das, J; Wityak, J; Spergel, SH; de Fex, H; Pang, S; Pitt, S; Shen, DR; Schieven, GL; Barrish, JC Synthesis and SAR of novel imidazoquinoxaline-based Lck inhibitors: improvement of cell potency. Bioorg Med Chem Lett12:3153-6 (2002) [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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BDBM50120090 |
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n/a |
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Name | BDBM50120090 |
Synonyms: | CHEMBL108686 | N*4*-(2-Chloro-6-methyl-phenyl)-N*8*,N*8*-diethyl-imidazo[1,5-a]quinoxaline-4,8-diamine | N4-(2-chloro-6-methylphenyl)-N8,N8-diethylimidazo[1,5-a]quinoxaline-4,8-diamine |
Type | Small organic molecule |
Emp. Form. | C21H22ClN5 |
Mol. Mass. | 379.886 |
SMILES | CCN(CC)c1ccc2nc(Nc3c(C)cccc3Cl)c3cncn3c2c1 |
Structure |
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