Reaction Details |
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Target | Tyrosine-protein kinase TXK |
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Ligand | BDBM50381092 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_814176 (CHEMBL2020890) |
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IC50 | 73.8±n/a nM |
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Citation | McLean, LR; Zhang, Y; Zaidi, N; Bi, X; Wang, R; Dharanipragada, R; Jurcak, JG; Gillespy, TA; Zhao, Z; Musick, KY; Choi, YM; Barrague, M; Peppard, J; Smicker, M; Duguid, M; Parkar, A; Fordham, J; Kominos, D X-ray crystallographic structure-based design of selective thienopyrazole inhibitors for interleukin-2-inducible tyrosine kinase. Bioorg Med Chem Lett22:3296-300 (2012) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Tyrosine-protein kinase TXK |
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Name: | Tyrosine-protein kinase TXK |
Synonyms: | PTK4 | Protein-tyrosine kinase 4 | RLK | Resting lymphocyte kinase | TXK | TXK_HUMAN | Tyrosine-protein kinase TXK (TXK) |
Type: | Protein |
Mol. Mass.: | 61268.80 |
Organism: | Homo sapiens (Human) |
Description: | P42681 |
Residue: | 527 |
Sequence: | MILSSYNTIQSVFCCCCCCSVQKRQMRTQISLSTDEELPEKYTQRRRPWLSQLSNKKQSN
TGRVQPSKRKPLPPLPPSEVAEEKIQVKALYDFLPREPCNLALRRAEEYLILEKYNPHWW
KARDRLGNEGLIPSNYVTENKITNLEIYEWYHRNITRNQAEHLLRQESKEGAFIVRDSRH
LGSYTISVFMGARRSTEAAIKHYQIKKNDSGQWYVAERHAFQSIPELIWYHQHNAAGLMT
RLRYPVGLMGSCLPATAGFSYEKWEIDPSELAFIKEIGSGQFGVVHLGEWRSHIQVAIKA
INEGSMSEEDFIEEAKVMMKLSHSKLVQLYGVCIQRKPLYIVTEFMENGCLLNYLRENKG
KLRKEMLLSVCQDICEGMEYLERNGYIHRDLAARNCLVSSTCIVKISDFGMTRYVLDDEY
VSSFGAKFPIKWSPPEVFLFNKYSSKSDVWSFGVLMWEVFTEGKMPFENKSNLQVVEAIS
EGFRLYRPHLAPMSIYEVMYSCWHEKPEGRPTFAELLRAVTEIAETW
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BDBM50381092 |
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n/a |
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Name | BDBM50381092 |
Synonyms: | CHEMBL2017552 |
Type | Small organic molecule |
Emp. Form. | C16H15N3OS |
Mol. Mass. | 297.375 |
SMILES | CC(C)(O)c1ccc2cc([nH]c2c1)-c1n[nH]c2ccsc12 |
Structure |
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