| Reaction Details |
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 | Report a problem with these data |
| Target | Tyrosine-protein kinase Srms |
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| Ligand | BDBM50269557 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | ChEMBL_1706739 (CHEMBL4057972) |
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| IC50 | 84±n/a nM |
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| Citation |  Boga, SB; Alhassan, AB; Liu, J; Guiadeen, D; Krikorian, A; Gao, X; Wang, J; Yu, Y; Anand, R; Liu, S; Yang, C; Wu, H; Cai, J; Zhu, H; Desai, J; Maloney, K; Gao, YD; Fischmann, TO; Presland, J; Mansueto, M; Xu, Z; Leccese, E; Knemeyer, I; Garlisi, CG; Bays, N; Stivers, P; Brandish, PE; Hicks, A; Cooper, A; Kim, RM; Kozlowski, JA Discovery of 3-morpholino-imidazole[1,5-a]pyrazine BTK inhibitors for rheumatoid arthritis. Bioorg Med Chem Lett27:3939-3943 (2017) [PubMed] Article |
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| More Info.: | Get all data from this article, Assay Method |
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| Tyrosine-protein kinase Srms |
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| Name: | Tyrosine-protein kinase Srms |
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| Synonyms: | C20orf148 | SRC | SRMS | SRMS_HUMAN |
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| Type: | Enzyme Catalytic Domain |
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| Mol. Mass.: | 54517.24 |
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| Organism: | Homo sapiens (Human) |
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| Description: | gi_18250298 |
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| Residue: | 488 |
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| Sequence: | MEPFLRRRLAFLSFFWDKIWPAGGEPDHGTPGSLDPNTDPVPTLPAEPCSPFPQLFLALY
DFTARCGGELSVRRGDRLCALEEGGGYIFARRLSGQPSAGLVPITHVAKASPETLSDQPW
YFSGVSRTQAQQLLLSPPNEPGAFLIRPSESSLGGYSLSVRAQAKVCHYRVSMAADGSLY
LQKGRLFPGLEELLTYYKANWKLIQNPLLQPCMPQKAPRQDVWERPHSEFALGRKLGEGY
FGEVWEGLWLGSLPVAIKVIKSANMKLTDLAKEIQTLKGLRHERLIRLHAVCSGGEPVYI
VTELMRKGNLQAFLGTPEGRALRLPPLLGFACQVAEGMSYLEEQRVVHRDLAARNVLVDD
GLACKVADFGLARLLKDDIYSPSSSSKIPVKWTAPEAANYRVFSQKSDVWSFGVLLHEVF
TYGQCPYEGMTNHETLQQIMRGYRLPRPAACPAEVYVLMLECWRSSPEERPSFATLREKL
HAIHRCHP
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| BDBM50269557 |
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| n/a |
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| Name | BDBM50269557 |
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| Synonyms: | CHEMBL4069387 |
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| Type | Small organic molecule |
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| Emp. Form. | C28H27F4N7O2 |
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| Mol. Mass. | 569.5533 |
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| SMILES | CC(C)C(=O)N1CCC[C@H](C1)c1nc(-c2ccc(cc2F)C(=O)Nc2cc(ccn2)C(F)(F)F)c2c(N)nccn12 |r| |
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| Structure | 
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