Reaction Details |
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Target | 5'-AMP-activated protein kinase catalytic subunit alpha-1 |
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Ligand | BDBM50123803 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1518900 (CHEMBL3625824) |
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IC50 | >10000±n/a nM |
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Citation | Lin, XD; Yang, HW; Ma, S; Li, WW; Zhang, CH; Wang, WJ; Xiang, R; Li, LL; Yang, SY Discovery of 6-phenylimidazo[2,1-b]thiazole derivatives as a new type of FLT3 inhibitors. Bioorg Med Chem Lett25:4534-8 (2015) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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5'-AMP-activated protein kinase catalytic subunit alpha-1 |
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Name: | 5'-AMP-activated protein kinase catalytic subunit alpha-1 |
Synonyms: | AAPK1_HUMAN | ACACA kinase | AMP-activated protein kinase alpha-1/beta-2/gamma-2 | AMP-activated protein kinase, alpha-1 subunit | AMPK subunit alpha-1 | AMPK-alpha1 | AMPK1 | Hydroxymethylglutaryl-CoA reductase kinase | PRKAA1 | Tau-protein kinase PRKAA1 |
Type: | Protein |
Mol. Mass.: | 64023.62 |
Organism: | Homo sapiens (Human) |
Description: | Q13131 |
Residue: | 559 |
Sequence: | MRRLSSWRKMATAEKQKHDGRVKIGHYILGDTLGVGTFGKVKVGKHELTGHKVAVKILNR
QKIRSLDVVGKIRREIQNLKLFRHPHIIKLYQVISTPSDIFMVMEYVSGGELFDYICKNG
RLDEKESRRLFQQILSGVDYCHRHMVVHRDLKPENVLLDAHMNAKIADFGLSNMMSDGEF
LRTSCGSPNYAAPEVISGRLYAGPEVDIWSSGVILYALLCGTLPFDDDHVPTLFKKICDG
IFYTPQYLNPSVISLLKHMLQVDPMKRATIKDIREHEWFKQDLPKYLFPEDPSYSSTMID
DEALKEVCEKFECSEEEVLSCLYNRNHQDPLAVAYHLIIDNRRIMNEAKDFYLATSPPDS
FLDDHHLTRPHPERVPFLVAETPRARHTLDELNPQKSKHQGVRKAKWHLGIRSQSRPNDI
MAEVCRAIKQLDYEWKVVNPYYLRVRRKNPVTSTYSKMSLQLYQVDSRTYLLDFRSIDDE
ITEAKSGTATPQRSGSVSNYRSCQRSDSDAEAQGKSSEVSLTSSVTSLDSSPVDLTPRPG
SHTIEFFEMCANLIKILAQ
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BDBM50123803 |
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n/a |
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Name | BDBM50123803 |
Synonyms: | CHEMBL3623375 |
Type | Small organic molecule |
Emp. Form. | C25H31N7O3S |
Mol. Mass. | 509.624 |
SMILES | CN(C)CCCNC(=O)c1csc2nc(cn12)-c1ccc(NC(=O)Nc2cc(on2)C(C)(C)C)cc1 |
Structure |
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