Reaction Details |
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Target | M-phase inducer phosphatase 2 |
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Ligand | BDBM50201807 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1625486 (CHEMBL3867955) |
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IC50 | 2470000±n/a nM |
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Citation | Meng, G; Zheng, M; Wang, M; Tong, J; Ge, W; Zhang, J; Zheng, A; Li, J; Gao, L; Li, J Design and synthesis of new potent PTP1B inhibitors with the skeleton of 2-substituted imino-3-substituted-5-heteroarylidene-1,3-thiazolidine-4-one: Part I. Eur J Med Chem122:756-769 (2016) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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M-phase inducer phosphatase 2 |
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Name: | M-phase inducer phosphatase 2 |
Synonyms: | CDC25B | CDC25HU2 | Dual specificity phosphatase (CDC25B) | Dual specificity phosphatase Cdc25B | M-phase inducer phosphatase 2 (CDC25B) | MPIP2_HUMAN |
Type: | Protein |
Mol. Mass.: | 64985.27 |
Organism: | Homo sapiens (Human) |
Description: | n/a |
Residue: | 580 |
Sequence: | MEVPQPEPAPGSALSPAGVCGGAQRPGHLPGLLLGSHGLLGSPVRAAASSPVTTLTQTMH
DLAGLGSETPKSQVGTLLFRSRSRLTHLSLSRRASESSLSSESSESSDAGLCMDSPSPMD
PHMAEQTFEQAIQAASRIIRNEQFAIRRFQSMPVRLLGHSPVLRNITNSQAPDGRRKSEA
GSGAASSSGEDKENDGFVFKMPWKPTHPSSTHALAEWASRREAFAQRPSSAPDLMCLSPD
RKMEVEELSPLALGRFSLTPAEGDTEEDDGFVDILESDLKDDDAVPPGMESLISAPLVKT
LEKEEEKDLVMYSKCQRLFRSPSMPCSVIRPILKRLERPQDRDTPVQNKRRRSVTPPEEQ
QEAEEPKARVLRSKSLCHDEIENLLDSDHRELIGDYSKAFLLQTVDGKHQDLKYISPETM
VALLTGKFSNIVDKFVIVDCRYPYEYEGGHIKTAVNLPLERDAESFLLKSPIAPCSLDKR
VILIFHCEFSSERGPRMCRFIRERDRAVNDYPSLYYPEMYILKGGYKEFFPQHPNFCEPQ
DYRPMNHEAFKDELKTFRLKTRSWAGERSRRELCSRLQDQ
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BDBM50201807 |
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n/a |
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Name | BDBM50201807 |
Synonyms: | CHEMBL3934071 |
Type | Small organic molecule |
Emp. Form. | C21H24N4O3S |
Mol. Mass. | 412.505 |
SMILES | CC(C)N1\C(S\C(=C/c2ccc(OCCN(C)c3ccccn3)cc2)C1=O)=N\O |
Structure |
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