Reaction Details |
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Target | M-phase inducer phosphatase 2 |
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Ligand | BDBM50351777 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_765399 (CHEMBL1828247) |
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IC50 | 8440±n/a nM |
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Citation | Sun, LP; Shen, Q; Piao, HH; Ma, WP; Gao, LX; Zhang, W; Nan, FJ; Li, J; Piao, HR Synthesis and biological evaluation of (±)-3-(2-(2-fluorobenzyloxy) naphthalen-6-yl)-2-aminopropanoic acid derivatives as novel PTP1B inhibitors. Eur J Med Chem46:3630-8 (2011) [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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BDBM50351777 |
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n/a |
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Name | BDBM50351777 |
Synonyms: | CHEMBL1823755 |
Type | Small organic molecule |
Emp. Form. | C28H23ClFNO4 |
Mol. Mass. | 491.938 |
SMILES | OC(=O)C(Cc1ccc2cc(OCc3ccccc3F)ccc2c1)NC(=O)Cc1ccc(Cl)cc1 |
Structure |
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