Reaction Details |
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Target | M-phase inducer phosphatase 1 |
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Ligand | BDBM50261055 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_552280 (CHEMBL995610) |
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IC50 | >100000±n/a nM |
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Citation | Shimazawa, R; Kuriyama, M; Shirai, R Design and synthesis of N-alkyl oxindolylidene acetic acids as a new class of potent Cdc25A inhibitors. Bioorg Med Chem Lett18:3350-3 (2008) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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M-phase inducer phosphatase 1 |
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Name: | M-phase inducer phosphatase 1 |
Synonyms: | CDC25A | Dual specificity phosphatase (Cdc25A) | Dual specificity phosphatase Cdc25A | M-phase inducer phosphatase 1 | MPIP1_HUMAN | phosphatase Cdc25 |
Type: | Protein |
Mol. Mass.: | 59090.18 |
Organism: | Homo sapiens (Human) |
Description: | P30304 |
Residue: | 524 |
Sequence: | MELGPEPPHRRRLLFACSPPPASQPVVKALFGASAAGGLSPVTNLTVTMDQLQGLGSDYE
QPLEVKNNSNLQRMGSSESTDSGFCLDSPGPLDSKENLENPMRRIHSLPQKLLGCSPALK
RSHSDSLDHDIFQLIDPDENKENEAFEFKKPVRPVSRGCLHSHGLQEGKDLFTQRQNSAP
ARMLSSNERDSSEPGNFIPLFTPQSPVTATLSDEDDGFVDLLDGENLKNEEETPSCMASL
WTAPLVMRTTNLDNRCKLFDSPSLCSSSTRSVLKRPERSQEESPPGSTKRRKSMSGASPK
ESTNPEKAHETLHQSLSLASSPKGTIENILDNDPRDLIGDFSKGYLFHTVAGKHQDLKYI
SPEIMASVLNGKFANLIKEFVIIDCRYPYEYEGGHIKGAVNLHMEEEVEDFLLKKPIVPT
DGKRVIVVFHCEFSSERGPRMCRYVRERDRLGNEYPKLHYPELYVLKGGYKEFFMKCQSY
CEPPSYRPMHHEDFKEDLKKFRTKSRTWAGEKSKREMYSRLKKL
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BDBM50261055 |
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n/a |
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Name | BDBM50261055 |
Synonyms: | (Z)-2-(1-hexyl-2-oxoindolin-3-ylidene)acetic acid | CHEMBL447811 |
Type | Small organic molecule |
Emp. Form. | C16H19NO3 |
Mol. Mass. | 273.327 |
SMILES | CCCCCCN1C(=O)\C(=C/C(O)=O)c2ccccc12 |
Structure |
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