Reaction Details |
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Target | Tyrosine-protein phosphatase non-receptor type 6 |
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Ligand | BDBM50351780 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_765400 (CHEMBL1828248) |
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pH | 8±n/a |
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IC50 | 2430±n/a nM |
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Comments | extracted |
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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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Tyrosine-protein phosphatase non-receptor type 6 |
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Name: | Tyrosine-protein phosphatase non-receptor type 6 |
Synonyms: | HCP | PTN6_HUMAN | PTP1C | PTPN6 | Protein tyrosine phosphatase SHP-1 (SHP-1) | Protein-tyrosine phosphatase 1C | Protein-tyrosine phosphatase SHP-1 | Src homology phosphatase 1 (SHP-1) | Tyrosine-protein phosphatase non-receptor type 6 | Tyrosine-protein phosphatase non-receptor type 6 (SHP1) |
Type: | Protein |
Mol. Mass.: | 67570.41 |
Organism: | Homo sapiens (Human) |
Description: | P29350 |
Residue: | 595 |
Sequence: | MVRWFHRDLSGLDAETLLKGRGVHGSFLARPSRKNQGDFSLSVRVGDQVTHIRIQNSGDF
YDLYGGEKFATLTELVEYYTQQQGVLQDRDGTIIHLKYPLNCSDPTSERWYHGHMSGGQA
ETLLQAKGEPWTFLVRESLSQPGDFVLSVLSDQPKAGPGSPLRVTHIKVMCEGGRYTVGG
LETFDSLTDLVEHFKKTGIEEASGAFVYLRQPYYATRVNAADIENRVLELNKKQESEDTA
KAGFWEEFESLQKQEVKNLHQRLEGQRPENKGKNRYKNILPFDHSRVILQGRDSNIPGSD
YINANYIKNQLLGPDENAKTYIASQGCLEATVNDFWQMAWQENSRVIVMTTREVEKGRNK
CVPYWPEVGMQRAYGPYSVTNCGEHDTTEYKLRTLQVSPLDNGDLIREIWHYQYLSWPDH
GVPSEPGGVLSFLDQINQRQESLPHAGPIIVHCSAGIGRTGTIIVIDMLMENISTKGLDC
DIDIQKTIQMVRAQRSGMVQTEAQYKFIYVAIAQFIETTKKKLEVLQSQKGQESEYGNIT
YPPAMKNAHAKASRTSSKHKEDVYENLHTKNKREEKVKKQRSADKEKSKGSLKRK
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BDBM50351780 |
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n/a |
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Name | BDBM50351780 |
Synonyms: | CHEMBL1823762 |
Type | Small organic molecule |
Emp. Form. | C29H23ClFNO4 |
Mol. Mass. | 503.949 |
SMILES | OC(=O)C(Cc1ccc2cc(OCc3ccccc3F)ccc2c1)NC(=O)\C=C\c1ccccc1Cl |
Structure |
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