Reaction Details |
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Target | Phosphomannomutase 2 |
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Ligand | BDBM44461 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_747526 (CHEMBL1777060) |
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IC50 | 9100±n/a nM |
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Citation | Dahl, R; Bravo, Y; Sharma, V; Ichikawa, M; Dhanya, RP; Hedrick, M; Brown, B; Rascon, J; Vicchiarelli, M; Mangravita-Novo, A; Yang, L; Stonich, D; Su, Y; Smith, LH; Sergienko, E; Freeze, HH; Cosford, ND Potent, selective, and orally available benzoisothiazolone phosphomannose isomerase inhibitors as probes for congenital disorder of glycosylation Ia. J Med Chem54:3661-8 (2011) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Phosphomannomutase 2 |
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Name: | Phosphomannomutase 2 |
Synonyms: | PMM2 | PMM2_HUMAN |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 28082.33 |
Organism: | Homo sapiens (Human) |
Description: | gi_4557839 |
Residue: | 246 |
Sequence: | MAAPGPALCLFDVDGTLTAPRQKITKEMDDFLQKLRQKIKIGVVGGSDFEKVQEQLGNDV
VEKYDYVFPENGLVAYKDGKLLCRQNIQSHLGEALIQDLINYCLSYIAKIKLPKKRGTFI
EFRNGMLNVSPIGRSCSQEERIEFYELDKKENIRQKFVADLRKEFAGKGLTFSIGGQISF
DVFPDGWDKRYCLRHVENDGYKTIYFFGDKTMPGGNDHEIFTDPRTMGYSVTAPEDTRRI
CELLFS
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BDBM44461 |
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n/a |
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Name | BDBM44461 |
Synonyms: | 5-[(2-methoxyphenyl)-oxomethoxy]-1-phenyl-3-pyrazolecarboxylic acid ethyl ester | 5-o-anisoyloxy-1-phenyl-pyrazole-3-carboxylic acid ethyl ester | MLS000538601 | SMR000144638 | cid_1256813 | ethyl 5-(2-methoxybenzoyl)oxy-1-phenylpyrazole-3-carboxylate | ethyl 5-(2-methoxyphenyl)carbonyloxy-1-phenyl-pyrazole-3-carboxylate | ethyl 5-[(2-methoxybenzoyl)oxy]-1-phenyl-1H-pyrazole-3-carboxylate |
Type | Small organic molecule |
Emp. Form. | C20H18N2O5 |
Mol. Mass. | 366.3673 |
SMILES | CCOC(=O)c1cc(OC(=O)c2ccccc2OC)n(n1)-c1ccccc1 |
Structure |
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