| Reaction Details |
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 | Report a problem with these data |
| Target | Phosphomannomutase 2 |
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| Ligand | BDBM44450 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | ChEMBL_747526 (CHEMBL1777060) |
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| IC50 | >20000±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 |
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| Synonyms: | PMM2 | PMM2_HUMAN |
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| Type: | Enzyme Catalytic Domain |
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| Mol. Mass.: | 28082.33 |
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| Organism: | Homo sapiens (Human) |
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| Description: | gi_4557839 |
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| Residue: | 246 |
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| Sequence: | MAAPGPALCLFDVDGTLTAPRQKITKEMDDFLQKLRQKIKIGVVGGSDFEKVQEQLGNDV
VEKYDYVFPENGLVAYKDGKLLCRQNIQSHLGEALIQDLINYCLSYIAKIKLPKKRGTFI
EFRNGMLNVSPIGRSCSQEERIEFYELDKKENIRQKFVADLRKEFAGKGLTFSIGGQISF
DVFPDGWDKRYCLRHVENDGYKTIYFFGDKTMPGGNDHEIFTDPRTMGYSVTAPEDTRRI
CELLFS
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| BDBM44450 |
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| n/a |
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| Name | BDBM44450 |
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| Synonyms: | (3,5-dimethylpyrazol-1-yl)methyl-[4-(trifluoromethyl)thiazol-2-yl]amine | MLS000085296 | N-[(3,5-dimethyl-1-pyrazolyl)methyl]-4-(trifluoromethyl)-2-thiazolamine | N-[(3,5-dimethyl-1H-pyrazol-1-yl)methyl]-4-(trifluoromethyl)-1,3-thiazol-2-amine | N-[(3,5-dimethylpyrazol-1-yl)methyl]-4-(trifluoromethyl)-1,3-thiazol-2-amine | SMR000020034 | cid_3244409 |
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| Type | Small organic molecule |
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| Emp. Form. | C10H11F3N4S |
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| Mol. Mass. | 276.281 |
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| SMILES | Cc1cc(C)n(CNc2nc(cs2)C(F)(F)F)n1 |
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| Structure | 
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