Reaction Details |
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Target | Deoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial |
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Ligand | BDBM50386612 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_826232 (CHEMBL2049243) |
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IC50 | >1000±n/a nM |
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Citation | Miyakoshi, H; Miyahara, S; Yokogawa, T; Chong, KT; Taguchi, J; Endoh, K; Yano, W; Wakasa, T; Ueno, H; Takao, Y; Nomura, M; Shuto, S; Nagasawa, H; Fukuoka, M Synthesis and discovery of N-carbonylpyrrolidine- or N-sulfonylpyrrolidine-containing uracil derivatives as potent human deoxyuridine triphosphatase inhibitors. J Med Chem55:2960-9 (2012) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Deoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial |
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Name: | Deoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial |
Synonyms: | DUT | DUT_HUMAN | Deoxyuridine 5'-triphosphate nucleotidohydrolase (dUTPase) | Deoxyuridine triphosphatase (dUTPase) | dUTP pyrophosphatase |
Type: | Enzyme |
Mol. Mass.: | 26574.03 |
Organism: | Homo sapiens (Human) |
Description: | P33316 |
Residue: | 252 |
Sequence: | MTPLCPRPALCYHFLTSLLRSAMQNARGARQRAEAAVLSGPGPPLGRAAQHGIPRPLSSA
GRLSQGCRGASTVGAAGWKGELPKAGGSPAPGPETPAISPSKRARPAEVGGMQLRFARLS
EHATAPTRGSARAAGYDLYSAYDYTIPPMEKAVVKTDIQIALPSGCYGRVAPRSGLAAKH
FIDVGAGVIDEDYRGNVGVVLFNFGKEKFEVKKGDRIAQLICERIFYPEIEEVQALDDTE
RGSGGFGSTGKN
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BDBM50386612 |
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n/a |
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Name | BDBM50386612 |
Synonyms: | CHEMBL2048478 |
Type | Small organic molecule |
Emp. Form. | C24H25N3O4 |
Mol. Mass. | 419.473 |
SMILES | OC([C@@H]1CCCN1C(=O)CCn1ccc(=O)[nH]c1=O)(c1ccccc1)c1ccccc1 |r| |
Structure |
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