| Reaction Details |
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 | Report a problem with these data |
| Target | UDP-glucuronosyltransferase 2B7 |
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| Ligand | BDBM21361 |
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| Substrate/Competitor | Diclofenac |
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| Meas. Tech. | UDP-glucuronosyltransferase Activity Assay |
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| IC50 | >3.00e+5±n/a nM |
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| Citation |  Liu, Y; She, M; Wu, Z; Dai, R The inhibition study of human UDP-glucuronosyltransferases with cytochrome P450 selective substrates and inhibitors. J Enzyme Inhib Med Chem26:386-93 (2011) [PubMed] Article |
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| More Info.: | Get all data from this article, Assay Method |
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| UDP-glucuronosyltransferase 2B7 |
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| Name: | UDP-glucuronosyltransferase 2B7 |
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| Synonyms: | 2.4.1.17 | 3,4-catechol estrogen-specific UDPGT | UD2B7_HUMAN | UDP-glucuronosyltransferase 2B7 | UDP-glucuronosyltransferase 2B9 | UDPGT 2B7 | UDPGT 2B9 | UDPGTh-2 | UGT2B7 | UGTB2B9 | Uridine-5'-diphosphoglucuronosyltransferase 2B7 |
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| Type: | Enzyme |
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| Mol. Mass.: | 60705.98 |
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| Organism: | Homo sapiens (Human) |
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| Description: | P16662 |
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| Residue: | 529 |
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| Sequence: | MSVKWTSVILLIQLSFCFSSGNCGKVLVWAAEYSHWMNIKTILDELIQRGHEVTVLASSA
SILFDPNNSSALKIEIYPTSLTKTELENFIMQQIKRWSDLPKDTFWLYFSQVQEIMSIFG
DITRKFCKDVVSNKKFMKKVQESRFDVIFADAIFPCSELLAELFNIPFVYSLSFSPGYTF
EKHSGGFIFPPSYVPVVMSELTDQMTFMERVKNMIYVLYFDFWFEIFDMKKWDQFYSEVL
GRPTTLSETMGKADVWLIRNSWNFQFPYPLLPNVDFVGGLHCKPAKPLPKEMEDFVQSSG
ENGVVVFSLGSMVSNMTEERANVIASALAQIPQKVLWRFDGNKPDTLGLNTRLYKWIPQN
DLLGHPKTRAFITHGGANGIYEAIYHGIPMVGIPLFADQPDNIAHMKARGAAVRVDFNTM
SSTDLLNALKRVINDPSYKENVMKLSRIQHDQPVKPLDRAVFWIEFVMRHKGAKHLRVAA
HDLTWFQYHSLDVIGFLLVCVATVIFIVTKCCLFCFWKFARKAKKGKND
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| BDBM21361 |
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| Diclofenac |
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| Name | BDBM21361 |
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| Synonyms: | (5S)-5-Ethyl-3-methyl-5-phenyl-2,4-imidazolidinedione | (5S)-5-ethyl-3-methyl-5-phenylimidazolidine-2,4-dione | Mephenytoin, D- | S-Mephenytoin | S-mephentoin |
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| Type | Small organic molecule |
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| Emp. Form. | C12H14N2O2 |
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| Mol. Mass. | 218.2518 |
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| SMILES | CC[C@]1(NC(=O)N(C)C1=O)c1ccccc1 |
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| Structure | 
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