Reaction Details |
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Target | UDP-glucuronosyltransferase 2B7 |
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Ligand | BDBM50211742 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_436438 (CHEMBL904746) |
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IC50 | 4000±n/a nM |
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Citation | Bichlmaier, I; Kurkela, M; Joshi, T; Siiskonen, A; Rüffer, T; Lang, H; Suchanova, B; Vahermo, M; Finel, M; Yli-Kauhaluoma, J Isoform-selective inhibition of the human UDP-glucuronosyltransferase 2B7 by isolongifolol derivatives. J Med Chem50:2655-64 (2007) [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 |
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 |
Type: | Enzyme |
Mol. Mass.: | 60705.98 |
Organism: | Homo sapiens (Human) |
Description: | P16662 |
Residue: | 529 |
Sequence: | MSVKWTSVILLIQLSFCFSSGNCGKVLVWAAEYSHWMNIKTILDELIQRGHEVTVLASSA
SILFDPNNSSALKIEIYPTSLTKTELENFIMQQIKRWSDLPKDTFWLYFSQVQEIMSIFG
DITRKFCKDVVSNKKFMKKVQESRFDVIFADAIFPCSELLAELFNIPFVYSLSFSPGYTF
EKHSGGFIFPPSYVPVVMSELTDQMTFMERVKNMIYVLYFDFWFEIFDMKKWDQFYSEVL
GRPTTLSETMGKADVWLIRNSWNFQFPYPLLPNVDFVGGLHCKPAKPLPKEMEDFVQSSG
ENGVVVFSLGSMVSNMTEERANVIASALAQIPQKVLWRFDGNKPDTLGLNTRLYKWIPQN
DLLGHPKTRAFITHGGANGIYEAIYHGIPMVGIPLFADQPDNIAHMKARGAAVRVDFNTM
SSTDLLNALKRVINDPSYKENVMKLSRIQHDQPVKPLDRAVFWIEFVMRHKGAKHLRVAA
HDLTWFQYHSLDVIGFLLVCVATVIFIVTKCCLFCFWKFARKAKKGKND
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BDBM50211742 |
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n/a |
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Name | BDBM50211742 |
Synonyms: | CHEMBL226459 | dimethyl {(3S)-3-hydroxy-3-[(1R,2S,7S,8S,9S)-3,3,7-trimethyltricyclo[5.4.0.02,9]undec-8-yl]propyl}phosphonate |
Type | Small organic molecule |
Emp. Form. | C19H35O4P |
Mol. Mass. | 358.4526 |
SMILES | COP(=O)(CC[C@H](O)[C@H]1[C@H]2CC[C@@H]3[C@H]2C(C)(C)CCC[C@]13C)OC |TLB:6:8:10.11:13,THB:19:20:10.11:13,14:13:10.11:8.20,21:20:10.11:13| |
Structure |
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