Reaction Details |
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Target | UDP-glucuronosyltransferase 1A1 |
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Ligand | BDBM50599144 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_2228974 (CHEMBL5142487) |
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IC50 | 2100±n/a nM |
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Citation | A M Subbaiah, M; Subramani, L; Ramar, T; Desai, S; Sinha, S; Mandlekar, S; Kadow, JF; Jenkins, S; Krystal, M; Subramanian, M; Sridhar, S; Padmanabhan, S; Bhutani, P; Arla, R; Meanwell, NA Improving Drug Delivery While Tailoring Prodrug Activation to Modulate J Med Chem65:11150-11176 (2022) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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UDP-glucuronosyltransferase 1A1 |
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Name: | UDP-glucuronosyltransferase 1A1 |
Synonyms: | Bilirubin-specific UDPGT isozyme 1 | GNT1 | UD11_HUMAN | UDP-glucuronosyltransferase 1-1 | UDP-glucuronosyltransferase 1-A | UDP-glucuronosyltransferase 1A1 | UDPGT 1-1 | UGT-1A | UGT1 | UGT1*1 | UGT1-01 | UGT1.1 | UGT1A | UGT1A1 | Uridine-5'-diphosphoglucuronosyltransferase 1A1 | hUG-BR1 |
Type: | Enzyme |
Mol. Mass.: | 59604.34 |
Organism: | Homo sapiens (Human) |
Description: | P22309 |
Residue: | 533 |
Sequence: | MAVESQGGRPLVLGLLLCVLGPVVSHAGKILLIPVDGSHWLSMLGAIQQLQQRGHEIVVL
APDASLYIRDGAFYTLKTYPVPFQREDVKESFVSLGHNVFENDSFLQRVIKTYKKIKKDS
AMLLSGCSHLLHNKELMASLAESSFDVMLTDPFLPCSPIVAQYLSLPTVFFLHALPCSLE
FEATQCPNPFSYVPRPLSSHSDHMTFLQRVKNMLIAFSQNFLCDVVYSPYATLASEFLQR
EVTVQDLLSSASVWLFRSDFVKDYPRPIMPNMVFVGGINCLHQNPLSQEFEAYINASGEH
GIVVFSLGSMVSEIPEKKAMAIADALGKIPQTVLWRYTGTRPSNLANNTILVKWLPQNDL
LGHPMTRAFITHAGSHGVYESICNGVPMVMMPLFGDQMDNAKRMETKGAGVTLNVLEMTS
EDLENALKAVINDKSYKENIMRLSSLHKDRPVEPLDLAVFWVEFVMRHKGAPHLRPAAHD
LTWYQYHSLDVIGFLLAVVLTVAFITFKCCAYGYRKCLGKKGRVKKAHKSKTH
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BDBM50599144 |
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n/a |
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Name | BDBM50599144 |
Synonyms: | CHEMBL5179012 |
Type | Small organic molecule |
Emp. Form. | C48H69N7O11 |
Mol. Mass. | 920.1018 |
SMILES | COC(=O)N[C@H](C(=O)N[C@@H](Cc1ccccc1)[C@H](CN(Cc1ccc(cc1)-c1ccccn1)NC(=O)[C@@H](NC(=O)OC)C(C)(C)C)OC(=O)OC(OC(=O)[C@H](N)C(C)C)C(C)C)C(C)(C)C |r| |
Structure |
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