Reaction Details |
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Target | Transcriptional activator protein LuxR |
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Ligand | BDBM50262517 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_490917 (CHEMBL989193) |
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IC50 | 6900±n/a nM |
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Citation | Estephane, J; Dauvergne, J; Soulère, L; Reverchon, S; Queneau, Y; Doutheau, A N-Acyl-3-amino-5H-furanone derivatives as new inhibitors of LuxR-dependent quorum sensing: Synthesis, biological evaluation and binding mode study. Bioorg Med Chem Lett18:4321-4 (2008) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Transcriptional activator protein LuxR |
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Name: | Transcriptional activator protein LuxR |
Synonyms: | LUXR_ALIFS | luxR |
Type: | PROTEIN |
Mol. Mass.: | 28563.86 |
Organism: | Vibrio fischeri |
Description: | ChEMBL_831639 |
Residue: | 250 |
Sequence: | MKNINADDTYRIINKIKACRSNNDINQCLSDMTKMVHCEYYLLAIIYPHSMVKSDISILD
NYPKKWRQYYDDANLIKYDPIVDYSNSNHSPINWNIFENNAVNKKSPNVIKEAKTSGLIT
GFSFPIHTANNGFGMLSFAHSEKDNYIDSLFLHACMNIPLIVPSLVDNYRKINIANNKSN
NDLTKREKECLAWACEGKSSWDISKILGCSERTVTFHLTNAQMKLNTTNRCQSISKAILT
GAIDCPYFKN
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BDBM50262517 |
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n/a |
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Name | BDBM50262517 |
Synonyms: | CHEMBL448263 | N-(4-chloro-2-oxo-2,5-dihydrofuran-3-yl)hexanamide |
Type | Small organic molecule |
Emp. Form. | C10H14ClNO3 |
Mol. Mass. | 231.676 |
SMILES | CCCCCC(=O)NC1=C(Cl)COC1=O |c:8| |
Structure |
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