Reaction Details |
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Target | CviR transcriptional regulator |
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Ligand | BDBM50136221 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1547614 (CHEMBL3755484) |
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IC50 | 66080±n/a nM |
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Citation | Bucio-Cano, A; Reyes-Arellano, A; Correa-Basurto, J; Bello, M; Torres-Jaramillo, J; Salgado-Zamora, H; Curiel-Quesada, E; Peralta-Cruz, J; Avila-Sorrosa, A Targeting quorum sensing by designing azoline derivatives to inhibit the N-hexanoyl homoserine lactone-receptor CviR: Synthesis as well as biological and theoretical evaluations. Bioorg Med Chem23:7565-77 (2015) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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CviR transcriptional regulator |
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Name: | CviR transcriptional regulator |
Synonyms: | n/a |
Type: | PROTEIN |
Mol. Mass.: | 29723.76 |
Organism: | Chromobacterium violaceum |
Description: | ChEMBL_765227 |
Residue: | 265 |
Sequence: | MVISKPINARPLPAGLTASQQWTLLEWIHMAGHIETENELKAFLDQVLSQAPSERLLLAL
GRLNNQNQIQRLERVLNVSYPSDWLDQYMKENYAQHDPILRIHLGQGPVMWEERFNRAKG
AEEKRFIAEATQNGMGSGITFSAASERNNIGSILSIAGREPGRNAALVAMLNCLTPHLHQ
AAIRVANLPPASPSNMPLSQREYDIFHWMSRGKTNWEIATILDISERTVKFHVANVIRKL
NANNRTHAIVLGMHLAMPPSTVANE
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BDBM50136221 |
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n/a |
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Name | BDBM50136221 |
Synonyms: | CHEMBL3754734 |
Type | Small organic molecule |
Emp. Form. | C17H17N3O2 |
Mol. Mass. | 295.3358 |
SMILES | O=C(COc1ccc(cc1)C1=NCCN1)Nc1ccccc1 |t:11| |
Structure |
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