Reaction Details |
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Target | Phospholipase C |
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Ligand | BDBM50332115 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_687789 (CHEMBL1291297) |
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Ki | 2500±n/a nM |
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Citation | González-Bulnes, P; González-Roura, A; Canals, D; Delgado, A; Casas, J; Llebaria, A 2-aminohydroxamic acid derivatives as inhibitors of Bacillus cereus phosphatidylcholine preferred phospholipase C PC-PLC(Bc). Bioorg Med Chem18:8549-55 (2010) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Phospholipase C |
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Name: | Phospholipase C |
Synonyms: | Cereolysin A | PHLC_BACCE | Phosphatidylcholine cholinephosphohydrolase | plc |
Type: | PROTEIN |
Mol. Mass.: | 32387.39 |
Organism: | Bacillus cereus |
Description: | ChEMBL_687786 |
Residue: | 283 |
Sequence: | MKKKVLALAAAITVVAPLQSVAFAHENDGGSKIKIVHRWSAEDKHKEGVNSHLWIVNRAI
DIMSRNTTLVKQDRVAQLNEWRTELENGIYAADYENPYYDNSTFASHFYDPDNGKTYIPF
AKQAKETGAKYFKLAGESYKNKDMKQAFFYLGLSLHYLGDVNQPMHAANFTNLSYPQGFH
SKYENFVDTIKDNYKVTDGNGYWNWKGTNPEEWIHGAAVVAKQDYSGIVNDNTKDWFVKA
AVSQEYADKWRAEVTPMTGKRLMDAQRVTAGYIQLWFDTYGDR
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BDBM50332115 |
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n/a |
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Name | BDBM50332115 |
Synonyms: | 3-(N-(benzyloxy)-2-(tert-butyloxycarbonylamino)dodecanamido-N,N,N-trimethylpropan-1-aminium iodide | CHEMBL1287946 |
Type | Small organic molecule |
Emp. Form. | C30H54N3O4 |
Mol. Mass. | 520.7669 |
SMILES | CCCCCCCCCCC(NC(=O)OC(C)(C)C)C(=O)N(CCC[N+](C)(C)C)OCc1ccccc1 |
Structure |
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