Reaction Details |
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Target | Enoyl-acyl-carrier protein reductase |
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Ligand | BDBM50211885 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_436470 (CHEMBL904775) |
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Ki | 32±n/a nM |
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Citation | Kumar, G; Parasuraman, P; Sharma, SK; Banerjee, T; Karmodiya, K; Surolia, N; Surolia, A Discovery of a rhodanine class of compounds as inhibitors of Plasmodium falciparum enoyl-acyl carrier protein reductase. J Med Chem50:2665-75 (2007) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Enoyl-acyl-carrier protein reductase |
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Name: | Enoyl-acyl-carrier protein reductase |
Synonyms: | n/a |
Type: | PROTEIN |
Mol. Mass.: | 49770.86 |
Organism: | Plasmodium falciparum |
Description: | ChEMBL_795989 |
Residue: | 432 |
Sequence: | MNKISQRLLFLFLHFYTTVCFIQNNTQKTFHNVLQNEQIRGKEKAFYRKEKRENIFIGNK
MKHVHNMNNTHNNNHYMEKEEQDASNINKIKEENKNEDICFIAGIGDTNGYGWGIAKELS
KRNVKIIFGIWPPVYNIFMKNYKNGKFDNDMIIDKDKKMNILDMLPFDASFDTANDIDEE
TKNNKRYNMLQNYPIEDVANLIHQKYGKINMLVHSLANAKEVQKDLLNTSRKGYLDALSK
SSYSLISLCKYFVNIMKPQSSIISLTYHASQKVVPGYGGGMSSAKAALESDTRVLAYHLG
RNYNIRINTISAGPLKSRAATAINKLNNTYENNTNQNKNRNSHDVHNIMNNSGEKEEKKN
SASQNYTFIDYAIEYSEKYAPLRQKLLSTDIGSVASFLLSRESRAITGQTIYVDNGLNIM
FLPDDIYRNENE
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BDBM50211885 |
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n/a |
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Name | BDBM50211885 |
Synonyms: | 5-(3,4-dihydroxybenzylidene)-3-phenyl-2-thioxothiazolidin-4-one | CHEMBL228097 |
Type | Small organic molecule |
Emp. Form. | C16H11NO3S2 |
Mol. Mass. | 329.393 |
SMILES | Oc1ccc(\C=C2/SC(=S)N(C2=O)c2ccccc2)cc1O |
Structure |
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