Reaction Details |
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Target | Enoyl-acyl carrier reductase ENR |
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Ligand | BDBM50431920 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_953658 (CHEMBL2352562) |
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IC50 | 58±n/a nM |
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Citation | Cheng, G; Muench, SP; Zhou, Y; Afanador, GA; Mui, EJ; Fomovska, A; Lai, BS; Prigge, ST; Woods, S; Roberts, CW; Hickman, MR; Lee, PJ; Leed, SE; Auschwitz, JM; Rice, DW; McLeod, R Design, synthesis, and biological activity of diaryl ether inhibitors of Toxoplasma gondii enoyl reductase. Bioorg Med Chem Lett23:2035-43 (2013) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Enoyl-acyl carrier reductase ENR |
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Name: | Enoyl-acyl carrier reductase ENR |
Synonyms: | Enoyl-acyl carrier reductase | Enoyl-acyl carrier reductase (ENR) | Enoyl-acyl carrier reductase, putative |
Type: | PROTEIN |
Mol. Mass.: | 43663.67 |
Organism: | Toxoplasma gondii |
Description: | ChEMBL_1290812 |
Residue: | 417 |
Sequence: | MVGFKLLTLGAFVAGELTLVGPAGTMAFTVPNATGAKPLVTSVSVRPSWSSARQNAFSSS
SSRSQSSVRPHSAFVTNRLETAGETGTQHRAADSAAGVGAAQSAFPIDLRGQTAFVAGVA
DSHGYGWAIAKHLASAGARVALGTWPPVLGLFQKSLQSGRLDEDRKLPDGSLIEFAGVYP
LDAAFDKPEDVPQDIKDNKRYAGVDGYTIKEVAVKVKQDLGNIDILVHSLANGPEVTKPL
LETSRKGYLAASSNSAYSFVSLLQHFGPIMNEGGSAVTLSYLAAERVVPGYGGGMSSAKA
ALESDTRTLAWEAGQKYGVRVNAISAGPLKSRAASAIGKSGEKSFIDYAIDYSYNNAPLR
RDLHSDDVGGAALFLLSPLARAVSGVTLYVDNGLHAMGQAVDSRSMPPLQRATQEIN
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BDBM50431920 |
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n/a |
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Name | BDBM50431920 |
Synonyms: | 5‐(4‐chloro‐2‐hydroxyphenoxy)‐N‐(5‐methyl‐1,2‐ oxazol‐3‐yl)furan‐2‐carboxamide (32) | CHEMBL2347835 |
Type | Small organic molecule |
Emp. Form. | C15H11ClN2O5 |
Mol. Mass. | 334.711 |
SMILES | Cc1cc(NC(=O)c2ccc(Oc3ccc(Cl)cc3O)o2)no1 |
Structure |
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