Reaction Details |
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Target | Lipoxygenase |
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Ligand | BDBM22334 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Colorimetric 5-LO Assay |
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IC50 | 1.71e+4±n/a nM |
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Citation | Richardson-Sanchez, T; Tieu, W; Codd, R Reverse Biosynthesis: Generating Combinatorial Pools of Drug Leads from Enzyme-Mediated Fragmentation of Natural Products. Chembiochem18:368-373 (2017) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Lipoxygenase |
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Name: | Lipoxygenase |
Synonyms: | 5-Lipoxygenase | 5-Lipoxygenase (5-LO) |
Type: | Enzyme |
Mol. Mass.: | 97294.59 |
Organism: | Solanum tuberosum (potato) |
Description: | n/a |
Residue: | 864 |
Sequence: | MNIGQIMGGRELFGGHDDSKKVKGTVVMMKKNALDFTDLAGSLTDIAFDVLGQKVSFQLI
SSVQGDPTNGLQGKHSNPAYLENSLFTLTPLTAGSETAFGVTFDWNEEFGVPGAFIIKNT
HINEFFLKSLTLEDVPNHGKVHFDCNSWVYPSFRYKSDRIFFANQPYLPSKTPELLRKYR
ENELLTLRGDGTGKREAWDRIYDYDIYNDLGNPDQGKENVRTTLGGSAEYPYPRRGRTGR
PPTRTDPKSESRIPLLLSLDIYVPRDERFGHLKMSDFLTYALKSIVQFILPELHALFDGT
PNEFDSFEDVLRLYEGGIKLPQGPLFKALTAAIPLEMIKELLRTDGEGILRFPTPLVIKD
SKTAWRTDEEFAREMLAGVNPIIISRLQEFPPKSKLDPEAYGNQNSTITAEHIEDKLDGL
TVDEAMNNNKLFILNHHDLLIPYLRRINTTITKSYASRTLLFLQDNGSLKPLAIELSLPH
PDGDQFGVTSKVYTPSDQGVESSIWQLAKAYVAVNDAGVHQLISHWLNTHAVIEPFVIAT
NRQLSVLHPIHKLLYPHFRDTMNINASARQILINAGGVLESTVFQSKFALEMSAVVYKDW
VFPDQALPADLVKRGVAVEDSSSPHGVRLLIEDYPYAVDGLEIWSAIKSWVTDYCSFYYG
SDEEILKDNELQAWWKELREVGHGDKKNEPWWPEMETPQELIDSCTTIIWIASALHAAVN
FGQYPYAGYLPNRPTVSRRFMPEPGTPEYEELKKNPDKAFLKTITAQLQTLLGVSLVEIL
SRHTTDEIYLGQRESPEWTKDKEPLAAFDKFGKKLTDIEKQIIQRNGDNILTNRSGPVNA
PYTLLFPTSEGGLTGKGIPNSVSI
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BDBM22334 |
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n/a |
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Name | BDBM22334 |
Synonyms: | BW A4C | BW4C | BWA4C | BWA4C, 10 | CHEMBL314360 | JMC515449 Compound 7 | N-(3-phenoxycinnamyl)acetohydroxamic acid | N-hydroxy-N-[(2E)-3-(3-phenoxyphenyl)prop-2-en-1-yl]acetamide |
Type | Small organic molecule |
Emp. Form. | C17H17NO3 |
Mol. Mass. | 283.3218 |
SMILES | CC(=O)N(O)C\C=C\c1cccc(Oc2ccccc2)c1 |
Structure |
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