Reaction Details |
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Target | Seed linoleate 9S-lipoxygenase |
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Ligand | BDBM50140137 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1547445 (CHEMBL3757564) |
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IC50 | 12000±n/a nM |
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Citation | Theodosis-Nobelos, P; Kourti, M; Gavalas, A; Rekka, EA Amides of non-steroidal anti-inflammatory drugs with thiomorpholine can yield hypolipidemic agents with improved anti-inflammatory activity. Bioorg Med Chem Lett26:910-3 (2016) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Seed linoleate 9S-lipoxygenase |
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Name: | Seed linoleate 9S-lipoxygenase |
Synonyms: | LOX1.4 | LOXX_SOYBN | SC514 |
Type: | PROTEIN |
Mol. Mass.: | 96810.33 |
Organism: | Glycine max |
Description: | ChEMBL_108041 |
Residue: | 864 |
Sequence: | MFGIFDKGQKIKGTVVLMPKNVLDFNAITSIGKGGVIDTATGILGQGVSLVGGVIDTATS
FLGRNISMQLISATQTDGSGNGKVGKEVYLEKHLPTLPTLGARQDAFSIFFEWDASFGIP
GAFYIKNFMTDEFFLVSVKLEDIPNHGTIEFVCNSWVYNFRSYKKNRIFFVNDTYLPSAT
PAPLLKYRKEELEVLRGDGTGKRKDFDRIYDYDVYNDLGNPDGGDPRPILGGSSIYPYPR
RVRTGRERTRTDPNSEKPGEVYVPRDENFGHLKSSDFLTYGIKSLSHDVIPLFKSAIFQL
RVTSSEFESFEDVRSLYEGGIKLPTDILSQISPLPALKEIFRTDGENVLQFPPPHVAKVS
KSGWMTDEEFAREVIAGVNPNVIRRLQEFPPKSTLDPTLYGDQTSTITKEQLEINMGGVT
VEEALSTQRLFILDYQDAFIPYLTRINSLPTAKAYATRTILFLKDDGTLKPLAIELSKPH
PDGDNLGPESIVVLPATEGVDSTIWLLAKAHVIVNDSGYHQLVSHWLNTHAVMEPFAIAT
NRHLSVLHPIYKLLYPHYRDTININGLARQSLINADGIIEKSFLPGKYSIEMSSSVYKNW
VFTDQALPADLVKRGLAIEDPSAPHGLRLVIEDYPYAVDGLEIWDAIKTWVHEYVSLYYP
TDAAVQQDTELQAWWKEAVEKGHGDLKEKPWWPKMQTTEDLIQSCSIIVWTASALHAAVN
FGQYPYGGLILNRPTLARRFIPAEGTPEYDEMVKNPQKAYLRTITPKFETLIDLSVIEIL
SRHASDEIYLGERETPNWTTDKKALEAFKRFGSKLTGIEGKINARNSDPSLRNRTGPVQL
PYTLLHRSSEEGLTFKGIPNSISI
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BDBM50140137 |
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n/a |
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Name | BDBM50140137 |
Synonyms: | CHEMBL3753908 |
Type | Small organic molecule |
Emp. Form. | C18H21NO2S |
Mol. Mass. | 315.43 |
SMILES | COc1ccc2cc(ccc2c1)C(C)C(=O)N1CCSCC1 |
Structure |
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