Reaction Details |
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Target | Lysyl oxidase homolog 3 |
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Ligand | BDBM50232678 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1901015 (CHEMBL4403237) |
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IC50 | 310±n/a nM |
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Citation | Smithen, DA; Leung, LMH; Challinor, M; Lawrence, R; Tang, H; Niculescu-Duvaz, D; Pearce, SP; Mcleary, R; Lopes, F; Aljarah, M; Brown, M; Johnson, L; Thomson, G; Marais, R; Springer, C 2-Aminomethylene-5-sulfonylthiazole Inhibitors of Lysyl Oxidase (LOX) and LOXL2 Show Significant Efficacy in Delaying Tumor Growth. J Med Chem63:2308-2324 (2020) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Lysyl oxidase homolog 3 |
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Name: | Lysyl oxidase homolog 3 |
Synonyms: | 1.4.3.- | 1.4.3.13 | LOXL | LOXL3 | LOXL3_HUMAN | Lysyl oxidase homolog 3 | Lysyl oxidase-like protein 3 | Synonyms=LOXL |
Type: | PROTEIN |
Mol. Mass.: | 83173.13 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_117594 |
Residue: | 753 |
Sequence: | MRPVSVWQWSPWGLLLCLLCSSCLGSPSPSTGPEKKAGSQGLRFRLAGFPRKPYEGRVEI
QRAGEWGTICDDDFTLQAAHILCRELGFTEATGWTHSAKYGPGTGRIWLDNLSCSGTEQS
VTECASRGWGNSDCTHDEDAGVICKDQRLPGFSDSNVIEVEHHLQVEEVRIRPAVGWGRR
PLPVTEGLVEVRLPDGWSQVCDKGWSAHNSHVVCGMLGFPSEKRVNAAFYRLLAQRQQHS
FGLHGVACVGTEAHLSLCSLEFYRANDTARCPGGGPAVVSCVPGPVYAASSGQKKQQQSK
PQGEARVRLKGGAHPGEGRVEVLKASTWGTVCDRKWDLHAASVVCRELGFGSAREALSGA
RMGQGMGAIHLSEVRCSGQELSLWKCPHKNITAEDCSHSQDAGVRCNLPYTGAETRIRLS
GGRSQHEGRVEVQIGGPGPLRWGLICGDDWGTLEAMVACRQLGLGYANHGLQETWYWDSG
NITEVVMSGVRCTGTELSLDQCAHHGTHITCKRTGTRFTAGVICSETASDLLLHSALVQE
TAYIEDRPLHMLYCAAEENCLASSARSANWPYGHRRLLRFSSQIHNLGRADFRPKAGRHS
WVWHECHGHYHSMDIFTHYDILTPNGTKVAEGHKASFCLEDTECQEDVSKRYECANFGEQ
GITVGCWDLYRHDIDCQWIDITDVKPGNYILQVVINPNFEVAESDFTNNAMKCNCKYDGH
RIWVHNCHIGDAFSEEANRRFERYPGQTSNQII
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BDBM50232678 |
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n/a |
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Name | BDBM50232678 |
Synonyms: | CHEBI:27413 | CHEMBL1618272 | US10717734, Compound BAPN | US11098045, Compound BAPN |
Type | Small organic molecule |
Emp. Form. | C3H6N2 |
Mol. Mass. | 70.0931 |
SMILES | NCCC#N |
Structure |
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