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TargetAmine oxidase [flavin-containing] B
LigandBDBM50327221
Substrate/Competitorn/a
Meas. Tech.ChEMBL_664237 (CHEMBL1261744)
IC50 86000±n/a nM
Citation Khattab, SNHassan, SYBekhit, AAEl Massry, AMLanger, VAmer, A Synthesis of new series of quinoxaline based MAO-inhibitors and docking studies. Eur J Med Chem45:4479-89 (2010) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Amine oxidase [flavin-containing] B
Name:Amine oxidase [flavin-containing] B
Synonyms:AOFB_HUMAN | MAO-B | MAOB | Monoamine oxidase type B | Monoamine oxidase type B (MAO B) | Monoamine oxidase type B (MAO B) | Monoamine oxidase type B (MAOB)
Type:Protein
Mol. Mass.:58768.76
Organism:Homo sapiens (Human)
Description:P27338
Residue:520
Sequence:
MSNKCDVVVVGGGISGMAAAKLLHDSGLNVVVLEARDRVGGRTYTLRNQKVKYVDLGGSY
VGPTQNRILRLAKELGLETYKVNEVERLIHHVKGKSYPFRGPFPPVWNPITYLDHNNFWR
TMDDMGREIPSDAPWKAPLAEEWDNMTMKELLDKLCWTESAKQLATLFVNLCVTAETHEV
SALWFLWYVKQCGGTTRIISTTNGGQERKFVGGSGQVSERIMDLLGDRVKLERPVIYIDQ
TRENVLVETLNHEMYEAKYVISAIPPTLGMKIHFNPPLPMMRNQMITRVPLGSVIKCIVY
YKEPFWRKKDYCGTMIIDGEEAPVAYTLDDTKPEGNYAAIMGFILAHKARKLARLTKEER
LKKLCELYAKVLGSLEALEPVHYEEKNWCEEQYSGGCYTTYFPPGILTQYGRVLRQPVDR
IYFAGTETATHWSGYMEGAVEAGERAAREILHAMGKIPEDEIWQSEPESVDVPAQPITTT
FLERHLPSVPGLLRLIGLTTIFSATALGFLAHKRGLLVRV
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  Blast E-value cutoff:
BDBM50327221
n/a
NameBDBM50327221
Synonyms:4-Benzoyl-1-(3,4-dimethoxyphenyl)-[1,2,4]triazolo[4,3-a]quinoxaline | CHEMBL1258955
TypeSmall organic molecule
Emp. Form.C24H18N4O3
Mol. Mass.410.4247
SMILESCOc1ccc(cc1OC)-c1nnc2c(nc3ccccc3n12)C(=O)c1ccccc1
Structure
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