Reaction Details |
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Target | Amine oxidase [flavin-containing] A |
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Ligand | BDBM50273660 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_536001 (CHEMBL988017) |
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Ki | 10±n/a nM |
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Citation | La Regina, G; Silvestri, R; Gatti, V; Lavecchia, A; Novellino, E; Befani, O; Turini, P; Agostinelli, E Synthesis, structure-activity relationships and molecular modeling studies of new indole inhibitors of monoamine oxidases A and B. Bioorg Med Chem16:9729-40 (2008) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Amine oxidase [flavin-containing] A |
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Name: | Amine oxidase [flavin-containing] A |
Synonyms: | AOFA_BOVIN | Amine oxidase [flavin-containing] A | MAO-A | MAOA | Monoamine Oxidase Type A (MAO-A) | Monoamine oxidase | Monoamine oxidase A | Monoamine oxidase type A |
Type: | PROTEIN |
Mol. Mass.: | 59764.63 |
Organism: | Bos taurus |
Description: | ChEMBL_1501477 |
Residue: | 527 |
Sequence: | MESLQKTSDAGQMFDVVVIGGGISGLSAAKLLAEHEVNVLVLEARERVGGRTYTVRNEHV
DYVDVGGAYVGPTQNRILRLSKQLGLETYKVNVNERLVHYVKGKTYPFRGAFPPVWNPIA
YLDYNNLWRTMDNMGKEIPADAPWEAPHAVEWDKMTMKDLIEKICWTKTARQFASLFVNI
NVTSEPHEVSALWFLWYVKQCGGTTRIFSITNGGQERKFVGGSGQVSERIMQLLGDRVKL
RSPVTYVDQSSENITVETLNRELYECRYVISAIPPTLTAKIHFRPELPSERNQLIQRLPM
GAVIKCMMYYKEAFWKKKDYCGCMIIEDEEAPISITLDDTKPDGSLPAIMGFILARKADR
LAKVHKDIRKRKICELYAKVLGSQEALHPVHYEEKNWCQEQYSGGCYTAYFPPGIMTQYG
RVIRQPVGRIYFAGTETATQWSGYMEGAVEAGERAAREVLNALGKLSAKDIWIQEPEAED
VPAVEITPSFWERNLPSVSGLLKIVGFSTSITALWFVMYRFRLLSRS
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BDBM50273660 |
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n/a |
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Name | BDBM50273660 |
Synonyms: | (R)-N-(alpha-Cyclohexylethyl)-N-(1H-indol-2-ylmethyl)amine | CHEMBL510210 |
Type | Small organic molecule |
Emp. Form. | C18H26N2 |
Mol. Mass. | 270.4124 |
SMILES | C[C@H](C1CCCCC1)N(C)Cc1cc2ccccc2[nH]1 |r| |
Structure |
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