Reaction Details |
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Target | Amine oxidase [flavin-containing] A |
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Ligand | BDBM50188724 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_364457 (CHEMBL862689) |
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IC50 | >1000±n/a nM |
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Citation | Frédérick, R; Dumont, W; Ooms, F; Aschenbach, L; Van der Schyf, CJ; Castagnoli, N; Wouters, J; Krief, A Synthesis, structural reassignment, and biological activity of type B MAO inhibitors based on the 5H-indeno[1,2-c]pyridazin-5-one core. J Med Chem49:3743-7 (2006) [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_RAT | Amine oxidase (flavin-containing) A | Amine oxidase [flavin-containing] A | Maoa | Monoamine Oxidase Type A (MAO-A) | Monoamine oxidase | Monoamine oxidase A (MAO-A) | Monoamine oxidase A (rMAO-A) | Monoamine oxidase type A (MAOA) |
Type: | Enzyme |
Mol. Mass.: | 59515.21 |
Organism: | Rattus norvegicus (rat) |
Description: | n/a |
Residue: | 526 |
Sequence: | MTDLEKPNLAGHMFDVGLIGGGISGLAAAKLLSEYKINVLVLEARDRVGGRTYTVRNEHV
KWVDVGGAYVGPTQNRILRLSKELGIETYKVNVNERLVQYVKGKTYPFRGAFPPVWNPLA
YLDYNNLWRTMDEMGKEIPVDAPWQARHAQEWDKMTMKDLIDKICWTKTAREFAYLFVNI
NVTSEPHEVSALWFLWYVRQCGGTARIFSVTNGGQERKFVGGSGQVSEQIMGLLGDKVKL
SSPVTYIDQTDDNIIVETLNHEHYECKYVISAIPPILTAKIHFKPELPPERNQLIQRLPM
GAVIKCMVYYKEAFWKKKDYCGCMIIEDEEAPIAITLDDTKPDGSLPAIMGFILARKADR
QAKLHKDIRKRKICELYAKVLGSQEALYPVHYEEKNWCEEQYSGGCYTAYFPPGIMTQYG
RVIRQPVGRIYFAGTETATQWSGYMEGAVEAGERAAREVLNALGKVAKKDIWVEEPESKD
VPAIEITHTFLERNLPSVPGLLKITGVSTSVALLCFVLYKIKKLPC
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BDBM50188724 |
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n/a |
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Name | BDBM50188724 |
Synonyms: | 3-methyl-8-methoxy-5H-indeno[1,2-c]pyridazin-5-one | CHEMBL210626 |
Type | Small organic molecule |
Emp. Form. | C13H10N2O2 |
Mol. Mass. | 226.2307 |
SMILES | COc1ccc2C(=O)c3cc(C)nnc3-c2c1 |
Structure |
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