Reaction Details |
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Target | Amine oxidase [flavin-containing] A |
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Ligand | BDBM50031035 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_122938 (CHEMBL733064) |
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IC50 | >1000±n/a nM |
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Citation | Kneubühler, S; Thull, U; Altomare, C; Carta, V; Gaillard, P; Carrupt, PA; Carotti, A; Testa, B Inhibition of monoamine oxidase-B by 5H-indeno[1,2-c]pyridazines: biological activities, quantitative structure-activity relationships (QSARs) and 3D-QSARs. J Med Chem38:3874-83 (1995) [PubMed] |
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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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BDBM50031035 |
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n/a |
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Name | BDBM50031035 |
Synonyms: | 3-((E)-Styryl)-indeno[1,2-c]pyridazin-5-one | CHEMBL125843 | trans-3-styryl-5H-indeno[1,2-c]pyridazin-5-one |
Type | Small organic molecule |
Emp. Form. | C19H12N2O |
Mol. Mass. | 284.3114 |
SMILES | O=C1c2ccccc2-c2nnc(\C=C\c3ccccc3)cc12 |
Structure |
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