Reaction Details |
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Target | Amine oxidase [flavin-containing] A |
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Ligand | BDBM50304152 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_601025 (CHEMBL1069162) |
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Ki | 3900±n/a nM |
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Citation | Gökhan-Kelekçi, N; Simsek, OO; Ercan, A; Yelekçi, K; Sahin, ZS; Isik, S; Uçar, G; Bilgin, AA Synthesis and molecular modeling of some novel hexahydroindazole derivatives as potent monoamine oxidase inhibitors. Bioorg Med Chem17:6761-72 (2009) [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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BDBM50304152 |
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n/a |
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Name | BDBM50304152 |
Synonyms: | 3-(2-Furyl)-2-thiocarbamoyl-2,3,4,5,6,7-hexahydro-1Hindazol | CHEMBL596453 |
Type | Small organic molecule |
Emp. Form. | C12H15N3OS |
Mol. Mass. | 249.332 |
SMILES | NC(=S)N1N=C2CCCCC2C1c1ccco1 |t:4| |
Structure |
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