Reaction Details |
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Target | Aldehyde dehydrogenase, mitochondrial |
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Ligand | BDBM50093532 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_31176 (CHEMBL641141) |
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IC50 | 300±n/a nM |
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Citation | Gao, GY; Li, DJ; Keung, WM Synthesis of potential antidipsotropic isoflavones: inhibitors of the mitochondrial monoamine oxidase-aldehyde dehydrogenase pathway. J Med Chem44:3320-8 (2001) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Aldehyde dehydrogenase, mitochondrial |
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Name: | Aldehyde dehydrogenase, mitochondrial |
Synonyms: | ALDH class 2 | ALDH-E2 | ALDH2 | ALDH2_HUMAN | ALDHI | ALDM | Aldehyde dehydrogenase (ALDH2) |
Type: | Enzyme |
Mol. Mass.: | 56382.67 |
Organism: | Homo sapiens (Human) |
Description: | P05091 |
Residue: | 517 |
Sequence: | MLRAAARFGPRLGRRLLSAAATQAVPAPNQQPEVFCNQIFINNEWHDAVSRKTFPTVNPS
TGEVICQVAEGDKEDVDKAVKAARAAFQLGSPWRRMDASHRGRLLNRLADLIERDRTYLA
ALETLDNGKPYVISYLVDLDMVLKCLRYYAGWADKYHGKTIPIDGDFFSYTRHEPVGVCG
QIIPWNFPLLMQAWKLGPALATGNVVVMKVAEQTPLTALYVANLIKEAGFPPGVVNIVPG
FGPTAGAAIASHEDVDKVAFTGSTEIGRVIQVAAGSSNLKRVTLELGGKSPNIIMSDADM
DWAVEQAHFALFFNQGQCCCAGSRTFVQEDIYDEFVERSVARAKSRVVGNPFDSKTEQGP
QVDETQFKKILGYINTGKQEGAKLLCGGGIAADRGYFIQPTVFGDVQDGMTIAKEEIFGP
VMQILKFKTIEEVVGRANNSTYGLAAAVFTKDLDKANYLSQALQAGTVWVNCYDVFGAQS
PFGGYKMSGSGRELGEYGLQAYTEVKTVTVKVPQKNS
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BDBM50093532 |
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n/a |
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Name | BDBM50093532 |
Synonyms: | 7-(6-Bromo-hexyloxy)-3-(4-hydroxy-phenyl)-chromen-4-one | CHEMBL112437 |
Type | Small organic molecule |
Emp. Form. | C21H21BrO4 |
Mol. Mass. | 417.293 |
SMILES | Oc1ccc(cc1)-c1coc2cc(OCCCCCCBr)ccc2c1=O |
Structure |
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