Reaction Details |
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Target | Alcohol dehydrogenase class-3 |
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Ligand | BDBM140261 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Binding Assay |
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pH | 7.4±n/a |
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Temperature | 295.15±n/a K |
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IC50 | 19720±n/a nM |
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Comments | extracted |
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Citation | Sun, X; Qiu, J Dihydropyrimidin-2(1H)-one compounds as neurokinin-3 receptor antagonists US Patent US8906933 Publication Date 12/9/2014 |
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More Info.: | Get all data from this article, Assay Method |
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Alcohol dehydrogenase class-3 |
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Name: | Alcohol dehydrogenase class-3 |
Synonyms: | 1.1.1.- | 1.1.1.1 | 1.1.1.284 | ADH5 | ADHX | ADHX_HUMAN | Alcohol dehydrogenase 5 | Alcohol dehydrogenase class chi chain | Alcohol dehydrogenase class-3 | Alcohol dehydrogenase class-III | FALDH | FDH | Glutathione-dependent formaldehyde dehydrogenase (GSH-FDH) | S-nitrosoglutathione reductase (GSNOR) | alcohol dehydrogenase 3 (ADH-3) |
Type: | n/a |
Mol. Mass.: | 39728.34 |
Organism: | Homo sapiens (Human) |
Description: | P11766 |
Residue: | 374 |
Sequence: | MANEVIKCKAAVAWEAGKPLSIEEIEVAPPKAHEVRIKIIATAVCHTDAYTLSGADPEGC
FPVILGHEGAGIVESVGEGVTKLKAGDTVIPLYIPQCGECKFCLNPKTNLCQKIRVTQGK
GLMPDGTSRFTCKGKTILHYMGTSTFSEYTVVADISVAKIDPLAPLDKVCLLGCGISTGY
GAAVNTAKLEPGSVCAVFGLGGVGLAVIMGCKVAGASRIIGVDINKDKFARAKEFGATEC
INPQDFSKPIQEVLIEMTDGGVDYSFECIGNVKVMRAALEACHKGWGVSVVVGVAASGEE
IATRPFQLVTGRTWKGTAFGGWKSVESVPKLVSEYMSKKIKVDEFVTHNLSFDEINKAFE
LMHSGKSIRTVVKI
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BDBM140261 |
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n/a |
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Name | BDBM140261 |
Synonyms: | US8906933, (R)-4-(3-ethoxy-4-hydroxy-5-nitrophenyl)-5,6-diphenyl-3,4-dihydropyrimidin-2(1H)-one |
Type | Small organic molecule |
Emp. Form. | C24H21N3O5 |
Mol. Mass. | 431.4406 |
SMILES | CCOc1cc(cc(c1O)[N+]([O-])=O)[C@H]1NC(=O)NC(=C1c1ccccc1)c1ccccc1 |c:19| |
Structure |
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