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TargetEstrogen receptor [298-554,Y537S]
LigandBDBM521273
Substrate/Competitorn/a
Meas. Tech.Biochemical Antagonist Activity on Wild Type (WT) and Mutants
IC50 18.0±n/a nM
Citation Bouaboula, MBrollo, MCertal, VEl-Ahmad, YFiloche-Romme, BHalley, FMcCort, GSchio, LTabart, MTerrier, CThompson, F Substituted N-(3-fluoropropyl)-pyrrolidine compounds, processes for their preparation and therapeutic uses thereof US Patent US11149031 Publication Date 10/19/2021
More Info.:Get all data from this article,  Assay Method
 
Estrogen receptor [298-554,Y537S]
Name:Estrogen receptor [298-554,Y537S]
Synonyms:ESR | ESR1 | ESR1_HUMAN | Estrogen Receptor alpha (aa 298-554, Y537S) | NR3A1
Type:Enzyme Catalytic Domain
Mol. Mass.:29151.56
Organism:Homo sapiens (Human)
Description:P03372[298-554,Y537S]
Residue:256
Sequence:
KRSKKNSLALSLTADQMVSALLDAEPPILYSEYDPTRPFSEASMMGLLTNLADRELVHMI
NWAKRVPGFVDLTLHDQVHLLECAWLEILMIGLVWRSMEHPGKLLFAPNLLLDRNQGKCV
EGMVEIFDMLLATSSRFRMMNLQGEEFVCLKSIILLNSGVYTFLSSTLKSLEEKDHIHRV
LDKITDTLIHLMAKAGLTLQQQHQRLAQLLLILSHIRHMSNKGMEHLYSMKCKNVVPLSD
LLLEMLDAHRLHAPTS
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  Blast E-value cutoff:
BDBM521273
n/a
NameBDBM521273
Synonyms:4-(4-chloro-3- fluoro-phenyl)- 5-[4-[(3S)-1-(3- fluoropropyl)pyr- rolidin-3- yl]oxyphenyl]- 2,3-dihydro-1- benzoxepin-8- ol | US11149031, Example 97
TypeSmall organic molecule
Emp. Form.C29H28ClF2NO3
Mol. Mass.511.987
SMILESOc1ccc2c(OCCC(c3ccc(Cl)c(F)c3)=C2c2ccc(O[C@H]3CCN(CCCF)C3)cc2)c1 |r,c:18|
Structure
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