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TargetOxysterols receptor LXR-beta
LigandBDBM50461063
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1770683 (CHEMBL4222795)
Kd>10000±n/a nM
Citation Ouvry, GBihl, FBouix-Peter, CChristin, ODefoin-Platel, CDeret, SFeret, CFroude, DHacini-Rachinel, FHarris, CSHervouet, CLafitte, GLuzy, APMusicki, BOrfila, DParnet, VPascau, CPascau, JPierre, RRaffin, CRossio, PSpiesse, DTaquet, NThoreau, EVatinel, RVial, EHennequin, LF Sulfoximines as potent ROR? inverse agonists. Bioorg Med Chem Lett28:1269-1273 (2018) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Oxysterols receptor LXR-beta
Name:Oxysterols receptor LXR-beta
Synonyms:LXRB | Liver X receptor beta (NR1H2) | Liver X, LXR beta | NER | NR1H2 | NR1H2_HUMAN | Nuclear receptor NER | UNR | Ubiquitously-expressed nuclear receptor
Type:Enzyme Catalytic Domain
Mol. Mass.:50978.79
Organism:Homo sapiens (Human)
Description:P55055
Residue:460
Sequence:
MSSPTTSSLDTPLPGNGPPQPGAPSSSPTVKEEGPEPWPGGPDPDVPGTDEASSACSTDW
VIPDPEEEPERKRKKGPAPKMLGHELCRVCGDKASGFHYNVLSCEGCKGFFRRSVVRGGA
RRYACRGGGTCQMDAFMRRKCQQCRLRKCKEAGMREQCVLSEEQIRKKKIRKQQQESQSQ
SQSPVGPQGSSSSASGPGASPGGSEAGSQGSGEGEGVQLTAAQELMIQQLVAAQLQCNKR
SFSDQPKVTPWPLGADPQSRDARQQRFAHFTELAIISVQEIVDFAKQVPGFLQLGREDQI
ALLKASTIEIMLLETARRYNHETECITFLKDFTYSKDDFHRAGLQVEFINPIFEFSRAMR
RLGLDDAEYALLIAINIFSADRPNVQEPGRVEALQQPYVEALLSYTRIKRPQDQLRFPRM
LMKLVSLRTLSSVHSEQVFALRLQDKKLPPLLSEIWDVHE
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50461063
n/a
NameBDBM50461063
Synonyms:CHEMBL4226803 | US10457637, Compound 8
TypeSmall organic molecule
Emp. Form.C25H36N2O5S2
Mol. Mass.508.694
SMILESCCc1ccc(cc1)N(CC(C)C)S(=O)(=O)c1ccc(OCC2CCOCC2)c(c1)[S@@](C)(=N)=O |r|
Structure
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