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TargetGlucocorticoid receptor
LigandBDBM50338732
Substrate/Competitorn/a
Meas. Tech.ChEMBL_726913 (CHEMBL1686702)
Ki 3±n/a nM
Citation Roach, SLHiguchi, RIHudson, ARVassar, AGrant, VHLamer, RHooper, CRungta, DSyka, PMMais, DEMarschke, KBZhi, L Tetrahydroquinolin-3-yl carbamate glucocorticoid receptor agonists with reduced PEPCK activation. Bioorg Med Chem Lett21:1658-62 (2011) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Glucocorticoid receptor
Name:Glucocorticoid receptor
Synonyms:GCR_HUMAN | GR | GRL | Glucocorticoid | Glucocorticoid receptor (GRFP) | NR3C1 | Nuclear receptor subfamily 3 group C member 1
Type:Enzyme
Mol. Mass.:85656.87
Organism:Homo sapiens (Human)
Description:P04150
Residue:777
Sequence:
MDSKESLTPGREENPSSVLAQERGDVMDFYKTLRGGATVKVSASSPSLAVASQSDSKQRR
LLVDFPKGSVSNAQQPDLSKAVSLSMGLYMGETETKVMGNDLGFPQQGQISLSSGETDLK
LLEESIANLNRSTSVPENPKSSASTAVSAAPTEKEFPKTHSDVSSEQQHLKGQTGTNGGN
VKLYTTDQSTFDILQDLEFSSGSPGKETNESPWRSDLLIDENCLLSPLAGEDDSFLLEGN
SNEDCKPLILPDTKPKIKDNGDLVLSSPSNVTLPQVKTEKEDFIELCTPGVIKQEKLGTV
YCQASFPGANIIGNKMSAISVHGVSTSGGQMYHYDMNTASLSQQQDQKPIFNVIPPIPVG
SENWNRCQGSGDDNLTSLGTLNFPGRTVFSNGYSSPSMRPDVSSPPSSSSTATTGPPPKL
CLVCSDEASGCHYGVLTCGSCKVFFKRAVEGQHNYLCAGRNDCIIDKIRRKNCPACRYRK
CLQAGMNLEARKTKKKIKGIQQATTGVSQETSENPGNKTIVPATLPQLTPTLVSLLEVIE
PEVLYAGYDSSVPDSTWRIMTTLNMLGGRQVIAAVKWAKAIPGFRNLHLDDQMTLLQYSW
MFLMAFALGWRSYRQSSANLLCFAPDLIINEQRMTLPCMYDQCKHMLYVSSELHRLQVSY
EEYLCMKTLLLLSSVPKDGLKSQELFDEIRMTYIKELGKAIVKREGNSSQNWQRFYQLTK
LLDSMHEVVENLLNYCFQTFLDKTMSIEFPEMLAEIITNQIPKYSNGNIKKLLFHQK
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50338732
n/a
NameBDBM50338732
Synonyms:(+/-)-(3R,4S)-5,7-difluoro-6-(1H-indol-7-yl)-2,2,4-trimethyl-1,2,3,4-tetrahydroquinolin-3-yl methylcarbamate | CHEMBL1684230
TypeSmall organic molecule
Emp. Form.C22H23F2N3O2
Mol. Mass.399.4337
SMILESCNC(=O)O[C@@H]1[C@@H](C)c2c(NC1(C)C)cc(F)c(c2F)-c1cccc2cc[nH]c12 |r,wU:5.4,wD:6.6,(14.22,-7.79,;12.89,-7.01,;11.56,-7.78,;11.55,-9.32,;10.22,-7.01,;8.89,-7.77,;7.55,-7,;7.55,-5.46,;6.22,-7.77,;6.21,-9.32,;7.54,-10.09,;8.89,-9.32,;9.65,-10.66,;10.43,-9.33,;4.88,-10.09,;3.55,-9.32,;2.22,-10.09,;3.55,-7.78,;4.88,-7.01,;4.88,-5.47,;2.22,-7.01,;2.22,-5.47,;.89,-4.7,;-.44,-5.47,;-.44,-7.02,;-1.57,-8.06,;-.93,-9.45,;.59,-9.28,;.9,-7.78,)|
Structure
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