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Reaction Details
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TargetSubstance-P receptor
LigandBDBM50114944
Substrate/Competitorn/a
Meas. Tech.ChEBML_205739
IC50 0.290000±n/a nM
Citation Elliott, JMCastro, JLChicchi, GGCooper, LCDinnell, KHollingworth, GJRidgill, MPRycroft, WKurtz, MMShaw, DESwain, CJTsao, KLYang, L 4,4-Disubstituted cyclohexylamine NK(1) receptor antagonists I. Bioorg Med Chem Lett12:1755-8 (2002) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Substance-P receptor
Name:Substance-P receptor
Synonyms:NK-1 receptor | NK-1R | NK1 Receptor | NK1R | NK1R_HUMAN | Neurokinin 1 receptor | Neurokinin-1 (NK-1) | Neuromedin-1 receptor (NK-1R) | SPR | TAC1R | TACR1 | Tachykinin receptor 1 | Tachykinin receptor 1 (NK1) | tachykinin
Type:G Protein-Coupled Receptor (GPCR)
Mol. Mass.:46254.43
Organism:Homo sapiens (Human)
Description:P25103
Residue:407
Sequence:
MDNVLPVDSDLSPNISTNTSEPNQFVQPAWQIVLWAAAYTVIVVTSVVGNVVVMWIILAH
KRMRTVTNYFLVNLAFAEASMAAFNTVVNFTYAVHNEWYYGLFYCKFHNFFPIAAVFASI
YSMTAVAFDRYMAIIHPLQPRLSATATKVVICVIWVLALLLAFPQGYYSTTETMPSRVVC
MIEWPEHPNKIYEKVYHICVTVLIYFLPLLVIGYAYTVVGITLWASEIPGDSSDRYHEQV
SAKRKVVKMMIVVVCTFAICWLPFHIFFLLPYINPDLYLKKFIQQVYLAIMWLAMSSTMY
NPIIYCCLNDRFRLGFKHAFRCCPFISAGDYEGLEMKSTRYLQTQGSVYKVSRLETTIST
VVGAHEEEPEDGPKATPSSLDLTSNCSSRSDSKTMTESFSFSSNVLS
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  Blast E-value cutoff:
BDBM50114944
n/a
NameBDBM50114944
Synonyms:4-[4-(4-Fluoro-phenyl)-piperidin-1-yl]-1-phenyl-cyclohexanecarboxylic acid [1-(3,5-bis-trifluoromethyl-phenyl)-2-hydroxy-ethyl]-amide | CHEMBL296583
TypeSmall organic molecule
Emp. Form.C34H35F7N2O2
Mol. Mass.636.6427
SMILESOCC(NC(=O)[C@]1(CC[C@@H](CC1)N1CCC(CC1)c1ccc(F)cc1)c1ccccc1)c1cc(cc(c1)C(F)(F)F)C(F)(F)F |wU:6.5,wD:9.12,(10.2,2.64,;9.45,1.31,;10.23,-.03,;8.9,-.8,;7.57,-.03,;7.56,1.51,;6.24,-.82,;7.57,-1.59,;7.57,-3.13,;6.21,-3.88,;4.88,-3.13,;4.9,-1.56,;6.21,-5.42,;4.9,-6.21,;4.9,-7.75,;6.21,-8.5,;7.54,-7.75,;7.54,-6.21,;6.21,-10.04,;4.88,-10.8,;4.88,-12.34,;6.21,-13.11,;6.21,-14.65,;7.56,-12.34,;7.54,-10.8,;4.9,-.05,;4.9,1.52,;3.55,2.29,;2.2,1.51,;2.22,-.05,;3.57,-.82,;11.56,-.8,;12.89,-.03,;14.22,-.79,;14.22,-2.34,;12.89,-3.11,;11.56,-2.34,;12.88,-4.65,;11.55,-5.42,;14.22,-5.42,;11.39,-4.25,;15.55,-.02,;15.94,-1.52,;16.88,-.79,;15.55,1.52,)|
Structure
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