Target
Nociceptin receptor
Ligand
BDBM469820
Substrate
n/a
Meas. Tech.
Human Nociceptin/Orphanin FQ Peptide (hNOP) Receptor Binding Assay
Ki
1.000±n/a nM
Citation
 Kuehnert, SKoenigs, RMJakob, FKless, ARatcliffe, PJostock, RKoch, TLinz, KSchroeder, WSchiene, KWegert, A 3-(carboxymethyl)-8-amino-2-oxo-1,3-diaza-spiro-[4.5]-decane derivatives US Patent  US10807989 Publication Date 10/20/2020 
Target
Name:
Nociceptin receptor
Synonyms:
KOR-3 | Kappa-type 3 opioid receptor | Mu-type opioid receptor (Mu) | NOP | Nociceptin Receptor (ORL1 Receptor) | Nociceptin receptor (NOP) | Nociceptin receptor (ORL-1) | Nociceptin receptor (ORL1) | Nociceptin/Orphanin FQ, NOP receptor | OOR | OPIATE ORL-1 | OPRL1 | OPRL1 protein | OPRX_HUMAN | ORL1 | ORL1 receptor | Opioid receptor like-1 | Orphanin FQ receptor | Orphanin FQ receptor (ORL1) | P41146
Type:
G Protein-Coupled Receptor (GPCR)
Mol. Mass.:
40702.87
Organism:
Homo sapiens (Human)
Description:
P41146
Residue:
370
Sequence:
MEPLFPAPFWEVIYGSHLQGNLSLLSPNHSLLPPHLLLNASHGAFLPLGLKVTIVGLYLAVCVGGLLGNCLVMYVILRHTKMKTATNIYIFNLALADTLVLLTLPFQGTDILLGFWPFGNALCKTVIAIDYYNMFTSTFTLTAMSVDRYVAICHPIRALDVRTSSKAQAVNVAIWALASVVGVPVAIMGSAQVEDEEIECLVEIPTPQDYWGPVFAICIFLFSFIVPVLVISVCYSLMIRRLRGVRLLSGSREKDRNLRRITRLVLVVVAVFVGCWTPVQVFVLAQGLGVQPSSETAVAILRFCTALGYVNSCLNPILYAFLDENFKACFRKFCCASALRRDVQVSDRVRSIAKDVALACKTSETVPRPA
  
Inhibitor
Name:
BDBM469820
Synonyms:
CIS-2-[1-(Cyclobutyl-methyl)-8-dimethylamino-2-oxo-8-phenyl-1,3- diazaspiro[4.5]decan-3-yl]-N-(3-methoxy-pyridin-4-yl)-acetamide | US10807989, Example SC_1048
Type:
Small organic molecule
Emp. Form.:
C29H39N5O3
Mol. Mass.:
505.6517
SMILES:
COc1cnccc1NC(=O)CN1C[C@]2(CC[C@@](CC2)(N(C)C)c2ccccc2)N(CC2CCC2)C1=O |r,wU:14.31,17.21,(-16.78,-14.08,;-18.26,-14.48,;-18.66,-15.97,;-20.15,-16.37,;-20.55,-17.86,;-19.46,-18.94,;-17.97,-18.55,;-17.57,-17.06,;-16.09,-16.66,;-15,-17.75,;-15.4,-19.24,;-13.51,-17.35,;-12.42,-18.44,;-10.96,-17.96,;-10.05,-19.21,;-9.28,-20.54,;-7.74,-20.54,;-6.97,-19.21,;-7.74,-17.88,;-9.28,-17.88,;-5.88,-18.12,;-4.39,-18.52,;-6.28,-16.63,;-5.88,-20.3,;-6.28,-21.79,;-5.19,-22.87,;-3.7,-22.48,;-3.3,-20.99,;-4.39,-19.9,;-10.96,-20.45,;-10.56,-21.94,;-11.65,-23.03,;-13.19,-23.03,;-13.19,-24.57,;-11.65,-24.57,;-12.42,-19.98,;-13.75,-20.75,)|
Structure:
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