Target
Nociceptin receptor
Ligand
BDBM464598
Substrate
n/a
Meas. Tech.
Receptor Binding Assay
Ki
57.0±n/a nM
Citation
 Kuehnert, SKoenigs, RMKless, AWegert, ARatcliffe, PJostock, RKoch, TLinz, KSchroeder, W 8-amino-2-oxo-1,3-diaza-spiro-[4.5]-decane derivatives US Patent  US10793556 Publication Date 10/6/2020 
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:
BDBM464598
Synonyms:
CIS-3-[1-[(1-Hydroxy-cyclobutyl)-methyl]-8-methylamino-2-oxo-8-phenyl-1,3- diazaspiro[4.5]decan-3-yl]-propionitrile | US10793556, Example SC_4022 | US10793556, Example SC_4024 | US10793556, Example SC_4025 | US10793556, Example SC_4026
Type:
Small organic molecule
Emp. Form.:
C27H42N4O3
Mol. Mass.:
470.6474
SMILES:
CN(C)[C@]1(CC[C@]2(CN(CCN3CCOCC3)C(=O)N2CC2(O)CCC2)CC1)c1ccccc1 |r,wU:3.2,6.20,(4.7,-19.56,;5.1,-21.04,;6.59,-21.44,;4.01,-22.13,;3.24,-23.47,;1.7,-23.47,;.93,-22.13,;.03,-20.89,;-1.44,-21.36,;-2.53,-20.27,;-4.01,-20.67,;-5.1,-19.58,;-4.7,-18.1,;-5.79,-17.01,;-7.28,-17.41,;-7.68,-18.89,;-6.59,-19.98,;-1.44,-22.9,;-2.68,-23.81,;.03,-23.38,;.5,-24.84,;-.53,-25.99,;1.01,-25.99,;-2.01,-26.39,;-1.62,-27.87,;-.13,-27.48,;1.7,-20.8,;3.24,-20.8,;5.1,-23.22,;4.7,-24.71,;5.79,-25.8,;7.28,-25.4,;7.68,-23.91,;6.59,-22.82,)|
Structure:
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