Target
Nociceptin receptor
Ligand
BDBM464643
Substrate
n/a
Meas. Tech.
Receptor Binding Assay
Ki
6.00±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:
BDBM464643
Synonyms:
CIS-1-(Cyclopropyl-methyl)-8-dimethylamino-3-[2-methyl-2-(2-oxo-pyrrolidin-1- yl)-propyl]-8-phenyl-1,3-diazaspiro[4.5]decan-2-one | US10793556, Example SC_4072 | US10793556, Example SC_4073 | US10793556, Example SC_4074 | US10793556, Example SC_4075 | US10793556, Example SC_4076
Type:
Small organic molecule
Emp. Form.:
C28H43N3O4S
Mol. Mass.:
517.724
SMILES:
CN(C)[C@]1(CC[C@]2(CN(CCC3(O)CCS(=O)(=O)CC3)C(=O)N2CC2CCC2)CC1)c1ccccc1 |r,wU:6.23,3.2,(5.31,-14.15,;3.77,-14.15,;3,-12.81,;3,-15.48,;2.23,-16.81,;.69,-16.81,;-.08,-15.48,;-.98,-14.23,;-2.45,-14.71,;-3.78,-13.94,;-5.12,-14.71,;-6.45,-13.94,;-7.78,-14.71,;-5.12,-13.17,;-5.12,-11.63,;-6.45,-10.86,;-7.22,-9.53,;-5.68,-9.53,;-7.78,-11.63,;-7.78,-13.17,;-2.45,-16.25,;-3.69,-17.16,;-.98,-16.73,;-.51,-18.19,;-1.54,-19.33,;-3.08,-19.33,;-3.08,-20.87,;-1.54,-20.87,;.69,-14.15,;2.23,-14.15,;3.77,-16.81,;3,-18.15,;3.77,-19.48,;5.31,-19.48,;6.08,-18.15,;5.31,-16.81,)|
Structure:
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