Reaction Details Report a problem with these data
Target
D(2) dopamine receptor
Ligand
BDBM50219941
Substrate
n/a
Meas. Tech.
ChEMBL_449064 (CHEMBL898269)
IC50
39±n/a nM
Citation
Agai-Csongor, E; Nógrádi, K; Galambos, J; Vágó, I; Bielik, A; Magdó, I; Ignácz-Szendrei, G; Keseru, GM; Greiner, I; Laszlovszky, I; Schmidt, E; Kiss, B; Sághy, K; Laszy, J; Gyertyán, I; Zájer-Balázs, M; Gémesi, L; Domány, G Novel sulfonamides having dual dopamine D2 and D3 receptor affinity show in vivo antipsychotic efficacy with beneficial cognitive and EPS profile. Bioorg Med Chem Lett 17:5340-4 (2007) [PubMed] Article
More Info.:
Target
Name:
D(2) dopamine receptor
Synonyms:
DOPAMINE D2 | DOPAMINE D2 Long | DOPAMINE D2 Short | DRD2_RAT | Dopamine D2 receptor | Dopamine2-like | Drd2
Type:
G Protein-Coupled Receptor (GPCR)
Mol. Mass.:
50931.60
Organism:
Rattus norvegicus (rat)
Description:
P61169
Residue:
444
Sequence:
MDPLNLSWYDDDLERQNWSRPFNGSEGKADRPHYNYYAMLLTLLIFIIVFGNVLVCMAVSREKALQTTTNYLIVSLAVADLLVATLVMPWVVYLEVVGEWKFSRIHCDIFVTLDVMMCTASILNLCAISIDRYTAVAMPMLYNTRYSSKRRVTVMIAIVWVLSFTISCPLLFGLNNTDQNECIIANPAFVVYSSIVSFYVPFIVTLLVYIKIYIVLRKRRKRVNTKRSSRAFRANLKTPLKGNCTHPEDMKLCTVIMKSNGSFPVNRRRMDAARRAQELEMEMLSSTSPPERTRYSPIPPSHHQLTLPDPSHHGLHSNPDSPAKPEKNGHAKIVNPRIAKFFEIQTMPNGKTRTSLKTMSRRKLSQQKEKKATQMLAIVLGVFIICWLPFFITHILNIHCDCNIPPVLYSAFTWLGYVNSAVNPIIYTTFNIEFRKAFMKILHC
Inhibitor
Name:
BDBM50219941
Synonyms:
CHEMBL240909 | N-((1r,4r)-4-(2-(4-(3-cyano-5-(trifluoromethyl)phenyl)piperazin-1-yl)ethyl)cyclohexyl)-6-methylpyridine-3-sulfonamide
Type:
Small organic molecule
Emp. Form.:
C26H32F3N5O2S
Mol. Mass.:
535.625
SMILES:
Cc1ccc(cn1)S(=O)(=O)N[C@H]1CC[C@H](CCN2CCN(CC2)c2cc(cc(c2)C(F)(F)F)C#N)CC1 |wU:11.11,wD:14.15,(-4.97,-20.83,;-3.63,-21.59,;-3.63,-23.15,;-2.29,-23.91,;-.96,-23.14,;-.95,-21.59,;-2.29,-20.83,;.38,-23.91,;-.38,-25.26,;1.14,-22.58,;1.72,-24.68,;3.06,-23.88,;3.06,-22.33,;4.4,-21.56,;5.73,-22.33,;7.07,-21.56,;8.4,-22.33,;9.74,-21.56,;11.07,-22.33,;12.39,-21.57,;12.4,-20.03,;11.07,-19.26,;9.73,-20.02,;13.74,-19.26,;13.74,-17.73,;15.06,-16.96,;16.41,-17.74,;16.4,-19.28,;15.06,-20.04,;17.73,-20.06,;19.06,-20.82,;16.96,-21.38,;18.51,-18.72,;15.06,-15.42,;15.05,-13.89,;5.73,-23.88,;4.4,-24.65,)|