Reaction Details Report a problem with these data
Target
Cannabinoid receptor 1
Ligand
BDBM50332881
Substrate
n/a
Meas. Tech.
ChEMBL_694005 (CHEMBL1636581)
Ki
372.3±n/a nM
Citation
Silvestri, R; Ligresti, A; La Regina, G; Piscitelli, F; Gatti, V; Lavecchia, A; Brizzi, A; Pasquini, S; Allarà, M; Fantini, N; Carai, MA; Bigogno, C; Rozio, MG; Sinisi, R; Novellino, E; Colombo, G; Di Marzo, V; Dondio, G; Corelli, F Synthesis and biological evaluation of new N-alkyl 1-aryl-5-(1H-pyrrol-1-yl)-1H-pyrazole-3-carboxamides as cannabinoid receptor ligands. Eur J Med Chem 45:5878-86 (2010) [PubMed] Article
More Info.:
Target
Name:
Cannabinoid receptor 1
Synonyms:
CANN6 | CANNABINOID CB1 | CB-R | CB1 | CNR | CNR1 | CNR1_HUMAN | Cannabinoid CB1 receptor | Cannabinoid receptor | Cannabinoid receptor 1 (CB1) | Cannabinoid receptor 1 (brain)
Type:
G Protein-Coupled Receptor (GPCR)
Mol. Mass.:
52868.96
Organism:
Homo sapiens (Human)
Description:
P21554
Residue:
472
Sequence:
MKSILDGLADTTFRTITTDLLYVGSNDIQYEDIKGDMASKLGYFPQKFPLTSFRGSPFQEKMTAGDNPQLVPADQVNITEFYNKSLSSFKENEENIQCGENFMDIECFMVLNPSQQLAIAVLSLTLGTFTVLENLLVLCVILHSRSLRCRPSYHFIGSLAVADLLGSVIFVYSFIDFHVFHRKDSRNVFLFKLGGVTASFTASVGSLFLTAIDRYISIHRPLAYKRIVTRPKAVVAFCLMWTIAIVIAVLPLLGWNCEKLQSVCSDIFPHIDETYLMFWIGVTSVLLLFIVYAYMYILWKAHSHAVRMIQRGTQKSIIIHTSEDGKVQVTRPDQARMDIRLAKTLVLILVVLIICWGPLLAIMVYDVFGKMNKLIKTVFAFCSMLCLLNSTVNPIIYALRSKDLRHAFRSMFPSCEGTAQPLDNSMGDSDCLHKHANNAASVHRAAESCIKSTVKIAKVTMSVSTDTSAEAL
Inhibitor
Name:
BDBM50332881
Synonyms:
1-(2,4-Dichlorophenyl)-5-(2,5-dimethyl-1H-pyrrol-1-yl)-N-(5-hydroxypentyl)-4-methyl-1H-pyrazole-3-carboxamide | CHEMBL1631169
Type:
Small organic molecule
Emp. Form.:
C22H26Cl2N4O2
Mol. Mass.:
449.373
SMILES:
Cc1ccc(C)n1-c1c(C)c(nn1-c1ccc(Cl)cc1Cl)C(=O)NCCCCCO |(-3.67,-7.38,;-3.57,-8.93,;-4.76,-9.88,;-4.24,-11.31,;-2.7,-11.26,;-2.08,-12.19,;-2.28,-9.79,;-.87,-9.18,;-.32,-7.75,;-1.15,-6.44,;1.19,-7.82,;1.61,-9.29,;.34,-10.15,;.33,-11.7,;-1,-12.47,;-1,-14.01,;.34,-14.78,;.34,-16.32,;1.67,-14.01,;1.67,-12.46,;3.01,-11.68,;1.94,-6.45,;1.15,-5.15,;3.49,-6.42,;4.29,-7.73,;5.83,-7.68,;6.63,-9,;8.17,-8.96,;8.98,-10.28,;10.52,-10.24,)|