Molecule Details
InChIKeyBKRGVLQUQGGVSM-RDTXWAMCSA-N
Compound Name3-[(6aR,9R)-7-methyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-yl]-1,1-diethylurea
Canonical SMILESCCN(CC)C(=O)N[C@@H]1C=C2c3cccc4[nH]cc(c34)C[C@H]2N(C)C1
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)18
Pfam Stratification Homologous
Avg pChEMBL8.6
SourceBindingDB
2D Structure
2D structure
Activity Profile
Target Activities (18)
Target Gene Organism Category Pfam pChEMBL Type Source
P08913 ADRA2A Homo sapiens Human PF00001 10.3 Ki BindingDB
P18089 ADRA2B Homo sapiens Human PF00001 9.9 Ki BindingDB
P35462 DRD3 Homo sapiens Human PF00001 9.6 Ki BindingDB
P08908 HTR1A Homo sapiens Human PF00001 9.4 Ki BindingDB
P14416 DRD2 Homo sapiens Human PF00001 9.3 Ki BindingDB
P28221 HTR1D Homo sapiens Human PF00001 9.0 Ki BindingDB
P41595 HTR2B Homo sapiens Human PF00001 8.9 Ki BindingDB
P28223 HTR2A Homo sapiens Human PF00001 8.7 Ki BindingDB
P25100 ADRA1D Homo sapiens Human PF00001 8.5 Ki BindingDB
P21918 DRD5 Homo sapiens Human PF00001 8.4 Ki BindingDB
P21917 DRD4 Homo sapiens Human PF00001 8.3 Ki BindingDB
P35348 ADRA1A Homo sapiens Human PF00001 8.3 Ki BindingDB
P28335 HTR2C Homo sapiens Human PF00001 8.2 Ki BindingDB
P07550 ADRB2 Homo sapiens Human PF00001 8.1 Ki BindingDB
P35368 ADRA1B Homo sapiens Human PF00001 7.8 Ki BindingDB
P28222 HTR1B Homo sapiens Human PF00001 7.7 Ki BindingDB
P21728 DRD1 Homo sapiens Human PF00001 7.2 Ki BindingDB
P08588 ADRB1 Homo sapiens Human PF00001 7.2 Ki BindingDB