Molecule Details
InChIKeyDUKNIHFTDAXJON-RCZCSUKSSA-N
Compound Name[(2R,4R)-2,4-dimethylazetidin-1-yl]-[(9R)-7-methyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinolin-9-yl]methanone
Canonical SMILESC[C@@H]1C[C@@H](C)N1C(=O)[C@@H]1C=C2c3cccc4[nH]cc(c34)CC2N(C)C1
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)11
Pfam Stratification Homologous
Avg pChEMBL7.23
SourceChEMBL;BindingDB
2D Structure
2D structure
Activity Profile
Target Activities (11)
Target Gene Organism Category Pfam pChEMBL Type Source
P28221 HTR1D Homo sapiens Human PF00001 8.7 Ki ChEMBL;BindingDB
P08908 HTR1A Homo sapiens Human PF00001 8.2 Ki ChEMBL;BindingDB
P47898 HTR5A Homo sapiens Human PF00001 7.9 Ki ChEMBL;BindingDB
P34969 HTR7 Homo sapiens Human PF00001 7.5 Ki ChEMBL;BindingDB
P50406 HTR6 Homo sapiens Human PF00001 7.2 Ki ChEMBL;BindingDB
P21917 DRD4 Homo sapiens Human PF00001 7.1 Ki ChEMBL;BindingDB
P28566 HTR1E Homo sapiens Human PF00001 6.8 Ki ChEMBL;BindingDB
P35462 DRD3 Homo sapiens Human PF00001 6.8 Ki ChEMBL;BindingDB
P41595 HTR2B Homo sapiens Human PF00001 6.5 Ki ChEMBL;BindingDB
P14416 DRD2 Homo sapiens Human PF00001 6.5 Ki ChEMBL;BindingDB
P21918 DRD5 Homo sapiens Human PF00001 6.2 Ki ChEMBL;BindingDB