Molecule Details
InChIKeyAWSRDDSRQUJMAJ-LCAJTWGOSA-N
Canonical SMILESC[C@H]1C[C@@H](N2C(=N)N[C@](C)(c3cccc(NC(=O)c4cccc(C#N)c4)c3Cl)CC2=O)CCO1
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)2
Pfam Stratification Homologous
Avg pChEMBL7.5
SourceChEMBL;BindingDB
2D Structure
2D structure
Activity Profile
DrugBank Annotations
DrugBank ID DB17096
Drug NameUCB7362
CAS Numbernan
Groups experimental
ATC Codes nan
DescriptionUCB7362 is an orally active plasmepsin X (PMX) inhibitor currently investigated for the treatment of malaria.[A254222] Plasmepsins are aspartyl proteases produced by the malaria parasite _Plasmodium falciparum_, and PMX is considered to be essential for parasite egress and invasion.[A254232] UCB7362...
Target Activities (2)
Target Gene Organism Category Pfam pChEMBL Type Source
Q8IAS0 PMX Plasmodium falciparum (isolate 3D7) Pathogen PF00026 8.2 IC50 ChEMBL;BindingDB
Q8ILG2 PMIX Plasmodium falciparum (isolate 3D7) Pathogen PF00026 6.8 IC50 ChEMBL;BindingDB
DrugBank Target Actions (4)
Target Gene Target Name Action Type
Q8IAS0 PMX Plasmepsin X binder targets
W7JWW5 W7JWW5 Plasmepsin X binder targets
Q8IAS0 PMX Plasmepsin X inhibitor targets
W7JWW5 W7JWW5 Plasmepsin X inhibitor targets