Molecule Details
InChIKeyKSERXGMCDHOLSS-LJQANCHMSA-N
Compound NameUlixertinib
Canonical SMILESCC(C)Nc1cc(-c2c[nH]c(C(=O)N[C@H](CO)c3cccc(Cl)c3)c2)c(Cl)cn1
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)3
Pfam Stratification Homologous
Avg pChEMBL7.07
SourceChEMBL;BindingDB
2D Structure
2D structure
Activity Profile
DrugBank Annotations
DrugBank ID DB13930
Drug NameUlixertinib
CAS Number869886-67-9
Groups investigational
ATC Codes nan
DescriptionUlixertinib is a a novel, reversible, ATP-competitive ERK1/2 inhibitor with high potency and ERK1/2 selectivity [A31474]. It is currently in clinical trials for the treatment of a wide range of tumors.

Categories: Amines Pyridines
Cross-references: CHEMBL3590106 ChemSpider: 9893722 PDB: EVK ZINC: ZINC000034642570
Target Activities (3)
Target Gene Organism Category Pfam pChEMBL Type Source
P28482 MAPK1 Homo sapiens Human PF00069 8.0 IC50 ChEMBL;BindingDB
P27361 MAPK3 Homo sapiens Human PF00069 6.8 IC50 ChEMBL
Q7L7X3 TAOK1 Homo sapiens Human PF00069 6.4 Kd ChEMBL
DrugBank Target Actions (3)
Target Gene Target Name Action Type
P27361 MAPK3 Mitogen-activated protein kinase 3 inhibitor targets
P28482 MAPK1 Mitogen-activated protein kinase 1 inhibitor targets
P29323 EPHB2 Ephrin type-B receptor 2 inhibitor targets