Molecule Details
| InChIKey | JTKFRFMSUBOCIQ-UHFFFAOYSA-N |
|---|---|
| Compound Name | 2-(2H-indazol-3-yl)-1H-1,3-benzodiazole |
| Canonical SMILES | c1ccc2[nH]c(-c3n[nH]c4ccccc34)nc2c1 |
| Clinical Status | Clinical Multi-Target |
| Targets (Human+Pathogen) | 4 |
| Pfam Stratification | Cross-Family |
| Avg pChEMBL | 6.12 |
| Source | BindingDB;ChEMBL;TTD_MultiTarget |
2D Structure
Activity Profile
DrugBank Annotations
| DrugBank ID | DB07959 |
|---|---|
| Drug Name | 3-(1H-BENZIMIDAZOL-2-YL)-1H-INDAZOLE |
| CAS Number | nan |
| Groups | experimental |
| ATC Codes | nan |
| Description | nan |
Cross-references: BindingDB: 16590 CHEMBL383990 ChemSpider: 10806321 PDB: IDZ PubChem:5327123 PubChem:99444430 ZINC: ZINC000014961821
Target Activities (4)
| Target | Gene | Organism | Category | Pfam | pChEMBL | Type | Source |
|---|---|---|---|---|---|---|---|
| P11362 | FGFR1 | Homo sapiens | Human | PF07679 PF00047 PF07714 | 6.1 | pIC50 | TTD_MultiTarget |
| P17948 | FLT1 | Homo sapiens | Human | PF07679 PF00047 PF13927 PF22971 PF07714 PF21339 PF17988 PF22854 | 6.1 | IC50 | ChEMBL;BindingDB |
| P49841 | GSK3B | Homo sapiens | Human | PF00069 | 6.1 | IC50 | BindingDB |
| P06493 | CDK1 | Homo sapiens | Human | PF00069 | 6.1 | IC50 | BindingDB |
DrugBank Target Actions (5)
| Target | Gene | Target Name | Action | Type |
|---|---|---|---|---|
| O14757 | CHEK1 | Serine/threonine-protein kinase Chk1 | binder | targets |
| P09619 | PDGFRB | Platelet-derived growth factor receptor beta | inhibitor | targets |
| P11362 | FGFR1 | Fibroblast growth factor receptor 1 | inhibitor | targets |
| P17948 | FLT1 | Vascular endothelial growth factor receptor 1 | inhibitor | targets |
| P35968 | KDR | Vascular endothelial growth factor receptor 2 | inhibitor | targets |