Compound Detail
CHEMBL5619878
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Basic Information
| ChEMBL ID | CHEMBL5619878 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | FRIOJNGETURVST-UHFFFAOYSA-N |
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names
Molecular Properties
355.4
MW (Da)
2.80
ALogP
7
HBA
1
HBD
83.3
PSA (Ų)
0.85
QED
0
Ro5 Violations
6
Rot. Bonds
Drug Information
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 1 meas. best 6.25
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Histone-lysine N-methyltransferase NSD2 CHEMBL3108645 | IC50 | 6.25 | 6.25 | 569.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Histone-lysine N-methyltransferase NSD2 | IC50 | = | 569.0 | nM | 6.25 | Inhibition of recombinant human NSD2 (941 to 1240 residues) using unmethylated h... | 39230932 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 39230932 | 10.1021/acs.jmedchem.4c00639 | Histone-lysine N-methyltransferase NSD2 | 1 |
Data from ChEMBL 36 via Core Engine