Compound Detail
CHEMBL5419719
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Basic Information
| ChEMBL ID | CHEMBL5419719 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | DGGOQICQTAGRMC-XMMPIXPASA-N |
3
Targets
3
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names
Molecular Properties
480.5
MW (Da)
2.74
ALogP
9
HBA
2
HBD
121.0
PSA (Ų)
0.43
QED
0
Ro5 Violations
6
Rot. Bonds
Drug Information
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 3 meas. best 9.0
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Histone-lysine N-methyltransferase NSD3 CHEMBL3108646 | IC50 | 9.0 | 9.0 | 1.0 | 1 |
| Histone-lysine N-methyltransferase NSD2 CHEMBL3108645 | IC50 | 8.26 | 8.26 | 5.5 | 1 |
| Histone-lysine N-methyltransferase, H3 lysine-36 specific CHEMBL3588738 | IC50 | 6.65 | 6.65 | 225.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Histone-lysine N-methyltransferase NSD3 | IC50 | = | 1.0 | nM | 9.0 | Inhibition of NSD3 degradation in human KMS-11 cells assessed as reduction in H3... | 37578463 |
| Histone-lysine N-methyltransferase NSD2 | IC50 | = | 5.5 | nM | 8.26 | LC-MS/MS-Based NSD2 Enzymatic Assay: This assay employed LC-MS/MS technology to ... | - |
| Histone-lysine N-methyltransferase, H3 lysine-36 specific | IC50 | = | 225.0 | nM | 6.65 | Inhibition of human recombinant NSD1 incubated for 2 hrs by AlphaLISA method | 37578463 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 37578463 | 10.1021/acs.jmedchem.3c00948 | Histone-lysine N-methyltransferase, H3 lysine-36 specific | 1 |
| 37578463 | 10.1021/acs.jmedchem.3c00948 | Histone-lysine N-methyltransferase NSD3 | 1 |
Data from ChEMBL 36 via Core Engine