Compound Detail
CHEMBL5398984
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Basic Information
| ChEMBL ID | CHEMBL5398984 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | UVVMAXSJVFOOMQ-VOTSOKGWSA-N |
2
Targets
2
Activities
1
Assay Types
1
PK Parameters
3
Publications
0
Known Names
Molecular Properties
447.6
MW (Da)
3.75
ALogP
7
HBA
2
HBD
88.0
PSA (Ų)
0.46
QED
0
Ro5 Violations
10
Rot. Bonds
Drug Information
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 2 meas. best 5.94
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Tyrosine-protein kinase JAK2 CHEMBL1649049 | IC50 | 5.94 | 5.94 | 1139.5 | 1 |
| Tyrosine-protein kinase JAK2 CHEMBL2971 | IC50 | 5.66 | 5.66 | 2189.8 | 1 |
Pharmacokinetic Data
| Parameter | Value | Units | Species |
|---|---|---|---|
| T1/2 | 0.9017 | hr | Homo sapiens |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Tyrosine-protein kinase JAK2 | IC50 | = | 1139.5 | nM | 5.94 | Inhibition of JAK2 V617F mutant in mouse BaF3 cells | 37583815 |
| Tyrosine-protein kinase JAK2 | IC50 | = | 2189.8 | nM | 5.66 | Inhibition of JAK2 V617F mutant in human SET2 cells | 37583815 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 37583815 | 10.1021/acsmedchemlett.3c00251 | Tyrosine-protein kinase JAK2 | 3 |
| 37583815 | 10.1021/acsmedchemlett.3c00251 | Receptor-type tyrosine-protein kinase FLT3 | 1 |
| 37583815 | 10.1021/acsmedchemlett.3c00251 | ADMET | 1 |
Data from ChEMBL 36 via Core Engine