Compound Detail
CHEMBL58436
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Basic Information
| ChEMBL ID | CHEMBL58436 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | LIMBOIOWYJOOIC-UHFFFAOYSA-N |
7
Targets
8
Activities
1
Assay Types
0
PK Parameters
9
Publications
0
Known Names
Molecular Properties
358.4
MW (Da)
3.56
ALogP
7
HBA
1
HBD
77.8
PSA (Ų)
0.54
QED
0
Ro5 Violations
7
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 8 meas. best 7.0
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Homo sapiens CHEMBL372 | IC50 | 7.0 | 7.0 | 100.0 | 1 |
| Tyrosine-protein kinase ABL1 CHEMBL1862 | IC50 | 6.0 | 6.0 | 1000.0 | 1 |
| Bcr/Abl fusion protein CHEMBL2096618 | IC50 | 6.0 | 6.0 | 1000.0 | 1 |
| Protein kinase C alpha type CHEMBL299 | IC50 | 5.82 | 5.82 | 1500.0 | 1 |
| Proto-oncogene tyrosine-protein kinase Src CHEMBL267 | IC50 | 5.31 | 5.31 | 4900.0 | 1 |
| Epidermal growth factor receptor CHEMBL203 | IC50 | 5.15 | 5.15 | 7100.0 | 1 |
| Protein kinase C delta type CHEMBL2996 | IC50 | 4.47 | 4.47 | 34000.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Homo sapiens | IC50 | = | 100.0 | nM | 7.0 | In vitro inhibition of histamine release from human basophils | 8410986 |
| Tyrosine-protein kinase ABL1 | IC50 | = | 1000.0 | nM | 6.0 | Inhibition of v-Abl tyrosine kinase. | - |
| Bcr/Abl fusion protein | IC50 | = | 1000.0 | nM | 6.0 | Inhibition of BCR-ABL kinase (unknown origin) | 23473682 |
| Protein kinase C alpha type | IC50 | = | 1500.0 | nM | 5.82 | Inhibition of protein kinase C alpha. | - |
| Proto-oncogene tyrosine-protein kinase Src | IC50 | = | 4900.0 | nM | 5.31 | Inhibition of c-Src-tyrosine kinase. | - |
| Epidermal growth factor receptor | IC50 | = | 7100.0 | nM | 5.15 | Inhibition of the epidermal growth factor receptor. | - |
| Protein kinase C delta type | IC50 | = | 34000.0 | nM | 4.47 | Inhibition of protein kinase C delta. | - |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 8410986 | 10.1021/jm00071a002 | Homo sapiens | 1 |
| - | 10.1016/S0960-894X(96)00601-4 | Tyrosine-protein kinase ABL1 | 1 |
| - | 10.1016/S0960-894X(96)00601-4 | Epidermal growth factor receptor | 1 |
| - | 10.1016/S0960-894X(96)00601-4 | Proto-oncogene tyrosine-protein kinase Src | 1 |
| - | 10.1016/S0960-894X(96)00601-4 | Platelet-derived growth factor receptor | 1 |
| - | 10.1016/S0960-894X(96)00601-4 | cAMP-dependent protein kinase (PKA) | 1 |
| - | 10.1016/S0960-894X(96)00601-4 | Protein kinase C alpha type | 1 |
| - | 10.1016/S0960-894X(96)00601-4 | Protein kinase C delta type | 1 |
| 23473682 | 10.1016/j.bmcl.2013.01.113 | Bcr/Abl fusion protein | 1 |
Data from ChEMBL 36 via Core Engine