Compound Detail
CHEMBL4281163
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Basic Information
| ChEMBL ID | CHEMBL4281163 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | AZFYXQQKGDXNAX-UHFFFAOYSA-N |
1
Targets
3
Activities
1
Assay Types
0
PK Parameters
0
Publications
0
Known Names
Molecular Properties
343.5
MW (Da)
3.43
ALogP
7
HBA
3
HBD
101.6
PSA (Ų)
0.71
QED
0
Ro5 Violations
7
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 3 meas. best 7.3
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Isocitrate dehydrogenase [NADP] cytoplasmic CHEMBL2007625 | IC50 | 7.3 | 7.3 | 50.0 | 3 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Isocitrate dehydrogenase [NADP] cytoplasmic | IC50 | = | 50.0 | nM | 7.3 | Inhibition of DH1 R132H mutant homodimer (unknown origin) expressed in Sf9 cells... | - |
| Isocitrate dehydrogenase [NADP] cytoplasmic | IC50 | = | 50.0 | nM | 7.3 | Inhibition of DH1 R132C mutant homodimer (unknown origin) expressed in Sf9 cells... | - |
| Isocitrate dehydrogenase [NADP] cytoplasmic | IC50 | = | 50.0 | nM | 7.3 | Inhibition of IDH1 R132H/R132C mutant in human HT1080 cells assessed as reductio... | - |
Data from ChEMBL 36 via Core Engine