Compound Detail
CHEMBL3765125
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Basic Information
| ChEMBL ID | CHEMBL3765125 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | GOMMADJURTTYPW-UHFFFAOYSA-N |
3
Targets
3
Activities
2
Assay Types
1
PK Parameters
5
Publications
0
Known Names
Molecular Properties
344.4
MW (Da)
2.35
ALogP
6
HBA
2
HBD
88.5
PSA (Ų)
0.58
QED
0
Ro5 Violations
2
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
EC50 2 meas. best 6.83
IC50 1 meas. best 8.62
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Poly [ADP-ribose] polymerase 1 CHEMBL3105 | IC50 | 8.62 | 8.62 | 2.4 | 1 |
| PARP 1, 2 and 3 CHEMBL3390820 | EC50 | 6.83 | 6.83 | 149.0 | 1 |
| NON-PROTEIN TARGET CHEMBL3879801 | EC50 | 6.77 | 6.77 | 170.0 | 1 |
Pharmacokinetic Data
| Parameter | Value | Units | Species |
|---|---|---|---|
| T1/2 | 6.9 | hr | Rattus norvegicus |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Poly [ADP-ribose] polymerase 1 | IC50 | = | 2.4 | nM | 8.62 | Inhibition of human PARP1 using [3H]NAD as substrate after 1 min by microplate s... | 26652717 |
| PARP 1, 2 and 3 | EC50 | = | 149.0 | nM | 6.83 | Inhibition of PARP in human LoVo cells assessed as inhibition of poly(ADP)-ribos... | 26652717 |
| NON-PROTEIN TARGET | EC50 | = | 170.0 | nM | 6.77 | Cytotoxicity against BRCA2-deficient human Capan1 cells | 26652717 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 26652717 | 10.1021/acs.jmedchem.5b01498 | Poly [ADP-ribose] polymerase 1 | 1 |
| 26652717 | 10.1021/acs.jmedchem.5b01498 | PARP 1, 2 and 3 | 1 |
| 26652717 | 10.1021/acs.jmedchem.5b01498 | LoVo | 1 |
| 26652717 | 10.1021/acs.jmedchem.5b01498 | NON-PROTEIN TARGET | 1 |
| 26652717 | 10.1021/acs.jmedchem.5b01498 | Liver microsome | 1 |
Data from ChEMBL 36 via Core Engine