Compound Detail
CHEMBL4282198
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CC[C@H](C)[C@@H]1C(=O)O[C@H]1C(=O)N[C@H](C(=O)N[C@H](C(=O)OCC(C)C)C(C)C)C(C)C
Basic Information
| ChEMBL ID | CHEMBL4282198 |
| Phase | Preclinical |
| Structure Type | MOL |
| InChI Key | PBBWGHXDMWKEJT-KFGODFMUSA-N |
4
Targets
4
Activities
1
Assay Types
0
PK Parameters
4
Publications
0
Known Names
Molecular Properties
426.6
MW (Da)
2.05
ALogP
6
HBA
2
HBD
110.8
PSA (Ų)
0.49
QED
0
Ro5 Violations
11
Rot. Bonds
Drug Information
| Molecule Type | Small molecule |
| Availability | Unknown |
| Chirality | Unknown |
Activity Summary
IC50 4 meas. best 8.06
Target Activity Profile
| Target | Type | Best pChEMBL | Mean pChEMBL | Best (nM) | # Data |
|---|---|---|---|---|---|
| Proteasome Macropain subunit MB1 CHEMBL4662 | IC50 | 8.06 | 8.06 | 8.8 | 1 |
| RPMI-8226 CHEMBL614882 | IC50 | 7.02 | 7.02 | 95.0 | 1 |
| MDA-MB-231 CHEMBL400 | IC50 | 6.5 | 6.5 | 317.0 | 1 |
| MCF7 CHEMBL387 | IC50 | 6.18 | 6.18 | 664.0 | 1 |
Activity Data Samples
Top measurements by pChEMBL value
| Target | Type | Rel. | Value | Units | pChEMBL | Assay | PubMed |
|---|---|---|---|---|---|---|---|
| Proteasome Macropain subunit MB1 | IC50 | = | 8.8 | nM | 8.06 | Inhibition of 20S proteasome beta5 subunit in human Jurkat cell lysate using Suc... | 30165344 |
| RPMI-8226 | IC50 | = | 95.0 | nM | 7.02 | Cytotoxicity against human RPMI8226 cells after 48 hrs by MTT assay | 30165344 |
| MDA-MB-231 | IC50 | = | 317.0 | nM | 6.5 | Cytotoxicity against human MDA-MB-231 cells after 48 hrs by MTT assay | 30165344 |
| MCF7 | IC50 | = | 664.0 | nM | 6.18 | Cytotoxicity against human MCF7 cells after 48 hrs by MTT assay | 30165344 |
Literature References
| PubMed | DOI | Target Context | # Activities |
|---|---|---|---|
| 30165344 | 10.1016/j.ejmech.2018.08.052 | MCF7 | 1 |
| 30165344 | 10.1016/j.ejmech.2018.08.052 | MDA-MB-231 | 1 |
| 30165344 | 10.1016/j.ejmech.2018.08.052 | RPMI-8226 | 1 |
| 30165344 | 10.1016/j.ejmech.2018.08.052 | Proteasome Macropain subunit MB1 | 1 |
Data from ChEMBL 36 via Core Engine