BDBM50242224 CHEMBL4070939
SMILES: CCCCCC[C@H]1[C@@H](OC1=O)C(=O)NCCCC[C@@H]1NC(=O)N([C@@H](C)C(=O)OCc2ccccc2)C1=O
InChI Key: InChIKey=HQACOVOVAYEUBW-JKLQHZFJSA-N
Data: 4 IC50
Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kcal/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Proteasome Macropain subunit (Homo sapiens (Human)) | BDBM50242224 (CHEMBL4070939) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | >1.00E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Baylor University Curated by ChEMBL | Assay Description Inhibition of trypsin-like activity of 20S proteasome in human red blood cells pretreated for 20 mins followed by Boc-Leu-Arg-Arg-AMC substrate addit... | Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Proteasome subunit beta type-1/beta type-5 (Homo sapiens (Human)) | BDBM50242224 (CHEMBL4070939) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 510 | n/a | n/a | n/a | n/a | n/a | n/a |
Baylor University Curated by ChEMBL | Assay Description Inhibition of chymotrypsin-like activity of 20S proteasome in human red blood cells pretreated for 20 mins followed by Suc-Leu-Leu-Val-Tyr-AMC substr... | Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Proteasome component C5 (Homo sapiens (Human)) | BDBM50242224 (CHEMBL4070939) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 7.93E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Baylor University Curated by ChEMBL | Assay Description Inhibition of caspase-like activity of 20S proteasome in human red blood cells pretreated for 20 mins followed by Z-Leu-Leu-Glu-AMC substrate additio... | Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Fatty acid synthase (Homo sapiens (Human)) | BDBM50242224 (CHEMBL4070939) | PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 5.55E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Baylor University Curated by ChEMBL | Assay Description Inhibition of human FAS thioster domain preincubated for 30 mins followed by 4-methylumbelliferyl heptanoate substrate addition measured every 5 mins... | Bioorg Med Chem 25: 2901-2916 (2017) Article DOI: 10.1016/j.bmc.2017.01.020 BindingDB Entry DOI: 10.7270/Q26W9DG3 | |||||||||||
More data for this Ligand-Target Pair |