Found 3 hits of ic50 for monomerid = 50452871 Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kJ/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
Cytochrome P450 3A4
(Homo sapiens (Human)) | BDBM50452871
![PNG](/data/jpeg/tenK5045/BindingDB_50452871.png) (CHEMBL4218256)Show SMILES N[C@H]1CCN(C1)c1cc2n(C3CC3)c(=O)c3ncnn3c2cc1F |r| Show InChI InChI=1S/C16H17FN6O/c17-11-5-14-13(6-12(11)21-4-3-9(18)7-21)22(10-1-2-10)16(24)15-19-8-20-23(14)15/h5-6,8-10H,1-4,7,18H2/t9-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | >3.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi R&D
Curated by ChEMBL
| Assay Description Inhibition of CYP3A4-mediated midazolam metabolism in human liver microsomes |
J Med Chem 61: 3565-3581 (2018)
Article DOI: 10.1021/acs.jmedchem.7b01892 BindingDB Entry DOI: 10.7270/Q2765HX2 |
More data for this Ligand-Target Pair | |
Cytochrome P450 3A4
(Homo sapiens (Human)) | BDBM50452871
![PNG](/data/jpeg/tenK5045/BindingDB_50452871.png) (CHEMBL4218256)Show SMILES N[C@H]1CCN(C1)c1cc2n(C3CC3)c(=O)c3ncnn3c2cc1F |r| Show InChI InChI=1S/C16H17FN6O/c17-11-5-14-13(6-12(11)21-4-3-9(18)7-21)22(10-1-2-10)16(24)15-19-8-20-23(14)15/h5-6,8-10H,1-4,7,18H2/t9-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | >3.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi R&D
Curated by ChEMBL
| Assay Description Inhibition of CYP3A4-mediated testosterone metabolism in human liver microsomes |
J Med Chem 61: 3565-3581 (2018)
Article DOI: 10.1021/acs.jmedchem.7b01892 BindingDB Entry DOI: 10.7270/Q2765HX2 |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily H member 2
(Homo sapiens (Human)) | BDBM50452871
![PNG](/data/jpeg/tenK5045/BindingDB_50452871.png) (CHEMBL4218256)Show SMILES N[C@H]1CCN(C1)c1cc2n(C3CC3)c(=O)c3ncnn3c2cc1F |r| Show InChI InChI=1S/C16H17FN6O/c17-11-5-14-13(6-12(11)21-4-3-9(18)7-21)22(10-1-2-10)16(24)15-19-8-20-23(14)15/h5-6,8-10H,1-4,7,18H2/t9-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | >3.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Sanofi R&D
Curated by ChEMBL
| Assay Description Inhibition of human ERG transfected in CHO cells by patch clamp method |
J Med Chem 61: 3565-3581 (2018)
Article DOI: 10.1021/acs.jmedchem.7b01892 BindingDB Entry DOI: 10.7270/Q2765HX2 |
More data for this Ligand-Target Pair | |