Found 6 hits for monomerid = 50393542 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 |
Macrophage colony stimulating factor receptor
(Homo sapiens (Human)) | BDBM50393542
(CHEMBL2158228)Show SMILES NC(=O)CN1CCC(CC1)c1ccc(NC(=O)c2ncc([nH]2)C#N)c(c1)C1=CCCCC1 |t:29| Show InChI InChI=1S/C24H28N6O2/c25-13-19-14-27-23(28-19)24(32)29-21-7-6-18(12-20(21)17-4-2-1-3-5-17)16-8-10-30(11-9-16)15-22(26)31/h4,6-7,12,14,16H,1-3,5,8-11,15H2,(H2,26,31)(H,27,28)(H,29,32) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.40 | n/a | n/a | n/a | n/a | n/a | n/a |
Johnson& Johnson Pharmaceutical Research& Development
Curated by ChEMBL
| Assay Description Inhibition of FMS mediated phosphorylation using SYEGNSYTFIDPTQ as substrate after 80 mins by fluorescence polarization |
J Med Chem 54: 7860-83 (2011)
Article DOI: 10.1021/jm200900q BindingDB Entry DOI: 10.7270/Q2VD70JB |
More data for this Ligand-Target Pair | |
Macrophage colony-stimulating factor 1 receptor (c-Fms)
(Mus musculus (Mouse)) | BDBM50393542
(CHEMBL2158228)Show SMILES NC(=O)CN1CCC(CC1)c1ccc(NC(=O)c2ncc([nH]2)C#N)c(c1)C1=CCCCC1 |t:29| Show InChI InChI=1S/C24H28N6O2/c25-13-19-14-27-23(28-19)24(32)29-21-7-6-18(12-20(21)17-4-2-1-3-5-17)16-8-10-30(11-9-16)15-22(26)31/h4,6-7,12,14,16H,1-3,5,8-11,15H2,(H2,26,31)(H,27,28)(H,29,32) | PDB MMDB
KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 11 | n/a | n/a | n/a | n/a | n/a | n/a |
Johnson& Johnson Pharmaceutical Research& Development
Curated by ChEMBL
| Assay Description Inhibition of FMS-mediated proliferation in CSF1-stimulated bone marrow-derived mouse macrophages assessed as inhibition of incorporation of bromodeo... |
J Med Chem 54: 7860-83 (2011)
Article DOI: 10.1021/jm200900q BindingDB Entry DOI: 10.7270/Q2VD70JB |
More data for this Ligand-Target Pair | |
Cytochrome P450 3A4
(Homo sapiens (Human)) | BDBM50393542
(CHEMBL2158228)Show SMILES NC(=O)CN1CCC(CC1)c1ccc(NC(=O)c2ncc([nH]2)C#N)c(c1)C1=CCCCC1 |t:29| Show InChI InChI=1S/C24H28N6O2/c25-13-19-14-27-23(28-19)24(32)29-21-7-6-18(12-20(21)17-4-2-1-3-5-17)16-8-10-30(11-9-16)15-22(26)31/h4,6-7,12,14,16H,1-3,5,8-11,15H2,(H2,26,31)(H,27,28)(H,29,32) | 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+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Johnson& Johnson Pharmaceutical Research& Development
Curated by ChEMBL
| Assay Description Inhibition of CYP3A4 |
J Med Chem 54: 7860-83 (2011)
Article DOI: 10.1021/jm200900q BindingDB Entry DOI: 10.7270/Q2VD70JB |
More data for this Ligand-Target Pair | |
Cytochrome P450 2C9
(Homo sapiens (Human)) | BDBM50393542
(CHEMBL2158228)Show SMILES NC(=O)CN1CCC(CC1)c1ccc(NC(=O)c2ncc([nH]2)C#N)c(c1)C1=CCCCC1 |t:29| Show InChI InChI=1S/C24H28N6O2/c25-13-19-14-27-23(28-19)24(32)29-21-7-6-18(12-20(21)17-4-2-1-3-5-17)16-8-10-30(11-9-16)15-22(26)31/h4,6-7,12,14,16H,1-3,5,8-11,15H2,(H2,26,31)(H,27,28)(H,29,32) | 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+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Johnson& Johnson Pharmaceutical Research& Development
Curated by ChEMBL
| Assay Description Inhibition of CYP2C9 |
J Med Chem 54: 7860-83 (2011)
Article DOI: 10.1021/jm200900q BindingDB Entry DOI: 10.7270/Q2VD70JB |
More data for this Ligand-Target Pair | |
Cytochrome P450 2C19
(Homo sapiens (Human)) | BDBM50393542
(CHEMBL2158228)Show SMILES NC(=O)CN1CCC(CC1)c1ccc(NC(=O)c2ncc([nH]2)C#N)c(c1)C1=CCCCC1 |t:29| Show InChI InChI=1S/C24H28N6O2/c25-13-19-14-27-23(28-19)24(32)29-21-7-6-18(12-20(21)17-4-2-1-3-5-17)16-8-10-30(11-9-16)15-22(26)31/h4,6-7,12,14,16H,1-3,5,8-11,15H2,(H2,26,31)(H,27,28)(H,29,32) | 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 | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Johnson& Johnson Pharmaceutical Research& Development
Curated by ChEMBL
| Assay Description Inhibition of CYP2C19 |
J Med Chem 54: 7860-83 (2011)
Article DOI: 10.1021/jm200900q BindingDB Entry DOI: 10.7270/Q2VD70JB |
More data for this Ligand-Target Pair | |
Cytochrome P450 1A
(Homo sapiens (Human)) | BDBM50393542
(CHEMBL2158228)Show SMILES NC(=O)CN1CCC(CC1)c1ccc(NC(=O)c2ncc([nH]2)C#N)c(c1)C1=CCCCC1 |t:29| Show InChI InChI=1S/C24H28N6O2/c25-13-19-14-27-23(28-19)24(32)29-21-7-6-18(12-20(21)17-4-2-1-3-5-17)16-8-10-30(11-9-16)15-22(26)31/h4,6-7,12,14,16H,1-3,5,8-11,15H2,(H2,26,31)(H,27,28)(H,29,32) | PDB MMDB
Reactome pathway KEGG
B.MOAD DrugBank GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Johnson& Johnson Pharmaceutical Research& Development
Curated by ChEMBL
| Assay Description Inhibition of CYP1A2 |
J Med Chem 54: 7860-83 (2011)
Article DOI: 10.1021/jm200900q BindingDB Entry DOI: 10.7270/Q2VD70JB |
More data for this Ligand-Target Pair | |