Found 6 hits for monomerid = 50007093 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 |
Tyrosine-protein kinase SYK
(Homo sapiens (Human)) | BDBM50007093
![PNG](/data/jpeg/tenK5000/BindingDB_50007093.png) (CHEMBL3237564)Show SMILES N[C@H]1CCCC[C@H]1Nc1cc(Nc2ccc3CCCc3n2)c(nn1)C(N)=O |r| Show InChI InChI=1S/C19H25N7O/c20-12-5-1-2-6-14(12)23-17-10-15(18(19(21)27)26-25-17)24-16-9-8-11-4-3-7-13(11)22-16/h8-10,12,14H,1-7,20H2,(H2,21,27)(H2,22,23,24,25)/t12-,14+/m0/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 10 | n/a | n/a | n/a | n/a | n/a | n/a |
Hoffmann-La Roche Inc.
Curated by ChEMBL
| Assay Description Inhibition of human SYK (360 to 635) using biotin-EPEGDYEEVLE as substrate preincubated for 10 mins followed by substrate/ATP/[33Pgamma]ATP addition ... |
J Med Chem 57: 2683-91 (2014)
Article DOI: 10.1021/jm401982j BindingDB Entry DOI: 10.7270/Q2HT2QTR |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase SYK
(Homo sapiens (Human)) | BDBM50007093
![PNG](/data/jpeg/tenK5000/BindingDB_50007093.png) (CHEMBL3237564)Show SMILES N[C@H]1CCCC[C@H]1Nc1cc(Nc2ccc3CCCc3n2)c(nn1)C(N)=O |r| Show InChI InChI=1S/C19H25N7O/c20-12-5-1-2-6-14(12)23-17-10-15(18(19(21)27)26-25-17)24-16-9-8-11-4-3-7-13(11)22-16/h8-10,12,14H,1-7,20H2,(H2,21,27)(H2,22,23,24,25)/t12-,14+/m0/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 251 | n/a | n/a | n/a | n/a | n/a | n/a |
Hoffmann-La Roche Inc.
Curated by ChEMBL
| Assay Description Inhibition of SYK in human whole blood assessed as anti-human IgM-induced CD69 protein expression preincubated for 30 mins followed by anti-human IgM... |
J Med Chem 57: 2683-91 (2014)
Article DOI: 10.1021/jm401982j BindingDB Entry DOI: 10.7270/Q2HT2QTR |
More data for this Ligand-Target Pair | |
Cytochrome P450 2D6
(Homo sapiens (Human)) | BDBM50007093
![PNG](/data/jpeg/tenK5000/BindingDB_50007093.png) (CHEMBL3237564)Show SMILES N[C@H]1CCCC[C@H]1Nc1cc(Nc2ccc3CCCc3n2)c(nn1)C(N)=O |r| Show InChI InChI=1S/C19H25N7O/c20-12-5-1-2-6-14(12)23-17-10-15(18(19(21)27)26-25-17)24-16-9-8-11-4-3-7-13(11)22-16/h8-10,12,14H,1-7,20H2,(H2,21,27)(H2,22,23,24,25)/t12-,14+/m0/s1 | PDB
UniProtKB/SwissProt UniProtKB/TrEMBL
GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Hoffmann-La Roche Inc.
Curated by ChEMBL
| Assay Description Inhibition of CYP2D6 in human liver microsomal fraction assessed as dextromethorphan O-demethylase preincubated for 10 mins followed by NADPH additio... |
J Med Chem 57: 2683-91 (2014)
Article DOI: 10.1021/jm401982j BindingDB Entry DOI: 10.7270/Q2HT2QTR |
More data for this Ligand-Target Pair | |
Cytochrome P450 3A4
(Homo sapiens (Human)) | BDBM50007093
![PNG](/data/jpeg/tenK5000/BindingDB_50007093.png) (CHEMBL3237564)Show SMILES N[C@H]1CCCC[C@H]1Nc1cc(Nc2ccc3CCCc3n2)c(nn1)C(N)=O |r| Show InChI InChI=1S/C19H25N7O/c20-12-5-1-2-6-14(12)23-17-10-15(18(19(21)27)26-25-17)24-16-9-8-11-4-3-7-13(11)22-16/h8-10,12,14H,1-7,20H2,(H2,21,27)(H2,22,23,24,25)/t12-,14+/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Hoffmann-La Roche Inc.
Curated by ChEMBL
| Assay Description Inhibition of CYP3A4 in human liver microsomal fraction assessed as midazolam-1'-hydroxylation preincubated for 10 mins followed by NADPH addition me... |
J Med Chem 57: 2683-91 (2014)
Article DOI: 10.1021/jm401982j BindingDB Entry DOI: 10.7270/Q2HT2QTR |
More data for this Ligand-Target Pair | |
Cytochrome P450 2C9
(Homo sapiens (Human)) | BDBM50007093
![PNG](/data/jpeg/tenK5000/BindingDB_50007093.png) (CHEMBL3237564)Show SMILES N[C@H]1CCCC[C@H]1Nc1cc(Nc2ccc3CCCc3n2)c(nn1)C(N)=O |r| Show InChI InChI=1S/C19H25N7O/c20-12-5-1-2-6-14(12)23-17-10-15(18(19(21)27)26-25-17)24-16-9-8-11-4-3-7-13(11)22-16/h8-10,12,14H,1-7,20H2,(H2,21,27)(H2,22,23,24,25)/t12-,14+/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | >5.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Hoffmann-La Roche Inc.
Curated by ChEMBL
| Assay Description Inhibition of CYP2C9 in human liver microsomal fraction assessed as diclofenac-4'-hydroxylation preincubated for 10 mins followed by NADPH addition m... |
J Med Chem 57: 2683-91 (2014)
Article DOI: 10.1021/jm401982j BindingDB Entry DOI: 10.7270/Q2HT2QTR |
More data for this Ligand-Target Pair | |
Potassium voltage-gated channel subfamily H member 2
(Homo sapiens (Human)) | BDBM50007093
![PNG](/data/jpeg/tenK5000/BindingDB_50007093.png) (CHEMBL3237564)Show SMILES N[C@H]1CCCC[C@H]1Nc1cc(Nc2ccc3CCCc3n2)c(nn1)C(N)=O |r| Show InChI InChI=1S/C19H25N7O/c20-12-5-1-2-6-14(12)23-17-10-15(18(19(21)27)26-25-17)24-16-9-8-11-4-3-7-13(11)22-16/h8-10,12,14H,1-7,20H2,(H2,21,27)(H2,22,23,24,25)/t12-,14+/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 7.94E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Hoffmann-La Roche Inc.
Curated by ChEMBL
| Assay Description Inhibition of human ERG expressed in CHO cells by patch clamp method |
J Med Chem 57: 2683-91 (2014)
Article DOI: 10.1021/jm401982j BindingDB Entry DOI: 10.7270/Q2HT2QTR |
More data for this Ligand-Target Pair | |