Found 3 hits for monomerid = 50007106 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)) | BDBM50007106
(CHEMBL3237574)Show SMILES CCCc1nc(Nc2cc(N[C@@H]3CCCC[C@@H]3N)nnc2C(N)=O)ccc1OC |r| Show InChI InChI=1S/C20H29N7O2/c1-3-6-14-16(29-2)9-10-17(24-14)25-15-11-18(26-27-19(15)20(22)28)23-13-8-5-4-7-12(13)21/h9-13H,3-8,21H2,1-2H3,(H2,22,28)(H2,23,24,25,26)/t12-,13+/m0/s1 | PDB MMDB
NCI pathway 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 | 5 | 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 | |
Potassium voltage-gated channel subfamily H member 2
(Homo sapiens (Human)) | BDBM50007106
(CHEMBL3237574)Show SMILES CCCc1nc(Nc2cc(N[C@@H]3CCCC[C@@H]3N)nnc2C(N)=O)ccc1OC |r| Show InChI InChI=1S/C20H29N7O2/c1-3-6-14-16(29-2)9-10-17(24-14)25-15-11-18(26-27-19(15)20(22)28)23-13-8-5-4-7-12(13)21/h9-13H,3-8,21H2,1-2H3,(H2,22,28)(H2,23,24,25,26)/t12-,13+/m0/s1 | 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 | 3.98E+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 | |
Tyrosine-protein kinase SYK
(Homo sapiens (Human)) | BDBM50007106
(CHEMBL3237574)Show SMILES CCCc1nc(Nc2cc(N[C@@H]3CCCC[C@@H]3N)nnc2C(N)=O)ccc1OC |r| Show InChI InChI=1S/C20H29N7O2/c1-3-6-14-16(29-2)9-10-17(24-14)25-15-11-18(26-27-19(15)20(22)28)23-13-8-5-4-7-12(13)21/h9-13H,3-8,21H2,1-2H3,(H2,22,28)(H2,23,24,25,26)/t12-,13+/m0/s1 | PDB MMDB
NCI pathway 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 | 200 | 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 | |