Found 4 hits for monomerid = 50456924 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 |
p110α/p85α
(Homo sapiens (Human)) | BDBM50456924
(CHEMBL4207685)Show SMILES COc1ncc(cc1NS(=O)(=O)c1ccc(F)cc1F)-c1ccc2ncc(C(=O)NCCCN3CCOCC3)n2c1 Show InChI InChI=1S/C27H28F2N6O5S/c1-39-27-22(33-41(37,38)24-5-4-20(28)14-21(24)29)13-19(15-32-27)18-3-6-25-31-16-23(35(25)17-18)26(36)30-7-2-8-34-9-11-40-12-10-34/h3-6,13-17,33H,2,7-12H2,1H3,(H,30,36) | PDB
UniProtKB/SwissProt UniProtKB/TrEMBL
antibodypedia antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 3.80 | n/a | n/a | n/a | n/a | n/a | n/a |
Shenyang Pharmaceutical University
Curated by ChEMBL
| Assay Description Inhibition of N-terminal His6-tagged recombinant full-length human p110alpha/untagged recombinant full length human p85alpha expressed in baculovirus... |
Eur J Med Chem 139: 95-106 (2017)
Article DOI: 10.1016/j.ejmech.2017.07.074 BindingDB Entry DOI: 10.7270/Q2KH0QXV |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
(Homo sapiens (Human)) | BDBM50456924
(CHEMBL4207685)Show SMILES COc1ncc(cc1NS(=O)(=O)c1ccc(F)cc1F)-c1ccc2ncc(C(=O)NCCCN3CCOCC3)n2c1 Show InChI InChI=1S/C27H28F2N6O5S/c1-39-27-22(33-41(37,38)24-5-4-20(28)14-21(24)29)13-19(15-32-27)18-3-6-25-31-16-23(35(25)17-18)26(36)30-7-2-8-34-9-11-40-12-10-34/h3-6,13-17,33H,2,7-12H2,1H3,(H,30,36) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 106 | n/a | n/a | n/a | n/a | n/a | n/a |
Shenyang Pharmaceutical University
Curated by ChEMBL
| Assay Description Inhibition of PI3Kbeta (unknown origin) using PIP2 as substrate by HTRF colorimetric assay |
Eur J Med Chem 139: 95-106 (2017)
Article DOI: 10.1016/j.ejmech.2017.07.074 BindingDB Entry DOI: 10.7270/Q2KH0QXV |
More data for this Ligand-Target Pair | |
Phosphoinositide 3-Kinase (PI3K), delta
(Homo sapiens (Human)) | BDBM50456924
(CHEMBL4207685)Show SMILES COc1ncc(cc1NS(=O)(=O)c1ccc(F)cc1F)-c1ccc2ncc(C(=O)NCCCN3CCOCC3)n2c1 Show InChI InChI=1S/C27H28F2N6O5S/c1-39-27-22(33-41(37,38)24-5-4-20(28)14-21(24)29)13-19(15-32-27)18-3-6-25-31-16-23(35(25)17-18)26(36)30-7-2-8-34-9-11-40-12-10-34/h3-6,13-17,33H,2,7-12H2,1H3,(H,30,36) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 101 | n/a | n/a | n/a | n/a | n/a | n/a |
Shenyang Pharmaceutical University
Curated by ChEMBL
| Assay Description Inhibition of p110delta/p85alpha (unknown origin) using PIP2 as substrate by HTRF colorimetric assay |
Eur J Med Chem 139: 95-106 (2017)
Article DOI: 10.1016/j.ejmech.2017.07.074 BindingDB Entry DOI: 10.7270/Q2KH0QXV |
More data for this Ligand-Target Pair | |
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform
(Homo sapiens (Human)) | BDBM50456924
(CHEMBL4207685)Show SMILES COc1ncc(cc1NS(=O)(=O)c1ccc(F)cc1F)-c1ccc2ncc(C(=O)NCCCN3CCOCC3)n2c1 Show InChI InChI=1S/C27H28F2N6O5S/c1-39-27-22(33-41(37,38)24-5-4-20(28)14-21(24)29)13-19(15-32-27)18-3-6-25-31-16-23(35(25)17-18)26(36)30-7-2-8-34-9-11-40-12-10-34/h3-6,13-17,33H,2,7-12H2,1H3,(H,30,36) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 37 | n/a | n/a | n/a | n/a | n/a | n/a |
Shenyang Pharmaceutical University
Curated by ChEMBL
| Assay Description Inhibition of N-terminal His6-tagged recombinant full-length human PI3Kgamma expressed in baculovirus infected Sf21 insect cells using PIP2 as substr... |
Eur J Med Chem 139: 95-106 (2017)
Article DOI: 10.1016/j.ejmech.2017.07.074 BindingDB Entry DOI: 10.7270/Q2KH0QXV |
More data for this Ligand-Target Pair | |