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)) | BDBM50169690 (CHEMBL3806137) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | 540 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Time dependent inhibition of CYP3A4 in human liver microsomes | ACS Med Chem Lett 7: 312-7 (2016) Article DOI: 10.1021/acsmedchemlett.5b00459 BindingDB Entry DOI: 10.7270/Q2W95C3K | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM9048 (US8536193, 10-5) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | US Patent | n/a | n/a | 0.340 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Sharp & Dohme Corp.; MSD K.K. US Patent | Assay Description Activated Akt isoforms and pleckstrin homology domain deletion constructs were assayed utilizing a GSK-derived biotinylated peptide substrate. The e... | US Patent US8536193 (2013) BindingDB Entry DOI: 10.7270/Q2NK3CP1 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM102310 (US8536193, 10-4) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | US Patent | n/a | n/a | 0.380 | n/a | n/a | n/a | n/a | 7.5 | n/a |
Merck Sharp & Dohme Corp.; MSD K.K. US Patent | Assay Description Activated Akt isoforms and pleckstrin homology domain deletion constructs were assayed utilizing a GSK-derived biotinylated peptide substrate. The e... | US Patent US8536193 (2013) BindingDB Entry DOI: 10.7270/Q2NK3CP1 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM8727 (US8536193, 7-26) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 0.700 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Sharp & Dohme Corp.; MSD K.K. US Patent | Assay Description Activated Akt isoforms and pleckstrin homology domain deletion constructs were assayed utilizing a GSK-derived biotinylated peptide substrate. The e... | US Patent US8536193 (2013) BindingDB Entry DOI: 10.7270/Q2NK3CP1 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-beta serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM102310 (US8536193, 10-4) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | US Patent | n/a | n/a | 1.70 | n/a | n/a | n/a | n/a | 7.5 | n/a |
Merck Sharp & Dohme Corp.; MSD K.K. US Patent | Assay Description Activated Akt isoforms and pleckstrin homology domain deletion constructs were assayed utilizing a GSK-derived biotinylated peptide substrate. The e... | US Patent US8536193 (2013) BindingDB Entry DOI: 10.7270/Q2NK3CP1 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM102311 (US8536193, 2-1) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | US Patent | n/a | n/a | 2.30 | n/a | n/a | n/a | n/a | 7.5 | n/a |
Merck Sharp & Dohme Corp.; MSD K.K. US Patent | Assay Description Activated Akt isoforms and pleckstrin homology domain deletion constructs were assayed utilizing a GSK-derived biotinylated peptide substrate. The e... | US Patent US8536193 (2013) BindingDB Entry DOI: 10.7270/Q2NK3CP1 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50256715 (9-phenyl-8-(4-((4-(5-(pyridin-2-yl)-1H-1,2,4-triaz...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 2.60 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of human cloned Akt1 expressed in Drosophila S2 cells by HTRF assay | Bioorg Med Chem Lett 19: 834-6 (2009) Article DOI: 10.1016/j.bmcl.2008.12.017 BindingDB Entry DOI: 10.7270/Q2PR7VT5 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50256714 (9-phenyl-8-(4-((4-(5-(pyridin-2-yl)-1H-1,2,4-triaz...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 2.80 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of human cloned Akt1 expressed in Drosophila S2 cells by HTRF assay | Bioorg Med Chem Lett 19: 834-6 (2009) Article DOI: 10.1016/j.bmcl.2008.12.017 BindingDB Entry DOI: 10.7270/Q2PR7VT5 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-beta serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50256723 (9-phenyl-8-(4-((4-(4-(pyridin-2-yl)-1H-imidazol-1-...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents | Article PubMed | n/a | n/a | 2.80 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of human cloned Akt2 expressed in Drosophila S2 cells by HTRF assay | Bioorg Med Chem Lett 19: 834-6 (2009) Article DOI: 10.1016/j.bmcl.2008.12.017 BindingDB Entry DOI: 10.7270/Q2PR7VT5 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50256723 (9-phenyl-8-(4-((4-(4-(pyridin-2-yl)-1H-imidazol-1-...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents | Article PubMed | n/a | n/a | 3.30 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of human cloned Akt1 expressed in Drosophila S2 cells by HTRF assay | Bioorg Med Chem Lett 19: 834-6 (2009) Article DOI: 10.1016/j.bmcl.2008.12.017 BindingDB Entry DOI: 10.7270/Q2PR7VT5 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50256718 (9-phenyl-8-(4-((4-(5-(pyridin-2-yl)-1H-1,2,4-triaz...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 4 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of human cloned Akt1 expressed in Drosophila S2 cells by HTRF assay | Bioorg Med Chem Lett 19: 834-6 (2009) Article DOI: 10.1016/j.bmcl.2008.12.017 BindingDB Entry DOI: 10.7270/Q2PR7VT5 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50256719 (3-methyl-9-phenyl-8-(4-((4-(5-(pyridin-2-yl)-1H-1,...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 4.60 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of human cloned Akt1 expressed in Drosophila S2 cells by HTRF assay | Bioorg Med Chem Lett 19: 834-6 (2009) Article DOI: 10.1016/j.bmcl.2008.12.017 BindingDB Entry DOI: 10.7270/Q2PR7VT5 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50256718 (9-phenyl-8-(4-((4-(5-(pyridin-2-yl)-1H-1,2,4-triaz...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 5 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of Akt1 (unknown origin) by cell based assay | Bioorg Med Chem Lett 19: 834-6 (2009) Article DOI: 10.1016/j.bmcl.2008.12.017 BindingDB Entry DOI: 10.7270/Q2PR7VT5 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM102307 (US8536193, 3-1) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | US Patent | n/a | n/a | 6.10 | n/a | n/a | n/a | n/a | 7.5 | n/a |
Merck Sharp & Dohme Corp.; MSD K.K. US Patent | Assay Description Activated Akt isoforms and pleckstrin homology domain deletion constructs were assayed utilizing a GSK-derived biotinylated peptide substrate. The e... | US Patent US8536193 (2013) BindingDB Entry DOI: 10.7270/Q2NK3CP1 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-beta serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50256715 (9-phenyl-8-(4-((4-(5-(pyridin-2-yl)-1H-1,2,4-triaz...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 6.70 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of human cloned Akt2 expressed in Drosophila S2 cells by HTRF assay | Bioorg Med Chem Lett 19: 834-6 (2009) Article DOI: 10.1016/j.bmcl.2008.12.017 BindingDB Entry DOI: 10.7270/Q2PR7VT5 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM102308 (US8536193, 4-1) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | US Patent | n/a | n/a | 8.20 | n/a | n/a | n/a | n/a | 7.5 | n/a |
Merck Sharp & Dohme Corp.; MSD K.K. US Patent | Assay Description Activated Akt isoforms and pleckstrin homology domain deletion constructs were assayed utilizing a GSK-derived biotinylated peptide substrate. The e... | US Patent US8536193 (2013) BindingDB Entry DOI: 10.7270/Q2NK3CP1 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50256717 (1-(9-phenyl-8-(4-((4-(5-(pyridin-2-yl)-1H-1,2,4-tr...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 8.5 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of human cloned Akt1 expressed in Drosophila S2 cells by HTRF assay | Bioorg Med Chem Lett 19: 834-6 (2009) Article DOI: 10.1016/j.bmcl.2008.12.017 BindingDB Entry DOI: 10.7270/Q2PR7VT5 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-beta serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50256714 (9-phenyl-8-(4-((4-(5-(pyridin-2-yl)-1H-1,2,4-triaz...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 9.40 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of human cloned Akt2 expressed in Drosophila S2 cells by HTRF assay | Bioorg Med Chem Lett 19: 834-6 (2009) Article DOI: 10.1016/j.bmcl.2008.12.017 BindingDB Entry DOI: 10.7270/Q2PR7VT5 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50256721 (3-((4-methylpiperazin-1-yl)methyl)-9-phenyl-8-(4-(...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 9.90 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of human cloned Akt1 expressed in Drosophila S2 cells by HTRF assay | Bioorg Med Chem Lett 19: 834-6 (2009) Article DOI: 10.1016/j.bmcl.2008.12.017 BindingDB Entry DOI: 10.7270/Q2PR7VT5 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM102309 (US8536193, 5-12) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | US Patent | n/a | n/a | 10 | n/a | n/a | n/a | n/a | 7.5 | n/a |
Merck Sharp & Dohme Corp.; MSD K.K. US Patent | Assay Description Activated Akt isoforms and pleckstrin homology domain deletion constructs were assayed utilizing a GSK-derived biotinylated peptide substrate. The e... | US Patent US8536193 (2013) BindingDB Entry DOI: 10.7270/Q2NK3CP1 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50256716 (9-phenyl-8-(4-((4-(5-(pyridin-2-yl)-1H-1,2,4-triaz...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 10 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of human cloned Akt1 expressed in Drosophila S2 cells by HTRF assay | Bioorg Med Chem Lett 19: 834-6 (2009) Article DOI: 10.1016/j.bmcl.2008.12.017 BindingDB Entry DOI: 10.7270/Q2PR7VT5 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-beta serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50256718 (9-phenyl-8-(4-((4-(5-(pyridin-2-yl)-1H-1,2,4-triaz...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 10 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of human cloned Akt2 expressed in Drosophila S2 cells by HTRF assay | Bioorg Med Chem Lett 19: 834-6 (2009) Article DOI: 10.1016/j.bmcl.2008.12.017 BindingDB Entry DOI: 10.7270/Q2PR7VT5 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-beta serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50256716 (9-phenyl-8-(4-((4-(5-(pyridin-2-yl)-1H-1,2,4-triaz...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 10.4 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of human cloned Akt2 expressed in Drosophila S2 cells by HTRF assay | Bioorg Med Chem Lett 19: 834-6 (2009) Article DOI: 10.1016/j.bmcl.2008.12.017 BindingDB Entry DOI: 10.7270/Q2PR7VT5 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-beta serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50256720 (3-(chloromethyl)-9-phenyl-8-(4-((4-(5-(pyridin-2-y...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 10.5 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of human cloned Akt2 expressed in Drosophila S2 cells by HTRF assay | Bioorg Med Chem Lett 19: 834-6 (2009) Article DOI: 10.1016/j.bmcl.2008.12.017 BindingDB Entry DOI: 10.7270/Q2PR7VT5 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Sodium channel protein type 9 subunit alpha (Mus musculus) | BDBM50242510 (CHEMBL4095146) | PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | Article PubMed | n/a | n/a | 11 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck& Co. Curated by ChEMBL | Assay Description Inhibition of 50% inactivated mouse Nav1.7alpha incubated for 5 mins measured at 10 secs interval by PatchXpress automated electrophysiology method | Bioorg Med Chem Lett 27: 2683-2688 (2017) Article DOI: 10.1016/j.bmcl.2017.04.040 BindingDB Entry DOI: 10.7270/Q2SN0CD7 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Sodium channel protein type 5 subunit alpha (Homo sapiens (Human)) | BDBM50240267 (CHEMBL2325014) | PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | Purchase CHEMBL MCE PC cid PC sid PDB UniChem Patents | Article PubMed | n/a | n/a | 11 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck& Co. Curated by ChEMBL | Assay Description Inhibition of 50% inactivated human Nav1.5alpha expressed in HEK293 cells measured after 5 to 10 mins post compound washout by PatchXpress automated ... | Bioorg Med Chem Lett 27: 2683-2688 (2017) Article DOI: 10.1016/j.bmcl.2017.04.040 BindingDB Entry DOI: 10.7270/Q2SN0CD7 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-beta serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50256719 (3-methyl-9-phenyl-8-(4-((4-(5-(pyridin-2-yl)-1H-1,...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 14.6 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of human cloned Akt2 expressed in Drosophila S2 cells by HTRF assay | Bioorg Med Chem Lett 19: 834-6 (2009) Article DOI: 10.1016/j.bmcl.2008.12.017 BindingDB Entry DOI: 10.7270/Q2PR7VT5 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50256716 (9-phenyl-8-(4-((4-(5-(pyridin-2-yl)-1H-1,2,4-triaz...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 17 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of Akt1 (unknown origin) by cell based assay | Bioorg Med Chem Lett 19: 834-6 (2009) Article DOI: 10.1016/j.bmcl.2008.12.017 BindingDB Entry DOI: 10.7270/Q2PR7VT5 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50256722 (2-((9-phenyl-8-(4-((4-(5-(pyridin-2-yl)-1H-1,2,4-t...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 17 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of human cloned Akt1 expressed in Drosophila S2 cells by HTRF assay | Bioorg Med Chem Lett 19: 834-6 (2009) Article DOI: 10.1016/j.bmcl.2008.12.017 BindingDB Entry DOI: 10.7270/Q2PR7VT5 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50256714 (9-phenyl-8-(4-((4-(5-(pyridin-2-yl)-1H-1,2,4-triaz...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 18.1 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of Akt1 (unknown origin) by cell based assay | Bioorg Med Chem Lett 19: 834-6 (2009) Article DOI: 10.1016/j.bmcl.2008.12.017 BindingDB Entry DOI: 10.7270/Q2PR7VT5 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50256723 (9-phenyl-8-(4-((4-(4-(pyridin-2-yl)-1H-imidazol-1-...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents | Article PubMed | n/a | n/a | 18.3 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of Akt1 (unknown origin) by cell based assay | Bioorg Med Chem Lett 19: 834-6 (2009) Article DOI: 10.1016/j.bmcl.2008.12.017 BindingDB Entry DOI: 10.7270/Q2PR7VT5 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Sodium channel protein type 9 subunit alpha (Homo sapiens (Human)) | BDBM50242509 (CHEMBL4068937) | PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | Article PubMed | n/a | n/a | 21 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck& Co. Curated by ChEMBL | Assay Description Inhibition of 50% inactivated human Nav1.7alpha expressed in HEK293 cells incubated for 5 mins measured at 10 secs interval by PatchXpress automated ... | Bioorg Med Chem Lett 27: 2683-2688 (2017) Article DOI: 10.1016/j.bmcl.2017.04.040 BindingDB Entry DOI: 10.7270/Q2SN0CD7 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-beta serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM102307 (US8536193, 3-1) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | US Patent | n/a | n/a | 24 | n/a | n/a | n/a | n/a | 7.5 | n/a |
Merck Sharp & Dohme Corp.; MSD K.K. US Patent | Assay Description Activated Akt isoforms and pleckstrin homology domain deletion constructs were assayed utilizing a GSK-derived biotinylated peptide substrate. The e... | US Patent US8536193 (2013) BindingDB Entry DOI: 10.7270/Q2NK3CP1 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-beta serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50256717 (1-(9-phenyl-8-(4-((4-(5-(pyridin-2-yl)-1H-1,2,4-tr...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 24.1 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of human cloned Akt2 expressed in Drosophila S2 cells by HTRF assay | Bioorg Med Chem Lett 19: 834-6 (2009) Article DOI: 10.1016/j.bmcl.2008.12.017 BindingDB Entry DOI: 10.7270/Q2PR7VT5 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50256719 (3-methyl-9-phenyl-8-(4-((4-(5-(pyridin-2-yl)-1H-1,...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 24.6 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of Akt1 (unknown origin) by cell based assay | Bioorg Med Chem Lett 19: 834-6 (2009) Article DOI: 10.1016/j.bmcl.2008.12.017 BindingDB Entry DOI: 10.7270/Q2PR7VT5 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50256720 (3-(chloromethyl)-9-phenyl-8-(4-((4-(5-(pyridin-2-y...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 26.7 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of human cloned Akt1 expressed in Drosophila S2 cells by HTRF assay | Bioorg Med Chem Lett 19: 834-6 (2009) Article DOI: 10.1016/j.bmcl.2008.12.017 BindingDB Entry DOI: 10.7270/Q2PR7VT5 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50256715 (9-phenyl-8-(4-((4-(5-(pyridin-2-yl)-1H-1,2,4-triaz...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 27 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of Akt1 (unknown origin) by cell based assay | Bioorg Med Chem Lett 19: 834-6 (2009) Article DOI: 10.1016/j.bmcl.2008.12.017 BindingDB Entry DOI: 10.7270/Q2PR7VT5 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Sodium channel protein type 2 subunit alpha (Homo sapiens (Human)) | BDBM50242509 (CHEMBL4068937) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | Article PubMed | n/a | n/a | 29 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck& Co. Curated by ChEMBL | Assay Description Inhibition of Nav1.2 (unknown origin) | Bioorg Med Chem Lett 27: 2683-2688 (2017) Article DOI: 10.1016/j.bmcl.2017.04.040 BindingDB Entry DOI: 10.7270/Q2SN0CD7 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Sodium channel protein type 9 subunit alpha (Mus musculus) | BDBM50242509 (CHEMBL4068937) | PDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | Article PubMed | n/a | n/a | 30 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck& Co. Curated by ChEMBL | Assay Description Inhibition of [3H]PIA binding to rat cortical adenosine A1 receptor | Bioorg Med Chem Lett 27: 2683-2688 (2017) Article DOI: 10.1016/j.bmcl.2017.04.040 BindingDB Entry DOI: 10.7270/Q2SN0CD7 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Sodium channel protein type 9 subunit alpha (Homo sapiens (Human)) | BDBM50242509 (CHEMBL4068937) | PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | Article PubMed | n/a | n/a | 31 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck& Co. Curated by ChEMBL | Assay Description Inhibition of NaV1.7 channel in human DRG neurons assessed as reduction of TTX-sensitive current by whole cell patch clamp assay | Bioorg Med Chem Lett 27: 2683-2688 (2017) Article DOI: 10.1016/j.bmcl.2017.04.040 BindingDB Entry DOI: 10.7270/Q2SN0CD7 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-beta serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM102311 (US8536193, 2-1) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | US Patent | n/a | n/a | 32 | n/a | n/a | n/a | n/a | 7.5 | n/a |
Merck Sharp & Dohme Corp.; MSD K.K. US Patent | Assay Description Activated Akt isoforms and pleckstrin homology domain deletion constructs were assayed utilizing a GSK-derived biotinylated peptide substrate. The e... | US Patent US8536193 (2013) BindingDB Entry DOI: 10.7270/Q2NK3CP1 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Sodium channel protein type 9 subunit alpha (Homo sapiens (Human)) | BDBM50242510 (CHEMBL4095146) | PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | Article PubMed | n/a | n/a | 39 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck& Co. Curated by ChEMBL | Assay Description Inhibition of 50% inactivated human Nav1.7alpha expressed in HEK293 cells incubated for 5 mins measured at 10 secs interval by PatchXpress automated ... | Bioorg Med Chem Lett 27: 2683-2688 (2017) Article DOI: 10.1016/j.bmcl.2017.04.040 BindingDB Entry DOI: 10.7270/Q2SN0CD7 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM102312 (US8536193, 1-9) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem | US Patent | n/a | n/a | 39 | n/a | n/a | n/a | n/a | 7.5 | n/a |
Merck Sharp & Dohme Corp.; MSD K.K. US Patent | Assay Description Activated Akt isoforms and pleckstrin homology domain deletion constructs were assayed utilizing a GSK-derived biotinylated peptide substrate. The e... | US Patent US8536193 (2013) BindingDB Entry DOI: 10.7270/Q2NK3CP1 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-beta serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50256718 (9-phenyl-8-(4-((4-(5-(pyridin-2-yl)-1H-1,2,4-triaz...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 41 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of Akt2 (unknown origin) by cell based assay | Bioorg Med Chem Lett 19: 834-6 (2009) Article DOI: 10.1016/j.bmcl.2008.12.017 BindingDB Entry DOI: 10.7270/Q2PR7VT5 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50256722 (2-((9-phenyl-8-(4-((4-(5-(pyridin-2-yl)-1H-1,2,4-t...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 41.8 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of Akt1 (unknown origin) by cell based assay | Bioorg Med Chem Lett 19: 834-6 (2009) Article DOI: 10.1016/j.bmcl.2008.12.017 BindingDB Entry DOI: 10.7270/Q2PR7VT5 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-beta serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50256714 (9-phenyl-8-(4-((4-(5-(pyridin-2-yl)-1H-1,2,4-triaz...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 47.7 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of Akt2 (unknown origin) by cell based assay | Bioorg Med Chem Lett 19: 834-6 (2009) Article DOI: 10.1016/j.bmcl.2008.12.017 BindingDB Entry DOI: 10.7270/Q2PR7VT5 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-beta serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM102308 (US8536193, 4-1) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | PC cid PC sid UniChem Similars | US Patent | n/a | n/a | 50 | n/a | n/a | n/a | n/a | 7.5 | n/a |
Merck Sharp & Dohme Corp.; MSD K.K. US Patent | Assay Description Activated Akt isoforms and pleckstrin homology domain deletion constructs were assayed utilizing a GSK-derived biotinylated peptide substrate. The e... | US Patent US8536193 (2013) BindingDB Entry DOI: 10.7270/Q2NK3CP1 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-beta serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50256721 (3-((4-methylpiperazin-1-yl)methyl)-9-phenyl-8-(4-(...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 55.1 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of human cloned Akt2 expressed in Drosophila S2 cells by HTRF assay | Bioorg Med Chem Lett 19: 834-6 (2009) Article DOI: 10.1016/j.bmcl.2008.12.017 BindingDB Entry DOI: 10.7270/Q2PR7VT5 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
RAC-alpha serine/threonine-protein kinase (Homo sapiens (Human)) | BDBM50256721 (3-((4-methylpiperazin-1-yl)methyl)-9-phenyl-8-(4-(...) | PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Patents Similars | Article PubMed | n/a | n/a | 62.5 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Research Laboratories Curated by ChEMBL | Assay Description Inhibition of Akt1 (unknown origin) by cell based assay | Bioorg Med Chem Lett 19: 834-6 (2009) Article DOI: 10.1016/j.bmcl.2008.12.017 BindingDB Entry DOI: 10.7270/Q2PR7VT5 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Sodium channel protein type 9 subunit alpha (Homo sapiens (Human)) | BDBM50242508 (CHEMBL4084948) | PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem | Article PubMed | n/a | n/a | 74 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck& Co. Curated by ChEMBL | Assay Description Inhibition of 50% inactivated human Nav1.7alpha expressed in HEK293 cells incubated for 5 mins measured at 10 secs interval by PatchXpress automated ... | Bioorg Med Chem Lett 27: 2683-2688 (2017) Article DOI: 10.1016/j.bmcl.2017.04.040 BindingDB Entry DOI: 10.7270/Q2SN0CD7 | |||||||||||
More data for this Ligand-Target Pair |
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