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SMILES: COc1ccc(-c2cn(Cc3nc4cccc(C)c4c(=O)n3-c3ccccc3C)nn2)c(C)c1

InChI Key: InChIKey=ZHEZUYRFPAASAR-UHFFFAOYSA-N

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50460340   
Target/Host
(Institution)
LigandTarget/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
pHTemp
°C
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform


(Homo sapiens (Human))
BDBM50460340
PNG
(CHEMBL4228200)
Show SMILES COc1ccc(-c2cn(Cc3nc4cccc(C)c4c(=O)n3-c3ccccc3C)nn2)c(C)c1 |(27.62,-21.79,;28.98,-21.07,;30.29,-21.88,;31.65,-21.16,;32.95,-21.98,;32.89,-23.52,;34.2,-24.34,;35.44,-23.43,;36.69,-24.32,;38.15,-23.84,;39.47,-24.63,;39.44,-26.17,;40.76,-26.97,;40.73,-28.51,;42.05,-29.3,;43.4,-28.56,;43.43,-27.02,;44.77,-26.28,;42.11,-26.22,;42.14,-24.69,;43.49,-23.94,;40.82,-23.89,;40.8,-22.35,;42.13,-21.56,;42.11,-20.02,;40.76,-19.27,;39.44,-20.06,;39.46,-21.6,;38.13,-22.38,;36.23,-25.79,;34.69,-25.8,;31.53,-24.24,;31.48,-25.78,;30.23,-23.42,)|
Show InChI InChI=1S/C27H25N5O2/c1-17-8-5-6-11-24(17)32-25(28-22-10-7-9-18(2)26(22)27(32)33)16-31-15-23(29-30-31)21-13-12-20(34-4)14-19(21)3/h5-15H,16H2,1-4H3
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MMDB

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PC sid
UniChem
Article
PubMed
n/an/a 3.00E+3n/an/an/an/an/an/a



India Academy of Scientific & Innovative Research (AcSIR)

Curated by ChEMBL


Assay Description
Inhibition of PI3K-gamma (unknown origin) by cell free biochemical assay


Bioorg Med Chem Lett 28: 1005-1010 (2018)


Article DOI: 10.1016/j.bmcl.2018.02.032
BindingDB Entry DOI: 10.7270/Q29S1TN5
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform


(Homo sapiens (Human))
BDBM50460340
PNG
(CHEMBL4228200)
Show SMILES COc1ccc(-c2cn(Cc3nc4cccc(C)c4c(=O)n3-c3ccccc3C)nn2)c(C)c1 |(27.62,-21.79,;28.98,-21.07,;30.29,-21.88,;31.65,-21.16,;32.95,-21.98,;32.89,-23.52,;34.2,-24.34,;35.44,-23.43,;36.69,-24.32,;38.15,-23.84,;39.47,-24.63,;39.44,-26.17,;40.76,-26.97,;40.73,-28.51,;42.05,-29.3,;43.4,-28.56,;43.43,-27.02,;44.77,-26.28,;42.11,-26.22,;42.14,-24.69,;43.49,-23.94,;40.82,-23.89,;40.8,-22.35,;42.13,-21.56,;42.11,-20.02,;40.76,-19.27,;39.44,-20.06,;39.46,-21.6,;38.13,-22.38,;36.23,-25.79,;34.69,-25.8,;31.53,-24.24,;31.48,-25.78,;30.23,-23.42,)|
Show InChI InChI=1S/C27H25N5O2/c1-17-8-5-6-11-24(17)32-25(28-22-10-7-9-18(2)26(22)27(32)33)16-31-15-23(29-30-31)21-13-12-20(34-4)14-19(21)3/h5-15H,16H2,1-4H3
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n/an/a 1.00E+4n/an/an/an/an/an/a



India Academy of Scientific & Innovative Research (AcSIR)

Curated by ChEMBL


Assay Description
Inhibition of PI3K-delta (unknown origin) by cell free biochemical assay


Bioorg Med Chem Lett 28: 1005-1010 (2018)


Article DOI: 10.1016/j.bmcl.2018.02.032
BindingDB Entry DOI: 10.7270/Q29S1TN5
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform


(Homo sapiens (Human))
BDBM50460340
PNG
(CHEMBL4228200)
Show SMILES COc1ccc(-c2cn(Cc3nc4cccc(C)c4c(=O)n3-c3ccccc3C)nn2)c(C)c1 |(27.62,-21.79,;28.98,-21.07,;30.29,-21.88,;31.65,-21.16,;32.95,-21.98,;32.89,-23.52,;34.2,-24.34,;35.44,-23.43,;36.69,-24.32,;38.15,-23.84,;39.47,-24.63,;39.44,-26.17,;40.76,-26.97,;40.73,-28.51,;42.05,-29.3,;43.4,-28.56,;43.43,-27.02,;44.77,-26.28,;42.11,-26.22,;42.14,-24.69,;43.49,-23.94,;40.82,-23.89,;40.8,-22.35,;42.13,-21.56,;42.11,-20.02,;40.76,-19.27,;39.44,-20.06,;39.46,-21.6,;38.13,-22.38,;36.23,-25.79,;34.69,-25.8,;31.53,-24.24,;31.48,-25.78,;30.23,-23.42,)|
Show InChI InChI=1S/C27H25N5O2/c1-17-8-5-6-11-24(17)32-25(28-22-10-7-9-18(2)26(22)27(32)33)16-31-15-23(29-30-31)21-13-12-20(34-4)14-19(21)3/h5-15H,16H2,1-4H3
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UniChem
Article
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n/an/a 3.55E+5n/an/an/an/an/an/a



India Academy of Scientific & Innovative Research (AcSIR)

Curated by ChEMBL


Assay Description
Inhibition of PI3K-beta (unknown origin) by cell free biochemical assay


Bioorg Med Chem Lett 28: 1005-1010 (2018)


Article DOI: 10.1016/j.bmcl.2018.02.032
BindingDB Entry DOI: 10.7270/Q29S1TN5
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform


(Homo sapiens (Human))
BDBM50460340
PNG
(CHEMBL4228200)
Show SMILES COc1ccc(-c2cn(Cc3nc4cccc(C)c4c(=O)n3-c3ccccc3C)nn2)c(C)c1 |(27.62,-21.79,;28.98,-21.07,;30.29,-21.88,;31.65,-21.16,;32.95,-21.98,;32.89,-23.52,;34.2,-24.34,;35.44,-23.43,;36.69,-24.32,;38.15,-23.84,;39.47,-24.63,;39.44,-26.17,;40.76,-26.97,;40.73,-28.51,;42.05,-29.3,;43.4,-28.56,;43.43,-27.02,;44.77,-26.28,;42.11,-26.22,;42.14,-24.69,;43.49,-23.94,;40.82,-23.89,;40.8,-22.35,;42.13,-21.56,;42.11,-20.02,;40.76,-19.27,;39.44,-20.06,;39.46,-21.6,;38.13,-22.38,;36.23,-25.79,;34.69,-25.8,;31.53,-24.24,;31.48,-25.78,;30.23,-23.42,)|
Show InChI InChI=1S/C27H25N5O2/c1-17-8-5-6-11-24(17)32-25(28-22-10-7-9-18(2)26(22)27(32)33)16-31-15-23(29-30-31)21-13-12-20(34-4)14-19(21)3/h5-15H,16H2,1-4H3
PDB
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NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

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PC cid
PC sid
UniChem
Article
PubMed
n/an/a 2.90E+5n/an/an/an/an/an/a



India Academy of Scientific & Innovative Research (AcSIR)

Curated by ChEMBL


Assay Description
Inhibition of PI3K-alpha (unknown origin) by cell free biochemical assay


Bioorg Med Chem Lett 28: 1005-1010 (2018)


Article DOI: 10.1016/j.bmcl.2018.02.032
BindingDB Entry DOI: 10.7270/Q29S1TN5
More data for this
Ligand-Target Pair