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Compile Data Set for Download or QSAR

Found 3 hits of ic50 for monomerid = 50537721   
Target/Host
(Institution)
LigandTarget/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
pHTemp
°C
Phosphatidylinositol 3-kinase regulatory subunit alpha/4,5-bisphosphate 3-kinase catalytic subunit delta isoform


(Homo sapiens (Human))
BDBM50537721
PNG
(CHEMBL4646478 | US11230547, Compound 1-17)
Show SMILES [H][C@]12CN(c3nc(ncc3C#N)-c3ccnc4[nH]ccc34)[C@]([H])(CN1c1cccc(F)c1)C2 |r|
Show InChI InChI=1S/C23H18FN7/c24-15-2-1-3-16(8-15)30-12-18-9-17(30)13-31(18)23-14(10-25)11-28-22(29-23)20-5-7-27-21-19(20)4-6-26-21/h1-8,11,17-18H,9,12-13H2,(H,26,27)/t17-,18-/m0/s1
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PC sid
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Article
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n/an/a 56n/an/an/an/an/an/a



Merck & Co.

Curated by ChEMBL


Assay Description
Inhibition of recombinant human full-length N-terminal GST-tagged p110delta/untagged full-length p85alpha expressed in baculovirus infected Sf21 cell...


Bioorg Med Chem Lett 30: (2020)


Article DOI: 10.1016/j.bmcl.2019.126715
BindingDB Entry DOI: 10.7270/Q2HM5CZG
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform


(Homo sapiens (Human))
BDBM50537721
PNG
(CHEMBL4646478 | US11230547, Compound 1-17)
Show SMILES [H][C@]12CN(c3nc(ncc3C#N)-c3ccnc4[nH]ccc34)[C@]([H])(CN1c1cccc(F)c1)C2 |r|
Show InChI InChI=1S/C23H18FN7/c24-15-2-1-3-16(8-15)30-12-18-9-17(30)13-31(18)23-14(10-25)11-28-22(29-23)20-5-7-27-21-19(20)4-6-26-21/h1-8,11,17-18H,9,12-13H2,(H,26,27)/t17-,18-/m0/s1
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US Patent
n/an/a 56n/an/an/an/an/an/a


TBA

Assay Description
This assay was developed and further optimized from a kit produced by Upstate (Millipore catalog #33-047) (Millipore Sigma, Billerica Mass., USA) and...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2K35XTR
More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform


(Homo sapiens (Human))
BDBM50537721
PNG
(CHEMBL4646478 | US11230547, Compound 1-17)
Show SMILES [H][C@]12CN(c3nc(ncc3C#N)-c3ccnc4[nH]ccc34)[C@]([H])(CN1c1cccc(F)c1)C2 |r|
Show InChI InChI=1S/C23H18FN7/c24-15-2-1-3-16(8-15)30-12-18-9-17(30)13-31(18)23-14(10-25)11-28-22(29-23)20-5-7-27-21-19(20)4-6-26-21/h1-8,11,17-18H,9,12-13H2,(H,26,27)/t17-,18-/m0/s1
PDB
MMDB

NCI pathway
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KEGG

UniProtKB/SwissProt

B.MOAD
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antibodypedia
GoogleScholar
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PC cid
PC sid
UniChem
Article
PubMed
n/an/a 1.00E+4n/an/an/an/an/an/a



Merck & Co.

Curated by ChEMBL


Assay Description
Inhibition of the fibroblast growth factor receptor (FGFR1)


Bioorg Med Chem Lett 30: (2020)


Article DOI: 10.1016/j.bmcl.2019.126715
BindingDB Entry DOI: 10.7270/Q2HM5CZG
More data for this
Ligand-Target Pair