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BDBM50389730 CHEMBL2069946::US10172858, Table 2.7::US10544104, Compound 24::US10844067, Example 44::US9765037, Compound 24::US9828378, # 7

SMILES: CC(C)n1nc(-c2cc3ccccc3[nH]2)c2c(N)ncnc12

InChI Key: InChIKey=SQZDJBNTERGDSI-UHFFFAOYSA-N

Data: 14 IC50

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 14 hits for monomerid = 50389730   
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
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50389730
PNG
(CHEMBL2069946 | US10172858, Table 2.7 | US10544104...)
Show SMILES CC(C)n1nc(-c2cc3ccccc3[nH]2)c2c(N)ncnc12
Show InChI InChI=1S/C16H16N6/c1-9(2)22-16-13(15(17)18-8-19-16)14(21-22)12-7-10-5-3-4-6-11(10)20-12/h3-9,20H,1-2H3,(H2,17,18,19)
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Article
PubMed
n/an/a 1.50E+3n/an/an/an/an/an/a



University of Washington

Curated by ChEMBL


Assay Description
Inhibition of human SRC using Ac-EIYGEFKKK-OH as substrate after 60 mins by phosphorimaging method


J Med Chem 55: 2416-26 (2012)


Article DOI: 10.1021/jm201713h
BindingDB Entry DOI: 10.7270/Q2P2706V
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase mTOR


(Homo sapiens (Human))
BDBM50389730
PNG
(CHEMBL2069946 | US10172858, Table 2.7 | US10544104...)
Show SMILES CC(C)n1nc(-c2cc3ccccc3[nH]2)c2c(N)ncnc12
Show InChI InChI=1S/C16H16N6/c1-9(2)22-16-13(15(17)18-8-19-16)14(21-22)12-7-10-5-3-4-6-11(10)20-12/h3-9,20H,1-2H3,(H2,17,18,19)
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n/an/a<100n/an/an/an/an/an/a



INTELLIKINE LLC

US Patent


Assay Description
This assay is relatively simple, reasonably sensitive, and the peptide substrate can be adjusted both in terms of sequence and concentration to meet ...


US Patent US10172858 (2019)


BindingDB Entry DOI: 10.7270/Q2736T01
More data for this
Ligand-Target Pair
PI3-kinase class I


(Homo sapiens (Human))
BDBM50389730
PNG
(CHEMBL2069946 | US10172858, Table 2.7 | US10544104...)
Show SMILES CC(C)n1nc(-c2cc3ccccc3[nH]2)c2c(N)ncnc12
Show InChI InChI=1S/C16H16N6/c1-9(2)22-16-13(15(17)18-8-19-16)14(21-22)12-7-10-5-3-4-6-11(10)20-12/h3-9,20H,1-2H3,(H2,17,18,19)
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n/an/a>500n/an/an/an/an/an/a



INTELLIKINE LLC

US Patent


Assay Description
This assay is relatively simple, reasonably sensitive, and the peptide substrate can be adjusted both in terms of sequence and concentration to meet ...


US Patent US10172858 (2019)


BindingDB Entry DOI: 10.7270/Q2736T01
More data for this
Ligand-Target Pair
Calmodulin-domain protein kinase 1 (CDPK1)


(Toxoplasma gondii)
BDBM50389730
PNG
(CHEMBL2069946 | US10172858, Table 2.7 | US10544104...)
Show SMILES CC(C)n1nc(-c2cc3ccccc3[nH]2)c2c(N)ncnc12
Show InChI InChI=1S/C16H16N6/c1-9(2)22-16-13(15(17)18-8-19-16)14(21-22)12-7-10-5-3-4-6-11(10)20-12/h3-9,20H,1-2H3,(H2,17,18,19)
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US Patent
n/an/a 11.9n/an/an/an/an/an/a



University of Washington Through its Center for Commercialization

US Patent


Assay Description
Most known kinase inhibitors bind in the ATP-binding pocket of the active site19,20. These inhibitors exploit many of the same hydrophobic contacts a...


US Patent US9765037 (2017)


BindingDB Entry DOI: 10.7270/Q2B56MVC
More data for this
Ligand-Target Pair
Calcium-dependent protein kinase 1 (CDPK1)


(Cryptosporidium parvum)
BDBM50389730
PNG
(CHEMBL2069946 | US10172858, Table 2.7 | US10544104...)
Show SMILES CC(C)n1nc(-c2cc3ccccc3[nH]2)c2c(N)ncnc12
Show InChI InChI=1S/C16H16N6/c1-9(2)22-16-13(15(17)18-8-19-16)14(21-22)12-7-10-5-3-4-6-11(10)20-12/h3-9,20H,1-2H3,(H2,17,18,19)
UniProtKB/TrEMBL

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US Patent
n/an/a 70.4n/an/an/an/an/an/a



University of Washington Through its Center for Commercialization

US Patent


Assay Description
Two types of enzyme assays were developed to follow TgCDPK1 activity, a radiometric scintillation proximity assay measured the labeled γ-phospha...


US Patent US9765037 (2017)


BindingDB Entry DOI: 10.7270/Q2B56MVC
More data for this
Ligand-Target Pair
Cytosolic arginine sensor for mTORC1 subunit 1


(Homo sapiens (Human))
BDBM50389730
PNG
(CHEMBL2069946 | US10172858, Table 2.7 | US10544104...)
Show SMILES CC(C)n1nc(-c2cc3ccccc3[nH]2)c2c(N)ncnc12
Show InChI InChI=1S/C16H16N6/c1-9(2)22-16-13(15(17)18-8-19-16)14(21-22)12-7-10-5-3-4-6-11(10)20-12/h3-9,20H,1-2H3,(H2,17,18,19)
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US Patent
n/an/a<100n/an/an/an/an/an/a



Intellikine LLC

US Patent


Assay Description
Class I PI3-Ks can be either purchased (p110α/p85α, p110β/p85α, p110δ/p85α from Upstate, and p110γ from Sigma) or...


US Patent US9828378 (2017)


BindingDB Entry DOI: 10.7270/Q2542QWN
More data for this
Ligand-Target Pair
RET kinase mutant (V804M)


(Homo sapiens (Human))
BDBM50389730
PNG
(CHEMBL2069946 | US10172858, Table 2.7 | US10544104...)
Show SMILES CC(C)n1nc(-c2cc3ccccc3[nH]2)c2c(N)ncnc12
Show InChI InChI=1S/C16H16N6/c1-9(2)22-16-13(15(17)18-8-19-16)14(21-22)12-7-10-5-3-4-6-11(10)20-12/h3-9,20H,1-2H3,(H2,17,18,19)
PDB

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PC cid
PC sid
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US Patent
n/an/a 1.87E+3n/an/an/an/an/an/a



Cancer Research Technology Limited

US Patent


Assay Description
RET and KDR: Kinase activity was detected using CisBio HTRF kinEASE kit based on time-resolved fluorescence transfer (FRET). The assay was performed ...


US Patent US10844067 (2020)

More data for this
Ligand-Target Pair
Calmodulin-domain protein kinase 1


(Toxoplasma gondii)
BDBM50389730
PNG
(CHEMBL2069946 | US10172858, Table 2.7 | US10544104...)
Show SMILES CC(C)n1nc(-c2cc3ccccc3[nH]2)c2c(N)ncnc12
Show InChI InChI=1S/C16H16N6/c1-9(2)22-16-13(15(17)18-8-19-16)14(21-22)12-7-10-5-3-4-6-11(10)20-12/h3-9,20H,1-2H3,(H2,17,18,19)
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US Patent
n/an/a 11.9n/an/an/an/an/an/a



UNIVERSITY OF WASHINGTON THROUGH ITS CENTER FOR CO

US Patent


Assay Description
Inhibition of TgCDPK1 and CpCDPK1 was determined using a luminescent kinase assay which measures ATP depletion in the presence of the Syntide 2 pepti...


US Patent US10544104 (2020)


BindingDB Entry DOI: 10.7270/Q2D79DSF
More data for this
Ligand-Target Pair
Calmodulin-domain protein kinase 1, putative


(Cryptosporidium parvum (strain Iowa II))
BDBM50389730
PNG
(CHEMBL2069946 | US10172858, Table 2.7 | US10544104...)
Show SMILES CC(C)n1nc(-c2cc3ccccc3[nH]2)c2c(N)ncnc12
Show InChI InChI=1S/C16H16N6/c1-9(2)22-16-13(15(17)18-8-19-16)14(21-22)12-7-10-5-3-4-6-11(10)20-12/h3-9,20H,1-2H3,(H2,17,18,19)
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US Patent
n/an/a 70.4n/an/an/an/an/an/a



UNIVERSITY OF WASHINGTON THROUGH ITS CENTER FOR CO

US Patent


Assay Description
Inhibition of TgCDPK1 and CpCDPK1 was determined using a luminescent kinase assay which measures ATP depletion in the presence of the Syntide 2 pepti...


US Patent US10544104 (2020)


BindingDB Entry DOI: 10.7270/Q2D79DSF
More data for this
Ligand-Target Pair
Calmodulin/Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50389730
PNG
(CHEMBL2069946 | US10172858, Table 2.7 | US10544104...)
Show SMILES CC(C)n1nc(-c2cc3ccccc3[nH]2)c2c(N)ncnc12
Show InChI InChI=1S/C16H16N6/c1-9(2)22-16-13(15(17)18-8-19-16)14(21-22)12-7-10-5-3-4-6-11(10)20-12/h3-9,20H,1-2H3,(H2,17,18,19)
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US Patent
n/an/a 1.45E+3n/an/an/an/an/an/a



UNIVERSITY OF WASHINGTON THROUGH ITS CENTER FOR CO

US Patent


Assay Description
Inhibition of TgCDPK1 and CpCDPK1 was determined using a luminescent kinase assay which measures ATP depletion in the presence of the Syntide 2 pepti...


US Patent US10544104 (2020)


BindingDB Entry DOI: 10.7270/Q2D79DSF
More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))
BDBM50389730
PNG
(CHEMBL2069946 | US10172858, Table 2.7 | US10544104...)
Show SMILES CC(C)n1nc(-c2cc3ccccc3[nH]2)c2c(N)ncnc12
Show InChI InChI=1S/C16H16N6/c1-9(2)22-16-13(15(17)18-8-19-16)14(21-22)12-7-10-5-3-4-6-11(10)20-12/h3-9,20H,1-2H3,(H2,17,18,19)
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US Patent
n/an/a 353n/an/an/an/an/an/a



UNIVERSITY OF WASHINGTON THROUGH ITS CENTER FOR CO

US Patent


Assay Description
Inhibition of TgCDPK1 and CpCDPK1 was determined using a luminescent kinase assay which measures ATP depletion in the presence of the Syntide 2 pepti...


US Patent US10544104 (2020)


BindingDB Entry DOI: 10.7270/Q2D79DSF
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase receptor Ret


(Homo sapiens (Human))
BDBM50389730
PNG
(CHEMBL2069946 | US10172858, Table 2.7 | US10544104...)
Show SMILES CC(C)n1nc(-c2cc3ccccc3[nH]2)c2c(N)ncnc12
Show InChI InChI=1S/C16H16N6/c1-9(2)22-16-13(15(17)18-8-19-16)14(21-22)12-7-10-5-3-4-6-11(10)20-12/h3-9,20H,1-2H3,(H2,17,18,19)
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US Patent
n/an/a 18.7n/an/an/an/an/an/a



Cancer Research Technology Limited

US Patent


Assay Description
RET and KDR: Kinase activity was detected using CisBio HTRF kinEASE kit based on time-resolved fluorescence transfer (FRET). The assay was performed ...


US Patent US10844067 (2020)

More data for this
Ligand-Target Pair
Vascular endothelial growth factor receptor 2


(Homo sapiens (Human))
BDBM50389730
PNG
(CHEMBL2069946 | US10172858, Table 2.7 | US10544104...)
Show SMILES CC(C)n1nc(-c2cc3ccccc3[nH]2)c2c(N)ncnc12
Show InChI InChI=1S/C16H16N6/c1-9(2)22-16-13(15(17)18-8-19-16)14(21-22)12-7-10-5-3-4-6-11(10)20-12/h3-9,20H,1-2H3,(H2,17,18,19)
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n/an/a 4.57E+3n/an/an/an/an/an/a



Cancer Research Technology Limited

US Patent


Assay Description
RET and KDR: Kinase activity was detected using CisBio HTRF kinEASE kit based on time-resolved fluorescence transfer (FRET). The assay was performed ...


US Patent US10844067 (2020)

More data for this
Ligand-Target Pair
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform


(Homo sapiens (Human))
BDBM50389730
PNG
(CHEMBL2069946 | US10172858, Table 2.7 | US10544104...)
Show SMILES CC(C)n1nc(-c2cc3ccccc3[nH]2)c2c(N)ncnc12
Show InChI InChI=1S/C16H16N6/c1-9(2)22-16-13(15(17)18-8-19-16)14(21-22)12-7-10-5-3-4-6-11(10)20-12/h3-9,20H,1-2H3,(H2,17,18,19)
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n/an/a>500n/an/an/an/an/an/a



Intellikine LLC

US Patent


Assay Description
Class I PI3-Ks can be either purchased (p110α/p85α, p110β/p85α, p110δ/p85α from Upstate, and p110γ from Sigma) or...


US Patent US9828378 (2017)


BindingDB Entry DOI: 10.7270/Q2542QWN
More data for this
Ligand-Target Pair