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Compile Data Set for Download or QSAR

Marvin 2D Structure

The following exact ligands are found in BindingDB

Wt: 369.4
BDBM50148647

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB (change energy unit to kcal/mol)

Found 7 hits in this display   
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
Calcium-dependent protein kinase 1


(Cryptosporidium parvum)
BDBM50148647
PNG
(CHEMBL3769570 | US9518026, Example 53 | US9956214,...)
Show SMILES CCOc1ccc2cc(cnc2c1)-c1nn(C(C)CCO)c(N)c1C(N)=O
Show InChI InChI=1S/C19H23N5O3/c1-3-27-14-5-4-12-8-13(10-22-15(12)9-14)17-16(19(21)26)18(20)24(23-17)11(2)6-7-25/h4-5,8-11,25H,3,6-7,20H2,1-2H3,(H2,21,26)
UniProtKB/TrEMBL

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US Patent
n/an/a 5n/an/an/an/an/an/a



Boehringer Ingelheim (Canada) Ltd.



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...


Bioorg Med Chem Lett 19: 1199-205 (2009)


BindingDB Entry DOI: 10.7270/Q23J3G91
More data for this
Ligand-Target Pair
Calmodulin-domain protein kinase 1


(Toxoplasma gondii)
BDBM50148647
PNG
(CHEMBL3769570 | US9518026, Example 53 | US9956214,...)
Show SMILES CCOc1ccc2cc(cnc2c1)-c1nn(C(C)CCO)c(N)c1C(N)=O
Show InChI InChI=1S/C19H23N5O3/c1-3-27-14-5-4-12-8-13(10-22-15(12)9-14)17-16(19(21)26)18(20)24(23-17)11(2)6-7-25/h4-5,8-11,25H,3,6-7,20H2,1-2H3,(H2,21,26)
PDB

UniProtKB/TrEMBL

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PC sid
UniChem

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US Patent
n/an/a 17n/an/an/an/an/an/a



Boehringer Ingelheim (Canada) Ltd.



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...


Bioorg Med Chem Lett 19: 1199-205 (2009)


BindingDB Entry DOI: 10.7270/Q23J3G91
More data for this
Ligand-Target Pair
Calmodulin-domain protein kinase 1


(Toxoplasma gondii)
BDBM50148647
PNG
(CHEMBL3769570 | US9518026, Example 53 | US9956214,...)
Show SMILES CCOc1ccc2cc(cnc2c1)-c1nn(C(C)CCO)c(N)c1C(N)=O
Show InChI InChI=1S/C19H23N5O3/c1-3-27-14-5-4-12-8-13(10-22-15(12)9-14)17-16(19(21)26)18(20)24(23-17)11(2)6-7-25/h4-5,8-11,25H,3,6-7,20H2,1-2H3,(H2,21,26)
PDB

UniProtKB/TrEMBL

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Article
PubMed
n/an/a 20n/an/an/an/an/an/a



University of Washington

Curated by ChEMBL


Assay Description
Inhibition of Toxoplasma gondii CDPK1 assessed as ATP consumption using (Biotin-C6-PLARTLSVAGLPGKK) as substrate after 90 mins by luciferase reporter...


ACS Med Chem Lett 6: 1184-1189 (2015)


Article DOI: 10.1021/acsmedchemlett.5b00319
BindingDB Entry DOI: 10.7270/Q2NK3GXD
More data for this
Ligand-Target Pair
Uncharacterized protein


(Cryptosporidium parvum)
BDBM50148647
PNG
(CHEMBL3769570 | US9518026, Example 53 | US9956214,...)
Show SMILES CCOc1ccc2cc(cnc2c1)-c1nn(C(C)CCO)c(N)c1C(N)=O
Show InChI InChI=1S/C19H23N5O3/c1-3-27-14-5-4-12-8-13(10-22-15(12)9-14)17-16(19(21)26)18(20)24(23-17)11(2)6-7-25/h4-5,8-11,25H,3,6-7,20H2,1-2H3,(H2,21,26)
PDB

UniProtKB/TrEMBL

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PC sid
UniChem

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US Patent
n/an/a 21n/an/an/an/an/an/a



University of Washington Through its Center For Commercialization

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 US9518026 (2016)


BindingDB Entry DOI: 10.7270/Q2BV7JN4
More data for this
Ligand-Target Pair
Calmodulin-domain protein kinase 1


(Toxoplasma gondii)
BDBM50148647
PNG
(CHEMBL3769570 | US9518026, Example 53 | US9956214,...)
Show SMILES CCOc1ccc2cc(cnc2c1)-c1nn(C(C)CCO)c(N)c1C(N)=O
Show InChI InChI=1S/C19H23N5O3/c1-3-27-14-5-4-12-8-13(10-22-15(12)9-14)17-16(19(21)26)18(20)24(23-17)11(2)6-7-25/h4-5,8-11,25H,3,6-7,20H2,1-2H3,(H2,21,26)
PDB

UniProtKB/TrEMBL

GoogleScholar
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CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

US Patent
n/an/a 41n/an/an/an/an/an/a



University of Washington Through its Center For Commercialization

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 US9518026 (2016)


BindingDB Entry DOI: 10.7270/Q2BV7JN4
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50148647
PNG
(CHEMBL3769570 | US9518026, Example 53 | US9956214,...)
Show SMILES CCOc1ccc2cc(cnc2c1)-c1nn(C(C)CCO)c(N)c1C(N)=O
Show InChI InChI=1S/C19H23N5O3/c1-3-27-14-5-4-12-8-13(10-22-15(12)9-14)17-16(19(21)26)18(20)24(23-17)11(2)6-7-25/h4-5,8-11,25H,3,6-7,20H2,1-2H3,(H2,21,26)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
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Article
PubMed
n/an/a 3.50E+3n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of SRC (unknown origin)


Citation and Details

Article DOI: 10.1021/acs.jmedchem.9b00069
BindingDB Entry DOI: 10.7270/Q2GT5RSJ
More data for this
Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2


(Homo sapiens (Human))
BDBM50148647
PNG
(CHEMBL3769570 | US9518026, Example 53 | US9956214,...)
Show SMILES CCOc1ccc2cc(cnc2c1)-c1nn(C(C)CCO)c(N)c1C(N)=O
Show InChI InChI=1S/C19H23N5O3/c1-3-27-14-5-4-12-8-13(10-22-15(12)9-14)17-16(19(21)26)18(20)24(23-17)11(2)6-7-25/h4-5,8-11,25H,3,6-7,20H2,1-2H3,(H2,21,26)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a>3.00E+4n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of human ERG by thallium flux assay


Citation and Details

Article DOI: 10.1021/acs.jmedchem.9b00069
BindingDB Entry DOI: 10.7270/Q2GT5RSJ
More data for this
Ligand-Target Pair