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Patent code US9765037

Compile Data Set for Download or QSAR

Found 344 hits of Enzyme Inhibition Constant Data   
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
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))
BDBM50345712
PNG
(3-(naphthalen-1-ylmethyl)-1-(piperidin-4-ylmethyl)...)
Show SMILES Nc1ncnc2n(CC3CCNCC3)nc(Cc3cccc4ccccc34)c12
Show InChI InChI=1S/C22H24N6/c23-21-20-19(12-17-6-3-5-16-4-1-2-7-18(16)17)27-28(22(20)26-14-25-21)13-15-8-10-24-11-9-15/h1-7,14-15,24H,8-13H2,(H2,23,25,26)
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n/an/a>2.00E+4n/an/an/an/an/an/a



University of Washington Through its Center for Commercialization

US Patent


Assay Description
Inhibition of human tyrosine kinases.


US Patent US9765037 (2017)

More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50345725
PNG
(3-(3,4-dichlorophenyl)-1-isopropyl-1H-pyrazolo[3,4...)
Show SMILES CC(C)n1nc(-c2ccc(Cl)c(Cl)c2)c2c(N)ncnc12
Show InChI InChI=1S/C14H13Cl2N5/c1-7(2)21-14-11(13(17)18-6-19-14)12(20-21)8-3-4-9(15)10(16)5-8/h3-7H,1-2H3,(H2,17,18,19)
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US Patent
n/an/a 35n/an/an/an/an/an/a



University of Washington Through its Center for Commercialization

US Patent


Assay Description
Inhibition of human tyrosine kinases.


US Patent US9765037 (2017)

More data for this
Ligand-Target Pair
Tyrosine-protein kinase HCK


(Homo sapiens (Human))
BDBM50345740
PNG
(3-(6-ethoxynaphthalen-2-yl)-1-isopropyl-1H-pyrazol...)
Show SMILES CCOc1ccc2cc(ccc2c1)-c1nn(C(C)C)c2ncnc(N)c12
Show InChI InChI=1S/C20H21N5O/c1-4-26-16-8-7-13-9-15(6-5-14(13)10-16)18-17-19(21)22-11-23-20(17)25(24-18)12(2)3/h5-12H,4H2,1-3H3,(H2,21,22,23)
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n/an/a 218n/an/an/an/an/an/a



University of Washington Through its Center for Commercialization

US Patent


Assay Description
Inhibition of human tyrosine kinases.


US Patent US9765037 (2017)

More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))
BDBM50345742
PNG
(1-isopropyl-3-(quinolin-3-yl)-1H-pyrazolo[3,4-d]py...)
Show SMILES CC(C)n1nc(-c2cnc3ccccc3c2)c2c(N)ncnc12
Show InChI InChI=1S/C17H16N6/c1-10(2)23-17-14(16(18)20-9-21-17)15(22-23)12-7-11-5-3-4-6-13(11)19-8-12/h3-10H,1-2H3,(H2,18,20,21)
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n/an/a 1.70E+3n/an/an/an/an/an/a



University of Washington Through its Center for Commercialization

US Patent


Assay Description
Inhibition of human tyrosine kinases.


US Patent US9765037 (2017)

More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50389685
PNG
(CHEMBL2070052 | US9765037, Compound 11)
Show SMILES CC(C)Oc1ccc2cc(ccc2c1)-c1nn(C(C)C)c2ncnc(N)c12
Show InChI InChI=1S/C21H23N5O/c1-12(2)26-21-18(20(22)23-11-24-21)19(25-26)16-6-5-15-10-17(27-13(3)4)8-7-14(15)9-16/h5-13H,1-4H3,(H2,22,23,24)
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n/an/a 475n/an/an/an/an/an/a



University of Washington Through its Center for Commercialization

US Patent


Assay Description
Inhibition of human tyrosine kinases.


US Patent US9765037 (2017)

More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))
BDBM50389689
PNG
(CHEMBL2070055 | US9765037, Compound 12)
Show SMILES CCCOc1ccc2cc(ccc2c1)-c1nn(C(C)C)c2ncnc(N)c12
Show InChI InChI=1S/C21H23N5O/c1-4-9-27-17-8-7-14-10-16(6-5-15(14)11-17)19-18-20(22)23-12-24-21(18)26(25-19)13(2)3/h5-8,10-13H,4,9H2,1-3H3,(H2,22,23,24)
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n/an/a 838n/an/an/an/an/an/a



University of Washington Through its Center for Commercialization

US Patent


Assay Description
Inhibition of human tyrosine kinases.


US Patent US9765037 (2017)

More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))
BDBM50383374
PNG
(CHEMBL2030555 | CHEMBL2069960 | US9765037, Compoun...)
Show SMILES Nc1ncnc2n(CC3CCNCC3)nc(-c3cnc4ccccc4c3)c12
Show InChI InChI=1S/C20H21N7/c21-19-17-18(15-9-14-3-1-2-4-16(14)23-10-15)26-27(20(17)25-12-24-19)11-13-5-7-22-8-6-13/h1-4,9-10,12-13,22H,5-8,11H2,(H2,21,24,25)
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n/an/a>2.00E+4n/an/an/an/an/an/a



University of Washington Through its Center for Commercialization

US Patent


Assay Description
Inhibition of human tyrosine kinases.


US Patent US9765037 (2017)

More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50389696
PNG
(CHEMBL2070063 | US9765037, Compound 34)
Show SMILES Nc1ncnc2n(CC3CCNCC3)nc(-c3ccc4cc(OCc5ccccc5)ccc4c3)c12
Show InChI InChI=1S/C28H28N6O/c29-27-25-26(33-34(28(25)32-18-31-27)16-19-10-12-30-13-11-19)23-7-6-22-15-24(9-8-21(22)14-23)35-17-20-4-2-1-3-5-20/h1-9,14-15,18-19,30H,10-13,16-17H2,(H2,29,31,32)
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n/an/a 3.06E+3n/an/an/an/an/an/a



University of Washington Through its Center for Commercialization

US Patent


Assay Description
Inhibition of human tyrosine kinases.


US Patent US9765037 (2017)

More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))
BDBM50389696
PNG
(CHEMBL2070063 | US9765037, Compound 34)
Show SMILES Nc1ncnc2n(CC3CCNCC3)nc(-c3ccc4cc(OCc5ccccc5)ccc4c3)c12
Show InChI InChI=1S/C28H28N6O/c29-27-25-26(33-34(28(25)32-18-31-27)16-19-10-12-30-13-11-19)23-7-6-22-15-24(9-8-21(22)14-23)35-17-20-4-2-1-3-5-20/h1-9,14-15,18-19,30H,10-13,16-17H2,(H2,29,31,32)
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n/an/a>1.00E+4n/an/an/an/an/an/a



University of Washington Through its Center for Commercialization

US Patent


Assay Description
Inhibition of human tyrosine kinases.


US Patent US9765037 (2017)

More data for this
Ligand-Target Pair
Tyrosine-protein kinase HCK


(Homo sapiens (Human))
BDBM50389746
PNG
(CHEMBL2070061 | US9765037, Compound 35)
Show SMILES CCCCOc1ccc2cc(ccc2c1)-c1nn(CC2CCNCC2)c2ncnc(N)c12
Show InChI InChI=1S/C25H30N6O/c1-2-3-12-32-21-7-6-18-13-20(5-4-19(18)14-21)23-22-24(26)28-16-29-25(22)31(30-23)15-17-8-10-27-11-9-17/h4-7,13-14,16-17,27H,2-3,8-12,15H2,1H3,(H2,26,28,29)
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n/an/a>1.00E+4n/an/an/an/an/an/a



University of Washington Through its Center for Commercialization

US Patent


Assay Description
Inhibition of human tyrosine kinases.


US Patent US9765037 (2017)

More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))
BDBM50389688
PNG
(CHEMBL2069315 | US9765037, Compound 36)
Show SMILES Nc1ncnc2n(CC3CCNCC3)nc(-c3ccc4cc(OCC=C)ccc4c3)c12
Show InChI InChI=1S/C24H26N6O/c1-2-11-31-20-6-5-17-12-19(4-3-18(17)13-20)22-21-23(25)27-15-28-24(21)30(29-22)14-16-7-9-26-10-8-16/h2-6,12-13,15-16,26H,1,7-11,14H2,(H2,25,27,28)
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n/an/a>1.00E+4n/an/an/an/an/an/a



University of Washington Through its Center for Commercialization

US Patent


Assay Description
Inhibition of human tyrosine kinases.


US Patent US9765037 (2017)

More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))
BDBM50389687
PNG
(CHEMBL2070054 | US9765037, Compound 41)
Show SMILES CC(C)n1nc(-c2ccc3cc(OCC=C)ccc3c2)c2c(N)ncnc12
Show InChI InChI=1S/C21H21N5O/c1-4-9-27-17-8-7-14-10-16(6-5-15(14)11-17)19-18-20(22)23-12-24-21(18)26(25-19)13(2)3/h4-8,10-13H,1,9H2,2-3H3,(H2,22,23,24)
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n/an/a 675n/an/an/an/an/an/a



University of Washington Through its Center for Commercialization

US Patent


Assay Description
Inhibition of human tyrosine kinases.


US Patent US9765037 (2017)

More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))
BDBM50389728
PNG
(CHEMBL2069944 | US9765037, Compound 132)
Show SMILES COc1ccc(cc1C)-c1nn(c2ncnc(N)c12)C(C)(C)C
Show InChI InChI=1S/C17H21N5O/c1-10-8-11(6-7-12(10)23-5)14-13-15(18)19-9-20-16(13)22(21-14)17(2,3)4/h6-9H,1-5H3,(H2,18,19,20)
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n/an/a 2.94E+3n/an/an/an/an/an/a



University of Washington Through its Center for Commercialization

US Patent


Assay Description
Inhibition of human tyrosine kinases.


US Patent US9765037 (2017)

More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))
BDBM50389679
PNG
(CHEMBL2070046 | US9765037, Compound 135)
Show SMILES COc1ccc2cc(ccc2c1)-c1nn(c2ncnc(N)c12)C(C)(C)C
Show InChI InChI=1S/C20H21N5O/c1-20(2,3)25-19-16(18(21)22-11-23-19)17(24-25)14-6-5-13-10-15(26-4)8-7-12(13)9-14/h5-11H,1-4H3,(H2,21,22,23)
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n/an/a 4.86E+3n/an/an/an/an/an/a



University of Washington Through its Center for Commercialization

US Patent


Assay Description
Inhibition of human tyrosine kinases.


US Patent US9765037 (2017)

More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))
BDBM50389682
PNG
(CHEMBL2070049 | US9518026, Example 4 | US9765037, ...)
Show SMILES CCOc1ccc2cc(ccc2c1)-c1nn(c2ncnc(N)c12)C(C)(C)C
Show InChI InChI=1S/C21H23N5O/c1-5-27-16-9-8-13-10-15(7-6-14(13)11-16)18-17-19(22)23-12-24-20(17)26(25-18)21(2,3)4/h6-12H,5H2,1-4H3,(H2,22,23,24)
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n/an/a 8.04E+3n/an/an/an/an/an/a



University of Washington Through its Center for Commercialization

US Patent


Assay Description
Inhibition of human tyrosine kinases.


US Patent US9765037 (2017)

More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50383376
PNG
(CHEMBL2030558 | CHEMBL2069945 | US9765037, Compoun...)
Show SMILES COc1ccc(cc1C)-c1nn(CC2CCNCC2)c2ncnc(N)c12
Show InChI InChI=1S/C19H24N6O/c1-12-9-14(3-4-15(12)26-2)17-16-18(20)22-11-23-19(16)25(24-17)10-13-5-7-21-8-6-13/h3-4,9,11,13,21H,5-8,10H2,1-2H3,(H2,20,22,23)
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n/an/a>1.00E+4n/an/an/an/an/an/a



University of Washington Through its Center for Commercialization

US Patent


Assay Description
Inhibition of human tyrosine kinases.


US Patent US9765037 (2017)

More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50142887
PNG
(1-(tert-butyl)-3-(4-chlorophenyl)-4-aminopyrazolo[...)
Show SMILES CC(C)(C)n1nc(-c2ccc(Cl)cc2)c2c(N)ncnc12
Show InChI InChI=1S/C15H16ClN5/c1-15(2,3)21-14-11(13(17)18-8-19-14)12(20-21)9-4-6-10(16)7-5-9/h4-8H,1-3H3,(H2,17,18,19)
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n/an/a 36.6n/an/an/an/an/an/a



University of Washington Through its Center for Commercialization

US Patent


Assay Description
Inhibition of human tyrosine kinases.


US Patent US9765037 (2017)

More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))
BDBM50389704
PNG
(CHEMBL2070081 | US9518026, Example 9 | US9765037, ...)
Show SMILES CCOc1ccc2cc(ccc2c1)-c1nn(CC2CCN(C)CC2)c2ncnc(N)c12
Show InChI InChI=1S/C24H28N6O/c1-3-31-20-7-6-17-12-19(5-4-18(17)13-20)22-21-23(25)26-15-27-24(21)30(28-22)14-16-8-10-29(2)11-9-16/h4-7,12-13,15-16H,3,8-11,14H2,1-2H3,(H2,25,26,27)
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n/an/a>3.00E+3n/an/an/an/an/an/a



University of Washington Through its Center for Commercialization

US Patent


Assay Description
Inhibition of human tyrosine kinases.


US Patent US9765037 (2017)

More data for this
Ligand-Target Pair
Calcium-dependent protein kinase 1 (CDPK1)


(Cryptosporidium parvum)
BDBM50345706
PNG
(1-methyl-3-(naphthalen-1-ylmethyl)-1H-pyrazolo[3,4...)
Show SMILES Cn1nc(Cc2cccc3ccccc23)c2c(N)ncnc12
Show InChI InChI=1S/C17H15N5/c1-22-17-15(16(18)19-10-20-17)14(21-22)9-12-7-4-6-11-5-2-3-8-13(11)12/h2-8,10H,9H2,1H3,(H2,18,19,20)
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n/an/a 413n/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)

More data for this
Ligand-Target Pair
Calmodulin-domain protein kinase 1 (CDPK1)


(Toxoplasma gondii)
BDBM50298225
PNG
(CHEMBL2069955 | CHEMBL573578 | NM-PP1 | US9765037,...)
Show SMILES CC(C)(C)n1nc(Cc2cccc3ccccc23)c2c(N)ncnc12
Show InChI InChI=1S/C20H21N5/c1-20(2,3)25-19-17(18(21)22-12-23-19)16(24-25)11-14-9-6-8-13-7-4-5-10-15(13)14/h4-10,12H,11H2,1-3H3,(H2,21,22,23)
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n/an/a 31n/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)

More data for this
Ligand-Target Pair
Calmodulin-domain protein kinase 1 (CDPK1)


(Toxoplasma gondii)
BDBM50345710
PNG
(1-cyclohexyl-3-(naphthalen-1-ylmethyl)-1H-pyrazolo...)
Show SMILES Nc1ncnc2n(nc(Cc3cccc4ccccc34)c12)C1CCCCC1
Show InChI InChI=1S/C22H23N5/c23-21-20-19(13-16-9-6-8-15-7-4-5-12-18(15)16)26-27(22(20)25-14-24-21)17-10-2-1-3-11-17/h4-9,12,14,17H,1-3,10-11,13H2,(H2,23,24,25)
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n/an/a 946n/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)

More data for this
Ligand-Target Pair
Calmodulin-domain protein kinase 1 (CDPK1)


(Toxoplasma gondii)
BDBM50345717
PNG
(1-(1-ethylpiperidin-4-yl)-3-(naphthalen-1-ylmethyl...)
Show SMILES CCN1CCC(CC1)n1nc(Cc2cccc3ccccc23)c2c(N)ncnc12
Show InChI InChI=1S/C23H26N6/c1-2-28-12-10-18(11-13-28)29-23-21(22(24)25-15-26-23)20(27-29)14-17-8-5-7-16-6-3-4-9-19(16)17/h3-9,15,18H,2,10-14H2,1H3,(H2,24,25,26)
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n/an/a 36n/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)

More data for this
Ligand-Target Pair
Calcium-dependent protein kinase 1 (CDPK1)


(Cryptosporidium parvum)
BDBM50345720
PNG
(1-(1-(methylsulfonyl)piperidin-4-yl)-3-(naphthalen...)
Show SMILES CS(=O)(=O)N1CCC(CC1)n1nc(Cc2cccc3ccccc23)c2c(N)ncnc12
Show InChI InChI=1S/C22H24N6O2S/c1-31(29,30)27-11-9-17(10-12-27)28-22-20(21(23)24-14-25-22)19(26-28)13-16-7-4-6-15-5-2-3-8-18(15)16/h2-8,14,17H,9-13H2,1H3,(H2,23,24,25)
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n/an/a 75n/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)

More data for this
Ligand-Target Pair
Calmodulin-domain protein kinase 1 (CDPK1)


(Toxoplasma gondii)
BDBM50345725
PNG
(3-(3,4-dichlorophenyl)-1-isopropyl-1H-pyrazolo[3,4...)
Show SMILES CC(C)n1nc(-c2ccc(Cl)c(Cl)c2)c2c(N)ncnc12
Show InChI InChI=1S/C14H13Cl2N5/c1-7(2)21-14-11(13(17)18-6-19-14)12(20-21)8-3-4-9(15)10(16)5-8/h3-7H,1-2H3,(H2,17,18,19)
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n/an/a 4n/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)

More data for this
Ligand-Target Pair
Calmodulin-domain protein kinase 1 (CDPK1)


(Toxoplasma gondii)
BDBM50345738
PNG
(1-isopropyl-3-(naphthalen-2-yl)-1H-pyrazolo[3,4-d]...)
Show SMILES CC(C)n1nc(-c2ccc3ccccc3c2)c2c(N)ncnc12
Show InChI InChI=1S/C18H17N5/c1-11(2)23-18-15(17(19)20-10-21-18)16(22-23)14-8-7-12-5-3-4-6-13(12)9-14/h3-11H,1-2H3,(H2,19,20,21)
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n/an/a 5n/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)

More data for this
Ligand-Target Pair
Calmodulin-domain protein kinase 1 (CDPK1)


(Toxoplasma gondii)
BDBM50345739
PNG
(1-isopropyl-3-(6-methoxynaphthalen-2-yl)-1H-pyrazo...)
Show SMILES COc1ccc2cc(ccc2c1)-c1nn(C(C)C)c2ncnc(N)c12
Show InChI InChI=1S/C19H19N5O/c1-11(2)24-19-16(18(20)21-10-22-19)17(23-24)14-5-4-13-9-15(25-3)7-6-12(13)8-14/h4-11H,1-3H3,(H2,20,21,22)
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n/an/a 6n/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)

More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Calcium-dependent protein kinase 1 (CDPK1)


(Cryptosporidium parvum)
BDBM50345740
PNG
(3-(6-ethoxynaphthalen-2-yl)-1-isopropyl-1H-pyrazol...)
Show SMILES CCOc1ccc2cc(ccc2c1)-c1nn(C(C)C)c2ncnc(N)c12
Show InChI InChI=1S/C20H21N5O/c1-4-26-16-8-7-13-9-15(6-5-14(13)10-16)18-17-19(21)22-11-23-20(17)25(24-18)12(2)3/h5-12H,4H2,1-3H3,(H2,21,22,23)
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n/an/a 12n/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)

More data for this
Ligand-Target Pair
Calmodulin-domain protein kinase 1 (CDPK1)


(Toxoplasma gondii)
BDBM50345749
PNG
(3-(3-(benzyloxy)phenyl)-1-isopropyl-1H-pyrazolo[3,...)
Show SMILES CC(C)n1nc(-c2cccc(OCc3ccccc3)c2)c2c(N)ncnc12
Show InChI InChI=1S/C21H21N5O/c1-14(2)26-21-18(20(22)23-13-24-21)19(25-26)16-9-6-10-17(11-16)27-12-15-7-4-3-5-8-15/h3-11,13-14H,12H2,1-2H3,(H2,22,23,24)
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n/an/a 1.06E+3n/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)

More data for this
Ligand-Target Pair
Calmodulin-domain protein kinase 1 (CDPK1)


(Toxoplasma gondii)
BDBM340883
PNG
(1-(6-ethoxynaphthalen-2-yl)-3- isopropylimidazo[1,...)
Show SMILES CCOc1ccc2cc(ccc2c1)-c1nc(C(C)C)n2ccnc(N)c12
Show InChI InChI=1S/C21H22N4O/c1-4-26-17-8-7-14-11-16(6-5-15(14)12-17)18-19-20(22)23-9-10-25(19)21(24-18)13(2)3/h5-13H,4H2,1-3H3,(H2,22,23)
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n/an/a 78n/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)

More data for this
Ligand-Target Pair
Calcium-dependent protein kinase 1 (CDPK1)


(Cryptosporidium parvum)
BDBM50389689
PNG
(CHEMBL2070055 | US9765037, Compound 12)
Show SMILES CCCOc1ccc2cc(ccc2c1)-c1nn(C(C)C)c2ncnc(N)c12
Show InChI InChI=1S/C21H23N5O/c1-4-9-27-17-8-7-14-10-16(6-5-15(14)11-17)19-18-20(22)23-12-24-21(18)26(25-19)13(2)3/h5-8,10-13H,4,9H2,1-3H3,(H2,22,23,24)
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n/an/a 53.2n/an/an/an/an/an/a



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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)

More data for this
Ligand-Target Pair
Calmodulin-domain protein kinase 1 (CDPK1)


(Toxoplasma gondii)
BDBM340886
PNG
(1-cyclopentyl-3-(naphthalen-1-ylmethyl)-1H- pyrazo...)
Show SMILES Nc1ncnc2n(nc(Cc3cccc4ccccc34)c12)C1CCCC1
Show InChI InChI=1S/C21H21N5/c22-20-19-18(12-15-8-5-7-14-6-1-4-11-17(14)15)25-26(16-9-2-3-10-16)21(19)24-13-23-20/h1,4-8,11,13,16H,2-3,9-10,12H2,(H2,22,23,24)
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n/an/a 553n/an/an/an/an/an/a



University of Washington Through its Center for Commercialization

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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)

More data for this
Ligand-Target Pair
Calcium-dependent protein kinase 1 (CDPK1)


(Cryptosporidium parvum)
BDBM340886
PNG
(1-cyclopentyl-3-(naphthalen-1-ylmethyl)-1H- pyrazo...)
Show SMILES Nc1ncnc2n(nc(Cc3cccc4ccccc34)c12)C1CCCC1
Show InChI InChI=1S/C21H21N5/c22-20-19-18(12-15-8-5-7-14-6-1-4-11-17(14)15)25-26(16-9-2-3-10-16)21(19)24-13-23-20/h1,4-8,11,13,16H,2-3,9-10,12H2,(H2,22,23,24)
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n/an/a 894n/an/an/an/an/an/a



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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)

More data for this
Ligand-Target Pair
Calcium-dependent protein kinase 1 (CDPK1)


(Cryptosporidium parvum)
BDBM340892
PNG
(3-(2-chloropyridin-4-yl)-1-isopropyl-1H- pyrazolo[...)
Show SMILES CC(C)n1nc(-c2ccnc(Cl)c2)c2c(N)ncnc12
Show InChI InChI=1S/C13H13ClN6/c1-7(2)20-13-10(12(15)17-6-18-13)11(19-20)8-3-4-16-9(14)5-8/h3-7H,1-2H3,(H2,15,17,18)
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n/an/a 370n/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)

More data for this
Ligand-Target Pair
Calmodulin-domain protein kinase 1 (CDPK1)


(Toxoplasma gondii)
BDBM340894
PNG
(3-(3-(2-chlorobenzyloxy)phenyl)-1-isopropyl-1H- py...)
Show SMILES CC(C)n1nc(-c2cccc(OCc3ccccc3Cl)c2)c2c(N)ncnc12
Show InChI InChI=1S/C21H20ClN5O/c1-13(2)27-21-18(20(23)24-12-25-21)19(26-27)14-7-5-8-16(10-14)28-11-15-6-3-4-9-17(15)22/h3-10,12-13H,11H2,1-2H3,(H2,23,24,25)
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n/an/a>3.00E+3n/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)

More data for this
Ligand-Target Pair
Calcium-dependent protein kinase 1 (CDPK1)


(Cryptosporidium parvum)
BDBM340896
PNG
(3-(3-(3,5-dimethoxybenzyloxy)phenyl)-1- isopropyl-...)
Show SMILES COc1cc(COc2cccc(c2)-c2nn(C(C)C)c3ncnc(N)c23)cc(OC)c1
Show InChI InChI=1S/C23H25N5O3/c1-14(2)28-23-20(22(24)25-13-26-23)21(27-28)16-6-5-7-17(10-16)31-12-15-8-18(29-3)11-19(9-15)30-4/h5-11,13-14H,12H2,1-4H3,(H2,24,25,26)
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n/an/a>3.00E+3n/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)

More data for this
Ligand-Target Pair
Calmodulin-domain protein kinase 1 (CDPK1)


(Toxoplasma gondii)
BDBM340899
PNG
(1-isopropyl-3-(4-methyl-1H-indol-2-yl)-1H- pyrazol...)
Show SMILES CC(C)n1nc(-c2cc3c(C)cccc3[nH]2)c2c(N)ncnc12
Show InChI InChI=1S/C17H18N6/c1-9(2)23-17-14(16(18)19-8-20-17)15(22-23)13-7-11-10(3)5-4-6-12(11)21-13/h4-9,21H,1-3H3,(H2,18,19,20)
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n/an/a 3.80n/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)

More data for this
Ligand-Target Pair
Calcium-dependent protein kinase 1 (CDPK1)


(Cryptosporidium parvum)
BDBM340919
PNG
(3-(4-chlorophenyl)-1-(piperidin-4-ylmethyl)-1H- py...)
Show SMILES Nc1ncnc2n(CC3CCNCC3)nc(-c3ccc(Cl)cc3)c12
Show InChI InChI=1S/C17H19ClN6/c18-13-3-1-12(2-4-13)15-14-16(19)21-10-22-17(14)24(23-15)9-11-5-7-20-8-6-11/h1-4,10-11,20H,5-9H2,(H2,19,21,22)
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n/an/a 92n/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)

More data for this
Ligand-Target Pair
Calmodulin-domain protein kinase 1 (CDPK1)


(Toxoplasma gondii)
BDBM340922
PNG
(3-(6-(2,5-dimethylbenzyloxy)naphthalen-2-yl)-1- is...)
Show SMILES CC(C)n1nc(-c2ccc3cc(OCc4cc(C)ccc4C)ccc3c2)c2c(N)ncnc12
Show InChI InChI=1S/C27H27N5O/c1-16(2)32-27-24(26(28)29-15-30-27)25(31-32)21-8-7-20-13-23(10-9-19(20)12-21)33-14-22-11-17(3)5-6-18(22)4/h5-13,15-16H,14H2,1-4H3,(H2,28,29,30)
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n/an/a 137n/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)

More data for this
Ligand-Target Pair
Calcium-dependent protein kinase 1 (CDPK1)


(Cryptosporidium parvum)
BDBM340925
PNG
(3-(6-(3-chloro-4-(2,2,2- trifluorethyl)benzyloxy)n...)
Show SMILES CC(C)n1nc(-c2ccc3cc(OCc4ccc(CC(F)(F)F)c(Cl)c4)ccc3c2)c2c(N)ncnc12
Show InChI InChI=1S/C27H23ClF3N5O/c1-15(2)36-26-23(25(32)33-14-34-26)24(35-36)19-6-5-18-11-21(8-7-17(18)10-19)37-13-16-3-4-20(22(28)9-16)12-27(29,30)31/h3-11,14-15H,12-13H2,1-2H3,(H2,32,33,34)
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n/an/a 262n/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)

More data for this
Ligand-Target Pair
Calmodulin-domain protein kinase 1 (CDPK1)


(Toxoplasma gondii)
BDBM340929
PNG
(3-(6-(4-tert-butylbenzyloxy)naphthalen-2-yl)-1- is...)
Show SMILES CC(C)n1nc(-c2ccc3cc(OCc4ccc(cc4)C(C)(C)C)ccc3c2)c2c(N)ncnc12
Show InChI InChI=1S/C29H31N5O/c1-18(2)34-28-25(27(30)31-17-32-28)26(33-34)22-9-8-21-15-24(13-10-20(21)14-22)35-16-19-6-11-23(12-7-19)29(3,4)5/h6-15,17-18H,16H2,1-5H3,(H2,30,31,32)
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n/an/a 15.9n/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)

More data for this
Ligand-Target Pair
Calmodulin-domain protein kinase 1 (CDPK1)


(Toxoplasma gondii)
BDBM340934
PNG
(N-(4-(4-amino-1-tert-butyl-1H-pyrazolo[3,4- d]pyri...)
Show SMILES CC(C)C(=O)Nc1ccc(cc1)-c1nn(c2ncnc(N)c12)C(C)(C)C
Show InChI InChI=1S/C19H24N6O/c1-11(2)18(26)23-13-8-6-12(7-9-13)15-14-16(20)21-10-22-17(14)25(24-15)19(3,4)5/h6-11H,1-5H3,(H,23,26)(H2,20,21,22)
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n/an/a 99.7n/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)

More data for this
Ligand-Target Pair
Calmodulin-domain protein kinase 1 (CDPK1)


(Toxoplasma gondii)
BDBM340935
PNG
(N-(4-(4-amino-1-tert-butyl-1H-pyrazolo[3,4- d]pyri...)
Show SMILES CC(C)(C)C(=O)Nc1ccc(cc1)-c1nn(c2ncnc(N)c12)C(C)(C)C
Show InChI InChI=1S/C20H26N6O/c1-19(2,3)18(27)24-13-9-7-12(8-10-13)15-14-16(21)22-11-23-17(14)26(25-15)20(4,5)6/h7-11H,1-6H3,(H,24,27)(H2,21,22,23)
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n/an/a 66.6n/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)

More data for this
Ligand-Target Pair
Calcium-dependent protein kinase 1 (CDPK1)


(Cryptosporidium parvum)
BDBM340942
PNG
(N-(4-(4-amino-1-tert-butyl-1H-pyrazolo[3,4- d]pyri...)
Show SMILES CCC(=O)Nc1ccc(cc1)-c1nn(c2ncnc(N)c12)C(C)(C)C
Show InChI InChI=1S/C18H22N6O/c1-5-13(25)22-12-8-6-11(7-9-12)15-14-16(19)20-10-21-17(14)24(23-15)18(2,3)4/h6-10H,5H2,1-4H3,(H,22,25)(H2,19,20,21)
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n/an/a 822n/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)

More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))
BDBM50345704
PNG
(1-(tert-butyl)-3-(naphthalen-2-yl)-1H-pyrazolo[3,4...)
Show SMILES CC(C)(C)n1nc(-c2ccc3ccccc3c2)c2c(N)ncnc12
Show InChI InChI=1S/C19H19N5/c1-19(2,3)24-18-15(17(20)21-11-22-18)16(23-24)14-9-8-12-6-4-5-7-13(12)10-14/h4-11H,1-3H3,(H2,20,21,22)
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n/an/a 6.00E+3n/an/an/an/an/an/a



University of Washington Through its Center for Commercialization

US Patent


Assay Description
Inhibition of human tyrosine kinases.


US Patent US9765037 (2017)

More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50298225
PNG
(CHEMBL2069955 | CHEMBL573578 | NM-PP1 | US9765037,...)
Show SMILES CC(C)(C)n1nc(Cc2cccc3ccccc23)c2c(N)ncnc12
Show InChI InChI=1S/C20H21N5/c1-20(2,3)25-19-17(18(21)22-12-23-19)16(24-25)11-14-9-6-8-13-7-4-5-10-15(13)14/h4-10,12H,11H2,1-3H3,(H2,21,22,23)
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n/an/a 2.20E+3n/an/an/an/an/an/a



University of Washington Through its Center for Commercialization

US Patent


Assay Description
Inhibition of human tyrosine kinases.


US Patent US9765037 (2017)

More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))
BDBM50345718
PNG
(1-((1-ethylpiperidin-4-yl)methyl)-3-(naphthalen-1-...)
Show SMILES CCN1CCC(Cn2nc(Cc3cccc4ccccc34)c3c(N)ncnc23)CC1
Show InChI InChI=1S/C24H28N6/c1-2-29-12-10-17(11-13-29)15-30-24-22(23(25)26-16-27-24)21(28-30)14-19-8-5-7-18-6-3-4-9-20(18)19/h3-9,16-17H,2,10-15H2,1H3,(H2,25,26,27)
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n/an/a>2.00E+4n/an/an/an/an/an/a



University of Washington Through its Center for Commercialization

US Patent


Assay Description
Inhibition of human tyrosine kinases.


US Patent US9765037 (2017)

More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50345739
PNG
(1-isopropyl-3-(6-methoxynaphthalen-2-yl)-1H-pyrazo...)
Show SMILES COc1ccc2cc(ccc2c1)-c1nn(C(C)C)c2ncnc(N)c12
Show InChI InChI=1S/C19H19N5O/c1-11(2)24-19-16(18(20)21-10-22-19)17(23-24)14-5-4-13-9-15(25-3)7-6-12(13)8-14/h4-11H,1-3H3,(H2,20,21,22)
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n/an/a 770n/an/an/an/an/an/a



University of Washington Through its Center for Commercialization

US Patent


Assay Description
Inhibition of human tyrosine kinases.


US Patent US9765037 (2017)

More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))
BDBM50383380
PNG
(CHEMBL2030553 | CHEMBL2070047 | US9765037, Compoun...)
Show SMILES COc1ccc2cc(ccc2c1)-c1nn(CC2CCNCC2)c2ncnc(N)c12
Show InChI InChI=1S/C22H24N6O/c1-29-18-5-4-15-10-17(3-2-16(15)11-18)20-19-21(23)25-13-26-22(19)28(27-20)12-14-6-8-24-9-7-14/h2-5,10-11,13-14,24H,6-9,12H2,1H3,(H2,23,25,26)
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n/an/a>2.00E+4n/an/an/an/an/an/a



University of Washington Through its Center for Commercialization

US Patent


Assay Description
Inhibition of human tyrosine kinases.


US Patent US9765037 (2017)

More data for this
Ligand-Target Pair
Tyrosine-protein kinase ABL1


(Homo sapiens (Human))
BDBM50389686
PNG
(CHEMBL2070053 | US9765037, Compound 32)
Show SMILES CC(C)Oc1ccc2cc(ccc2c1)-c1nn(CC2CCNCC2)c2ncnc(N)c12
Show InChI InChI=1S/C24H28N6O/c1-15(2)31-20-6-5-17-11-19(4-3-18(17)12-20)22-21-23(25)27-14-28-24(21)30(29-22)13-16-7-9-26-10-8-16/h3-6,11-12,14-16,26H,7-10,13H2,1-2H3,(H2,25,27,28)
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n/an/a>1.00E+4n/an/an/an/an/an/a



University of Washington Through its Center for Commercialization

US Patent


Assay Description
Inhibition of human tyrosine kinases.


US Patent US9765037 (2017)

More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50389688
PNG
(CHEMBL2069315 | US9765037, Compound 36)
Show SMILES Nc1ncnc2n(CC3CCNCC3)nc(-c3ccc4cc(OCC=C)ccc4c3)c12
Show InChI InChI=1S/C24H26N6O/c1-2-11-31-20-6-5-17-12-19(4-3-18(17)13-20)22-21-23(25)27-15-28-24(21)30(29-22)14-16-7-9-26-10-8-16/h2-6,12-13,15-16,26H,1,7-11,14H2,(H2,25,27,28)
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n/an/a>1.00E+4n/an/an/an/an/an/a



University of Washington Through its Center for Commercialization

US Patent


Assay Description
Inhibition of human tyrosine kinases.


US Patent US9765037 (2017)

More data for this
Ligand-Target Pair
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* indicates data uncertainty>20%