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Compile Data Set for Download or QSAR

Found 4 hits Enz. Inhib. hit(s) with Target = 'Tyrosine-protein kinase BTK' and Ligand = 'BDBM259431'   
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 BTK


(Homo sapiens (Human))
BDBM259431
PNG
(US10457647, Example 30 | US11180460, Example 30 | ...)
Show SMILES CO[C@H]1C[C@@H](COc2c(N)ncnc2-c2cc(F)cc(NC(=O)c3ccc(cc3F)C3CC3)c2C)N(C1)C(=O)C#CC |r|
Show InChI InChI=1S/C31H31F2N5O4/c1-4-5-27(39)38-14-22(41-3)13-21(38)15-42-29-28(35-16-36-30(29)34)24-11-20(32)12-26(17(24)2)37-31(40)23-9-8-19(10-25(23)33)18-6-7-18/h8-12,16,18,21-22H,6-7,13-15H2,1-3H3,(H,37,40)(H2,34,35,36)/t21-,22-/m0/s1
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US Patent
n/an/a 6n/an/an/an/a7.530



Novartis AG

US Patent


Assay Description
The inhibitory activity of the present compounds against Btk was assessed in a biochemical enzyme assay. Assay plates in 384 well format were prepare...


US Patent US9512084 (2016)


BindingDB Entry DOI: 10.7270/Q2ZK5FMH
More data for this
Ligand-Target Pair
Tyrosine-protein kinase BTK


(Homo sapiens (Human))
BDBM259431
PNG
(US10457647, Example 30 | US11180460, Example 30 | ...)
Show SMILES CO[C@H]1C[C@@H](COc2c(N)ncnc2-c2cc(F)cc(NC(=O)c3ccc(cc3F)C3CC3)c2C)N(C1)C(=O)C#CC |r|
Show InChI InChI=1S/C31H31F2N5O4/c1-4-5-27(39)38-14-22(41-3)13-21(38)15-42-29-28(35-16-36-30(29)34)24-11-20(32)12-26(17(24)2)37-31(40)23-9-8-19(10-25(23)33)18-6-7-18/h8-12,16,18,21-22H,6-7,13-15H2,1-3H3,(H,37,40)(H2,34,35,36)/t21-,22-/m0/s1
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n/an/a 6n/an/an/an/an/an/a


TBA



Citation and Details

BindingDB Entry DOI: 10.7270/Q2PV6Q9F
More data for this
Ligand-Target Pair
Tyrosine-protein kinase BTK


(Homo sapiens (Human))
BDBM259431
PNG
(US10457647, Example 30 | US11180460, Example 30 | ...)
Show SMILES CO[C@H]1C[C@@H](COc2c(N)ncnc2-c2cc(F)cc(NC(=O)c3ccc(cc3F)C3CC3)c2C)N(C1)C(=O)C#CC |r|
Show InChI InChI=1S/C31H31F2N5O4/c1-4-5-27(39)38-14-22(41-3)13-21(38)15-42-29-28(35-16-36-30(29)34)24-11-20(32)12-26(17(24)2)37-31(40)23-9-8-19(10-25(23)33)18-6-7-18/h8-12,16,18,21-22H,6-7,13-15H2,1-3H3,(H,37,40)(H2,34,35,36)/t21-,22-/m0/s1
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n/an/a 6n/an/an/an/an/an/a


TBA

Assay Description
The inhibitory activity of the present compounds against Btk was assessed in a biochemical enzyme assay. Assay plates in 384 well format were prepare...


Citation and Details

BindingDB Entry DOI: 10.7270/Q20R9SKR
More data for this
Ligand-Target Pair
Tyrosine-protein kinase BTK


(Homo sapiens (Human))
BDBM259431
PNG
(US10457647, Example 30 | US11180460, Example 30 | ...)
Show SMILES CO[C@H]1C[C@@H](COc2c(N)ncnc2-c2cc(F)cc(NC(=O)c3ccc(cc3F)C3CC3)c2C)N(C1)C(=O)C#CC |r|
Show InChI InChI=1S/C31H31F2N5O4/c1-4-5-27(39)38-14-22(41-3)13-21(38)15-42-29-28(35-16-36-30(29)34)24-11-20(32)12-26(17(24)2)37-31(40)23-9-8-19(10-25(23)33)18-6-7-18/h8-12,16,18,21-22H,6-7,13-15H2,1-3H3,(H,37,40)(H2,34,35,36)/t21-,22-/m0/s1
PDB
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PC sid
UniChem
US Patent
n/an/a 6n/an/an/an/an/an/a



Novartis AG

US Patent


Assay Description
The inhibitory activity of the present compounds against Btk was assessed in a biochemical enzyme assay. Assay plates in 384 well format were prepare...


US Patent US10457647 (2019)


BindingDB Entry DOI: 10.7270/Q2KH0QPQ
More data for this
Ligand-Target Pair