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Compile Data Set for Download or QSAR

Found 3 hits Enz. Inhib. hit(s) with Target = 'Tyrosine-protein kinase JAK2' and Ligand = 'BDBM419640'   
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 JAK2


(Homo sapiens (Human))
BDBM419640
PNG
(US10463675, Example 83 | US10980815, Ex. No. 83 | ...)
Show SMILES Cn1cc(Nc2nccc(n2)N2C[C@@H]3CC[C@H](C2)N3C2(CC#N)CN(C2)S(C)(=O)=O)cn1 |r,TLB:9:11:18:15.14|
Show InChI InChI=1S/C20H27N9O2S/c1-26-10-15(9-23-26)24-19-22-8-5-18(25-19)27-11-16-3-4-17(12-27)29(16)20(6-7-21)13-28(14-20)32(2,30)31/h5,8-10,16-17H,3-4,6,11-14H2,1-2H3,(H,22,24,25)/t16-,17+
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n/an/a 21n/an/an/an/an/an/a



Pfizer Inc.

US Patent


Assay Description
Compounds were added to a 384-well plate. Reaction mixtures contained 10 mM HEPES, pH 7.4, 10 mM MgCl2, 0.01% BSA, 0.0005% Tween 20, 1 mM ATP and 1 &...


US Patent US10463675 (2019)


BindingDB Entry DOI: 10.7270/Q2VT1VGN
More data for this
Ligand-Target Pair
Tyrosine-protein kinase JAK2


(Homo sapiens (Human))
BDBM419640
PNG
(US10463675, Example 83 | US10980815, Ex. No. 83 | ...)
Show SMILES Cn1cc(Nc2nccc(n2)N2C[C@@H]3CC[C@H](C2)N3C2(CC#N)CN(C2)S(C)(=O)=O)cn1 |r,TLB:9:11:18:15.14|
Show InChI InChI=1S/C20H27N9O2S/c1-26-10-15(9-23-26)24-19-22-8-5-18(25-19)27-11-16-3-4-17(12-27)29(16)20(6-7-21)13-28(14-20)32(2,30)31/h5,8-10,16-17H,3-4,6,11-14H2,1-2H3,(H,22,24,25)/t16-,17+
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PC sid
UniChem
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n/an/a 21n/an/an/an/an/an/a


TBA

Assay Description
Compounds were added to a 384-well plate. Reaction mixtures contained 10 mM HEPES, pH 7.4, 10 mM MgCl2, 0.01% BSA, 0.0005% Tween 20, 1 mM ATP and 1 M...


Citation and Details

BindingDB Entry DOI: 10.7270/Q2PC35J0
More data for this
Ligand-Target Pair
Tyrosine-protein kinase JAK2


(Homo sapiens (Human))
BDBM419640
PNG
(US10463675, Example 83 | US10980815, Ex. No. 83 | ...)
Show SMILES Cn1cc(Nc2nccc(n2)N2C[C@@H]3CC[C@H](C2)N3C2(CC#N)CN(C2)S(C)(=O)=O)cn1 |r,TLB:9:11:18:15.14|
Show InChI InChI=1S/C20H27N9O2S/c1-26-10-15(9-23-26)24-19-22-8-5-18(25-19)27-11-16-3-4-17(12-27)29(16)20(6-7-21)13-28(14-20)32(2,30)31/h5,8-10,16-17H,3-4,6,11-14H2,1-2H3,(H,22,24,25)/t16-,17+
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a 21n/an/an/an/an/an/a



Pfizer Inc.

US Patent


Assay Description
Compounds were added to a 384-well plate. Reaction mixtures contained 10 mM HEPES, pH 7.4, 10 mM MgCl2, 0.01% BSA, 0.0005% Tween 20, 1 mM ATP and 1 &...


US Patent US10980815 (2021)


BindingDB Entry DOI: 10.7270/Q2XD14SG
More data for this
Ligand-Target Pair