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Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Tyrosine-protein kinase BTK' and Ligand = 'BDBM50063963'   
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))
BDBM50063963
PNG
(CHEMBL3402585)
Show SMILES OCc1c(cccc1-n1ccc2cc(cc(F)c2c1=O)C1CC1)-c1ncnc2[nH]c(cc12)C1=CCN(CC1)C(=O)N1CCOCC1 |t:38|
Show InChI InChI=1S/C35H33FN6O4/c36-28-17-24(21-4-5-21)16-23-8-11-42(34(44)31(23)28)30-3-1-2-25(27(30)19-43)32-26-18-29(39-33(26)38-20-37-32)22-6-9-40(10-7-22)35(45)41-12-14-46-15-13-41/h1-3,6,8,11,16-18,20-21,43H,4-5,7,9-10,12-15,19H2,(H,37,38,39)
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PC cid
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Similars

Article
PubMed
n/an/a 4.80n/an/an/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Inhibition of BTK (unknown origin) after 1 hr by TR-FRET analysis


Bioorg Med Chem 23: 891-901 (2015)


Article DOI: 10.1016/j.bmc.2014.10.043
BindingDB Entry DOI: 10.7270/Q2SN0BNZ
More data for this
Ligand-Target Pair
Tyrosine-protein kinase BTK


(Homo sapiens (Human))
BDBM50063963
PNG
(CHEMBL3402585)
Show SMILES OCc1c(cccc1-n1ccc2cc(cc(F)c2c1=O)C1CC1)-c1ncnc2[nH]c(cc12)C1=CCN(CC1)C(=O)N1CCOCC1 |t:38|
Show InChI InChI=1S/C35H33FN6O4/c36-28-17-24(21-4-5-21)16-23-8-11-42(34(44)31(23)28)30-3-1-2-25(27(30)19-43)32-26-18-29(39-33(26)38-20-37-32)22-6-9-40(10-7-22)35(45)41-12-14-46-15-13-41/h1-3,6,8,11,16-18,20-21,43H,4-5,7,9-10,12-15,19H2,(H,37,38,39)
PDB
MMDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 17n/an/an/an/an/an/a



China Pharmaceutical University

Curated by ChEMBL


Assay Description
Inhibition of BTK in human Ramos cells after 20 mins by fluorescence assay


Bioorg Med Chem 23: 891-901 (2015)


Article DOI: 10.1016/j.bmc.2014.10.043
BindingDB Entry DOI: 10.7270/Q2SN0BNZ
More data for this
Ligand-Target Pair