BindingDB logo
myBDB logout
Compile Data Set for Download or QSAR

Found 522 hits with Last Name = 'lazo' and Initial = 'js'   
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
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50084504
PNG
(CHEMBL3426991)
Show SMILES Nc1cccc(c1)-c1ccc2c(cc(Nc3ccccc3)[nH]c2=O)c1
Show InChI InChI=1S/C21H17N3O/c22-17-6-4-5-14(12-17)15-9-10-19-16(11-15)13-20(24-21(19)25)23-18-7-2-1-3-8-18/h1-13H,22H2,(H2,23,24,25)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
1.90E+3n/an/an/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Competitive inhibition of His6-tagged human recombinant Cdc25B catalytic domain (350 to 566 residues) expressed in Escherichia coli BL21 (D3) after 2...


Bioorg Med Chem 23: 2810-8 (2015)


Article DOI: 10.1016/j.bmc.2015.01.043
BindingDB Entry DOI: 10.7270/Q2CJ8G62
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50096680
PNG
((E)-2-(2-Chloro-phenyl)-ethenesulfonic acid [4-(4-...)
Show SMILES CCCc1sc(NS(=O)(=O)\C=C\c2ccccc2Cl)nc1-c1ccc(Cl)cc1
Show InChI InChI=1S/C20H18Cl2N2O2S2/c1-2-5-18-19(15-8-10-16(21)11-9-15)23-20(27-18)24-28(25,26)13-12-14-6-3-4-7-17(14)22/h3-4,6-13H,2,5H2,1H3,(H,23,24)/b13-12+
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

PubMed
4.60E+3n/an/an/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against human recombinant Cdc25B phosphatase enzyme


Bioorg Med Chem Lett 11: 313-7 (2001)


BindingDB Entry DOI: 10.7270/Q2DR2TRG
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50096693
PNG
((E)-2-Naphthalen-2-yl-ethenesulfonic acid (4,5-dip...)
Show SMILES O=S(=O)(Nc1nc(c(s1)-c1ccccc1)-c1ccccc1)\C=C\c1ccc2ccccc2c1
Show InChI InChI=1S/C27H20N2O2S2/c30-33(31,18-17-20-15-16-21-9-7-8-14-24(21)19-20)29-27-28-25(22-10-3-1-4-11-22)26(32-27)23-12-5-2-6-13-23/h1-19H,(H,28,29)/b18-17+
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

PubMed
3.60E+4n/an/an/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibitory activity against human recombinant Cdc25B phosphatase enzyme


Bioorg Med Chem Lett 11: 313-7 (2001)


BindingDB Entry DOI: 10.7270/Q2DR2TRG
More data for this
Ligand-Target Pair
Cytochrome P450 3A4


(Homo sapiens (Human))
BDBM50479538
PNG
(CAS 381679-98-5 | CHEMBL490678)
Show SMILES CCc1ccc(CCNS(=O)(=O)c2ccc(SC)cc2)cc1
Show InChI InChI=1S/C17H21NO2S2/c1-3-14-4-6-15(7-5-14)12-13-18-22(19,20)17-10-8-16(21-2)9-11-17/h4-11,18H,3,12-13H2,1-2H3
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
<5.00E+7n/an/an/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibition of CYP3A4


J Med Chem 52: 1247-50 (2009)


Article DOI: 10.1021/jm801278g
BindingDB Entry DOI: 10.7270/Q23T9M14
More data for this
Ligand-Target Pair
Cytochrome P450 3A4


(Homo sapiens (Human))
BDBM50479539
PNG
(CAS 307545-04-6 | CHEMBL491275)
Show SMILES CC(C)c1ccc(OCC(=O)Nc2nc3ccccc3s2)cc1
Show InChI InChI=1S/C18H18N2O2S/c1-12(2)13-7-9-14(10-8-13)22-11-17(21)20-18-19-15-5-3-4-6-16(15)23-18/h3-10,12H,11H2,1-2H3,(H,19,20,21)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
Purchase

PC cid
PC sid
UniChem
Article
PubMed
<5.00E+7n/an/an/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibition of CYP3A4


J Med Chem 52: 1247-50 (2009)


Article DOI: 10.1021/jm801278g
BindingDB Entry DOI: 10.7270/Q23T9M14
More data for this
Ligand-Target Pair
Cytochrome P450 3A4


(Homo sapiens (Human))
BDBM50479540
PNG
(CAS 329920-60-7 | CHEMBL452613)
Show SMILES CCc1ccc(OCC(=O)NCc2cccc3ccccc23)cc1
Show InChI InChI=1S/C21H21NO2/c1-2-16-10-12-19(13-11-16)24-15-21(23)22-14-18-8-5-7-17-6-3-4-9-20(17)18/h3-13H,2,14-15H2,1H3,(H,22,23)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
Purchase

PC cid
PC sid
UniChem
Article
PubMed
<5.00E+7n/an/an/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibition of CYP3A4


J Med Chem 52: 1247-50 (2009)


Article DOI: 10.1021/jm801278g
BindingDB Entry DOI: 10.7270/Q23T9M14
More data for this
Ligand-Target Pair
Cytochrome P450 3A4


(Homo sapiens (Human))
BDBM50479541
PNG
(CAS 303796-42-1 | CHEMBL446965)
Show SMILES CCc1ccc(OCC(=O)NCCc2ccccc2)cc1
Show InChI InChI=1S/C18H21NO2/c1-2-15-8-10-17(11-9-15)21-14-18(20)19-13-12-16-6-4-3-5-7-16/h3-11H,2,12-14H2,1H3,(H,19,20)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
Purchase

PC cid
PC sid
UniChem
Article
PubMed
<5.00E+7n/an/an/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibition of CYP3A4


J Med Chem 52: 1247-50 (2009)


Article DOI: 10.1021/jm801278g
BindingDB Entry DOI: 10.7270/Q23T9M14
More data for this
Ligand-Target Pair
Cytochrome P450 3A4


(Homo sapiens (Human))
BDBM50479542
PNG
(CAS 31122-64-2 | CHEMBL491273)
Show SMILES O=C(CCN1C(=O)c2ccccc2C1=O)N1CCCCC1
Show InChI InChI=1S/C16H18N2O3/c19-14(17-9-4-1-5-10-17)8-11-18-15(20)12-6-2-3-7-13(12)16(18)21/h2-3,6-7H,1,4-5,8-11H2
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
Purchase

PC cid
PC sid
UniChem
Article
PubMed
<5.00E+7n/an/an/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibition of CYP3A4


J Med Chem 52: 1247-50 (2009)


Article DOI: 10.1021/jm801278g
BindingDB Entry DOI: 10.7270/Q23T9M14
More data for this
Ligand-Target Pair
Cytochrome P450 3A4


(Homo sapiens (Human))
BDBM50479536
PNG
(CHEMBL489096)
Show SMILES CCc1ccc(OCC(=O)Nc2ccc(C)cc2Br)cc1
Show InChI InChI=1S/C17H18BrNO2/c1-3-13-5-7-14(8-6-13)21-11-17(20)19-16-9-4-12(2)10-15(16)18/h4-10H,3,11H2,1-2H3,(H,19,20)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
Purchase

PC cid
PC sid
UniChem
Article
PubMed
<5.00E+7n/an/an/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibition of CYP3A4


J Med Chem 52: 1247-50 (2009)


Article DOI: 10.1021/jm801278g
BindingDB Entry DOI: 10.7270/Q23T9M14
More data for this
Ligand-Target Pair
Cytochrome P450 3A4


(Homo sapiens (Human))
BDBM50479535
PNG
(CAS 160693-53-8 | CHEMBL491274)
Show SMILES CCc1ccc(cc1)N1CC(CC1=O)C(=O)OC
Show InChI InChI=1S/C14H17NO3/c1-3-10-4-6-12(7-5-10)15-9-11(8-13(15)16)14(17)18-2/h4-7,11H,3,8-9H2,1-2H3
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
Purchase

PC cid
PC sid
UniChem
Article
PubMed
<5.00E+7n/an/an/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibition of CYP3A4


J Med Chem 52: 1247-50 (2009)


Article DOI: 10.1021/jm801278g
BindingDB Entry DOI: 10.7270/Q23T9M14
More data for this
Ligand-Target Pair
Cytochrome P450 3A4


(Homo sapiens (Human))
BDBM50479537
PNG
(CHEMBL504747)
Show SMILES Cc1ccc(C)c(OCN2Cc3ccccc3C2C=O)c1
Show InChI InChI=1S/C18H19NO2/c1-13-7-8-14(2)18(9-13)21-12-19-10-15-5-3-4-6-16(15)17(19)11-20/h3-9,11,17H,10,12H2,1-2H3
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
<5.00E+7n/an/an/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibition of CYP3A4


J Med Chem 52: 1247-50 (2009)


Article DOI: 10.1021/jm801278g
BindingDB Entry DOI: 10.7270/Q23T9M14
More data for this
Ligand-Target Pair
Protein tyrosine phosphatase type IVA 3


(Homo sapiens (Human))
BDBM396097
PNG
(US10308663, JMS-631-053)
Show SMILES N=C1c2sc(cc2C(=O)NC1=O)-c1ccccc1
Show InChI InChI=1S/C13H8N2O2S/c14-10-11-8(12(16)15-13(10)17)6-9(18-11)7-4-2-1-3-5-7/h1-6,14H,(H,15,16,17)
PDB
MMDB

NCI pathway
KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
Purchase

MCE
PC cid
PC sid
PDB
UniChem
US Patent
n/an/a 18n/an/an/an/an/an/a



Boehringer Ingelheim Pharmaceuticals Inc.



Assay Description
The in vitro biochemical evaluation of all compounds was carried out using recombinant human PTP4A3, overexpressed as a His6-tag fusion protein in E....


Bioorg Med Chem Lett 17: 4664-9 (2007)


BindingDB Entry DOI: 10.7270/Q20867N2
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase D1


(Homo sapiens (Human))
BDBM50336960
PNG
(3,4-Dihydro-9-hydroxy-[1]benzothieno[2,3-f]-1,4-th...)
Show SMILES Oc1ccc2sc3c(SCCNC3=O)c2c1
Show InChI InChI=1S/C11H9NO2S2/c13-6-1-2-8-7(5-6)9-10(16-8)11(14)12-3-4-15-9/h1-2,5,13H,3-4H2,(H,12,14)
NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
MCE
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 28.3n/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PKD1 after 10 mins by radiometric assay


ACS Med Chem Lett 2: 154-159 (2012)


Article DOI: 10.1021/ml100230n
BindingDB Entry DOI: 10.7270/Q29G5NTR
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase D1


(Homo sapiens (Human))
BDBM50336960
PNG
(3,4-Dihydro-9-hydroxy-[1]benzothieno[2,3-f]-1,4-th...)
Show SMILES Oc1ccc2sc3c(SCCNC3=O)c2c1
Show InChI InChI=1S/C11H9NO2S2/c13-6-1-2-8-7(5-6)9-10(16-8)11(14)12-3-4-15-9/h1-2,5,13H,3-4H2,(H,12,14)
NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
MCE
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 28.3n/an/an/an/a7.530



University of Pittsburgh



Assay Description
In vitro radiometric kinase assay were conducted using PKD1 from Biomol International, PKD2 from SignalChem and PKD3 Enzo Life Sciences.


BMC Chem Biol 10: 5 (2010)


Article DOI: 10.1186/1472-6769-10-5
BindingDB Entry DOI: 10.7270/Q2VQ315D
More data for this
Ligand-Target Pair
Protein tyrosine phosphatase type IVA 3


(Homo sapiens (Human))
BDBM50535759
PNG
(CHEMBL4471843)
Show SMILES O=C1NC(=O)C(=O)c2sc(cc12)-c1ccccc1
Show InChI InChI=1S/C13H7NO3S/c15-10-11-8(12(16)14-13(10)17)6-9(18-11)7-4-2-1-3-5-7/h1-6H,(H,14,16,17)
PDB
MMDB

NCI pathway
KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 30n/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibition of recombinant human His-6-tagged PTP4A3 expressed in Escherichia coli assessed as reduction in hydrolysis using DIFMUP as substrate incub...


Bioorg Med Chem Lett 29: 2008-2015 (2019)


Article DOI: 10.1016/j.bmcl.2019.06.048
BindingDB Entry DOI: 10.7270/Q2VH5SBF
More data for this
Ligand-Target Pair
Protein tyrosine phosphatase type IVA 3


(Homo sapiens (Human))
BDBM396097
PNG
(US10308663, JMS-631-053)
Show SMILES N=C1c2sc(cc2C(=O)NC1=O)-c1ccccc1
Show InChI InChI=1S/C13H8N2O2S/c14-10-11-8(12(16)15-13(10)17)6-9(18-11)7-4-2-1-3-5-7/h1-6,14H,(H,15,16,17)
PDB
MMDB

NCI pathway
KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
Purchase

MCE
PC cid
PC sid
PDB
UniChem
Article
PubMed
n/an/a 35n/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibition of recombinant human His-6-tagged PTP4A3 expressed in Escherichia coli assessed as reduction in hydrolysis using DIFMUP as substrate incub...


Bioorg Med Chem Lett 29: 2008-2015 (2019)


Article DOI: 10.1016/j.bmcl.2019.06.048
BindingDB Entry DOI: 10.7270/Q2VH5SBF
More data for this
Ligand-Target Pair
Polycystin-2


(Homo sapiens (Human))
BDBM50336958
PNG
(2-Methoxy-7H,8H,9H-1,4-thiazepino[7',6'-5,4]thioph...)
Show SMILES COc1ncc2sc3c(SCCNC3=O)c2n1
Show InChI InChI=1S/C10H9N3O2S2/c1-15-10-12-4-5-6(13-10)7-8(17-5)9(14)11-2-3-16-7/h4H,2-3H2,1H3,(H,11,14)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 50n/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PKD2 after 10 mins by radiometric assay


ACS Med Chem Lett 2: 154-159 (2012)


Article DOI: 10.1021/ml100230n
BindingDB Entry DOI: 10.7270/Q29G5NTR
More data for this
Ligand-Target Pair
Protein tyrosine phosphatase type IVA 1


(Homo sapiens (Human))
BDBM396097
PNG
(US10308663, JMS-631-053)
Show SMILES N=C1c2sc(cc2C(=O)NC1=O)-c1ccccc1
Show InChI InChI=1S/C13H8N2O2S/c14-10-11-8(12(16)15-13(10)17)6-9(18-11)7-4-2-1-3-5-7/h1-6,14H,(H,15,16,17)
PDB
MMDB

NCI pathway
KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
Purchase

MCE
PC cid
PC sid
PDB
UniChem
Article
PubMed
n/an/a 50n/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibition of PTP4A1 (unknown origin) expressed in Escherichia coli assessed as reduction in hydrolysis using DIFMUP as substrate incubated for 30 mi...


Bioorg Med Chem Lett 29: 2008-2015 (2019)


Article DOI: 10.1016/j.bmcl.2019.06.048
BindingDB Entry DOI: 10.7270/Q2VH5SBF
More data for this
Ligand-Target Pair
Protein tyrosine phosphatase type IVA 2


(Homo sapiens (Human))
BDBM396097
PNG
(US10308663, JMS-631-053)
Show SMILES N=C1c2sc(cc2C(=O)NC1=O)-c1ccccc1
Show InChI InChI=1S/C13H8N2O2S/c14-10-11-8(12(16)15-13(10)17)6-9(18-11)7-4-2-1-3-5-7/h1-6,14H,(H,15,16,17)
PDB
MMDB

NCI pathway
KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
Purchase

MCE
PC cid
PC sid
PDB
UniChem
Article
PubMed
n/an/a 52n/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibition of PTP4A2 (unknown origin) expressed in Escherichia coli assessed as reduction in hydrolysis using DIFMUP as substrate incubated for 30 mi...


Bioorg Med Chem Lett 29: 2008-2015 (2019)


Article DOI: 10.1016/j.bmcl.2019.06.048
BindingDB Entry DOI: 10.7270/Q2VH5SBF
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase D3


(Homo sapiens (Human))
BDBM50336960
PNG
(3,4-Dihydro-9-hydroxy-[1]benzothieno[2,3-f]-1,4-th...)
Show SMILES Oc1ccc2sc3c(SCCNC3=O)c2c1
Show InChI InChI=1S/C11H9NO2S2/c13-6-1-2-8-7(5-6)9-10(16-8)11(14)12-3-4-15-9/h1-2,5,13H,3-4H2,(H,12,14)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
MCE
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 53.2n/an/an/an/a7.530



University of Pittsburgh



Assay Description
In vitro radiometric kinase assay were conducted using PKD1 from Biomol International, PKD2 from SignalChem and PKD3 Enzo Life Sciences.


BMC Chem Biol 10: 5 (2010)


Article DOI: 10.1186/1472-6769-10-5
BindingDB Entry DOI: 10.7270/Q2VQ315D
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase D2


(Homo sapiens (Human))
BDBM50336960
PNG
(3,4-Dihydro-9-hydroxy-[1]benzothieno[2,3-f]-1,4-th...)
Show SMILES Oc1ccc2sc3c(SCCNC3=O)c2c1
Show InChI InChI=1S/C11H9NO2S2/c13-6-1-2-8-7(5-6)9-10(16-8)11(14)12-3-4-15-9/h1-2,5,13H,3-4H2,(H,12,14)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
MCE
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 58.7n/an/an/an/a7.530



University of Pittsburgh



Assay Description
In vitro radiometric kinase assay were conducted using PKD1 from Biomol International, PKD2 from SignalChem and PKD3 Enzo Life Sciences.


BMC Chem Biol 10: 5 (2010)


Article DOI: 10.1186/1472-6769-10-5
BindingDB Entry DOI: 10.7270/Q2VQ315D
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase D3


(Homo sapiens (Human))
BDBM50336962
PNG
(2,3,4,5-Tetrahydro-10-hydroxybenzo[b]thieno[2,3-f]...)
Show SMILES Oc1ccc2sc3c(SCCCNC3=O)c2c1
Show InChI InChI=1S/C12H11NO2S2/c14-7-2-3-9-8(6-7)10-11(17-9)12(15)13-4-1-5-16-10/h2-3,6,14H,1,4-5H2,(H,13,15)
PDB
MMDB

KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 58.8n/an/an/an/a7.530



University of Pittsburgh



Assay Description
In vitro radiometric kinase assay were conducted using PKD1 from Biomol International, PKD2 from SignalChem and PKD3 Enzo Life Sciences.


BMC Chem Biol 10: 5 (2010)


Article DOI: 10.1186/1472-6769-10-5
BindingDB Entry DOI: 10.7270/Q2VQ315D
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase D1


(Homo sapiens (Human))
BDBM50336961
PNG
(3,4-Dihydro-9-azido-[1]benzothieno[2,3-f]-1,4-thia...)
Show SMILES [N-]=[N+]=Nc1ccc2sc3c(SCCNC3=O)c2c1
Show InChI InChI=1S/C11H8N4OS2/c12-15-14-6-1-2-8-7(5-6)9-10(18-8)11(16)13-3-4-17-9/h1-2,5H,3-4H2,(H,13,16)
NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 74.9n/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PKD1 after 10 mins by radiometric assay


ACS Med Chem Lett 2: 154-159 (2012)


Article DOI: 10.1021/ml100230n
BindingDB Entry DOI: 10.7270/Q29G5NTR
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50267086
PNG
(Adociaquinone B | CHEMBL476648)
Show SMILES C[C@@]12CCCc3coc(c13)C(=O)c1cc3C(=O)C4=NCCS(=O)(=O)C4C(=O)c3cc21 |r,t:19|
Show InChI InChI=1S/C22H17NO6S/c1-22-4-2-3-10-9-29-20(15(10)22)18(25)13-7-11-12(8-14(13)22)19(26)21-16(17(11)24)23-5-6-30(21,27)28/h7-9,21H,2-6H2,1H3/t21?,22-/m0/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 80n/an/an/an/an/an/a



Virginia Polytechnic Institute and State University

Curated by ChEMBL


Assay Description
Inhibition of histidine-tagged full length human Cdc25B expressed in Escherichia coli


Bioorg Med Chem 17: 2276-81 (2009)


Article DOI: 10.1016/j.bmc.2008.10.090
BindingDB Entry DOI: 10.7270/Q21J99MN
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase D1


(Homo sapiens (Human))
BDBM50119286
PNG
(3-Methoxy-7,8-dihydro-6H-5,10-dithia-8-aza-benzo[a...)
Show SMILES COc1ccc2sc3c(SCCNC3=O)c2c1
Show InChI InChI=1S/C12H11NO2S2/c1-15-7-2-3-9-8(6-7)10-11(17-9)12(14)13-4-5-16-10/h2-3,6H,4-5H2,1H3,(H,13,14)
NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 82.5n/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PKD1 after 10 mins by radiometric assay


ACS Med Chem Lett 2: 154-159 (2012)


Article DOI: 10.1021/ml100230n
BindingDB Entry DOI: 10.7270/Q29G5NTR
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase D1


(Homo sapiens (Human))
BDBM50119286
PNG
(3-Methoxy-7,8-dihydro-6H-5,10-dithia-8-aza-benzo[a...)
Show SMILES COc1ccc2sc3c(SCCNC3=O)c2c1
Show InChI InChI=1S/C12H11NO2S2/c1-15-7-2-3-9-8(6-7)10-11(17-9)12(14)13-4-5-16-10/h2-3,6H,4-5H2,1H3,(H,13,14)
NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 82.5n/an/an/an/a7.530



University of Pittsburgh



Assay Description
In vitro radiometric kinase assay were conducted using PKD1 from Biomol International, PKD2 from SignalChem and PKD3 Enzo Life Sciences.


BMC Chem Biol 10: 5 (2010)


Article DOI: 10.1186/1472-6769-10-5
BindingDB Entry DOI: 10.7270/Q2VQ315D
More data for this
Ligand-Target Pair
Protein tyrosine phosphatase type IVA 3


(Homo sapiens (Human))
BDBM396097
PNG
(US10308663, JMS-631-053)
Show SMILES N=C1c2sc(cc2C(=O)NC1=O)-c1ccccc1
Show InChI InChI=1S/C13H8N2O2S/c14-10-11-8(12(16)15-13(10)17)6-9(18-11)7-4-2-1-3-5-7/h1-6,14H,(H,15,16,17)
PDB
MMDB

NCI pathway
KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
Purchase

MCE
PC cid
PC sid
PDB
UniChem
Article
PubMed
n/an/a 84n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant human PTP4A3


Citation and Details

Article DOI: 10.1016/j.bmcl.2021.128167
BindingDB Entry DOI: 10.7270/Q23X8BDD
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase D3


(Homo sapiens (Human))
BDBM81614
PNG
(kb-NB165-31)
Show SMILES Oc1ccc2sc3c(SCCNC3=O)c2c1I
Show InChI InChI=1S/C11H8INO2S2/c12-8-5(14)1-2-6-7(8)9-10(17-6)11(15)13-3-4-16-9/h1-2,14H,3-4H2,(H,13,15)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 91.1n/an/an/an/a7.530



University of Pittsburgh



Assay Description
In vitro radiometric kinase assay were conducted using PKD1 from Biomol International, PKD2 from SignalChem and PKD3 Enzo Life Sciences.


BMC Chem Biol 10: 5 (2010)


Article DOI: 10.1186/1472-6769-10-5
BindingDB Entry DOI: 10.7270/Q2VQ315D
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase D3


(Homo sapiens (Human))
BDBM50119286
PNG
(3-Methoxy-7,8-dihydro-6H-5,10-dithia-8-aza-benzo[a...)
Show SMILES COc1ccc2sc3c(SCCNC3=O)c2c1
Show InChI InChI=1S/C12H11NO2S2/c1-15-7-2-3-9-8(6-7)10-11(17-9)12(14)13-4-5-16-10/h2-3,6H,4-5H2,1H3,(H,13,14)
PDB
MMDB

KEGG

UniProtKB/SwissProt

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

Patents


Similars

Article
PubMed
n/an/a 98.5n/an/an/an/a7.530



University of Pittsburgh



Assay Description
In vitro radiometric kinase assay were conducted using PKD1 from Biomol International, PKD2 from SignalChem and PKD3 Enzo Life Sciences.


BMC Chem Biol 10: 5 (2010)


Article DOI: 10.1186/1472-6769-10-5
BindingDB Entry DOI: 10.7270/Q2VQ315D
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase D2


(Homo sapiens (Human))
BDBM50336962
PNG
(2,3,4,5-Tetrahydro-10-hydroxybenzo[b]thieno[2,3-f]...)
Show SMILES Oc1ccc2sc3c(SCCCNC3=O)c2c1
Show InChI InChI=1S/C12H11NO2S2/c14-7-2-3-9-8(6-7)10-11(17-9)12(15)13-4-1-5-16-10/h2-3,6,14H,1,4-5H2,(H,13,15)
PDB
MMDB

KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 101n/an/an/an/a7.530



University of Pittsburgh



Assay Description
In vitro radiometric kinase assay were conducted using PKD1 from Biomol International, PKD2 from SignalChem and PKD3 Enzo Life Sciences.


BMC Chem Biol 10: 5 (2010)


Article DOI: 10.1186/1472-6769-10-5
BindingDB Entry DOI: 10.7270/Q2VQ315D
More data for this
Ligand-Target Pair
Protein tyrosine phosphatase type IVA 3


(Homo sapiens (Human))
BDBM50571230
PNG
(CHEMBL4862721)
Show SMILES N=C1c2sc(cc2C(=O)NC1=O)-c1ccc(OCC(=O)NCCOCCOCCNC(=O)CC23CC4CC(CC(C4)C2)C3)cc1 |TLB:32:33:36.35.40:38,THB:34:35:38:42.33.41,34:33:36.35.40:38,41:33:36:40.39.38,41:39:36:42.34.33,32:33:36:40.39.38|
PDB
MMDB

NCI pathway
KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 107n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant human PTP4A3


Citation and Details

Article DOI: 10.1016/j.bmcl.2021.128167
BindingDB Entry DOI: 10.7270/Q23X8BDD
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50267086
PNG
(Adociaquinone B | CHEMBL476648)
Show SMILES C[C@@]12CCCc3coc(c13)C(=O)c1cc3C(=O)C4=NCCS(=O)(=O)C4C(=O)c3cc21 |r,t:19|
Show InChI InChI=1S/C22H17NO6S/c1-22-4-2-3-10-9-29-20(15(10)22)18(25)13-7-11-12(8-14(13)22)19(26)21-16(17(11)24)23-5-6-30(21,27)28/h7-9,21H,2-6H2,1H3/t21?,22-/m0/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 110n/an/an/an/an/an/a



Virginia Polytechnic Institute and State University

Curated by ChEMBL


Assay Description
Inhibition of histidine-tagged human recombinant Cdc25B catalytic domain expressed in Escherichia coli


Bioorg Med Chem 17: 2276-81 (2009)


Article DOI: 10.1016/j.bmc.2008.10.090
BindingDB Entry DOI: 10.7270/Q21J99MN
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase D1


(Homo sapiens (Human))
BDBM50336962
PNG
(2,3,4,5-Tetrahydro-10-hydroxybenzo[b]thieno[2,3-f]...)
Show SMILES Oc1ccc2sc3c(SCCCNC3=O)c2c1
Show InChI InChI=1S/C12H11NO2S2/c14-7-2-3-9-8(6-7)10-11(17-9)12(15)13-4-1-5-16-10/h2-3,6,14H,1,4-5H2,(H,13,15)
NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 111n/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PKD1 after 10 mins by radiometric assay


ACS Med Chem Lett 2: 154-159 (2012)


Article DOI: 10.1021/ml100230n
BindingDB Entry DOI: 10.7270/Q29G5NTR
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase D1


(Homo sapiens (Human))
BDBM50336962
PNG
(2,3,4,5-Tetrahydro-10-hydroxybenzo[b]thieno[2,3-f]...)
Show SMILES Oc1ccc2sc3c(SCCCNC3=O)c2c1
Show InChI InChI=1S/C12H11NO2S2/c14-7-2-3-9-8(6-7)10-11(17-9)12(15)13-4-1-5-16-10/h2-3,6,14H,1,4-5H2,(H,13,15)
NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 111n/an/an/an/a7.530



University of Pittsburgh



Assay Description
In vitro radiometric kinase assay were conducted using PKD1 from Biomol International, PKD2 from SignalChem and PKD3 Enzo Life Sciences.


BMC Chem Biol 10: 5 (2010)


Article DOI: 10.1186/1472-6769-10-5
BindingDB Entry DOI: 10.7270/Q2VQ315D
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase D1


(Homo sapiens (Human))
BDBM81614
PNG
(kb-NB165-31)
Show SMILES Oc1ccc2sc3c(SCCNC3=O)c2c1I
Show InChI InChI=1S/C11H8INO2S2/c12-8-5(14)1-2-6-7(8)9-10(17-6)11(15)13-3-4-16-9/h1-2,14H,3-4H2,(H,13,15)
NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 114n/an/an/an/a7.530



University of Pittsburgh



Assay Description
In vitro radiometric kinase assay were conducted using PKD1 from Biomol International, PKD2 from SignalChem and PKD3 Enzo Life Sciences.


BMC Chem Biol 10: 5 (2010)


Article DOI: 10.1186/1472-6769-10-5
BindingDB Entry DOI: 10.7270/Q2VQ315D
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase D1


(Homo sapiens (Human))
BDBM50336958
PNG
(2-Methoxy-7H,8H,9H-1,4-thiazepino[7',6'-5,4]thioph...)
Show SMILES COc1ncc2sc3c(SCCNC3=O)c2n1
Show InChI InChI=1S/C10H9N3O2S2/c1-15-10-12-4-5-6(13-10)7-8(17-5)9(14)11-2-3-16-7/h4H,2-3H2,1H3,(H,11,14)
NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 124n/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PKD1 after 10 mins by radiometric assay


ACS Med Chem Lett 2: 154-159 (2012)


Article DOI: 10.1021/ml100230n
BindingDB Entry DOI: 10.7270/Q29G5NTR
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase D1


(Homo sapiens (Human))
BDBM50336959
PNG
(3,4,5,10-Tetrahydro-7-hydroxy-azepino[3,4-b]indol-...)
Show SMILES Oc1ccc2[nH]c3c(CCCNC3=O)c2c1
Show InChI InChI=1S/C12H12N2O2/c15-7-3-4-10-9(6-7)8-2-1-5-13-12(16)11(8)14-10/h3-4,6,14-15H,1-2,5H2,(H,13,16)
NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 130n/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PKD1 after 10 mins by radiometric assay


ACS Med Chem Lett 2: 154-159 (2012)


Article DOI: 10.1021/ml100230n
BindingDB Entry DOI: 10.7270/Q29G5NTR
More data for this
Ligand-Target Pair
Protein tyrosine phosphatase type IVA 3


(Homo sapiens (Human))
BDBM50059084
PNG
(CHEMBL3393171 | US10308663, Thienopyridone (5))
Show SMILES Nc1c[nH]c(=O)c2cc(sc12)-c1ccccc1
Show InChI InChI=1S/C13H10N2OS/c14-10-7-15-13(16)9-6-11(17-12(9)10)8-4-2-1-3-5-8/h1-7H,14H2,(H,15,16)
PDB
MMDB

NCI pathway
KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
Purchase

CHEMBL
MCE
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 130n/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibition of recombinant human His-6-tagged PTP4A3 expressed in Escherichia coli assessed as increase in polarization using TAMRAThr-Ala-Asp-Ile-Tyr...


Bioorg Med Chem Lett 29: 2008-2015 (2019)


Article DOI: 10.1016/j.bmcl.2019.06.048
BindingDB Entry DOI: 10.7270/Q2VH5SBF
More data for this
Ligand-Target Pair
Protein tyrosine phosphatase type IVA 3


(Homo sapiens (Human))
BDBM50059084
PNG
(CHEMBL3393171 | US10308663, Thienopyridone (5))
Show SMILES Nc1c[nH]c(=O)c2cc(sc12)-c1ccccc1
Show InChI InChI=1S/C13H10N2OS/c14-10-7-15-13(16)9-6-11(17-12(9)10)8-4-2-1-3-5-8/h1-7H,14H2,(H,15,16)
PDB
MMDB

NCI pathway
KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
Purchase

CHEMBL
MCE
PC cid
PC sid
UniChem

Similars

US Patent
n/an/a 132n/an/an/an/an/an/a



Boehringer Ingelheim Pharmaceuticals Inc.



Assay Description
The in vitro biochemical evaluation of all compounds was carried out using recombinant human PTP4A3, overexpressed as a His6-tag fusion protein in E....


Bioorg Med Chem Lett 17: 4664-9 (2007)


BindingDB Entry DOI: 10.7270/Q20867N2
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase D2


(Homo sapiens (Human))
BDBM50119286
PNG
(3-Methoxy-7,8-dihydro-6H-5,10-dithia-8-aza-benzo[a...)
Show SMILES COc1ccc2sc3c(SCCNC3=O)c2c1
Show InChI InChI=1S/C12H11NO2S2/c1-15-7-2-3-9-8(6-7)10-11(17-9)12(14)13-4-5-16-10/h2-3,6H,4-5H2,1H3,(H,13,14)
PDB
MMDB

KEGG

UniProtKB/SwissProt

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

Patents


Similars

Article
PubMed
n/an/a 142n/an/an/an/a7.530



University of Pittsburgh



Assay Description
In vitro radiometric kinase assay were conducted using PKD1 from Biomol International, PKD2 from SignalChem and PKD3 Enzo Life Sciences.


BMC Chem Biol 10: 5 (2010)


Article DOI: 10.1186/1472-6769-10-5
BindingDB Entry DOI: 10.7270/Q2VQ315D
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase D2


(Homo sapiens (Human))
BDBM81614
PNG
(kb-NB165-31)
Show SMILES Oc1ccc2sc3c(SCCNC3=O)c2c1I
Show InChI InChI=1S/C11H8INO2S2/c12-8-5(14)1-2-6-7(8)9-10(17-6)11(15)13-3-4-16-9/h1-2,14H,3-4H2,(H,13,15)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 163n/an/an/an/a7.530



University of Pittsburgh



Assay Description
In vitro radiometric kinase assay were conducted using PKD1 from Biomol International, PKD2 from SignalChem and PKD3 Enzo Life Sciences.


BMC Chem Biol 10: 5 (2010)


Article DOI: 10.1186/1472-6769-10-5
BindingDB Entry DOI: 10.7270/Q2VQ315D
More data for this
Ligand-Target Pair
Protein tyrosine phosphatase type IVA 1


(Homo sapiens (Human))
BDBM50059084
PNG
(CHEMBL3393171 | US10308663, Thienopyridone (5))
Show SMILES Nc1c[nH]c(=O)c2cc(sc12)-c1ccccc1
Show InChI InChI=1S/C13H10N2OS/c14-10-7-15-13(16)9-6-11(17-12(9)10)8-4-2-1-3-5-8/h1-7H,14H2,(H,15,16)
PDB
MMDB

NCI pathway
KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
MCE
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 170n/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibition of recombinant human His-6-tagged PTP4A1 expressed in Escherichia coli assessed as increase in polarization using TAMRAThr-Ala-Asp-Ile-Tyr...


Bioorg Med Chem Lett 29: 2008-2015 (2019)


Article DOI: 10.1016/j.bmcl.2019.06.048
BindingDB Entry DOI: 10.7270/Q2VH5SBF
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase D1


(Homo sapiens (Human))
BDBM32334
PNG
(7-hydroxy-2,3,4,5-tetrahydro-1H-[1]benzofuro[2,3-c...)
Show SMILES Oc1ccc2oc3c(CCCNC3=O)c2c1
Show InChI InChI=1S/C12H11NO3/c14-7-3-4-10-9(6-7)8-2-1-5-13-12(15)11(8)16-10/h3-4,6,14H,1-2,5H2,(H,13,15)
NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
Purchase

MCE
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 182n/an/an/an/a7.530



University of Pittsburgh



Assay Description
The radiometric kinase assay using PKD kinase.


J Biol Chem 283: 33516-26 (2008)


Article DOI: 10.1074/jbc.M805358200
BindingDB Entry DOI: 10.7270/Q20863WJ
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase D1


(Homo sapiens (Human))
BDBM32334
PNG
(7-hydroxy-2,3,4,5-tetrahydro-1H-[1]benzofuro[2,3-c...)
Show SMILES Oc1ccc2oc3c(CCCNC3=O)c2c1
Show InChI InChI=1S/C12H11NO3/c14-7-3-4-10-9(6-7)8-2-1-5-13-12(15)11(8)16-10/h3-4,6,14H,1-2,5H2,(H,13,15)
NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
Purchase

MCE
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 182n/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PKD1 after 10 mins by radiometric assay


ACS Med Chem Lett 2: 154-159 (2012)


Article DOI: 10.1021/ml100230n
BindingDB Entry DOI: 10.7270/Q29G5NTR
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase D1


(Homo sapiens (Human))
BDBM32334
PNG
(7-hydroxy-2,3,4,5-tetrahydro-1H-[1]benzofuro[2,3-c...)
Show SMILES Oc1ccc2oc3c(CCCNC3=O)c2c1
Show InChI InChI=1S/C12H11NO3/c14-7-3-4-10-9(6-7)8-2-1-5-13-12(15)11(8)16-10/h3-4,6,14H,1-2,5H2,(H,13,15)
NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
Purchase

MCE
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 182n/an/an/an/a7.530



University of Pittsburgh



Assay Description
In vitro radiometric kinase assay were conducted using PKD1 from Biomol International, PKD2 from SignalChem and PKD3 Enzo Life Sciences.


BMC Chem Biol 10: 5 (2010)


Article DOI: 10.1186/1472-6769-10-5
BindingDB Entry DOI: 10.7270/Q2VQ315D
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase D1


(Homo sapiens (Human))
BDBM50336963
PNG
(2,3,4,5-Tetrahydro-10-methoxybenzo[b]thieno[2,3-f]...)
Show SMILES COc1ccc2sc3c(SCCCNC3=O)c2c1
Show InChI InChI=1S/C13H13NO2S2/c1-16-8-3-4-10-9(7-8)11-12(18-10)13(15)14-5-2-6-17-11/h3-4,7H,2,5-6H2,1H3,(H,14,15)
NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 193n/an/an/an/a7.530



University of Pittsburgh



Assay Description
In vitro radiometric kinase assay were conducted using PKD1 from Biomol International, PKD2 from SignalChem and PKD3 Enzo Life Sciences.


BMC Chem Biol 10: 5 (2010)


Article DOI: 10.1186/1472-6769-10-5
BindingDB Entry DOI: 10.7270/Q2VQ315D
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase D1


(Homo sapiens (Human))
BDBM50336963
PNG
(2,3,4,5-Tetrahydro-10-methoxybenzo[b]thieno[2,3-f]...)
Show SMILES COc1ccc2sc3c(SCCCNC3=O)c2c1
Show InChI InChI=1S/C13H13NO2S2/c1-16-8-3-4-10-9(7-8)11-12(18-10)13(15)14-5-2-6-17-11/h3-4,7H,2,5-6H2,1H3,(H,14,15)
NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 193n/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PKD1 after 10 mins by radiometric assay


ACS Med Chem Lett 2: 154-159 (2012)


Article DOI: 10.1021/ml100230n
BindingDB Entry DOI: 10.7270/Q29G5NTR
More data for this
Ligand-Target Pair
Protein tyrosine phosphatase type IVA 3


(Homo sapiens (Human))
BDBM50571225
PNG
(CHEMBL4862502)
Show SMILES N=C1c2sc(cc2C(=O)NC1=O)-c1ccc(OCC(=O)NCCCNC(=O)CC23CC4CC(CC(C4)C2)C3)cc1 |TLB:27:28:31.30.35:33,THB:29:30:33:37.28.36,29:28:31.30.35:33,36:28:31:35.34.33,36:34:31:37.29.28,27:28:31:35.34.33|
PDB
MMDB

NCI pathway
KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 206n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of recombinant human PTP4A3


Citation and Details

Article DOI: 10.1016/j.bmcl.2021.128167
BindingDB Entry DOI: 10.7270/Q23X8BDD
More data for this
Ligand-Target Pair
M-phase inducer phosphatase 2


(Homo sapiens (Human))
BDBM50106497
PNG
(6-Chloro-7-(2-morpholin-4-yl-ethylamino)-quinoline...)
Show SMILES Oc1c(Cl)c(N=CCN2CCOCC2)c(O)c2ncccc12 |w:6.6|
Show InChI InChI=1S/C15H16ClN3O3/c16-11-13(18-4-5-19-6-8-22-9-7-19)15(21)12-10(14(11)20)2-1-3-17-12/h1-4,20-21H,5-9H2
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

PubMed
n/an/a 210n/an/an/an/an/an/a



University of Pittsburgh

Curated by ChEMBL


Assay Description
Inhibitory activity against recombinant human cell division cycle 25B


J Med Chem 44: 4042-9 (2001)


BindingDB Entry DOI: 10.7270/Q2X34WR5
More data for this
Ligand-Target Pair
Serine/threonine-protein kinase D3


(Homo sapiens (Human))
BDBM32334
PNG
(7-hydroxy-2,3,4,5-tetrahydro-1H-[1]benzofuro[2,3-c...)
Show SMILES Oc1ccc2oc3c(CCCNC3=O)c2c1
Show InChI InChI=1S/C12H11NO3/c14-7-3-4-10-9(6-7)8-2-1-5-13-12(15)11(8)16-10/h3-4,6,14H,1-2,5H2,(H,13,15)
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
Purchase

MCE
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 227n/an/an/an/a7.530



University of Pittsburgh



Assay Description
The radiometric kinase assay using PKD kinase.


J Biol Chem 283: 33516-26 (2008)


Article DOI: 10.1074/jbc.M805358200
BindingDB Entry DOI: 10.7270/Q20863WJ
More data for this
Ligand-Target Pair
Displayed 1 to 50 (of 522 total )  |  Next  |  Last  >>
Jump to: