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Compile Data Set for Download or QSAR

Found 51 hits with Last Name = 'hirahara' and Initial = 'k'   
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
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM14774
PNG
(3-(cyclopropylmethoxy)-N-(3,5-dichloropyridin-4-yl...)
Show SMILES FC(F)Oc1ccc(cc1OCC1CC1)C(=O)Nc1c(Cl)cncc1Cl
Show InChI InChI=1S/C17H14Cl2F2N2O3/c18-11-6-22-7-12(19)15(11)23-16(24)10-3-4-13(26-17(20)21)14(5-10)25-8-9-1-2-9/h3-7,9,17H,1-2,8H2,(H,22,23,24)
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n/an/a 0.490n/an/an/an/an/an/a



Kyushu University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human PDE4B using cAMP as substrate after 30 mins


Bioorg Med Chem 21: 7025-37 (2013)


Article DOI: 10.1016/j.bmc.2013.09.013
BindingDB Entry DOI: 10.7270/Q2DZ0C84
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM14774
PNG
(3-(cyclopropylmethoxy)-N-(3,5-dichloropyridin-4-yl...)
Show SMILES FC(F)Oc1ccc(cc1OCC1CC1)C(=O)Nc1c(Cl)cncc1Cl
Show InChI InChI=1S/C17H14Cl2F2N2O3/c18-11-6-22-7-12(19)15(11)23-16(24)10-3-4-13(26-17(20)21)14(5-10)25-8-9-1-2-9/h3-7,9,17H,1-2,8H2,(H,22,23,24)
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n/an/a 0.490n/an/an/an/an/an/a



Daiichi Sankyo Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PDE4B (152 to 564 amino acids) using cAMP as substrate after 30 mins by plate reader analysis


Bioorg Med Chem Lett 23: 3325-8 (2013)


Article DOI: 10.1016/j.bmcl.2013.03.104
BindingDB Entry DOI: 10.7270/Q2QF8WSQ
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50493949
PNG
(CHEMBL2442479)
Show SMILES CC(=C)c1ncc(C(N)=O)c(Nc2ccc(CC(=O)NCC(C)(C)C)cc2)n1
Show InChI InChI=1S/C21H27N5O2/c1-13(2)19-23-11-16(18(22)28)20(26-19)25-15-8-6-14(7-9-15)10-17(27)24-12-21(3,4)5/h6-9,11H,1,10,12H2,2-5H3,(H2,22,28)(H,24,27)(H,23,25,26)
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Kyushu University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human PDE4B using cAMP as substrate after 30 mins


Bioorg Med Chem 21: 7025-37 (2013)


Article DOI: 10.1016/j.bmc.2013.09.013
BindingDB Entry DOI: 10.7270/Q2DZ0C84
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50491736
PNG
(CHEMBL2385759)
Show SMILES CC(C)(C)CNC(=O)Cc1ccc(Nc2nc(nc3CCCS(=O)(=O)c23)-c2ccccc2)cc1
Show InChI InChI=1S/C26H30N4O3S/c1-26(2,3)17-27-22(31)16-18-11-13-20(14-12-18)28-25-23-21(10-7-15-34(23,32)33)29-24(30-25)19-8-5-4-6-9-19/h4-6,8-9,11-14H,7,10,15-17H2,1-3H3,(H,27,31)(H,28,29,30)
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Daiichi Sankyo Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PDE4B (152 to 564 amino acids) using cAMP as substrate after 30 mins by plate reader analysis


Bioorg Med Chem Lett 23: 3325-8 (2013)


Article DOI: 10.1016/j.bmcl.2013.03.104
BindingDB Entry DOI: 10.7270/Q2QF8WSQ
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50491737
PNG
(CHEMBL2385757)
Show SMILES CC(C)CNC(=O)Cc1ccc(Nc2nc(nc3CCCS(=O)(=O)c23)-c2ccccc2)cc1
Show InChI InChI=1S/C25H28N4O3S/c1-17(2)16-26-22(30)15-18-10-12-20(13-11-18)27-25-23-21(9-6-14-33(23,31)32)28-24(29-25)19-7-4-3-5-8-19/h3-5,7-8,10-13,17H,6,9,14-16H2,1-2H3,(H,26,30)(H,27,28,29)
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n/an/a 6.60n/an/an/an/an/an/a



Daiichi Sankyo Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PDE4B (152 to 564 amino acids) using cAMP as substrate after 30 mins by plate reader analysis


Bioorg Med Chem Lett 23: 3325-8 (2013)


Article DOI: 10.1016/j.bmcl.2013.03.104
BindingDB Entry DOI: 10.7270/Q2QF8WSQ
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50493958
PNG
(CHEMBL2442473)
Show SMILES NC(=O)c1cnc(nc1Nc1ccc(CC(=O)NO)cc1)-c1ccccc1
Show InChI InChI=1S/C19H17N5O3/c20-17(26)15-11-21-18(13-4-2-1-3-5-13)23-19(15)22-14-8-6-12(7-9-14)10-16(25)24-27/h1-9,11,27H,10H2,(H2,20,26)(H,24,25)(H,21,22,23)
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Kyushu University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human PDE4B using cAMP as substrate after 30 mins


Bioorg Med Chem 21: 7025-37 (2013)


Article DOI: 10.1016/j.bmc.2013.09.013
BindingDB Entry DOI: 10.7270/Q2DZ0C84
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50493947
PNG
(CHEMBL2442465)
Show SMILES CC(C)CNC(=O)Cc1ccc(Nc2nc(nc3CCNC(=O)c23)-c2ccccc2)cc1
Show InChI InChI=1S/C25H27N5O2/c1-16(2)15-27-21(31)14-17-8-10-19(11-9-17)28-24-22-20(12-13-26-25(22)32)29-23(30-24)18-6-4-3-5-7-18/h3-11,16H,12-15H2,1-2H3,(H,26,32)(H,27,31)(H,28,29,30)
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Kyushu University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human PDE4B using cAMP as substrate after 30 mins


Bioorg Med Chem 21: 7025-37 (2013)


Article DOI: 10.1016/j.bmc.2013.09.013
BindingDB Entry DOI: 10.7270/Q2DZ0C84
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50491759
PNG
(CHEMBL2385755 | US11401286, Example 270)
Show SMILES CCCNC(=O)Cc1ccc(Nc2nc(nc3CCCS(=O)(=O)c23)-c2ccccc2)cc1
Show InChI InChI=1S/C24H26N4O3S/c1-2-14-25-21(29)16-17-10-12-19(13-11-17)26-24-22-20(9-6-15-32(22,30)31)27-23(28-24)18-7-4-3-5-8-18/h3-5,7-8,10-13H,2,6,9,14-16H2,1H3,(H,25,29)(H,26,27,28)
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Daiichi Sankyo Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PDE4B (152 to 564 amino acids) using cAMP as substrate after 30 mins by plate reader analysis


Bioorg Med Chem Lett 23: 3325-8 (2013)


Article DOI: 10.1016/j.bmcl.2013.03.104
BindingDB Entry DOI: 10.7270/Q2QF8WSQ
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50493961
PNG
(CHEMBL2442478)
Show SMILES CC(C)(C)CNC(=O)Cc1ccc(Nc2nc(ncc2C(N)=O)-c2ccc3[nH]ccc3c2)cc1
Show InChI InChI=1S/C26H28N6O2/c1-26(2,3)15-30-22(33)12-16-4-7-19(8-5-16)31-25-20(23(27)34)14-29-24(32-25)18-6-9-21-17(13-18)10-11-28-21/h4-11,13-14,28H,12,15H2,1-3H3,(H2,27,34)(H,30,33)(H,29,31,32)
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Kyushu University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human PDE4B using cAMP as substrate after 30 mins


Bioorg Med Chem 21: 7025-37 (2013)


Article DOI: 10.1016/j.bmc.2013.09.013
BindingDB Entry DOI: 10.7270/Q2DZ0C84
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50493946
PNG
(CHEMBL2442472)
Show SMILES CC(C)(C)CNC(=O)Cc1ccc(Nc2nc(ncc2C(N)=O)-c2ccccc2)cc1
Show InChI InChI=1S/C24H27N5O2/c1-24(2,3)15-27-20(30)13-16-9-11-18(12-10-16)28-23-19(21(25)31)14-26-22(29-23)17-7-5-4-6-8-17/h4-12,14H,13,15H2,1-3H3,(H2,25,31)(H,27,30)(H,26,28,29)
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n/an/a 8.30n/an/an/an/an/an/a



Kyushu University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human PDE4B using cAMP as substrate after 30 mins


Bioorg Med Chem 21: 7025-37 (2013)


Article DOI: 10.1016/j.bmc.2013.09.013
BindingDB Entry DOI: 10.7270/Q2DZ0C84
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50493950
PNG
(CHEMBL2442477)
Show SMILES CC(C)(C)CNC(=O)Cc1ccc(Nc2nc(ncc2C(N)=O)-c2ccoc2)cc1
Show InChI InChI=1S/C22H25N5O3/c1-22(2,3)13-25-18(28)10-14-4-6-16(7-5-14)26-21-17(19(23)29)11-24-20(27-21)15-8-9-30-12-15/h4-9,11-12H,10,13H2,1-3H3,(H2,23,29)(H,25,28)(H,24,26,27)
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Kyushu University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human PDE4B using cAMP as substrate after 30 mins


Bioorg Med Chem 21: 7025-37 (2013)


Article DOI: 10.1016/j.bmc.2013.09.013
BindingDB Entry DOI: 10.7270/Q2DZ0C84
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50491753
PNG
(CHEMBL2385758)
Show SMILES CC(C)(C)NC(=O)Cc1ccc(Nc2nc(nc3CCCS(=O)(=O)c23)-c2ccccc2)cc1
Show InChI InChI=1S/C25H28N4O3S/c1-25(2,3)29-21(30)16-17-11-13-19(14-12-17)26-24-22-20(10-7-15-33(22,31)32)27-23(28-24)18-8-5-4-6-9-18/h4-6,8-9,11-14H,7,10,15-16H2,1-3H3,(H,29,30)(H,26,27,28)
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Daiichi Sankyo Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PDE4B (152 to 564 amino acids) using cAMP as substrate after 30 mins by plate reader analysis


Bioorg Med Chem Lett 23: 3325-8 (2013)


Article DOI: 10.1016/j.bmcl.2013.03.104
BindingDB Entry DOI: 10.7270/Q2QF8WSQ
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50493962
PNG
(CHEMBL2442470)
Show SMILES CC(C)CNC(=O)Cc1ccc(Nc2nc(ncc2C(N)=O)-c2ccccc2)cc1
Show InChI InChI=1S/C23H25N5O2/c1-15(2)13-25-20(29)12-16-8-10-18(11-9-16)27-23-19(21(24)30)14-26-22(28-23)17-6-4-3-5-7-17/h3-11,14-15H,12-13H2,1-2H3,(H2,24,30)(H,25,29)(H,26,27,28)
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Kyushu University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human PDE4B using cAMP as substrate after 30 mins


Bioorg Med Chem 21: 7025-37 (2013)


Article DOI: 10.1016/j.bmc.2013.09.013
BindingDB Entry DOI: 10.7270/Q2DZ0C84
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50493948
PNG
(CHEMBL2442462)
Show SMILES CC(C)(C)CNC(=O)Cc1ccc(Nc2nc(ncc2C(N)=O)N2CCCC2)cc1
Show InChI InChI=1S/C22H30N6O2/c1-22(2,3)14-25-18(29)12-15-6-8-16(9-7-15)26-20-17(19(23)30)13-24-21(27-20)28-10-4-5-11-28/h6-9,13H,4-5,10-12,14H2,1-3H3,(H2,23,30)(H,25,29)(H,24,26,27)
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Kyushu University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human PDE4B using cAMP as substrate after 30 mins


Bioorg Med Chem 21: 7025-37 (2013)


Article DOI: 10.1016/j.bmc.2013.09.013
BindingDB Entry DOI: 10.7270/Q2DZ0C84
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50493953
PNG
(CHEMBL2442469)
Show SMILES NC(=O)c1cnc(nc1Nc1ccc(CC(=O)NCC2CC2)cc1)-c1ccccc1
Show InChI InChI=1S/C23H23N5O2/c24-21(30)19-14-26-22(17-4-2-1-3-5-17)28-23(19)27-18-10-8-15(9-11-18)12-20(29)25-13-16-6-7-16/h1-5,8-11,14,16H,6-7,12-13H2,(H2,24,30)(H,25,29)(H,26,27,28)
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Kyushu University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human PDE4B using cAMP as substrate after 30 mins


Bioorg Med Chem 21: 7025-37 (2013)


Article DOI: 10.1016/j.bmc.2013.09.013
BindingDB Entry DOI: 10.7270/Q2DZ0C84
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50493957
PNG
(CHEMBL2442461)
Show SMILES CN(C)c1ncc(C(N)=O)c(Nc2ccc(CC(=O)NCC(C)(C)C)cc2)n1
Show InChI InChI=1S/C20H28N6O2/c1-20(2,3)12-23-16(27)10-13-6-8-14(9-7-13)24-18-15(17(21)28)11-22-19(25-18)26(4)5/h6-9,11H,10,12H2,1-5H3,(H2,21,28)(H,23,27)(H,22,24,25)
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Kyushu University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human PDE4B using cAMP as substrate after 30 mins


Bioorg Med Chem 21: 7025-37 (2013)


Article DOI: 10.1016/j.bmc.2013.09.013
BindingDB Entry DOI: 10.7270/Q2DZ0C84
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50491738
PNG
(CHEMBL2385753 | US11401286, Example 269)
Show SMILES NC(=O)Cc1ccc(Nc2nc(nc3CCCS(=O)(=O)c23)-c2ccccc2)cc1
Show InChI InChI=1S/C21H20N4O3S/c22-18(26)13-14-8-10-16(11-9-14)23-21-19-17(7-4-12-29(19,27)28)24-20(25-21)15-5-2-1-3-6-15/h1-3,5-6,8-11H,4,7,12-13H2,(H2,22,26)(H,23,24,25)
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Daiichi Sankyo Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PDE4B (152 to 564 amino acids) using cAMP as substrate after 30 mins by plate reader analysis


Bioorg Med Chem Lett 23: 3325-8 (2013)


Article DOI: 10.1016/j.bmcl.2013.03.104
BindingDB Entry DOI: 10.7270/Q2QF8WSQ
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50491754
PNG
(CHEMBL2385756)
Show SMILES CCCCNC(=O)Cc1ccc(Nc2nc(nc3CCCS(=O)(=O)c23)-c2ccccc2)cc1
Show InChI InChI=1S/C25H28N4O3S/c1-2-3-15-26-22(30)17-18-11-13-20(14-12-18)27-25-23-21(10-7-16-33(23,31)32)28-24(29-25)19-8-5-4-6-9-19/h4-6,8-9,11-14H,2-3,7,10,15-17H2,1H3,(H,26,30)(H,27,28,29)
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Daiichi Sankyo Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PDE4B (152 to 564 amino acids) using cAMP as substrate after 30 mins by plate reader analysis


Bioorg Med Chem Lett 23: 3325-8 (2013)


Article DOI: 10.1016/j.bmcl.2013.03.104
BindingDB Entry DOI: 10.7270/Q2QF8WSQ
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50491740
PNG
(CHEMBL2385749)
Show SMILES OC(=O)Cc1ccc(Nc2nc(nc3CCCS(=O)(=O)c23)-c2ccccc2)cc1
Show InChI InChI=1S/C21H19N3O4S/c25-18(26)13-14-8-10-16(11-9-14)22-21-19-17(7-4-12-29(19,27)28)23-20(24-21)15-5-2-1-3-6-15/h1-3,5-6,8-11H,4,7,12-13H2,(H,25,26)(H,22,23,24)
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Daiichi Sankyo Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PDE4B (152 to 564 amino acids) using cAMP as substrate after 30 mins by plate reader analysis


Bioorg Med Chem Lett 23: 3325-8 (2013)


Article DOI: 10.1016/j.bmcl.2013.03.104
BindingDB Entry DOI: 10.7270/Q2QF8WSQ
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50491751
PNG
(CHEMBL2385754)
Show SMILES CNC(=O)Cc1ccc(Nc2nc(nc3CCCS(=O)(=O)c23)-c2ccccc2)cc1
Show InChI InChI=1S/C22H22N4O3S/c1-23-19(27)14-15-9-11-17(12-10-15)24-22-20-18(8-5-13-30(20,28)29)25-21(26-22)16-6-3-2-4-7-16/h2-4,6-7,9-12H,5,8,13-14H2,1H3,(H,23,27)(H,24,25,26)
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Daiichi Sankyo Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PDE4B (152 to 564 amino acids) using cAMP as substrate after 30 mins by plate reader analysis


Bioorg Med Chem Lett 23: 3325-8 (2013)


Article DOI: 10.1016/j.bmcl.2013.03.104
BindingDB Entry DOI: 10.7270/Q2QF8WSQ
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50491739
PNG
(CHEMBL2385750)
Show SMILES OC(=O)Cc1ccc(Nc2nc(nc3CS(=O)(=O)CCc23)-c2ccccc2)cc1
Show InChI InChI=1S/C21H19N3O4S/c25-19(26)12-14-6-8-16(9-7-14)22-21-17-10-11-29(27,28)13-18(17)23-20(24-21)15-4-2-1-3-5-15/h1-9H,10-13H2,(H,25,26)(H,22,23,24)
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Daiichi Sankyo Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PDE4B (152 to 564 amino acids) using cAMP as substrate after 30 mins by plate reader analysis


Bioorg Med Chem Lett 23: 3325-8 (2013)


Article DOI: 10.1016/j.bmcl.2013.03.104
BindingDB Entry DOI: 10.7270/Q2QF8WSQ
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50491746
PNG
(CHEMBL2385559)
Show SMILES OC(=O)Cc1ccc(Nc2nc(nc3CSCc23)-c2ccccc2)cc1
Show InChI InChI=1S/C20H17N3O2S/c24-18(25)10-13-6-8-15(9-7-13)21-20-16-11-26-12-17(16)22-19(23-20)14-4-2-1-3-5-14/h1-9H,10-12H2,(H,24,25)(H,21,22,23)
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Daiichi Sankyo Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PDE4B (152 to 564 amino acids) using cAMP as substrate after 30 mins by plate reader analysis


Bioorg Med Chem Lett 23: 3325-8 (2013)


Article DOI: 10.1016/j.bmcl.2013.03.104
BindingDB Entry DOI: 10.7270/Q2QF8WSQ
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50493966
PNG
(CHEMBL2442475)
Show SMILES CC(C)(C)CNC(=O)Cc1ccc(Nc2nc(ncc2C(N)=O)-c2cccnc2)cc1
Show InChI InChI=1S/C23H26N6O2/c1-23(2,3)14-27-19(30)11-15-6-8-17(9-7-15)28-22-18(20(24)31)13-26-21(29-22)16-5-4-10-25-12-16/h4-10,12-13H,11,14H2,1-3H3,(H2,24,31)(H,27,30)(H,26,28,29)
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Kyushu University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human PDE4B using cAMP as substrate after 30 mins


Bioorg Med Chem 21: 7025-37 (2013)


Article DOI: 10.1016/j.bmc.2013.09.013
BindingDB Entry DOI: 10.7270/Q2DZ0C84
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50491761
PNG
(CHEMBL2385573)
Show SMILES OC(=O)Cc1ccc(Nc2nc(nc3CCCSc23)-c2ccccc2)cc1
Show InChI InChI=1S/C21H19N3O2S/c25-18(26)13-14-8-10-16(11-9-14)22-21-19-17(7-4-12-27-19)23-20(24-21)15-5-2-1-3-6-15/h1-3,5-6,8-11H,4,7,12-13H2,(H,25,26)(H,22,23,24)
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Daiichi Sankyo Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PDE4B (152 to 564 amino acids) using cAMP as substrate after 30 mins by plate reader analysis


Bioorg Med Chem Lett 23: 3325-8 (2013)


Article DOI: 10.1016/j.bmcl.2013.03.104
BindingDB Entry DOI: 10.7270/Q2QF8WSQ
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50491735
PNG
(CHEMBL2385761)
Show SMILES CN(C)C(=O)Cc1ccc(Nc2nc(nc3CCCS(=O)(=O)c23)-c2ccccc2)cc1
Show InChI InChI=1S/C23H24N4O3S/c1-27(2)20(28)15-16-10-12-18(13-11-16)24-23-21-19(9-6-14-31(21,29)30)25-22(26-23)17-7-4-3-5-8-17/h3-5,7-8,10-13H,6,9,14-15H2,1-2H3,(H,24,25,26)
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Daiichi Sankyo Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PDE4B (152 to 564 amino acids) using cAMP as substrate after 30 mins by plate reader analysis


Bioorg Med Chem Lett 23: 3325-8 (2013)


Article DOI: 10.1016/j.bmcl.2013.03.104
BindingDB Entry DOI: 10.7270/Q2QF8WSQ
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50491750
PNG
(CHEMBL2385760)
Show SMILES O=C(Cc1ccc(Nc2nc(nc3CCCS(=O)(=O)c23)-c2ccccc2)cc1)Nc1ccccc1
Show InChI InChI=1S/C27H24N4O3S/c32-24(28-21-10-5-2-6-11-21)18-19-13-15-22(16-14-19)29-27-25-23(12-7-17-35(25,33)34)30-26(31-27)20-8-3-1-4-9-20/h1-6,8-11,13-16H,7,12,17-18H2,(H,28,32)(H,29,30,31)
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Daiichi Sankyo Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PDE4B (152 to 564 amino acids) using cAMP as substrate after 30 mins by plate reader analysis


Bioorg Med Chem Lett 23: 3325-8 (2013)


Article DOI: 10.1016/j.bmcl.2013.03.104
BindingDB Entry DOI: 10.7270/Q2QF8WSQ
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50493959
PNG
(CHEMBL2442464)
Show SMILES OC(=O)Cc1ccc(Nc2nc(nc3CCNC(=O)c23)-c2ccccc2)cc1
Show InChI InChI=1S/C21H18N4O3/c26-17(27)12-13-6-8-15(9-7-13)23-20-18-16(10-11-22-21(18)28)24-19(25-20)14-4-2-1-3-5-14/h1-9H,10-12H2,(H,22,28)(H,26,27)(H,23,24,25)
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Kyushu University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human PDE4B using cAMP as substrate after 30 mins


Bioorg Med Chem 21: 7025-37 (2013)


Article DOI: 10.1016/j.bmc.2013.09.013
BindingDB Entry DOI: 10.7270/Q2DZ0C84
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50493952
PNG
(CHEMBL2442471)
Show SMILES CC(C)(C)NC(=O)Cc1ccc(Nc2nc(ncc2C(N)=O)-c2ccccc2)cc1
Show InChI InChI=1S/C23H25N5O2/c1-23(2,3)28-19(29)13-15-9-11-17(12-10-15)26-22-18(20(24)30)14-25-21(27-22)16-7-5-4-6-8-16/h4-12,14H,13H2,1-3H3,(H2,24,30)(H,28,29)(H,25,26,27)
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Kyushu University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human PDE4B using cAMP as substrate after 30 mins


Bioorg Med Chem 21: 7025-37 (2013)


Article DOI: 10.1016/j.bmc.2013.09.013
BindingDB Entry DOI: 10.7270/Q2DZ0C84
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50493951
PNG
(CHEMBL2440142)
Show SMILES CC(C)(C)CNC(=O)Cc1ccc(Nc2nc(ncc2C(N)=O)-c2cncnc2)cc1
Show InChI InChI=1S/C22H25N7O2/c1-22(2,3)12-27-18(30)8-14-4-6-16(7-5-14)28-21-17(19(23)31)11-26-20(29-21)15-9-24-13-25-10-15/h4-7,9-11,13H,8,12H2,1-3H3,(H2,23,31)(H,27,30)(H,26,28,29)
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Kyushu University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human PDE4B using cAMP as substrate after 30 mins


Bioorg Med Chem 21: 7025-37 (2013)


Article DOI: 10.1016/j.bmc.2013.09.013
BindingDB Entry DOI: 10.7270/Q2DZ0C84
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50493955
PNG
(CHEMBL2442467)
Show SMILES NC(=O)Cc1ccc(Nc2nc(ncc2C(N)=O)-c2ccccc2)cc1
Show InChI InChI=1S/C19H17N5O2/c20-16(25)10-12-6-8-14(9-7-12)23-19-15(17(21)26)11-22-18(24-19)13-4-2-1-3-5-13/h1-9,11H,10H2,(H2,20,25)(H2,21,26)(H,22,23,24)
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Kyushu University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human PDE4B using cAMP as substrate after 30 mins


Bioorg Med Chem 21: 7025-37 (2013)


Article DOI: 10.1016/j.bmc.2013.09.013
BindingDB Entry DOI: 10.7270/Q2DZ0C84
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50493954
PNG
(CHEMBL2442468)
Show SMILES CCCNC(=O)Cc1ccc(Nc2nc(ncc2C(N)=O)-c2ccccc2)cc1
Show InChI InChI=1S/C22H23N5O2/c1-2-12-24-19(28)13-15-8-10-17(11-9-15)26-22-18(20(23)29)14-25-21(27-22)16-6-4-3-5-7-16/h3-11,14H,2,12-13H2,1H3,(H2,23,29)(H,24,28)(H,25,26,27)
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Kyushu University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human PDE4B using cAMP as substrate after 30 mins


Bioorg Med Chem 21: 7025-37 (2013)


Article DOI: 10.1016/j.bmc.2013.09.013
BindingDB Entry DOI: 10.7270/Q2DZ0C84
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50491744
PNG
(CHEMBL2385563)
Show SMILES OC(=O)Cc1ccc(Nc2nc(nc3CS(=O)(=O)Cc23)-c2ccccc2)cc1
Show InChI InChI=1S/C20H17N3O4S/c24-18(25)10-13-6-8-15(9-7-13)21-20-16-11-28(26,27)12-17(16)22-19(23-20)14-4-2-1-3-5-14/h1-9H,10-12H2,(H,24,25)(H,21,22,23)
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Daiichi Sankyo Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PDE4B (152 to 564 amino acids) using cAMP as substrate after 30 mins by plate reader analysis


Bioorg Med Chem Lett 23: 3325-8 (2013)


Article DOI: 10.1016/j.bmcl.2013.03.104
BindingDB Entry DOI: 10.7270/Q2QF8WSQ
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50491747
PNG
(CHEMBL2385558)
Show SMILES OC(=O)CC1CCN(CC1)c1nc(nc2CSCc12)-c1ccccc1
Show InChI InChI=1S/C19H21N3O2S/c23-17(24)10-13-6-8-22(9-7-13)19-15-11-25-12-16(15)20-18(21-19)14-4-2-1-3-5-14/h1-5,13H,6-12H2,(H,23,24)
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Daiichi Sankyo Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PDE4B (152 to 564 amino acids) using cAMP as substrate after 30 mins by plate reader analysis


Bioorg Med Chem Lett 23: 3325-8 (2013)


Article DOI: 10.1016/j.bmcl.2013.03.104
BindingDB Entry DOI: 10.7270/Q2QF8WSQ
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50491745
PNG
(CHEMBL2385560)
Show SMILES OC(=O)CC1CCN(CC1)c1nc(nc2CS(=O)(=O)Cc12)-c1ccccc1
Show InChI InChI=1S/C19H21N3O4S/c23-17(24)10-13-6-8-22(9-7-13)19-15-11-27(25,26)12-16(15)20-18(21-19)14-4-2-1-3-5-14/h1-5,13H,6-12H2,(H,23,24)
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Daiichi Sankyo Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PDE4B (152 to 564 amino acids) using cAMP as substrate after 30 mins by plate reader analysis


Bioorg Med Chem Lett 23: 3325-8 (2013)


Article DOI: 10.1016/j.bmcl.2013.03.104
BindingDB Entry DOI: 10.7270/Q2QF8WSQ
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50493967
PNG
(CHEMBL2442480)
Show SMILES NC(=O)c1cnc(nc1Nc1ccc(CC(O)=O)cc1)-c1ccccc1
Show InChI InChI=1S/C19H16N4O3/c20-17(26)15-11-21-18(13-4-2-1-3-5-13)23-19(15)22-14-8-6-12(7-9-14)10-16(24)25/h1-9,11H,10H2,(H2,20,26)(H,24,25)(H,21,22,23)
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Kyushu University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human PDE4B using cAMP as substrate after 30 mins


Bioorg Med Chem 21: 7025-37 (2013)


Article DOI: 10.1016/j.bmc.2013.09.013
BindingDB Entry DOI: 10.7270/Q2DZ0C84
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50491741
PNG
(CHEMBL2385572)
Show SMILES OC(=O)Cc1ccc(Nc2nc(nc3sccc23)-c2ccccc2)cc1
Show InChI InChI=1S/C20H15N3O2S/c24-17(25)12-13-6-8-15(9-7-13)21-19-16-10-11-26-20(16)23-18(22-19)14-4-2-1-3-5-14/h1-11H,12H2,(H,24,25)(H,21,22,23)
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Daiichi Sankyo Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PDE4B (152 to 564 amino acids) using cAMP as substrate after 30 mins by plate reader analysis


Bioorg Med Chem Lett 23: 3325-8 (2013)


Article DOI: 10.1016/j.bmcl.2013.03.104
BindingDB Entry DOI: 10.7270/Q2QF8WSQ
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50491752
PNG
(CHEMBL2385751)
Show SMILES OC(=O)Cc1ccc(Nc2nc(nc3CCS(=O)(=O)c23)-c2ccccc2)cc1
Show InChI InChI=1S/C20H17N3O4S/c24-17(25)12-13-6-8-15(9-7-13)21-20-18-16(10-11-28(18,26)27)22-19(23-20)14-4-2-1-3-5-14/h1-9H,10-12H2,(H,24,25)(H,21,22,23)
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Daiichi Sankyo Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PDE4B (152 to 564 amino acids) using cAMP as substrate after 30 mins by plate reader analysis


Bioorg Med Chem Lett 23: 3325-8 (2013)


Article DOI: 10.1016/j.bmcl.2013.03.104
BindingDB Entry DOI: 10.7270/Q2QF8WSQ
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50491742
PNG
(CHEMBL2385567)
Show SMILES OC(=O)Cc1ccc(Nc2nc(nc3CCCCc23)-c2ccccc2)cc1
Show InChI InChI=1S/C22H21N3O2/c26-20(27)14-15-10-12-17(13-11-15)23-22-18-8-4-5-9-19(18)24-21(25-22)16-6-2-1-3-7-16/h1-3,6-7,10-13H,4-5,8-9,14H2,(H,26,27)(H,23,24,25)
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Daiichi Sankyo Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PDE4B (152 to 564 amino acids) using cAMP as substrate after 30 mins by plate reader analysis


Bioorg Med Chem Lett 23: 3325-8 (2013)


Article DOI: 10.1016/j.bmcl.2013.03.104
BindingDB Entry DOI: 10.7270/Q2QF8WSQ
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50491748
PNG
(CHEMBL2385570)
Show SMILES OC(=O)Cc1ccc(Nc2nc(nc3ccccc23)-c2ccccc2)cc1
Show InChI InChI=1S/C22H17N3O2/c26-20(27)14-15-10-12-17(13-11-15)23-22-18-8-4-5-9-19(18)24-21(25-22)16-6-2-1-3-7-16/h1-13H,14H2,(H,26,27)(H,23,24,25)
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Daiichi Sankyo Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PDE4B (152 to 564 amino acids) using cAMP as substrate after 30 mins by plate reader analysis


Bioorg Med Chem Lett 23: 3325-8 (2013)


Article DOI: 10.1016/j.bmcl.2013.03.104
BindingDB Entry DOI: 10.7270/Q2QF8WSQ
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50493964
PNG
(CHEMBL2442474)
Show SMILES CS(=O)(=O)NC(=O)Cc1ccc(Nc2nc(ncc2C(N)=O)-c2ccccc2)cc1
Show InChI InChI=1S/C20H19N5O4S/c1-30(28,29)25-17(26)11-13-7-9-15(10-8-13)23-20-16(18(21)27)12-22-19(24-20)14-5-3-2-4-6-14/h2-10,12H,11H2,1H3,(H2,21,27)(H,25,26)(H,22,23,24)
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Kyushu University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human PDE4B using cAMP as substrate after 30 mins


Bioorg Med Chem 21: 7025-37 (2013)


Article DOI: 10.1016/j.bmc.2013.09.013
BindingDB Entry DOI: 10.7270/Q2DZ0C84
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50491756
PNG
(CHEMBL2385566)
Show SMILES OC(=O)Cc1ccc(Nc2nc(nc3CCCc23)-c2ccccc2)cc1
Show InChI InChI=1S/C21H19N3O2/c25-19(26)13-14-9-11-16(12-10-14)22-21-17-7-4-8-18(17)23-20(24-21)15-5-2-1-3-6-15/h1-3,5-6,9-12H,4,7-8,13H2,(H,25,26)(H,22,23,24)
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Daiichi Sankyo Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PDE4B (152 to 564 amino acids) using cAMP as substrate after 30 mins by plate reader analysis


Bioorg Med Chem Lett 23: 3325-8 (2013)


Article DOI: 10.1016/j.bmcl.2013.03.104
BindingDB Entry DOI: 10.7270/Q2QF8WSQ
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50491743
PNG
(CHEMBL2385565)
Show SMILES OC(=O)CCc1ccc(Nc2nc(nc3CS(=O)(=O)Cc23)-c2ccccc2)cc1
Show InChI InChI=1S/C21H19N3O4S/c25-19(26)11-8-14-6-9-16(10-7-14)22-21-17-12-29(27,28)13-18(17)23-20(24-21)15-4-2-1-3-5-15/h1-7,9-10H,8,11-13H2,(H,25,26)(H,22,23,24)
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Daiichi Sankyo Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PDE4B (152 to 564 amino acids) using cAMP as substrate after 30 mins by plate reader analysis


Bioorg Med Chem Lett 23: 3325-8 (2013)


Article DOI: 10.1016/j.bmcl.2013.03.104
BindingDB Entry DOI: 10.7270/Q2QF8WSQ
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50493963
PNG
(CHEMBL2442482)
Show SMILES CSc1nc(nc(Nc2ccc(CC(O)=O)cc2)c1C(N)=O)-c1ccccc1
Show InChI InChI=1S/C20H18N4O3S/c1-28-20-16(17(21)27)19(23-18(24-20)13-5-3-2-4-6-13)22-14-9-7-12(8-10-14)11-15(25)26/h2-10H,11H2,1H3,(H2,21,27)(H,25,26)(H,22,23,24)
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Kyushu University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human PDE4B using cAMP as substrate after 30 mins


Bioorg Med Chem 21: 7025-37 (2013)


Article DOI: 10.1016/j.bmc.2013.09.013
BindingDB Entry DOI: 10.7270/Q2DZ0C84
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50491760
PNG
(CHEMBL2385569)
Show SMILES OC(=O)Cc1ccc(Nc2nc(nc3COCc23)-c2ccccc2)cc1
Show InChI InChI=1S/C20H17N3O3/c24-18(25)10-13-6-8-15(9-7-13)21-20-16-11-26-12-17(16)22-19(23-20)14-4-2-1-3-5-14/h1-9H,10-12H2,(H,24,25)(H,21,22,23)
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n/an/a 2.20E+3n/an/an/an/an/an/a



Daiichi Sankyo Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PDE4B (152 to 564 amino acids) using cAMP as substrate after 30 mins by plate reader analysis


Bioorg Med Chem Lett 23: 3325-8 (2013)


Article DOI: 10.1016/j.bmcl.2013.03.104
BindingDB Entry DOI: 10.7270/Q2QF8WSQ
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50491758
PNG
(CHEMBL2385564)
Show SMILES OC(=O)Cc1cccc(Nc2nc(nc3CS(=O)(=O)Cc23)-c2ccccc2)c1
Show InChI InChI=1S/C20H17N3O4S/c24-18(25)10-13-5-4-8-15(9-13)21-20-16-11-28(26,27)12-17(16)22-19(23-20)14-6-2-1-3-7-14/h1-9H,10-12H2,(H,24,25)(H,21,22,23)
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n/an/a 2.50E+3n/an/an/an/an/an/a



Daiichi Sankyo Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PDE4B (152 to 564 amino acids) using cAMP as substrate after 30 mins by plate reader analysis


Bioorg Med Chem Lett 23: 3325-8 (2013)


Article DOI: 10.1016/j.bmcl.2013.03.104
BindingDB Entry DOI: 10.7270/Q2QF8WSQ
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50491757
PNG
(CHEMBL2385562)
Show SMILES OC(=O)CN1CCC(CC1)Nc1nc(nc2CS(=O)(=O)Cc12)-c1ccccc1
Show InChI InChI=1S/C19H22N4O4S/c24-17(25)10-23-8-6-14(7-9-23)20-19-15-11-28(26,27)12-16(15)21-18(22-19)13-4-2-1-3-5-13/h1-5,14H,6-12H2,(H,24,25)(H,20,21,22)
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n/an/a 3.00E+3n/an/an/an/an/an/a



Daiichi Sankyo Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PDE4B (152 to 564 amino acids) using cAMP as substrate after 30 mins by plate reader analysis


Bioorg Med Chem Lett 23: 3325-8 (2013)


Article DOI: 10.1016/j.bmcl.2013.03.104
BindingDB Entry DOI: 10.7270/Q2QF8WSQ
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50493956
PNG
(CHEMBL2442481)
Show SMILES Cc1nc(nc(Nc2ccc(CC(O)=O)cc2)c1C(N)=O)-c1ccccc1
Show InChI InChI=1S/C20H18N4O3/c1-12-17(18(21)27)20(24-19(22-12)14-5-3-2-4-6-14)23-15-9-7-13(8-10-15)11-16(25)26/h2-10H,11H2,1H3,(H2,21,27)(H,25,26)(H,22,23,24)
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Kyushu University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human PDE4B using cAMP as substrate after 30 mins


Bioorg Med Chem 21: 7025-37 (2013)


Article DOI: 10.1016/j.bmc.2013.09.013
BindingDB Entry DOI: 10.7270/Q2DZ0C84
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50491749
PNG
(CHEMBL2385561)
Show SMILES OC(=O)CN1CCN(CC1)c1nc(nc2CS(=O)(=O)Cc12)-c1ccccc1
Show InChI InChI=1S/C18H20N4O4S/c23-16(24)10-21-6-8-22(9-7-21)18-14-11-27(25,26)12-15(14)19-17(20-18)13-4-2-1-3-5-13/h1-5H,6-12H2,(H,23,24)
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n/an/a 5.00E+3n/an/an/an/an/an/a



Daiichi Sankyo Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PDE4B (152 to 564 amino acids) using cAMP as substrate after 30 mins by plate reader analysis


Bioorg Med Chem Lett 23: 3325-8 (2013)


Article DOI: 10.1016/j.bmcl.2013.03.104
BindingDB Entry DOI: 10.7270/Q2QF8WSQ
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50493960
PNG
(CHEMBL2442463)
Show SMILES CC(C)(C)CNC(=O)Cc1ccc(Nc2nc(NN3CCCCC3)ncc2C(N)=O)cc1
Show InChI InChI=1S/C23H33N7O2/c1-23(2,3)15-26-19(31)13-16-7-9-17(10-8-16)27-21-18(20(24)32)14-25-22(28-21)29-30-11-5-4-6-12-30/h7-10,14H,4-6,11-13,15H2,1-3H3,(H2,24,32)(H,26,31)(H2,25,27,28,29)
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n/an/a 6.50E+3n/an/an/an/an/an/a



Kyushu University

Curated by ChEMBL


Assay Description
Inhibition of recombinant human PDE4B using cAMP as substrate after 30 mins


Bioorg Med Chem 21: 7025-37 (2013)


Article DOI: 10.1016/j.bmc.2013.09.013
BindingDB Entry DOI: 10.7270/Q2DZ0C84
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50491755
PNG
(CHEMBL2385752)
Show SMILES OC(=O)Cc1ccc(Nc2nc(nc3CCS(=O)(=O)Cc23)-c2ccccc2)cc1
Show InChI InChI=1S/C21H19N3O4S/c25-19(26)12-14-6-8-16(9-7-14)22-21-17-13-29(27,28)11-10-18(17)23-20(24-21)15-4-2-1-3-5-15/h1-9H,10-13H2,(H,25,26)(H,22,23,24)
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n/an/a 7.90E+3n/an/an/an/an/an/a



Daiichi Sankyo Co., Ltd

Curated by ChEMBL


Assay Description
Inhibition of human recombinant PDE4B (152 to 564 amino acids) using cAMP as substrate after 30 mins by plate reader analysis


Bioorg Med Chem Lett 23: 3325-8 (2013)


Article DOI: 10.1016/j.bmcl.2013.03.104
BindingDB Entry DOI: 10.7270/Q2QF8WSQ
More data for this
Ligand-Target Pair
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