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Compile Data Set for Download or QSAR

Found 979 hits with Last Name = 'hagen' and Initial = 'tj'   
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 4D


(Homo sapiens (Human))
BDBM50049413
PNG
(CHEMBL3313945 | US11401286, Example 52)
Show SMILES CCc1nc(Nc2ccc(CC#N)cc2)nc(n1)-c1cccc(Cl)c1
Show InChI InChI=1S/C19H16ClN5/c1-2-17-23-18(14-4-3-5-15(20)12-14)25-19(24-17)22-16-8-6-13(7-9-16)10-11-21/h3-9,12H,2,10H2,1H3,(H,22,23,24,25)
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n/an/a 7n/an/an/an/an/an/a



Northern Illinois University

Curated by ChEMBL


Assay Description
Inhibition of human PDE4D


Bioorg Med Chem Lett 24: 4031-4 (2014)


Article DOI: 10.1016/j.bmcl.2014.06.002
BindingDB Entry DOI: 10.7270/Q2KD20KD
More data for this
Ligand-Target Pair
Methionine aminopeptidase 2


(Homo sapiens (Human))
BDBM50437324
PNG
(CHEMBL2407597)
Show SMILES Cc1ccc(cc1)S(=O)(=O)Nc1ccc(Br)cc1C(O)=O
Show InChI InChI=1S/C14H12BrNO4S/c1-9-2-5-11(6-3-9)21(19,20)16-13-7-4-10(15)8-12(13)14(17)18/h2-8,16H,1H3,(H,17,18)
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n/an/a 9n/an/an/an/an/an/a



Northern Illinois University

Curated by ChEMBL


Assay Description
Inhibition of human methionine aminopeptidase 2


ACS Med Chem Lett 4: (2013)


Article DOI: 10.1021/ml400034m
BindingDB Entry DOI: 10.7270/Q2XW4M72
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50525013
PNG
(CHEMBL4476440 | US11401286, Example 81)
Show SMILES CCc1nc(Nc2ccc(CCCO)cc2)nc(n1)-c1cccc(Cl)c1
Show InChI InChI=1S/C20H21ClN4O/c1-2-18-23-19(15-6-3-7-16(21)13-15)25-20(24-18)22-17-10-8-14(9-11-17)5-4-12-26/h3,6-11,13,26H,2,4-5,12H2,1H3,(H,22,23,24,25)
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n/an/a 11n/an/an/an/an/an/a



Tetra Discovery Partners, Inc.

Curated by ChEMBL


Assay Description
Inhibition of recombinant human His6-tagged PDE4B1 UCR1 S133D mutant expressed in baculovirus infected Sf9 insect cells using cAMP as substrate prein...


J Med Chem 62: 4884-4901 (2019)


Article DOI: 10.1021/acs.jmedchem.9b00193
BindingDB Entry DOI: 10.7270/Q26H4MVT
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50049407
PNG
(CHEMBL3315271 | US11401286, Example 51)
Show SMILES CCc1nc(Nc2ccc(cc2)C#N)nc(n1)-c1cccc(Cl)c1
Show InChI InChI=1S/C18H14ClN5/c1-2-16-22-17(13-4-3-5-14(19)10-13)24-18(23-16)21-15-8-6-12(11-20)7-9-15/h3-10H,2H2,1H3,(H,21,22,23,24)
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n/an/a 12n/an/an/an/an/an/a



Northern Illinois University

Curated by ChEMBL


Assay Description
Inhibition of human PDE4B


Bioorg Med Chem Lett 24: 4031-4 (2014)


Article DOI: 10.1016/j.bmcl.2014.06.002
BindingDB Entry DOI: 10.7270/Q2KD20KD
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4D


(Homo sapiens (Human))
BDBM50049407
PNG
(CHEMBL3315271 | US11401286, Example 51)
Show SMILES CCc1nc(Nc2ccc(cc2)C#N)nc(n1)-c1cccc(Cl)c1
Show InChI InChI=1S/C18H14ClN5/c1-2-16-22-17(13-4-3-5-14(19)10-13)24-18(23-16)21-15-8-6-12(11-20)7-9-15/h3-10H,2H2,1H3,(H,21,22,23,24)
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n/an/a 13n/an/an/an/an/an/a



Northern Illinois University

Curated by ChEMBL


Assay Description
Inhibition of human PDE4D


Bioorg Med Chem Lett 24: 4031-4 (2014)


Article DOI: 10.1016/j.bmcl.2014.06.002
BindingDB Entry DOI: 10.7270/Q2KD20KD
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4D


(Homo sapiens (Human))
BDBM50049410
PNG
(CHEMBL3315265 | US11401286, Example 41)
Show SMILES OC(=O)c1ccc(Nc2nc(nc(n2)-c2cccc(Cl)c2)C2CC2)cc1
Show InChI InChI=1S/C19H15ClN4O2/c20-14-3-1-2-13(10-14)17-22-16(11-4-5-11)23-19(24-17)21-15-8-6-12(7-9-15)18(25)26/h1-3,6-11H,4-5H2,(H,25,26)(H,21,22,23,24)
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n/an/a 20n/an/an/an/an/an/a



Northern Illinois University

Curated by ChEMBL


Assay Description
Inhibition of human PDE4D


Bioorg Med Chem Lett 24: 4031-4 (2014)


Article DOI: 10.1016/j.bmcl.2014.06.002
BindingDB Entry DOI: 10.7270/Q2KD20KD
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50524997
PNG
(CHEMBL4570605 | US11401286, Example 58)
Show SMILES CCc1nc(Nc2ccc(CCO)cc2)nc(n1)-c1cccc(Cl)c1
Show InChI InChI=1S/C19H19ClN4O/c1-2-17-22-18(14-4-3-5-15(20)12-14)24-19(23-17)21-16-8-6-13(7-9-16)10-11-25/h3-9,12,25H,2,10-11H2,1H3,(H,21,22,23,24)
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n/an/a 24n/an/an/an/an/an/a



Tetra Discovery Partners, Inc.

Curated by ChEMBL


Assay Description
Inhibition of recombinant human His6-tagged PDE4B1 UCR1 S133D mutant expressed in baculovirus infected Sf9 insect cells using cAMP as substrate prein...


J Med Chem 62: 4884-4901 (2019)


Article DOI: 10.1021/acs.jmedchem.9b00193
BindingDB Entry DOI: 10.7270/Q26H4MVT
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50248919
PNG
((S)-N-(2-(1-(3-ethoxy-4-methoxyphenyl)-2-(methylsu...)
Show SMILES CCOc1cc(ccc1OC)[C@@H](CS(C)(=O)=O)N1C(=O)c2cccc(NC(C)=O)c2C1=O |r|
Show InChI InChI=1S/C22H24N2O7S/c1-5-31-19-11-14(9-10-18(19)30-3)17(12-32(4,28)29)24-21(26)15-7-6-8-16(23-13(2)25)20(15)22(24)27/h6-11,17H,5,12H2,1-4H3,(H,23,25)/t17-/m1/s1
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Tetra Discovery Partners, Inc.

Curated by ChEMBL


Assay Description
Inhibition of recombinant human His6-tagged PDE4B1 UCR1 S133D mutant expressed in baculovirus infected Sf9 insect cells using cAMP as substrate prein...


J Med Chem 62: 4884-4901 (2019)


Article DOI: 10.1021/acs.jmedchem.9b00193
BindingDB Entry DOI: 10.7270/Q26H4MVT
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4D


(Homo sapiens (Human))
BDBM50248919
PNG
((S)-N-(2-(1-(3-ethoxy-4-methoxyphenyl)-2-(methylsu...)
Show SMILES CCOc1cc(ccc1OC)[C@@H](CS(C)(=O)=O)N1C(=O)c2cccc(NC(C)=O)c2C1=O |r|
Show InChI InChI=1S/C22H24N2O7S/c1-5-31-19-11-14(9-10-18(19)30-3)17(12-32(4,28)29)24-21(26)15-7-6-8-16(23-13(2)25)20(15)22(24)27/h6-11,17H,5,12H2,1-4H3,(H,23,25)/t17-/m1/s1
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n/an/a 35n/an/an/an/an/an/a



Tetra Discovery Partners, Inc.

Curated by ChEMBL


Assay Description
Inhibition of recombinant human His6-tagged PDE4D2 expressed in baculovirus infected Sf9 insect cells using cAMP as substrate preincubated for 5 to 1...


J Med Chem 62: 4884-4901 (2019)


Article DOI: 10.1021/acs.jmedchem.9b00193
BindingDB Entry DOI: 10.7270/Q26H4MVT
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50525005
PNG
(CHEMBL4459298 | US11401286, Example 171)
Show SMILES CCc1cc(Nc2ccc(CC(N)=O)cc2)nc(n1)-c1cccc(Cl)c1
Show InChI InChI=1S/C20H19ClN4O/c1-2-16-12-19(23-17-8-6-13(7-9-17)10-18(22)26)25-20(24-16)14-4-3-5-15(21)11-14/h3-9,11-12H,2,10H2,1H3,(H2,22,26)(H,23,24,25)
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n/an/a 43n/an/an/an/an/an/a



Tetra Discovery Partners, Inc.

Curated by ChEMBL


Assay Description
Inhibition of recombinant human His6-tagged PDE4B1 UCR1 S133D mutant expressed in baculovirus infected Sf9 insect cells using cAMP as substrate prein...


J Med Chem 62: 4884-4901 (2019)


Article DOI: 10.1021/acs.jmedchem.9b00193
BindingDB Entry DOI: 10.7270/Q26H4MVT
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50524998
PNG
(CHEMBL4564798 | US11401286, Example 62)
Show SMILES CCc1nc(Nc2ccc(cc2)C(N)=O)nc(n1)-c1cccc(Cl)c1
Show InChI InChI=1S/C18H16ClN5O/c1-2-15-22-17(12-4-3-5-13(19)10-12)24-18(23-15)21-14-8-6-11(7-9-14)16(20)25/h3-10H,2H2,1H3,(H2,20,25)(H,21,22,23,24)
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n/an/a 44n/an/an/an/an/an/a



Tetra Discovery Partners, Inc.

Curated by ChEMBL


Assay Description
Inhibition of recombinant human His6-tagged PDE4B1 UCR1 S133D mutant expressed in baculovirus infected Sf9 insect cells using cAMP as substrate prein...


J Med Chem 62: 4884-4901 (2019)


Article DOI: 10.1021/acs.jmedchem.9b00193
BindingDB Entry DOI: 10.7270/Q26H4MVT
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50049410
PNG
(CHEMBL3315265 | US11401286, Example 41)
Show SMILES OC(=O)c1ccc(Nc2nc(nc(n2)-c2cccc(Cl)c2)C2CC2)cc1
Show InChI InChI=1S/C19H15ClN4O2/c20-14-3-1-2-13(10-14)17-22-16(11-4-5-11)23-19(24-17)21-15-8-6-12(7-9-15)18(25)26/h1-3,6-11H,4-5H2,(H,25,26)(H,21,22,23,24)
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n/an/a 46n/an/an/an/an/an/a



Northern Illinois University

Curated by ChEMBL


Assay Description
Inhibition of human PDE4B


Bioorg Med Chem Lett 24: 4031-4 (2014)


Article DOI: 10.1016/j.bmcl.2014.06.002
BindingDB Entry DOI: 10.7270/Q2KD20KD
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50524991
PNG
(CHEMBL4544243 | US11401286, Example 57)
Show SMILES CCc1nc(Nc2ccc(CC(N)=O)cc2)nc(n1)-c1cccc(Cl)c1
Show InChI InChI=1S/C19H18ClN5O/c1-2-17-23-18(13-4-3-5-14(20)11-13)25-19(24-17)22-15-8-6-12(7-9-15)10-16(21)26/h3-9,11H,2,10H2,1H3,(H2,21,26)(H,22,23,24,25)
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n/an/a 48n/an/an/an/an/an/a



Tetra Discovery Partners, Inc.

Curated by ChEMBL


Assay Description
Inhibition of recombinant human His6-tagged PDE4B1 UCR1 S133D mutant expressed in baculovirus infected Sf9 insect cells using cAMP as substrate prein...


J Med Chem 62: 4884-4901 (2019)


Article DOI: 10.1021/acs.jmedchem.9b00193
BindingDB Entry DOI: 10.7270/Q26H4MVT
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50346121
PNG
(2-(4-(2-(5-chlorothiophen-2-yl)-5-ethyl-6-methylpy...)
Show SMILES CCc1c(C)nc(nc1Nc1ccc(CC(O)=O)cc1)-c1ccc(Cl)s1
Show InChI InChI=1S/C19H18ClN3O2S/c1-3-14-11(2)21-19(15-8-9-16(20)26-15)23-18(14)22-13-6-4-12(5-7-13)10-17(24)25/h4-9H,3,10H2,1-2H3,(H,24,25)(H,21,22,23)
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n/an/a 55n/an/an/an/an/an/a



Northern Illinois University

Curated by ChEMBL


Assay Description
Inhibition of human PDE4B1


Bioorg Med Chem Lett 24: 4031-4 (2014)


Article DOI: 10.1016/j.bmcl.2014.06.002
BindingDB Entry DOI: 10.7270/Q2KD20KD
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Methionine aminopeptidase 2


(Homo sapiens (Human))
BDBM64987
PNG
(5-nitro-8-quinolinol | 5-nitroquinolin-8-ol | 8-HY...)
Show SMILES Oc1ccc([N+]([O-])=O)c2cccnc12
Show InChI InChI=1S/C9H6N2O3/c12-8-4-3-7(11(13)14)6-2-1-5-10-9(6)8/h1-5,12H
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n/an/a 55n/an/an/an/an/an/a



Northern Illinois University

Curated by ChEMBL


Assay Description
Inhibition of human methionine aminopeptidase 2


ACS Med Chem Lett 4: (2013)


Article DOI: 10.1021/ml400034m
BindingDB Entry DOI: 10.7270/Q2XW4M72
More data for this
Ligand-Target Pair
Methionine aminopeptidase 2


(Homo sapiens (Human))
BDBM76305
PNG
(5-chloranylquinolin-8-ol | 5-chloro-8-quinolinol |...)
Show SMILES Oc1ccc(Cl)c2cccnc12
Show InChI InChI=1S/C9H6ClNO/c10-7-3-4-8(12)9-6(7)2-1-5-11-9/h1-5,12H
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n/an/a 55n/an/an/an/an/an/a



Northern Illinois University

Curated by ChEMBL


Assay Description
Inhibition of recombinant full length human N-terminal GST/His6-tagged methionine aminopeptidase 2 expressed in baculovirus infected sf9 cells using ...


Bioorg Med Chem 25: 813-824 (2017)


Article DOI: 10.1016/j.bmc.2016.11.013
BindingDB Entry DOI: 10.7270/Q2125VV2
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50525009
PNG
(CHEMBL4437670 | US11401286, Example 191)
Show SMILES CCc1cc(Nc2ccc(CCO)cc2)nc(n1)-c1cccc(Cl)c1
Show InChI InChI=1S/C20H20ClN3O/c1-2-17-13-19(22-18-8-6-14(7-9-18)10-11-25)24-20(23-17)15-4-3-5-16(21)12-15/h3-9,12-13,25H,2,10-11H2,1H3,(H,22,23,24)
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Tetra Discovery Partners, Inc.

Curated by ChEMBL


Assay Description
Inhibition of recombinant human His6-tagged PDE4B1 UCR1 S133D mutant expressed in baculovirus infected Sf9 insect cells using cAMP as substrate prein...


J Med Chem 62: 4884-4901 (2019)


Article DOI: 10.1021/acs.jmedchem.9b00193
BindingDB Entry DOI: 10.7270/Q26H4MVT
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50525003
PNG
(CHEMBL4449185 | US11401286, Example 182)
Show SMILES CCc1cc(Oc2ccc(CCO)cc2)nc(n1)-c1cccc(Cl)c1
Show InChI InChI=1S/C20H19ClN2O2/c1-2-17-13-19(25-18-8-6-14(7-9-18)10-11-24)23-20(22-17)15-4-3-5-16(21)12-15/h3-9,12-13,24H,2,10-11H2,1H3
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Tetra Discovery Partners, Inc.

Curated by ChEMBL


Assay Description
Inhibition of recombinant human His6-tagged PDE4B1 UCR1 S133D mutant expressed in baculovirus infected Sf9 insect cells using cAMP as substrate prein...


J Med Chem 62: 4884-4901 (2019)


Article DOI: 10.1021/acs.jmedchem.9b00193
BindingDB Entry DOI: 10.7270/Q26H4MVT
More data for this
Ligand-Target Pair
Nitric oxide synthase, brain


(Homo sapiens (Human))
BDBM50062142
PNG
(4,6-Dimethyl-piperidin-(2Z)-ylideneamine | CHEMBL2...)
Show SMILES CC1CC(C)N=C(N)C1 |t:5|
Show InChI InChI=1S/C7H14N2/c1-5-3-6(2)9-7(8)4-5/h5-6H,3-4H2,1-2H3,(H2,8,9)
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n/an/a 60n/an/an/an/an/an/a



G. D. Searle Research and Development

Curated by ChEMBL


Assay Description
Inhibition of human Neuronal nitric oxide synthase


J Med Chem 41: 96-101 (1998)


Article DOI: 10.1021/jm9705059
BindingDB Entry DOI: 10.7270/Q2GM86D2
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4D


(Homo sapiens (Human))
BDBM50049416
PNG
(CHEMBL3315273)
Show SMILES CCc1nc(Nc2ccc(Cc3nnn[nH]3)cc2)nc(n1)-c1cccc(Cl)c1
Show InChI InChI=1S/C19H17ClN8/c1-2-16-22-18(13-4-3-5-14(20)11-13)24-19(23-16)21-15-8-6-12(7-9-15)10-17-25-27-28-26-17/h3-9,11H,2,10H2,1H3,(H,21,22,23,24)(H,25,26,27,28)
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n/an/a 63n/an/an/an/an/an/a



Northern Illinois University

Curated by ChEMBL


Assay Description
Inhibition of human PDE4D


Bioorg Med Chem Lett 24: 4031-4 (2014)


Article DOI: 10.1016/j.bmcl.2014.06.002
BindingDB Entry DOI: 10.7270/Q2KD20KD
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50049416
PNG
(CHEMBL3315273)
Show SMILES CCc1nc(Nc2ccc(Cc3nnn[nH]3)cc2)nc(n1)-c1cccc(Cl)c1
Show InChI InChI=1S/C19H17ClN8/c1-2-16-22-18(13-4-3-5-14(20)11-13)24-19(23-16)21-15-8-6-12(7-9-15)10-17-25-27-28-26-17/h3-9,11H,2,10H2,1H3,(H,21,22,23,24)(H,25,26,27,28)
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n/an/a 69n/an/an/an/an/an/a



Northern Illinois University

Curated by ChEMBL


Assay Description
Inhibition of human PDE4B


Bioorg Med Chem Lett 24: 4031-4 (2014)


Article DOI: 10.1016/j.bmcl.2014.06.002
BindingDB Entry DOI: 10.7270/Q2KD20KD
More data for this
Ligand-Target Pair
Nitric oxide synthase, inducible


(Homo sapiens (Human))
BDBM50062142
PNG
(4,6-Dimethyl-piperidin-(2Z)-ylideneamine | CHEMBL2...)
Show SMILES CC1CC(C)N=C(N)C1 |t:5|
Show InChI InChI=1S/C7H14N2/c1-5-3-6(2)9-7(8)4-5/h5-6H,3-4H2,1-2H3,(H2,8,9)
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n/an/a 80n/an/an/an/an/an/a



G. D. Searle Research and Development

Curated by ChEMBL


Assay Description
Inhibition of human Inducible nitric oxide synthase


J Med Chem 41: 96-101 (1998)


Article DOI: 10.1021/jm9705059
BindingDB Entry DOI: 10.7270/Q2GM86D2
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4D


(Homo sapiens (Human))
BDBM50049418
PNG
(CHEMBL3315275 | US11401286, Example 59)
Show SMILES CCc1nc(Nc2ccc(cc2)C(C)C(O)=O)nc(n1)-c1cccc(Cl)c1
Show InChI InChI=1S/C20H19ClN4O2/c1-3-17-23-18(14-5-4-6-15(21)11-14)25-20(24-17)22-16-9-7-13(8-10-16)12(2)19(26)27/h4-12H,3H2,1-2H3,(H,26,27)(H,22,23,24,25)
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n/an/a 96n/an/an/an/an/an/a



Northern Illinois University

Curated by ChEMBL


Assay Description
Inhibition of human PDE4D


Bioorg Med Chem Lett 24: 4031-4 (2014)


Article DOI: 10.1016/j.bmcl.2014.06.002
BindingDB Entry DOI: 10.7270/Q2KD20KD
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50525000
PNG
(CHEMBL4561428 | US11401286, Example 120)
Show SMILES CNC(=O)Cc1ccc(Nc2cc(nc3CCCc23)-c2cccc(Cl)c2)cc1
Show InChI InChI=1S/C23H22ClN3O/c1-25-23(28)12-15-8-10-18(11-9-15)26-22-14-21(16-4-2-5-17(24)13-16)27-20-7-3-6-19(20)22/h2,4-5,8-11,13-14H,3,6-7,12H2,1H3,(H,25,28)(H,26,27)
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n/an/a 98n/an/an/an/an/an/a



Tetra Discovery Partners, Inc.

Curated by ChEMBL


Assay Description
Inhibition of recombinant human His6-tagged PDE4B1 UCR1 S133D mutant expressed in baculovirus infected Sf9 insect cells using cAMP as substrate prein...


J Med Chem 62: 4884-4901 (2019)


Article DOI: 10.1021/acs.jmedchem.9b00193
BindingDB Entry DOI: 10.7270/Q26H4MVT
More data for this
Ligand-Target Pair
Nitric oxide synthase, inducible


(Homo sapiens (Human))
BDBM50062133
PNG
(4-Methyl-piperidin-(2E)-ylideneamine | 4-Methyl-pi...)
Show SMILES CC1CCN=C(N)C1 |t:4|
Show InChI InChI=1S/C6H12N2/c1-5-2-3-8-6(7)4-5/h5H,2-4H2,1H3,(H2,7,8)
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n/an/a 100n/an/an/an/an/an/a



G. D. Searle Research and Development

Curated by ChEMBL


Assay Description
Inhibition of human Inducible nitric oxide synthase


J Med Chem 41: 96-101 (1998)


Article DOI: 10.1021/jm9705059
BindingDB Entry DOI: 10.7270/Q2GM86D2
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50525006
PNG
(CHEMBL4434783 | US11401286, Example 80)
Show SMILES CCc1nc(Nc2ccc(CO)cc2)nc(n1)-c1cccc(Cl)c1
Show InChI InChI=1S/C18H17ClN4O/c1-2-16-21-17(13-4-3-5-14(19)10-13)23-18(22-16)20-15-8-6-12(11-24)7-9-15/h3-10,24H,2,11H2,1H3,(H,20,21,22,23)
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n/an/a 105n/an/an/an/an/an/a



Tetra Discovery Partners, Inc.

Curated by ChEMBL


Assay Description
Inhibition of recombinant human His6-tagged PDE4B1 UCR1 S133D mutant expressed in baculovirus infected Sf9 insect cells using cAMP as substrate prein...


J Med Chem 62: 4884-4901 (2019)


Article DOI: 10.1021/acs.jmedchem.9b00193
BindingDB Entry DOI: 10.7270/Q26H4MVT
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50049417
PNG
(CHEMBL3315272)
Show SMILES CCc1nc(Nc2ccc(cc2)-c2nnn[nH]2)nc(n1)-c1cccc(Cl)c1
Show InChI InChI=1S/C18H15ClN8/c1-2-15-21-16(12-4-3-5-13(19)10-12)23-18(22-15)20-14-8-6-11(7-9-14)17-24-26-27-25-17/h3-10H,2H2,1H3,(H,20,21,22,23)(H,24,25,26,27)
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n/an/a 126n/an/an/an/an/an/a



Northern Illinois University

Curated by ChEMBL


Assay Description
Inhibition of human PDE4B


Bioorg Med Chem Lett 24: 4031-4 (2014)


Article DOI: 10.1016/j.bmcl.2014.06.002
BindingDB Entry DOI: 10.7270/Q2KD20KD
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4D


(Homo sapiens (Human))
BDBM50524994
PNG
(CHEMBL4541964 | US11401286, Example 142)
Show SMILES OC(=O)Cc1ccc(Cc2cc(nc(c2)C(F)(F)F)-c2cccc(Cl)c2)cc1
Show InChI InChI=1S/C21H15ClF3NO2/c22-17-3-1-2-16(12-17)18-9-15(10-19(26-18)21(23,24)25)8-13-4-6-14(7-5-13)11-20(27)28/h1-7,9-10,12H,8,11H2,(H,27,28)
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n/an/a 127n/an/an/an/an/an/a



Tetra Discovery Partners, Inc.

Curated by ChEMBL


Assay Description
Inhibition of recombinant human His6-tagged PDE4D2 expressed in baculovirus infected Sf9 insect cells using cAMP as substrate preincubated for 5 to 1...


J Med Chem 62: 4884-4901 (2019)


Article DOI: 10.1021/acs.jmedchem.9b00193
BindingDB Entry DOI: 10.7270/Q26H4MVT
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50524995
PNG
(CHEMBL4593524 | US11401286, Example 195)
Show SMILES CCc1cc(Cc2ccc(CC(=O)NCCO)cc2)nc(n1)-c1cccc(Cl)c1
Show InChI InChI=1S/C23H24ClN3O2/c1-2-20-15-21(27-23(26-20)18-4-3-5-19(24)14-18)12-16-6-8-17(9-7-16)13-22(29)25-10-11-28/h3-9,14-15,28H,2,10-13H2,1H3,(H,25,29)
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n/an/a 128n/an/an/an/an/an/a



Tetra Discovery Partners, Inc.

Curated by ChEMBL


Assay Description
Inhibition of recombinant human His6-tagged PDE4B1 UCR1 S133D mutant expressed in baculovirus infected Sf9 insect cells using cAMP as substrate prein...


J Med Chem 62: 4884-4901 (2019)


Article DOI: 10.1021/acs.jmedchem.9b00193
BindingDB Entry DOI: 10.7270/Q26H4MVT
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4D


(Homo sapiens (Human))
BDBM50049417
PNG
(CHEMBL3315272)
Show SMILES CCc1nc(Nc2ccc(cc2)-c2nnn[nH]2)nc(n1)-c1cccc(Cl)c1
Show InChI InChI=1S/C18H15ClN8/c1-2-15-21-16(12-4-3-5-13(19)10-12)23-18(22-15)20-14-8-6-11(7-9-14)17-24-26-27-25-17/h3-10H,2H2,1H3,(H,20,21,22,23)(H,24,25,26,27)
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n/an/a 132n/an/an/an/an/an/a



Northern Illinois University

Curated by ChEMBL


Assay Description
Inhibition of human PDE4D


Bioorg Med Chem Lett 24: 4031-4 (2014)


Article DOI: 10.1016/j.bmcl.2014.06.002
BindingDB Entry DOI: 10.7270/Q2KD20KD
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50049415
PNG
(CHEMBL3315267 | US11401286, Example 49)
Show SMILES Clc1cccc(c1)C1=NC(NC2CCC(=O)NC2)=NC(N1)C1CC1 |c:19,t:8|
Show InChI InChI=1S/C17H20ClN5O/c18-12-3-1-2-11(8-12)16-21-15(10-4-5-10)22-17(23-16)20-13-6-7-14(24)19-9-13/h1-3,8,10,13,15H,4-7,9H2,(H,19,24)(H2,20,21,22,23)
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n/an/a 135n/an/an/an/an/an/a



Northern Illinois University

Curated by ChEMBL


Assay Description
Inhibition of human PDE4B


Bioorg Med Chem Lett 24: 4031-4 (2014)


Article DOI: 10.1016/j.bmcl.2014.06.002
BindingDB Entry DOI: 10.7270/Q2KD20KD
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50049411
PNG
(CHEMBL3315266 | US11401286, Example 38)
Show SMILES OC(=O)c1ccc(Nc2nc(nc(n2)-c2ccc(Cl)cc2)C2CC2)cc1
Show InChI InChI=1S/C19H15ClN4O2/c20-14-7-3-12(4-8-14)17-22-16(11-1-2-11)23-19(24-17)21-15-9-5-13(6-10-15)18(25)26/h3-11H,1-2H2,(H,25,26)(H,21,22,23,24)
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n/an/a 135n/an/an/an/an/an/a



Northern Illinois University

Curated by ChEMBL


Assay Description
Inhibition of human PDE4B


Bioorg Med Chem Lett 24: 4031-4 (2014)


Article DOI: 10.1016/j.bmcl.2014.06.002
BindingDB Entry DOI: 10.7270/Q2KD20KD
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50525004
PNG
(CHEMBL4553222 | US11401286, Example 3)
Show SMILES NC(=O)Cc1ccc(Nc2cc(nc3CCCc23)-c2cccc(Cl)c2)cc1
Show InChI InChI=1S/C22H20ClN3O/c23-16-4-1-3-15(12-16)20-13-21(18-5-2-6-19(18)26-20)25-17-9-7-14(8-10-17)11-22(24)27/h1,3-4,7-10,12-13H,2,5-6,11H2,(H2,24,27)(H,25,26)
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n/an/a 136n/an/an/an/an/an/a



Tetra Discovery Partners, Inc.

Curated by ChEMBL


Assay Description
Inhibition of recombinant human His6-tagged PDE4B1 UCR1 S133D mutant expressed in baculovirus infected Sf9 insect cells using cAMP as substrate prein...


J Med Chem 62: 4884-4901 (2019)


Article DOI: 10.1021/acs.jmedchem.9b00193
BindingDB Entry DOI: 10.7270/Q26H4MVT
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50525008
PNG
(CHEMBL4567525 | US11401286, Example 125)
Show SMILES NC(=O)Cc1ccc(Cc2cc(nc3CCCc23)-c2cccc(Cl)c2)cc1
Show InChI InChI=1S/C23H21ClN2O/c24-19-4-1-3-17(13-19)22-14-18(20-5-2-6-21(20)26-22)11-15-7-9-16(10-8-15)12-23(25)27/h1,3-4,7-10,13-14H,2,5-6,11-12H2,(H2,25,27)
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n/an/a 137n/an/an/an/an/an/a



Tetra Discovery Partners, Inc.

Curated by ChEMBL


Assay Description
Inhibition of recombinant human His6-tagged PDE4B1 UCR1 S133D mutant expressed in baculovirus infected Sf9 insect cells using cAMP as substrate prein...


J Med Chem 62: 4884-4901 (2019)


Article DOI: 10.1021/acs.jmedchem.9b00193
BindingDB Entry DOI: 10.7270/Q26H4MVT
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4D


(Homo sapiens (Human))
BDBM50049412
PNG
(CHEMBL3315274)
Show SMILES CCc1nc(Nc2ccc(NS(N)(=O)=O)cc2)nc(n1)-c1cccc(Cl)c1
Show InChI InChI=1S/C17H17ClN6O2S/c1-2-15-21-16(11-4-3-5-12(18)10-11)23-17(22-15)20-13-6-8-14(9-7-13)24-27(19,25)26/h3-10,24H,2H2,1H3,(H2,19,25,26)(H,20,21,22,23)
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n/an/a 160n/an/an/an/an/an/a



Northern Illinois University

Curated by ChEMBL


Assay Description
Inhibition of human PDE4D


Bioorg Med Chem Lett 24: 4031-4 (2014)


Article DOI: 10.1016/j.bmcl.2014.06.002
BindingDB Entry DOI: 10.7270/Q2KD20KD
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50049413
PNG
(CHEMBL3313945 | US11401286, Example 52)
Show SMILES CCc1nc(Nc2ccc(CC#N)cc2)nc(n1)-c1cccc(Cl)c1
Show InChI InChI=1S/C19H16ClN5/c1-2-17-23-18(14-4-3-5-15(20)12-14)25-19(24-17)22-16-8-6-13(7-9-16)10-11-21/h3-9,12H,2,10H2,1H3,(H,22,23,24,25)
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n/an/a 165n/an/an/an/an/an/a



Northern Illinois University

Curated by ChEMBL


Assay Description
Inhibition of human PDE4B


Bioorg Med Chem Lett 24: 4031-4 (2014)


Article DOI: 10.1016/j.bmcl.2014.06.002
BindingDB Entry DOI: 10.7270/Q2KD20KD
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50525011
PNG
(CHEMBL4569780 | US11401286, Example 119)
Show SMILES NC(=O)CCc1ccc(Nc2cc(nc3CCCc23)-c2cccc(Cl)c2)cc1
Show InChI InChI=1S/C23H22ClN3O/c24-17-4-1-3-16(13-17)21-14-22(19-5-2-6-20(19)27-21)26-18-10-7-15(8-11-18)9-12-23(25)28/h1,3-4,7-8,10-11,13-14H,2,5-6,9,12H2,(H2,25,28)(H,26,27)
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n/an/a 166n/an/an/an/an/an/a



Tetra Discovery Partners, Inc.

Curated by ChEMBL


Assay Description
Inhibition of recombinant human His6-tagged PDE4B1 UCR1 S133D mutant expressed in baculovirus infected Sf9 insect cells using cAMP as substrate prein...


J Med Chem 62: 4884-4901 (2019)


Article DOI: 10.1021/acs.jmedchem.9b00193
BindingDB Entry DOI: 10.7270/Q26H4MVT
More data for this
Ligand-Target Pair
Nitric oxide synthase, inducible


(Homo sapiens (Human))
BDBM50066778
PNG
(5-Ethyl-4-methyl-pyrrolidin-(2E)-ylideneamine; hyd...)
Show SMILES CCC1N=C(N)CC1C |t:3|
Show InChI InChI=1S/C7H14N2/c1-3-6-5(2)4-7(8)9-6/h5-6H,3-4H2,1-2H3,(H2,8,9)
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n/an/a 170n/an/an/an/an/an/a



Pfizer Inc.

Curated by ChEMBL


Assay Description
Inhibition of cloned (from RNA) human inducible nitric oxide synthase (hiNOS)


J Med Chem 41: 3675-83 (1998)


Article DOI: 10.1021/jm970840x
BindingDB Entry DOI: 10.7270/Q2XP75MP
More data for this
Ligand-Target Pair
Nitric oxide synthase, brain


(Homo sapiens (Human))
BDBM50066778
PNG
(5-Ethyl-4-methyl-pyrrolidin-(2E)-ylideneamine; hyd...)
Show SMILES CCC1N=C(N)CC1C |t:3|
Show InChI InChI=1S/C7H14N2/c1-3-6-5(2)4-7(8)9-6/h5-6H,3-4H2,1-2H3,(H2,8,9)
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n/an/a 170n/an/an/an/an/an/a



Pfizer Inc.

Curated by ChEMBL


Assay Description
Inhibition of cloned (from RNA) human Neuronal nitric oxide synthase


J Med Chem 41: 3675-83 (1998)


Article DOI: 10.1021/jm970840x
BindingDB Entry DOI: 10.7270/Q2XP75MP
More data for this
Ligand-Target Pair
Nitric oxide synthase, inducible


(Homo sapiens (Human))
BDBM50062132
PNG
(6-Propyl-piperidin-(2Z)-ylideneamine | CHEMBL6760)
Show SMILES CCCC1CCCC(N)=N1 |c:8|
Show InChI InChI=1S/C8H16N2/c1-2-4-7-5-3-6-8(9)10-7/h7H,2-6H2,1H3,(H2,9,10)
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n/an/a 200n/an/an/an/an/an/a



G. D. Searle Research and Development

Curated by ChEMBL


Assay Description
Inhibition of human Inducible nitric oxide synthase


J Med Chem 41: 96-101 (1998)


Article DOI: 10.1021/jm9705059
BindingDB Entry DOI: 10.7270/Q2GM86D2
More data for this
Ligand-Target Pair
Nitric oxide synthase, brain


(Homo sapiens (Human))
BDBM50062133
PNG
(4-Methyl-piperidin-(2E)-ylideneamine | 4-Methyl-pi...)
Show SMILES CC1CCN=C(N)C1 |t:4|
Show InChI InChI=1S/C6H12N2/c1-5-2-3-8-6(7)4-5/h5H,2-4H2,1H3,(H2,7,8)
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n/an/a 200n/an/an/an/an/an/a



G. D. Searle Research and Development

Curated by ChEMBL


Assay Description
Inhibition of human Neuronal nitric oxide synthase


J Med Chem 41: 96-101 (1998)


Article DOI: 10.1021/jm9705059
BindingDB Entry DOI: 10.7270/Q2GM86D2
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4D


(Homo sapiens (Human))
BDBM50049253
PNG
(CHEMBL3315262 | US11401286, Example 28)
Show SMILES CCc1nc(Nc2ccc(F)cc2)nc(n1)-c1ccc(Cl)s1
Show InChI InChI=1S/C15H12ClFN4S/c1-2-13-19-14(11-7-8-12(16)22-11)21-15(20-13)18-10-5-3-9(17)4-6-10/h3-8H,2H2,1H3,(H,18,19,20,21)
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n/an/a 207n/an/an/an/an/an/a



Northern Illinois University

Curated by ChEMBL


Assay Description
Inhibition of human PDE4D


Bioorg Med Chem Lett 24: 4031-4 (2014)


Article DOI: 10.1016/j.bmcl.2014.06.002
BindingDB Entry DOI: 10.7270/Q2KD20KD
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4D


(Homo sapiens (Human))
BDBM50049408
PNG
(CHEMBL3315270 | US11401286, Example 40)
Show SMILES CCc1nc(Nc2ccc(cc2)C(O)=O)nc(n1)-c1cccc(Cl)c1
Show InChI InChI=1S/C18H15ClN4O2/c1-2-15-21-16(12-4-3-5-13(19)10-12)23-18(22-15)20-14-8-6-11(7-9-14)17(24)25/h3-10H,2H2,1H3,(H,24,25)(H,20,21,22,23)
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n/an/a 213n/an/an/an/an/an/a



Northern Illinois University

Curated by ChEMBL


Assay Description
Inhibition of human PDE4D


Bioorg Med Chem Lett 24: 4031-4 (2014)


Article DOI: 10.1016/j.bmcl.2014.06.002
BindingDB Entry DOI: 10.7270/Q2KD20KD
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4D


(Homo sapiens (Human))
BDBM50049406
PNG
(CHEMBL3315263 | US11401286, Example 29)
Show SMILES CC(C)c1nc(Nc2ccc(cc2)C(O)=O)nc(n1)-c1ccc(Cl)s1
Show InChI InChI=1S/C17H15ClN4O2S/c1-9(2)14-20-15(12-7-8-13(18)25-12)22-17(21-14)19-11-5-3-10(4-6-11)16(23)24/h3-9H,1-2H3,(H,23,24)(H,19,20,21,22)
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n/an/a 219n/an/an/an/an/an/a



Northern Illinois University

Curated by ChEMBL


Assay Description
Inhibition of human PDE4D


Bioorg Med Chem Lett 24: 4031-4 (2014)


Article DOI: 10.1016/j.bmcl.2014.06.002
BindingDB Entry DOI: 10.7270/Q2KD20KD
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50049406
PNG
(CHEMBL3315263 | US11401286, Example 29)
Show SMILES CC(C)c1nc(Nc2ccc(cc2)C(O)=O)nc(n1)-c1ccc(Cl)s1
Show InChI InChI=1S/C17H15ClN4O2S/c1-9(2)14-20-15(12-7-8-13(18)25-12)22-17(21-14)19-11-5-3-10(4-6-11)16(23)24/h3-9H,1-2H3,(H,23,24)(H,19,20,21,22)
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n/an/a 220n/an/an/an/an/an/a



Northern Illinois University

Curated by ChEMBL


Assay Description
Inhibition of human PDE4B


Bioorg Med Chem Lett 24: 4031-4 (2014)


Article DOI: 10.1016/j.bmcl.2014.06.002
BindingDB Entry DOI: 10.7270/Q2KD20KD
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50524996
PNG
(CHEMBL4573171 | US11401286, Example 65)
Show SMILES CCc1cc(Cc2ccc(CC(N)=O)cc2)nc(n1)-c1cccc(Cl)c1
Show InChI InChI=1S/C21H20ClN3O/c1-2-18-13-19(10-14-6-8-15(9-7-14)11-20(23)26)25-21(24-18)16-4-3-5-17(22)12-16/h3-9,12-13H,2,10-11H2,1H3,(H2,23,26)
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n/an/a 225n/an/an/an/an/an/a



Tetra Discovery Partners, Inc.

Curated by ChEMBL


Assay Description
Inhibition of recombinant human His6-tagged PDE4B1 UCR1 S133D mutant expressed in baculovirus infected Sf9 insect cells using cAMP as substrate prein...


J Med Chem 62: 4884-4901 (2019)


Article DOI: 10.1021/acs.jmedchem.9b00193
BindingDB Entry DOI: 10.7270/Q26H4MVT
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Nitric oxide synthase, inducible


(Homo sapiens (Human))
BDBM50066775
PNG
(5-Pentyl-4-trifluoromethyl-pyrrolidin-(2E)-ylidene...)
Show SMILES CCCCCC1N=C(N)CC1C(F)(F)F |t:6|
Show InChI InChI=1S/C10H17F3N2/c1-2-3-4-5-8-7(10(11,12)13)6-9(14)15-8/h7-8H,2-6H2,1H3,(H2,14,15)
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n/an/a 230n/an/an/an/an/an/a



Pfizer Inc.

Curated by ChEMBL


Assay Description
Inhibition of cloned (from RNA) human inducible nitric oxide synthase (hiNOS)


J Med Chem 41: 3675-83 (1998)


Article DOI: 10.1021/jm970840x
BindingDB Entry DOI: 10.7270/Q2XP75MP
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50049146
PNG
(CHEMBL3315251 | US11401286, Example 36)
Show SMILES OC(=O)Cc1ccc(Nc2nc(nc(n2)-c2cccc(Cl)c2)C2CC2)cc1
Show InChI InChI=1S/C20H17ClN4O2/c21-15-3-1-2-14(11-15)19-23-18(13-6-7-13)24-20(25-19)22-16-8-4-12(5-9-16)10-17(26)27/h1-5,8-9,11,13H,6-7,10H2,(H,26,27)(H,22,23,24,25)
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n/an/a 237n/an/an/an/an/an/a



Northern Illinois University

Curated by ChEMBL


Assay Description
Inhibition of human PDE4B


Bioorg Med Chem Lett 24: 4031-4 (2014)


Article DOI: 10.1016/j.bmcl.2014.06.002
BindingDB Entry DOI: 10.7270/Q2KD20KD
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50049408
PNG
(CHEMBL3315270 | US11401286, Example 40)
Show SMILES CCc1nc(Nc2ccc(cc2)C(O)=O)nc(n1)-c1cccc(Cl)c1
Show InChI InChI=1S/C18H15ClN4O2/c1-2-15-21-16(12-4-3-5-13(19)10-12)23-18(22-15)20-14-8-6-11(7-9-14)17(24)25/h3-10H,2H2,1H3,(H,24,25)(H,20,21,22,23)
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n/an/a 241n/an/an/an/an/an/a



Tetra Discovery Partners, Inc.

Curated by ChEMBL


Assay Description
Inhibition of recombinant human His6-tagged PDE4B1 UCR1 S133D mutant expressed in baculovirus infected Sf9 insect cells using cAMP as substrate prein...


J Med Chem 62: 4884-4901 (2019)


Article DOI: 10.1021/acs.jmedchem.9b00193
BindingDB Entry DOI: 10.7270/Q26H4MVT
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4B


(Homo sapiens (Human))
BDBM50049408
PNG
(CHEMBL3315270 | US11401286, Example 40)
Show SMILES CCc1nc(Nc2ccc(cc2)C(O)=O)nc(n1)-c1cccc(Cl)c1
Show InChI InChI=1S/C18H15ClN4O2/c1-2-15-21-16(12-4-3-5-13(19)10-12)23-18(22-15)20-14-8-6-11(7-9-14)17(24)25/h3-10H,2H2,1H3,(H,24,25)(H,20,21,22,23)
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n/an/a 241n/an/an/an/an/an/a



Northern Illinois University

Curated by ChEMBL


Assay Description
Inhibition of human PDE4B


Bioorg Med Chem Lett 24: 4031-4 (2014)


Article DOI: 10.1016/j.bmcl.2014.06.002
BindingDB Entry DOI: 10.7270/Q2KD20KD
More data for this
Ligand-Target Pair
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