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10 similar compounds to monomer 50219169

Compile data set for download or QSAR
Wt: 387.4
BDBM50219178
Wt: 339.3
BDBM50219189
Wt: 387.4
BDBM50219182
Wt: 793.1
BDBM50219173
Wt: 781.1
BDBM50219174
Wt: 765.1
BDBM50219175
Wt: 361.3
BDBM50219177
Wt: 411.3
BDBM50219185
Wt: 242.2
BDBM50219171
Wt: 256.3
BDBM50219172

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 22 hits for monomerid = 50219178,50219189,50219182,50219173,50219174,50219175,50219177,50219185,50219171,50219172   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50219174
PNG
(CHEMBL2112274)
Show SMILES [Zn++].NS(=O)(=O)c1nnc(NC(=O)CN(CCN(CCN(CC([O-])=O)CC(=O)Nc2nnc(s2)S(N)(=O)=O)CC([O-])=O)CC(O)=O)s1
Show InChI InChI=1S/C18H27N11O12S4.Zn/c19-44(38,39)17-25-23-15(42-17)21-10(30)5-28(8-13(34)35)3-1-27(7-12(32)33)2-4-29(9-14(36)37)6-11(31)22-16-24-26-18(43-16)45(20,40)41;/h1-9H2,(H,32,33)(H,34,35)(H,36,37)(H2,19,38,39)(H2,20,40,41)(H,21,23,30)(H,22,24,31);/q;+2/p-2
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0.5n/an/an/an/an/an/an/an/a



Universit£ degli Studi

Curated by ChEMBL


Assay Description
Inhibition of hepatitis c virus Non structural protein 3 protease/Non structural protein 4A protease


Bioorg Med Chem Lett 11: 575-82 (2001)


Article DOI: 10.1016/s0960-894x(00)00722-8
BindingDB Entry DOI: 10.7270/Q2KW5GJQ
More data for this
Ligand-Target Pair
Carbonic anhydrase 4


(Homo sapiens (Human))
BDBM50219174
PNG
(CHEMBL2112274)
Show SMILES [Zn++].NS(=O)(=O)c1nnc(NC(=O)CN(CCN(CCN(CC([O-])=O)CC(=O)Nc2nnc(s2)S(N)(=O)=O)CC([O-])=O)CC(O)=O)s1
Show InChI InChI=1S/C18H27N11O12S4.Zn/c19-44(38,39)17-25-23-15(42-17)21-10(30)5-28(8-13(34)35)3-1-27(7-12(32)33)2-4-29(9-14(36)37)6-11(31)22-16-24-26-18(43-16)45(20,40)41;/h1-9H2,(H,32,33)(H,34,35)(H,36,37)(H2,19,38,39)(H2,20,40,41)(H,21,23,30)(H,22,24,31);/q;+2/p-2
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4n/an/an/an/an/an/an/an/a



Universit£ degli Studi

Curated by ChEMBL


Assay Description
In vitro binding affinity of the compound towards cloned human Dopamine receptor D2A using [3H]- Raclopride as radioligand.


Bioorg Med Chem Lett 11: 575-82 (2001)


Article DOI: 10.1016/s0960-894x(00)00722-8
BindingDB Entry DOI: 10.7270/Q2KW5GJQ
More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50219173
PNG
(CHEMBL2112276)
Show SMILES [Zn++].NS(=O)(=O)c1ccc(CNC(=O)CN(CCN(CCN(CC([O-])=O)CC(=O)NCc2ccc(cc2)S(N)(=O)=O)CC([O-])=O)CC(O)=O)cc1
Show InChI InChI=1S/C28H39N7O12S2.Zn/c29-48(44,45)22-5-1-20(2-6-22)13-31-24(36)15-34(18-27(40)41)11-9-33(17-26(38)39)10-12-35(19-28(42)43)16-25(37)32-14-21-3-7-23(8-4-21)49(30,46)47;/h1-8H,9-19H2,(H,31,36)(H,32,37)(H,38,39)(H,40,41)(H,42,43)(H2,29,44,45)(H2,30,46,47);/q;+2/p-2
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9n/an/an/an/an/an/an/an/a



Universit£ degli Studi

Curated by ChEMBL


Assay Description
Inhibition of hepatitis c virus Non structural protein 3 protease/Non structural protein 4A protease


Bioorg Med Chem Lett 11: 575-82 (2001)


Article DOI: 10.1016/s0960-894x(00)00722-8
BindingDB Entry DOI: 10.7270/Q2KW5GJQ
More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50219175
PNG
(CHEMBL2112275)
Show SMILES [Zn++].NS(=O)(=O)c1ccc(NC(=O)CN(CCN(CCN(CC([O-])=O)CC(=O)Nc2ccc(cc2)S(N)(=O)=O)CC([O-])=O)CC(O)=O)cc1
Show InChI InChI=1S/C26H35N7O12S2.Zn/c27-46(42,43)20-5-1-18(2-6-20)29-22(34)13-32(16-25(38)39)11-9-31(15-24(36)37)10-12-33(17-26(40)41)14-23(35)30-19-3-7-21(8-4-19)47(28,44)45;/h1-8H,9-17H2,(H,29,34)(H,30,35)(H,36,37)(H,38,39)(H,40,41)(H2,27,42,43)(H2,28,44,45);/q;+2/p-2
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16n/an/an/an/an/an/an/an/a



Universit£ degli Studi

Curated by ChEMBL


Assay Description
Inhibition of hepatitis c virus Non structural protein 3 protease/Non structural protein 4A protease


Bioorg Med Chem Lett 11: 575-82 (2001)


Article DOI: 10.1016/s0960-894x(00)00722-8
BindingDB Entry DOI: 10.7270/Q2KW5GJQ
More data for this
Ligand-Target Pair
Carbonic anhydrase 4


(Homo sapiens (Human))
BDBM50219173
PNG
(CHEMBL2112276)
Show SMILES [Zn++].NS(=O)(=O)c1ccc(CNC(=O)CN(CCN(CCN(CC([O-])=O)CC(=O)NCc2ccc(cc2)S(N)(=O)=O)CC([O-])=O)CC(O)=O)cc1
Show InChI InChI=1S/C28H39N7O12S2.Zn/c29-48(44,45)22-5-1-20(2-6-22)13-31-24(36)15-34(18-27(40)41)11-9-33(17-26(38)39)10-12-35(19-28(42)43)16-25(37)32-14-21-3-7-23(8-4-21)49(30,46)47;/h1-8H,9-19H2,(H,31,36)(H,32,37)(H,38,39)(H,40,41)(H,42,43)(H2,29,44,45)(H2,30,46,47);/q;+2/p-2
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21n/an/an/an/an/an/an/an/a



Universit£ degli Studi

Curated by ChEMBL


Assay Description
In vitro binding affinity of the compound towards cloned human 5-hydroxytryptamine 1A receptor expressed in Chinese hamster ovary (CHO) cells using [...


Bioorg Med Chem Lett 11: 575-82 (2001)


Article DOI: 10.1016/s0960-894x(00)00722-8
BindingDB Entry DOI: 10.7270/Q2KW5GJQ
More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM50219173
PNG
(CHEMBL2112276)
Show SMILES [Zn++].NS(=O)(=O)c1ccc(CNC(=O)CN(CCN(CCN(CC([O-])=O)CC(=O)NCc2ccc(cc2)S(N)(=O)=O)CC([O-])=O)CC(O)=O)cc1
Show InChI InChI=1S/C28H39N7O12S2.Zn/c29-48(44,45)22-5-1-20(2-6-22)13-31-24(36)15-34(18-27(40)41)11-9-33(17-26(38)39)10-12-35(19-28(42)43)16-25(37)32-14-21-3-7-23(8-4-21)49(30,46)47;/h1-8H,9-19H2,(H,31,36)(H,32,37)(H,38,39)(H,40,41)(H,42,43)(H2,29,44,45)(H2,30,46,47);/q;+2/p-2
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39n/an/an/an/an/an/an/an/a



Universit£ degli Studi

Curated by ChEMBL


Assay Description
Inhibition of hepatitis c virus Non structural protein 3 protease/Non structural protein 4A protease


Bioorg Med Chem Lett 11: 575-82 (2001)


Article DOI: 10.1016/s0960-894x(00)00722-8
BindingDB Entry DOI: 10.7270/Q2KW5GJQ
More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM50219174
PNG
(CHEMBL2112274)
Show SMILES [Zn++].NS(=O)(=O)c1nnc(NC(=O)CN(CCN(CCN(CC([O-])=O)CC(=O)Nc2nnc(s2)S(N)(=O)=O)CC([O-])=O)CC(O)=O)s1
Show InChI InChI=1S/C18H27N11O12S4.Zn/c19-44(38,39)17-25-23-15(42-17)21-10(30)5-28(8-13(34)35)3-1-27(7-12(32)33)2-4-29(9-14(36)37)6-11(31)22-16-24-26-18(43-16)45(20,40)41;/h1-9H2,(H,32,33)(H,34,35)(H,36,37)(H2,19,38,39)(H2,20,40,41)(H,21,23,30)(H,22,24,31);/q;+2/p-2
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40n/an/an/an/an/an/an/an/a



Universit£ degli Studi

Curated by ChEMBL


Assay Description
In vitro binding affinity of the compound towards cloned human 5-hydroxytryptamine 1A receptor expressed in Chinese hamster ovary (CHO) cells using [...


Bioorg Med Chem Lett 11: 575-82 (2001)


Article DOI: 10.1016/s0960-894x(00)00722-8
BindingDB Entry DOI: 10.7270/Q2KW5GJQ
More data for this
Ligand-Target Pair
Carbonic anhydrase 4


(Homo sapiens (Human))
BDBM50219175
PNG
(CHEMBL2112275)
Show SMILES [Zn++].NS(=O)(=O)c1ccc(NC(=O)CN(CCN(CCN(CC([O-])=O)CC(=O)Nc2ccc(cc2)S(N)(=O)=O)CC([O-])=O)CC(O)=O)cc1
Show InChI InChI=1S/C26H35N7O12S2.Zn/c27-46(42,43)20-5-1-18(2-6-20)29-22(34)13-32(16-25(38)39)11-9-31(15-24(36)37)10-12-33(17-26(40)41)14-23(35)30-19-3-7-21(8-4-19)47(28,44)45;/h1-8H,9-17H2,(H,29,34)(H,30,35)(H,36,37)(H,38,39)(H,40,41)(H2,27,42,43)(H2,28,44,45);/q;+2/p-2
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100n/an/an/an/an/an/an/an/a



Universit£ degli Studi

Curated by ChEMBL


Assay Description
In vitro binding affinity of the compound towards cloned human Dopamine receptor D2A using [3H]- Raclopride as radioligand.


Bioorg Med Chem Lett 11: 575-82 (2001)


Article DOI: 10.1016/s0960-894x(00)00722-8
BindingDB Entry DOI: 10.7270/Q2KW5GJQ
More data for this
Ligand-Target Pair
Carbonic anhydrase 1


(Homo sapiens (Human))
BDBM50219175
PNG
(CHEMBL2112275)
Show SMILES [Zn++].NS(=O)(=O)c1ccc(NC(=O)CN(CCN(CCN(CC([O-])=O)CC(=O)Nc2ccc(cc2)S(N)(=O)=O)CC([O-])=O)CC(O)=O)cc1
Show InChI InChI=1S/C26H35N7O12S2.Zn/c27-46(42,43)20-5-1-18(2-6-20)29-22(34)13-32(16-25(38)39)11-9-31(15-24(36)37)10-12-33(17-26(40)41)14-23(35)30-19-3-7-21(8-4-19)47(28,44)45;/h1-8H,9-17H2,(H,29,34)(H,30,35)(H,36,37)(H,38,39)(H,40,41)(H2,27,42,43)(H2,28,44,45);/q;+2/p-2
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350n/an/an/an/an/an/an/an/a



Universit£ degli Studi

Curated by ChEMBL


Assay Description
Inhibition of hepatitis c virus Non structural protein 3 protease/Non structural protein 4A protease


Bioorg Med Chem Lett 11: 575-82 (2001)


Article DOI: 10.1016/s0960-894x(00)00722-8
BindingDB Entry DOI: 10.7270/Q2KW5GJQ
More data for this
Ligand-Target Pair
Adrenergic receptor alpha


(Homo sapiens (Human))
BDBM50219171
PNG
(CHEMBL154346)
Show SMILES C(Nc1ccccc1-c1cnoc1)C1=NCCN1
Show InChI InChI=1S/C13H14N4O/c1-2-4-12(16-8-13-14-5-6-15-13)11(3-1)10-7-17-18-9-10/h1-4,7,9,16H,5-6,8H2,(H,14,15)
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n/an/an/an/a<1.00E+5n/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
In vitro activation of human Alpha-1B receptor expressed in rat-1 fibroblasts via calcium mobilization through the Gq coupled PLC pathway as function...


Bioorg Med Chem Lett 12: 575-9 (2002)


Article DOI: 10.1016/s0960-894x(01)00822-8
BindingDB Entry DOI: 10.7270/Q2Z320ZN
More data for this
Ligand-Target Pair
Adrenergic receptor alpha


(Homo sapiens (Human))
BDBM50219172
PNG
(CHEMBL152154)
Show SMILES Cc1nc(co1)-c1ccccc1NCC1=NCCN1
Show InChI InChI=1S/C14H16N4O/c1-10-18-13(9-19-10)11-4-2-3-5-12(11)17-8-14-15-6-7-16-14/h2-5,9,17H,6-8H2,1H3,(H,15,16)
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n/an/an/an/a<5.01E+3n/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
In vitro activation of human Alpha-1B receptor expressed in rat-1 fibroblasts via calcium mobilization through the Gq coupled PLC pathway as function...


Bioorg Med Chem Lett 12: 575-9 (2002)


Article DOI: 10.1016/s0960-894x(01)00822-8
BindingDB Entry DOI: 10.7270/Q2Z320ZN
More data for this
Ligand-Target Pair
Alpha adrenergic receptor (1a and 1d)


(Homo sapiens (Human))
BDBM50219172
PNG
(CHEMBL152154)
Show SMILES Cc1nc(co1)-c1ccccc1NCC1=NCCN1
Show InChI InChI=1S/C14H16N4O/c1-10-18-13(9-19-10)11-4-2-3-5-12(11)17-8-14-15-6-7-16-14/h2-5,9,17H,6-8H2,1H3,(H,15,16)
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n/an/an/an/a<5.01E+3n/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
In vitro activation of human alpha-1D receptor expressed in rat-1 fibroblasts via calcium using mobilization through the Gq coupled PLC pathway as fu...


Bioorg Med Chem Lett 12: 575-9 (2002)


Article DOI: 10.1016/s0960-894x(01)00822-8
BindingDB Entry DOI: 10.7270/Q2Z320ZN
More data for this
Ligand-Target Pair
Alpha-1A adrenergic receptor


(Homo sapiens (Human))
BDBM50219171
PNG
(CHEMBL154346)
Show SMILES C(Nc1ccccc1-c1cnoc1)C1=NCCN1
Show InChI InChI=1S/C13H14N4O/c1-2-4-12(16-8-13-14-5-6-15-13)11(3-1)10-7-17-18-9-10/h1-4,7,9,16H,5-6,8H2,(H,14,15)
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n/an/an/an/a 46n/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
In vitro activation of human alpha-1A receptor expressed in rat-1 fibroblasts via calcium mobilization through the Gq coupled PLC pathway as function...


Bioorg Med Chem Lett 12: 575-9 (2002)


Article DOI: 10.1016/s0960-894x(01)00822-8
BindingDB Entry DOI: 10.7270/Q2Z320ZN
More data for this
Ligand-Target Pair
Alpha-1A adrenergic receptor


(Homo sapiens (Human))
BDBM50219172
PNG
(CHEMBL152154)
Show SMILES Cc1nc(co1)-c1ccccc1NCC1=NCCN1
Show InChI InChI=1S/C14H16N4O/c1-10-18-13(9-19-10)11-4-2-3-5-12(11)17-8-14-15-6-7-16-14/h2-5,9,17H,6-8H2,1H3,(H,15,16)
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n/an/an/an/a 324n/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
In vitro activation of human alpha-1A receptor expressed in rat-1 fibroblasts via calcium mobilization through the Gq coupled PLC pathway as function...


Bioorg Med Chem Lett 12: 575-9 (2002)


Article DOI: 10.1016/s0960-894x(01)00822-8
BindingDB Entry DOI: 10.7270/Q2Z320ZN
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4C


(Rattus norvegicus)
BDBM50219177
PNG
(CHEMBL347478)
Show SMILES Cn1c2nccc(-c3ccccc3F)c2c(=O)n(Cc2ccccc2)c1=O
Show InChI InChI=1S/C21H16FN3O2/c1-24-19-18(16(11-12-23-19)15-9-5-6-10-17(15)22)20(26)25(21(24)27)13-14-7-3-2-4-8-14/h2-12H,13H2,1H3
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n/an/a 240n/an/an/an/an/an/a



Korea Institute of Science and Technology

Curated by ChEMBL


Assay Description
Concentration for inhibitory activity against phosphodiesterase 4 from rat liver


Bioorg Med Chem Lett 11: 611-4 (2001)


Article DOI: 10.1016/s0960-894x(00)00681-8
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4C


(Rattus norvegicus)
BDBM50219189
PNG
(CHEMBL436416)
Show SMILES CCCOCc1cnc2n(C)c(=O)n(Cc3ccccc3)c(=O)c2c1
Show InChI InChI=1S/C19H21N3O3/c1-3-9-25-13-15-10-16-17(20-11-15)21(2)19(24)22(18(16)23)12-14-7-5-4-6-8-14/h4-8,10-11H,3,9,12-13H2,1-2H3
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n/an/a 4.48E+3n/an/an/an/an/an/a



Korea Institute of Science and Technology

Curated by ChEMBL


Assay Description
Concentration for inhibitory activity against phosphodiesterase 4 from rat liver


Bioorg Med Chem Lett 11: 611-4 (2001)


Article DOI: 10.1016/s0960-894x(00)00681-8
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4C


(Rattus norvegicus)
BDBM50219185
PNG
(CHEMBL157550)
Show SMILES Cn1c2nccc(-c3cccc(c3)C(F)(F)F)c2c(=O)n(Cc2ccccc2)c1=O
Show InChI InChI=1S/C22H16F3N3O2/c1-27-19-18(20(29)28(21(27)30)13-14-6-3-2-4-7-14)17(10-11-26-19)15-8-5-9-16(12-15)22(23,24)25/h2-12H,13H2,1H3
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n/an/a 950n/an/an/an/an/an/a



Korea Institute of Science and Technology

Curated by ChEMBL


Assay Description
Binding affinity to rolipram binding site in isolated rat brain by rolipram binding assay


Bioorg Med Chem Lett 11: 611-4 (2001)


Article DOI: 10.1016/s0960-894x(00)00681-8
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4C


(Rattus norvegicus)
BDBM50219185
PNG
(CHEMBL157550)
Show SMILES Cn1c2nccc(-c3cccc(c3)C(F)(F)F)c2c(=O)n(Cc2ccccc2)c1=O
Show InChI InChI=1S/C22H16F3N3O2/c1-27-19-18(20(29)28(21(27)30)13-14-6-3-2-4-7-14)17(10-11-26-19)15-8-5-9-16(12-15)22(23,24)25/h2-12H,13H2,1H3
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n/an/a 950n/an/an/an/an/an/a



Korea Institute of Science and Technology

Curated by ChEMBL


Assay Description
Concentration for inhibitory activity against phosphodiesterase 4 from rat liver


Bioorg Med Chem Lett 11: 611-4 (2001)


Article DOI: 10.1016/s0960-894x(00)00681-8
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4C


(Rattus norvegicus)
BDBM50219182
PNG
(CHEMBL156054)
Show SMILES CCOc1ccc(cc1)-c1ccnc2n(C)c(=O)n(Cc3ccccc3)c(=O)c12
Show InChI InChI=1S/C23H21N3O3/c1-3-29-18-11-9-17(10-12-18)19-13-14-24-21-20(19)22(27)26(23(28)25(21)2)15-16-7-5-4-6-8-16/h4-14H,3,15H2,1-2H3
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n/an/a>1.00E+4n/an/an/an/an/an/a



Korea Institute of Science and Technology

Curated by ChEMBL


Assay Description
Concentration for inhibitory activity against phosphodiesterase 4 from rat liver


Bioorg Med Chem Lett 11: 611-4 (2001)


Article DOI: 10.1016/s0960-894x(00)00681-8
More data for this
Ligand-Target Pair
Alpha adrenergic receptor (1a and 1d)


(Homo sapiens (Human))
BDBM50219171
PNG
(CHEMBL154346)
Show SMILES C(Nc1ccccc1-c1cnoc1)C1=NCCN1
Show InChI InChI=1S/C13H14N4O/c1-2-4-12(16-8-13-14-5-6-15-13)11(3-1)10-7-17-18-9-10/h1-4,7,9,16H,5-6,8H2,(H,14,15)
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n/an/an/an/a<1.00E+5n/an/an/an/a



GlaxoSmithKline

Curated by ChEMBL


Assay Description
In vitro activation of human alpha-1D receptor expressed in rat-1 fibroblasts via calcium using mobilization through the Gq coupled PLC pathway as fu...


Bioorg Med Chem Lett 12: 575-9 (2002)


Article DOI: 10.1016/s0960-894x(01)00822-8
BindingDB Entry DOI: 10.7270/Q2Z320ZN
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4C


(Rattus norvegicus)
BDBM50219177
PNG
(CHEMBL347478)
Show SMILES Cn1c2nccc(-c3ccccc3F)c2c(=O)n(Cc2ccccc2)c1=O
Show InChI InChI=1S/C21H16FN3O2/c1-24-19-18(16(11-12-23-19)15-9-5-6-10-17(15)22)20(26)25(21(24)27)13-14-7-3-2-4-8-14/h2-12H,13H2,1H3
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n/an/a 491n/an/an/an/an/an/a



Korea Institute of Science and Technology

Curated by ChEMBL


Assay Description
Binding affinity to rolipram binding site in isolated rat brain by rolipram binding assay


Bioorg Med Chem Lett 11: 611-4 (2001)


Article DOI: 10.1016/s0960-894x(00)00681-8
More data for this
Ligand-Target Pair
cAMP-specific 3',5'-cyclic phosphodiesterase 4C


(Rattus norvegicus)
BDBM50219178
PNG
(CHEMBL157832)
Show SMILES Cn1c2ncc(COCc3ccccc3)cc2c(=O)n(Cc2ccccc2)c1=O
Show InChI InChI=1S/C23H21N3O3/c1-25-21-20(22(27)26(23(25)28)14-17-8-4-2-5-9-17)12-19(13-24-21)16-29-15-18-10-6-3-7-11-18/h2-13H,14-16H2,1H3
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n/an/a 3.05E+3n/an/an/an/an/an/a



Korea Institute of Science and Technology

Curated by ChEMBL


Assay Description
Concentration for inhibitory activity against phosphodiesterase 4 from rat liver


Bioorg Med Chem Lett 11: 611-4 (2001)


Article DOI: 10.1016/s0960-894x(00)00681-8
More data for this
Ligand-Target Pair