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Compile Data Set for Download or QSAR

Found 45 hits Enz. Inhib. hit(s) with all data for entry = 50041033   
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
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090430
PNG
(4-(3-Methyl-2,5-dioxo-2,5-dihydro-pyrrol-1-ylamino...)
Show SMILES CCOC(=O)c1cnc(nc1NN1C(=O)C=C(C)C1=O)-c1cccs1 |t:16|
Show InChI InChI=1S/C16H14N4O4S/c1-3-24-16(23)10-8-17-14(11-5-4-6-25-11)18-13(10)19-20-12(21)7-9(2)15(20)22/h4-8H,3H2,1-2H3,(H,17,18,19)
PDB

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n/an/a 20n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090444
PNG
(4-(3-Methyl-2,5-dioxo-2,5-dihydro-pyrrol-1-ylamino...)
Show SMILES CCOC(=O)c1cnc(nc1NN1C(=O)C=C(C)C1=O)-c1ccccc1 |t:16|
Show InChI InChI=1S/C18H16N4O4/c1-3-26-18(25)13-10-19-15(12-7-5-4-6-8-12)20-16(13)21-22-14(23)9-11(2)17(22)24/h4-10H,3H2,1-2H3,(H,19,20,21)
PDB

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n/an/a 100n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090407
PNG
(4-(3-Methyl-2,5-dioxo-2,5-dihydro-pyrrol-1-ylamino...)
Show SMILES CCOC(=O)c1cnc(nc1NN1C(=O)C=C(C)C1=O)-c1ccsc1 |t:16|
Show InChI InChI=1S/C16H14N4O4S/c1-3-24-16(23)11-7-17-13(10-4-5-25-8-10)18-14(11)19-20-12(21)6-9(2)15(20)22/h4-8H,3H2,1-2H3,(H,17,18,19)
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n/an/a 100n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090420
PNG
(4-(3-Methyl-2,5-dioxo-2,5-dihydro-pyrrol-1-ylamino...)
Show SMILES CCOC(=O)c1cnc(nc1NN1C(=O)C=C(C)C1=O)-c1ccc(C)s1 |t:16|
Show InChI InChI=1S/C17H16N4O4S/c1-4-25-17(24)11-8-18-15(12-6-5-10(3)26-12)19-14(11)20-21-13(22)7-9(2)16(21)23/h5-8H,4H2,1-3H3,(H,18,19,20)
PDB

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n/an/a 200n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090406
PNG
(1-(5-(4,5-dihydrooxazol-2-yl)-2-(thiophen-2-yl)pyr...)
Show SMILES CC1=CC(=O)N(Nc2nc(ncc2C2=NCCO2)-c2cccs2)C1=O |t:1,14|
Show InChI InChI=1S/C16H13N5O3S/c1-9-7-12(22)21(16(9)23)20-13-10(15-17-4-5-24-15)8-18-14(19-13)11-3-2-6-25-11/h2-3,6-8H,4-5H2,1H3,(H,18,19,20)
PDB

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n/an/a 200n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090443
PNG
(4-(3-Methyl-2,5-dioxo-2,5-dihydro-pyrrol-1-ylamino...)
Show SMILES CCOC(=O)c1cnc(SC)nc1NN1C(=O)C=C(C)C1=O |t:18|
Show InChI InChI=1S/C13H14N4O4S/c1-4-21-12(20)8-6-14-13(22-3)15-10(8)16-17-9(18)5-7(2)11(17)19/h5-6H,4H2,1-3H3,(H,14,15,16)
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n/an/a 200n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090442
PNG
(3-Methyl-1-[5-(2-methyl-2H-tetrazol-5-yl)-2-thioph...)
Show SMILES CC1=CC(=O)N(Nc2nc(ncc2-c2nnn(C)n2)-c2cccs2)C1=O |t:1|
Show InChI InChI=1S/C15H12N8O2S/c1-8-6-11(24)23(15(8)25)20-12-9(13-18-21-22(2)19-13)7-16-14(17-12)10-4-3-5-26-10/h3-7H,1-2H3,(H,16,17,20)
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n/an/a 200n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090431
PNG
(3-Methyl-1-[5-(4-methyl-oxazol-2-yl)-2-thiophen-2-...)
Show SMILES CC1=CC(=O)N(Nc2nc(ncc2-c2nc(C)co2)-c2cccs2)C1=O |t:1|
Show InChI InChI=1S/C17H13N5O3S/c1-9-6-13(23)22(17(9)24)21-14-11(16-19-10(2)8-25-16)7-18-15(20-14)12-4-3-5-26-12/h3-8H,1-2H3,(H,18,20,21)
PDB

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n/an/a 200n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090433
PNG
(2-(5-Chloro-thiophen-2-yl)-4-(3-methyl-2,5-dioxo-2...)
Show SMILES CCOC(=O)c1cnc(nc1NN1C(=O)C=C(C)C1=O)-c1ccc(Cl)s1 |t:16|
Show InChI InChI=1S/C16H13ClN4O4S/c1-3-25-16(24)9-7-18-14(10-4-5-11(17)26-10)19-13(9)20-21-12(22)6-8(2)15(21)23/h4-7H,3H2,1-2H3,(H,18,19,20)
PDB

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n/an/a 300n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090449
PNG
(2-(4-Chloro-phenyl)-4-(3-methyl-2,5-dioxo-2,5-dihy...)
Show SMILES CCOC(=O)c1cnc(nc1NN1C(=O)C=C(C)C1=O)-c1ccc(Cl)cc1 |t:16|
Show InChI InChI=1S/C18H15ClN4O4/c1-3-27-18(26)13-9-20-15(11-4-6-12(19)7-5-11)21-16(13)22-23-14(24)8-10(2)17(23)25/h4-9H,3H2,1-2H3,(H,20,21,22)
PDB

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n/an/a 300n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090450
PNG
(3-Methyl-1-[5-(5-methyl-[1,3,4]oxadiazol-2-yl)-2-t...)
Show SMILES CC1=CC(=O)N(Nc2nc(ncc2-c2nnc(C)o2)-c2cccs2)C1=O |t:1|
Show InChI InChI=1S/C16H12N6O3S/c1-8-6-12(23)22(16(8)24)21-13-10(15-20-19-9(2)25-15)7-17-14(18-13)11-4-3-5-26-11/h3-7H,1-2H3,(H,17,18,21)
PDB

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n/an/a 300n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090429
PNG
(2-(3,5-Dichloro-phenyl)-4-(3-methyl-2,5-dioxo-2,5-...)
Show SMILES CCOC(=O)c1cnc(nc1NN1C(=O)C=C(C)C1=O)-c1cc(Cl)cc(Cl)c1 |t:16|
Show InChI InChI=1S/C18H14Cl2N4O4/c1-3-28-18(27)13-8-21-15(10-5-11(19)7-12(20)6-10)22-16(13)23-24-14(25)4-9(2)17(24)26/h4-8H,3H2,1-2H3,(H,21,22,23)
PDB

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n/an/a 300n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090435
PNG
(3-Methyl-1-[5-(3-methyl-isoxazol-5-yl)-2-thiophen-...)
Show SMILES CC1=CC(=O)N(Nc2nc(ncc2-c2cc(C)no2)-c2cccs2)C1=O |t:1|
Show InChI InChI=1S/C17H13N5O3S/c1-9-6-14(23)22(17(9)24)20-15-11(12-7-10(2)21-25-12)8-18-16(19-15)13-4-3-5-26-13/h3-8H,1-2H3,(H,18,19,20)
PDB

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UniChem
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n/an/a 300n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090440
PNG
(4-(3-Methyl-2,5-dioxo-2,5-dihydro-pyrrol-1-ylamino...)
Show SMILES CCOC(=O)c1cnc(nc1NN1C(=O)C=C(C)C1=O)-c1ccc(cc1)C(F)(F)F |t:16|
Show InChI InChI=1S/C19H15F3N4O4/c1-3-30-18(29)13-9-23-15(11-4-6-12(7-5-11)19(20,21)22)24-16(13)25-26-14(27)8-10(2)17(26)28/h4-9H,3H2,1-2H3,(H,23,24,25)
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n/an/a 400n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090426
PNG
(2-(4-Fluoro-phenyl)-4-(3-methyl-2,5-dioxo-2,5-dihy...)
Show SMILES CCOC(=O)c1cnc(nc1NN1C(=O)C=C(C)C1=O)-c1ccc(F)cc1 |t:16|
Show InChI InChI=1S/C18H15FN4O4/c1-3-27-18(26)13-9-20-15(11-4-6-12(19)7-5-11)21-16(13)22-23-14(24)8-10(2)17(23)25/h4-9H,3H2,1-2H3,(H,20,21,22)
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n/an/a 700n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090441
PNG
(2-(3-Bromo-phenyl)-4-(3-methyl-2,5-dioxo-2,5-dihyd...)
Show SMILES CCOC(=O)c1cnc(nc1NN1C(=O)C=C(C)C1=O)-c1cccc(Br)c1 |t:16|
Show InChI InChI=1S/C18H15BrN4O4/c1-3-27-18(26)13-9-20-15(11-5-4-6-12(19)8-11)21-16(13)22-23-14(24)7-10(2)17(23)25/h4-9H,3H2,1-2H3,(H,20,21,22)
PDB

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n/an/a 700n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090421
PNG
(2-(Furan-2-carbonyl)-4-(3-methyl-2,5-dioxo-2,5-dih...)
Show SMILES CCOC(=O)c1cnc(nc1NN1C(=O)C=C(C)C1=O)C(=O)c1ccco1 |t:16|
Show InChI InChI=1S/C17H14N4O6/c1-3-26-17(25)10-8-18-15(13(23)11-5-4-6-27-11)19-14(10)20-21-12(22)7-9(2)16(21)24/h4-8H,3H2,1-2H3,(H,18,19,20)
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n/an/a 700n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090409
PNG
(2-(4-Methoxy-phenyl)-4-(3-methyl-2,5-dioxo-2,5-dih...)
Show SMILES CCOC(=O)c1cnc(nc1NN1C(=O)C=C(C)C1=O)-c1ccc(OC)cc1 |t:16|
Show InChI InChI=1S/C19H18N4O5/c1-4-28-19(26)14-10-20-16(12-5-7-13(27-3)8-6-12)21-17(14)22-23-15(24)9-11(2)18(23)25/h5-10H,4H2,1-3H3,(H,20,21,22)
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n/an/a 900n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090410
PNG
(4-[Methyl-(3-methyl-2,5-dioxo-2,5-dihydro-pyrrol-1...)
Show SMILES CCOC(=O)c1cnc(nc1N(C)N1C(=O)C=C(C)C1=O)-c1cccs1 |t:17|
Show InChI InChI=1S/C17H16N4O4S/c1-4-25-17(24)11-9-18-14(12-6-5-7-26-12)19-15(11)20(3)21-13(22)8-10(2)16(21)23/h5-9H,4H2,1-3H3
PDB

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n/an/a 1.00E+3n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090408
PNG
(4-(3-Methyl-2,5-dioxo-2,5-dihydro-pyrrol-1-ylamino...)
Show SMILES CCOC(=O)c1cnc(nc1NN1C(=O)C=C(C)C1=O)C(F)(F)F |t:16|
Show InChI InChI=1S/C13H11F3N4O4/c1-3-24-11(23)7-5-17-12(13(14,15)16)18-9(7)19-20-8(21)4-6(2)10(20)22/h4-5H,3H2,1-2H3,(H,17,18,19)
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n/an/a 1.00E+3n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090432
PNG
(2-Cyclopropyl-4-(3-methyl-2,5-dioxo-2,5-dihydro-py...)
Show SMILES CCOC(=O)c1cnc(nc1NN1C(=O)C=C(C)C1=O)C1CC1 |t:16|
Show InChI InChI=1S/C15H16N4O4/c1-3-23-15(22)10-7-16-12(9-4-5-9)17-13(10)18-19-11(20)6-8(2)14(19)21/h6-7,9H,3-5H2,1-2H3,(H,16,17,18)
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n/an/a 1.00E+3n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090415
PNG
(4-(3-Methyl-2,5-dioxo-2,5-dihydro-pyrrol-1-ylamino...)
Show SMILES CCOC(=O)c1cnc(Sc2ccccc2)nc1NN1C(=O)C=C(C)C1=O |t:24|
Show InChI InChI=1S/C18H16N4O4S/c1-3-26-17(25)13-10-19-18(27-12-7-5-4-6-8-12)20-15(13)21-22-14(23)9-11(2)16(22)24/h4-10H,3H2,1-2H3,(H,19,20,21)
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n/an/a 1.00E+3n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL




Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090447
PNG
(2-tert-Butyl-4-(3-methyl-2,5-dioxo-2,5-dihydro-pyr...)
Show SMILES CCOC(=O)c1cnc(nc1NN1C(=O)C=C(C)C1=O)C(C)(C)C |t:16|
Show InChI InChI=1S/C16H20N4O4/c1-6-24-14(23)10-8-17-15(16(3,4)5)18-12(10)19-20-11(21)7-9(2)13(20)22/h7-8H,6H2,1-5H3,(H,17,18,19)
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n/an/a 1.00E+3n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090437
PNG
(2-Cyclohex-1-enylmethyl-4-(3-methyl-2,5-dioxo-2,5-...)
Show SMILES CCOC(=O)c1cnc(CC2=CCCCC2)nc1NN1C(=O)C=C(C)C1=O |t:10,24|
Show InChI InChI=1S/C19H22N4O4/c1-3-27-19(26)14-11-20-15(10-13-7-5-4-6-8-13)21-17(14)22-23-16(24)9-12(2)18(23)25/h7,9,11H,3-6,8,10H2,1-2H3,(H,20,21,22)
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n/an/a 2.00E+3n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090411
PNG
(2-(2,6-Dichloro-pyridin-4-yl)-4-(3-methyl-2,5-diox...)
Show SMILES CCOC(=O)c1cnc(nc1NN1C(=O)C=C(C)C1=O)-c1cc(Cl)nc(Cl)c1 |t:16|
Show InChI InChI=1S/C17H13Cl2N5O4/c1-3-28-17(27)10-7-20-14(9-5-11(18)21-12(19)6-9)22-15(10)23-24-13(25)4-8(2)16(24)26/h4-7H,3H2,1-2H3,(H,20,22,23)
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n/an/a 2.00E+3n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090436
PNG
(4-[Methyl-(3-methyl-2,5-dioxo-2,5-dihydro-pyrrol-1...)
Show SMILES CCOC(=O)c1cnc(nc1N(C)N1C(=O)C=C(C)C1=O)-c1ccccc1 |t:17|
Show InChI InChI=1S/C19H18N4O4/c1-4-27-19(26)14-11-20-16(13-8-6-5-7-9-13)21-17(14)22(3)23-15(24)10-12(2)18(23)25/h5-11H,4H2,1-3H3
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n/an/a 2.00E+3n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090445
PNG
(2-(4-Fluoro-phenyl)-4-[methyl-(3-methyl-2,5-dioxo-...)
Show SMILES CCOC(=O)c1cnc(nc1N(C)N1C(=O)C=C(C)C1=O)-c1ccc(F)cc1 |t:17|
Show InChI InChI=1S/C19H17FN4O4/c1-4-28-19(27)14-10-21-16(12-5-7-13(20)8-6-12)22-17(14)23(3)24-15(25)9-11(2)18(24)26/h5-10H,4H2,1-3H3
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n/an/a 3.00E+3n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090439
PNG
(2-Benzo[b]thiophen-2-yl-4-(3-methyl-2,5-dioxo-2,5-...)
Show SMILES CCOC(=O)c1cnc(nc1NN1C(=O)C=C(C)C1=O)-c1cc2ccccc2s1 |t:16|
Show InChI InChI=1S/C20H16N4O4S/c1-3-28-20(27)13-10-21-18(15-9-12-6-4-5-7-14(12)29-15)22-17(13)23-24-16(25)8-11(2)19(24)26/h4-10H,3H2,1-2H3,(H,21,22,23)
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n/an/a 4.00E+3n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090425
PNG
(4-[Acetyl-(3-methyl-2,5-dioxo-2,5-dihydro-pyrrol-1...)
Show SMILES CCOC(=O)c1cnc(nc1N(N1C(=O)C=C(C)C1=O)C(C)=O)-c1ccccc1 |t:16|
Show InChI InChI=1S/C20H18N4O5/c1-4-29-20(28)15-11-21-17(14-8-6-5-7-9-14)22-18(15)23(13(3)25)24-16(26)10-12(2)19(24)27/h5-11H,4H2,1-3H3
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n/an/a 4.00E+3n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090427
PNG
(2-(3-Methoxy-phenyl)-4-(3-methyl-2,5-dioxo-2,5-dih...)
Show SMILES CCOC(=O)c1cnc(nc1NN1C(=O)C=C(C)C1=O)-c1cccc(OC)c1 |t:16|
Show InChI InChI=1S/C19H18N4O5/c1-4-28-19(26)14-10-20-16(12-6-5-7-13(9-12)27-3)21-17(14)22-23-15(24)8-11(2)18(23)25/h5-10H,4H2,1-3H3,(H,20,21,22)
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n/an/a 5.00E+3n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090428
PNG
(4-(3-Methyl-2,5-dioxo-2,5-dihydro-pyrrol-1-ylamino...)
Show SMILES CC1=CC(=O)N(Nc2nc(ncc2C#N)-c2cccs2)C1=O |t:1|
Show InChI InChI=1S/C14H9N5O2S/c1-8-5-11(20)19(14(8)21)18-12-9(6-15)7-16-13(17-12)10-3-2-4-22-10/h2-5,7H,1H3,(H,16,17,18)
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n/an/a 5.00E+3n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090423
PNG
(4-(3-Methyl-2,5-dioxo-2,5-dihydro-pyrrol-1-ylamino...)
Show SMILES CCOC(=O)c1cnc(nc1NN1C(=O)C=C(C)C1=O)-c1cnc2ccccc2c1 |t:16|
Show InChI InChI=1S/C21H17N5O4/c1-3-30-21(29)15-11-23-18(14-9-13-6-4-5-7-16(13)22-10-14)24-19(15)25-26-17(27)8-12(2)20(26)28/h4-11H,3H2,1-2H3,(H,23,24,25)
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n/an/a 6.00E+3n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090446
PNG
(4-(3-Methyl-2,5-dioxo-2,5-dihydro-pyrrol-1-ylamino...)
Show SMILES CCOC(=O)c1cnc(nc1NN1C(=O)C=C(C)C1=O)-c1ccncc1 |t:16|
Show InChI InChI=1S/C17H15N5O4/c1-3-26-17(25)12-9-19-14(11-4-6-18-7-5-11)20-15(12)21-22-13(23)8-10(2)16(22)24/h4-9H,3H2,1-2H3,(H,19,20,21)
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n/an/a 6.00E+3n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090422
PNG
(4-(3-Methyl-2,5-dioxo-2,5-dihydro-pyrrol-1-ylamino...)
Show SMILES CCOC(=O)c1cnc(nc1NN1C(=O)C=C(C)C1=O)-c1cccc(c1)[N+]([O-])=O |t:16|
Show InChI InChI=1S/C18H15N5O6/c1-3-29-18(26)13-9-19-15(11-5-4-6-12(8-11)23(27)28)20-16(13)21-22-14(24)7-10(2)17(22)25/h4-9H,3H2,1-2H3,(H,19,20,21)
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n/an/a 7.00E+3n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090414
PNG
(2-Benzyl-4-(3-methyl-2,5-dioxo-2,5-dihydro-pyrrol-...)
Show SMILES CCOC(=O)c1cnc(Cc2ccccc2)nc1NN1C(=O)C=C(C)C1=O |t:24|
Show InChI InChI=1S/C19H18N4O4/c1-3-27-19(26)14-11-20-15(10-13-7-5-4-6-8-13)21-17(14)22-23-16(24)9-12(2)18(23)25/h4-9,11H,3,10H2,1-2H3,(H,20,21,22)
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n/an/a 7.00E+3n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090417
PNG
(4-(3-Methyl-2,5-dioxo-2,5-dihydro-pyrrol-1-ylamino...)
Show SMILES CCOC(=O)c1cnc(nc1NN1C(=O)C=C(C)C1=O)-c1csc(C)n1 |t:16|
Show InChI InChI=1S/C16H15N5O4S/c1-4-25-16(24)10-6-17-14(11-7-26-9(3)18-11)19-13(10)20-21-12(22)5-8(2)15(21)23/h5-7H,4H2,1-3H3,(H,17,19,20)
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n/an/a 8.00E+3n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090419
PNG
(4-(2,5-Dioxo-2,5-dihydro-pyrrol-1-ylamino)-2-trifl...)
Show SMILES CCOC(=O)c1cnc(nc1NN1C(=O)C=CC1=O)C(F)(F)F |c:16|
Show InChI InChI=1S/C12H9F3N4O4/c1-2-23-10(22)6-5-16-11(12(13,14)15)17-9(6)18-19-7(20)3-4-8(19)21/h3-5H,2H2,1H3,(H,16,17,18)
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n/an/a 1.00E+4n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090434
PNG
(4-(3,4-Dimethyl-2,5-dioxo-2,5-dihydro-pyrrol-1-yla...)
Show SMILES CCOC(=O)c1cnc(nc1NN1C(=O)C(C)=C(C)C1=O)C(F)(F)F |t:17|
Show InChI InChI=1S/C14H13F3N4O4/c1-4-25-12(24)8-5-18-13(14(15,16)17)19-9(8)20-21-10(22)6(2)7(3)11(21)23/h5H,4H2,1-3H3,(H,18,19,20)
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n/an/a 1.00E+4n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090424
PNG
(2-Benzenesulfonyl-4-(3-methyl-2,5-dioxo-2,5-dihydr...)
Show SMILES CCOC(=O)c1cnc(nc1NN1C(=O)C=C(C)C1=O)S(=O)(=O)c1ccccc1 |t:16|
Show InChI InChI=1S/C18H16N4O6S/c1-3-28-17(25)13-10-19-18(29(26,27)12-7-5-4-6-8-12)20-15(13)21-22-14(23)9-11(2)16(22)24/h4-10H,3H2,1-2H3,(H,19,20,21)
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n/an/a 1.00E+4n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090438
PNG
(2-(3,5-Dimethyl-pyrazol-1-yl)-4-(3-methyl-2,5-diox...)
Show SMILES CCOC(=O)c1cnc(nc1NN1C(=O)C=C(C)C1=O)-n1nc(C)cc1C |t:16|
Show InChI InChI=1S/C17H18N6O4/c1-5-27-16(26)12-8-18-17(22-11(4)7-10(3)20-22)19-14(12)21-23-13(24)6-9(2)15(23)25/h6-8H,5H2,1-4H3,(H,18,19,21)
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CHEMBL
PC cid
PC sid
UniChem
PubMed
n/an/a 1.00E+4n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090413
PNG
(2-Ethyl-4-[methyl-(3-methyl-2,5-dioxo-2,5-dihydro-...)
Show SMILES CCOC(=O)c1cnc(CC)nc1N(C)N1C(=O)C=C(C)C1=O |t:19|
Show InChI InChI=1S/C15H18N4O4/c1-5-11-16-8-10(15(22)23-6-2)13(17-11)18(4)19-12(20)7-9(3)14(19)21/h7-8H,5-6H2,1-4H3
PDB

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UniProtKB/SwissProt

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GoogleScholar
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CHEMBL
PC cid
PC sid
UniChem
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n/an/a 1.00E+4n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090416
PNG
(2-Ethyl-4-(3-methyl-2,5-dioxo-2,5-dihydro-pyrrol-1...)
Show SMILES CCOC(=O)c1cnc(CC)nc1NN1C(=O)C=C(C)C1=O |t:18|
Show InChI InChI=1S/C14H16N4O4/c1-4-10-15-7-9(14(21)22-5-2)12(16-10)17-18-11(19)6-8(3)13(18)20/h6-7H,4-5H2,1-3H3,(H,15,16,17)
PDB

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UniProtKB/SwissProt

antibodypedia
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PC sid
UniChem
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n/an/a 1.00E+4n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090418
PNG
(4-(3-Methyl-2,5-dioxo-2,5-dihydro-pyrrol-1-ylamino...)
Show SMILES CCOC(=O)c1cnc(Oc2ccccc2)nc1NN1C(=O)C=C(C)C1=O |t:24|
Show InChI InChI=1S/C18H16N4O5/c1-3-26-17(25)13-10-19-18(27-12-7-5-4-6-8-12)20-15(13)21-22-14(23)9-11(2)16(22)24/h4-10H,3H2,1-2H3,(H,19,20,21)
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n/an/a 1.50E+4n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090448
PNG
(2-Methyl-4-(3-methyl-2,5-dioxo-2,5-dihydro-pyrrol-...)
Show SMILES CCOC(=O)c1cnc(C)nc1NN1C(=O)C=C(C)C1=O |t:17|
Show InChI InChI=1S/C13H14N4O4/c1-4-21-13(20)9-6-14-8(3)15-11(9)16-17-10(18)5-7(2)12(17)19/h5-6H,4H2,1-3H3,(H,14,15,16)
PDB

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n/an/a 1.60E+4n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair
Proto-oncogene c-JUN/protein c-fos


(Homo sapiens (Human))
BDBM50090412
PNG
(4-(2,5-Dioxo-3-phenyl-2,5-dihydro-pyrrol-1-ylamino...)
Show SMILES CCOC(=O)c1cnc(nc1NN1C(=O)C=C(C1=O)c1ccccc1)C(F)(F)F |c:16|
Show InChI InChI=1S/C18H13F3N4O4/c1-2-29-16(28)12-9-22-17(18(19,20)21)23-14(12)24-25-13(26)8-11(15(25)27)10-6-4-3-5-7-10/h3-9H,2H2,1H3,(H,22,23,24)
PDB

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UniProtKB/SwissProt

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GoogleScholar
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UniChem
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n/an/a 2.00E+4n/an/an/an/an/an/a



Signal Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of AP-1 (activator protein-1) mediated transcriptional activation in Jurkat T-cells


Bioorg Med Chem Lett 10: 1645-8 (2000)


BindingDB Entry DOI: 10.7270/Q2F190XH
More data for this
Ligand-Target Pair