Compile Data Set for Download or QSAR

Found 3287 hits with Last Name = 'ericsson' and Initial = 'a'   

Target/Host (Institution)	Ligand	Target/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	pH	Temp °C
Isocitrate dehydrogenase [NADP] cytoplasmic (Homo sapiens (Human))	BDBM383860 (US10280150, Cmpd No I-143 | US10550099, Compound I...) Show SMILES COc1cc2[nH]c(=O)c(cc2cc1Cl)[C@H](C)Nc1ncc(C#N)c(OC)n1 |r| Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1	n/a	n/a	n/a	n/a	n/a	n/a
Forma Therapeutics, Inc. Curated by ChEMBL					Assay Description Inhibition of human Myc-DDK-tagged IDH1 R132H mutant expressed in human U87MG cells assessed as reduction in 2-HG levels after 24 hrs by RapidFire hi...				J Med Chem 62: 6575-6596 (2019) Article DOI: 10.1021/acs.jmedchem.9b00362 BindingDB Entry DOI: 10.7270/Q2VD72TR
					More data for this Ligand-Target Pair
Isocitrate dehydrogenase [NADP] cytoplasmic (Homo sapiens (Human))	BDBM50503280 (CHEMBL4469055 | US11311527, Cpd ID I-26 | US113762...) Show SMILES C[C@H](Nc1ccc(C#N)n(C)c1=O)c1cc2cc(Cl)c(O[C@H](C)c3ccccn3)cc2[nH]c1=O |r| Show InChI InChI=1S/C25H22ClN5O3/c1-14(29-21-8-7-17(13-27)31(3)25(21)33)18-10-16-11-19(26)23(12-22(16)30-24(18)32)34-15(2)20-6-4-5-9-28-20/h4-12,14-15,29H,1-3H3,(H,30,32)/t14-,15+/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	<2	n/a	n/a	n/a	n/a	n/a	n/a
FORMA Therapeutics, Inc. Curated by ChEMBL					Assay Description Inhibition of IDH1 R132C mutant in human HCT116 cells assessed as reduction in 2-HG levels after 24 hrs by RapidFire high-throughput mass spectrometr...				J Med Chem 63: 1612-1623 (2020) Article DOI: 10.1021/acs.jmedchem.9b01423 BindingDB Entry DOI: 10.7270/Q2J106F7
					More data for this Ligand-Target Pair
Isocitrate dehydrogenase [NADP] cytoplasmic (Homo sapiens (Human))	BDBM50503263 (CHEMBL4464313 | US11311527, Cpd ID I-23 | US113762...) Show SMILES C[C@H](Nc1ccc(C#N)n(C)c1=O)c1cc2cc(Cl)c(OCc3ccccn3)cc2[nH]c1=O |r| Show InChI InChI=1S/C24H20ClN5O3/c1-14(28-20-7-6-17(12-26)30(2)24(20)32)18-9-15-10-19(25)22(11-21(15)29-23(18)31)33-13-16-5-3-4-8-27-16/h3-11,14,28H,13H2,1-2H3,(H,29,31)/t14-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	<2	n/a	n/a	n/a	n/a	n/a	n/a
FORMA Therapeutics, Inc. Curated by ChEMBL					Assay Description Inhibition of IDH1 R132H mutant in human HCT116 cells assessed as reduction in 2-HG levels after 24 hrs by RapidFire high-throughput mass spectrometr...				J Med Chem 63: 1612-1623 (2020) Article DOI: 10.1021/acs.jmedchem.9b01423 BindingDB Entry DOI: 10.7270/Q2J106F7
					More data for this Ligand-Target Pair
Isocitrate dehydrogenase [NADP] cytoplasmic (Homo sapiens (Human))	BDBM50503260 (CHEMBL4456610 | US11311527, Cpd ID I-27 | US113762...) Show SMILES C[C@H](Nc1ccc(C#N)n(C)c1=O)c1cc2cc(Cl)c(OCC3CC3)cc2[nH]c1=O |r| Show InChI InChI=1S/C22H21ClN4O3/c1-12(25-18-6-5-15(10-24)27(2)22(18)29)16-7-14-8-17(23)20(30-11-13-3-4-13)9-19(14)26-21(16)28/h5-9,12-13,25H,3-4,11H2,1-2H3,(H,26,28)/t12-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
FORMA Therapeutics, Inc. Curated by ChEMBL					Assay Description Inhibition of IDH1 R132H mutant in human HCT116 cells assessed as reduction in 2-HG levels after 24 hrs by RapidFire high-throughput mass spectrometr...				J Med Chem 63: 1612-1623 (2020) Article DOI: 10.1021/acs.jmedchem.9b01423 BindingDB Entry DOI: 10.7270/Q2J106F7
					More data for this Ligand-Target Pair
Isocitrate dehydrogenase [NADP] cytoplasmic (Homo sapiens (Human))	BDBM50503280 (CHEMBL4469055 | US11311527, Cpd ID I-26 | US113762...) Show SMILES C[C@H](Nc1ccc(C#N)n(C)c1=O)c1cc2cc(Cl)c(O[C@H](C)c3ccccn3)cc2[nH]c1=O |r| Show InChI InChI=1S/C25H22ClN5O3/c1-14(29-21-8-7-17(13-27)31(3)25(21)33)18-10-16-11-19(26)23(12-22(16)30-24(18)32)34-15(2)20-6-4-5-9-28-20/h4-12,14-15,29H,1-3H3,(H,30,32)/t14-,15+/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	<2	n/a	n/a	n/a	n/a	n/a	n/a
FORMA Therapeutics, Inc. Curated by ChEMBL					Assay Description Inhibition of IDH1 R132H mutant in human HCT116 cells assessed as reduction in 2-HG levels after 24 hrs by RapidFire high-throughput mass spectrometr...				J Med Chem 63: 1612-1623 (2020) Article DOI: 10.1021/acs.jmedchem.9b01423 BindingDB Entry DOI: 10.7270/Q2J106F7
					More data for this Ligand-Target Pair
Tyrosine-protein kinase JAK1 (Homo sapiens (Human))	BDBM50426739 (CHEMBL2322135) Show SMILES C1CCC(CC1)c1n[nH]c2cnc3[nH]ccc3c12 Show InChI InChI=1S/C14H16N4/c1-2-4-9(5-3-1)13-12-10-6-7-15-14(10)16-8-11(12)17-18-13/h6-9H,1-5H2,(H,15,16)(H,17,18)	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of JAK1 in human TF1 cells assessed as inhibition of IL6-dependent STAT3 phosphorylation				Bioorg Med Chem Lett 23: 693-8 (2013) Article DOI: 10.1016/j.bmcl.2012.11.108 BindingDB Entry DOI: 10.7270/Q2DN46CT
					More data for this Ligand-Target Pair
Isocitrate dehydrogenase [NADP] cytoplasmic (Homo sapiens (Human))	BDBM383860 (US10280150, Cmpd No I-143 | US10550099, Compound I...) Show SMILES COc1cc2[nH]c(=O)c(cc2cc1Cl)[C@H](C)Nc1ncc(C#N)c(OC)n1 |r| Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
Forma Therapeutics, Inc. Curated by ChEMBL					Assay Description Inhibition of human Myc-DDK-tagged IDH1 R132G mutant expressed in human U87MG cells assessed as reduction in 2-HG levels after 24 hrs by RapidFire hi...				J Med Chem 62: 6575-6596 (2019) Article DOI: 10.1021/acs.jmedchem.9b00362 BindingDB Entry DOI: 10.7270/Q2VD72TR
					More data for this Ligand-Target Pair
Isocitrate dehydrogenase [NADP] cytoplasmic (Homo sapiens (Human))	BDBM383892 (US10280150, Cmpd No I-175 | US10550099, Compound I...) Show SMILES COc1nc(N[C@@H](C)c2cc3cc(Cl)c(OC(C)C)cc3[nH]c2=O)ncc1C#N |r| Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4	n/a	n/a	n/a	n/a	n/a	n/a
Forma Therapeutics, Inc. Curated by ChEMBL					Assay Description Inhibition of IDH1 R132H mutant in human HCT116 cells assessed as reduction in 2-HG levels after 24 hrs by RapidFire high-throughput mass spectrometr...				J Med Chem 62: 6575-6596 (2019) Article DOI: 10.1021/acs.jmedchem.9b00362 BindingDB Entry DOI: 10.7270/Q2VD72TR
					More data for this Ligand-Target Pair
Isocitrate dehydrogenase [NADP] cytoplasmic (Homo sapiens (Human))	BDBM383860 (US10280150, Cmpd No I-143 | US10550099, Compound I...) Show SMILES COc1cc2[nH]c(=O)c(cc2cc1Cl)[C@H](C)Nc1ncc(C#N)c(OC)n1 |r| Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4	n/a	n/a	n/a	n/a	n/a	n/a
Forma Therapeutics, Inc. Curated by ChEMBL					Assay Description Inhibition of human Myc-DDK-tagged IDH1 R132C mutant expressed in human U87MG cells assessed as reduction in 2-HG levels after 24 hrs by RapidFire hi...				J Med Chem 62: 6575-6596 (2019) Article DOI: 10.1021/acs.jmedchem.9b00362 BindingDB Entry DOI: 10.7270/Q2VD72TR
					More data for this Ligand-Target Pair
Tyrosine-protein kinase JAK1 (Homo sapiens (Human))	BDBM50426734 (CHEMBL2322142) Show SMILES C1CCC(CC1)c1cnc2cnc3[nH]ccc3n12 Show InChI InChI=1S/C14H16N4/c1-2-4-10(5-3-1)12-8-16-13-9-17-14-11(18(12)13)6-7-15-14/h6-10,15H,1-5H2	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	4	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Bioresearch Center Curated by ChEMBL					Assay Description Inhibition of JAK1 in human TF1 cells assessed as inhibition of IL6-dependent STAT3 phosphorylation				Bioorg Med Chem Lett 23: 693-8 (2013) Article DOI: 10.1016/j.bmcl.2012.11.108 BindingDB Entry DOI: 10.7270/Q2DN46CT
					More data for this Ligand-Target Pair
Isocitrate dehydrogenase [NADP] cytoplasmic (Homo sapiens (Human))	BDBM50503280 (CHEMBL4469055 | US11311527, Cpd ID I-26 | US113762...) Show SMILES C[C@H](Nc1ccc(C#N)n(C)c1=O)c1cc2cc(Cl)c(O[C@H](C)c3ccccn3)cc2[nH]c1=O |r| Show InChI InChI=1S/C25H22ClN5O3/c1-14(29-21-8-7-17(13-27)31(3)25(21)33)18-10-16-11-19(26)23(12-22(16)30-24(18)32)34-15(2)20-6-4-5-9-28-20/h4-12,14-15,29H,1-3H3,(H,30,32)/t14-,15+/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4	n/a	n/a	n/a	n/a	n/a	n/a
FORMA Therapeutics, Inc. Curated by ChEMBL					Assay Description Inhibition of recombinant human Myc-DDK-tagged IDH1 R132C mutant using alpha-ketoglutarate as substrate preincubated for 15 mins followed by substrat...				J Med Chem 63: 1612-1623 (2020) Article DOI: 10.1021/acs.jmedchem.9b01423 BindingDB Entry DOI: 10.7270/Q2J106F7
					More data for this Ligand-Target Pair
Isocitrate dehydrogenase [NADP] cytoplasmic (Homo sapiens (Human))	BDBM50506480 (CHEMBL4437754 | US11311527, Cpd ID I-20 | US113762...) Show SMILES COc1cc2[nH]c(=O)c(cc2cc1Cl)[C@H](C)Nc1ccc(C#N)n(C)c1=O |r| Show InChI InChI=1S/C19H17ClN4O3/c1-10(22-15-5-4-12(9-21)24(2)19(15)26)13-6-11-7-14(20)17(27-3)8-16(11)23-18(13)25/h4-8,10,22H,1-3H3,(H,23,25)/t10-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4	n/a	n/a	n/a	n/a	n/a	n/a
FORMA Therapeutics, Inc. Curated by ChEMBL					Assay Description Inhibition of IDH1 R132H mutant in human HCT116 cells assessed as reduction in 2-HG levels after 24 hrs by RapidFire high-throughput mass spectrometr...				J Med Chem 63: 1612-1623 (2020) Article DOI: 10.1021/acs.jmedchem.9b01423 BindingDB Entry DOI: 10.7270/Q2J106F7
					More data for this Ligand-Target Pair
Isocitrate dehydrogenase [NADP] cytoplasmic (Homo sapiens (Human))	BDBM383892 (US10280150, Cmpd No I-175 | US10550099, Compound I...) Show SMILES COc1nc(N[C@@H](C)c2cc3cc(Cl)c(OC(C)C)cc3[nH]c2=O)ncc1C#N |r| Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4	n/a	n/a	n/a	n/a	n/a	n/a
Forma Therapeutics, Inc. Curated by ChEMBL					Assay Description Inhibition of human Myc-DDK-tagged IDH1 R132H mutant assessed as reduction in NADPH consumption pre-incubated for 15 mins followed by alpha-ketogluta...				J Med Chem 62: 6575-6596 (2019) Article DOI: 10.1021/acs.jmedchem.9b00362 BindingDB Entry DOI: 10.7270/Q2VD72TR
					More data for this Ligand-Target Pair
Isocitrate dehydrogenase [NADP] cytoplasmic (Homo sapiens (Human))	BDBM383860 (US10280150, Cmpd No I-143 | US10550099, Compound I...) Show SMILES COc1cc2[nH]c(=O)c(cc2cc1Cl)[C@H](C)Nc1ncc(C#N)c(OC)n1 |r| Show InChI	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	5	n/a	n/a	n/a	n/a	n/a	n/a
Forma Therapeutics, Inc. Curated by ChEMBL					Assay Description Inhibition of human Myc-DDK-tagged IDH1 R132L mutant expressed in human U87MG cells assessed as reduction in 2-HG levels after 24 hrs by RapidFire hi...				J Med Chem 62: 6575-6596 (2019) Article DOI: 10.1021/acs.jmedchem.9b00362 BindingDB Entry DOI: 10.7270/Q2VD72TR
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM546787 (US11292791, Example 60 | cis-4-((S)-6-(methoxycarb...) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n([C@@H]3CC[C@@H](CC3)C(O)=O)c(nc21)[C@H](C)Cc1ccccc1 |r,wU:5.5,15.15,18.22,27.31,(-5.67,4.63,;-5.67,6.17,;-7,6.94,;-8.34,6.17,;-7,8.48,;-8.34,9.25,;-9.67,8.48,;-8.34,10.79,;-7,11.56,;-5.67,10.79,;-5.67,9.25,;-4.34,8.48,;-3,9.25,;-3,10.79,;-1.86,11.82,;-.37,11.42,;.03,9.94,;1.51,9.54,;2.6,10.63,;2.2,12.11,;.72,12.51,;4.09,10.23,;5.18,11.32,;4.49,8.74,;-2.49,13.23,;-4.02,13.07,;-4.34,11.56,;-2.09,14.72,;-.6,15.12,;-3.18,15.81,;-2.78,17.29,;-1.29,17.69,;-.89,19.18,;-1.98,20.27,;-3.47,19.87,;-3.87,18.38,)| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547131 (US11292791, Example 404 | US11292791, Example 455 ...) Show SMILES COC1CCCC(C1)n1c(CC(C(O)=O)c2ccccc2)nc2c3CC[C@H](C)N(C(=O)OC)c3ccc12 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547132 (US11292791, Example 405 | US11292791, Example 720) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n(C3CCCC(C3)C(O)=O)c(nc21)C(C)Cc1ccc(F)c(F)c1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547133 (US11292791, Example 406 | US11292791, Example 763) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n(C3CCCC(C3)C(O)=O)c(nc21)C(C)Cc1ccccc1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547134 (US11292791, Example 407 | US11292791, Example 446 ...) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n(C3CCCOC3)c(CC(C(O)=O)c3ccc(C)c(F)c3)nc21 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547135 (US11292791, Example 408) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n(C3CC[C@@H](CC3)C(O)=O)c(Cc3ccc(OC(F)F)c(F)c3)nc21 |r,wU:5.5,18.22,(-6.09,-8.3,;-6.09,-6.76,;-4.76,-5.99,;-3.42,-6.76,;-4.76,-4.45,;-6.09,-3.68,;-7.43,-4.45,;-6.09,-2.14,;-4.76,-1.37,;-3.42,-2.14,;-3.42,-3.68,;-2.09,-4.45,;-.76,-3.68,;-.76,-2.14,;.39,-1.11,;1.87,-1.51,;2.27,-3,;3.76,-3.39,;4.85,-2.3,;4.45,-.82,;2.96,-.42,;6.34,-2.7,;7.43,-1.61,;6.74,-4.19,;-.24,.3,;.53,1.63,;-.24,2.97,;-1.78,2.97,;-2.55,4.3,;-1.78,5.63,;-2.55,6.97,;-4.09,6.97,;-4.86,8.3,;-4.86,5.63,;-.24,5.63,;.53,6.97,;.53,4.3,;-1.77,.14,;-2.09,-1.37,)| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547136 (US11292791, Example 409) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n([C@@H]3CCC[C@H](C3)C(O)=O)c(nc21)C1(CC1)Oc1ccccc1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547137 (US11292791, Example 410) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n([C@@H]3CCC[C@H](C3)C(O)=O)c(Cc3ccc(Cl)c(OC)n3)nc21 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547138 (US11292791, Example 411) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n(C3CCC[C@H](C3)C(O)=O)c(nc21)C(C)Oc1ccccc1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547139 (US11292791, Example 412) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n([C@H]3CC[C@@H](CC3)C(O)=O)c(Cc3ccc(OC(C)C)c(F)c3)nc21 |r,wU:5.5,18.22,wD:15.15,(-6.09,-8.3,;-6.09,-6.76,;-4.76,-5.99,;-3.42,-6.76,;-4.76,-4.45,;-6.09,-3.68,;-7.43,-4.45,;-6.09,-2.14,;-4.76,-1.37,;-3.42,-2.14,;-3.42,-3.68,;-2.09,-4.45,;-.76,-3.68,;-.76,-2.14,;.39,-1.11,;1.87,-1.51,;2.27,-3,;3.76,-3.39,;4.85,-2.3,;4.45,-.82,;2.96,-.42,;6.34,-2.7,;7.43,-1.61,;6.74,-4.19,;-.24,.3,;.53,1.63,;-.24,2.97,;-1.78,2.97,;-2.55,4.3,;-1.78,5.63,;-2.55,6.97,;-4.09,6.97,;-4.86,8.3,;-4.86,5.63,;-.24,5.63,;.53,6.97,;.53,4.3,;-1.77,.14,;-2.09,-1.37,)| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547140 ((1R,3R)-3-[(7S)-2-[(R)-(4-chlorophenyl)(hydroxy)me...) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n(C3CCCC(C3)C(O)=O)c(nc21)C(O)c1ccc(Cl)cn1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547141 (US11292791, Example 414 | US11292791, Example 415) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n(C3CCCC(C3)C(O)=O)c(nc21)C(O)c1ccc(C)c(F)c1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547141 (US11292791, Example 414 | US11292791, Example 415) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n(C3CCCC(C3)C(O)=O)c(nc21)C(O)c1ccc(C)c(F)c1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547143 (US11292791, Example 416 | US11292791, Example 437) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n(C3CCCC(C3)C(O)=O)c(nc21)C(O)c1ccc(OC)c(Cl)c1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547144 (US11292791, Example 417 | US11292791, Example 418) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n(C3CCCC(C3)C(O)=O)c(nc21)C(O)c1cc(F)cc(OC)c1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547144 (US11292791, Example 417 | US11292791, Example 418) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n(C3CCCC(C3)C(O)=O)c(nc21)C(O)c1cc(F)cc(OC)c1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547146 (US11292791, Example 419 | US11292791, Example 460) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n(C3CCCC(C3)C(O)=O)c(nc21)C(O)c1ccc2OCCc2c1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547147 (US11292791, Example 420 | US11292791, Example 438) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n(C3CCCC(C3)C(O)=O)c(nc21)C(O)c1ccc(OC)c(F)c1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547148 (US11292791, Example 421 | US11292791, Example 433) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n(C3CCCC(C3)C(O)=O)c(nc21)C(O)c1cc(Cl)cc(OC)c1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547149 (US11292791, Example 422) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n([C@@H]3CCC[C@H](C3)C(O)=O)c(nc21)C1(CC1)Nc1ccccn1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547150 (US11292791, Example 423 | US11292791, Example 523) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n(C3CCCC(C3)C(O)=O)c(nc21)C(O)c1cccc(Cl)c1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547151 (Intermediate 2-(5-fluoro-2-methoxyphenyl)-2-hydrox...) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n(C3CCCC(C3)C(O)=O)c(nc21)C(O)c1cc(F)ccc1OC |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547152 (US11292791, Example 425 | US11292791, Example 545) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n(C3CCCC(C3)C(O)=O)c(nc21)C(C)C(O)c1ccccc1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547153 (US11292791, Example 426 | US11292791, Example 461) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n(C3CCCC(C3)C(O)=O)c(nc21)C(O)c1cc2CCOc2c(Cl)c1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547154 (US11292791, Example 427 | US11292791, Example 474) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n(C3CCCC(C3)C(O)=O)c(nc21)C(O)c1cc2CCOc2c(F)c1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547155 (US11292791, Example 428 | US11292791, Example 638) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n(C3CCCC(C3)C(O)=O)c(nc21)C(O)c1c(OC)ccc(F)c1F |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547156 (US11292791, Example 429) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n(C3CCC[C@H](C3)C(O)=O)c(nc21)[C@@H](O)c1cc(F)cc2cn[nH]c12 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547157 (US11292791, Example 430 | US11292791, Example 431) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n(C3CCCC(C3)C(O)=O)c(nc21)C(O)c1ccc(OC)cc1Cl |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547157 (US11292791, Example 430 | US11292791, Example 431) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n(C3CCCC(C3)C(O)=O)c(nc21)C(O)c1ccc(OC)cc1Cl |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547159 (US11292791, Example 432 | US11292791, Example 479) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n(C3CCCC(C3)C(O)=O)c(nc21)C(O)c1ccc(F)c(F)c1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547148 (US11292791, Example 421 | US11292791, Example 433) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n(C3CCCC(C3)C(O)=O)c(nc21)C(O)c1cc(Cl)cc(OC)c1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547161 (US11292791, Example 434 | US11292791, Example 448) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n(C3CCCC(C3)C(O)=O)c(nc21)C(O)c1cc(F)cc2cc[nH]c12 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547162 (US11292791, Example 435) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n([C@@H]3CCC[C@H](C3)C(O)=O)c(nc21)C1(CC1)Oc1ccccn1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547163 (US11292791, Example 436 | US11292791, Example 730) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n(C3CCCC(C3)C(O)=O)c(nc21)C(O)Cn1cc(Cl)cn1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547143 (US11292791, Example 416 | US11292791, Example 437) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n(C3CCCC(C3)C(O)=O)c(nc21)C(O)c1ccc(OC)c(Cl)c1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair
CREB-binding protein (Homo sapiens (Human))	BDBM547147 (US11292791, Example 420 | US11292791, Example 438) Show SMILES COC(=O)N1[C@@H](C)CCc2c1ccc1n(C3CCCC(C3)C(O)=O)c(nc21)C(O)c1ccc(OC)c(F)c1 |r| Show InChI	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	5.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description The assay was performed in a final volume of 6 μL in assay buffer containing 50 mM Hepes (pH 7.5, (0.5M Hepes, pH 7.5 solution; Teknova H1575)),...				Citation and Details BindingDB Entry DOI: 10.7270/Q2MG7SQM
					More data for this Ligand-Target Pair

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