Compile Data Set for Download or QSAR

Found 155 hits with Last Name = 'zhang' and Initial = 'xk'   

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
Androgen receptor (Rattus norvegicus (Rat))	BDBM78433 (2-[4-[3-[2-(trifluoromethyl)-10-phenothiazinyl]pro...) Show SMILES OCCN1CCN(CCCN2c3ccccc3Sc3ccc(cc23)C(F)(F)F)CC1 Show InChI InChI=1S/C22H26F3N3OS/c23-22(24,25)17-6-7-21-19(16-17)28(18-4-1-2-5-20(18)30-21)9-3-8-26-10-12-27(13-11-26)14-15-29/h1-2,4-7,16,29H,3,8-15H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase DrugBank MCE KEGG PC cid PC sid UniChem Similars	Article PubMed	800	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Scripps Research Institute Curated by ChEMBL					Assay Description Displacement of [3H]mibolerone from rat androgen receptor				Proc Natl Acad Sci USA 104: 11927-32 (2007) Article DOI: 10.1073/pnas.0609752104 BindingDB Entry DOI: 10.7270/Q2MP544F
					More data for this Ligand-Target Pair
Androgen receptor (Rattus norvegicus (Rat))	BDBM82475 (ACETOPHENAZINE | CAS_5714-00-1 | NSC_17676 | med.2...) Show SMILES CC(=O)c1ccc2Sc3ccccc3N(CCCN3CCN(CCO)CC3)c2c1 Show InChI InChI=1S/C23H29N3O2S/c1-18(28)19-7-8-23-21(17-19)26(20-5-2-3-6-22(20)29-23)10-4-9-24-11-13-25(14-12-24)15-16-27/h2-3,5-8,17,27H,4,9-16H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase DrugBank MCE PC cid PC sid UniChem Patents Similars	Article PubMed	800	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Scripps Research Institute Curated by ChEMBL					Assay Description Displacement of [3H]mibolerone from rat androgen receptor				Proc Natl Acad Sci USA 104: 11927-32 (2007) Article DOI: 10.1073/pnas.0609752104 BindingDB Entry DOI: 10.7270/Q2MP544F
					More data for this Ligand-Target Pair
Androgen receptor (Rattus norvegicus (Rat))	BDBM50346422 (10-(3-(4-hydroxypiperidin-1-yl)propyl)-10H-phenoth...) Show SMILES OC1CCN(CCCN2c3ccccc3Sc3ccc(cc23)C#N)CC1 Show InChI InChI=1S/C21H23N3OS/c22-15-16-6-7-21-19(14-16)24(18-4-1-2-5-20(18)26-21)11-3-10-23-12-8-17(25)9-13-23/h1-2,4-7,14,17,25H,3,8-13H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE PC cid PC sid UniChem Similars	Article PubMed	3.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Scripps Research Institute Curated by ChEMBL					Assay Description Displacement of [3H]mibolerone from rat androgen receptor				Proc Natl Acad Sci USA 104: 11927-32 (2007) Article DOI: 10.1073/pnas.0609752104 BindingDB Entry DOI: 10.7270/Q2MP544F
					More data for this Ligand-Target Pair
Retinoic acid receptor gamma (Mus musculus)	BDBM31883 (9-cis-retinoic acid (9cRA) | ALL-TRANS-RETINOIC AC...) Show SMILES C\C(\C=C\C1=C(C)CCCC1(C)C)=C/C=C/C(/C)=C/C(O)=O |c:4| Show InChI InChI=1S/C20H28O2/c1-15(8-6-9-16(2)14-19(21)22)11-12-18-17(3)10-7-13-20(18,4)5/h6,8-9,11-12,14H,7,10,13H2,1-5H3,(H,21,22)/b9-6+,12-11+,15-8+,16-14+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG MMDB PC cid PC sid UniChem Patents Similars	MMDB PubMed	n/a	n/a	4	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of binding to murine Retinoic acid receptor RAR gamma				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair
Retinoic acid receptor beta (Mus musculus)	BDBM31883 (9-cis-retinoic acid (9cRA) | ALL-TRANS-RETINOIC AC...) Show SMILES C\C(\C=C\C1=C(C)CCCC1(C)C)=C/C=C/C(/C)=C/C(O)=O |c:4| Show InChI InChI=1S/C20H28O2/c1-15(8-6-9-16(2)14-19(21)22)11-12-18-17(3)10-7-13-20(18,4)5/h6,8-9,11-12,14H,7,10,13H2,1-5H3,(H,21,22)/b9-6+,12-11+,15-8+,16-14+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG MMDB PC cid PC sid UniChem Patents Similars	MMDB PubMed	n/a	n/a	5	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of murine Retinoic acid receptor RAR beta				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair
Retinoic acid receptor alpha (Mus musculus)	BDBM31883 (9-cis-retinoic acid (9cRA) | ALL-TRANS-RETINOIC AC...) Show SMILES C\C(\C=C\C1=C(C)CCCC1(C)C)=C/C=C/C(/C)=C/C(O)=O |c:4| Show InChI InChI=1S/C20H28O2/c1-15(8-6-9-16(2)14-19(21)22)11-12-18-17(3)10-7-13-20(18,4)5/h6,8-9,11-12,14H,7,10,13H2,1-5H3,(H,21,22)/b9-6+,12-11+,15-8+,16-14+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG MMDB PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	5	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of murine Retinoic acid receptor RAR alpha				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair
Retinoic acid receptor RXR-alpha (Homo sapiens (Human))	BDBM50151228 (6-[Cyclopropylidene-(5,5,8,8-tetramethyl-3-propoxy...) Show SMILES [#6]-[#6]-[#6]-[#8]-c1cc2c(cc1\[#6](=[#6]-1\[#6]-[#6]-1)-c1ccc(cn1)-[#6](-[#8])=O)C([#6])([#6])[#6]-[#6]C2([#6])[#6] Show InChI InChI=1S/C27H33NO3/c1-6-13-31-23-15-21-20(26(2,3)11-12-27(21,4)5)14-19(23)24(17-7-8-17)22-10-9-18(16-28-22)25(29)30/h9-10,14-16H,6-8,11-13H2,1-5H3,(H,29,30)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6	n/a	n/a	n/a	n/a	n/a	n/a
Institute Curated by ChEMBL					Assay Description Inhibition of [3H]-9-cis-retinoic acid binding to human retinoid X receptor alpha ligand-binding domain expressed in E. coli				J Med Chem 47: 4360-72 (2004) Article DOI: 10.1021/jm030651g BindingDB Entry DOI: 10.7270/Q24749B0
					More data for this Ligand-Target Pair
Retinoic acid receptor beta (Mus musculus)	BDBM50031460 ((2E,4E,6E)-8-[3-Ethyl-2-isopropyl-cyclohex-2-en-(E...) Show SMILES CCC1=C(C(C)C)\C(CCC1)=C\C(\C)=C\C=C\C(\C)=C\C(O)=O |c:2| Show InChI InChI=1S/C21H30O2/c1-6-18-11-8-12-19(21(18)15(2)3)13-16(4)9-7-10-17(5)14-20(22)23/h7,9-10,13-15H,6,8,11-12H2,1-5H3,(H,22,23)/b10-7+,16-9+,17-14+,19-13+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	6	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of murine Retinoic acid receptor RAR beta				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair
Retinoic acid receptor beta (Mus musculus)	BDBM50031458 ((2Z,5E)-7-Methyl-3-[(E)-2-(2,6,6-trimethyl-cyclohe...) Show SMILES CCC(C)\C=C\C\C(\C=C\C1=C(C)CCCC1(C)C)=C\C(O)=O |c:10| Show InChI InChI=1S/C21H32O2/c1-6-16(2)9-7-11-18(15-20(22)23)12-13-19-17(3)10-8-14-21(19,4)5/h7,9,12-13,15-16H,6,8,10-11,14H2,1-5H3,(H,22,23)/b9-7+,13-12+,18-15-	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	8	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of murine Retinoic acid receptor RAR beta				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair
Retinoic acid receptor gamma (Mus musculus)	BDBM50031460 ((2E,4E,6E)-8-[3-Ethyl-2-isopropyl-cyclohex-2-en-(E...) Show SMILES CCC1=C(C(C)C)\C(CCC1)=C\C(\C)=C\C=C\C(\C)=C\C(O)=O |c:2| Show InChI InChI=1S/C21H30O2/c1-6-18-11-8-12-19(21(18)15(2)3)13-16(4)9-7-10-17(5)14-20(22)23/h7,9-10,13-15H,6,8,11-12H2,1-5H3,(H,22,23)/b10-7+,16-9+,17-14+,19-13+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	10	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of binding to murine Retinoic acid receptor RAR gamma				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair
Retinoic acid receptor RXR-alpha (Homo sapiens (Human))	BDBM50151230 (6-[(3-Butoxy-5,5,8,8-tetramethyl-5,6,7,8-tetrahydr...) Show SMILES [#6]-[#6]-[#6]-[#6]-[#8]-c1cc2c(cc1\[#6](=[#6]-1\[#6]-[#6]-1)-c1ccc(cn1)-[#6](-[#8])=O)C([#6])([#6])[#6]-[#6]C2([#6])[#6] Show InChI InChI=1S/C28H35NO3/c1-6-7-14-32-24-16-22-21(27(2,3)12-13-28(22,4)5)15-20(24)25(18-8-9-18)23-11-10-19(17-29-23)26(30)31/h10-11,15-17H,6-9,12-14H2,1-5H3,(H,30,31)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	10	n/a	n/a	n/a	n/a	n/a	n/a
Institute Curated by ChEMBL					Assay Description Inhibition of [3H]-9-cis-retinoic acid binding to human retinoid X receptor alpha ligand-binding domain expressed in E. coli				J Med Chem 47: 4360-72 (2004) Article DOI: 10.1021/jm030651g BindingDB Entry DOI: 10.7270/Q24749B0
					More data for this Ligand-Target Pair
Retinoic acid receptor alpha (Mus musculus)	BDBM50031460 ((2E,4E,6E)-8-[3-Ethyl-2-isopropyl-cyclohex-2-en-(E...) Show SMILES CCC1=C(C(C)C)\C(CCC1)=C\C(\C)=C\C=C\C(\C)=C\C(O)=O |c:2| Show InChI InChI=1S/C21H30O2/c1-6-18-11-8-12-19(21(18)15(2)3)13-16(4)9-7-10-17(5)14-20(22)23/h7,9-10,13-15H,6,8,11-12H2,1-5H3,(H,22,23)/b10-7+,16-9+,17-14+,19-13+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	11	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of murine Retinoic acid receptor RAR alpha				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair
Retinoic acid receptor RXR-alpha (Homo sapiens (Human))	BDBM50151229 (4-[Cyclopropylidene-(3,5,5,8,8-pentamethyl-5,6,7,8...) Show SMILES [#6]-c1cc2c(cc1\[#6](=[#6]-1\[#6]-[#6]-1)-c1ccc(cc1)-[#6](-[#8])=O)C([#6])([#6])[#6]-[#6]C2([#6])[#6] Show InChI InChI=1S/C26H30O2/c1-16-14-21-22(26(4,5)13-12-25(21,2)3)15-20(16)23(17-6-7-17)18-8-10-19(11-9-18)24(27)28/h8-11,14-15H,6-7,12-13H2,1-5H3,(H,27,28)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	21	n/a	n/a	n/a	n/a	n/a	n/a
Institute Curated by ChEMBL					Assay Description Inhibition of [3H]-9-cis-retinoic acid binding to human retinoid X receptor alpha ligand-binding domain expressed in E. coli				J Med Chem 47: 4360-72 (2004) Article DOI: 10.1021/jm030651g BindingDB Entry DOI: 10.7270/Q24749B0
					More data for this Ligand-Target Pair
Retinoic acid receptor RXR-alpha (Homo sapiens (Human))	BDBM31892 (9-cis retinoic acid | 9C-RA | CHEMBL705 | Panretin...) Show SMILES C\C(\C=C\C1=C(C)CCCC1(C)C)=C\C=C\C(\C)=C\C(O)=O |c:4| Show InChI InChI=1S/C20H28O2/c1-15(8-6-9-16(2)14-19(21)22)11-12-18-17(3)10-7-13-20(18,4)5/h6,8-9,11-12,14H,7,10,13H2,1-5H3,(H,21,22)/b9-6+,12-11+,15-8-,16-14+	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	DrugBank MMDB PDB Article PubMed	n/a	n/a	29	n/a	n/a	n/a	n/a	n/a	n/a
Institute Curated by ChEMBL					Assay Description Inhibition of [3H]-9-cis-retinoic acid binding to human retinoid X receptor alpha ligand-binding domain expressed in E. coli				J Med Chem 47: 4360-72 (2004) Article DOI: 10.1021/jm030651g BindingDB Entry DOI: 10.7270/Q24749B0
					More data for this Ligand-Target Pair				3D Structure (crystal)
Retinoic acid receptor alpha (Mus musculus)	BDBM50031458 ((2Z,5E)-7-Methyl-3-[(E)-2-(2,6,6-trimethyl-cyclohe...) Show SMILES CCC(C)\C=C\C\C(\C=C\C1=C(C)CCCC1(C)C)=C\C(O)=O |c:10| Show InChI InChI=1S/C21H32O2/c1-6-16(2)9-7-11-18(15-20(22)23)12-13-19-17(3)10-8-14-21(19,4)5/h7,9,12-13,15-16H,6,8,10-11,14H2,1-5H3,(H,22,23)/b9-7+,13-12+,18-15-	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	31	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of murine Retinoic acid receptor RAR alpha				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair
Retinoic acid receptor gamma (Mus musculus)	BDBM50031458 ((2Z,5E)-7-Methyl-3-[(E)-2-(2,6,6-trimethyl-cyclohe...) Show SMILES CCC(C)\C=C\C\C(\C=C\C1=C(C)CCCC1(C)C)=C\C(O)=O |c:10| Show InChI InChI=1S/C21H32O2/c1-6-16(2)9-7-11-18(15-20(22)23)12-13-19-17(3)10-8-14-21(19,4)5/h7,9,12-13,15-16H,6,8,10-11,14H2,1-5H3,(H,22,23)/b9-7+,13-12+,18-15-	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	60	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of binding to murine Retinoic acid receptor RAR gamma				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair
Retinoic acid receptor RXR-alpha (Mus musculus)	BDBM50031458 ((2Z,5E)-7-Methyl-3-[(E)-2-(2,6,6-trimethyl-cyclohe...) Show SMILES CCC(C)\C=C\C\C(\C=C\C1=C(C)CCCC1(C)C)=C\C(O)=O |c:10| Show InChI InChI=1S/C21H32O2/c1-6-16(2)9-7-11-18(15-20(22)23)12-13-19-17(3)10-8-14-21(19,4)5/h7,9,12-13,15-16H,6,8,10-11,14H2,1-5H3,(H,22,23)/b9-7+,13-12+,18-15-	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	73	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of binding to murine Retinoid X receptor RXR alpha				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair
Retinoic acid receptor RXR-gamma (Mus musculus)	BDBM50031458 ((2Z,5E)-7-Methyl-3-[(E)-2-(2,6,6-trimethyl-cyclohe...) Show SMILES CCC(C)\C=C\C\C(\C=C\C1=C(C)CCCC1(C)C)=C\C(O)=O |c:10| Show InChI InChI=1S/C21H32O2/c1-6-16(2)9-7-11-18(15-20(22)23)12-13-19-17(3)10-8-14-21(19,4)5/h7,9,12-13,15-16H,6,8,10-11,14H2,1-5H3,(H,22,23)/b9-7+,13-12+,18-15-	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	85	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of binding to murine Retinoid X receptor RXR gamma				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair
Retinoic acid receptor RXR-beta (Mus musculus)	BDBM50031458 ((2Z,5E)-7-Methyl-3-[(E)-2-(2,6,6-trimethyl-cyclohe...) Show SMILES CCC(C)\C=C\C\C(\C=C\C1=C(C)CCCC1(C)C)=C\C(O)=O |c:10| Show InChI InChI=1S/C21H32O2/c1-6-16(2)9-7-11-18(15-20(22)23)12-13-19-17(3)10-8-14-21(19,4)5/h7,9,12-13,15-16H,6,8,10-11,14H2,1-5H3,(H,22,23)/b9-7+,13-12+,18-15-	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	117	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of binding to murine Retinoid X receptor RXR beta				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair
Retinoic acid receptor RXR-alpha (Homo sapiens (Human))	BDBM50151231 (4-[Cyclopropylidene-(5,5,8,8-tetramethyl-3-propoxy...) Show SMILES [#6]-[#6]-[#6]-[#8]-c1cc2c(cc1\[#6](=[#6]-1\[#6]-[#6]-1)-c1ccc(cc1)-[#6](-[#8])=O)C([#6])([#6])[#6]-[#6]C2([#6])[#6] Show InChI InChI=1S/C28H34O3/c1-6-15-31-24-17-23-22(27(2,3)13-14-28(23,4)5)16-21(24)25(18-7-8-18)19-9-11-20(12-10-19)26(29)30/h9-12,16-17H,6-8,13-15H2,1-5H3,(H,29,30)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	120	n/a	n/a	n/a	n/a	n/a	n/a
Institute Curated by ChEMBL					Assay Description Inhibition of [3H]-9-cis-retinoic acid binding to human retinoid X receptor alpha ligand-binding domain expressed in E. coli				J Med Chem 47: 4360-72 (2004) Article DOI: 10.1021/jm030651g BindingDB Entry DOI: 10.7270/Q24749B0
					More data for this Ligand-Target Pair
Androgen receptor (Homo sapiens (Human))	BDBM50376214 (CHEMBL263660) Show SMILES FC(F)(F)c1ccc2Sc3ccccc3N(CC(=O)c3cccc4ccccc34)c2c1 Show InChI InChI=1S/C25H16F3NOS/c26-25(27,28)17-12-13-24-21(14-17)29(20-10-3-4-11-23(20)31-24)15-22(30)19-9-5-7-16-6-1-2-8-18(16)19/h1-14H,15H2	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	250	n/a	n/a	n/a	n/a	n/a	n/a
The Scripps Research Institute Curated by ChEMBL					Assay Description Inhibition of wild type androgen receptor expressed in CV1 cells assessed as dihydrotestosterone-stimulated transactivation by CAT reporter gene assa...				Proc Natl Acad Sci USA 104: 11927-32 (2007) Article DOI: 10.1073/pnas.0609752104 BindingDB Entry DOI: 10.7270/Q2MP544F
					More data for this Ligand-Target Pair
Retinoic acid receptor RXR-alpha (Homo sapiens (Human))	BDBM50151227 (4-[(3-Butoxy-5,5,8,8-tetramethyl-5,6,7,8-tetrahydr...) Show SMILES [#6]-[#6]-[#6]-[#6]-[#8]-c1cc2c(cc1\[#6](=[#6]-1\[#6]-[#6]-1)-c1ccc(cc1)-[#6](-[#8])=O)C([#6])([#6])[#6]-[#6]C2([#6])[#6] Show InChI InChI=1S/C29H36O3/c1-6-7-16-32-25-18-24-23(28(2,3)14-15-29(24,4)5)17-22(25)26(19-8-9-19)20-10-12-21(13-11-20)27(30)31/h10-13,17-18H,6-9,14-16H2,1-5H3,(H,30,31)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	270	n/a	n/a	n/a	n/a	n/a	n/a
Institute Curated by ChEMBL					Assay Description Inhibition of [3H]-9-cis-retinoic acid binding to human retinoid X receptor alpha ligand-binding domain expressed in E. coli				J Med Chem 47: 4360-72 (2004) Article DOI: 10.1021/jm030651g BindingDB Entry DOI: 10.7270/Q24749B0
					More data for this Ligand-Target Pair
Retinoic acid receptor beta (Mus musculus)	BDBM50407395 (CHEMBL2111557) Show SMILES CCC1=C(C(C)C)\C(CCC1)=C\C(\C)=C/C=C/C=C/C(=C/C)/C(O)=O |c:2| Show InChI InChI=1S/C23H32O2/c1-6-19-14-11-15-21(22(19)17(3)4)16-18(5)12-9-8-10-13-20(7-2)23(24)25/h7-10,12-13,16-17H,6,11,14-15H2,1-5H3,(H,24,25)/b9-8+,13-10+,18-12-,20-7-,21-16+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	371	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of murine Retinoic acid receptor RAR beta				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 11 [205-593] (Homo sapiens (Human))	BDBM25127 ((2E)-3-{3-chloro-4-[3-(3,3-dimethylbut-1-yn-1-yl)-...) Show SMILES CC(C)(C)C#Cc1cc(ccc1O)-c1ccc(\C=C\C(O)=O)cc1Cl Show InChI InChI=1S/C21H19ClO3/c1-21(2,3)11-10-16-13-15(6-8-19(16)23)17-7-4-14(12-18(17)22)5-9-20(24)25/h4-9,12-13,23H,1-3H3,(H,24,25)/b9-5+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	450	n/a	n/a	n/a	n/a	6.0	30
Burnham Institute for Medical Research					Assay Description The phosphatase-catalyzed hydrolysis of 6,8-difluoro-4-methylumbelliferyl phosphate was assayed in the presence of each test compound. The fluorescen...				J Med Chem 51: 5650-62 (2008) Article DOI: 10.1021/jm800456k BindingDB Entry DOI: 10.7270/Q24T6GNQ
					More data for this Ligand-Target Pair
Retinoic acid receptor RXR-alpha (Homo sapiens (Human))	BDBM50151226 (4-[(3-Butyl-5,5,8,8-tetramethyl-5,6,7,8-tetrahydro...) Show SMILES [#6]-[#6]-[#6]-[#6]-c1cc2c(cc1\[#6](=[#6]-1\[#6]-[#6]-1)-c1ccc(cc1)-[#6](-[#8])=O)C([#6])([#6])[#6]-[#6]C2([#6])[#6] Show InChI InChI=1S/C29H36O2/c1-6-7-8-22-17-24-25(29(4,5)16-15-28(24,2)3)18-23(22)26(19-9-10-19)20-11-13-21(14-12-20)27(30)31/h11-14,17-18H,6-10,15-16H2,1-5H3,(H,30,31)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	500	n/a	n/a	n/a	n/a	n/a	n/a
Institute Curated by ChEMBL					Assay Description Inhibition of [3H]-9-cis-retinoic acid binding to human retinoid X receptor alpha ligand-binding domain expressed in E. coli				J Med Chem 47: 4360-72 (2004) Article DOI: 10.1021/jm030651g BindingDB Entry DOI: 10.7270/Q24749B0
					More data for this Ligand-Target Pair
Cellular retinoic acid-binding protein 1 (Gallus gallus)	BDBM31883 (9-cis-retinoic acid (9cRA) | ALL-TRANS-RETINOIC AC...) Show SMILES C\C(\C=C\C1=C(C)CCCC1(C)C)=C/C=C/C(/C)=C/C(O)=O |c:4| Show InChI InChI=1S/C20H28O2/c1-15(8-6-9-16(2)14-19(21)22)11-12-18-17(3)10-7-13-20(18,4)5/h6,8-9,11-12,14H,7,10,13H2,1-5H3,(H,21,22)/b9-6+,12-11+,15-8+,16-14+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG MMDB PC cid PC sid UniChem Patents Similars	MMDB PubMed	n/a	n/a	600	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of binding to chick skin Cytoplasmic retinoic acid binding protein				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair
Retinoic acid receptor RXR-beta (Mus musculus)	BDBM50031457 ((2Z,5E)-3-{(E)-3-[3-Ethyl-2-isopropyl-cyclohex-2-e...) Show SMILES CCC1=C(C(C)C)\C(CCC1)=C\C(\C)=C\C(\C\C(C)=C\C)=C/C(O)=O |c:2| Show InChI InChI=1S/C23H34O2/c1-7-17(5)12-19(15-22(24)25)13-18(6)14-21-11-9-10-20(8-2)23(21)16(3)4/h7,13-16H,8-12H2,1-6H3,(H,24,25)/b17-7+,18-13+,19-15-,21-14+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	640	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of binding to murine Retinoid X receptor RXR beta				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair
Cellular retinoic acid-binding protein 1 (Gallus gallus)	BDBM50031460 ((2E,4E,6E)-8-[3-Ethyl-2-isopropyl-cyclohex-2-en-(E...) Show SMILES CCC1=C(C(C)C)\C(CCC1)=C\C(\C)=C\C=C\C(\C)=C\C(O)=O |c:2| Show InChI InChI=1S/C21H30O2/c1-6-18-11-8-12-19(21(18)15(2)3)13-16(4)9-7-10-17(5)14-20(22)23/h7,9-10,13-15H,6,8,11-12H2,1-5H3,(H,22,23)/b10-7+,16-9+,17-14+,19-13+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	700	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of binding to chick skin Cytoplasmic retinoic acid binding protein				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair
Retinoic acid receptor gamma (Mus musculus)	BDBM50407395 (CHEMBL2111557) Show SMILES CCC1=C(C(C)C)\C(CCC1)=C\C(\C)=C/C=C/C=C/C(=C/C)/C(O)=O |c:2| Show InChI InChI=1S/C23H32O2/c1-6-19-14-11-15-21(22(19)17(3)4)16-18(5)12-9-8-10-13-20(7-2)23(24)25/h7-10,12-13,16-17H,6,11,14-15H2,1-5H3,(H,24,25)/b9-8+,13-10+,18-12-,20-7-,21-16+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	708	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of binding to murine Retinoic acid receptor RAR gamma				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair
Cellular retinoic acid-binding protein 1 (Gallus gallus)	BDBM50031459 ((2Z,4E6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcycloh...) Show SMILES C\C(\C=C\C1=C(C)CCCC1(C)C)=C/C=C/C(/C)=C\C(O)=O |c:4| Show InChI InChI=1S/C20H28O2/c1-15(8-6-9-16(2)14-19(21)22)11-12-18-17(3)10-7-13-20(18,4)5/h6,8-9,11-12,14H,7,10,13H2,1-5H3,(H,21,22)/b9-6+,12-11+,15-8+,16-14-	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars	PDB PubMed	n/a	n/a	900	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of binding to chick skin Cytoplasmic retinoic acid binding protein				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair				3D Structure (crystal)
Retinoic acid receptor alpha (Mus musculus)	BDBM50407395 (CHEMBL2111557) Show SMILES CCC1=C(C(C)C)\C(CCC1)=C\C(\C)=C/C=C/C=C/C(=C/C)/C(O)=O |c:2| Show InChI InChI=1S/C23H32O2/c1-6-19-14-11-15-21(22(19)17(3)4)16-18(5)12-9-8-10-13-20(7-2)23(24)25/h7-10,12-13,16-17H,6,11,14-15H2,1-5H3,(H,24,25)/b9-8+,13-10+,18-12-,20-7-,21-16+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	900	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of murine Retinoic acid receptor RAR alpha				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair
Retinoic acid receptor RXR-alpha (Mus musculus)	BDBM50031460 ((2E,4E,6E)-8-[3-Ethyl-2-isopropyl-cyclohex-2-en-(E...) Show SMILES CCC1=C(C(C)C)\C(CCC1)=C\C(\C)=C\C=C\C(\C)=C\C(O)=O |c:2| Show InChI InChI=1S/C21H30O2/c1-6-18-11-8-12-19(21(18)15(2)3)13-16(4)9-7-10-17(5)14-20(22)23/h7,9-10,13-15H,6,8,11-12H2,1-5H3,(H,22,23)/b10-7+,16-9+,17-14+,19-13+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of binding to murine Retinoid X receptor RXR alpha				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair
Retinoic acid receptor gamma (Mus musculus)	BDBM50031459 ((2Z,4E6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcycloh...) Show SMILES C\C(\C=C\C1=C(C)CCCC1(C)C)=C/C=C/C(/C)=C\C(O)=O |c:4| Show InChI InChI=1S/C20H28O2/c1-15(8-6-9-16(2)14-19(21)22)11-12-18-17(3)10-7-13-20(18,4)5/h6,8-9,11-12,14H,7,10,13H2,1-5H3,(H,21,22)/b9-6+,12-11+,15-8+,16-14-	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars	PDB PubMed	n/a	n/a	>1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of binding to murine Retinoic acid receptor RAR gamma				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair				3D Structure (crystal)
Retinoic acid receptor alpha (Mus musculus)	BDBM50031459 ((2Z,4E6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcycloh...) Show SMILES C\C(\C=C\C1=C(C)CCCC1(C)C)=C/C=C/C(/C)=C\C(O)=O |c:4| Show InChI InChI=1S/C20H28O2/c1-15(8-6-9-16(2)14-19(21)22)11-12-18-17(3)10-7-13-20(18,4)5/h6,8-9,11-12,14H,7,10,13H2,1-5H3,(H,21,22)/b9-6+,12-11+,15-8+,16-14-	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars	PDB PubMed	n/a	n/a	>1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of murine Retinoic acid receptor RAR alpha				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair				3D Structure (crystal)
Retinoic acid receptor RXR-alpha (Mus musculus)	BDBM50407395 (CHEMBL2111557) Show SMILES CCC1=C(C(C)C)\C(CCC1)=C\C(\C)=C/C=C/C=C/C(=C/C)/C(O)=O |c:2| Show InChI InChI=1S/C23H32O2/c1-6-19-14-11-15-21(22(19)17(3)4)16-18(5)12-9-8-10-13-20(7-2)23(24)25/h7-10,12-13,16-17H,6,11,14-15H2,1-5H3,(H,24,25)/b9-8+,13-10+,18-12-,20-7-,21-16+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	>1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of binding to murine Retinoid X receptor RXR alpha				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair
Cellular retinoic acid-binding protein 1 (Gallus gallus)	BDBM50407395 (CHEMBL2111557) Show SMILES CCC1=C(C(C)C)\C(CCC1)=C\C(\C)=C/C=C/C=C/C(=C/C)/C(O)=O |c:2| Show InChI InChI=1S/C23H32O2/c1-6-19-14-11-15-21(22(19)17(3)4)16-18(5)12-9-8-10-13-20(7-2)23(24)25/h7-10,12-13,16-17H,6,11,14-15H2,1-5H3,(H,24,25)/b9-8+,13-10+,18-12-,20-7-,21-16+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of binding to chick skin Cytoplasmic retinoic acid binding protein				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair
Retinoic acid receptor RXR-alpha (Mus musculus)	BDBM50407395 (CHEMBL2111557) Show SMILES CCC1=C(C(C)C)\C(CCC1)=C\C(\C)=C/C=C/C=C/C(=C/C)/C(O)=O |c:2| Show InChI InChI=1S/C23H32O2/c1-6-19-14-11-15-21(22(19)17(3)4)16-18(5)12-9-8-10-13-20(7-2)23(24)25/h7-10,12-13,16-17H,6,11,14-15H2,1-5H3,(H,24,25)/b9-8+,13-10+,18-12-,20-7-,21-16+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	>1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of binding to murine Retinoid X receptor RXR alpha				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair
Retinoic acid receptor alpha (Mus musculus)	BDBM50407395 (CHEMBL2111557) Show SMILES CCC1=C(C(C)C)\C(CCC1)=C\C(\C)=C/C=C/C=C/C(=C/C)/C(O)=O |c:2| Show InChI InChI=1S/C23H32O2/c1-6-19-14-11-15-21(22(19)17(3)4)16-18(5)12-9-8-10-13-20(7-2)23(24)25/h7-10,12-13,16-17H,6,11,14-15H2,1-5H3,(H,24,25)/b9-8+,13-10+,18-12-,20-7-,21-16+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	>1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of murine Retinoic acid receptor RAR alpha				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair
Retinoic acid receptor beta (Mus musculus)	BDBM50031459 ((2Z,4E6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcycloh...) Show SMILES C\C(\C=C\C1=C(C)CCCC1(C)C)=C/C=C/C(/C)=C\C(O)=O |c:4| Show InChI InChI=1S/C20H28O2/c1-15(8-6-9-16(2)14-19(21)22)11-12-18-17(3)10-7-13-20(18,4)5/h6,8-9,11-12,14H,7,10,13H2,1-5H3,(H,21,22)/b9-6+,12-11+,15-8+,16-14-	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem Patents Similars	PDB PubMed	n/a	n/a	>1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of murine Retinoic acid receptor RAR beta				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair				3D Structure (crystal)
Retinoic acid receptor alpha (Mus musculus)	BDBM50031457 ((2Z,5E)-3-{(E)-3-[3-Ethyl-2-isopropyl-cyclohex-2-e...) Show SMILES CCC1=C(C(C)C)\C(CCC1)=C\C(\C)=C\C(\C\C(C)=C\C)=C/C(O)=O |c:2| Show InChI InChI=1S/C23H34O2/c1-7-17(5)12-19(15-22(24)25)13-18(6)14-21-11-9-10-20(8-2)23(21)16(3)4/h7,13-16H,8-12H2,1-6H3,(H,24,25)/b17-7+,18-13+,19-15-,21-14+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.05E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of murine Retinoic acid receptor RAR alpha				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair
Retinoic acid receptor RXR-gamma (Mus musculus)	BDBM50031457 ((2Z,5E)-3-{(E)-3-[3-Ethyl-2-isopropyl-cyclohex-2-e...) Show SMILES CCC1=C(C(C)C)\C(CCC1)=C\C(\C)=C\C(\C\C(C)=C\C)=C/C(O)=O |c:2| Show InChI InChI=1S/C23H34O2/c1-7-17(5)12-19(15-22(24)25)13-18(6)14-21-11-9-10-20(8-2)23(21)16(3)4/h7,13-16H,8-12H2,1-6H3,(H,24,25)/b17-7+,18-13+,19-15-,21-14+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.08E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of binding to murine Retinoid X receptor RXR gamma				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair
Retinoic acid receptor beta (Mus musculus)	BDBM50031457 ((2Z,5E)-3-{(E)-3-[3-Ethyl-2-isopropyl-cyclohex-2-e...) Show SMILES CCC1=C(C(C)C)\C(CCC1)=C\C(\C)=C\C(\C\C(C)=C\C)=C/C(O)=O |c:2| Show InChI InChI=1S/C23H34O2/c1-7-17(5)12-19(15-22(24)25)13-18(6)14-21-11-9-10-20(8-2)23(21)16(3)4/h7,13-16H,8-12H2,1-6H3,(H,24,25)/b17-7+,18-13+,19-15-,21-14+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.13E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of murine Retinoic acid receptor RAR beta				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair
Protein tyrosine phosphatase receptor type C-associated protein (Homo sapiens (Human))	BDBM50212333 (5-[3'-(1-adamantyl)-2-chloro-4'-hydroxy-4-biphenyl...) Show SMILES Oc1ccc(cc1C12CC3CC(CC(C3)C1)C2)-c1ccc(cc1Cl)-c1nnn[nH]1 |TLB:6:7:10:14.13.12,THB:8:9:12:16.7.15,8:7:10.9.14:12,15:7:10:14.13.12,15:13:10:16.8.7| Show InChI InChI=1S/C23H23ClN4O/c24-20-9-17(22-25-27-28-26-22)1-3-18(20)16-2-4-21(29)19(8-16)23-10-13-5-14(11-23)7-15(6-13)12-23/h1-4,8-9,13-15,29H,5-7,10-12H2,(H,25,26,27,28)	KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Burnham Institute for Medical Research Curated by ChEMBL					Assay Description Inhibition of CD45 PTP by fluorescence spectrometry				J Med Chem 50: 2622-39 (2007) Article DOI: 10.1021/jm0613323 BindingDB Entry DOI: 10.7270/Q2XS5V3H
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 11 (Homo sapiens (Human))	BDBM50212333 (5-[3'-(1-adamantyl)-2-chloro-4'-hydroxy-4-biphenyl...) Show SMILES Oc1ccc(cc1C12CC3CC(CC(C3)C1)C2)-c1ccc(cc1Cl)-c1nnn[nH]1 |TLB:6:7:10:14.13.12,THB:8:9:12:16.7.15,8:7:10.9.14:12,15:7:10:14.13.12,15:13:10:16.8.7| Show InChI InChI=1S/C23H23ClN4O/c24-20-9-17(22-25-27-28-26-22)1-3-18(20)16-2-4-21(29)19(8-16)23-10-13-5-14(11-23)7-15(6-13)12-23/h1-4,8-9,13-15,29H,5-7,10-12H2,(H,25,26,27,28)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Burnham Institute for Medical Research Curated by ChEMBL					Assay Description Inhibition of SHP2 PTP by fluorescence spectroscopy				J Med Chem 50: 2622-39 (2007) Article DOI: 10.1021/jm0613323 BindingDB Entry DOI: 10.7270/Q2XS5V3H
					More data for this Ligand-Target Pair
Retinoic acid receptor RXR-alpha (Mus musculus)	BDBM50031457 ((2Z,5E)-3-{(E)-3-[3-Ethyl-2-isopropyl-cyclohex-2-e...) Show SMILES CCC1=C(C(C)C)\C(CCC1)=C\C(\C)=C\C(\C\C(C)=C\C)=C/C(O)=O |c:2| Show InChI InChI=1S/C23H34O2/c1-7-17(5)12-19(15-22(24)25)13-18(6)14-21-11-9-10-20(8-2)23(21)16(3)4/h7,13-16H,8-12H2,1-6H3,(H,24,25)/b17-7+,18-13+,19-15-,21-14+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of binding to murine Retinoid X receptor RXR alpha				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair
Retinoic acid receptor gamma (Mus musculus)	BDBM50031457 ((2Z,5E)-3-{(E)-3-[3-Ethyl-2-isopropyl-cyclohex-2-e...) Show SMILES CCC1=C(C(C)C)\C(CCC1)=C\C(\C)=C\C(\C\C(C)=C\C)=C/C(O)=O |c:2| Show InChI InChI=1S/C23H34O2/c1-7-17(5)12-19(15-22(24)25)13-18(6)14-21-11-9-10-20(8-2)23(21)16(3)4/h7,13-16H,8-12H2,1-6H3,(H,24,25)/b17-7+,18-13+,19-15-,21-14+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.59E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Alabama at Birmingham Curated by ChEMBL					Assay Description Inhibition of binding to murine Retinoic acid receptor RAR gamma				J Med Chem 38: 2302-10 (1995) BindingDB Entry DOI: 10.7270/Q2S181H8
					More data for this Ligand-Target Pair
Retinoic acid receptor RXR-alpha (Homo sapiens (Human))	BDBM50430582 (CHEMBL2337792) Show SMILES CC(C)c1ccc(\C=C2/C=C(CC(O)=O)c3cc(F)ccc23)cc1 |t:9| Show InChI InChI=1S/C21H19FO2/c1-13(2)15-5-3-14(4-6-15)9-16-10-17(11-21(23)24)20-12-18(22)7-8-19(16)20/h3-10,12-13H,11H2,1-2H3,(H,23,24)/b16-9+	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
Xiamen University Curated by ChEMBL					Assay Description Displacement of [3H]-9-cis-RA from human GST-tagged N-terminal truncated RXRalpha after 1 hr by liquid scintillation counting				Eur J Med Chem 62: 632-48 (2013) Article DOI: 10.1016/j.ejmech.2013.01.012 BindingDB Entry DOI: 10.7270/Q2J104JR
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 11 [205-593] (Homo sapiens (Human))	BDBM25124 ((2E)-3-{4-[3-(adamantan-1-yl)-4-aminophenyl]-3-chl...) Show SMILES Nc1ccc(cc1C12CC3CC(CC(C3)C1)C2)-c1ccc(\C=C\C(O)=O)cc1Cl |TLB:14:9:16:13.12.15,14:13:9.10.8:16,THB:12:11:8:13.14.15,12:13:8:11.10.16| Show InChI InChI=1S/C25H26ClNO2/c26-22-10-15(2-6-24(28)29)1-4-20(22)19-3-5-23(27)21(11-19)25-12-16-7-17(13-25)9-18(8-16)14-25/h1-6,10-11,16-18H,7-9,12-14,27H2,(H,28,29)/b6-2+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.83E+3	n/a	n/a	n/a	n/a	6.0	30
Burnham Institute for Medical Research					Assay Description The phosphatase-catalyzed hydrolysis of 6,8-difluoro-4-methylumbelliferyl phosphate was assayed in the presence of each test compound. The fluorescen...				J Med Chem 51: 5650-62 (2008) Article DOI: 10.1021/jm800456k BindingDB Entry DOI: 10.7270/Q24T6GNQ
					More data for this Ligand-Target Pair
Prostaglandin G/H synthase 2 (Homo sapiens (Human))	BDBM50110164 ((Z)-2-(3-(4-(methylthio)benzylidene)-6-fluoro-2-me...) Show SMILES CSc1ccc(\C=C2\C(C)=C(CC(O)=O)c3cc(F)ccc23)cc1 |t:9| Show InChI InChI=1S/C20H17FO2S/c1-12-17(9-13-3-6-15(24-2)7-4-13)16-8-5-14(21)10-19(16)18(12)11-20(22)23/h3-10H,11H2,1-2H3,(H,22,23)/b17-9-	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	1.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of COX-2 (unknown origin) using arachidonic acid as substrate preincubated for 10 mins followed by substrate addition by microplate reader...				Citation and Details Article DOI: 10.1016/j.ejmech.2021.113542 BindingDB Entry DOI: 10.7270/Q2NG4VGG
					More data for this Ligand-Target Pair
Tyrosine-protein phosphatase non-receptor type 11 [205-593] (Homo sapiens (Human))	BDBM25122 ((2E)-3-{4-[3-(adamantan-1-yl)-4-hydroxyphenyl]-3-c...) Show SMILES OC(=O)\C=C\c1ccc(c(Cl)c1)-c1ccc(O)c(c1)C12CC3CC(CC(C3)C1)C2 |TLB:26:21:28:25.24.27,26:25:21.22.20:28,THB:24:23:20:25.26.27,24:25:20:23.22.28| Show InChI InChI=1S/C25H25ClO3/c26-22-10-15(2-6-24(28)29)1-4-20(22)19-3-5-23(27)21(11-19)25-12-16-7-17(13-25)9-18(8-16)14-25/h1-6,10-11,16-18,27H,7-9,12-14H2,(H,28,29)/b6-2+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.10E+3	n/a	n/a	n/a	n/a	6.0	30
Burnham Institute for Medical Research					Assay Description The phosphatase-catalyzed hydrolysis of 6,8-difluoro-4-methylumbelliferyl phosphate was assayed in the presence of each test compound. The fluorescen...				J Med Chem 51: 5650-62 (2008) Article DOI: 10.1021/jm800456k BindingDB Entry DOI: 10.7270/Q24T6GNQ
					More data for this Ligand-Target Pair

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