Compile Data Set for Download or QSAR

Found 136 hits Enz. Inhib. hit(s) with all data for entry = 9322   

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
Retinoic acid receptor beta (Homo sapiens (Human))	BDBM323588 (Retinoic Acid | US10188615, at-RA | US10752616, Co...) Show SMILES CC(C=CC1=C(C)CCCC1(C)C)=CC=CC(C)=CC(O)=O |w:3.3,13.14,15.16,18.19,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 antibodypedia GoogleScholar AffyNet	Purchase PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	1.88	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor alpha (Homo sapiens (Human))	BDBM323588 (Retinoic Acid | US10188615, at-RA | US10752616, Co...) Show SMILES CC(C=CC1=C(C)CCCC1(C)C)=CC=CC(C)=CC(O)=O |w:3.3,13.14,15.16,18.19,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 PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	1.20	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor gamma (Homo sapiens (Human))	BDBM323588 (Retinoic Acid | US10188615, at-RA | US10752616, Co...) Show SMILES CC(C=CC1=C(C)CCCC1(C)C)=CC=CC(C)=CC(O)=O |w:3.3,13.14,15.16,18.19,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 antibodypedia GoogleScholar AffyNet	Purchase PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	0.900	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor beta (Homo sapiens (Human))	BDBM50526314 (CHEMBL4459692 | US10752616, Code No. BHBA-001) Show SMILES Cc1ccc(C)c2oc(cc12)-c1nc(no1)-c1ccc(cc1)C(O)=O Show InChI InChI=1S/C19H14N2O4/c1-10-3-4-11(2)16-14(10)9-15(24-16)18-20-17(21-25-18)12-5-7-13(8-6-12)19(22)23/h3-9H,1-2H3,(H,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	1.94	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor alpha (Homo sapiens (Human))	BDBM50526314 (CHEMBL4459692 | US10752616, Code No. BHBA-001) Show SMILES Cc1ccc(C)c2oc(cc12)-c1nc(no1)-c1ccc(cc1)C(O)=O Show InChI InChI=1S/C19H14N2O4/c1-10-3-4-11(2)16-14(10)9-15(24-16)18-20-17(21-25-18)12-5-7-13(8-6-12)19(22)23/h3-9H,1-2H3,(H,22,23)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	26	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor gamma (Homo sapiens (Human))	BDBM50526314 (CHEMBL4459692 | US10752616, Code No. BHBA-001) Show SMILES Cc1ccc(C)c2oc(cc12)-c1nc(no1)-c1ccc(cc1)C(O)=O Show InChI InChI=1S/C19H14N2O4/c1-10-3-4-11(2)16-14(10)9-15(24-16)18-20-17(21-25-18)12-5-7-13(8-6-12)19(22)23/h3-9H,1-2H3,(H,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	11	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor beta (Homo sapiens (Human))	BDBM458121 (US10752616, Code No. BHBA-002) Show SMILES Cc1ccc(C)c2oc(cc12)-c1nc(no1)-c1ccc(cc1Cl)C(O)=O Show InChI InChI=1S/C19H13ClN2O4/c1-9-3-4-10(2)16-13(9)8-15(25-16)18-21-17(22-26-18)12-6-5-11(19(23)24)7-14(12)20/h3-8H,1-2H3,(H,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	11.4	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor alpha (Homo sapiens (Human))	BDBM458121 (US10752616, Code No. BHBA-002) Show SMILES Cc1ccc(C)c2oc(cc12)-c1nc(no1)-c1ccc(cc1Cl)C(O)=O Show InChI InChI=1S/C19H13ClN2O4/c1-9-3-4-10(2)16-13(9)8-15(25-16)18-21-17(22-26-18)12-6-5-11(19(23)24)7-14(12)20/h3-8H,1-2H3,(H,23,24)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	136	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor gamma (Homo sapiens (Human))	BDBM458121 (US10752616, Code No. BHBA-002) Show SMILES Cc1ccc(C)c2oc(cc12)-c1nc(no1)-c1ccc(cc1Cl)C(O)=O Show InChI InChI=1S/C19H13ClN2O4/c1-9-3-4-10(2)16-13(9)8-15(25-16)18-21-17(22-26-18)12-6-5-11(19(23)24)7-14(12)20/h3-8H,1-2H3,(H,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	29	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor beta (Homo sapiens (Human))	BDBM458124 (US10752616, Code No. BHBA-003) Show SMILES Cc1ccc(C)c2oc(cc12)-c1nc(no1)-c1ccc(cc1Br)C(O)=O Show InChI InChI=1S/C19H13BrN2O4/c1-9-3-4-10(2)16-13(9)8-15(25-16)18-21-17(22-26-18)12-6-5-11(19(23)24)7-14(12)20/h3-8H,1-2H3,(H,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	16	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor alpha (Homo sapiens (Human))	BDBM458124 (US10752616, Code No. BHBA-003) Show SMILES Cc1ccc(C)c2oc(cc12)-c1nc(no1)-c1ccc(cc1Br)C(O)=O Show InChI InChI=1S/C19H13BrN2O4/c1-9-3-4-10(2)16-13(9)8-15(25-16)18-21-17(22-26-18)12-6-5-11(19(23)24)7-14(12)20/h3-8H,1-2H3,(H,23,24)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	160	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor gamma (Homo sapiens (Human))	BDBM458124 (US10752616, Code No. BHBA-003) Show SMILES Cc1ccc(C)c2oc(cc12)-c1nc(no1)-c1ccc(cc1Br)C(O)=O Show InChI InChI=1S/C19H13BrN2O4/c1-9-3-4-10(2)16-13(9)8-15(25-16)18-21-17(22-26-18)12-6-5-11(19(23)24)7-14(12)20/h3-8H,1-2H3,(H,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	36	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor beta (Homo sapiens (Human))	BDBM458127 (US10752616, Code No. BHBA-004) Show SMILES Cc1ccc(C)c2oc(cc12)-c1nc(no1)-c1ccc(cc1C(F)(F)F)C(O)=O Show InChI InChI=1S/C20H13F3N2O4/c1-9-3-4-10(2)16-13(9)8-15(28-16)18-24-17(25-29-18)12-6-5-11(19(26)27)7-14(12)20(21,22)23/h3-8H,1-2H3,(H,26,27)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	10	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor beta (Homo sapiens (Human))	BDBM458133 (US10752616, Code No. BHBA-005) Show SMILES Cc1ccc(C)c2oc(cc12)-c1nc(no1)-c1ccc(cc1N)C(O)=O Show InChI InChI=1S/C19H15N3O4/c1-9-3-4-10(2)16-13(9)8-15(25-16)18-21-17(22-26-18)12-6-5-11(19(23)24)7-14(12)20/h3-8H,20H2,1-2H3,(H,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	23	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor alpha (Homo sapiens (Human))	BDBM458133 (US10752616, Code No. BHBA-005) Show SMILES Cc1ccc(C)c2oc(cc12)-c1nc(no1)-c1ccc(cc1N)C(O)=O Show InChI InChI=1S/C19H15N3O4/c1-9-3-4-10(2)16-13(9)8-15(25-16)18-21-17(22-26-18)12-6-5-11(19(23)24)7-14(12)20/h3-8H,20H2,1-2H3,(H,23,24)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	130	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor gamma (Homo sapiens (Human))	BDBM458133 (US10752616, Code No. BHBA-005) Show SMILES Cc1ccc(C)c2oc(cc12)-c1nc(no1)-c1ccc(cc1N)C(O)=O Show InChI InChI=1S/C19H15N3O4/c1-9-3-4-10(2)16-13(9)8-15(25-16)18-21-17(22-26-18)12-6-5-11(19(23)24)7-14(12)20/h3-8H,20H2,1-2H3,(H,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	55	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor beta (Homo sapiens (Human))	BDBM50526313 (CHEMBL4469143 | US10752616, Code No. BHBA-006) Show SMILES Cc1cc(ccc1C(O)=O)-c1noc(n1)-c1cc2c(C)ccc(C)c2o1 Show InChI InChI=1S/C20H16N2O4/c1-10-4-5-11(2)17-15(10)9-16(25-17)19-21-18(22-26-19)13-6-7-14(20(23)24)12(3)8-13/h4-9H,1-3H3,(H,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	14	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor alpha (Homo sapiens (Human))	BDBM50526313 (CHEMBL4469143 | US10752616, Code No. BHBA-006) Show SMILES Cc1cc(ccc1C(O)=O)-c1noc(n1)-c1cc2c(C)ccc(C)c2o1 Show InChI InChI=1S/C20H16N2O4/c1-10-4-5-11(2)17-15(10)9-16(25-17)19-21-18(22-26-19)13-6-7-14(20(23)24)12(3)8-13/h4-9H,1-3H3,(H,23,24)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	89	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor gamma (Homo sapiens (Human))	BDBM50526313 (CHEMBL4469143 | US10752616, Code No. BHBA-006) Show SMILES Cc1cc(ccc1C(O)=O)-c1noc(n1)-c1cc2c(C)ccc(C)c2o1 Show InChI InChI=1S/C20H16N2O4/c1-10-4-5-11(2)17-15(10)9-16(25-17)19-21-18(22-26-19)13-6-7-14(20(23)24)12(3)8-13/h4-9H,1-3H3,(H,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	25	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor beta (Homo sapiens (Human))	BDBM50526312 (CHEMBL4449668 | US10752616, Code No. BHBA-007) Show SMILES Cc1ccc(C)c2oc(cc12)-c1nc(no1)-c1ccc(C(O)=O)c(F)c1 Show InChI InChI=1S/C19H13FN2O4/c1-9-3-4-10(2)16-13(9)8-15(25-16)18-21-17(22-26-18)11-5-6-12(19(23)24)14(20)7-11/h3-8H,1-2H3,(H,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	2.20	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor alpha (Homo sapiens (Human))	BDBM50526312 (CHEMBL4449668 | US10752616, Code No. BHBA-007) Show SMILES Cc1ccc(C)c2oc(cc12)-c1nc(no1)-c1ccc(C(O)=O)c(F)c1 Show InChI InChI=1S/C19H13FN2O4/c1-9-3-4-10(2)16-13(9)8-15(25-16)18-21-17(22-26-18)11-5-6-12(19(23)24)14(20)7-11/h3-8H,1-2H3,(H,23,24)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	16	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor gamma (Homo sapiens (Human))	BDBM50526312 (CHEMBL4449668 | US10752616, Code No. BHBA-007) Show SMILES Cc1ccc(C)c2oc(cc12)-c1nc(no1)-c1ccc(C(O)=O)c(F)c1 Show InChI InChI=1S/C19H13FN2O4/c1-9-3-4-10(2)16-13(9)8-15(25-16)18-21-17(22-26-18)11-5-6-12(19(23)24)14(20)7-11/h3-8H,1-2H3,(H,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	8.40	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor beta (Homo sapiens (Human))	BDBM458145 (US10752616, Code No. BHBA-008) Show SMILES Cc1c(oc2c(C)ccc(C)c12)-c1nc(no1)-c1ccc(cc1)C(O)=O Show InChI InChI=1S/C20H16N2O4/c1-10-4-5-11(2)16-15(10)12(3)17(25-16)19-21-18(22-26-19)13-6-8-14(9-7-13)20(23)24/h4-9H,1-3H3,(H,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	1.90	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor alpha (Homo sapiens (Human))	BDBM458145 (US10752616, Code No. BHBA-008) Show SMILES Cc1c(oc2c(C)ccc(C)c12)-c1nc(no1)-c1ccc(cc1)C(O)=O Show InChI InChI=1S/C20H16N2O4/c1-10-4-5-11(2)16-15(10)12(3)17(25-16)19-21-18(22-26-19)13-6-8-14(9-7-13)20(23)24/h4-9H,1-3H3,(H,23,24)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	17	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor gamma (Homo sapiens (Human))	BDBM458145 (US10752616, Code No. BHBA-008) Show SMILES Cc1c(oc2c(C)ccc(C)c12)-c1nc(no1)-c1ccc(cc1)C(O)=O Show InChI InChI=1S/C20H16N2O4/c1-10-4-5-11(2)16-15(10)12(3)17(25-16)19-21-18(22-26-19)13-6-8-14(9-7-13)20(23)24/h4-9H,1-3H3,(H,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	6.80	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor beta (Homo sapiens (Human))	BDBM458150 (US10752616, Code No. BHBA-009) Show SMILES Cc1c(oc2c(C)ccc(C)c12)-c1nc(no1)-c1ccc(cc1Cl)C(O)=O Show InChI InChI=1S/C20H15ClN2O4/c1-9-4-5-10(2)16-15(9)11(3)17(26-16)19-22-18(23-27-19)13-7-6-12(20(24)25)8-14(13)21/h4-8H,1-3H3,(H,24,25)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	4.20	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor alpha (Homo sapiens (Human))	BDBM458150 (US10752616, Code No. BHBA-009) Show SMILES Cc1c(oc2c(C)ccc(C)c12)-c1nc(no1)-c1ccc(cc1Cl)C(O)=O Show InChI InChI=1S/C20H15ClN2O4/c1-9-4-5-10(2)16-15(9)11(3)17(26-16)19-22-18(23-27-19)13-7-6-12(20(24)25)8-14(13)21/h4-8H,1-3H3,(H,24,25)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	32	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor gamma (Homo sapiens (Human))	BDBM458150 (US10752616, Code No. BHBA-009) Show SMILES Cc1c(oc2c(C)ccc(C)c12)-c1nc(no1)-c1ccc(cc1Cl)C(O)=O Show InChI InChI=1S/C20H15ClN2O4/c1-9-4-5-10(2)16-15(9)11(3)17(26-16)19-22-18(23-27-19)13-7-6-12(20(24)25)8-14(13)21/h4-8H,1-3H3,(H,24,25)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	11	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor beta (Homo sapiens (Human))	BDBM458152 (US10752616, Code No. BHBA-010) Show SMILES CC(C)c1ccc(C)c2oc(cc12)-c1nc(no1)-c1ccc(cc1)C(O)=O Show InChI InChI=1S/C21H18N2O4/c1-11(2)15-9-4-12(3)18-16(15)10-17(26-18)20-22-19(23-27-20)13-5-7-14(8-6-13)21(24)25/h4-11H,1-3H3,(H,24,25)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	2.90	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor alpha (Homo sapiens (Human))	BDBM458152 (US10752616, Code No. BHBA-010) Show SMILES CC(C)c1ccc(C)c2oc(cc12)-c1nc(no1)-c1ccc(cc1)C(O)=O Show InChI InChI=1S/C21H18N2O4/c1-11(2)15-9-4-12(3)18-16(15)10-17(26-18)20-22-19(23-27-20)13-5-7-14(8-6-13)21(24)25/h4-11H,1-3H3,(H,24,25)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	25	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor gamma (Homo sapiens (Human))	BDBM458152 (US10752616, Code No. BHBA-010) Show SMILES CC(C)c1ccc(C)c2oc(cc12)-c1nc(no1)-c1ccc(cc1)C(O)=O Show InChI InChI=1S/C21H18N2O4/c1-11(2)15-9-4-12(3)18-16(15)10-17(26-18)20-22-19(23-27-20)13-5-7-14(8-6-13)21(24)25/h4-11H,1-3H3,(H,24,25)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	0.530	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor beta (Homo sapiens (Human))	BDBM458158 (US10752616, Code No. BHBA-011) Show SMILES OC(=O)c1ccc(cc1)-c1noc(n1)-c1cc2c(Cl)ccc(Cl)c2o1 Show InChI InChI=1S/C17H8Cl2N2O4/c18-11-5-6-12(19)14-10(11)7-13(24-14)16-20-15(21-25-16)8-1-3-9(4-2-8)17(22)23/h1-7H,(H,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	4.30	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor alpha (Homo sapiens (Human))	BDBM458158 (US10752616, Code No. BHBA-011) Show SMILES OC(=O)c1ccc(cc1)-c1noc(n1)-c1cc2c(Cl)ccc(Cl)c2o1 Show InChI InChI=1S/C17H8Cl2N2O4/c18-11-5-6-12(19)14-10(11)7-13(24-14)16-20-15(21-25-16)8-1-3-9(4-2-8)17(22)23/h1-7H,(H,22,23)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	26	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor gamma (Homo sapiens (Human))	BDBM458158 (US10752616, Code No. BHBA-011) Show SMILES OC(=O)c1ccc(cc1)-c1noc(n1)-c1cc2c(Cl)ccc(Cl)c2o1 Show InChI InChI=1S/C17H8Cl2N2O4/c18-11-5-6-12(19)14-10(11)7-13(24-14)16-20-15(21-25-16)8-1-3-9(4-2-8)17(22)23/h1-7H,(H,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	14	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor beta (Homo sapiens (Human))	BDBM458165 (US10752616, Code No. BHBA-012) Show SMILES OC(=O)c1ccc(-c2noc(n2)-c2cc3c(Cl)ccc(Cl)c3o2)c(Cl)c1 Show InChI InChI=1S/C17H7Cl3N2O4/c18-10-3-4-11(19)14-9(10)6-13(25-14)16-21-15(22-26-16)8-2-1-7(17(23)24)5-12(8)20/h1-6H,(H,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	17	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor alpha (Homo sapiens (Human))	BDBM458165 (US10752616, Code No. BHBA-012) Show SMILES OC(=O)c1ccc(-c2noc(n2)-c2cc3c(Cl)ccc(Cl)c3o2)c(Cl)c1 Show InChI InChI=1S/C17H7Cl3N2O4/c18-10-3-4-11(19)14-9(10)6-13(25-14)16-21-15(22-26-16)8-2-1-7(17(23)24)5-12(8)20/h1-6H,(H,23,24)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	67	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor gamma (Homo sapiens (Human))	BDBM458165 (US10752616, Code No. BHBA-012) Show SMILES OC(=O)c1ccc(-c2noc(n2)-c2cc3c(Cl)ccc(Cl)c3o2)c(Cl)c1 Show InChI InChI=1S/C17H7Cl3N2O4/c18-10-3-4-11(19)14-9(10)6-13(25-14)16-21-15(22-26-16)8-2-1-7(17(23)24)5-12(8)20/h1-6H,(H,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	17	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor beta (Homo sapiens (Human))	BDBM458201 (US10752616, Code No. BHBA-013) Show SMILES Cc1cc(ccc1C(O)=O)-c1noc(n1)-c1cc2c(Cl)ccc(Cl)c2o1 Show InChI InChI=1S/C18H10Cl2N2O4/c1-8-6-9(2-3-10(8)18(23)24)16-21-17(26-22-16)14-7-11-12(19)4-5-13(20)15(11)25-14/h2-7H,1H3,(H,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	16	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor alpha (Homo sapiens (Human))	BDBM458201 (US10752616, Code No. BHBA-013) Show SMILES Cc1cc(ccc1C(O)=O)-c1noc(n1)-c1cc2c(Cl)ccc(Cl)c2o1 Show InChI InChI=1S/C18H10Cl2N2O4/c1-8-6-9(2-3-10(8)18(23)24)16-21-17(26-22-16)14-7-11-12(19)4-5-13(20)15(11)25-14/h2-7H,1H3,(H,23,24)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	140	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor gamma (Homo sapiens (Human))	BDBM458201 (US10752616, Code No. BHBA-013) Show SMILES Cc1cc(ccc1C(O)=O)-c1noc(n1)-c1cc2c(Cl)ccc(Cl)c2o1 Show InChI InChI=1S/C18H10Cl2N2O4/c1-8-6-9(2-3-10(8)18(23)24)16-21-17(26-22-16)14-7-11-12(19)4-5-13(20)15(11)25-14/h2-7H,1H3,(H,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	110	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor beta (Homo sapiens (Human))	BDBM458233 (US10752616, Code No. BHBA-014) Show SMILES OC(=O)c1ccc(cc1F)-c1noc(n1)-c1cc2c(Cl)ccc(Cl)c2o1 Show InChI InChI=1S/C17H7Cl2FN2O4/c18-10-3-4-11(19)14-9(10)6-13(25-14)16-21-15(22-26-16)7-1-2-8(17(23)24)12(20)5-7/h1-6H,(H,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	2	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor alpha (Homo sapiens (Human))	BDBM458233 (US10752616, Code No. BHBA-014) Show SMILES OC(=O)c1ccc(cc1F)-c1noc(n1)-c1cc2c(Cl)ccc(Cl)c2o1 Show InChI InChI=1S/C17H7Cl2FN2O4/c18-10-3-4-11(19)14-9(10)6-13(25-14)16-21-15(22-26-16)7-1-2-8(17(23)24)12(20)5-7/h1-6H,(H,23,24)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	12	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor gamma (Homo sapiens (Human))	BDBM458233 (US10752616, Code No. BHBA-014) Show SMILES OC(=O)c1ccc(cc1F)-c1noc(n1)-c1cc2c(Cl)ccc(Cl)c2o1 Show InChI InChI=1S/C17H7Cl2FN2O4/c18-10-3-4-11(19)14-9(10)6-13(25-14)16-21-15(22-26-16)7-1-2-8(17(23)24)12(20)5-7/h1-6H,(H,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	11	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor beta (Homo sapiens (Human))	BDBM458240 (US10752616, Code No. BHBA-015) Show SMILES Cc1ccc(Cl)c2oc(cc12)-c1nc(no1)-c1ccc(cc1)C(O)=O Show InChI InChI=1S/C18H11ClN2O4/c1-9-2-7-13(19)15-12(9)8-14(24-15)17-20-16(21-25-17)10-3-5-11(6-4-10)18(22)23/h2-8H,1H3,(H,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	2.90	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor alpha (Homo sapiens (Human))	BDBM458240 (US10752616, Code No. BHBA-015) Show SMILES Cc1ccc(Cl)c2oc(cc12)-c1nc(no1)-c1ccc(cc1)C(O)=O Show InChI InChI=1S/C18H11ClN2O4/c1-9-2-7-13(19)15-12(9)8-14(24-15)17-20-16(21-25-17)10-3-5-11(6-4-10)18(22)23/h2-8H,1H3,(H,22,23)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	23	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor gamma (Homo sapiens (Human))	BDBM458240 (US10752616, Code No. BHBA-015) Show SMILES Cc1ccc(Cl)c2oc(cc12)-c1nc(no1)-c1ccc(cc1)C(O)=O Show InChI InChI=1S/C18H11ClN2O4/c1-9-2-7-13(19)15-12(9)8-14(24-15)17-20-16(21-25-17)10-3-5-11(6-4-10)18(22)23/h2-8H,1H3,(H,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	12	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor beta (Homo sapiens (Human))	BDBM458251 (US10752616, Code No. BHBA-016) Show SMILES Cc1ccc(Cl)c2cc(oc12)-c1nc(no1)-c1ccc(cc1)C(O)=O Show InChI InChI=1S/C18H11ClN2O4/c1-9-2-7-13(19)12-8-14(24-15(9)12)17-20-16(21-25-17)10-3-5-11(6-4-10)18(22)23/h2-8H,1H3,(H,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	2.70	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor alpha (Homo sapiens (Human))	BDBM458251 (US10752616, Code No. BHBA-016) Show SMILES Cc1ccc(Cl)c2cc(oc12)-c1nc(no1)-c1ccc(cc1)C(O)=O Show InChI InChI=1S/C18H11ClN2O4/c1-9-2-7-13(19)12-8-14(24-15(9)12)17-20-16(21-25-17)10-3-5-11(6-4-10)18(22)23/h2-8H,1H3,(H,22,23)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	18	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor gamma (Homo sapiens (Human))	BDBM458251 (US10752616, Code No. BHBA-016) Show SMILES Cc1ccc(Cl)c2cc(oc12)-c1nc(no1)-c1ccc(cc1)C(O)=O Show InChI InChI=1S/C18H11ClN2O4/c1-9-2-7-13(19)12-8-14(24-15(9)12)17-20-16(21-25-17)10-3-5-11(6-4-10)18(22)23/h2-8H,1H3,(H,22,23)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	6	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair
Retinoic acid receptor beta (Homo sapiens (Human))	BDBM458259 (US10752616, Code No. BHBA-017) Show SMILES Cc1ccc(Cl)c2oc(cc12)-c1nc(no1)-c1ccc(cc1Cl)C(O)=O Show InChI InChI=1S/C18H10Cl2N2O4/c1-8-2-5-12(19)15-11(8)7-14(25-15)17-21-16(22-26-17)10-4-3-9(18(23)24)6-13(10)20/h2-7H,1H3,(H,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	n/a	n/a	n/a	n/a	7.40	n/a	n/a	n/a	n/a
King''s College London US Patent					Assay Description Transcriptional transactivation assays were performed with gal4 fusion receptor constructs, created using each of the RAR ligand binding domains of e...				US Patent US10752616 (2020) BindingDB Entry DOI: 10.7270/Q2B85C6M
					More data for this Ligand-Target Pair

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