Compile Data Set for Download or QSAR

Found 93 hits with Last Name = 'meyer' and Initial = 'jh'   

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
Sodium-dependent serotonin transporter (Homo sapiens (Human))	BDBM50091096 (5-Chloro-2-(2-dimethylaminomethyl-phenylsulfanyl)-...) Show SMILES CN(C)Cc1ccccc1Sc1ccc(Cl)cc1N Show InChI InChI=1S/C15H17ClN2S/c1-18(2)10-11-5-3-4-6-14(11)19-15-8-7-12(16)9-13(15)17/h3-9H,10,17H2,1-2H3	PDB KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.270	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Centre for Addiction and Mental Health Curated by ChEMBL					Assay Description In vitro binding affinity on cloned Serotonin transporter				J Med Chem 43: 3103-10 (2000) BindingDB Entry DOI: 10.7270/Q2J67G4W
					More data for this Ligand-Target Pair
Sodium-dependent serotonin transporter (Homo sapiens (Human))	BDBM50091098 (2-(2-Dimethylaminomethyl-phenylsulfanyl)-5-trifluo...) Show SMILES CN(C)Cc1ccccc1Sc1ccc(cc1N)C(F)(F)F Show InChI InChI=1S/C16H17F3N2S/c1-21(2)10-11-5-3-4-6-14(11)22-15-8-7-12(9-13(15)20)16(17,18)19/h3-9H,10,20H2,1-2H3	PDB KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	0.330	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Centre for Addiction and Mental Health Curated by ChEMBL					Assay Description In vitro binding affinity on cloned Serotonin transporter				J Med Chem 43: 3103-10 (2000) BindingDB Entry DOI: 10.7270/Q2J67G4W
					More data for this Ligand-Target Pair
Sodium-dependent serotonin transporter (Homo sapiens (Human))	BDBM50091097 (3-Amino-4-(2-dimethylaminomethyl-phenylsulfanyl)-b...) Show SMILES CN(C)Cc1ccccc1Sc1ccc(cc1N)C#N Show InChI InChI=1S/C16H17N3S/c1-19(2)11-13-5-3-4-6-15(13)20-16-8-7-12(10-17)9-14(16)18/h3-9H,11,18H2,1-2H3	PDB KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Centre for Addiction and Mental Health Curated by ChEMBL					Assay Description In vitro binding affinity on cloned Serotonin transporter				J Med Chem 43: 3103-10 (2000) BindingDB Entry DOI: 10.7270/Q2J67G4W
					More data for this Ligand-Target Pair
Sodium-dependent serotonin transporter (Homo sapiens (Human))	BDBM50091095 (2-(2-Dimethylaminomethyl-phenylsulfanyl)-5-methoxy...) Show SMILES COc1ccc(Sc2ccccc2CN(C)C)c(N)c1 Show InChI InChI=1S/C16H20N2OS/c1-18(2)11-12-6-4-5-7-15(12)20-16-9-8-13(19-3)10-14(16)17/h4-10H,11,17H2,1-3H3	PDB KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.89	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Centre for Addiction and Mental Health Curated by ChEMBL					Assay Description In vitro binding affinity on cloned Serotonin transporter				J Med Chem 43: 3103-10 (2000) BindingDB Entry DOI: 10.7270/Q2J67G4W
					More data for this Ligand-Target Pair
Sodium-dependent dopamine transporter (Homo sapiens (Human))	BDBM50091096 (5-Chloro-2-(2-dimethylaminomethyl-phenylsulfanyl)-...) Show SMILES CN(C)Cc1ccccc1Sc1ccc(Cl)cc1N Show InChI InChI=1S/C15H17ClN2S/c1-18(2)10-11-5-3-4-6-14(11)19-15-8-7-12(16)9-13(15)17/h3-9H,10,17H2,1-2H3	NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	115	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Centre for Addiction and Mental Health Curated by ChEMBL					Assay Description In vitro binding affinity on cloned Dopamine transporter				J Med Chem 43: 3103-10 (2000) BindingDB Entry DOI: 10.7270/Q2J67G4W
					More data for this Ligand-Target Pair
Sodium-dependent noradrenaline transporter (Homo sapiens (Human))	BDBM50091096 (5-Chloro-2-(2-dimethylaminomethyl-phenylsulfanyl)-...) Show SMILES CN(C)Cc1ccccc1Sc1ccc(Cl)cc1N Show InChI InChI=1S/C15H17ClN2S/c1-18(2)10-11-5-3-4-6-14(11)19-15-8-7-12(16)9-13(15)17/h3-9H,10,17H2,1-2H3	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	230	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Centre for Addiction and Mental Health Curated by ChEMBL					Assay Description In vitro binding affinity on cloned Norepinephrine transporter				J Med Chem 43: 3103-10 (2000) BindingDB Entry DOI: 10.7270/Q2J67G4W
					More data for this Ligand-Target Pair
Sodium-dependent noradrenaline transporter (Homo sapiens (Human))	BDBM50091098 (2-(2-Dimethylaminomethyl-phenylsulfanyl)-5-trifluo...) Show SMILES CN(C)Cc1ccccc1Sc1ccc(cc1N)C(F)(F)F Show InChI InChI=1S/C16H17F3N2S/c1-21(2)10-11-5-3-4-6-14(11)22-15-8-7-12(9-13(15)20)16(17,18)19/h3-9H,10,20H2,1-2H3	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	1.21E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Centre for Addiction and Mental Health Curated by ChEMBL					Assay Description In vitro binding affinity on cloned Norepinephrine transporter				J Med Chem 43: 3103-10 (2000) BindingDB Entry DOI: 10.7270/Q2J67G4W
					More data for this Ligand-Target Pair
Sodium-dependent noradrenaline transporter (Homo sapiens (Human))	BDBM50091097 (3-Amino-4-(2-dimethylaminomethyl-phenylsulfanyl)-b...) Show SMILES CN(C)Cc1ccccc1Sc1ccc(cc1N)C#N Show InChI InChI=1S/C16H17N3S/c1-19(2)11-13-5-3-4-6-15(13)20-16-8-7-12(10-17)9-14(16)18/h3-9H,11,18H2,1-2H3	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.35E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Centre for Addiction and Mental Health Curated by ChEMBL					Assay Description In vitro binding affinity on cloned Norepinephrine transporter				J Med Chem 43: 3103-10 (2000) BindingDB Entry DOI: 10.7270/Q2J67G4W
					More data for this Ligand-Target Pair
Sodium-dependent dopamine transporter (Homo sapiens (Human))	BDBM50091097 (3-Amino-4-(2-dimethylaminomethyl-phenylsulfanyl)-b...) Show SMILES CN(C)Cc1ccccc1Sc1ccc(cc1N)C#N Show InChI InChI=1S/C16H17N3S/c1-19(2)11-13-5-3-4-6-15(13)20-16-8-7-12(10-17)9-14(16)18/h3-9H,11,18H2,1-2H3	NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.42E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Centre for Addiction and Mental Health Curated by ChEMBL					Assay Description In vitro binding affinity on cloned Dopamine transporter				J Med Chem 43: 3103-10 (2000) BindingDB Entry DOI: 10.7270/Q2J67G4W
					More data for this Ligand-Target Pair
Sodium-dependent noradrenaline transporter (Homo sapiens (Human))	BDBM50091095 (2-(2-Dimethylaminomethyl-phenylsulfanyl)-5-methoxy...) Show SMILES COc1ccc(Sc2ccccc2CN(C)C)c(N)c1 Show InChI InChI=1S/C16H20N2OS/c1-18(2)11-12-6-4-5-7-15(12)20-16-9-8-13(19-3)10-14(16)17/h4-10H,11,17H2,1-3H3	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.99E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Centre for Addiction and Mental Health Curated by ChEMBL					Assay Description In vitro binding affinity on cloned Norepinephrine transporter				J Med Chem 43: 3103-10 (2000) BindingDB Entry DOI: 10.7270/Q2J67G4W
					More data for this Ligand-Target Pair
Sodium-dependent dopamine transporter (Homo sapiens (Human))	BDBM50091098 (2-(2-Dimethylaminomethyl-phenylsulfanyl)-5-trifluo...) Show SMILES CN(C)Cc1ccccc1Sc1ccc(cc1N)C(F)(F)F Show InChI InChI=1S/C16H17F3N2S/c1-21(2)10-11-5-3-4-6-14(11)22-15-8-7-12(9-13(15)20)16(17,18)19/h3-9H,10,20H2,1-2H3	NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	2.04E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Centre for Addiction and Mental Health Curated by ChEMBL					Assay Description In vitro binding affinity on cloned Dopamine transporter				J Med Chem 43: 3103-10 (2000) BindingDB Entry DOI: 10.7270/Q2J67G4W
					More data for this Ligand-Target Pair
Sodium-dependent dopamine transporter (Homo sapiens (Human))	BDBM50091095 (2-(2-Dimethylaminomethyl-phenylsulfanyl)-5-methoxy...) Show SMILES COc1ccc(Sc2ccccc2CN(C)C)c(N)c1 Show InChI InChI=1S/C16H20N2OS/c1-18(2)11-12-6-4-5-7-15(12)20-16-9-8-13(19-3)10-14(16)17/h4-10H,11,17H2,1-3H3	NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	2.65E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Centre for Addiction and Mental Health Curated by ChEMBL					Assay Description In vitro binding affinity on cloned Dopamine transporter				J Med Chem 43: 3103-10 (2000) BindingDB Entry DOI: 10.7270/Q2J67G4W
					More data for this Ligand-Target Pair
Fusion glycoprotein F0 (Human respiratory syncytial virus A (strain A2))	BDBM50572440 (CHEMBL4469438) Show SMILES CC(C)CCn1c(CN2C(=O)C3(CC3)c3ccccc23)nc2cc(CN)ccc12 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.400	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of Respiratory syncytial virus A2 fusion protein expressed in HEK293T cells harboring GAL4-NF-kappaB assessed as reduction in cell-cell fu...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01882 BindingDB Entry DOI: 10.7270/Q2QF8XNB
					More data for this Ligand-Target Pair
Fusion glycoprotein F0 (Human respiratory syncytial virus A (strain A2))	BDBM50572444 (CHEMBL4878302) Show SMILES CC(C)CCn1c(CN2C(=O)C3(CC3)c3ccc(F)cc23)nc2cc(CN)ccc12 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of Respiratory syncytial virus A2 fusion protein expressed in HEK293T cells harboring GAL4-NF-kappaB assessed as reduction in cell-cell fu...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01882 BindingDB Entry DOI: 10.7270/Q2QF8XNB
					More data for this Ligand-Target Pair
Fusion glycoprotein F0 (Human respiratory syncytial virus A (strain A2))	BDBM50572466 (CHEMBL4876200) Show SMILES CC(C)CCn1c(CN2C(=O)C3(CCOCC3)c3ccccc23)nc2cc(CN)ccc12 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.690	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of Respiratory syncytial virus fusion protein				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01882 BindingDB Entry DOI: 10.7270/Q2QF8XNB
					More data for this Ligand-Target Pair
Fusion glycoprotein F0 (Human respiratory syncytial virus A (strain A2))	BDBM50572442 (CHEMBL4872095) Show SMILES CC(C)CCn1c(CN2C(=O)C3(CC3)c3cc(F)ccc23)nc2cc(CN)ccc12 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.700	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of Respiratory syncytial virus A2 fusion protein expressed in HEK293T cells harboring GAL4-NF-kappaB assessed as reduction in cell-cell fu...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01882 BindingDB Entry DOI: 10.7270/Q2QF8XNB
					More data for this Ligand-Target Pair
Fusion glycoprotein F0 (Human respiratory syncytial virus A (strain A2))	BDBM50572464 (CHEMBL4858040) Show SMILES CC(C)CCn1c(CN2C(=O)C3(CC3)c3ccncc23)nc2cc(CN)ccc12 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.900	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of Respiratory syncytial virus fusion protein				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01882 BindingDB Entry DOI: 10.7270/Q2QF8XNB
					More data for this Ligand-Target Pair
Fusion glycoprotein F0 (Human respiratory syncytial virus A (strain A2))	BDBM50572463 (CHEMBL4871101) Show SMILES CC(C)CCn1c(CN2C(=O)C3(CC3)c3cccnc23)nc2cc(CN)ccc12 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	0.900	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of Respiratory syncytial virus fusion protein				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01882 BindingDB Entry DOI: 10.7270/Q2QF8XNB
					More data for this Ligand-Target Pair
Fusion glycoprotein F0 (Human respiratory syncytial virus A (strain A2))	BDBM50572450 (Rv-521 | Rv521 | Sisunatovir) Show SMILES NCc1ccc2n(CCCC(F)(F)F)c(CN3C(=O)C4(CC4)c4ccc(F)cc34)nc2c1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase MCE PC cid PC sid PDB UniChem	PDB Article PubMed	n/a	n/a	0.900	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of Respiratory syncytial virus A2 fusion protein expressed in HEK293T cells harboring GAL4-NF-kappaB assessed as reduction in cell-cell fu...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01882 BindingDB Entry DOI: 10.7270/Q2QF8XNB
					More data for this Ligand-Target Pair				3D Structure (crystal)
Fusion glycoprotein F0 (Human respiratory syncytial virus A (strain A2))	BDBM50572451 (CHEMBL4867108) Show SMILES NCc1ccc2n(CCCC(F)(F)F)c(CN3C(=O)C4(CC4)c4cccc(F)c34)nc2c1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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
TBA					Assay Description Inhibition of Respiratory syncytial virus A2 fusion protein expressed in HEK293T cells harboring GAL4-NF-kappaB assessed as reduction in cell-cell fu...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01882 BindingDB Entry DOI: 10.7270/Q2QF8XNB
					More data for this Ligand-Target Pair
Fusion glycoprotein F0 (Human respiratory syncytial virus A (strain A2))	BDBM50572465 (CHEMBL4858949) Show SMILES CC(C)CCn1c(CN2C(=O)C3(CN(C3)C(C)=O)c3ccccc23)nc2cc(CN)ccc12 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.10	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of Respiratory syncytial virus fusion protein				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01882 BindingDB Entry DOI: 10.7270/Q2QF8XNB
					More data for this Ligand-Target Pair
Fusion glycoprotein F0 (Human respiratory syncytial virus A (strain A2))	BDBM50572453 (CHEMBL4874709) Show SMILES NCc1ccc2n(C3CCOCC3)c(CN3C(=O)C4(CC4)c4ccc(F)cc34)nc2c1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.20	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of Respiratory syncytial virus A2 fusion protein expressed in HEK293T cells harboring GAL4-NF-kappaB assessed as reduction in cell-cell fu...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01882 BindingDB Entry DOI: 10.7270/Q2QF8XNB
					More data for this Ligand-Target Pair
Fusion glycoprotein F0 (Human respiratory syncytial virus A (strain A2))	BDBM50572445 (CHEMBL4865906) Show SMILES CC(C)CCn1c(CN2C(=O)C3(CC3)c3ccc(Cl)cc23)nc2cc(CN)ccc12 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.20	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of Respiratory syncytial virus A2 fusion protein expressed in HEK293T cells harboring GAL4-NF-kappaB assessed as reduction in cell-cell fu...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01882 BindingDB Entry DOI: 10.7270/Q2QF8XNB
					More data for this Ligand-Target Pair
Fusion glycoprotein F0 (Human respiratory syncytial virus A (strain A2))	BDBM50572447 (CHEMBL4860271) Show SMILES CC(C)CCn1c(CN2C(=O)C3(CC3)c3cccc(F)c23)nc2cc(CN)ccc12 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.30	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of Respiratory syncytial virus A2 fusion protein expressed in HEK293T cells harboring GAL4-NF-kappaB assessed as reduction in cell-cell fu...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01882 BindingDB Entry DOI: 10.7270/Q2QF8XNB
					More data for this Ligand-Target Pair
Fusion glycoprotein F0 (Human respiratory syncytial virus A (strain A2))	BDBM50572449 (CHEMBL4853602) Show SMILES NCc1ccc2n(CCCCO)c(CN3C(=O)C4(CC4)c4ccc(F)cc34)nc2c1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of Respiratory syncytial virus A2 fusion protein expressed in HEK293T cells harboring GAL4-NF-kappaB assessed as reduction in cell-cell fu...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01882 BindingDB Entry DOI: 10.7270/Q2QF8XNB
					More data for this Ligand-Target Pair
Fusion glycoprotein F0 (Human respiratory syncytial virus A (strain A2))	BDBM50572448 (CHEMBL4863172) Show SMILES CS(=O)(=O)CCCn1c(CN2C(=O)C3(CC3)c3ccc(F)cc23)nc2cc(CN)ccc12 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.60	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of Respiratory syncytial virus A2 fusion protein expressed in HEK293T cells harboring GAL4-NF-kappaB assessed as reduction in cell-cell fu...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01882 BindingDB Entry DOI: 10.7270/Q2QF8XNB
					More data for this Ligand-Target Pair
Fusion glycoprotein F0 (Human respiratory syncytial virus A (strain A2))	BDBM50572452 (CHEMBL4873528) Show SMILES NCc1ccc2n(C3CCC(O)CC3)c(CN3C(=O)C4(CC4)c4ccc(F)cc34)nc2c1 |(23.93,-12.4,;22.59,-11.64,;21.26,-12.41,;21.26,-13.96,;19.93,-14.74,;18.59,-13.97,;17.13,-14.45,;16.66,-15.91,;15.16,-16.23,;14.69,-17.69,;15.72,-18.84,;15.24,-20.3,;17.23,-18.52,;17.7,-17.05,;16.22,-13.21,;14.68,-13.21,;13.91,-11.88,;14.52,-10.48,;16.02,-10.15,;13.36,-9.45,;12.58,-8.11,;14.13,-8.11,;12.04,-10.23,;10.58,-9.76,;9.44,-10.79,;9.77,-12.3,;8.64,-13.34,;11.23,-12.76,;12.37,-11.73,;17.12,-11.96,;18.59,-12.43,;19.92,-11.65,)| Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.60	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of Respiratory syncytial virus A2 fusion protein expressed in HEK293T cells harboring GAL4-NF-kappaB assessed as reduction in cell-cell fu...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01882 BindingDB Entry DOI: 10.7270/Q2QF8XNB
					More data for this Ligand-Target Pair
Fusion glycoprotein F0 (Human respiratory syncytial virus A (strain A2))	BDBM50572454 (CHEMBL4855358) Show SMILES NC(=N)c1ccc2n(CCCC(F)(F)F)c(CN3C(=O)C4(CC4)c4ccc(F)cc34)nc2c1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank 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
TBA					Assay Description Inhibition of Respiratory syncytial virus A2 fusion protein expressed in HEK293T cells harboring GAL4-NF-kappaB assessed as reduction in cell-cell fu...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01882 BindingDB Entry DOI: 10.7270/Q2QF8XNB
					More data for this Ligand-Target Pair
Fusion glycoprotein F0 (Human respiratory syncytial virus A (strain A2))	BDBM50572443 (CHEMBL4872263) Show SMILES CC(C)CCn1c(CN2C(=O)C3(CC3)c3cc(Cl)ccc23)nc2cc(CN)ccc12 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.5	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of Respiratory syncytial virus A2 fusion protein expressed in HEK293T cells harboring GAL4-NF-kappaB assessed as reduction in cell-cell fu...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01882 BindingDB Entry DOI: 10.7270/Q2QF8XNB
					More data for this Ligand-Target Pair
Fusion glycoprotein F0 (Human respiratory syncytial virus A (strain A2))	BDBM50572462 (CHEMBL4876843) Show SMILES Fc1ccc2c(c1)N(Cc1nc3cc(Cl)ccc3n1CCCC(F)(F)F)C(=O)C21CC1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.20	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of Respiratory syncytial virus A2 fusion protein expressed in HEK293T cells harboring GAL4-NF-kappaB assessed as reduction in cell-cell fu...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01882 BindingDB Entry DOI: 10.7270/Q2QF8XNB
					More data for this Ligand-Target Pair
Fusion glycoprotein F0 (Human respiratory syncytial virus A (strain A2))	BDBM50572441 (CHEMBL4862291) Show SMILES CC(C)CCn1c(CN2C(=O)C3(CC3)c3c2cccc3Cl)nc2cc(CN)ccc12 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	11	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of Respiratory syncytial virus A2 fusion protein expressed in HEK293T cells harboring GAL4-NF-kappaB assessed as reduction in cell-cell fu...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01882 BindingDB Entry DOI: 10.7270/Q2QF8XNB
					More data for this Ligand-Target Pair
Fusion glycoprotein F0 (Human respiratory syncytial virus A (strain A2))	BDBM50572461 (CHEMBL4859694) Show SMILES Fc1ccc2c(c1)N(Cc1nc3ccccc3n1CCCC(F)(F)F)C(=O)C21CC1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	37	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of Respiratory syncytial virus A2 fusion protein expressed in HEK293T cells harboring GAL4-NF-kappaB assessed as reduction in cell-cell fu...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01882 BindingDB Entry DOI: 10.7270/Q2QF8XNB
					More data for this Ligand-Target Pair
Fusion glycoprotein F0 (Human respiratory syncytial virus A (strain A2))	BDBM50572446 (CHEMBL4878086) Show SMILES CC(C)CCn1c(CN2C(=O)C3(CC3)c3cccc(Cl)c23)nc2cc(CN)ccc12 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	47	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of Respiratory syncytial virus A2 fusion protein expressed in HEK293T cells harboring GAL4-NF-kappaB assessed as reduction in cell-cell fu...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01882 BindingDB Entry DOI: 10.7270/Q2QF8XNB
					More data for this Ligand-Target Pair
Fusion glycoprotein F0 (Human respiratory syncytial virus A (strain A2))	BDBM50572457 (CHEMBL4847062) Show SMILES NC(=O)c1ccc2n(CCCC(F)(F)F)c(CN3C(=O)C4(CC4)c4ccc(F)cc34)nc2c1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	71	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of Respiratory syncytial virus A2 fusion protein expressed in HEK293T cells harboring GAL4-NF-kappaB assessed as reduction in cell-cell fu...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01882 BindingDB Entry DOI: 10.7270/Q2QF8XNB
					More data for this Ligand-Target Pair
Fusion glycoprotein F0 (Human respiratory syncytial virus A (strain A2))	BDBM50572456 (CHEMBL4866951) Show SMILES NC(=N)NCc1ccc2n(CCCC(F)(F)F)c(CN3C(=O)C4(CC4)c4ccc(F)cc34)nc2c1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	183	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of Respiratory syncytial virus A2 fusion protein expressed in HEK293T cells harboring GAL4-NF-kappaB assessed as reduction in cell-cell fu...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01882 BindingDB Entry DOI: 10.7270/Q2QF8XNB
					More data for this Ligand-Target Pair
Fusion glycoprotein F0 (Human respiratory syncytial virus A (strain A2))	BDBM50572460 (CHEMBL4871056) Show SMILES CC(=O)NCc1ccc2n(CCCC(F)(F)F)c(CN3C(=O)C4(CC4)c4ccc(F)cc34)nc2c1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	365	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of Respiratory syncytial virus A2 fusion protein expressed in HEK293T cells harboring GAL4-NF-kappaB assessed as reduction in cell-cell fu...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01882 BindingDB Entry DOI: 10.7270/Q2QF8XNB
					More data for this Ligand-Target Pair
Fusion glycoprotein F0 (Human respiratory syncytial virus A (strain A2))	BDBM50572455 (CHEMBL4869353) Show SMILES CCNC(=N)c1ccc2n(CCCC(F)(F)F)c(CN3C(=O)C4(CC4)c4ccc(F)cc34)nc2c1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	641	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of Respiratory syncytial virus A2 fusion protein expressed in HEK293T cells harboring GAL4-NF-kappaB assessed as reduction in cell-cell fu...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01882 BindingDB Entry DOI: 10.7270/Q2QF8XNB
					More data for this Ligand-Target Pair
Fusion glycoprotein F0 (Human respiratory syncytial virus A (strain A2))	BDBM50572459 (CHEMBL4873987) Show SMILES CS(=O)(=O)c1ccc2n(CCCC(F)(F)F)c(CN3C(=O)C4(CC4)c4ccc(F)cc34)nc2c1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.07E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of Respiratory syncytial virus A2 fusion protein expressed in HEK293T cells harboring GAL4-NF-kappaB assessed as reduction in cell-cell fu...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01882 BindingDB Entry DOI: 10.7270/Q2QF8XNB
					More data for this Ligand-Target Pair
Fusion glycoprotein F0 (Human respiratory syncytial virus A (strain A2))	BDBM50572458 (CHEMBL4878851) Show SMILES OC(=O)c1ccc2n(CCCC(F)(F)F)c(CN3C(=O)C4(CC4)c4ccc(F)cc34)nc2c1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>2.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of Respiratory syncytial virus A2 fusion protein expressed in HEK293T cells harboring GAL4-NF-kappaB assessed as reduction in cell-cell fu...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01882 BindingDB Entry DOI: 10.7270/Q2QF8XNB
					More data for this Ligand-Target Pair
Estrogen receptor (Homo sapiens (Human))	BDBM50161598 (2-Methyl-4-((1R,2R,5R)-4,4,8-trimethyl-3-oxa-bicyc...) Show SMILES CC1=CC[C@@H]2C[C@H]1[C@@H](OC2(C)C)c1ccc(O)c(C)c1 |t:1| Show InChI InChI=1S/C18H24O2/c1-11-5-7-14-10-15(11)17(20-18(14,3)4)13-6-8-16(19)12(2)9-13/h5-6,8-9,14-15,17,19H,7,10H2,1-4H3/t14?,15?,17-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	143	n/a	n/a	n/a	n/a
Ligand Pharmaceuticals Curated by ChEMBL					Assay Description In vitro agonist activity for estrogen receptor alpha expressed in COS-1 cells				Bioorg Med Chem Lett 15: 1463-6 (2005) Article DOI: 10.1016/j.bmcl.2004.12.077 BindingDB Entry DOI: 10.7270/Q25H7FR7
					More data for this Ligand-Target Pair
Estrogen receptor beta (Homo sapiens (Human))	BDBM50161604 (4-((1R,2R,5R)-5-Hydroxymethyl-8-methyl-3-oxa-bicyc...) Show SMILES CC1=CC[C@@]2(CO)CO[C@H]([C@@H]1C2)c1ccc(O)cc1 |t:1| Show InChI InChI=1S/C16H20O3/c1-11-6-7-16(9-17)8-14(11)15(19-10-16)12-2-4-13(18)5-3-12/h2-6,14-15,17-18H,7-10H2,1H3/t14?,15-,16+/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	38	n/a	n/a	n/a	n/a
Ligand Pharmaceuticals Curated by ChEMBL					Assay Description In vitro agonist activity for estrogen receptor beta expressed in COS-1 cells				Bioorg Med Chem Lett 15: 1463-6 (2005) Article DOI: 10.1016/j.bmcl.2004.12.077 BindingDB Entry DOI: 10.7270/Q25H7FR7
					More data for this Ligand-Target Pair
Estrogen receptor beta (Homo sapiens (Human))	BDBM50161615 (4-((1R,2R,5R)-5-Hydroxymethyl-8-methyl-3-oxa-bicyc...) Show SMILES CC1=CC[C@@]2(CO)CO[C@H]([C@@H]1C2)c1ccc(O)cc1C |t:1| Show InChI InChI=1S/C17H22O3/c1-11-5-6-17(9-18)8-15(11)16(20-10-17)14-4-3-13(19)7-12(14)2/h3-5,7,15-16,18-19H,6,8-10H2,1-2H3/t15?,16-,17+/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	79	n/a	n/a	n/a	n/a
Ligand Pharmaceuticals Curated by ChEMBL					Assay Description In vitro agonist activity for estrogen receptor beta expressed in COS-1 cells				Bioorg Med Chem Lett 15: 1463-6 (2005) Article DOI: 10.1016/j.bmcl.2004.12.077 BindingDB Entry DOI: 10.7270/Q25H7FR7
					More data for this Ligand-Target Pair
Estrogen receptor beta (Homo sapiens (Human))	BDBM50161611 (4-((1R,2R,5R)-5-Hydroxymethyl-8-methyl-3-oxa-bicyc...) Show SMILES CC1=CC[C@@]2(CO)CO[C@H]([C@@H]1C2)c1ccc(O)cc1O |t:1| Show InChI InChI=1S/C16H20O4/c1-10-4-5-16(8-17)7-13(10)15(20-9-16)12-3-2-11(18)6-14(12)19/h2-4,6,13,15,17-19H,5,7-9H2,1H3/t13?,15-,16+/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	275	n/a	n/a	n/a	n/a
Ligand Pharmaceuticals Curated by ChEMBL					Assay Description In vitro agonist activity for estrogen receptor beta expressed in COS-1 cells				Bioorg Med Chem Lett 15: 1463-6 (2005) Article DOI: 10.1016/j.bmcl.2004.12.077 BindingDB Entry DOI: 10.7270/Q25H7FR7
					More data for this Ligand-Target Pair
Estrogen receptor (Homo sapiens (Human))	BDBM50161611 (4-((1R,2R,5R)-5-Hydroxymethyl-8-methyl-3-oxa-bicyc...) Show SMILES CC1=CC[C@@]2(CO)CO[C@H]([C@@H]1C2)c1ccc(O)cc1O |t:1| Show InChI InChI=1S/C16H20O4/c1-10-4-5-16(8-17)7-13(10)15(20-9-16)12-3-2-11(18)6-14(12)19/h2-4,6,13,15,17-19H,5,7-9H2,1H3/t13?,15-,16+/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	173	n/a	n/a	n/a	n/a
Ligand Pharmaceuticals Curated by ChEMBL					Assay Description In vitro agonist activity for estrogen receptor alpha expressed in COS-1 cells				Bioorg Med Chem Lett 15: 1463-6 (2005) Article DOI: 10.1016/j.bmcl.2004.12.077 BindingDB Entry DOI: 10.7270/Q25H7FR7
					More data for this Ligand-Target Pair
Estrogen receptor beta (Homo sapiens (Human))	BDBM50161606 (4-((1R,2R,5R)-5-Hydroxymethyl-8-methyl-3-oxa-bicyc...) Show SMILES CC1=CC[C@@]2(CO)CO[C@H]([C@@H]1C2)c1ccc(O)c(C)c1 |t:1| Show InChI InChI=1S/C17H22O3/c1-11-5-6-17(9-18)8-14(11)16(20-10-17)13-3-4-15(19)12(2)7-13/h3-5,7,14,16,18-19H,6,8-10H2,1-2H3/t14?,16-,17+/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	305	n/a	n/a	n/a	n/a
Ligand Pharmaceuticals Curated by ChEMBL					Assay Description In vitro agonist activity for estrogen receptor beta expressed in COS-1 cells				Bioorg Med Chem Lett 15: 1463-6 (2005) Article DOI: 10.1016/j.bmcl.2004.12.077 BindingDB Entry DOI: 10.7270/Q25H7FR7
					More data for this Ligand-Target Pair
Estrogen receptor (Homo sapiens (Human))	BDBM50161604 (4-((1R,2R,5R)-5-Hydroxymethyl-8-methyl-3-oxa-bicyc...) Show SMILES CC1=CC[C@@]2(CO)CO[C@H]([C@@H]1C2)c1ccc(O)cc1 |t:1| Show InChI InChI=1S/C16H20O3/c1-11-6-7-16(9-17)8-14(11)15(19-10-16)12-2-4-13(18)5-3-12/h2-6,14-15,17-18H,7-10H2,1H3/t14?,15-,16+/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	835	n/a	n/a	n/a	n/a
Ligand Pharmaceuticals Curated by ChEMBL					Assay Description In vitro agonist activity for estrogen receptor alpha expressed in COS-1 cells				Bioorg Med Chem Lett 15: 1463-6 (2005) Article DOI: 10.1016/j.bmcl.2004.12.077 BindingDB Entry DOI: 10.7270/Q25H7FR7
					More data for this Ligand-Target Pair
Estrogen receptor beta (Homo sapiens (Human))	BDBM50161613 (3-Chloro-4-((1R,2R,5R)-5-hydroxymethyl-1,8-dimethy...) Show SMILES CC1=CC[C@@]2(CO)CO[C@@H](c3ccc(O)cc3Cl)[C@]1(C)C2 |t:1| Show InChI InChI=1S/C17H21ClO3/c1-11-5-6-17(9-19)8-16(11,2)15(21-10-17)13-4-3-12(20)7-14(13)18/h3-5,7,15,19-20H,6,8-10H2,1-2H3/t15-,16+,17+/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	67	n/a	n/a	n/a	n/a
Ligand Pharmaceuticals Curated by ChEMBL					Assay Description In vitro agonist activity for estrogen receptor beta expressed in COS-1 cells				Bioorg Med Chem Lett 15: 1463-6 (2005) Article DOI: 10.1016/j.bmcl.2004.12.077 BindingDB Entry DOI: 10.7270/Q25H7FR7
					More data for this Ligand-Target Pair
Estrogen receptor beta (Homo sapiens (Human))	BDBM17292 ((1S,10R,11S,14S,15S)-15-methyltetracyclo[8.7.0.0^{...) Show SMILES [H][C@@]12CC[C@H](O)[C@@]1(C)CC[C@]1([H])c3ccc(O)cc3CC[C@@]21[H] Show InChI InChI=1S/C18H24O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-17,19-20H,2,4,6-9H2,1H3/t14-,15-,16+,17+,18+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	n/a	n/a	n/a	n/a	9.70	n/a	n/a	n/a	n/a
Ligand Pharmaceuticals Curated by ChEMBL					Assay Description In vitro agonist activity for estrogen receptor beta expressed in COS-1 cells				Bioorg Med Chem Lett 15: 1463-6 (2005) Article DOI: 10.1016/j.bmcl.2004.12.077 BindingDB Entry DOI: 10.7270/Q25H7FR7
					More data for this Ligand-Target Pair				3D Structure (crystal)
Estrogen receptor beta (Homo sapiens (Human))	BDBM50161594 (2-Fluoro-4-((1R,2S,5R)-5-hydroxymethyl-1,8-dimethy...) Show SMILES CC1=CC[C@@]2(CO)CO[C@@H](c3ccc(O)c(F)c3)[C@]1(C)C2 |t:1| Show InChI InChI=1S/C17H21FO3/c1-11-5-6-17(9-19)8-16(11,2)15(21-10-17)12-3-4-14(20)13(18)7-12/h3-5,7,15,19-20H,6,8-10H2,1-2H3/t15-,16+,17+/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	6	n/a	n/a	n/a	n/a
Ligand Pharmaceuticals Curated by ChEMBL					Assay Description In vitro agonist activity for estrogen receptor beta expressed in COS-1 cells				Bioorg Med Chem Lett 15: 1463-6 (2005) Article DOI: 10.1016/j.bmcl.2004.12.077 BindingDB Entry DOI: 10.7270/Q25H7FR7
					More data for this Ligand-Target Pair
Estrogen receptor (Homo sapiens (Human))	BDBM50161613 (3-Chloro-4-((1R,2R,5R)-5-hydroxymethyl-1,8-dimethy...) Show SMILES CC1=CC[C@@]2(CO)CO[C@@H](c3ccc(O)cc3Cl)[C@]1(C)C2 |t:1| Show InChI InChI=1S/C17H21ClO3/c1-11-5-6-17(9-19)8-16(11,2)15(21-10-17)13-4-3-12(20)7-14(13)18/h3-5,7,15,19-20H,6,8-10H2,1-2H3/t15-,16+,17+/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	43	n/a	n/a	n/a	n/a
Ligand Pharmaceuticals Curated by ChEMBL					Assay Description In vitro agonist activity for estrogen receptor alpha expressed in COS-1 cells				Bioorg Med Chem Lett 15: 1463-6 (2005) Article DOI: 10.1016/j.bmcl.2004.12.077 BindingDB Entry DOI: 10.7270/Q25H7FR7
					More data for this Ligand-Target Pair

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