Compile Data Set for Download or QSAR

Found 7 hits with Last Name = 'baiocchi' and Initial = 'l'   

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
5-hydroxytryptamine receptor 2A (Rattus norvegicus (rat))	BDBM50073443 (2-{3-[4-(3-Chloro-phenyl)-piperazin-1-yl]-butyl}-2...) Show SMILES CC(CCn1nc2ccccn2c1=O)N1CCN(CC1)c1cccc(Cl)c1 Show InChI InChI=1S/C20H24ClN5O/c1-16(8-10-26-20(27)25-9-3-2-7-19(25)22-26)23-11-13-24(14-12-23)18-6-4-5-17(21)15-18/h2-7,9,15-16H,8,10-14H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	17	n/a	n/a	n/a	n/a	n/a	n/a
Angelini Ricerche S.p.A. Curated by ChEMBL					Assay Description Compound was tested for the inhibition of [3H]-ketanserin binding to 5-hydroxytryptamine 2A receptor				J Med Chem 42: 336-45 (1999) Article DOI: 10.1021/jm970700n BindingDB Entry DOI: 10.7270/Q2Q52NSS
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 2A (Rattus norvegicus (rat))	BDBM50073444 (2-{3-[4-(3-chlorophenyl)piperazin-1-yl]propyl}[1,2...) Show SMILES Clc1cccc(c1)N1CCN(CCCn2nc3ccccn3c2=O)CC1 Show InChI InChI=1S/C19H22ClN5O/c20-16-5-3-6-17(15-16)23-13-11-22(12-14-23)8-4-10-25-19(26)24-9-2-1-7-18(24)21-25/h1-3,5-7,9,15H,4,8,10-14H2	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	17	n/a	n/a	n/a	n/a	n/a	n/a
Angelini Ricerche S.p.A. Curated by ChEMBL					Assay Description Compound was tested for the inhibition of [3H]-ketanserin binding to 5-hydroxytryptamine 2A receptor				J Med Chem 42: 336-45 (1999) Article DOI: 10.1021/jm970700n BindingDB Entry DOI: 10.7270/Q2Q52NSS
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 2A (Rattus norvegicus (rat))	BDBM50073445 (2-{3-[(S)-4-(3-Chloro-phenyl)-2-methyl-piperazin-1...) Show SMILES C[C@H]1CN(CCN1CCCn1nc2ccccn2c1=O)c1cccc(Cl)c1 Show InChI InChI=1S/C20H24ClN5O/c1-16-15-24(18-7-4-6-17(21)14-18)13-12-23(16)9-5-11-26-20(27)25-10-3-2-8-19(25)22-26/h2-4,6-8,10,14,16H,5,9,11-13,15H2,1H3/t16-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	25.4	n/a	n/a	n/a	n/a	n/a	n/a
Angelini Ricerche S.p.A. Curated by ChEMBL					Assay Description Compound was tested for it's binding affinity towards 5-hydroxytryptamine 2A receptor				J Med Chem 42: 336-45 (1999) Article DOI: 10.1021/jm970700n BindingDB Entry DOI: 10.7270/Q2Q52NSS
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 2A (Rattus norvegicus (rat))	BDBM50073439 (2-{3-[4-(3-Chloro-phenyl)-2-methyl-piperazin-1-yl]...) Show SMILES CC1CN(CCN1CCCn1nc2ccccn2c1=O)c1cccc(Cl)c1 Show InChI InChI=1S/C20H24ClN5O/c1-16-15-24(18-7-4-6-17(21)14-18)13-12-23(16)9-5-11-26-20(27)25-10-3-2-8-19(25)22-26/h2-4,6-8,10,14,16H,5,9,11-13,15H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	31	n/a	n/a	n/a	n/a	n/a	n/a
Angelini Ricerche S.p.A. Curated by ChEMBL					Assay Description Compound was tested for the inhibition of [3H]-ketanserin binding to 5-hydroxytryptamine 2A receptor				J Med Chem 42: 336-45 (1999) Article DOI: 10.1021/jm970700n BindingDB Entry DOI: 10.7270/Q2Q52NSS
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 2A (Rattus norvegicus (rat))	BDBM50073442 (2-{3-[4-(3-Chloro-phenyl)-piperazin-1-yl]-2-methyl...) Show SMILES CC(CN1CCN(CC1)c1cccc(Cl)c1)Cn1nc2ccccn2c1=O Show InChI InChI=1S/C20H24ClN5O/c1-16(15-26-20(27)25-8-3-2-7-19(25)22-26)14-23-9-11-24(12-10-23)18-6-4-5-17(21)13-18/h2-8,13,16H,9-12,14-15H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	94	n/a	n/a	n/a	n/a	n/a	n/a
Angelini Ricerche S.p.A. Curated by ChEMBL					Assay Description Compound was tested for the inhibition of [3H]-ketanserin binding to 5-hydroxytryptamine 2A receptor				J Med Chem 42: 336-45 (1999) Article DOI: 10.1021/jm970700n BindingDB Entry DOI: 10.7270/Q2Q52NSS
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 2A (Rattus norvegicus (rat))	BDBM50073441 (2-{3-[4-(3-Chloro-phenyl)-2-ethyl-piperazin-1-yl]-...) Show SMILES CCC1CN(CCN1CCCn1nc2ccccn2c1=O)c1cccc(Cl)c1 Show InChI InChI=1S/C21H26ClN5O/c1-2-18-16-25(19-8-5-7-17(22)15-19)14-13-24(18)10-6-12-27-21(28)26-11-4-3-9-20(26)23-27/h3-5,7-9,11,15,18H,2,6,10,12-14,16H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	169	n/a	n/a	n/a	n/a	n/a	n/a
Angelini Ricerche S.p.A. Curated by ChEMBL					Assay Description Compound was tested for the inhibition of [3H]-ketanserin binding to 5-hydroxytryptamine 2A receptor				J Med Chem 42: 336-45 (1999) Article DOI: 10.1021/jm970700n BindingDB Entry DOI: 10.7270/Q2Q52NSS
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 2A (Rattus norvegicus (rat))	BDBM50073440 (2-{3-[(R)-4-(3-Chloro-phenyl)-2-methyl-piperazin-1...) Show SMILES C[C@@H]1CN(CCN1CCCn1nc2ccccn2c1=O)c1cccc(Cl)c1 Show InChI InChI=1S/C20H24ClN5O/c1-16-15-24(18-7-4-6-17(21)14-18)13-12-23(16)9-5-11-26-20(27)25-10-3-2-8-19(25)22-26/h2-4,6-8,10,14,16H,5,9,11-13,15H2,1H3/t16-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	234	n/a	n/a	n/a	n/a	n/a	n/a
Angelini Ricerche S.p.A. Curated by ChEMBL					Assay Description Compound was tested for it's binding affinity towards 5-hydroxytryptamine 2A receptor				J Med Chem 42: 336-45 (1999) Article DOI: 10.1021/jm970700n BindingDB Entry DOI: 10.7270/Q2Q52NSS
					More data for this Ligand-Target Pair