Compile Data Set for Download or QSAR

Found 204 hits with Last Name = 'pietras' and Initial = 'm'   

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
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50130561 ((R)-N-((S)-1-((3R,4R)-4-(3-hydroxyphenyl)-3,4-dime...) Show SMILES CC(C)[C@@H](CN1CC[C@](C)([C@@H](C)C1)c1cccc(O)c1)NC(=O)[C@H]1Cc2ccccc2CN1 Show InChI InChI=1S/C28H39N3O2/c1-19(2)26(30-27(33)25-14-21-8-5-6-9-22(21)16-29-25)18-31-13-12-28(4,20(3)17-31)23-10-7-11-24(32)15-23/h5-11,15,19-20,25-26,29,32H,12-14,16-18H2,1-4H3,(H,30,33)/t20-,25+,26+,28+/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	0.300	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Pharmaceuticals Curated by ChEMBL					Assay Description Binding affinity to kappa opioid receptor				Bioorg Med Chem Lett 20: 5847-52 (2010) Article DOI: 10.1016/j.bmcl.2010.07.113 BindingDB Entry DOI: 10.7270/Q23F4PV1
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50327257 (3-(1-(cyclopropylmethyl)piperidin-4-yloxy)-N-(3-(3...) Show SMILES O=C(Nc1cccc(NC(=O)c2cccc(c2)N2CCOCC2)c1)c1cccc(OC2CCN(CC3CC3)CC2)c1 Show InChI InChI=1S/C33H38N4O4/c38-32(25-4-1-8-29(20-25)37-16-18-40-19-17-37)34-27-6-3-7-28(22-27)35-33(39)26-5-2-9-31(21-26)41-30-12-14-36(15-13-30)23-24-10-11-24/h1-9,20-22,24,30H,10-19,23H2,(H,34,38)(H,35,39)	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	0.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Pharmaceuticals Curated by ChEMBL					Assay Description Binding affinity to kappa opioid receptor				Bioorg Med Chem Lett 20: 5847-52 (2010) Article DOI: 10.1016/j.bmcl.2010.07.113 BindingDB Entry DOI: 10.7270/Q23F4PV1
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM82551 (C18130 | CAS_105618-26-6 | NOR-BNI (HCI)2 | NORBNI) Show SMILES Oc1ccc2C[C@H]3N(CC4CC4)CC[C@@]45[C@@H](Oc1c24)c1[nH]c2[C@@H]4Oc6c7c(C[C@H]8N(CC9CC9)CC[C@@]47[C@@]8(O)Cc2c1C[C@@]35O)ccc6O |r| Show InChI InChI=1S/C40H43N3O6/c44-25-7-5-21-13-27-39(46)15-23-24-16-40(47)28-14-22-6-8-26(45)34-30(22)38(40,10-12-43(28)18-20-3-4-20)36(49-34)32(24)41-31(23)35-37(39,29(21)33(25)48-35)9-11-42(27)17-19-1-2-19/h5-8,19-20,27-28,35-36,41,44-47H,1-4,9-18H2/t27-,28-,35+,36+,37+,38+,39-,40-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE KEGG PC cid PC sid UniChem Similars	Article PubMed	0.900	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Pharmaceuticals Curated by ChEMBL					Assay Description Binding affinity to kappa opioid receptor				Bioorg Med Chem Lett 20: 5847-52 (2010) Article DOI: 10.1016/j.bmcl.2010.07.113 BindingDB Entry DOI: 10.7270/Q23F4PV1
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Rattus norvegicus (rat))	BDBM21393 (7-(dipropylamino)-5,6,7,8-tetrahydronaphthalen-1-o...) Show SMILES CCCN(CCC)C1CCc2cccc(O)c2C1 Show InChI InChI=1S/C16H25NO/c1-3-10-17(11-4-2)14-9-8-13-6-5-7-16(18)15(13)12-14/h5-7,14,18H,3-4,8-12H2,1-2H3	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	PubMed	1.40	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description Compound was evaluated in vitro for its ability to displace [3H]-8-hydroxy-2-(di-n-propylamino) tetralin binding from 5-hydroxytryptamine 1A receptor...				J Med Chem 35: 2369-74 (1992) BindingDB Entry DOI: 10.7270/Q2F18XP5
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Rattus norvegicus (rat))	BDBM50005135 (1-(3-Chloro-phenyl)-4-hexyl-piperazine | CHEMBL279...) Show SMILES CCCCCCN1CCN(CC1)c1cccc(Cl)c1 Show InChI InChI=1S/C16H25ClN2/c1-2-3-4-5-9-18-10-12-19(13-11-18)16-8-6-7-15(17)14-16/h6-8,14H,2-5,9-13H2,1H3	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	2.70	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description In vitro ability to displace [3H]-8-hydroxy-2-(di-n-propylamino) tetralin binding from 5-hydroxytryptamine 1A receptor site in rat brain hippocampus				J Med Chem 35: 2369-74 (1992) BindingDB Entry DOI: 10.7270/Q2F18XP5
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Rattus norvegicus (rat))	BDBM50005127 (1,1-Dioxo-2-[4-(4-pyrimidin-2-yl-piperazin-1-yl)-b...) Show SMILES O=C1N(CCCCN2CCN(CC2)c2ncccn2)S(=O)(=O)c2ccccc12 Show InChI InChI=1S/C19H23N5O3S/c25-18-16-6-1-2-7-17(16)28(26,27)24(18)11-4-3-10-22-12-14-23(15-13-22)19-20-8-5-9-21-19/h1-2,5-9H,3-4,10-15H2	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	PubMed	3.40	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description In vitro ability to displace [3H]-8-hydroxy-2-(di-n-propylamino) tetralin binding from 5-hydroxytryptamine 1A receptor site in rat brain hippocampus				J Med Chem 35: 2369-74 (1992) BindingDB Entry DOI: 10.7270/Q2F18XP5
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Rattus norvegicus (rat))	BDBM50005140 (1-(3-Chloro-phenyl)-4-pentyl-piperazine | CHEMBL27...) Show SMILES CCCCCN1CCN(CC1)c1cccc(Cl)c1 Show InChI InChI=1S/C15H23ClN2/c1-2-3-4-8-17-9-11-18(12-10-17)15-7-5-6-14(16)13-15/h5-7,13H,2-4,8-12H2,1H3	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	5.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description In vitro ability to displace [3H]-8-hydroxy-2-(di-n-propylamino) tetralin binding from 5-hydroxytryptamine 1A receptor site in rat brain hippocampus				J Med Chem 35: 2369-74 (1992) BindingDB Entry DOI: 10.7270/Q2F18XP5
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Rattus norvegicus (rat))	BDBM50005129 (1-(3-Chloro-phenyl)-4-octyl-piperazine | CHEMBL805...) Show SMILES CCCCCCCCN1CCN(CC1)c1cccc(Cl)c1 Show InChI InChI=1S/C18H29ClN2/c1-2-3-4-5-6-7-11-20-12-14-21(15-13-20)18-10-8-9-17(19)16-18/h8-10,16H,2-7,11-15H2,1H3	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	11	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description Compound was evaluated in vitro for its ability to displace [3H]-8-hydroxy-2-(di-n-propylamino) tetralin binding from 5-hydroxytryptamine 1A receptor...				J Med Chem 35: 2369-74 (1992) BindingDB Entry DOI: 10.7270/Q2F18XP5
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Rattus norvegicus (rat))	BDBM50005134 (1-Butyl-4-(3-chloro-phenyl)-piperazine | CHEMBL266...) Show SMILES CCCCN1CCN(CC1)c1cccc(Cl)c1 Show InChI InChI=1S/C14H21ClN2/c1-2-3-7-16-8-10-17(11-9-16)14-6-4-5-13(15)12-14/h4-6,12H,2-3,7-11H2,1H3	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	18	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description In vitro ability to displace [3H]-8-hydroxy-2-(di-n-propylamino) tetralin binding from 5-hydroxytryptamine 1A receptor site in rat brain hippocampus				J Med Chem 35: 2369-74 (1992) BindingDB Entry DOI: 10.7270/Q2F18XP5
					More data for this Ligand-Target Pair
Orphan methyltransferase M.SssI (Spiroplasma monobiae strain MQ-1)	BDBM50070942 ((-)-Epigallocatechin gallate | (-)-Epigallocatechi...) Show SMILES Oc1cc(O)c2C[C@@H](OC(=O)c3cc(O)c(O)c(O)c3)[C@H](Oc2c1)c1cc(O)c(O)c(O)c1 |r| Show InChI InChI=1S/C22H18O11/c23-10-5-12(24)11-7-18(33-22(31)9-3-15(27)20(30)16(28)4-9)21(32-17(11)6-10)8-1-13(25)19(29)14(26)2-8/h1-6,18,21,23-30H,7H2/t18-,21-/m1/s1	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG MMDB PC cid PC sid UniChem Patents Similars	Article PubMed	28	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description Competitive inhibition of Spiroplasma sp. MQ1 SssI methyltransferase using pUC18 as substrate measured for 10 mins by Dixon plot analysis				Eur J Med Chem 55: 243-54 (2012) Article DOI: 10.1016/j.ejmech.2012.07.024 BindingDB Entry DOI: 10.7270/Q2GH9K11
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Rattus norvegicus (rat))	BDBM50005132 (4,4-Dimethyl-1-[4-(4-pyrimidin-2-yl-piperazin-1-yl...) Show SMILES CC1(C)CC(=O)N(CCCCN2CCN(CC2)c2ncccn2)C(=O)C1 Show InChI InChI=1S/C19H29N5O2/c1-19(2)14-16(25)24(17(26)15-19)9-4-3-8-22-10-12-23(13-11-22)18-20-6-5-7-21-18/h5-7H,3-4,8-15H2,1-2H3	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	PubMed	32	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description In vitro ability to displace [3H]-8-hydroxy-2-(di-n-propylamino) tetralin binding from 5-hydroxytryptamine 1A receptor site in rat brain hippocampus				J Med Chem 35: 2369-74 (1992) BindingDB Entry DOI: 10.7270/Q2F18XP5
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50325855 (CHEMBL1223951 | exo-3-((1R,3s,5S)-8-benzyl-8-azabi...) Show SMILES NC(=O)c1cccc(O[C@H]2C[C@@H]3CC[C@H](C2)N3Cc2ccccc2)c1 |r,TLB:17:16:15.9.10:13.12| Show InChI InChI=1S/C21H24N2O2/c22-21(24)16-7-4-8-19(11-16)25-20-12-17-9-10-18(13-20)23(17)14-15-5-2-1-3-6-15/h1-8,11,17-18,20H,9-10,12-14H2,(H2,22,24)/t17-,18+,20-	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	40	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Pharmaceuticals Curated by ChEMBL					Assay Description Binding affinity to kappa opioid receptor				Bioorg Med Chem Lett 20: 5847-52 (2010) Article DOI: 10.1016/j.bmcl.2010.07.113 BindingDB Entry DOI: 10.7270/Q23F4PV1
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50327259 (3-(1-benzylpiperidin-4-yloxy)benzamide | CHEMBL125...) Show SMILES NC(=O)c1cccc(OC2CCN(Cc3ccccc3)CC2)c1 Show InChI InChI=1S/C19H22N2O2/c20-19(22)16-7-4-8-18(13-16)23-17-9-11-21(12-10-17)14-15-5-2-1-3-6-15/h1-8,13,17H,9-12,14H2,(H2,20,22)	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	75	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Pharmaceuticals Curated by ChEMBL					Assay Description Binding affinity to kappa opioid receptor				Bioorg Med Chem Lett 20: 5847-52 (2010) Article DOI: 10.1016/j.bmcl.2010.07.113 BindingDB Entry DOI: 10.7270/Q23F4PV1
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Rattus norvegicus (rat))	BDBM50005123 (1-(3-Chloro-phenyl)-4-propyl-piperazine | 1-(3-Chl...) Show SMILES CCCN1CCN(CC1)c1cccc(Cl)c1 Show InChI InChI=1S/C13H19ClN2/c1-2-6-15-7-9-16(10-8-15)13-5-3-4-12(14)11-13/h3-5,11H,2,6-10H2,1H3	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	122	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description In vitro ability to displace [3H]-8-hydroxy-2-(di-n-propylamino) tetralin binding from 5-hydroxytryptamine 1A receptor site in rat brain hippocampus				J Med Chem 35: 2369-74 (1992) BindingDB Entry DOI: 10.7270/Q2F18XP5
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Rattus norvegicus (rat))	BDBM50005133 (1-sec-Butyl-4-(3-chloro-phenyl)-piperazine | CHEMB...) Show SMILES CCC(C)N1CCN(CC1)c1cccc(Cl)c1 Show InChI InChI=1S/C14H21ClN2/c1-3-12(2)16-7-9-17(10-8-16)14-6-4-5-13(15)11-14/h4-6,11-12H,3,7-10H2,1-2H3	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	127	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description In vitro ability to displace [3H]-8-hydroxy-2-(di-n-propylamino) tetralin binding from 5-hydroxytryptamine 1A receptor site in rat brain hippocampus				J Med Chem 35: 2369-74 (1992) BindingDB Entry DOI: 10.7270/Q2F18XP5
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Rattus norvegicus (rat))	BDBM50001915 (1-(3-chlorophenyl)piperazine | CHEMBL478 | m-Chlor...) Show SMILES Clc1cccc(c1)N1CCNCC1 Show InChI InChI=1S/C10H13ClN2/c11-9-2-1-3-10(8-9)13-6-4-12-5-7-13/h1-3,8,12H,4-7H2	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL KEGG PC cid PC sid UniChem Patents Similars	PubMed	143	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description In vitro ability to displace [3H]-8-hydroxy-2-(di-n-propylamino) tetralin binding from 5-hydroxytryptamine 1A receptor site in rat brain hippocampus				J Med Chem 35: 2369-74 (1992) BindingDB Entry DOI: 10.7270/Q2F18XP5
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50327258 (3-(1-(cyclopropylmethyl)piperidin-4-yloxy)benzamid...) Show SMILES NC(=O)c1cccc(OC2CCN(CC3CC3)CC2)c1 Show InChI InChI=1S/C16H22N2O2/c17-16(19)13-2-1-3-15(10-13)20-14-6-8-18(9-7-14)11-12-4-5-12/h1-3,10,12,14H,4-9,11H2,(H2,17,19)	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	146	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Pharmaceuticals Curated by ChEMBL					Assay Description Binding affinity to kappa opioid receptor				Bioorg Med Chem Lett 20: 5847-52 (2010) Article DOI: 10.1016/j.bmcl.2010.07.113 BindingDB Entry DOI: 10.7270/Q23F4PV1
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Rattus norvegicus (rat))	BDBM50005124 (1-(3-Chloro-phenyl)-4-methyl-piperazine | CHEMBL26...) Show SMILES CN1CCN(CC1)c1cccc(Cl)c1 Show InChI InChI=1S/C11H15ClN2/c1-13-5-7-14(8-6-13)11-4-2-3-10(12)9-11/h2-4,9H,5-8H2,1H3	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	152	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description In vitro ability to displace [3H]-8-hydroxy-2-(di-n-propylamino) tetralin binding from 5-hydroxytryptamine 1A receptor site in rat brain hippocampus				J Med Chem 35: 2369-74 (1992) BindingDB Entry DOI: 10.7270/Q2F18XP5
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Rattus norvegicus (rat))	BDBM50005142 (1-(3-Chloro-phenyl)-4-isopropyl-piperazine | CHEMB...) Show SMILES CC(C)N1CCN(CC1)c1cccc(Cl)c1 Show InChI InChI=1S/C13H19ClN2/c1-11(2)15-6-8-16(9-7-15)13-5-3-4-12(14)10-13/h3-5,10-11H,6-9H2,1-2H3	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	159	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description In vitro ability to displace [3H]-8-hydroxy-2-(di-n-propylamino) tetralin binding from 5-hydroxytryptamine 1A receptor site in rat brain hippocampus				J Med Chem 35: 2369-74 (1992) BindingDB Entry DOI: 10.7270/Q2F18XP5
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Rattus norvegicus (rat))	BDBM50005131 (1-Benzyl-4-(3-chloro-phenyl)-piperazine | CHEMBL27...) Show SMILES Clc1cccc(c1)N1CCN(Cc2ccccc2)CC1 Show InChI InChI=1S/C17H19ClN2/c18-16-7-4-8-17(13-16)20-11-9-19(10-12-20)14-15-5-2-1-3-6-15/h1-8,13H,9-12,14H2	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	166	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description In vitro ability to displace [3H]-8-hydroxy-2-(di-n-propylamino) tetralin binding from 5-hydroxytryptamine 1A receptor site in rat brain hippocampus				J Med Chem 35: 2369-74 (1992) BindingDB Entry DOI: 10.7270/Q2F18XP5
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Rattus norvegicus (rat))	BDBM50005143 (2-[4-(3-Chloro-phenyl)-piperazin-1-yl]-ethanol | C...) Show SMILES OCCN1CCN(CC1)c1cccc(Cl)c1 Show InChI InChI=1S/C12H17ClN2O/c13-11-2-1-3-12(10-11)15-6-4-14(5-7-15)8-9-16/h1-3,10,16H,4-9H2	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	202	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description In vitro ability to displace [3H]-8-hydroxy-2-(di-n-propylamino) tetralin binding from 5-hydroxytryptamine 1A receptor site in rat brain hippocampus				J Med Chem 35: 2369-74 (1992) BindingDB Entry DOI: 10.7270/Q2F18XP5
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Rattus norvegicus (rat))	BDBM50005139 (1-(3-Chloro-phenyl)-4-ethyl-piperazine | CHEMBL413...) Show SMILES CCN1CCN(CC1)c1cccc(Cl)c1 Show InChI InChI=1S/C12H17ClN2/c1-2-14-6-8-15(9-7-14)12-5-3-4-11(13)10-12/h3-5,10H,2,6-9H2,1H3	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	220	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description In vitro ability to displace [3H]-8-hydroxy-2-(di-n-propylamino) tetralin binding from 5-hydroxytryptamine 1A receptor site in rat brain hippocampus				J Med Chem 35: 2369-74 (1992) BindingDB Entry DOI: 10.7270/Q2F18XP5
					More data for this Ligand-Target Pair
Orphan methyltransferase M.SssI (Spiroplasma monobiae strain MQ-1)	BDBM50389497 (CHEMBL1564869) Show SMILES OC(=O)[C@H](Cc1c[nH]c2ccccc12)N1C(=O)c2ccccc2C1=O Show InChI InChI=1S/C19H14N2O4/c22-17-13-6-1-2-7-14(13)18(23)21(17)16(19(24)25)9-11-10-20-15-8-4-3-5-12(11)15/h1-8,10,16,20H,9H2,(H,24,25)/t16-/m0/s1	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	230	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description Competitive inhibition of Spiroplasma sp. MQ1 SssI methyltransferase using pUC18 as substrate measured for 10 mins by Dixon plot analysis				Eur J Med Chem 55: 243-54 (2012) Article DOI: 10.1016/j.ejmech.2012.07.024 BindingDB Entry DOI: 10.7270/Q2GH9K11
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Rattus norvegicus (rat))	BDBM50005126 (1-Allyl-4-(3-chloro-phenyl)-piperazine | CHEMBL767...) Show SMILES Clc1cccc(c1)N1CCN(CC=C)CC1 Show InChI InChI=1S/C13H17ClN2/c1-2-6-15-7-9-16(10-8-15)13-5-3-4-12(14)11-13/h2-5,11H,1,6-10H2	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	251	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description In vitro ability to displace [3H]-8-hydroxy-2-(di-n-propylamino) tetralin binding from 5-hydroxytryptamine 1A receptor site in rat brain hippocampus				J Med Chem 35: 2369-74 (1992) BindingDB Entry DOI: 10.7270/Q2F18XP5
					More data for this Ligand-Target Pair
Orphan methyltransferase M.SssI (Spiroplasma monobiae strain MQ-1)	BDBM50389487 (CHEMBL2063048) Show SMILES O=C1NCNC(NCc2ccco2)=N1 |c:13| Show InChI InChI=1S/C8H10N4O2/c13-8-11-5-10-7(12-8)9-4-6-2-1-3-14-6/h1-3H,4-5H2,(H3,9,10,11,12,13)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	700	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description Competitive inhibition of Spiroplasma sp. MQ1 SssI methyltransferase using pUC18 as substrate measured for 10 mins by Dixon plot analysis				Eur J Med Chem 55: 243-54 (2012) Article DOI: 10.1016/j.ejmech.2012.07.024 BindingDB Entry DOI: 10.7270/Q2GH9K11
					More data for this Ligand-Target Pair
Orphan methyltransferase M.SssI (Spiroplasma monobiae strain MQ-1)	BDBM50389488 (CHEMBL2063060) Show SMILES Cc1cnc(=O)[nH]c1NCc1ccccc1 Show InChI InChI=1S/C12H13N3O/c1-9-7-14-12(16)15-11(9)13-8-10-5-3-2-4-6-10/h2-7H,8H2,1H3,(H2,13,14,15,16)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.60E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description Competitive inhibition of Spiroplasma sp. MQ1 SssI methyltransferase using pUC18 as substrate measured for 10 mins by Dixon plot analysis				Eur J Med Chem 55: 243-54 (2012) Article DOI: 10.1016/j.ejmech.2012.07.024 BindingDB Entry DOI: 10.7270/Q2GH9K11
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Rattus norvegicus (rat))	BDBM50005130 (8-(3-Chloro-phenyl)-8-aza-5-azonia-spiro[4.5]decan...) Show SMILES Clc1cccc(c1)N1CC[N+]2(CCCC2)CC1 Show InChI InChI=1S/C14H20ClN2/c15-13-4-3-5-14(12-13)16-6-10-17(11-7-16)8-1-2-9-17/h3-5,12H,1-2,6-11H2/q+1	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	7.22E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description In vitro ability to displace [3H]-8-hydroxy-2-(di-n-propylamino) tetralin binding from 5-hydroxytryptamine 1A receptor site in rat brain hippocampus				J Med Chem 35: 2369-74 (1992) BindingDB Entry DOI: 10.7270/Q2F18XP5
					More data for this Ligand-Target Pair
Orphan methyltransferase M.SssI (Spiroplasma monobiae strain MQ-1)	BDBM50389495 (CHEMBL2063052) Show SMILES O=c1nccc(NCc2ccccc2)[nH]1 Show InChI InChI=1S/C11H11N3O/c15-11-12-7-6-10(14-11)13-8-9-4-2-1-3-5-9/h1-7H,8H2,(H2,12,13,14,15)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description Competitive inhibition of Spiroplasma sp. MQ1 SssI methyltransferase using pUC18 as substrate measured for 10 mins by Dixon plot analysis				Eur J Med Chem 55: 243-54 (2012) Article DOI: 10.1016/j.ejmech.2012.07.024 BindingDB Entry DOI: 10.7270/Q2GH9K11
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Rattus norvegicus (rat))	BDBM50005138 (1-[4-(3-Chloro-phenyl)-piperazin-1-yl]-2-phenyl-et...) Show SMILES Clc1cccc(c1)N1CCN(CC1)C(=O)Cc1ccccc1 Show InChI InChI=1S/C18H19ClN2O/c19-16-7-4-8-17(14-16)20-9-11-21(12-10-20)18(22)13-15-5-2-1-3-6-15/h1-8,14H,9-13H2	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	1.48E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description In vitro ability to displace [3H]-8-hydroxy-2-(di-n-propylamino) tetralin binding from 5-hydroxytryptamine 1A receptor site in rat brain hippocampus				J Med Chem 35: 2369-74 (1992) BindingDB Entry DOI: 10.7270/Q2F18XP5
					More data for this Ligand-Target Pair
Orphan methyltransferase M.SssI (Spiroplasma monobiae strain MQ-1)	BDBM50389498 (CHEMBL2063050) Show SMILES Cc1cnc(=O)[nH]c1NCc1ccco1 Show InChI InChI=1S/C10H11N3O2/c1-7-5-12-10(14)13-9(7)11-6-8-3-2-4-15-8/h2-5H,6H2,1H3,(H2,11,12,13,14)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.50E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description Competitive inhibition of Spiroplasma sp. MQ1 SssI methyltransferase using pUC18 as substrate measured for 10 mins by Dixon plot analysis				Eur J Med Chem 55: 243-54 (2012) Article DOI: 10.1016/j.ejmech.2012.07.024 BindingDB Entry DOI: 10.7270/Q2GH9K11
					More data for this Ligand-Target Pair
Orphan methyltransferase M.SssI (Spiroplasma monobiae strain MQ-1)	BDBM50389489 (CHEMBL2063059) Show SMILES O=C1NCNC(NCc2ccccc2)=N1 |c:14| Show InChI InChI=1S/C10H12N4O/c15-10-13-7-12-9(14-10)11-6-8-4-2-1-3-5-8/h1-5H,6-7H2,(H3,11,12,13,14,15)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	2.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description Competitive inhibition of Spiroplasma sp. MQ1 SssI methyltransferase using pUC18 as substrate measured for 10 mins by Dixon plot analysis				Eur J Med Chem 55: 243-54 (2012) Article DOI: 10.1016/j.ejmech.2012.07.024 BindingDB Entry DOI: 10.7270/Q2GH9K11
					More data for this Ligand-Target Pair
Orphan methyltransferase M.SssI (Spiroplasma monobiae strain MQ-1)	BDBM50389481 (CHEMBL2063056) Show SMILES CC(=O)OCc1cnc(=O)[nH]c1NCc1ccccc1 Show InChI InChI=1S/C14H15N3O3/c1-10(18)20-9-12-8-16-14(19)17-13(12)15-7-11-5-3-2-4-6-11/h2-6,8H,7,9H2,1H3,(H2,15,16,17,19)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.30E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description Competitive inhibition of Spiroplasma sp. MQ1 SssI methyltransferase using pUC18 as substrate measured for 10 mins by Dixon plot analysis				Eur J Med Chem 55: 243-54 (2012) Article DOI: 10.1016/j.ejmech.2012.07.024 BindingDB Entry DOI: 10.7270/Q2GH9K11
					More data for this Ligand-Target Pair
Orphan methyltransferase M.SssI (Spiroplasma monobiae strain MQ-1)	BDBM50389494 (CHEMBL2063053) Show SMILES Cc1ccc(CNc2ccnc(=O)[nH]2)cc1 Show InChI InChI=1S/C12H13N3O/c1-9-2-4-10(5-3-9)8-14-11-6-7-13-12(16)15-11/h2-7H,8H2,1H3,(H2,13,14,15,16)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.60E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description Competitive inhibition of Spiroplasma sp. MQ1 SssI methyltransferase using pUC18 as substrate measured for 10 mins by Dixon plot analysis				Eur J Med Chem 55: 243-54 (2012) Article DOI: 10.1016/j.ejmech.2012.07.024 BindingDB Entry DOI: 10.7270/Q2GH9K11
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Rattus norvegicus (rat))	BDBM50005141 (1-[4-(3-Chloro-phenyl)-piperazin-1-yl]-propan-1-on...) Show SMILES CCC(=O)N1CCN(CC1)c1cccc(Cl)c1 Show InChI InChI=1S/C13H17ClN2O/c1-2-13(17)16-8-6-15(7-9-16)12-5-3-4-11(14)10-12/h3-5,10H,2,6-9H2,1H3	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	3.08E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description In vitro ability to displace [3H]-8-hydroxy-2-(di-n-propylamino) tetralin binding from 5-hydroxytryptamine 1A receptor site in rat brain hippocampus				J Med Chem 35: 2369-74 (1992) BindingDB Entry DOI: 10.7270/Q2F18XP5
					More data for this Ligand-Target Pair
Orphan methyltransferase M.SssI (Spiroplasma monobiae strain MQ-1)	BDBM50389491 (CHEMBL2063057) Show SMILES OS(=O)(=O)Cc1cnc(=O)[nH]c1NCc1ccccc1 Show InChI InChI=1S/C12H13N3O4S/c16-12-14-7-10(8-20(17,18)19)11(15-12)13-6-9-4-2-1-3-5-9/h1-5,7H,6,8H2,(H,17,18,19)(H2,13,14,15,16)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem	Article PubMed	3.30E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description Competitive inhibition of Spiroplasma sp. MQ1 SssI methyltransferase using pUC18 as substrate measured for 10 mins by Dixon plot analysis				Eur J Med Chem 55: 243-54 (2012) Article DOI: 10.1016/j.ejmech.2012.07.024 BindingDB Entry DOI: 10.7270/Q2GH9K11
					More data for this Ligand-Target Pair
Orphan methyltransferase M.SssI (Spiroplasma monobiae strain MQ-1)	BDBM50389490 (CHEMBL2063058) Show SMILES O=Cc1cnc(=O)[nH]c1NCc1ccccc1 Show InChI InChI=1S/C12H11N3O2/c16-8-10-7-14-12(17)15-11(10)13-6-9-4-2-1-3-5-9/h1-5,7-8H,6H2,(H2,13,14,15,17)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.50E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description Competitive inhibition of Spiroplasma sp. MQ1 SssI methyltransferase using pUC18 as substrate measured for 10 mins by Dixon plot analysis				Eur J Med Chem 55: 243-54 (2012) Article DOI: 10.1016/j.ejmech.2012.07.024 BindingDB Entry DOI: 10.7270/Q2GH9K11
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Rattus norvegicus (rat))	BDBM50005122 (1-[4-(3-Chloro-phenyl)-piperazin-1-yl]-butan-1-one...) Show SMILES CCCC(=O)N1CCN(CC1)c1cccc(Cl)c1 Show InChI InChI=1S/C14H19ClN2O/c1-2-4-14(18)17-9-7-16(8-10-17)13-6-3-5-12(15)11-13/h3,5-6,11H,2,4,7-10H2,1H3	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	4.90E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description In vitro ability to displace [3H]-8-hydroxy-2-(di-n-propylamino) tetralin binding from 5-hydroxytryptamine 1A receptor site in rat brain hippocampus				J Med Chem 35: 2369-74 (1992) BindingDB Entry DOI: 10.7270/Q2F18XP5
					More data for this Ligand-Target Pair
Orphan methyltransferase M.SssI (Spiroplasma monobiae strain MQ-1)	BDBM50389503 (CHEMBL2063044) Show SMILES CC(=O)OCc1cnc(=O)[nH]c1NCc1ccco1 Show InChI InChI=1S/C12H13N3O4/c1-8(16)19-7-9-5-14-12(17)15-11(9)13-6-10-3-2-4-18-10/h2-5H,6-7H2,1H3,(H2,13,14,15,17)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description Competitive inhibition of Spiroplasma sp. MQ1 SssI methyltransferase using pUC18 as substrate measured for 10 mins by Dixon plot analysis				Eur J Med Chem 55: 243-54 (2012) Article DOI: 10.1016/j.ejmech.2012.07.024 BindingDB Entry DOI: 10.7270/Q2GH9K11
					More data for this Ligand-Target Pair
Orphan methyltransferase M.SssI (Spiroplasma monobiae strain MQ-1)	BDBM50389482 (CHEMBL1699292) Show SMILES O=c1nccc(NCc2ccco2)[nH]1 Show InChI InChI=1S/C9H9N3O2/c13-9-10-4-3-8(12-9)11-6-7-2-1-5-14-7/h1-5H,6H2,(H2,10,11,12,13)	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid PDB UniChem Similars	Article PubMed	7.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description Competitive inhibition of Spiroplasma sp. MQ1 SssI methyltransferase using pUC18 as substrate measured for 10 mins by Dixon plot analysis				Eur J Med Chem 55: 243-54 (2012) Article DOI: 10.1016/j.ejmech.2012.07.024 BindingDB Entry DOI: 10.7270/Q2GH9K11
					More data for this Ligand-Target Pair
Orphan methyltransferase M.SssI (Spiroplasma monobiae strain MQ-1)	BDBM50389501 (CHEMBL2063046) Show SMILES O=Cc1cnc(=O)[nH]c1NCc1ccco1 Show InChI InChI=1S/C10H9N3O3/c14-6-7-4-12-10(15)13-9(7)11-5-8-2-1-3-16-8/h1-4,6H,5H2,(H2,11,12,13,15)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	8.30E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description Competitive inhibition of Spiroplasma sp. MQ1 SssI methyltransferase using pUC18 as substrate measured for 10 mins by Dixon plot analysis				Eur J Med Chem 55: 243-54 (2012) Article DOI: 10.1016/j.ejmech.2012.07.024 BindingDB Entry DOI: 10.7270/Q2GH9K11
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Rattus norvegicus (rat))	BDBM50005128 (1-[4-(3-Chloro-phenyl)-piperazin-1-yl]-ethanone | ...) Show SMILES CC(=O)N1CCN(CC1)c1cccc(Cl)c1 Show InChI InChI=1S/C12H15ClN2O/c1-10(16)14-5-7-15(8-6-14)12-4-2-3-11(13)9-12/h2-4,9H,5-8H2,1H3	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description In vitro ability to displace [3H]-8-hydroxy-2-(di-n-propylamino) tetralin binding from 5-hydroxytryptamine 1A receptor site in rat brain hippocampus				J Med Chem 35: 2369-74 (1992) BindingDB Entry DOI: 10.7270/Q2F18XP5
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Rattus norvegicus (rat))	BDBM50005136 (4-(3-Chloro-phenyl)-morpholine | CHEMBL77181) Show SMILES Clc1cccc(c1)N1CCOCC1 Show InChI InChI=1S/C10H12ClNO/c11-9-2-1-3-10(8-9)12-4-6-13-7-5-12/h1-3,8H,4-7H2	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents	PubMed	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description In vitro ability to displace [3H]-8-hydroxy-2-(di-n-propylamino) tetralin binding from 5-hydroxytryptamine 1A receptor site in rat brain hippocampus				J Med Chem 35: 2369-74 (1992) BindingDB Entry DOI: 10.7270/Q2F18XP5
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Rattus norvegicus (rat))	BDBM50005125 (1-[4-(3-Chloro-phenyl)-piperazin-1-yl]-2-methyl-pr...) Show SMILES CC(C)C(=O)N1CCN(CC1)c1cccc(Cl)c1 Show InChI InChI=1S/C14H19ClN2O/c1-11(2)14(18)17-8-6-16(7-9-17)13-5-3-4-12(15)10-13/h3-5,10-11H,6-9H2,1-2H3	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description In vitro ability to displace [3H]-8-hydroxy-2-(di-n-propylamino) tetralin binding from 5-hydroxytryptamine 1A receptor site in rat brain hippocampus				J Med Chem 35: 2369-74 (1992) BindingDB Entry DOI: 10.7270/Q2F18XP5
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Rattus norvegicus (rat))	BDBM50005137 (CHEMBL418386 | [4-(3-Chloro-phenyl)-piperazin-1-yl...) Show SMILES Clc1cccc(c1)N1CCN(CC1)C(=O)c1ccccc1 Show InChI InChI=1S/C17H17ClN2O/c18-15-7-4-8-16(13-15)19-9-11-20(12-10-19)17(21)14-5-2-1-3-6-14/h1-8,13H,9-12H2	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description In vitro ability to displace [3H]-8-hydroxy-2-(di-n-propylamino) tetralin binding from 5-hydroxytryptamine 1A receptor site in rat brain hippocampus				J Med Chem 35: 2369-74 (1992) BindingDB Entry DOI: 10.7270/Q2F18XP5
					More data for this Ligand-Target Pair
Orphan methyltransferase M.SssI (Spiroplasma monobiae strain MQ-1)	BDBM50389502 (CHEMBL2063045) Show SMILES OS(=O)(=O)Cc1cnc(=O)[nH]c1NCc1ccco1 Show InChI InChI=1S/C10H11N3O5S/c14-10-12-4-7(6-19(15,16)17)9(13-10)11-5-8-2-1-3-18-8/h1-4H,5-6H2,(H,15,16,17)(H2,11,12,13,14)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem	Article PubMed	1.12E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description Competitive inhibition of Spiroplasma sp. MQ1 SssI methyltransferase using pUC18 as substrate measured for 10 mins by Dixon plot analysis				Eur J Med Chem 55: 243-54 (2012) Article DOI: 10.1016/j.ejmech.2012.07.024 BindingDB Entry DOI: 10.7270/Q2GH9K11
					More data for this Ligand-Target Pair
Orphan methyltransferase M.SssI (Spiroplasma monobiae strain MQ-1)	BDBM50389492 (CHEMBL2063055) Show SMILES OCc1cnc(=O)[nH]c1NCc1ccccc1 Show InChI InChI=1S/C12H13N3O2/c16-8-10-7-14-12(17)15-11(10)13-6-9-4-2-1-3-5-9/h1-5,7,16H,6,8H2,(H2,13,14,15,17)	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.35E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description Competitive inhibition of Spiroplasma sp. MQ1 SssI methyltransferase using pUC18 as substrate measured for 10 mins by Dixon plot analysis				Eur J Med Chem 55: 243-54 (2012) Article DOI: 10.1016/j.ejmech.2012.07.024 BindingDB Entry DOI: 10.7270/Q2GH9K11
					More data for this Ligand-Target Pair
Orphan methyltransferase M.SssI (Spiroplasma monobiae strain MQ-1)	BDBM50389505 (CHEMBL2063041) Show SMILES OC[C@H]1O[C@H](C[C@@H]1O)n1ccc(NCc2ccco2)nc1=O |r| Show InChI InChI=1S/C14H17N3O5/c18-8-11-10(19)6-13(22-11)17-4-3-12(16-14(17)20)15-7-9-2-1-5-21-9/h1-5,10-11,13,18-19H,6-8H2,(H,15,16,20)/t10-,11+,13+/m0/s1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.70E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description Competitive inhibition of Spiroplasma sp. MQ1 SssI methyltransferase using pUC18 as substrate measured for 10 mins by Dixon plot analysis				Eur J Med Chem 55: 243-54 (2012) Article DOI: 10.1016/j.ejmech.2012.07.024 BindingDB Entry DOI: 10.7270/Q2GH9K11
					More data for this Ligand-Target Pair
Orphan methyltransferase M.SssI (Spiroplasma monobiae strain MQ-1)	BDBM50389499 (CHEMBL2063049) Show SMILES Cc1cn([C@H]2C[C@H](O)[C@@H](CO)O2)c(=O)nc1NCc1ccco1 |r| Show InChI InChI=1S/C15H19N3O5/c1-9-7-18(13-5-11(20)12(8-19)23-13)15(21)17-14(9)16-6-10-3-2-4-22-10/h2-4,7,11-13,19-20H,5-6,8H2,1H3,(H,16,17,21)/t11-,12+,13+/m0/s1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.50E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description Competitive inhibition of Spiroplasma sp. MQ1 SssI methyltransferase using pUC18 as substrate measured for 10 mins by Dixon plot analysis				Eur J Med Chem 55: 243-54 (2012) Article DOI: 10.1016/j.ejmech.2012.07.024 BindingDB Entry DOI: 10.7270/Q2GH9K11
					More data for this Ligand-Target Pair
Orphan methyltransferase M.SssI (Spiroplasma monobiae strain MQ-1)	BDBM50389493 (CHEMBL2063054) Show SMILES O=c1nccc(NCc2cccnc2)[nH]1 Show InChI InChI=1S/C10H10N4O/c15-10-12-5-3-9(14-10)13-7-8-2-1-4-11-6-8/h1-6H,7H2,(H2,12,13,14,15)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	4.00E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description Competitive inhibition of Spiroplasma sp. MQ1 SssI methyltransferase using pUC18 as substrate measured for 10 mins by Dixon plot analysis				Eur J Med Chem 55: 243-54 (2012) Article DOI: 10.1016/j.ejmech.2012.07.024 BindingDB Entry DOI: 10.7270/Q2GH9K11
					More data for this Ligand-Target Pair
Orphan methyltransferase M.SssI (Spiroplasma monobiae strain MQ-1)	BDBM50389504 (CHEMBL2063043) Show SMILES OCc1cnc(=O)[nH]c1NCc1ccco1 Show InChI InChI=1S/C10H11N3O3/c14-6-7-4-12-10(15)13-9(7)11-5-8-2-1-3-16-8/h1-4,14H,5-6H2,(H2,11,12,13,15)	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.40E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Polish Academy of Sciences Curated by ChEMBL					Assay Description Competitive inhibition of Spiroplasma sp. MQ1 SssI methyltransferase using pUC18 as substrate measured for 10 mins by Dixon plot analysis				Eur J Med Chem 55: 243-54 (2012) Article DOI: 10.1016/j.ejmech.2012.07.024 BindingDB Entry DOI: 10.7270/Q2GH9K11
					More data for this Ligand-Target Pair

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