Compile Data Set for Download or QSAR

Found 45 hits with Last Name = 'salo' and Initial = 'om'   

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
Thymidylate synthase (Homo sapiens (Human))	BDBM18796 ((2S)-2-{[4-(2-{2-amino-4-oxo-1H,4H,7H-pyrrolo[2,3-...) Show SMILES Nc1nc2[nH]cc(CCc3ccc(cc3)C(=O)N[C@@H](CCC(O)=O)C(O)=O)c2c(=O)[nH]1 |r| Show InChI InChI=1S/C20H21N5O6/c21-20-24-16-15(18(29)25-20)12(9-22-16)6-3-10-1-4-11(5-2-10)17(28)23-13(19(30)31)7-8-14(26)27/h1-2,4-5,9,13H,3,6-8H2,(H,23,28)(H,26,27)(H,30,31)(H4,21,22,24,25,29)/t13-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE MMDB PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	1.30	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Theoretical Studies gGmbH Curated by ChEMBL					Assay Description Inhibition of thymidin synthase				J Med Chem 53: 6539-49 (2010) Article DOI: 10.1021/jm901869w BindingDB Entry DOI: 10.7270/Q24J0F9S
					More data for this Ligand-Target Pair				3D Structure (crystal)
Dihydrofolate reductase (Homo sapiens (Human))	BDBM18796 ((2S)-2-{[4-(2-{2-amino-4-oxo-1H,4H,7H-pyrrolo[2,3-...) Show SMILES Nc1nc2[nH]cc(CCc3ccc(cc3)C(=O)N[C@@H](CCC(O)=O)C(O)=O)c2c(=O)[nH]1 |r| Show InChI InChI=1S/C20H21N5O6/c21-20-24-16-15(18(29)25-20)12(9-22-16)6-3-10-1-4-11(5-2-10)17(28)23-13(19(30)31)7-8-14(26)27/h1-2,4-5,9,13H,3,6-8H2,(H,23,28)(H,26,27)(H,30,31)(H4,21,22,24,25,29)/t13-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	7.20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Theoretical Studies gGmbH Curated by ChEMBL					Assay Description Inhibition of DHFR				J Med Chem 53: 6539-49 (2010) Article DOI: 10.1021/jm901869w BindingDB Entry DOI: 10.7270/Q24J0F9S
					More data for this Ligand-Target Pair
Thymidylate synthase (Homo sapiens (Human))	BDBM50326711 (1,3-propanediphosphonic acid | CHEMBL1230579 | PRO...) Show SMILES OP(O)(=O)CCCP(O)(O)=O Show InChI InChI=1S/C3H10O6P2/c4-10(5,6)2-1-3-11(7,8)9/h1-3H2,(H2,4,5,6)(H2,7,8,9)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE MMDB PC cid PC sid PDB UniChem Patents	MMDB PDB Article PubMed	260	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Theoretical Studies gGmbH Curated by ChEMBL					Assay Description Inhibition of human Thymidylate synthase by uncompetitive binding				J Med Chem 53: 6539-49 (2010) Article DOI: 10.1021/jm901869w BindingDB Entry DOI: 10.7270/Q24J0F9S
					More data for this Ligand-Target Pair				3D Structure (crystal)
Trifunctional purine biosynthetic protein adenosine-3 (Homo sapiens (Human))	BDBM18796 ((2S)-2-{[4-(2-{2-amino-4-oxo-1H,4H,7H-pyrrolo[2,3-...) Show SMILES Nc1nc2[nH]cc(CCc3ccc(cc3)C(=O)N[C@@H](CCC(O)=O)C(O)=O)c2c(=O)[nH]1 |r| Show InChI InChI=1S/C20H21N5O6/c21-20-24-16-15(18(29)25-20)12(9-22-16)6-3-10-1-4-11(5-2-10)17(28)23-13(19(30)31)7-8-14(26)27/h1-2,4-5,9,13H,3,6-8H2,(H,23,28)(H,26,27)(H,30,31)(H4,21,22,24,25,29)/t13-/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase MCE MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	380	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Theoretical Studies gGmbH Curated by ChEMBL					Assay Description Inhibition of GARFT				J Med Chem 53: 6539-49 (2010) Article DOI: 10.1021/jm901869w BindingDB Entry DOI: 10.7270/Q24J0F9S
					More data for this Ligand-Target Pair
Thymidylate synthase (Homo sapiens (Human))	BDBM50326711 (1,3-propanediphosphonic acid | CHEMBL1230579 | PRO...) Show SMILES OP(O)(=O)CCCP(O)(O)=O Show InChI InChI=1S/C3H10O6P2/c4-10(5,6)2-1-3-11(7,8)9/h1-3H2,(H2,4,5,6)(H2,7,8,9)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE MMDB PC cid PC sid PDB UniChem Patents	MMDB PDB Article PubMed	2.70E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Theoretical Studies gGmbH Curated by ChEMBL					Assay Description Inhibition of human Thymidylate synthase by noncompetitive binding				J Med Chem 53: 6539-49 (2010) Article DOI: 10.1021/jm901869w BindingDB Entry DOI: 10.7270/Q24J0F9S
					More data for this Ligand-Target Pair				3D Structure (crystal)
Estrogen receptor (Homo sapiens (Human))	BDBM50326712 (2(R)-[4(S)-carboxy-4-[4-[N-(2-hydroxymethyl-4-oxo-...) Show SMILES OCc1nc2cc3CCC(N(CC#C)c4ccc(cc4)C(=O)N[C@@H](CCC(=O)N[C@H](CCC(O)=O)C(O)=O)C(O)=O)c3cc2c(=O)[nH]1 |r| Show InChI InChI=1S/C32H33N5O10/c1-2-13-37(25-10-5-18-14-24-21(15-20(18)25)30(43)36-26(16-38)33-24)19-6-3-17(4-7-19)29(42)35-23(32(46)47)8-11-27(39)34-22(31(44)45)9-12-28(40)41/h1,3-4,6-7,14-15,22-23,25,38H,5,8-13,16H2,(H,34,39)(H,35,42)(H,40,41)(H,44,45)(H,46,47)(H,33,36,43)/t22-,23+,25?/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Theoretical Studies gGmbH Curated by ChEMBL					Assay Description Inhibition of ERalpha expressed in human tumor cells				J Med Chem 53: 6539-49 (2010) Article DOI: 10.1021/jm901869w BindingDB Entry DOI: 10.7270/Q24J0F9S
					More data for this Ligand-Target Pair
Thymidylate synthase (Homo sapiens (Human))	BDBM50326712 (2(R)-[4(S)-carboxy-4-[4-[N-(2-hydroxymethyl-4-oxo-...) Show SMILES OCc1nc2cc3CCC(N(CC#C)c4ccc(cc4)C(=O)N[C@@H](CCC(=O)N[C@H](CCC(O)=O)C(O)=O)C(O)=O)c3cc2c(=O)[nH]1 |r| Show InChI InChI=1S/C32H33N5O10/c1-2-13-37(25-10-5-18-14-24-21(15-20(18)25)30(43)36-26(16-38)33-24)19-6-3-17(4-7-19)29(42)35-23(32(46)47)8-11-27(39)34-22(31(44)45)9-12-28(40)41/h1,3-4,6-7,14-15,22-23,25,38H,5,8-13,16H2,(H,34,39)(H,35,42)(H,40,41)(H,44,45)(H,46,47)(H,33,36,43)/t22-,23+,25?/m1/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.20	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Theoretical Studies gGmbH Curated by ChEMBL					Assay Description Inhibition of thymidin synthase				J Med Chem 53: 6539-49 (2010) Article DOI: 10.1021/jm901869w BindingDB Entry DOI: 10.7270/Q24J0F9S
					More data for this Ligand-Target Pair				3D Structure (docked)
Fatty-acid amide hydrolase 1 [30-579] (Rattus norvegicus (rat))	BDBM26739 (3-(3-carbamoylphenyl)phenyl N-cyclohexylcarbamate ...) Show SMILES NC(=O)c1cccc(c1)-c1cccc(OC(=O)NC2CCCCC2)c1 Show InChI InChI=1S/C20H22N2O3/c21-19(23)16-8-4-6-14(12-16)15-7-5-11-18(13-15)25-20(24)22-17-9-2-1-3-10-17/h4-8,11-13,17H,1-3,9-10H2,(H2,21,23)(H,22,24)	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	3.80	n/a	n/a	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Inhibition of Wistar rat brain FAAH				J Med Chem 49: 4650-6 (2006) Article DOI: 10.1021/jm060394q BindingDB Entry DOI: 10.7270/Q2Q52P8G
					More data for this Ligand-Target Pair
Fatty-acid amide hydrolase 1 [30-579] (Rattus norvegicus (rat))	BDBM50191457 (4-(thiazol-2-yl)phenyl butylcarbamate | CHEMBL3767...) Show SMILES CCCCNC(=O)Oc1ccc(cc1)-c1nccs1 Show InChI InChI=1S/C14H16N2O2S/c1-2-3-8-16-14(17)18-12-6-4-11(5-7-12)13-15-9-10-19-13/h4-7,9-10H,2-3,8H2,1H3,(H,16,17)	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	520	n/a	n/a	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Inhibition of Wistar rat brain FAAH				J Med Chem 49: 4650-6 (2006) Article DOI: 10.1021/jm060394q BindingDB Entry DOI: 10.7270/Q2Q52P8G
					More data for this Ligand-Target Pair
Fatty-acid amide hydrolase 1 [30-579] (Rattus norvegicus (rat))	BDBM50191456 (1-(2-phenyl-1,3-thiazol-4-yl)ethanone [4-(4-methyl...) Show SMILES CC(N=Nc1nc(cs1)-c1ccc(C)cc1)c1csc(n1)-c1ccccc1 |w:3.3| Show InChI InChI=1S/C21H18N4S2/c1-14-8-10-16(11-9-14)19-13-27-21(23-19)25-24-15(2)18-12-26-20(22-18)17-6-4-3-5-7-17/h3-13,15H,1-2H3	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	690	n/a	n/a	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Inhibition of Wistar rat brain FAAH				J Med Chem 49: 4650-6 (2006) Article DOI: 10.1021/jm060394q BindingDB Entry DOI: 10.7270/Q2Q52P8G
					More data for this Ligand-Target Pair
Fatty-acid amide hydrolase 1 [30-579] (Rattus norvegicus (rat))	BDBM60419 (BDBM50295658 | NAM) Show SMILES CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCCN1C(=O)C=CC1=O |c:23| Show InChI InChI=1S/C24H35NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-22-25-23(26)20-21-24(25)27/h6-7,9-10,12-13,15-16,20-21H,2-5,8,11,14,17-19,22H2,1H3/b7-6-,10-9-,13-12-,16-15-	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Inhibition of Wistar rat brain FAAH				J Med Chem 49: 4650-6 (2006) Article DOI: 10.1021/jm060394q BindingDB Entry DOI: 10.7270/Q2Q52P8G
					More data for this Ligand-Target Pair
Fatty-acid amide hydrolase 1 [30-579] (Rattus norvegicus (rat))	BDBM50191459 (4-[4-(benzyloxy)phenyl]-5-[(5-nitro-1,3-thiazol-2-...) Show SMILES [O-][N+](=O)c1cnc(Sc2n[n-]c(=[OH+])n2-c2ccc(OCc3ccccc3)cc2)s1 Show InChI InChI=1S/C18H13N5O4S2/c24-16-20-21-17(29-18-19-10-15(28-18)23(25)26)22(16)13-6-8-14(9-7-13)27-11-12-4-2-1-3-5-12/h1-10H,11H2,(H,20,24)	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Inhibition of Wistar rat brain FAAH				J Med Chem 49: 4650-6 (2006) Article DOI: 10.1021/jm060394q BindingDB Entry DOI: 10.7270/Q2Q52P8G
					More data for this Ligand-Target Pair
Fatty-acid amide hydrolase 1 [30-579] (Rattus norvegicus (rat))	BDBM50191462 (1-(3-methyl-1-benzothien-2-yl)ethanone O-(anilinoc...) Show SMILES C\C(=N/OC(=O)Nc1ccccc1)c1sc2ccccc2c1C Show InChI InChI=1S/C18H16N2O2S/c1-12-15-10-6-7-11-16(15)23-17(12)13(2)20-22-18(21)19-14-8-4-3-5-9-14/h3-11H,1-2H3,(H,19,21)/b20-13+	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Inhibition of Wistar rat brain FAAH				J Med Chem 49: 4650-6 (2006) Article DOI: 10.1021/jm060394q BindingDB Entry DOI: 10.7270/Q2Q52P8G
					More data for this Ligand-Target Pair
Fatty-acid amide hydrolase 1 [30-579] (Rattus norvegicus (rat))	BDBM50191461 (1-(4-fluorophenyl)-2-(1-(4-hydroxyphenyl)-1H-tetra...) Show SMILES Oc1ccc(cc1)-n1nnnc1SCC(=O)c1ccc(F)cc1 Show InChI InChI=1S/C15H11FN4O2S/c16-11-3-1-10(2-4-11)14(22)9-23-15-17-18-19-20(15)12-5-7-13(21)8-6-12/h1-8,21H,9H2	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Inhibition of Wistar rat brain FAAH				J Med Chem 49: 4650-6 (2006) Article DOI: 10.1021/jm060394q BindingDB Entry DOI: 10.7270/Q2Q52P8G
					More data for this Ligand-Target Pair
Fatty-acid amide hydrolase 1 [30-579] (Rattus norvegicus (rat))	BDBM50191454 (1-(4-((4-(2,5-dimethyl-1-(thiophen-2-ylmethyl)-1H-...) Show SMILES CC(=O)c1ccc(OCC2CN(CCO2)C(=O)c2cc(C)n(Cc3cccs3)c2C)cc1F Show InChI InChI=1S/C25H27FN2O4S/c1-16-11-23(17(2)28(16)14-21-5-4-10-33-21)25(30)27-8-9-31-20(13-27)15-32-19-6-7-22(18(3)29)24(26)12-19/h4-7,10-12,20H,8-9,13-15H2,1-3H3	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	8.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Inhibition of Wistar rat brain FAAH				J Med Chem 49: 4650-6 (2006) Article DOI: 10.1021/jm060394q BindingDB Entry DOI: 10.7270/Q2Q52P8G
					More data for this Ligand-Target Pair
Fatty-acid amide hydrolase 1 [30-579] (Rattus norvegicus (rat))	BDBM50191455 (CHEMBL213901 | ethyl 2-(2-(3-(styrylthio)propanami...) Show SMILES CCOC(=O)Cc1csc(NC(=O)CCS\C=C\c2ccccc2)n1 Show InChI InChI=1S/C18H20N2O3S2/c1-2-23-17(22)12-15-13-25-18(19-15)20-16(21)9-11-24-10-8-14-6-4-3-5-7-14/h3-8,10,13H,2,9,11-12H2,1H3,(H,19,20,21)/b10-8+	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Inhibition of Wistar rat brain FAAH				J Med Chem 49: 4650-6 (2006) Article DOI: 10.1021/jm060394q BindingDB Entry DOI: 10.7270/Q2Q52P8G
					More data for this Ligand-Target Pair
Monoglyceride lipase (Rattus norvegicus (Rat))	BDBM50191457 (4-(thiazol-2-yl)phenyl butylcarbamate | CHEMBL3767...) Show SMILES CCCCNC(=O)Oc1ccc(cc1)-c1nccs1 Show InChI InChI=1S/C14H16N2O2S/c1-2-3-8-16-14(17)18-12-6-4-11(5-7-12)13-15-9-10-19-13/h4-7,9-10H,2-3,8H2,1H3,(H,16,17)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Inhibition of MGL-like activity in Wistar rat cerebellar membranes				J Med Chem 49: 4650-6 (2006) Article DOI: 10.1021/jm060394q BindingDB Entry DOI: 10.7270/Q2Q52P8G
					More data for this Ligand-Target Pair
Fatty-acid amide hydrolase 1 [30-579] (Rattus norvegicus (rat))	BDBM50191458 (4-[4-(benzyloxy)phenyl]-3-methyl-5-[(5-nitro-1,3-t...) Show SMILES Cc1nnc(Sc2ncc(s2)[N+]([O-])=O)n1-c1ccc(OCc2ccccc2)cc1 Show InChI InChI=1S/C19H15N5O3S2/c1-13-21-22-18(29-19-20-11-17(28-19)24(25)26)23(13)15-7-9-16(10-8-15)27-12-14-5-3-2-4-6-14/h2-11H,12H2,1H3	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Inhibition of Wistar rat brain FAAH				J Med Chem 49: 4650-6 (2006) Article DOI: 10.1021/jm060394q BindingDB Entry DOI: 10.7270/Q2Q52P8G
					More data for this Ligand-Target Pair
Fatty-acid amide hydrolase 1 [30-579] (Rattus norvegicus (rat))	BDBM50191460 ((2-((6-methylpyridin-3-yloxy)methyl)morpholino)(2-...) Show SMILES Cc1ccc(OCC2CN(CCO2)C(=O)C2CC2c2ccccc2)cn1 Show InChI InChI=1S/C21H24N2O3/c1-15-7-8-17(12-22-15)26-14-18-13-23(9-10-25-18)21(24)20-11-19(20)16-5-3-2-4-6-16/h2-8,12,18-20H,9-11,13-14H2,1H3	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Inhibition of Wistar rat brain FAAH				J Med Chem 49: 4650-6 (2006) Article DOI: 10.1021/jm060394q BindingDB Entry DOI: 10.7270/Q2Q52P8G
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50475554 (CHEMBL200113) Show SMILES CCCCCCC(C)(C)\C=C/C\C=C/C\C=C/C\C=C/CCCCOC(CO)CO Show InChI InChI=1S/C27H48O3/c1-4-5-6-18-21-27(2,3)22-19-16-14-12-10-8-7-9-11-13-15-17-20-23-30-26(24-28)25-29/h7-8,11-14,19,22,26,28-29H,4-6,9-10,15-18,20-21,23-25H2,1-3H3/b8-7-,13-11-,14-12-,22-19-	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	3.98E+4	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Displacement of [35S]GTP-gamma-S from rat cerebellar CB1 receptor				J Med Chem 49: 554-66 (2006) Article DOI: 10.1021/jm0505157 BindingDB Entry DOI: 10.7270/Q2PN98DG
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50475555 (CHEMBL199668) Show SMILES CCCCCCC(C)(C)\C=C/C\C=C/C\C=C/C\C=C/CCC(=O)OC(CO)CO Show InChI InChI=1S/C26H44O4/c1-4-5-6-17-20-26(2,3)21-18-15-13-11-9-7-8-10-12-14-16-19-25(29)30-24(22-27)23-28/h7-8,11-14,18,21,24,27-28H,4-6,9-10,15-17,19-20,22-23H2,1-3H3/b8-7-,13-11-,14-12-,21-18-	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	5.01E+4	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Displacement of [35S]GTP-gamma-S from rat cerebellar CB1 receptor				J Med Chem 49: 554-66 (2006) Article DOI: 10.1021/jm0505157 BindingDB Entry DOI: 10.7270/Q2PN98DG
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50006255 (CHEMBL418353) Show SMILES CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(=O)NC1CC1 Show InChI InChI=1S/C23H37NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-23(25)24-22-20-21-22/h6-7,9-10,12-13,15-16,22H,2-5,8,11,14,17-21H2,1H3,(H,24,25)/b7-6-,10-9-,13-12-,16-15-	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	398	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Displacement of [35S]GTP-gamma-S from rat cerebellar CB1 receptor				J Med Chem 49: 554-66 (2006) Article DOI: 10.1021/jm0505157 BindingDB Entry DOI: 10.7270/Q2PN98DG
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50072775 (2-((1R,2R,5R)-5-hydroxy-2-(3-hydroxypropyl)cyclohe...) Show SMILES CCCCCCC(C)(C)c1ccc([C@@H]2C[C@H](O)CC[C@H]2CCCO)c(O)c1 |r| Show InChI InChI=1S/C24H40O3/c1-4-5-6-7-14-24(2,3)19-11-13-21(23(27)16-19)22-17-20(26)12-10-18(22)9-8-15-25/h11,13,16,18,20,22,25-27H,4-10,12,14-15,17H2,1-3H3/t18-,20-,22-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	n/a	n/a	n/a	n/a	100	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Displacement of [35S]GTP-gamma-S from rat cerebellar CB1 receptor				J Med Chem 49: 554-66 (2006) Article DOI: 10.1021/jm0505157 BindingDB Entry DOI: 10.7270/Q2PN98DG
					More data for this Ligand-Target Pair				3D Structure (crystal)
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50072760 (3-Hydroxy-N-((5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetra...) Show SMILES CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCCNC(=O)CCO Show InChI InChI=1S/C23H39NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-21-24-23(26)20-22-25/h6-7,9-10,12-13,15-16,25H,2-5,8,11,14,17-22H2,1H3,(H,24,26)/b7-6-,10-9-,13-12-,16-15-	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	7.94E+3	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Displacement of [35S]GTP-gamma-S from rat cerebellar CB1 receptor				J Med Chem 49: 554-66 (2006) Article DOI: 10.1021/jm0505157 BindingDB Entry DOI: 10.7270/Q2PN98DG
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50067498 ((6aS,10aS)-3-(1,1-Dimethyl-heptyl)-9-hydroxymethyl...) Show SMILES CCCCCCC(C)(C)c1cc(O)c2[C@H]3CC(CO)=CC[C@@H]3C(C)(C)Oc2c1 |c:18| Show InChI InChI=1S/C25H38O3/c1-6-7-8-9-12-24(2,3)18-14-21(27)23-19-13-17(16-26)10-11-20(19)25(4,5)28-22(23)15-18/h10,14-15,19-20,26-27H,6-9,11-13,16H2,1-5H3/t19-,20-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	0.251	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Agonist activity at human CB2 receptor transfected in CHO cells by [35]GTPgamma binding assay				J Med Chem 48: 7166-71 (2005) Article DOI: 10.1021/jm050565b BindingDB Entry DOI: 10.7270/Q2PC3552
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50061117 (6,6,9-Trimethyl-3-pentyl-6H-benzo[c]chromen-1-ol |...) Show SMILES CCCCCc1cc(O)c-2c(OC(C)(C)c3ccc(C)cc-23)c1 Show InChI InChI=1S/C21H26O2/c1-5-6-7-8-15-12-18(22)20-16-11-14(2)9-10-17(16)21(3,4)23-19(20)13-15/h9-13,22H,5-8H2,1-4H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	316	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Displacement of [35S]GTP-gamma-S from rat cerebellar CB1 receptor				J Med Chem 49: 554-66 (2006) Article DOI: 10.1021/jm0505157 BindingDB Entry DOI: 10.7270/Q2PN98DG
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50072769 ((5Z,8Z,11Z,14Z)-Icosa-5,8,11,14-tetraenoic acid (2...) Show SMILES CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(=O)NCCCl Show InChI InChI=1S/C22H36ClNO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-22(25)24-21-20-23/h6-7,9-10,12-13,15-16H,2-5,8,11,14,17-21H2,1H3,(H,24,25)/b7-6-,10-9-,13-12-,16-15-	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	316	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Displacement of [35S]GTP-gamma-S from rat cerebellar CB1 receptor				J Med Chem 49: 554-66 (2006) Article DOI: 10.1021/jm0505157 BindingDB Entry DOI: 10.7270/Q2PN98DG
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50475553 (CHEMBL371953) Show SMILES CCCCCCC(C)(C)\C=C/C\C=C/C\C=C/C\C=C/CCCC(=O)OC(CO)CO Show InChI InChI=1S/C27H46O4/c1-4-5-6-18-21-27(2,3)22-19-16-14-12-10-8-7-9-11-13-15-17-20-26(30)31-25(23-28)24-29/h7-8,11-14,19,22,25,28-29H,4-6,9-10,15-18,20-21,23-24H2,1-3H3/b8-7-,13-11-,14-12-,22-19-	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	5.01E+4	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Displacement of [35S]GTP-gamma-S from rat cerebellar CB1 receptor				J Med Chem 49: 554-66 (2006) Article DOI: 10.1021/jm0505157 BindingDB Entry DOI: 10.7270/Q2PN98DG
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50067499 ((6aR,10aR)-3(1,1-dimethylheptyl)-9-hydroxymethyl)-...) Show SMILES CCCCCCC(C)(C)c1cc(O)c2[C@@H]3CC(CO)=CC[C@H]3C(C)(C)Oc2c1 |r,c:18| Show InChI InChI=1S/C25H38O3/c1-6-7-8-9-12-24(2,3)18-14-21(27)23-19-13-17(16-26)10-11-20(19)25(4,5)28-22(23)15-18/h10,14-15,19-20,26-27H,6-9,11-13,16H2,1-5H3/t19-,20-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	5	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Displacement of [35S]GTP-gamma-S from rat cerebellar CB1 receptor				J Med Chem 49: 554-66 (2006) Article DOI: 10.1021/jm0505157 BindingDB Entry DOI: 10.7270/Q2PN98DG
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50404269 (CHEMBL320549) Show SMILES CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCCOC(=O)[C@@H](O)CO Show InChI InChI=1S/C23H38O4/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-27-23(26)22(25)21-24/h6-7,9-10,12-13,15-16,22,24-25H,2-5,8,11,14,17-21H2,1H3/b7-6-,10-9-,13-12-,16-15-/t22-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	3.98E+4	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Displacement of [35S]GTP-gamma-S from rat cerebellar CB1 receptor				J Med Chem 49: 554-66 (2006) Article DOI: 10.1021/jm0505157 BindingDB Entry DOI: 10.7270/Q2PN98DG
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50475552 (CHEMBL201758) Show SMILES CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCNC(=O)CCC Show InChI InChI=1S/C23H39NO/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-22-24-23(25)21-4-2/h8-9,11-12,14-15,17-18H,3-7,10,13,16,19-22H2,1-2H3,(H,24,25)/b9-8-,12-11-,15-14-,18-17-	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	1.26E+3	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Displacement of [35S]GTP-gamma-S from rat cerebellar CB1 receptor				J Med Chem 49: 554-66 (2006) Article DOI: 10.1021/jm0505157 BindingDB Entry DOI: 10.7270/Q2PN98DG
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM22988 ((5Z,8Z,11Z,14Z)-N-(2-hydroxyethyl)icosa-5,8,11,14-...) Show SMILES CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(=O)NCCO Show InChI InChI=1S/C22H37NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-22(25)23-20-21-24/h6-7,9-10,12-13,15-16,24H,2-5,8,11,14,17-21H2,1H3,(H,23,25)/b7-6-,10-9-,13-12-,16-15-	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL KEGG PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	1.58E+4	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Displacement of [35S]GTP-gamma-S from rat cerebellar CB1 receptor				J Med Chem 49: 554-66 (2006) Article DOI: 10.1021/jm0505157 BindingDB Entry DOI: 10.7270/Q2PN98DG
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50404270 (CHEMBL113473) Show SMILES CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCCOC(=O)[C@H](O)CO Show InChI InChI=1S/C23H38O4/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-27-23(26)22(25)21-24/h6-7,9-10,12-13,15-16,22,24-25H,2-5,8,11,14,17-21H2,1H3/b7-6-,10-9-,13-12-,16-15-/t22-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	2.51E+4	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Displacement of [35S]GTP-gamma-S from rat cerebellar CB1 receptor				J Med Chem 49: 554-66 (2006) Article DOI: 10.1021/jm0505157 BindingDB Entry DOI: 10.7270/Q2PN98DG
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50067740 (6-((6aR,10aR)-1-Hydroxy-6,6,9-trimethyl-6a,7,10,10...) Show SMILES CC1=CC[C@@H]2[C@@H](C1)c1c(O)cc(cc1OC2(C)C)C(C)(C)CCCCC#N |t:1| Show InChI InChI=1S/C24H33NO2/c1-16-9-10-19-18(13-16)22-20(26)14-17(15-21(22)27-24(19,4)5)23(2,3)11-7-6-8-12-25/h9,14-15,18-19,26H,6-8,10-11,13H2,1-5H3/t18-,19-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	10	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Displacement of [35S]GTP-gamma-S from rat cerebellar CB1 receptor				J Med Chem 49: 554-66 (2006) Article DOI: 10.1021/jm0505157 BindingDB Entry DOI: 10.7270/Q2PN98DG
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50067734 ((-)-(6aR-trans)-6,6,9-trimethyl-3-pentyl-6a,7,10,1...) Show SMILES CCCCCc1cc(O)c2[C@@H]3CC(C)=CC[C@H]3C(C)(C)Oc2c1 |r,c:13| Show InChI InChI=1S/C21H30O2/c1-5-6-7-8-15-12-18(22)20-16-11-14(2)9-10-17(16)21(3,4)23-19(20)13-15/h9,12-13,16-17,22H,5-8,10-11H2,1-4H3/t16-,17-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE MMDB PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	631	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Displacement of [35S]GTP-gamma-S from rat cerebellar CB1 receptor				J Med Chem 49: 554-66 (2006) Article DOI: 10.1021/jm0505157 BindingDB Entry DOI: 10.7270/Q2PN98DG
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50059523 ((6Z,9Z,12Z,15Z)-1,1,1-trifluorohenicosa-6,9,12,15-...) Show SMILES CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(=O)C(F)(F)F Show InChI InChI=1S/C21H31F3O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(25)21(22,23)24/h6-7,9-10,12-13,15-16H,2-5,8,11,14,17-19H2,1H3/b7-6-,10-9-,13-12-,16-15-	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	2.51E+4	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Displacement of [35S]GTP-gamma-S from rat cerebellar CB1 receptor				J Med Chem 49: 554-66 (2006) Article DOI: 10.1021/jm0505157 BindingDB Entry DOI: 10.7270/Q2PN98DG
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50213599 ((6aR,10aR)-3-(6-bromo-2-methylhexan-2-yl)-6,6,9-tr...) Show SMILES CC1=CC[C@@H]2[C@@H](C1)c1c(O)cc(cc1OC2(C)C)C(C)(C)CCCCBr |t:1| Show InChI InChI=1S/C23H33BrO2/c1-15-8-9-18-17(12-15)21-19(25)13-16(14-20(21)26-23(18,4)5)22(2,3)10-6-7-11-24/h8,13-14,17-18,25H,6-7,9-12H2,1-5H3/t17-,18-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	10	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Displacement of [35S]GTP-gamma-S from rat cerebellar CB1 receptor				J Med Chem 49: 554-66 (2006) Article DOI: 10.1021/jm0505157 BindingDB Entry DOI: 10.7270/Q2PN98DG
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50475551 (CHEMBL380923) Show SMILES CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCNC(=O)CC Show InChI InChI=1S/C22H37NO/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-23-22(24)4-2/h8-9,11-12,14-15,17-18H,3-7,10,13,16,19-21H2,1-2H3,(H,23,24)/b9-8-,12-11-,15-14-,18-17-	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	2.00E+3	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Displacement of [35S]GTP-gamma-S from rat cerebellar CB1 receptor				J Med Chem 49: 554-66 (2006) Article DOI: 10.1021/jm0505157 BindingDB Entry DOI: 10.7270/Q2PN98DG
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50475550 (CHEMBL199911) Show SMILES CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCCNC(=O)CC Show InChI InChI=1S/C23H39NO/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-24-23(25)4-2/h8-9,11-12,14-15,17-18H,3-7,10,13,16,19-22H2,1-2H3,(H,24,25)/b9-8-,12-11-,15-14-,18-17-	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	3.16E+3	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Displacement of [35S]GTP-gamma-S from rat cerebellar CB1 receptor				J Med Chem 49: 554-66 (2006) Article DOI: 10.1021/jm0505157 BindingDB Entry DOI: 10.7270/Q2PN98DG
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM60994 ((10R,10aR)-6,6,9-Trimethyl-3-pentyl-6a,7,8,10a-tet...) Show SMILES CCCCCc1cc(O)c2[C@@H]3C=C(C)CC[C@H]3C(C)(C)Oc2c1 |r,t:11| Show InChI InChI=1S/C21H30O2/c1-5-6-7-8-15-12-18(22)20-16-11-14(2)9-10-17(16)21(3,4)23-19(20)13-15/h11-13,16-17,22H,5-10H2,1-4H3/t16-,17-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL DrugBank KEGG PC cid PC sid PDB UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	200	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Displacement of [35S]GTP-gamma-S from rat cerebellar CB1 receptor				J Med Chem 49: 554-66 (2006) Article DOI: 10.1021/jm0505157 BindingDB Entry DOI: 10.7270/Q2PN98DG
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50414522 (CHEMBL224137) Show SMILES FC(F)(F)c1cccc(c1)C(=O)c1nccc2ccccc12 Show InChI InChI=1S/C17H10F3NO/c18-17(19,20)13-6-3-5-12(10-13)16(22)15-14-7-2-1-4-11(14)8-9-21-15/h1-10H	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	5.01E+3	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Agonist activity at human CB2 receptor transfected in CHO cells by [35]GTPgamma binding assay				J Med Chem 48: 7166-71 (2005) Article DOI: 10.1021/jm050565b BindingDB Entry DOI: 10.7270/Q2PC3552
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50475548 (CHEMBL381893) Show SMILES CCCCCCC(C)(C)\C=C/C\C=C/C\C=C/C\C=C/CCCOC(CO)CO Show InChI InChI=1S/C26H46O3/c1-4-5-6-17-20-26(2,3)21-18-15-13-11-9-7-8-10-12-14-16-19-22-29-25(23-27)24-28/h7-8,11-14,18,21,25,27-28H,4-6,9-10,15-17,19-20,22-24H2,1-3H3/b8-7-,13-11-,14-12-,21-18-	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	5.01E+4	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Displacement of [35S]GTP-gamma-S from rat cerebellar CB1 receptor				J Med Chem 49: 554-66 (2006) Article DOI: 10.1021/jm0505157 BindingDB Entry DOI: 10.7270/Q2PN98DG
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50180036 ((6aR,10aR)-3-(1,1-dimethylbutyl)-6a,7,10,10a-tetra...) Show SMILES CCCC(C)(C)c1ccc2[C@@H]3CC(C)=CC[C@H]3C(C)(C)Oc2c1 |r,c:13| Show InChI InChI=1S/C22H32O/c1-7-12-21(3,4)16-9-10-17-18-13-15(2)8-11-19(18)22(5,6)23-20(17)14-16/h8-10,14,18-19H,7,11-13H2,1-6H3/t18-,19+/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	2.00E+3	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Displacement of [35S]GTP-gamma-S from rat cerebellar CB1 receptor				J Med Chem 49: 554-66 (2006) Article DOI: 10.1021/jm0505157 BindingDB Entry DOI: 10.7270/Q2PN98DG
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50475547 (CHEMBL201260) Show SMILES CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCCNC(=O)CCC Show InChI InChI=1S/C24H41NO/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-23-25-24(26)22-4-2/h8-9,11-12,14-15,17-18H,3-7,10,13,16,19-23H2,1-2H3,(H,25,26)/b9-8-,12-11-,15-14-,18-17-	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	3.16E+3	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Displacement of [35S]GTP-gamma-S from rat cerebellar CB1 receptor				J Med Chem 49: 554-66 (2006) Article DOI: 10.1021/jm0505157 BindingDB Entry DOI: 10.7270/Q2PN98DG
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Rattus norvegicus (rat))	BDBM50475549 (CHEMBL203474) Show SMILES CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCNC(=O)CCO Show InChI InChI=1S/C22H37NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-20-23-22(25)19-21-24/h6-7,9-10,12-13,15-16,24H,2-5,8,11,14,17-21H2,1H3,(H,23,25)/b7-6-,10-9-,13-12-,16-15-	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	1.58E+4	n/a	n/a	n/a	n/a
University of Kuopio Curated by ChEMBL					Assay Description Displacement of [35S]GTP-gamma-S from rat cerebellar CB1 receptor				J Med Chem 49: 554-66 (2006) Article DOI: 10.1021/jm0505157 BindingDB Entry DOI: 10.7270/Q2PN98DG
					More data for this Ligand-Target Pair