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Compile Data Set for Download or QSAR

Found 96 hits with Last Name = 'sherwood' and Initial = 'am'   
Target/Host
(Institution)
LigandTarget/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
pHTemp
°C
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM50265927
PNG
(CHEMBL4093687)
Show SMILES [H][C@@]12CC[C@@](C)([C@@H](CC(OC)OC)C(=O)OC)[C@H](C(=O)OC)[C@@]1(C)C[C@H](OC2=O)c1ccoc1 |r|
Show InChI InChI=1S/C24H34O9/c1-23(16(20(25)30-5)11-18(28-3)29-4)9-7-15-21(26)33-17(14-8-10-32-13-14)12-24(15,2)19(23)22(27)31-6/h8,10,13,15-19H,7,9,11-12H2,1-6H3/t15-,16-,17-,19-,23-,24-/m0/s1
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n/an/an/an/a 12n/an/an/an/a



The University of Kansas

Curated by ChEMBL


Assay Description
Agonist activity at human kappa-type opioid receptor expressed in CHO-K1 cells assessed as forskolin-induced cAMP accumulation after 30 mins in prese...


J Med Chem 60: 3866-3878 (2017)


Article DOI: 10.1021/acs.jmedchem.7b00148
BindingDB Entry DOI: 10.7270/Q2K93B08
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM50265928
PNG
(CHEMBL4086641)
Show SMILES [H][C@@]12CC[C@@]3(C)[C@@H](CC(=O)C(O)=C3[C@@]1(C)C[C@H](OC2=O)c1ccoc1)C(=O)OC |r,c:11|
Show InChI InChI=1S/C21H24O7/c1-20-6-4-12-19(25)28-15(11-5-7-27-10-11)9-21(12,2)17(20)16(23)14(22)8-13(20)18(24)26-3/h5,7,10,12-13,15,23H,4,6,8-9H2,1-3H3/t12-,13-,15-,20-,21-/m0/s1
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n/an/an/an/a>1.00E+4n/an/an/an/a



The University of Kansas

Curated by ChEMBL


Assay Description
Agonist activity at human kappa-type opioid receptor expressed in CHO-K1 cells assessed as forskolin-induced cAMP accumulation after 30 mins in prese...


J Med Chem 60: 3866-3878 (2017)


Article DOI: 10.1021/acs.jmedchem.7b00148
BindingDB Entry DOI: 10.7270/Q2K93B08
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM50265929
PNG
(CHEMBL4105286)
Show SMILES [H][C@@]12CC[C@@](C)([C@@H](CC(O)=O)C(=O)OC)[C@H](C(=O)OC)[C@@]1(C)C[C@H](OC2=O)c1ccoc1 |r|
Show InChI InChI=1S/C22H28O9/c1-21(14(9-16(23)24)18(25)28-3)7-5-13-19(26)31-15(12-6-8-30-11-12)10-22(13,2)17(21)20(27)29-4/h6,8,11,13-15,17H,5,7,9-10H2,1-4H3,(H,23,24)/t13-,14-,15-,17-,21-,22-/m0/s1
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n/an/an/an/a>1.00E+4n/an/an/an/a



The University of Kansas

Curated by ChEMBL


Assay Description
Agonist activity at human kappa-type opioid receptor expressed in CHO-K1 cells assessed as forskolin-induced cAMP accumulation after 30 mins in prese...


J Med Chem 60: 3866-3878 (2017)


Article DOI: 10.1021/acs.jmedchem.7b00148
BindingDB Entry DOI: 10.7270/Q2K93B08
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM50265930
PNG
(CHEMBL4083444)
Show SMILES [H][C@@]12CC[C@@]3(C)[C@@H](C[C@]4(CCC(=O)O4)C(=O)[C@]3([H])[C@@]1(C)C[C@H](OC2=O)c1ccoc1)C(=O)OC |r|
Show InChI InChI=1S/C24H28O8/c1-22-7-4-14-21(28)31-16(13-6-9-30-12-13)11-23(14,2)18(22)19(26)24(8-5-17(25)32-24)10-15(22)20(27)29-3/h6,9,12,14-16,18H,4-5,7-8,10-11H2,1-3H3/t14-,15-,16-,18-,22-,23-,24+/m0/s1
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n/an/an/an/a 0.600n/an/an/an/a



The University of Kansas

Curated by ChEMBL


Assay Description
Agonist activity at human kappa-type opioid receptor expressed in CHO-K1 cells assessed as forskolin-induced cAMP accumulation after 30 mins in prese...


J Med Chem 60: 3866-3878 (2017)


Article DOI: 10.1021/acs.jmedchem.7b00148
BindingDB Entry DOI: 10.7270/Q2K93B08
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM50189136
PNG
(CHEMBL424698 | Salvinorin B)
Show SMILES COC(=O)[C@@H]1C[C@H](O)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@@H](C[C@]21C)c1ccoc1
Show InChI InChI=1S/C21H26O7/c1-20-6-4-12-19(25)28-15(11-5-7-27-10-11)9-21(12,2)17(20)16(23)14(22)8-13(20)18(24)26-3/h5,7,10,12-15,17,22H,4,6,8-9H2,1-3H3/t12-,13-,14-,15-,17-,20-,21-/m0/s1
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n/an/an/an/a 2.40n/an/an/an/a



The University of Kansas

Curated by ChEMBL


Assay Description
Agonist activity at human kappa-type opioid receptor expressed in CHO-K1 cells assessed as forskolin-induced cAMP accumulation after 30 mins in prese...


J Med Chem 60: 3866-3878 (2017)


Article DOI: 10.1021/acs.jmedchem.7b00148
BindingDB Entry DOI: 10.7270/Q2K93B08
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM50327505
PNG
((3S,4aR,4bS,8R,8aR,10aR)-3-Furan-3-yl-4a,8a-dimeth...)
Show SMILES COC(=O)[C@@H]1CCC(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@@H](C[C@]21C)c1ccoc1 |r|
Show InChI InChI=1S/C21H26O6/c1-20-8-6-14-19(24)27-16(12-7-9-26-11-12)10-21(14,2)17(20)15(22)5-4-13(20)18(23)25-3/h7,9,11,13-14,16-17H,4-6,8,10H2,1-3H3/t13-,14-,16-,17-,20-,21-/m0/s1
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n/an/an/an/a>1.00E+4n/an/an/an/a



The University of Kansas

Curated by ChEMBL


Assay Description
Agonist activity at human kappa-type opioid receptor expressed in CHO-K1 cells assessed as forskolin-induced cAMP accumulation after 30 mins in prese...


J Med Chem 60: 3866-3878 (2017)


Article DOI: 10.1021/acs.jmedchem.7b00148
BindingDB Entry DOI: 10.7270/Q2K93B08
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM50265931
PNG
(CHEMBL4094854)
Show SMILES [H][C@@]12CC[C@@](C)([C@@H](CCOC(C)=O)C(=O)OC)[C@H](C(=O)OC)[C@@]1(C)C[C@H](OC2=O)c1ccoc1 |r|
Show InChI InChI=1S/C24H32O9/c1-14(25)32-11-8-17(20(26)29-4)23(2)9-6-16-21(27)33-18(15-7-10-31-13-15)12-24(16,3)19(23)22(28)30-5/h7,10,13,16-19H,6,8-9,11-12H2,1-5H3/t16-,17-,18-,19-,23-,24-/m0/s1
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n/an/an/an/a 13n/an/an/an/a



The University of Kansas

Curated by ChEMBL


Assay Description
Agonist activity at human kappa-type opioid receptor expressed in CHO-K1 cells assessed as forskolin-induced cAMP accumulation after 30 mins in prese...


J Med Chem 60: 3866-3878 (2017)


Article DOI: 10.1021/acs.jmedchem.7b00148
BindingDB Entry DOI: 10.7270/Q2K93B08
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM50265932
PNG
(CHEMBL4076437)
Show SMILES [H][C@@]12CC[C@@](C)([C@@H](CCO)C(=O)OC)[C@H](C(=O)OC)[C@@]1(C)C[C@H](OC2=O)c1ccoc1 |r|
Show InChI InChI=1S/C22H30O8/c1-21(15(6-9-23)18(24)27-3)8-5-14-19(25)30-16(13-7-10-29-12-13)11-22(14,2)17(21)20(26)28-4/h7,10,12,14-17,23H,5-6,8-9,11H2,1-4H3/t14-,15-,16-,17-,21-,22-/m0/s1
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n/an/an/an/a>1.00E+4n/an/an/an/a



The University of Kansas

Curated by ChEMBL


Assay Description
Agonist activity at human kappa-type opioid receptor expressed in CHO-K1 cells assessed as forskolin-induced cAMP accumulation after 30 mins in prese...


J Med Chem 60: 3866-3878 (2017)


Article DOI: 10.1021/acs.jmedchem.7b00148
BindingDB Entry DOI: 10.7270/Q2K93B08
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM50265933
PNG
(CHEMBL4075281)
Show SMILES [H][C@@]12CC[C@@](C)([C@@H](CC=O)C(=O)OC)[C@H](C(=O)OC)[C@@]1(C)C[C@H](OC2=O)c1ccoc1 |r|
Show InChI InChI=1S/C22H28O8/c1-21(15(6-9-23)18(24)27-3)8-5-14-19(25)30-16(13-7-10-29-12-13)11-22(14,2)17(21)20(26)28-4/h7,9-10,12,14-17H,5-6,8,11H2,1-4H3/t14-,15-,16-,17-,21-,22-/m0/s1
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n/an/an/an/a 30n/an/an/an/a



The University of Kansas

Curated by ChEMBL


Assay Description
Agonist activity at human kappa-type opioid receptor expressed in CHO-K1 cells assessed as forskolin-induced cAMP accumulation after 30 mins in prese...


J Med Chem 60: 3866-3878 (2017)


Article DOI: 10.1021/acs.jmedchem.7b00148
BindingDB Entry DOI: 10.7270/Q2K93B08
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM50159165
PNG
((2S,4aR,6aR,7R,9S,10aS,10bR)-9-(acetyloxy)-2-(fura...)
Show SMILES COC(=O)[C@@H]1C[C@H](OC(C)=O)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@@H](C[C@]21C)c1ccoc1 |r|
Show InChI InChI=1S/C23H28O8/c1-12(24)30-16-9-15(20(26)28-4)22(2)7-5-14-21(27)31-17(13-6-8-29-11-13)10-23(14,3)19(22)18(16)25/h6,8,11,14-17,19H,5,7,9-10H2,1-4H3/t14-,15-,16-,17-,19-,22-,23-/m0/s1
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n/an/an/an/a 0.210n/an/an/an/a



The University of Kansas

Curated by ChEMBL


Assay Description
Agonist activity at human kappa-type opioid receptor expressed in CHO-K1 cells assessed as forskolin-induced cAMP accumulation after 30 mins in prese...


J Med Chem 60: 3866-3878 (2017)


Article DOI: 10.1021/acs.jmedchem.7b00148
BindingDB Entry DOI: 10.7270/Q2K93B08
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM50456634
PNG
(CHEMBL4213827)
Show SMILES [H][C@@]12CC[C@]3(C)[C@@]([H])([C@]4([H])OC(=O)[C@@]3(O)[C@@H](Br)[C@@H]4Br)[C@]1(C)C[C@@H](OC2=O)c1ccoc1Br |r,TLB:5:4:17.15:11.10,3:4:17.15:11.10,18:17:6.4:11.10,THB:12:11:17.15:6.4,19:6:17.15:11.10,16:15:6.4:11.10|
Show InChI InChI=1S/C20H21Br3O6/c1-18-7-10(8-4-6-27-15(8)23)28-16(24)9(18)3-5-19(2)13(18)12-11(21)14(22)20(19,26)17(25)29-12/h4,6,9-14,26H,3,5,7H2,1-2H3/t9-,10+,11+,12+,13-,14-,18+,19+,20-/m0/s1
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n/an/an/an/a>5.00E+4n/an/an/an/a



Istanbul Technical University

Curated by ChEMBL


Assay Description
Agonist activity at human kappa-type opioid receptor expressed in CHO-K1 cells assessed as inhibition of forskolin-induced cAMP accumulation after 30...


J Nat Prod 80: 2094-2100 (2017)


Article DOI: 10.1021/acs.jnatprod.7b00327
BindingDB Entry DOI: 10.7270/Q21N83RM
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM50456635
PNG
(CHEMBL4213388)
Show SMILES [H][C@@]12OC(=O)[C@@](O)([C@H](OC(C)=O)[C@@H]1OC(C)=O)[C@]1(C)CC[C@@]3([H])C(=O)O[C@H](C[C@@]3(C)[C@]21[H])c1ccoc1 |r,TLB:4:3:12.7:30.17,18:17:12.7:3.2,19:17:12.7:3.2,8:7:30.17:3.2,THB:28:30:12.7:3.2,13:12:30.17:3.2|
Show InChI InChI=1S/C24H28O10/c1-11(25)31-17-16-18-22(3)9-15(13-6-8-30-10-13)33-20(27)14(22)5-7-23(18,4)24(29,21(28)34-16)19(17)32-12(2)26/h6,8,10,14-19,29H,5,7,9H2,1-4H3/t14-,15+,16+,17+,18-,19+,22+,23+,24-/m0/s1
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n/an/an/an/a>5.00E+4n/an/an/an/a



Istanbul Technical University

Curated by ChEMBL


Assay Description
Agonist activity at human kappa-type opioid receptor expressed in CHO-K1 cells assessed as inhibition of forskolin-induced cAMP accumulation after 30...


J Nat Prod 80: 2094-2100 (2017)


Article DOI: 10.1021/acs.jnatprod.7b00327
BindingDB Entry DOI: 10.7270/Q21N83RM
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM50456636
PNG
(CHEMBL4208735)
Show SMILES [H][C@@]12OC(=O)[C@@](OC(C)=O)(C=C1)[C@]1(C)CC[C@@]3([H])C(=O)O[C@H](C[C@@]3(C)[C@]21[H])c1ccoc1 |r,c:10,TLB:4:3:11.10:25.12,13:12:11.10:3.2,14:12:11.10:3.2,THB:23:25:11.10:3.2|
Show InChI InChI=1S/C22H24O7/c1-12(23)29-22-8-5-15(28-19(22)25)17-20(2)10-16(13-6-9-26-11-13)27-18(24)14(20)4-7-21(17,22)3/h5-6,8-9,11,14-17H,4,7,10H2,1-3H3/t14-,15+,16+,17-,20+,21+,22-/m0/s1
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n/an/an/an/a 8.00E+3n/an/an/an/a



Istanbul Technical University

Curated by ChEMBL


Assay Description
Agonist activity at human kappa-type opioid receptor expressed in CHO-K1 cells assessed as inhibition of forskolin-induced cAMP accumulation after 30...


J Nat Prod 80: 2094-2100 (2017)


Article DOI: 10.1021/acs.jnatprod.7b00327
BindingDB Entry DOI: 10.7270/Q21N83RM
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM50456637
PNG
(CHEMBL4208460)
Show SMILES [H][C@@]12OC(=O)[C@@](O)([C@H](O)[C@@H]1O)[C@]1(C)CC[C@@]3([H])C(=O)O[C@H](C[C@@]3(C)[C@]21[H])c1ccoc1 |r,TLB:4:3:9.7:24.11,12:11:9.7:3.2,13:11:9.7:3.2,8:7:24.11:3.2,THB:22:24:9.7:3.2,10:9:24.11:3.2|
Show InChI InChI=1S/C20H24O8/c1-18-7-11(9-4-6-26-8-9)27-16(23)10(18)3-5-19(2)14(18)13-12(21)15(22)20(19,25)17(24)28-13/h4,6,8,10-15,21-22,25H,3,5,7H2,1-2H3/t10-,11+,12+,13+,14-,15+,18+,19+,20-/m0/s1
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n/an/an/an/a 1.60E+4n/an/an/an/a



Istanbul Technical University

Curated by ChEMBL


Assay Description
Agonist activity at human kappa-type opioid receptor expressed in CHO-K1 cells assessed as inhibition of forskolin-induced cAMP accumulation after 30...


J Nat Prod 80: 2094-2100 (2017)


Article DOI: 10.1021/acs.jnatprod.7b00327
BindingDB Entry DOI: 10.7270/Q21N83RM
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM50456638
PNG
(CHEMBL4205563)
Show SMILES [H][C@@]12OC(=O)[C@@](OCOC)(C=C1)[C@]1(C)CC[C@@]3([H])C(=O)O[C@H](C[C@@]3(C)[C@]21[H])c1ccoc1 |r,c:10,TLB:4:3:11.10:25.12,13:12:11.10:3.2,14:12:11.10:3.2,THB:23:25:11.10:3.2|
Show InChI InChI=1S/C22H26O7/c1-20-10-16(13-6-9-26-11-13)28-18(23)14(20)4-7-21(2)17(20)15-5-8-22(21,19(24)29-15)27-12-25-3/h5-6,8-9,11,14-17H,4,7,10,12H2,1-3H3/t14-,15+,16+,17-,20+,21+,22-/m0/s1
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n/an/an/an/a 1.20E+4n/an/an/an/a



Istanbul Technical University

Curated by ChEMBL


Assay Description
Agonist activity at human kappa-type opioid receptor expressed in CHO-K1 cells assessed as inhibition of forskolin-induced cAMP accumulation after 30...


J Nat Prod 80: 2094-2100 (2017)


Article DOI: 10.1021/acs.jnatprod.7b00327
BindingDB Entry DOI: 10.7270/Q21N83RM
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM50456639
PNG
(CHEMBL4218745)
Show SMILES [H][C@@]12OC(=O)[C@@](O)(C=C1)[C@]1(C)CC[C@@]3([H])C(=O)O[C@H](C[C@@]3(C)[C@]21[H])c1ccoc1 |r,c:7,TLB:4:3:8.7:22.9,10:9:8.7:3.2,11:9:8.7:3.2,THB:20:22:8.7:3.2|
Show InChI InChI=1S/C20H22O6/c1-18-9-14(11-5-8-24-10-11)25-16(21)12(18)3-6-19(2)15(18)13-4-7-20(19,23)17(22)26-13/h4-5,7-8,10,12-15,23H,3,6,9H2,1-2H3/t12-,13+,14+,15-,18+,19+,20-/m0/s1
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n/an/an/an/a>5.00E+4n/an/an/an/a



Istanbul Technical University

Curated by ChEMBL


Assay Description
Agonist activity at human kappa-type opioid receptor expressed in CHO-K1 cells assessed as inhibition of forskolin-induced cAMP accumulation after 30...


J Nat Prod 80: 2094-2100 (2017)


Article DOI: 10.1021/acs.jnatprod.7b00327
BindingDB Entry DOI: 10.7270/Q21N83RM
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM50456640
PNG
(CHEMBL4214547)
Show SMILES [H][C@]12CC[C@](O)(C(=O)O1)[C@]1(C)CC[C@@]3([H])C(=O)O[C@H](C[C@@]3(C)[C@]21[H])c1ccoc1 |r,TLB:7:6:2.3:22.9,20:22:2.3:6.8,THB:10:9:2.3:6.8,11:9:2.3:6.8|
Show InChI InChI=1S/C20H24O6/c1-18-9-14(11-5-8-24-10-11)25-16(21)12(18)3-6-19(2)15(18)13-4-7-20(19,23)17(22)26-13/h5,8,10,12-15,23H,3-4,6-7,9H2,1-2H3/t12-,13+,14+,15-,18+,19+,20-/m0/s1
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n/an/an/an/a 2.00E+3n/an/an/an/a



Istanbul Technical University

Curated by ChEMBL


Assay Description
Agonist activity at human kappa-type opioid receptor expressed in CHO-K1 cells assessed as inhibition of forskolin-induced cAMP accumulation after 30...


J Nat Prod 80: 2094-2100 (2017)


Article DOI: 10.1021/acs.jnatprod.7b00327
BindingDB Entry DOI: 10.7270/Q21N83RM
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM50456641
PNG
(CHEMBL4218758)
Show SMILES [H][C@@]12OC(=O)[C@@](O)(C=C1)[C@]1(C)CC[C@@]3([H])C(=O)O[C@H](C[C@@]3(C)[C@]21[H])c1ccoc1Br |r,c:7,TLB:4:3:8.7:22.9,10:9:8.7:3.2,11:9:8.7:3.2,THB:20:22:8.7:3.2|
Show InChI InChI=1S/C20H21BrO6/c1-18-9-13(10-5-8-25-15(10)21)26-16(22)11(18)3-6-19(2)14(18)12-4-7-20(19,24)17(23)27-12/h4-5,7-8,11-14,24H,3,6,9H2,1-2H3/t11-,12+,13+,14-,18+,19+,20-/m0/s1
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n/an/an/an/a>5.00E+4n/an/an/an/a



Istanbul Technical University

Curated by ChEMBL


Assay Description
Agonist activity at human kappa-type opioid receptor expressed in CHO-K1 cells assessed as inhibition of forskolin-induced cAMP accumulation after 30...


J Nat Prod 80: 2094-2100 (2017)


Article DOI: 10.1021/acs.jnatprod.7b00327
BindingDB Entry DOI: 10.7270/Q21N83RM
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM50456642
PNG
(CHEMBL4211267)
Show SMILES [H][C@@]12OC(=O)[C@@](OC(=O)\C=C\c3ccccc3)(C=C1)[C@]1(C)CC[C@@]3([H])C(=O)O[C@H](C[C@@]3(C)[C@]21[H])c1ccoc1 |r,c:18,TLB:4:3:18.17:32.19,20:19:18.17:3.2,21:19:18.17:3.2,THB:30:32:18.17:3.2|
Show InChI InChI=1S/C29H28O7/c1-27-16-22(19-12-15-33-17-19)34-25(31)20(27)10-13-28(2)24(27)21-11-14-29(28,26(32)35-21)36-23(30)9-8-18-6-4-3-5-7-18/h3-9,11-12,14-15,17,20-22,24H,10,13,16H2,1-2H3/b9-8+/t20-,21+,22+,24-,27+,28+,29-/m0/s1
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n/an/an/an/a 6.00E+3n/an/an/an/a



Istanbul Technical University

Curated by ChEMBL


Assay Description
Agonist activity at human kappa-type opioid receptor expressed in CHO-K1 cells assessed as inhibition of forskolin-induced cAMP accumulation after 30...


J Nat Prod 80: 2094-2100 (2017)


Article DOI: 10.1021/acs.jnatprod.7b00327
BindingDB Entry DOI: 10.7270/Q21N83RM
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM50159165
PNG
((2S,4aR,6aR,7R,9S,10aS,10bR)-9-(acetyloxy)-2-(fura...)
Show SMILES COC(=O)[C@@H]1C[C@H](OC(C)=O)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@@H](C[C@]21C)c1ccoc1 |r|
Show InChI InChI=1S/C23H28O8/c1-12(24)30-16-9-15(20(26)28-4)22(2)7-5-14-21(27)31-17(13-6-8-29-11-13)10-23(14,3)19(22)18(16)25/h6,8,11,14-17,19H,5,7,9-10H2,1-4H3/t14-,15-,16-,17-,19-,22-,23-/m0/s1
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n/an/an/an/a 0.0420n/an/an/an/a



Istanbul Technical University

Curated by ChEMBL


Assay Description
Agonist activity at human kappa-type opioid receptor expressed in CHO-K1 cells assessed as inhibition of forskolin-induced cAMP accumulation after 30...


J Nat Prod 80: 2094-2100 (2017)


Article DOI: 10.1021/acs.jnatprod.7b00327
BindingDB Entry DOI: 10.7270/Q21N83RM
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Homo sapiens (Human))
BDBM50081701
PNG
(3-[2-(dimethylamino)ethyl]-1H-indol-4-ol | 4-hydro...)
Show SMILES CN(C)CCc1c[nH]c2cccc(O)c12
Show InChI InChI=1S/C12H16N2O/c1-14(2)7-6-9-8-13-10-4-3-5-11(15)12(9)10/h3-5,8,13,15H,6-7H2,1-2H3
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n/an/an/an/a 4.30n/an/an/an/a



Usona Institute

Curated by ChEMBL


Assay Description
Agonist activity at human 5-HT2A receptor expressed in Flp-In T-REx 293 cells assessed as induction of Gq-mediated calcium flux incubated for 1 hr by...


J Nat Prod 83: 461-467 (2020)


Article DOI: 10.1021/acs.jnatprod.9b01061
BindingDB Entry DOI: 10.7270/Q2RX9GM1
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Homo sapiens (Human))
BDBM50081701
PNG
(3-[2-(dimethylamino)ethyl]-1H-indol-4-ol | 4-hydro...)
Show SMILES CN(C)CCc1c[nH]c2cccc(O)c12
Show InChI InChI=1S/C12H16N2O/c1-14(2)7-6-9-8-13-10-4-3-5-11(15)12(9)10/h3-5,8,13,15H,6-7H2,1-2H3
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n/an/an/an/a 4.30n/an/an/an/a



Usona Institute

Curated by ChEMBL


Assay Description
Agonist activity at human 5-HT2A receptor expressed in Flp-In T-REx 293 cells assessed as induction of Gq-mediated calcium flux incubated for 1 hr by...


J Nat Prod 83: 461-467 (2020)


Article DOI: 10.1021/acs.jnatprod.9b01061
BindingDB Entry DOI: 10.7270/Q2RX9GM1
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Mus musculus (Mouse))
BDBM50081701
PNG
(3-[2-(dimethylamino)ethyl]-1H-indol-4-ol | 4-hydro...)
Show SMILES CN(C)CCc1c[nH]c2cccc(O)c12
Show InChI InChI=1S/C12H16N2O/c1-14(2)7-6-9-8-13-10-4-3-5-11(15)12(9)10/h3-5,8,13,15H,6-7H2,1-2H3
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n/an/an/an/a 9.90n/an/an/an/a



Usona Institute

Curated by ChEMBL


Assay Description
Agonist activity at mouse 5-HT2A receptor expressed in Flp-In T-REx 293 cells assessed as induction of Gq-mediated calcium flux incubated for 1 hr by...


J Nat Prod 83: 461-467 (2020)


Article DOI: 10.1021/acs.jnatprod.9b01061
BindingDB Entry DOI: 10.7270/Q2RX9GM1
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Mus musculus (Mouse))
BDBM50081701
PNG
(3-[2-(dimethylamino)ethyl]-1H-indol-4-ol | 4-hydro...)
Show SMILES CN(C)CCc1c[nH]c2cccc(O)c12
Show InChI InChI=1S/C12H16N2O/c1-14(2)7-6-9-8-13-10-4-3-5-11(15)12(9)10/h3-5,8,13,15H,6-7H2,1-2H3
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n/an/an/an/a 9.80n/an/an/an/a



Usona Institute

Curated by ChEMBL


Assay Description
Agonist activity at mouse 5-HT2A receptor expressed in Flp-In T-REx 293 cells assessed as induction of Gq-mediated calcium flux incubated for 1 hr by...


J Nat Prod 83: 461-467 (2020)


Article DOI: 10.1021/acs.jnatprod.9b01061
BindingDB Entry DOI: 10.7270/Q2RX9GM1
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Homo sapiens (Human))
BDBM50538100
PNG
(CHEMBL4648350)
Show SMILES CNCCc1c[nH]c2cccc(O)c12
Show InChI InChI=1S/C11H14N2O/c1-12-6-5-8-7-13-9-3-2-4-10(14)11(8)9/h2-4,7,12-14H,5-6H2,1H3
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n/an/an/an/a 8.40n/an/an/an/a



Usona Institute

Curated by ChEMBL


Assay Description
Agonist activity at human 5-HT2A receptor expressed in Flp-In T-REx 293 cells assessed as induction of Gq-mediated calcium flux incubated for 1 hr by...


J Nat Prod 83: 461-467 (2020)


Article DOI: 10.1021/acs.jnatprod.9b01061
BindingDB Entry DOI: 10.7270/Q2RX9GM1
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Homo sapiens (Human))
BDBM50538100
PNG
(CHEMBL4648350)
Show SMILES CNCCc1c[nH]c2cccc(O)c12
Show InChI InChI=1S/C11H14N2O/c1-12-6-5-8-7-13-9-3-2-4-10(14)11(8)9/h2-4,7,12-14H,5-6H2,1H3
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n/an/an/an/a 8.30n/an/an/an/a



Usona Institute

Curated by ChEMBL


Assay Description
Agonist activity at human 5-HT2A receptor expressed in Flp-In T-REx 293 cells assessed as induction of Gq-mediated calcium flux incubated for 1 hr by...


J Nat Prod 83: 461-467 (2020)


Article DOI: 10.1021/acs.jnatprod.9b01061
BindingDB Entry DOI: 10.7270/Q2RX9GM1
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Mus musculus (Mouse))
BDBM50538100
PNG
(CHEMBL4648350)
Show SMILES CNCCc1c[nH]c2cccc(O)c12
Show InChI InChI=1S/C11H14N2O/c1-12-6-5-8-7-13-9-3-2-4-10(14)11(8)9/h2-4,7,12-14H,5-6H2,1H3
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n/an/an/an/a 19n/an/an/an/a



Usona Institute

Curated by ChEMBL


Assay Description
Agonist activity at mouse 5-HT2A receptor expressed in Flp-In T-REx 293 cells assessed as induction of Gq-mediated calcium flux incubated for 1 hr by...


J Nat Prod 83: 461-467 (2020)


Article DOI: 10.1021/acs.jnatprod.9b01061
BindingDB Entry DOI: 10.7270/Q2RX9GM1
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Mus musculus (Mouse))
BDBM50538100
PNG
(CHEMBL4648350)
Show SMILES CNCCc1c[nH]c2cccc(O)c12
Show InChI InChI=1S/C11H14N2O/c1-12-6-5-8-7-13-9-3-2-4-10(14)11(8)9/h2-4,7,12-14H,5-6H2,1H3
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n/an/an/an/a 19n/an/an/an/a



Usona Institute

Curated by ChEMBL


Assay Description
Agonist activity at mouse 5-HT2A receptor expressed in Flp-In T-REx 293 cells assessed as induction of Gq-mediated calcium flux incubated for 1 hr by...


J Nat Prod 83: 461-467 (2020)


Article DOI: 10.1021/acs.jnatprod.9b01061
BindingDB Entry DOI: 10.7270/Q2RX9GM1
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Homo sapiens (Human))
BDBM10755
PNG
(14C-5-hydroxy tryptamine creatinine disulfate | 2-...)
Show SMILES NCCc1c[nH]c2ccc(O)cc12
Show InChI InChI=1S/C10H12N2O/c11-4-3-7-6-12-10-2-1-8(13)5-9(7)10/h1-2,5-6,12-13H,3-4,11H2
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n/an/an/an/a 0.510n/an/an/an/a



Usona Institute

Curated by ChEMBL


Assay Description
Agonist activity at human 5-HT2A receptor expressed in Flp-In T-REx 293 cells assessed as induction of Gq-mediated calcium flux incubated for 1 hr by...


J Nat Prod 83: 461-467 (2020)


Article DOI: 10.1021/acs.jnatprod.9b01061
BindingDB Entry DOI: 10.7270/Q2RX9GM1
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Homo sapiens (Human))
BDBM10755
PNG
(14C-5-hydroxy tryptamine creatinine disulfate | 2-...)
Show SMILES NCCc1c[nH]c2ccc(O)cc12
Show InChI InChI=1S/C10H12N2O/c11-4-3-7-6-12-10-2-1-8(13)5-9(7)10/h1-2,5-6,12-13H,3-4,11H2
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n/an/an/an/a 0.513n/an/an/an/a



Usona Institute

Curated by ChEMBL


Assay Description
Agonist activity at human 5-HT2A receptor expressed in Flp-In T-REx 293 cells assessed as induction of Gq-mediated calcium flux incubated for 1 hr by...


J Nat Prod 83: 461-467 (2020)


Article DOI: 10.1021/acs.jnatprod.9b01061
BindingDB Entry DOI: 10.7270/Q2RX9GM1
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Mus musculus (Mouse))
BDBM10755
PNG
(14C-5-hydroxy tryptamine creatinine disulfate | 2-...)
Show SMILES NCCc1c[nH]c2ccc(O)cc12
Show InChI InChI=1S/C10H12N2O/c11-4-3-7-6-12-10-2-1-8(13)5-9(7)10/h1-2,5-6,12-13H,3-4,11H2
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n/an/an/an/a 0.525n/an/an/an/a



Usona Institute

Curated by ChEMBL


Assay Description
Agonist activity at mouse 5-HT2A receptor expressed in Flp-In T-REx 293 cells assessed as induction of Gq-mediated calcium flux incubated for 1 hr by...


J Nat Prod 83: 461-467 (2020)


Article DOI: 10.1021/acs.jnatprod.9b01061
BindingDB Entry DOI: 10.7270/Q2RX9GM1
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2A


(Mus musculus (Mouse))
BDBM10755
PNG
(14C-5-hydroxy tryptamine creatinine disulfate | 2-...)
Show SMILES NCCc1c[nH]c2ccc(O)cc12
Show InChI InChI=1S/C10H12N2O/c11-4-3-7-6-12-10-2-1-8(13)5-9(7)10/h1-2,5-6,12-13H,3-4,11H2
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n/an/an/an/a 0.530n/an/an/an/a



Usona Institute

Curated by ChEMBL


Assay Description
Agonist activity at mouse 5-HT2A receptor expressed in Flp-In T-REx 293 cells assessed as induction of Gq-mediated calcium flux incubated for 1 hr by...


J Nat Prod 83: 461-467 (2020)


Article DOI: 10.1021/acs.jnatprod.9b01061
BindingDB Entry DOI: 10.7270/Q2RX9GM1
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Homo sapiens (Human))
BDBM50000092
PNG
((-)-(etorphine) | (-)-morphine | (1S,5R,13R,14S)-1...)
Show SMILES CN1CC[C@@]23[C@H]4Oc5c2c(C[C@@H]1[C@@H]3C=C[C@@H]4O)ccc5O |r,c:16,TLB:13:12:8.9.10:3.2.1|
Show InChI InChI=1S/C17H19NO3/c1-18-7-6-17-10-3-5-13(20)16(17)21-15-12(19)4-2-9(14(15)17)8-11(10)18/h2-5,10-11,13,16,19-20H,6-8H2,1H3/t10-,11+,13-,16-,17-/m0/s1
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n/an/an/an/a 5n/an/an/an/a


TBA

Assay Description
Agonist activity at human mu opiod receptor expressed in CHO-K1 cells assessed as increase in forskolin induced cAMP production measured after 30 min...


Citation and Details

Article DOI: 10.1021/acs.jmedchem.6b01235
BindingDB Entry DOI: 10.7270/Q2FJ2MH3
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Mu-type opioid receptor


(Homo sapiens (Human))
BDBM21015
PNG
((2S)-2-{2-[(2R)-2-[(2S)-2-amino-3-(4-hydroxyphenyl...)
Show SMILES C[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)NCC(=O)N(C)[C@@H](Cc1ccccc1)C(=O)NCCO
Show InChI InChI=1S/C26H35N5O6/c1-17(30-25(36)21(27)14-19-8-10-20(33)11-9-19)24(35)29-16-23(34)31(2)22(26(37)28-12-13-32)15-18-6-4-3-5-7-18/h3-11,17,21-22,32-33H,12-16,27H2,1-2H3,(H,28,37)(H,29,35)(H,30,36)/t17-,21+,22+/m1/s1
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n/an/an/an/a 0.600n/an/an/an/a


TBA

Assay Description
Agonist activity at human mu opiod receptor expressed in CHO-K1 cells assessed as increase in forskolin induced cAMP production measured after 30 min...


Citation and Details

Article DOI: 10.1021/acs.jmedchem.6b01235
BindingDB Entry DOI: 10.7270/Q2FJ2MH3
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Homo sapiens (Human))
BDBM50558750
PNG
(CHEMBL4790712)
Show SMILES [H][C@@]12CC[C@@]3(C)[C@@H](C=C(OC(=O)c4ccc(OC)cc4)C(=O)[C@]3([H])[C@@]1(C)C[C@H](OC2=O)c1ccoc1)C(=O)OC |r,t:7|
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n/an/an/an/a 8n/an/an/an/a


TBA

Assay Description
Agonist activity at human mu opiod receptor expressed in CHO-K1 cells assessed as increase in forskolin induced cAMP production measured after 30 min...


Citation and Details

Article DOI: 10.1021/acs.jmedchem.6b01235
BindingDB Entry DOI: 10.7270/Q2FJ2MH3
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Homo sapiens (Human))
BDBM50558751
PNG
(CHEMBL4745430)
Show SMILES [H][C@@]12CC[C@@]3(C)[C@@H](C=C(OC(=O)c4cccc(OC)c4)C(=O)[C@]3([H])[C@@]1(C)C[C@H](OC2=O)c1ccoc1)C(=O)OC |r,t:7|
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n/an/an/an/a 11n/an/an/an/a


TBA

Assay Description
Agonist activity at human mu opiod receptor expressed in CHO-K1 cells assessed as increase in forskolin induced cAMP production measured after 30 min...


Citation and Details

Article DOI: 10.1021/acs.jmedchem.6b01235
BindingDB Entry DOI: 10.7270/Q2FJ2MH3
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Homo sapiens (Human))
BDBM50558752
PNG
(CHEMBL4760942)
Show SMILES [H][C@@]12CC[C@@]3(C)[C@@H](C=C(OC(=O)c4ccc(cc4)[N+]([O-])=O)C(=O)[C@]3([H])[C@@]1(C)C[C@H](OC2=O)c1ccoc1)C(=O)OC |r,t:7|
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n/an/an/an/a 31n/an/an/an/a


TBA

Assay Description
Agonist activity at human mu opiod receptor expressed in CHO-K1 cells assessed as increase in forskolin induced cAMP production measured after 30 min...


Citation and Details

Article DOI: 10.1021/acs.jmedchem.6b01235
BindingDB Entry DOI: 10.7270/Q2FJ2MH3
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Homo sapiens (Human))
BDBM50558753
PNG
(CHEMBL4741711)
Show SMILES [H][C@@]12CC[C@@]3(C)[C@@H](C=C(OC(=O)c4ccc(C)cc4)C(=O)[C@]3([H])[C@@]1(C)C[C@H](OC2=O)c1ccoc1)C(=O)OC |r,t:7|
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n/an/an/an/a 22n/an/an/an/a


TBA

Assay Description
Agonist activity at human mu opiod receptor expressed in CHO-K1 cells assessed as increase in forskolin induced cAMP production measured after 30 min...


Citation and Details

Article DOI: 10.1021/acs.jmedchem.6b01235
BindingDB Entry DOI: 10.7270/Q2FJ2MH3
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Homo sapiens (Human))
BDBM50558754
PNG
(CHEMBL4799292)
Show SMILES [H][C@@]12CC[C@@]3(C)[C@@H](C=C(OC(=O)c4ccc(Cl)cc4)C(=O)[C@]3([H])[C@@]1(C)C[C@H](OC2=O)c1ccoc1)C(=O)OC |r,t:7|
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n/an/an/an/a 30n/an/an/an/a


TBA

Assay Description
Agonist activity at human mu opiod receptor expressed in CHO-K1 cells assessed as increase in forskolin induced cAMP production measured after 30 min...


Citation and Details

Article DOI: 10.1021/acs.jmedchem.6b01235
BindingDB Entry DOI: 10.7270/Q2FJ2MH3
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Homo sapiens (Human))
BDBM50558755
PNG
(CHEMBL4756271)
Show SMILES [H][C@@]12CC[C@@]3(C)[C@@H](C=C(OC(=O)c4ccc(F)cc4)C(=O)[C@]3([H])[C@@]1(C)C[C@H](OC2=O)c1ccoc1)C(=O)OC |r,t:7|
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n/an/an/an/a 15n/an/an/an/a


TBA

Assay Description
Agonist activity at human mu opiod receptor expressed in CHO-K1 cells assessed as increase in forskolin induced cAMP production measured after 30 min...


Citation and Details

Article DOI: 10.1021/acs.jmedchem.6b01235
BindingDB Entry DOI: 10.7270/Q2FJ2MH3
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Homo sapiens (Human))
BDBM50558756
PNG
(CHEMBL4782368)
Show SMILES [H][C@@]12CC[C@@]3(C)[C@H](OC(C)=O)C=C(OC(=O)c4cccc(F)c4)C(=O)[C@]3([H])[C@@]1(C)C[C@H](OC2=O)c1ccoc1 |r,t:11|
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n/an/an/an/a 4.70n/an/an/an/a


TBA

Assay Description
Agonist activity at human mu opiod receptor expressed in CHO-K1 cells assessed as increase in forskolin induced cAMP production measured after 30 min...


Citation and Details

Article DOI: 10.1021/acs.jmedchem.6b01235
BindingDB Entry DOI: 10.7270/Q2FJ2MH3
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Homo sapiens (Human))
BDBM50558757
PNG
(CHEMBL4763725)
Show SMILES [H][C@@]12CC[C@@]3(C)[C@@H](C=C(OC(=O)c4ccccc4F)C(=O)[C@]3([H])[C@@]1(C)C[C@H](OC2=O)c1ccoc1)C(=O)OC |r,t:7|
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n/an/an/an/a 4.80n/an/an/an/a


TBA

Assay Description
Agonist activity at human mu opiod receptor expressed in CHO-K1 cells assessed as increase in forskolin induced cAMP production measured after 30 min...


Citation and Details

Article DOI: 10.1021/acs.jmedchem.6b01235
BindingDB Entry DOI: 10.7270/Q2FJ2MH3
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Homo sapiens (Human))
BDBM50265928
PNG
(CHEMBL4086641)
Show SMILES [H][C@@]12CC[C@@]3(C)[C@@H](CC(=O)C(O)=C3[C@@]1(C)C[C@H](OC2=O)c1ccoc1)C(=O)OC |r,c:11|
Show InChI InChI=1S/C21H24O7/c1-20-6-4-12-19(25)28-15(11-5-7-27-10-11)9-21(12,2)17(20)16(23)14(22)8-13(20)18(24)26-3/h5,7,10,12-13,15,23H,4,6,8-9H2,1-3H3/t12-,13-,15-,20-,21-/m0/s1
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PubMed
n/an/an/an/a>1.00E+4n/an/an/an/a


TBA

Assay Description
Agonist activity at human mu opiod receptor expressed in CHO-K1 cells assessed as increase in forskolin induced cAMP production measured after 30 min...


Citation and Details

Article DOI: 10.1021/acs.jmedchem.6b01235
BindingDB Entry DOI: 10.7270/Q2FJ2MH3
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Homo sapiens (Human))
BDBM50558758
PNG
(CHEMBL4787274)
Show SMILES [H][C@@]12CC[C@@]3(C)[C@@H](C=C(O)C(=O)[C@]3([H])[C@@]1(C)C[C@H](OC2=O)c1ccoc1)C(=O)OC |r,t:7|
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n/an/an/an/a>1.00E+4n/an/an/an/a


TBA

Assay Description
Agonist activity at human mu opiod receptor expressed in CHO-K1 cells assessed as increase in forskolin induced cAMP production measured after 30 min...


Citation and Details

Article DOI: 10.1021/acs.jmedchem.6b01235
BindingDB Entry DOI: 10.7270/Q2FJ2MH3
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Homo sapiens (Human))
BDBM50558759
PNG
(CHEMBL4786506)
Show SMILES [H][C@@]12CC[C@@]3(C)[C@@H](C=C(OC(=O)c4ccccc4)C(=O)[C@]3([H])[C@@]1(C)C[C@H](OC2=O)c1ccoc1)C(=O)OC |r,t:7|
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n/an/an/an/a 1.20n/an/an/an/a


TBA

Assay Description
Agonist activity at human mu opiod receptor expressed in CHO-K1 cells assessed as increase in forskolin induced cAMP production measured after 30 min...


Citation and Details

Article DOI: 10.1021/acs.jmedchem.6b01235
BindingDB Entry DOI: 10.7270/Q2FJ2MH3
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Homo sapiens (Human))
BDBM50558760
PNG
(CHEMBL4752988)
Show SMILES [H][C@@]12CC[C@@]3(C)[C@@H](C[C@@H](OC(=O)c4ccccc4)C(=O)[C@]3([H])[C@@]1(C)C[C@H](OC2=O)c1ccoc1)C(=O)OC |r|
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n/an/an/an/a>1.00E+4n/an/an/an/a


TBA

Assay Description
Agonist activity at human mu opiod receptor expressed in CHO-K1 cells assessed as increase in forskolin induced cAMP production measured after 30 min...


Citation and Details

Article DOI: 10.1021/acs.jmedchem.6b01235
BindingDB Entry DOI: 10.7270/Q2FJ2MH3
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Homo sapiens (Human))
BDBM50558761
PNG
(CHEMBL4783674)
Show SMILES [H][C@@]12CC[C@@]3(C)[C@@H](C[C@H](NC(=O)c4ccccc4)C(=O)[C@]3([H])[C@@]1(C)C[C@H](OC2=O)c1ccoc1)OC(C)=O |r|
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n/an/an/an/a 3n/an/an/an/a


TBA

Assay Description
Agonist activity at human mu opiod receptor expressed in CHO-K1 cells assessed as increase in forskolin induced cAMP production measured after 30 min...


Citation and Details

Article DOI: 10.1021/acs.jmedchem.6b01235
BindingDB Entry DOI: 10.7270/Q2FJ2MH3
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Homo sapiens (Human))
BDBM50170678
PNG
((3S,4aR,4bS,6S,8R,8aR,10aR)-6-Benzoyloxy-3-furan-3...)
Show SMILES COC(=O)[C@@H]1C[C@H](OC(=O)c2ccccc2)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@@H](C[C@]21C)c1ccoc1 |r|
Show InChI InChI=1S/C28H30O8/c1-27-11-9-18-26(32)36-21(17-10-12-34-15-17)14-28(18,2)23(27)22(29)20(13-19(27)25(31)33-3)35-24(30)16-7-5-4-6-8-16/h4-8,10,12,15,18-21,23H,9,11,13-14H2,1-3H3/t18-,19-,20-,21-,23-,27-,28-/m0/s1
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n/an/an/an/a 40n/an/an/an/a


TBA

Assay Description
Agonist activity at human mu opiod receptor expressed in CHO-K1 cells assessed as increase in forskolin induced cAMP production measured after 30 min...


Citation and Details

Article DOI: 10.1021/acs.jmedchem.6b01235
BindingDB Entry DOI: 10.7270/Q2FJ2MH3
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Homo sapiens (Human))
BDBM50189145
PNG
((2S,4aR,6aR,7R,9R,10aS,10bR)-9-(Acetyloxy)-2-(3-fu...)
Show SMILES COC(=O)[C@@H]1C[C@@H](OC(C)=O)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@@H](C[C@]21C)c1ccoc1 |r|
Show InChI InChI=1S/C23H28O8/c1-12(24)30-16-9-15(20(26)28-4)22(2)7-5-14-21(27)31-17(13-6-8-29-11-13)10-23(14,3)19(22)18(16)25/h6,8,11,14-17,19H,5,7,9-10H2,1-4H3/t14-,15-,16+,17-,19-,22-,23-/m0/s1
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n/an/an/an/a>1.00E+4n/an/an/an/a


TBA

Assay Description
Agonist activity at human mu opiod receptor expressed in CHO-K1 cells assessed as increase in forskolin induced cAMP production measured after 30 min...


Citation and Details

Article DOI: 10.1021/acs.jmedchem.6b01235
BindingDB Entry DOI: 10.7270/Q2FJ2MH3
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Homo sapiens (Human))
BDBM50558762
PNG
(CHEMBL4749616)
Show SMILES [H][C@@]12CC[C@@]3(C)[C@@H](C=C(OC(C)=O)C(=O)[C@]3([H])[C@@]1(C)C[C@H](OC2=O)c1ccoc1)C(=O)OC |r,t:7|
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n/an/an/an/a>1.00E+4n/an/an/an/a


TBA

Assay Description
Agonist activity at human mu opiod receptor expressed in CHO-K1 cells assessed as increase in forskolin induced cAMP production measured after 30 min...


Citation and Details

Article DOI: 10.1021/acs.jmedchem.6b01235
BindingDB Entry DOI: 10.7270/Q2FJ2MH3
More data for this
Ligand-Target Pair
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