Ligand source activities (1 row/activity)





Ligands (move mouse cursor over ligand name to see structure) Receptor Assay information Chemical information
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name
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p-value
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Activity
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DOI

56707820 2910 39 None - 1 Human 6.8 pEC50 = 6.8 Functional
Affinity Phenotypic Cellular interaction (FLIPR-TETRA assay (proton-mediated calcium mobilization in HEK293T cells)) EUB0000354a GPR68Affinity Phenotypic Cellular interaction (FLIPR-TETRA assay (proton-mediated calcium mobilization in HEK293T cells)) EUB0000354a GPR68
ChEMBL 307 5 3 6 2.2 OCc1ccccc1c1nc(NCc2ccccc2)nc(n1)N 10.6019/CHEMBL5209897
9155 2910 39 None - 1 Human 6.8 pEC50 = 6.8 Functional
Affinity Phenotypic Cellular interaction (FLIPR-TETRA assay (proton-mediated calcium mobilization in HEK293T cells)) EUB0000354a GPR68Affinity Phenotypic Cellular interaction (FLIPR-TETRA assay (proton-mediated calcium mobilization in HEK293T cells)) EUB0000354a GPR68
ChEMBL 307 5 3 6 2.2 OCc1ccccc1c1nc(NCc2ccccc2)nc(n1)N 10.6019/CHEMBL5209897
CHEMBL4548689 2910 39 None - 1 Human 6.8 pEC50 = 6.8 Functional
Affinity Phenotypic Cellular interaction (FLIPR-TETRA assay (proton-mediated calcium mobilization in HEK293T cells)) EUB0000354a GPR68Affinity Phenotypic Cellular interaction (FLIPR-TETRA assay (proton-mediated calcium mobilization in HEK293T cells)) EUB0000354a GPR68
ChEMBL 307 5 3 6 2.2 OCc1ccccc1c1nc(NCc2ccccc2)nc(n1)N 10.6019/CHEMBL5209897
10572 3148 0 None - 1 Human 5.9 pEC50 = 5.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 31675498
145996515 3148 0 None - 1 Human 5.9 pEC50 = 5.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 31675498
10571 802 0 None - 1 Human 6.0 pEC50 = 6.0 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 31675498
145996514 802 0 None - 1 Human 6.0 pEC50 = 6.0 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 31675498
10570 2971 0 None - 1 Human 6.4 pEC50 = 6.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 31675498
145996513 2971 0 None - 1 Human 6.4 pEC50 = 6.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 31675498
56707820 2910 39 None - 1 Human 5.0 pKB = 5.0 Functional
Allosteric ligand biochemical binding affinity in the presence of protons (H<sup>+</sup>. Affinity cannot be measured in the absence of endogenous ligand for this receptor.Allosteric ligand biochemical binding affinity in the presence of protons (H<sup>+</sup>. Affinity cannot be measured in the absence of endogenous ligand for this receptor.
Guide to Pharmacology 307 5 3 6 2.2 OCc1ccccc1c1nc(NCc2ccccc2)nc(n1)N 26550826
9155 2910 39 None - 1 Human 5.0 pKB = 5.0 Functional
Allosteric ligand biochemical binding affinity in the presence of protons (H<sup>+</sup>. Affinity cannot be measured in the absence of endogenous ligand for this receptor.Allosteric ligand biochemical binding affinity in the presence of protons (H<sup>+</sup>. Affinity cannot be measured in the absence of endogenous ligand for this receptor.
Guide to Pharmacology 307 5 3 6 2.2 OCc1ccccc1c1nc(NCc2ccccc2)nc(n1)N 26550826
CHEMBL4548689 2910 39 None - 1 Human 5.0 pKB = 5.0 Functional
Allosteric ligand biochemical binding affinity in the presence of protons (H<sup>+</sup>. Affinity cannot be measured in the absence of endogenous ligand for this receptor.Allosteric ligand biochemical binding affinity in the presence of protons (H<sup>+</sup>. Affinity cannot be measured in the absence of endogenous ligand for this receptor.
Guide to Pharmacology 307 5 3 6 2.2 OCc1ccccc1c1nc(NCc2ccccc2)nc(n1)N 26550826
10440 2680 20 None -4 3 Human 5.9 pKB = 5.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology 417 7 3 7 4.2 OCc1cccc(c1c1nc(NCc2ccc(cc2)Oc2ccccc2)nc(n1)N)F 31298539
139030523 2680 20 None -4 3 Human 5.9 pKB = 5.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology 417 7 3 7 4.2 OCc1cccc(c1c1nc(NCc2ccc(cc2)Oc2ccccc2)nc(n1)N)F 31298539
CHEMBL4449712 2680 20 None -4 3 Human 5.9 pKB = 5.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology 417 7 3 7 4.2 OCc1cccc(c1c1nc(NCc2ccc(cc2)Oc2ccccc2)nc(n1)N)F 31298539




Ligands (move mouse cursor over ligand name to see structure) Receptor Assay information Chemical information
Sel. page Similar-
ity
Common
name
GPCRdb
ID
#Vendors

Reference
ligand
Fold
selectivity
# Tested
GPCRs
Species

p-value
(-log)
Activity
Type
Activity
Relation
Activity
Value
Assay
Type
Assay
Description
Source

Mol
weight
Rot
Bonds
H don

H acc

LogP

Smiles

DOI