Found 7 hits in this display 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 |
|---|
Adenosine receptor A2a
(Rattus norvegicus (rat)) | BDBM50221680
(9-(2-(1H-indol-3-yl)ethyl)-1,3-dipropyl-6,7,8,9-te...)Show SMILES CCCn1c2nc3N(CCc4c[nH]c5ccccc45)CCCn3c2c(=O)n(CCC)c1=O Show InChI InChI=1S/C24H30N6O2/c1-3-11-29-21-20(22(31)30(12-4-2)24(29)32)28-14-7-13-27(23(28)26-21)15-10-17-16-25-19-9-6-5-8-18(17)19/h5-6,8-9,16,25H,3-4,7,10-15H2,1-2H3 | PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
GoogleScholar
AffyNet 
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| 900 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Jagiellonian University Medical College
Curated by ChEMBL
| Assay Description
Displacement of [3H]MSX2 from adenosine A2A receptor in rat brain striatal membrane |
Bioorg Med Chem 15: 6956-74 (2007)
Article DOI: 10.1016/j.bmc.2007.07.051
BindingDB Entry DOI: 10.7270/Q26W99TB |
More data for this
Ligand-Target Pair | |
Adenosine receptor A3
(Homo sapiens (Human)) | BDBM50221680
(9-(2-(1H-indol-3-yl)ethyl)-1,3-dipropyl-6,7,8,9-te...)Show SMILES CCCn1c2nc3N(CCc4c[nH]c5ccccc45)CCCn3c2c(=O)n(CCC)c1=O Show InChI InChI=1S/C24H30N6O2/c1-3-11-29-21-20(22(31)30(12-4-2)24(29)32)28-14-7-13-27(23(28)26-21)15-10-17-16-25-19-9-6-5-8-18(17)19/h5-6,8-9,16,25H,3-4,7,10-15H2,1-2H3 | PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| >1.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Jagiellonian University Medical College
Curated by ChEMBL
| Assay Description
Displacement of [3H]PSB11 from human adenosine A3 receptor expressed in CHO cells |
Bioorg Med Chem 15: 6956-74 (2007)
Article DOI: 10.1016/j.bmc.2007.07.051
BindingDB Entry DOI: 10.7270/Q26W99TB |
More data for this
Ligand-Target Pair | |
Adenosine receptor A1
(Rattus norvegicus (rat)) | BDBM50221680
(9-(2-(1H-indol-3-yl)ethyl)-1,3-dipropyl-6,7,8,9-te...)Show SMILES CCCn1c2nc3N(CCc4c[nH]c5ccccc45)CCCn3c2c(=O)n(CCC)c1=O Show InChI InChI=1S/C24H30N6O2/c1-3-11-29-21-20(22(31)30(12-4-2)24(29)32)28-14-7-13-27(23(28)26-21)15-10-17-16-25-19-9-6-5-8-18(17)19/h5-6,8-9,16,25H,3-4,7,10-15H2,1-2H3 | PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| 1.79E+3 | n/a | n/a | n/a | n/a | n/a | n/a | n/a | n/a |
Jagiellonian University Medical College
Curated by ChEMBL
| Assay Description
Displacement of [3H]CCPA from adenosine A1 receptor in rat brain cortical membrane |
Bioorg Med Chem 15: 6956-74 (2007)
Article DOI: 10.1016/j.bmc.2007.07.051
BindingDB Entry DOI: 10.7270/Q26W99TB |
More data for this
Ligand-Target Pair | |
G-protein coupled receptor 55
(Homo sapiens (Human)) | BDBM50221680
(9-(2-(1H-indol-3-yl)ethyl)-1,3-dipropyl-6,7,8,9-te...)Show SMILES CCCn1c2nc3N(CCc4c[nH]c5ccccc45)CCCn3c2c(=O)n(CCC)c1=O Show InChI InChI=1S/C24H30N6O2/c1-3-11-29-21-20(22(31)30(12-4-2)24(29)32)28-14-7-13-27(23(28)26-21)15-10-17-16-25-19-9-6-5-8-18(17)19/h5-6,8-9,16,25H,3-4,7,10-15H2,1-2H3 | Reactome pathway
KEGG
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Antagonist activity at Prolink1-tagged human GPR55 receptor expressed in CHO cells assessed as inhibition of lysophosphatidylinositol-induced beta ar... |
Citation and Details
Article DOI: 10.1021/acsmedchemlett.0c00208
BindingDB Entry DOI: 10.7270/Q2PZ5DJH |
More data for this
Ligand-Target Pair | |
N-arachidonyl glycine receptor
(Homo sapiens (Human)) | BDBM50221680
(9-(2-(1H-indol-3-yl)ethyl)-1,3-dipropyl-6,7,8,9-te...)Show SMILES CCCn1c2nc3N(CCc4c[nH]c5ccccc45)CCCn3c2c(=O)n(CCC)c1=O Show InChI InChI=1S/C24H30N6O2/c1-3-11-29-21-20(22(31)30(12-4-2)24(29)32)28-14-7-13-27(23(28)26-21)15-10-17-16-25-19-9-6-5-8-18(17)19/h5-6,8-9,16,25H,3-4,7,10-15H2,1-2H3 | Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Antagonist activity at Prolink1-tagged human GPR18 receptor expressed in CHO cells assessed as inhibition of THC-induced beta arrestin recruitment af... |
Citation and Details
Article DOI: 10.1021/acsmedchemlett.0c00208
BindingDB Entry DOI: 10.7270/Q2PZ5DJH |
More data for this
Ligand-Target Pair | |
G-protein coupled receptor 55
(Homo sapiens (Human)) | BDBM50221680
(9-(2-(1H-indol-3-yl)ethyl)-1,3-dipropyl-6,7,8,9-te...)Show SMILES CCCn1c2nc3N(CCc4c[nH]c5ccccc45)CCCn3c2c(=O)n(CCC)c1=O Show InChI InChI=1S/C24H30N6O2/c1-3-11-29-21-20(22(31)30(12-4-2)24(29)32)28-14-7-13-27(23(28)26-21)15-10-17-16-25-19-9-6-5-8-18(17)19/h5-6,8-9,16,25H,3-4,7,10-15H2,1-2H3 | Reactome pathway
KEGG
UniProtKB/SwissProt
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Agonist activity at Prolink1-tagged human GPR55 receptor expressed in CHO cells assessed as induction of beta-arrestin recruitment after 90 mins by b... |
Citation and Details
Article DOI: 10.1021/acsmedchemlett.0c00208
BindingDB Entry DOI: 10.7270/Q2PZ5DJH |
More data for this
Ligand-Target Pair | |
N-arachidonyl glycine receptor
(Homo sapiens (Human)) | BDBM50221680
(9-(2-(1H-indol-3-yl)ethyl)-1,3-dipropyl-6,7,8,9-te...)Show SMILES CCCn1c2nc3N(CCc4c[nH]c5ccccc45)CCCn3c2c(=O)n(CCC)c1=O Show InChI InChI=1S/C24H30N6O2/c1-3-11-29-21-20(22(31)30(12-4-2)24(29)32)28-14-7-13-27(23(28)26-21)15-10-17-16-25-19-9-6-5-8-18(17)19/h5-6,8-9,16,25H,3-4,7,10-15H2,1-2H3 | Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a |
TBA
| Assay Description
Agonist activity at Prolink1-tagged human GPR18 receptor expressed in CHO cells assessed as induction of beta-arrestin recruitment after 90 mins by b... |
Citation and Details
Article DOI: 10.1021/acsmedchemlett.0c00208
BindingDB Entry DOI: 10.7270/Q2PZ5DJH |
More data for this
Ligand-Target Pair | |