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Compile Data Set for Download or QSAR

Found 3 hits Enz. Inhib. hit(s) with Target = 'Delta-type opioid receptor' and Ligand = 'BDBM50010658'   
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
Delta-type opioid receptor


(MOUSE)
BDBM50010658
PNG
(CHEMBL3264747)
Show SMILES [H][C@]12O[C@]34CC[C@@]5(OCOc6c(O)ccc7C[C@@]3([H])N(CC3CC3)CC[C@]4(c67)[C@]15[H])N(C2=O)c1ccccc1 |r,TLB:20:19:3:27.15.16,THB:7:6:26:1.2|
Show InChI InChI=1S/C29H30N2O5/c32-20-9-8-18-14-21-28-10-11-29-25(24(36-28)26(33)31(29)19-4-2-1-3-5-19)27(28,22(18)23(20)34-16-35-29)12-13-30(21)15-17-6-7-17/h1-5,8-9,17,21,24-25,32H,6-7,10-16H2/t21-,24+,25+,27+,28-,29+/m1/s1
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Article
PubMed
0.534n/an/an/an/an/an/an/an/a



Kitasato University

Curated by ChEMBL


Assay Description
Displacement of [3H]DPDPE from delta opioid receptor in mouse whole brain cerebellum membrane


ACS Med Chem Lett 5: 368-72 (2014)


Article DOI: 10.1021/ml400491k
BindingDB Entry DOI: 10.7270/Q2GF0W23
More data for this
Ligand-Target Pair
Delta-type opioid receptor


(Homo sapiens (Human))
BDBM50010658
PNG
(CHEMBL3264747)
Show SMILES [H][C@]12O[C@]34CC[C@@]5(OCOc6c(O)ccc7C[C@@]3([H])N(CC3CC3)CC[C@]4(c67)[C@]15[H])N(C2=O)c1ccccc1 |r,TLB:20:19:3:27.15.16,THB:7:6:26:1.2|
Show InChI InChI=1S/C29H30N2O5/c32-20-9-8-18-14-21-28-10-11-29-25(24(36-28)26(33)31(29)19-4-2-1-3-5-19)27(28,22(18)23(20)34-16-35-29)12-13-30(21)15-17-6-7-17/h1-5,8-9,17,21,24-25,32H,6-7,10-16H2/t21-,24+,25+,27+,28-,29+/m1/s1
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PC sid
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Article
PubMed
n/an/an/an/a 0.390n/an/an/an/a



Kitasato University

Curated by ChEMBL


Assay Description
Agonist activity at human delta opioid receptor expressed in HEK293 cells by CellKey method


ACS Med Chem Lett 5: 368-72 (2014)


Article DOI: 10.1021/ml400491k
BindingDB Entry DOI: 10.7270/Q2GF0W23
More data for this
Ligand-Target Pair
Delta-type opioid receptor


(Homo sapiens (Human))
BDBM50010658
PNG
(CHEMBL3264747)
Show SMILES [H][C@]12O[C@]34CC[C@@]5(OCOc6c(O)ccc7C[C@@]3([H])N(CC3CC3)CC[C@]4(c67)[C@]15[H])N(C2=O)c1ccccc1 |r,TLB:20:19:3:27.15.16,THB:7:6:26:1.2|
Show InChI InChI=1S/C29H30N2O5/c32-20-9-8-18-14-21-28-10-11-29-25(24(36-28)26(33)31(29)19-4-2-1-3-5-19)27(28,22(18)23(20)34-16-35-29)12-13-30(21)15-17-6-7-17/h1-5,8-9,17,21,24-25,32H,6-7,10-16H2/t21-,24+,25+,27+,28-,29+/m1/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/an/an/a 0.980n/an/an/an/a



Kitasato University

Curated by ChEMBL


Assay Description
Agonist activity at human delta opioid receptor expressed in CHO cells assessed as [35S]-GTP[gammaS] binding


ACS Med Chem Lett 5: 368-72 (2014)


Article DOI: 10.1021/ml400491k
BindingDB Entry DOI: 10.7270/Q2GF0W23
More data for this
Ligand-Target Pair