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Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Opioid receptors; mu/kappa/delta' and Ligand = 'BDBM50430606'   
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
Opioid receptors; mu/kappa/delta


(Homo sapiens (Human))
BDBM50430606
PNG
(CHEMBL2338714 | Isopentyl Orvinol M320)
Show SMILES CO[C@]12C=C[C@@]3(C[C@@H]1[C@](C)(O)CCC(C)C)[C@H]1Cc4ccc(O)c5O[C@@H]2[C@]3(CCN1CC1CC1)c45 |r,wU:8.9,5.5,16.32,wD:8.10,26.38,25.25,7.8,2.1,c:3,THB:8:7:26.25:4.3,(43.61,-49.36,;42.29,-48.59,;42.3,-47.05,;40.92,-46.19,;41.8,-45.37,;40.79,-44.38,;42.31,-44.38,;43.08,-45.72,;44.62,-45.72,;44.61,-44.16,;45.96,-44.94,;45.4,-47.07,;44.61,-48.42,;45.39,-49.77,;44.61,-51.11,;46.94,-49.77,;39.97,-43.06,;38.47,-43.06,;37.73,-44.38,;36.19,-44.38,;35.41,-45.71,;36.19,-47.02,;35.39,-48.38,;37.73,-47.02,;39.17,-47.94,;40.76,-47.02,;40,-45.71,;39.22,-44.38,;39.22,-42.49,;40,-41.52,;40.78,-40.17,;42.33,-40.14,;43.68,-40.89,;43.66,-39.34,;38.47,-45.71,)|
Show InChI InChI=1S/C30H41NO4/c1-18(2)9-10-27(3,33)22-16-28-11-12-30(22,34-4)26-29(28)13-14-31(17-19-5-6-19)23(28)15-20-7-8-21(32)25(35-26)24(20)29/h7-8,11-12,18-19,22-23,26,32-33H,5-6,9-10,13-17H2,1-4H3/t22-,23-,26-,27-,28-,29+,30-/m1/s1
PDB

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UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
0.0820n/an/an/an/an/an/an/an/a



University of Bath

Curated by ChEMBL


Assay Description
Displacement of [3H]-diprenorphine from human KOR expressed in CHO cells


J Med Chem 56: 3207-16 (2013)


Article DOI: 10.1021/jm301543e
BindingDB Entry DOI: 10.7270/Q28G8N2Q
More data for this
Ligand-Target Pair
Opioid receptors; mu/kappa/delta


(Homo sapiens (Human))
BDBM50430606
PNG
(CHEMBL2338714 | Isopentyl Orvinol M320)
Show SMILES CO[C@]12C=C[C@@]3(C[C@@H]1[C@](C)(O)CCC(C)C)[C@H]1Cc4ccc(O)c5O[C@@H]2[C@]3(CCN1CC1CC1)c45 |r,wU:8.9,5.5,16.32,wD:8.10,26.38,25.25,7.8,2.1,c:3,THB:8:7:26.25:4.3,(43.61,-49.36,;42.29,-48.59,;42.3,-47.05,;40.92,-46.19,;41.8,-45.37,;40.79,-44.38,;42.31,-44.38,;43.08,-45.72,;44.62,-45.72,;44.61,-44.16,;45.96,-44.94,;45.4,-47.07,;44.61,-48.42,;45.39,-49.77,;44.61,-51.11,;46.94,-49.77,;39.97,-43.06,;38.47,-43.06,;37.73,-44.38,;36.19,-44.38,;35.41,-45.71,;36.19,-47.02,;35.39,-48.38,;37.73,-47.02,;39.17,-47.94,;40.76,-47.02,;40,-45.71,;39.22,-44.38,;39.22,-42.49,;40,-41.52,;40.78,-40.17,;42.33,-40.14,;43.68,-40.89,;43.66,-39.34,;38.47,-45.71,)|
Show InChI InChI=1S/C30H41NO4/c1-18(2)9-10-27(3,33)22-16-28-11-12-30(22,34-4)26-29(28)13-14-31(17-19-5-6-19)23(28)15-20-7-8-21(32)25(35-26)24(20)29/h7-8,11-12,18-19,22-23,26,32-33H,5-6,9-10,13-17H2,1-4H3/t22-,23-,26-,27-,28-,29+,30-/m1/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/an/a 0.0510n/an/an/an/a



University of Bath

Curated by ChEMBL


Assay Description
Agonist activity at human KOR expressed in CHO cells assessed as stimulation of [35S]GTPgammaS binding


J Med Chem 56: 3207-16 (2013)


Article DOI: 10.1021/jm301543e
BindingDB Entry DOI: 10.7270/Q28G8N2Q
More data for this
Ligand-Target Pair