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BDBM50381668 CHEMBL2022019

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)C(=O)c1ccccc1

InChI Key: InChIKey=UAZABUMKRADYLE-CGPRNCPCSA-N

Data: 3 KI  1 EC50

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50381668   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM50381668
PNG
(CHEMBL2022019)
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)C(=O)c1ccccc1 |r|
Show InChI InChI=1S/C26H30O8/c1-14(27)33-18-12-17(23(30)32-4)25(2)11-10-16-24(31)34-19(13-26(16,3)22(25)21(18)29)20(28)15-8-6-5-7-9-15/h5-9,16-19,22H,10-13H2,1-4H3/t16-,17-,18-,19-,22-,25-,26-/m0/s1
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PC cid
PC sid
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Article
PubMed
70n/an/an/an/an/an/an/an/a



The University of Kansas

Curated by ChEMBL


Assay Description
Displacement of [3H]U69593 from human recombinant kappa opioid receptor expressed in CHO cells after 2 hrs by liquid scintillation counting


Bioorg Med Chem 20: 3100-10 (2012)


Article DOI: 10.1016/j.bmc.2012.02.040
BindingDB Entry DOI: 10.7270/Q27H1KK0
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Homo sapiens (Human))
BDBM50381668
PNG
(CHEMBL2022019)
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)C(=O)c1ccccc1 |r|
Show InChI InChI=1S/C26H30O8/c1-14(27)33-18-12-17(23(30)32-4)25(2)11-10-16-24(31)34-19(13-26(16,3)22(25)21(18)29)20(28)15-8-6-5-7-9-15/h5-9,16-19,22H,10-13H2,1-4H3/t16-,17-,18-,19-,22-,25-,26-/m0/s1
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Article
PubMed
1.49E+3n/an/an/an/an/an/an/an/a



The University of Kansas

Curated by ChEMBL


Assay Description
Displacement of [3H]DAMGO from human recombinant mu opioid receptor expressed in CHO cells after 2 hrs by liquid scintillation counting


Bioorg Med Chem 20: 3100-10 (2012)


Article DOI: 10.1016/j.bmc.2012.02.040
BindingDB Entry DOI: 10.7270/Q27H1KK0
More data for this
Ligand-Target Pair
Delta-type opioid receptor


(Homo sapiens (Human))
BDBM50381668
PNG
(CHEMBL2022019)
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)C(=O)c1ccccc1 |r|
Show InChI InChI=1S/C26H30O8/c1-14(27)33-18-12-17(23(30)32-4)25(2)11-10-16-24(31)34-19(13-26(16,3)22(25)21(18)29)20(28)15-8-6-5-7-9-15/h5-9,16-19,22H,10-13H2,1-4H3/t16-,17-,18-,19-,22-,25-,26-/m0/s1
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PubMed
>1.00E+4n/an/an/an/an/an/an/an/a



The University of Kansas

Curated by ChEMBL


Assay Description
Displacement of [3H]DADLE from human recombinant delta opioid receptor expressed in CHO cells after 2 hrs by liquid scintillation counting


Bioorg Med Chem 20: 3100-10 (2012)


Article DOI: 10.1016/j.bmc.2012.02.040
BindingDB Entry DOI: 10.7270/Q27H1KK0
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM50381668
PNG
(CHEMBL2022019)
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)C(=O)c1ccccc1 |r|
Show InChI InChI=1S/C26H30O8/c1-14(27)33-18-12-17(23(30)32-4)25(2)11-10-16-24(31)34-19(13-26(16,3)22(25)21(18)29)20(28)15-8-6-5-7-9-15/h5-9,16-19,22H,10-13H2,1-4H3/t16-,17-,18-,19-,22-,25-,26-/m0/s1
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Article
PubMed
n/an/an/an/a 2.28E+3n/an/an/an/a



The University of Kansas

Curated by ChEMBL


Assay Description
Partial agonist activity at human recombinant kappa opioid receptor expressed in CHO cells assessed as [35S]GTP-gamma-S binding after 3 hrs by liquid...


Bioorg Med Chem 20: 3100-10 (2012)


Article DOI: 10.1016/j.bmc.2012.02.040
BindingDB Entry DOI: 10.7270/Q27H1KK0
More data for this
Ligand-Target Pair