BindingDB logo
myBDB logout

null

SMILES: CN(C)[C@@H](Cc1c(C)cc(O)cc1C)C(=O)N1Cc2ccccc2C[C@H]1C(=O)OC1=C2O[C@H]3[C@@H](O)C=C[C@H]4[C@H]5CC(C=C1)C2[C@@]34CCN5C

InChI Key: InChIKey=XCSVQYRKBHKRNV-VTSRCMDQSA-N

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 6 hits for monomerid = 50378890   
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
Mu-type opioid receptor


(Homo sapiens (Human))
BDBM50378890
PNG
(CHEMBL1743604)
Show SMILES CN(C)[C@@H](Cc1c(C)cc(O)cc1C)C(=O)N1Cc2ccccc2C[C@H]1C(=O)OC1=C2O[C@H]3[C@@H](O)C=C[C@H]4[C@H]5CC(C=C1)C2[C@@]34CCN5C |r,c:32,38,44,TLB:48:47:37:39.40.43|
Show InChI InChI=1S/C40H47N3O6/c1-22-16-27(44)17-23(2)28(22)20-31(41(3)4)38(46)43-21-26-9-7-6-8-24(26)18-32(43)39(47)48-34-13-10-25-19-30-29-11-12-33(45)37-40(29,14-15-42(30)5)35(25)36(34)49-37/h6-13,16-17,25,29-33,35,37,44-45H,14-15,18-21H2,1-5H3/t25?,29-,30+,31-,32-,33-,35?,37-,40-/m0/s1
PDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
1.10n/an/an/an/an/an/an/an/a



University of Cagliari

Curated by ChEMBL


Assay Description
Displacement of [3H]DAMGO from human mu opioid receptor expressed in CHO cells after 60 mins by scintillation counting


Eur J Med Chem 46: 799-803 (2011)


Article DOI: 10.1016/j.ejmech.2010.12.001
BindingDB Entry DOI: 10.7270/Q2CF9R3C
More data for this
Ligand-Target Pair
Delta-type opioid receptor


(Homo sapiens (Human))
BDBM50378890
PNG
(CHEMBL1743604)
Show SMILES CN(C)[C@@H](Cc1c(C)cc(O)cc1C)C(=O)N1Cc2ccccc2C[C@H]1C(=O)OC1=C2O[C@H]3[C@@H](O)C=C[C@H]4[C@H]5CC(C=C1)C2[C@@]34CCN5C |r,c:32,38,44,TLB:48:47:37:39.40.43|
Show InChI InChI=1S/C40H47N3O6/c1-22-16-27(44)17-23(2)28(22)20-31(41(3)4)38(46)43-21-26-9-7-6-8-24(26)18-32(43)39(47)48-34-13-10-25-19-30-29-11-12-33(45)37-40(29,14-15-42(30)5)35(25)36(34)49-37/h6-13,16-17,25,29-33,35,37,44-45H,14-15,18-21H2,1-5H3/t25?,29-,30+,31-,32-,33-,35?,37-,40-/m0/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
1.60n/an/an/an/an/an/an/an/a



University of Cagliari

Curated by ChEMBL


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


Eur J Med Chem 46: 799-803 (2011)


Article DOI: 10.1016/j.ejmech.2010.12.001
BindingDB Entry DOI: 10.7270/Q2CF9R3C
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM50378890
PNG
(CHEMBL1743604)
Show SMILES CN(C)[C@@H](Cc1c(C)cc(O)cc1C)C(=O)N1Cc2ccccc2C[C@H]1C(=O)OC1=C2O[C@H]3[C@@H](O)C=C[C@H]4[C@H]5CC(C=C1)C2[C@@]34CCN5C |r,c:32,38,44,TLB:48:47:37:39.40.43|
Show InChI InChI=1S/C40H47N3O6/c1-22-16-27(44)17-23(2)28(22)20-31(41(3)4)38(46)43-21-26-9-7-6-8-24(26)18-32(43)39(47)48-34-13-10-25-19-30-29-11-12-33(45)37-40(29,14-15-42(30)5)35(25)36(34)49-37/h6-13,16-17,25,29-33,35,37,44-45H,14-15,18-21H2,1-5H3/t25?,29-,30+,31-,32-,33-,35?,37-,40-/m0/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
12n/an/an/an/an/an/an/an/a



University of Cagliari

Curated by ChEMBL


Assay Description
Displacement of [3H]U69593 from human kappa opioid receptor expressed in CHO cells after 60 mins by scintillation counting


Eur J Med Chem 46: 799-803 (2011)


Article DOI: 10.1016/j.ejmech.2010.12.001
BindingDB Entry DOI: 10.7270/Q2CF9R3C
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Homo sapiens (Human))
BDBM50378890
PNG
(CHEMBL1743604)
Show SMILES CN(C)[C@@H](Cc1c(C)cc(O)cc1C)C(=O)N1Cc2ccccc2C[C@H]1C(=O)OC1=C2O[C@H]3[C@@H](O)C=C[C@H]4[C@H]5CC(C=C1)C2[C@@]34CCN5C |r,c:32,38,44,TLB:48:47:37:39.40.43|
Show InChI InChI=1S/C40H47N3O6/c1-22-16-27(44)17-23(2)28(22)20-31(41(3)4)38(46)43-21-26-9-7-6-8-24(26)18-32(43)39(47)48-34-13-10-25-19-30-29-11-12-33(45)37-40(29,14-15-42(30)5)35(25)36(34)49-37/h6-13,16-17,25,29-33,35,37,44-45H,14-15,18-21H2,1-5H3/t25?,29-,30+,31-,32-,33-,35?,37-,40-/m0/s1
PDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 13n/an/an/an/an/an/a



University of Cagliari

Curated by ChEMBL


Assay Description
Agonist activity at human mu opioid receptor expressed in CHO cells by [35S]GTPgammaS binding assay


Eur J Med Chem 46: 799-803 (2011)


Article DOI: 10.1016/j.ejmech.2010.12.001
BindingDB Entry DOI: 10.7270/Q2CF9R3C
More data for this
Ligand-Target Pair
Delta-type opioid receptor


(Homo sapiens (Human))
BDBM50378890
PNG
(CHEMBL1743604)
Show SMILES CN(C)[C@@H](Cc1c(C)cc(O)cc1C)C(=O)N1Cc2ccccc2C[C@H]1C(=O)OC1=C2O[C@H]3[C@@H](O)C=C[C@H]4[C@H]5CC(C=C1)C2[C@@]34CCN5C |r,c:32,38,44,TLB:48:47:37:39.40.43|
Show InChI InChI=1S/C40H47N3O6/c1-22-16-27(44)17-23(2)28(22)20-31(41(3)4)38(46)43-21-26-9-7-6-8-24(26)18-32(43)39(47)48-34-13-10-25-19-30-29-11-12-33(45)37-40(29,14-15-42(30)5)35(25)36(34)49-37/h6-13,16-17,25,29-33,35,37,44-45H,14-15,18-21H2,1-5H3/t25?,29-,30+,31-,32-,33-,35?,37-,40-/m0/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 1.70n/an/an/an/an/an/a



University of Cagliari

Curated by ChEMBL


Assay Description
Antagonist activity at human delta opioid receptor expressed in CHO cells assessed as inhibition of U50488-induced [35S]GTPgammaS binding


Eur J Med Chem 46: 799-803 (2011)


Article DOI: 10.1016/j.ejmech.2010.12.001
BindingDB Entry DOI: 10.7270/Q2CF9R3C
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Homo sapiens (Human))
BDBM50378890
PNG
(CHEMBL1743604)
Show SMILES CN(C)[C@@H](Cc1c(C)cc(O)cc1C)C(=O)N1Cc2ccccc2C[C@H]1C(=O)OC1=C2O[C@H]3[C@@H](O)C=C[C@H]4[C@H]5CC(C=C1)C2[C@@]34CCN5C |r,c:32,38,44,TLB:48:47:37:39.40.43|
Show InChI InChI=1S/C40H47N3O6/c1-22-16-27(44)17-23(2)28(22)20-31(41(3)4)38(46)43-21-26-9-7-6-8-24(26)18-32(43)39(47)48-34-13-10-25-19-30-29-11-12-33(45)37-40(29,14-15-42(30)5)35(25)36(34)49-37/h6-13,16-17,25,29-33,35,37,44-45H,14-15,18-21H2,1-5H3/t25?,29-,30+,31-,32-,33-,35?,37-,40-/m0/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

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

Similars

Article
PubMed
n/an/a 3.10E+3n/an/an/an/an/an/a



University of Cagliari

Curated by ChEMBL


Assay Description
Antagonist activity at human kappa opioid receptor expressed in CHO cells assessed as inhibition of SNC80-induced [35S]GTPgammaS binding


Eur J Med Chem 46: 799-803 (2011)


Article DOI: 10.1016/j.ejmech.2010.12.001
BindingDB Entry DOI: 10.7270/Q2CF9R3C
More data for this
Ligand-Target Pair