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BDBM50395067 CHEMBL2163922

SMILES: N[C@@H](Cc1ccc(O)cc1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C(=C)C(=O)N[C@H](C(=C)C(N)=O)c1ccccc1)c1ccccc1

InChI Key: InChIKey=ZKOITTBBWXMGMR-VZNYXHRGSA-N

Data: 2 KI  2 IC50  1 EC50

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 5 hits for monomerid = 50395067   
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))
BDBM50395067
PNG
(CHEMBL2163922)
Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C(=C)C(=O)N[C@H](C(=C)C(N)=O)c1ccccc1)c1ccccc1 |r|
Show InChI InChI=1S/C34H37N5O5/c1-21(31(36)41)29(24-10-5-3-6-11-24)37-32(42)22(2)30(25-12-7-4-8-13-25)38-33(43)28-14-9-19-39(28)34(44)27(35)20-23-15-17-26(40)18-16-23/h3-8,10-13,15-18,27-30,40H,1-2,9,14,19-20,35H2,(H2,36,41)(H,37,42)(H,38,43)/t27-,28-,29+,30+/m0/s1
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Article
PubMed
16n/an/an/an/an/an/an/an/a



Lanzhou University

Curated by ChEMBL


Assay Description
Displacement of [3H]DAMGO from FLAG-tagged mu opioid receptor expressed in HEK293 cells after 60 mins by liquid scintillation counter


J Med Chem 55: 6224-36 (2012)


Article DOI: 10.1021/jm300664y
BindingDB Entry DOI: 10.7270/Q2T154S8
More data for this
Ligand-Target Pair
Delta-type opioid receptor


(Homo sapiens (Human))
BDBM50395067
PNG
(CHEMBL2163922)
Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C(=C)C(=O)N[C@H](C(=C)C(N)=O)c1ccccc1)c1ccccc1 |r|
Show InChI InChI=1S/C34H37N5O5/c1-21(31(36)41)29(24-10-5-3-6-11-24)37-32(42)22(2)30(25-12-7-4-8-13-25)38-33(43)28-14-9-19-39(28)34(44)27(35)20-23-15-17-26(40)18-16-23/h3-8,10-13,15-18,27-30,40H,1-2,9,14,19-20,35H2,(H2,36,41)(H,37,42)(H,38,43)/t27-,28-,29+,30+/m0/s1
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1.10E+4n/an/an/an/an/an/an/an/a



Lanzhou University

Curated by ChEMBL


Assay Description
Displacement of [3H]DPDPE from Myc-tagged delta opioid receptor expressed in HEK293 cells after 60 mins by liquid scintillation counter


J Med Chem 55: 6224-36 (2012)


Article DOI: 10.1021/jm300664y
BindingDB Entry DOI: 10.7270/Q2T154S8
More data for this
Ligand-Target Pair
Delta-type opioid receptor


(MOUSE)
BDBM50395067
PNG
(CHEMBL2163922)
Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C(=C)C(=O)N[C@H](C(=C)C(N)=O)c1ccccc1)c1ccccc1 |r|
Show InChI InChI=1S/C34H37N5O5/c1-21(31(36)41)29(24-10-5-3-6-11-24)37-32(42)22(2)30(25-12-7-4-8-13-25)38-33(43)28-14-9-19-39(28)34(44)27(35)20-23-15-17-26(40)18-16-23/h3-8,10-13,15-18,27-30,40H,1-2,9,14,19-20,35H2,(H2,36,41)(H,37,42)(H,38,43)/t27-,28-,29+,30+/m0/s1
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Article
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n/an/a 166n/an/an/an/an/an/a



Lanzhou University

Curated by ChEMBL


Assay Description
Agonist activity at delta opioid receptor in Kunming mouse vas deferens assessed as inhibition of electrically-stimulated muscle contraction


J Med Chem 55: 6224-36 (2012)


Article DOI: 10.1021/jm300664y
BindingDB Entry DOI: 10.7270/Q2T154S8
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(GUINEA PIG)
BDBM50395067
PNG
(CHEMBL2163922)
Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C(=C)C(=O)N[C@H](C(=C)C(N)=O)c1ccccc1)c1ccccc1 |r|
Show InChI InChI=1S/C34H37N5O5/c1-21(31(36)41)29(24-10-5-3-6-11-24)37-32(42)22(2)30(25-12-7-4-8-13-25)38-33(43)28-14-9-19-39(28)34(44)27(35)20-23-15-17-26(40)18-16-23/h3-8,10-13,15-18,27-30,40H,1-2,9,14,19-20,35H2,(H2,36,41)(H,37,42)(H,38,43)/t27-,28-,29+,30+/m0/s1
UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 38n/an/an/an/an/an/a



Lanzhou University

Curated by ChEMBL


Assay Description
Agonist activity at mu opioid receptor in guinea pig ileum assessed as inhibition of electrically-stimulated muscle contraction


J Med Chem 55: 6224-36 (2012)


Article DOI: 10.1021/jm300664y
BindingDB Entry DOI: 10.7270/Q2T154S8
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Homo sapiens (Human))
BDBM50395067
PNG
(CHEMBL2163922)
Show SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N1CCC[C@H]1C(=O)N[C@H](C(=C)C(=O)N[C@H](C(=C)C(N)=O)c1ccccc1)c1ccccc1 |r|
Show InChI InChI=1S/C34H37N5O5/c1-21(31(36)41)29(24-10-5-3-6-11-24)37-32(42)22(2)30(25-12-7-4-8-13-25)38-33(43)28-14-9-19-39(28)34(44)27(35)20-23-15-17-26(40)18-16-23/h3-8,10-13,15-18,27-30,40H,1-2,9,14,19-20,35H2,(H2,36,41)(H,37,42)(H,38,43)/t27-,28-,29+,30+/m0/s1
PDB

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PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 45n/an/an/an/a



Lanzhou University

Curated by ChEMBL


Assay Description
Agonist activity at mu opioid receptor expressed in HEK293 cells assessed as inhibition of forskolin-induced cAMP accumulation after 30 mins by liqui...


J Med Chem 55: 6224-36 (2012)


Article DOI: 10.1021/jm300664y
BindingDB Entry DOI: 10.7270/Q2T154S8
More data for this
Ligand-Target Pair