BindingDB logo
myBDB logout

null

SMILES: CCC(=O)N(CC1CCCCN1Cc1ccc2[C@@H](CCCc2c1)N[C@H](Cc1ccccc1)C(=O)NCC(=O)N[C@H](C)C(=O)N[C@@H](Cc1ccc(O)cc1)C(O)=O)c1ccccc1

InChI Key: InChIKey=OHXAATBRYBMJJL-HDPIZSEHSA-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 = 50500611   
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


(Rattus norvegicus (rat))
BDBM50500611
PNG
(CHEMBL4299482)
Show SMILES CCC(=O)N(CC1CCCCN1Cc1ccc2[C@@H](CCCc2c1)N[C@H](Cc1ccccc1)C(=O)NCC(=O)N[C@H](C)C(=O)N[C@@H](Cc1ccc(O)cc1)C(O)=O)c1ccccc1 |r|
Show InChI InChI=1S/C49H60N6O7/c1-3-46(58)55(38-16-8-5-9-17-38)32-39-18-10-11-26-54(39)31-36-22-25-41-37(27-36)15-12-19-42(41)52-43(28-34-13-6-4-7-14-34)48(60)50-30-45(57)51-33(2)47(59)53-44(49(61)62)29-35-20-23-40(56)24-21-35/h4-9,13-14,16-17,20-25,27,33,39,42-44,52,56H,3,10-12,15,18-19,26,28-32H2,1-2H3,(H,50,60)(H,51,57)(H,53,59)(H,61,62)/t33-,39?,42-,43-,44+/m1/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
1n/an/an/an/an/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Displacement of [3H]DAMGO from mu-opioid receptor in Sprague-Dawley rat brain membrane after 180 mins by scintillation counting analysis


Bioorg Med Chem Lett 26: 222-7 (2016)


Article DOI: 10.1016/j.bmcl.2015.10.081
BindingDB Entry DOI: 10.7270/Q2W66PSM
More data for this
Ligand-Target Pair
Delta-type opioid receptor


(Homo sapiens (Human))
BDBM50500611
PNG
(CHEMBL4299482)
Show SMILES CCC(=O)N(CC1CCCCN1Cc1ccc2[C@@H](CCCc2c1)N[C@H](Cc1ccccc1)C(=O)NCC(=O)N[C@H](C)C(=O)N[C@@H](Cc1ccc(O)cc1)C(O)=O)c1ccccc1 |r|
Show InChI InChI=1S/C49H60N6O7/c1-3-46(58)55(38-16-8-5-9-17-38)32-39-18-10-11-26-54(39)31-36-22-25-41-37(27-36)15-12-19-42(41)52-43(28-34-13-6-4-7-14-34)48(60)50-30-45(57)51-33(2)47(59)53-44(49(61)62)29-35-20-23-40(56)24-21-35/h4-9,13-14,16-17,20-25,27,33,39,42-44,52,56H,3,10-12,15,18-19,26,28-32H2,1-2H3,(H,50,60)(H,51,57)(H,53,59)(H,61,62)/t33-,39?,42-,43-,44+/m1/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
160n/an/an/an/an/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Displacement of [3H]DPDPE from human delta opioid receptor after 180 mins by scintillation counting analysis


Bioorg Med Chem Lett 26: 222-7 (2016)


Article DOI: 10.1016/j.bmcl.2015.10.081
BindingDB Entry DOI: 10.7270/Q2W66PSM
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Rattus norvegicus (rat))
BDBM50500611
PNG
(CHEMBL4299482)
Show SMILES CCC(=O)N(CC1CCCCN1Cc1ccc2[C@@H](CCCc2c1)N[C@H](Cc1ccccc1)C(=O)NCC(=O)N[C@H](C)C(=O)N[C@@H](Cc1ccc(O)cc1)C(O)=O)c1ccccc1 |r|
Show InChI InChI=1S/C49H60N6O7/c1-3-46(58)55(38-16-8-5-9-17-38)32-39-18-10-11-26-54(39)31-36-22-25-41-37(27-36)15-12-19-42(41)52-43(28-34-13-6-4-7-14-34)48(60)50-30-45(57)51-33(2)47(59)53-44(49(61)62)29-35-20-23-40(56)24-21-35/h4-9,13-14,16-17,20-25,27,33,39,42-44,52,56H,3,10-12,15,18-19,26,28-32H2,1-2H3,(H,50,60)(H,51,57)(H,53,59)(H,61,62)/t33-,39?,42-,43-,44+/m1/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 2n/an/an/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Displacement of [3H]DAMGO from mu-opioid receptor in Sprague-Dawley rat brain membrane after 180 mins by scintillation counting analysis


Bioorg Med Chem Lett 26: 222-7 (2016)


Article DOI: 10.1016/j.bmcl.2015.10.081
BindingDB Entry DOI: 10.7270/Q2W66PSM
More data for this
Ligand-Target Pair
Delta-type opioid receptor


(MOUSE)
BDBM50500611
PNG
(CHEMBL4299482)
Show SMILES CCC(=O)N(CC1CCCCN1Cc1ccc2[C@@H](CCCc2c1)N[C@H](Cc1ccccc1)C(=O)NCC(=O)N[C@H](C)C(=O)N[C@@H](Cc1ccc(O)cc1)C(O)=O)c1ccccc1 |r|
Show InChI InChI=1S/C49H60N6O7/c1-3-46(58)55(38-16-8-5-9-17-38)32-39-18-10-11-26-54(39)31-36-22-25-41-37(27-36)15-12-19-42(41)52-43(28-34-13-6-4-7-14-34)48(60)50-30-45(57)51-33(2)47(59)53-44(49(61)62)29-35-20-23-40(56)24-21-35/h4-9,13-14,16-17,20-25,27,33,39,42-44,52,56H,3,10-12,15,18-19,26,28-32H2,1-2H3,(H,50,60)(H,51,57)(H,53,59)(H,61,62)/t33-,39?,42-,43-,44+/m1/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 540n/an/an/an/an/an/a



University of Arizona

Curated by ChEMBL


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


Bioorg Med Chem Lett 26: 222-7 (2016)


Article DOI: 10.1016/j.bmcl.2015.10.081
BindingDB Entry DOI: 10.7270/Q2W66PSM
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(GUINEA PIG)
BDBM50500611
PNG
(CHEMBL4299482)
Show SMILES CCC(=O)N(CC1CCCCN1Cc1ccc2[C@@H](CCCc2c1)N[C@H](Cc1ccccc1)C(=O)NCC(=O)N[C@H](C)C(=O)N[C@@H](Cc1ccc(O)cc1)C(O)=O)c1ccccc1 |r|
Show InChI InChI=1S/C49H60N6O7/c1-3-46(58)55(38-16-8-5-9-17-38)32-39-18-10-11-26-54(39)31-36-22-25-41-37(27-36)15-12-19-42(41)52-43(28-34-13-6-4-7-14-34)48(60)50-30-45(57)51-33(2)47(59)53-44(49(61)62)29-35-20-23-40(56)24-21-35/h4-9,13-14,16-17,20-25,27,33,39,42-44,52,56H,3,10-12,15,18-19,26,28-32H2,1-2H3,(H,50,60)(H,51,57)(H,53,59)(H,61,62)/t33-,39?,42-,43-,44+/m1/s1
UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 95n/an/an/an/an/an/a



University of Arizona

Curated by ChEMBL


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


Bioorg Med Chem Lett 26: 222-7 (2016)


Article DOI: 10.1016/j.bmcl.2015.10.081
BindingDB Entry DOI: 10.7270/Q2W66PSM
More data for this
Ligand-Target Pair
Delta-type opioid receptor


(Homo sapiens (Human))
BDBM50500611
PNG
(CHEMBL4299482)
Show SMILES CCC(=O)N(CC1CCCCN1Cc1ccc2[C@@H](CCCc2c1)N[C@H](Cc1ccccc1)C(=O)NCC(=O)N[C@H](C)C(=O)N[C@@H](Cc1ccc(O)cc1)C(O)=O)c1ccccc1 |r|
Show InChI InChI=1S/C49H60N6O7/c1-3-46(58)55(38-16-8-5-9-17-38)32-39-18-10-11-26-54(39)31-36-22-25-41-37(27-36)15-12-19-42(41)52-43(28-34-13-6-4-7-14-34)48(60)50-30-45(57)51-33(2)47(59)53-44(49(61)62)29-35-20-23-40(56)24-21-35/h4-9,13-14,16-17,20-25,27,33,39,42-44,52,56H,3,10-12,15,18-19,26,28-32H2,1-2H3,(H,50,60)(H,51,57)(H,53,59)(H,61,62)/t33-,39?,42-,43-,44+/m1/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 339n/an/an/an/an/an/a



University of Arizona

Curated by ChEMBL


Assay Description
Displacement of [3H]DPDPE from human delta opioid receptor after 180 mins by scintillation counting analysis


Bioorg Med Chem Lett 26: 222-7 (2016)


Article DOI: 10.1016/j.bmcl.2015.10.081
BindingDB Entry DOI: 10.7270/Q2W66PSM
More data for this
Ligand-Target Pair