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SMILES: CC(=O)N[C@H](Cc1ccc2ccccc2c1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@H](Cc1ccc2ccccc2c1)C(=O)N[C@@H](CCCNC(N)=N)C(N)=O

InChI Key:

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 = 50574242   
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
Melanocortin receptor 3


(Mus musculus)
BDBM50574242
PNG
(CHEMBL4859395)
Show SMILES CC(=O)N[C@H](Cc1ccc2ccccc2c1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@H](Cc1ccc2ccccc2c1)C(=O)N[C@@H](CCCNC(N)=N)C(N)=O |r|
PDB

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UniProtKB/SwissProt

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UniChem
Article
PubMed
5n/an/an/an/an/an/an/an/a


TBA

Assay Description
Antagonist activity at mouse melanocortin receptor 4 expressed in HEK293 cells assessed as inhibition of NDP-MSH-induced cAMP accumulation incubated ...


Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c01417
BindingDB Entry DOI: 10.7270/Q2RR231G
More data for this
Ligand-Target Pair
Melanocortin receptor 3


(Mus musculus)
BDBM50574242
PNG
(CHEMBL4859395)
Show SMILES CC(=O)N[C@H](Cc1ccc2ccccc2c1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@H](Cc1ccc2ccccc2c1)C(=O)N[C@@H](CCCNC(N)=N)C(N)=O |r|
PDB

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UniProtKB/SwissProt

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PC cid
PC sid
UniChem
Article
PubMed
790n/an/an/an/an/an/an/an/a


TBA

Assay Description
Antagonist activity at mouse melanocortin receptor 3 expressed in HEK293 cells assessed as inhibition of NDP-MSH-induced cAMP accumulation incubated ...


Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c01417
BindingDB Entry DOI: 10.7270/Q2RR231G
More data for this
Ligand-Target Pair
Melanocortin receptor 4


(Mus musculus)
BDBM50574242
PNG
(CHEMBL4859395)
Show SMILES CC(=O)N[C@H](Cc1ccc2ccccc2c1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@H](Cc1ccc2ccccc2c1)C(=O)N[C@@H](CCCNC(N)=N)C(N)=O |r|
PDB

KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/an/a>1.00E+5n/an/an/an/a


TBA

Assay Description
Agonist activity at mouse MC4R expressed in HEK293 cells assessed as induction of cAMP level incubated for 2 hr by alphaScreen assay


Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c01417
BindingDB Entry DOI: 10.7270/Q2RR231G
More data for this
Ligand-Target Pair
Melanocortin receptor 3


(Mus musculus)
BDBM50574242
PNG
(CHEMBL4859395)
Show SMILES CC(=O)N[C@H](Cc1ccc2ccccc2c1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@H](Cc1ccc2ccccc2c1)C(=O)N[C@@H](CCCNC(N)=N)C(N)=O |r|
PDB

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UniProtKB/SwissProt

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PC cid
PC sid
UniChem
Article
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n/an/an/an/a>1.00E+5n/an/an/an/a


TBA

Assay Description
Agonist activity at mouse MC3R expressed in HEK293 cells assessed as induction of cAMP level incubated for 2 hr by alphaScreen assay


Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c01417
BindingDB Entry DOI: 10.7270/Q2RR231G
More data for this
Ligand-Target Pair
Melanocyte-stimulating hormone receptor


(Mus musculus)
BDBM50574242
PNG
(CHEMBL4859395)
Show SMILES CC(=O)N[C@H](Cc1ccc2ccccc2c1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@H](Cc1ccc2ccccc2c1)C(=O)N[C@@H](CCCNC(N)=N)C(N)=O |r|
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/an/a 1.00E+3n/an/an/an/a


TBA

Assay Description
Partial agonist activity at mouse MC1R expressed in HEK293 cells assessed as induction of cAMP level incubated for 2 hr by alphaScreen assay


Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c01417
BindingDB Entry DOI: 10.7270/Q2RR231G
More data for this
Ligand-Target Pair
Melanocortin receptor 5


(Mus musculus (Mouse))
BDBM50574242
PNG
(CHEMBL4859395)
Show SMILES CC(=O)N[C@H](Cc1ccc2ccccc2c1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@H](Cc1ccc2ccccc2c1)C(=O)N[C@@H](CCCNC(N)=N)C(N)=O |r|
UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/an/an/a>1.00E+5n/an/an/an/a


TBA

Assay Description
Agonist activity at mouse MC5R expressed in HEK293 cells assessed as induction of cAMP level at 100 uM incubated for 2 hr by alphaScreen assay


Citation and Details

Article DOI: 10.1021/acs.jmedchem.1c01417
BindingDB Entry DOI: 10.7270/Q2RR231G
More data for this
Ligand-Target Pair