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SMILES: Cc1ccc(NC(=O)N[C@@H]2CCCN(C2=O)c2ccc(cc2)-c2ccccc2C(N)=O)c(C)c1

InChI Key: InChIKey=PZTCWIODTRRXCQ-XMMPIXPASA-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 4 hits for monomerid = 454199   
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
N-formyl peptide receptor 2


(Homo sapiens (Human))
BDBM454199
PNG
(US10717708, Example 175 | US11186544, Example 175)
Show SMILES Cc1ccc(NC(=O)N[C@@H]2CCCN(C2=O)c2ccc(cc2)-c2ccccc2C(N)=O)c(C)c1 |r|
Show InChI InChI=1S/C27H28N4O3/c1-17-9-14-23(18(2)16-17)29-27(34)30-24-8-5-15-31(26(24)33)20-12-10-19(11-13-20)21-6-3-4-7-22(21)25(28)32/h3-4,6-7,9-14,16,24H,5,8,15H2,1-2H3,(H2,28,32)(H2,29,30,34)/t24-/m1/s1
PDB

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PC cid
PC sid
UniChem
US Patent
n/an/an/an/a 520n/an/an/an/a



Bristol-Myers Squibb Company

US Patent


Assay Description
FPR2 and FPR1 Cyclic Adenosine Monophosphate (cAMP) Assays. A mixture of forskolin (5 μM final for FPR2 or 10 μM final for FPR1) and IBMX (...


US Patent US10717708 (2020)

More data for this
Ligand-Target Pair
fMet-Leu-Phe receptor


(Homo sapiens (Human))
BDBM454199
PNG
(US10717708, Example 175 | US11186544, Example 175)
Show SMILES Cc1ccc(NC(=O)N[C@@H]2CCCN(C2=O)c2ccc(cc2)-c2ccccc2C(N)=O)c(C)c1 |r|
Show InChI InChI=1S/C27H28N4O3/c1-17-9-14-23(18(2)16-17)29-27(34)30-24-8-5-15-31(26(24)33)20-12-10-19(11-13-20)21-6-3-4-7-22(21)25(28)32/h3-4,6-7,9-14,16,24H,5,8,15H2,1-2H3,(H2,28,32)(H2,29,30,34)/t24-/m1/s1
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PC sid
UniChem
n/an/an/an/a 2.60E+3n/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
N-formyl peptide receptor 2


(Homo sapiens (Human))
BDBM454199
PNG
(US10717708, Example 175 | US11186544, Example 175)
Show SMILES Cc1ccc(NC(=O)N[C@@H]2CCCN(C2=O)c2ccc(cc2)-c2ccccc2C(N)=O)c(C)c1 |r|
Show InChI InChI=1S/C27H28N4O3/c1-17-9-14-23(18(2)16-17)29-27(34)30-24-8-5-15-31(26(24)33)20-12-10-19(11-13-20)21-6-3-4-7-22(21)25(28)32/h3-4,6-7,9-14,16,24H,5,8,15H2,1-2H3,(H2,28,32)(H2,29,30,34)/t24-/m1/s1
PDB

NCI pathway
Reactome pathway
KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
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PC cid
PC sid
UniChem
n/an/an/an/a 520n/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
fMet-Leu-Phe receptor


(Homo sapiens (Human))
BDBM454199
PNG
(US10717708, Example 175 | US11186544, Example 175)
Show SMILES Cc1ccc(NC(=O)N[C@@H]2CCCN(C2=O)c2ccc(cc2)-c2ccccc2C(N)=O)c(C)c1 |r|
Show InChI InChI=1S/C27H28N4O3/c1-17-9-14-23(18(2)16-17)29-27(34)30-24-8-5-15-31(26(24)33)20-12-10-19(11-13-20)21-6-3-4-7-22(21)25(28)32/h3-4,6-7,9-14,16,24H,5,8,15H2,1-2H3,(H2,28,32)(H2,29,30,34)/t24-/m1/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/an/an/a 2.60E+3n/an/an/an/a



Bristol-Myers Squibb Company

US Patent


Assay Description
FPR2 and FPR1 Cyclic Adenosine Monophosphate (cAMP) Assays. A mixture of forskolin (5 μM final for FPR2 or 10 μM final for FPR1) and IBMX (...


US Patent US10717708 (2020)

More data for this
Ligand-Target Pair