Target
fMet-Leu-Phe receptor
Ligand
BDBM450271
Substrate
n/a
Meas. Tech.
FPR2 and FPR1 Cyclic Adenosine Monophosphate (cAMP) Assays
EC50
26.0±n/a nM
Citation
 Shirude, PSBaligar, VSeshadri, BChattopadhyay, AKWurtz, NRKick, EK Phenylpyrrolidinone formyl peptide 2 receptor agonists US Patent  US10676431 Publication Date 6/9/2020 
Target
Name:
fMet-Leu-Phe receptor
Synonyms:
FPR | FPR1 | FPR1_HUMAN | Formyl peptide Receptor | N-formyl peptide receptor 1 | N-formylpeptide chemoattractant receptor | fMLP receptor | fMet-Leu-Phe receptor | formyl peptide receptor 1
Type:
Enzyme Catalytic Domain
Mol. Mass.:
38456.14
Organism:
Homo sapiens (Human)
Description:
gi_4503779
Residue:
350
Sequence:
METNSSLPTNISGGTPAVSAGYLFLDIITYLVFAVTFVLGVLGNGLVIWVAGFRMTHTVTTISYLNLAVADFCFTSTLPFFMVRKAMGGHWPFGWFLCKFVFTIVDINLFGSVFLIALIALDRCVCVLHPVWTQNHRTVSLAKKVIIGPWVMALLLTLPVIIRVTTVPGKTGTVACTFNFSPWTNDPKERINVAVAMLTVRGIIRFIIGFSAPMSIVAVSYGLIATKIHKQGLIKSSRPLRVLSFVAAAFFLCWSPYQVVALIATVRIRELLQGMYKEIGIAVDVTSALAFFNSCLNPMLYVFMGQDFRERLIHALPASLERALTEDSTQTSDTATNSTLPSAEVELQAK
  
Inhibitor
Name:
BDBM450271
Synonyms:
US10676431, Example 34 | US11117861, Example 34
Type:
Small organic molecule
Emp. Form.:
C25H23ClF2N4O5S
Mol. Mass.:
564.989
SMILES:
COc1c(F)c(ccc1-c1ccccc1NS(C)(=O)=O)N1CC[C@@H](NC(=O)Nc2ccc(Cl)cc2F)C1=O |r|
Structure:
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