General
Preferred name
TC-FPR 43
Synonyms
pyrazolone, 1 ()
FPR Agonist 43 ()
P&D ID
PD038314
CAS
903895-98-7
Tags
available
drug candidate
Drug indication
Discovery agent
Structure
Probe scores
P&D probe-likeness score
[[ v.score ]]%
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
Description
(extracted from source data)
DESCRIPTION Potent FPR2 agonist (Tocriscreen Plus)
DESCRIPTION Potent non-peptide oxytocin receptor partial agonist; also V1a receptor antagonist (Tocris Bioactive Compound Library)
DESCRIPTION TC-FPR 43 is a potent formyl peptide receptor 2 (FPR2) agonist (EC50 = 44 nM) that inhibits fMLP- and IL-8-induced neutrophil migration and induces calcium mobilization. TC-FPR 43 was shown to suppress inflammation in a mouse model of acute inflammation. It also acts as an ALX agonist. (BOC Sciences Bioactive Compounds)
Cell lines
1
Organisms
0
Compound Sets
12
BOC Sciences Bioactive Compounds
Cayman Chemical Bioactives
CZ-OPENSCREEN Bioactive Library
Drug Repurposing Hub
DrugMAP
EU-OPENSCREEN Bioactive Compound Library
EUbOPEN Chemogenomics Library
Guide to Pharmacology
MedChem Express Bioactive Compound Library
Novartis Chemogenetic Library (NIBR MoA Box)
Tocris Bioactive Compound Library
Tocriscreen Plus
External IDs
16
Properties
(calculated by RDKit )
Molecular Weight
384.14
Hydrogen Bond Acceptors
4
Hydrogen Bond Donors
2
Rotatable Bonds
4
Ring Count
3
Aromatic Ring Count
3
cLogP
4.6
TPSA
68.06
Fraction CSP3
0.2
Chiral centers
0.0
Largest ring
6.0
QED
0.69
Structural alerts
0
No structural alerts detected
Custom attributes
(extracted from source data)
Target Type
7-TM Receptors
Primary Target
Formyl Peptide Receptors
MOA
Agonist
FPR1 agonist
FPR2 agonist
formyl peptide receptor agonist
Member status
member
Target
FPR2
formyl peptide receptor (FPR)
Pathway
GPCR/G protein
Recommended Cell Concentration
None
Source data