FPR Agonist 43

CAS No. 903895-98-7

FPR Agonist 43( —— )

Catalog No. M33510 CAS No. 903895-98-7

FPR Agonist 43 is a dual agonist of formyl peptide receptor 1 and formyl peptide receptor 2 (FPR2)/ALX.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 97 Get Quote
5MG 147 Get Quote
10MG 227 Get Quote
25MG 434 Get Quote
50MG 638 Get Quote
100MG 889 Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    FPR Agonist 43
  • Note
    Research use only, not for human use.
  • Brief Description
    FPR Agonist 43 is a dual agonist of formyl peptide receptor 1 and formyl peptide receptor 2 (FPR2)/ALX.
  • Description
    FPR Agonist 43 (compound 43) is a dual formyl peptide receptor 1 (FPR1) and formyl peptide receptor 2 (FPR2)/ALX agonist.
  • In Vitro
    FPR Agonist 43 (10-5-107 nM) is actively potent in the cAMP assay in FPR2/ALX over-expressing CHO cells. FPR Agonist 43 is also active in the GTPγ binding assay (IC50=207±51 nM).FPR1 is the preferred receptor for FPR Agonist 43 in in both human neutrophils and possibly also in mouse cells.Cell Viability Assay Cell Line:Chinese hamster ovary (CHO) over-expressing human FPR2/ALX receptors Concentration:10-5, 10-3, 0.1, 10, 1000, 105, 107 nM Incubation Time:Result:Actively potent in the cAMP assay in FPR2/ALX over-expressing CHO cells (IC50 =11.6±1.9 nM).
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    903895-98-7
  • Formula Weight
    384.86
  • Molecular Formula
    C20H21ClN4O2
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 37.5 mg/mL (97.44 mM; Ultrasonic )H2O : < 0.1 mg/mL (insoluble)
  • SMILES
    CC(C)c1c(NC(=O)Nc2ccc(Cl)cc2)c(=O)n(-c2ccccc2)n1C
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Planagumà A, et al. Lack of activity of 15-epi-lipoxin A? on FPR2/ALX and CysLT1 receptors in interleukin-8-driven human neutrophil function. Clin Exp Immunol. 2013 Aug;173(2):298-309.?
molnova catalog
related products
  • Valeramide

    Valeramide is an amide compound isolated from the roots of Ottonia anisum Spreng.

  • Pedalitin

    Pedalitin is a mixed-type inhibitor of tyrosinase. In the assay of α-glucosidase inhibition, rosmarinic acid is a competitive inhibitor, whereas both methyl rosmarinate and Pedalitin are mixed-type inhibitors.

  • Protocatechuic acid ...

    The herbs of Gastrodia elata BL.