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HomeProduct name listSB 290157 trifluoroacetate salt

SB 290157 trifluoroacetate salt

Synonym(s):N²-[(2,2-Diphenylethoxy)acetyl]-L-arginine, TFA;N2-[2-(2,2-Diphenylethoxy)acetyl]-L-arginine trifluoroacetate salt;SB 290157 - CAS 1140525-25-2 - Calbiochem;SB 290157 trifluoroacetate salt

  • CAS NO.:1140525-25-2
  • Empirical Formula: C24H29F3N4O6
  • Molecular Weight: 526.51
  • MDL number: MFCD04974198
  • Update Date: 2026-02-02 18:10:39
SB 290157 trifluoroacetate salt Structural

What is SB 290157 trifluoroacetate salt?

The Uses of SB 290157 trifluoroacetate salt

SB 290157 Trifluoroacetate Salt is a selective, high affinity, competitive antagonist of anaphylatoxin C3a receptor.

What are the applications of Application

SB 290157 trifluoroacetate salt is a selective, high affinity, competitive antagonist of anaphylatoxin C3a receptor

General Description

A non-peptide with anti-inflammatory properties that acts as a selective, high affinity, competitive antagonist of the anaphylatoxin C3a receptor (C3aR; IC50 = 200 nM). Does not antagonize C5aR or other chemotactic G-protein coupled receptors. Blocks C3a-induced internalization of C3aR in human neutrophils and C3a-induced Ca2+ mobilization in basophilic leukemia RBL-2H3 cells expressing murine, guinea pig, or human C3aR (IC50 = 7, 12.5, and 27.7 nM, respectively). Also blocks C3a-mediated ATP release from guinea pig platelets (IC50 = 30 nM).

Biological Activity

sb 290157 is a c3ar antagonist.the anaphylatoxin c3a, a potent chemotactic peptide and inflammatory mediator, binds to and activates a g-protein-coupled receptor. molecular cloning of the c3ar has facilitated the identification of the non-peptide c3ar antagonists.

Biochem/physiol Actions

Target IC50: 200 nM against the anaphylatoxin C3a receptor; 7, 12.5, and 27.7 nM, in blocking C3a-induced internalization of C3aR in human neutrophils and C3a-induced Ca2+ mobilization in basophilic leukemia RBL-2H3 cells expressing murine, guinea pig, or human C3aR

in vitro

sb 290157 was a competitive antagonist of 125i-c3a and binding to rat basophilic leukemia (rbl)-2h3 cells expressing the human c3ar , with an ic50 of 200 nm. sb 290157 could also block the c3a-induced c3ar internalization concentration-dependently and c3a-induced ca21 mobilization in rbl-c3ar cells and human neutrophils. sb 290157 was founf to be selective for the c3ar in that it did not antagonize the c5ar or six other chemotactic g protein-coupled receptors. in addition, sb 290157 could also inhibit c3a induced ca21 mobilization of rbl-2h3 cells expressing the mouse and guinea pig c3ars [1].

in vivo

in animal models, sb 290157 was able to inhibit neutrophil recruitment in a guinea pig lps-induced airway neutrophilia model and decrease paw edema in a rat adjuvant-induced arthritis model [1].

Storage

Desiccate at RT

References

[1] r. s. ames, d. lee, j. j. foley, et al. identification of a selective nonpeptide antagonist of the anaphylatoxin c3a receptor that demonstrates antiinflammatory activity in animal models. journal of immunology 166(10), 6341-6348 (2001).

Properties of SB 290157 trifluoroacetate salt

Melting point: >43°C (dec.)
storage temp.  -20°C
solubility  Ethanol (Slightly, Sonicated), Methanol (Slightly), Water (Slightly)
form  powder
color  white to beige
optical activity [α]/D +1.5 to +5°, c = 1.0 in DMSO
Stability: Hygroscopic

Safety information for SB 290157 trifluoroacetate salt

Signal word Warning
Pictogram(s)
ghs
Exclamation Mark
Irritant
GHS07
GHS Hazard Statements H302:Acute toxicity,oral
H315:Skin corrosion/irritation
H319:Serious eye damage/eye irritation
H335:Specific target organ toxicity, single exposure;Respiratory tract irritation
Precautionary Statement Codes P261:Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

Computed Descriptors for SB 290157 trifluoroacetate salt

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