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SB 328437

Cat. No. 3650 2 Citations Submit a Review Datasheet / COA / SDS
Pricing Availability   Qty
Description: Potent and selective CCR3 antagonist
Chemical Name: N-(1-Naphthalenylcarbonyl)-4-nitro-L-phenylalanine methyl ester
Purity: ≥99% (HPLC)
Datasheet
Citations (2)
Reviews
Literature (1)
Biological Activity Technical Data Solubility Calculators Datasheets References

Biological Activity for SB 328437

SB 328437 is a potent and selective CCR3 antagonist (IC50 = 4 nM). Displays > 2500-fold selectivity over C5aR, LTD4, CCR7, CXCR1 and CXCR2 receptors. Inhibits eotaxin-, eotaxin-2- and MCP-4-induced Ca2+ mobilization (IC50 values are 38, 35 and 20 nM respectively) and inhibits eotaxin-, eotaxin-2- and MCP-4-induced eosinophil chemotaxis with similar potencies.

Compound Libraries for SB 328437

SB 328437 is also offered as part of the Tocriscreen 2.0 Max. Find out more about compound libraries available from Tocris.

Technical Data for SB 328437

M. Wt 378.38
Formula C21H18N2O5
Storage Store at +4°C
Purity ≥99% (HPLC)
CAS Number 247580-43-4
PubChem ID 10474776
InChI Key VMFGCGRAIBLAFY-IBGZPJMESA-N
Smiles O=C(C2=CC=CC3=C2C=CC=C3)N[C@H](C(OC)=O)CC1=CC=C([N+]([O-])=O)C=C1

The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.

Tocris products are intended for laboratory research use only, unless stated otherwise.

Solubility Data for SB 328437

Solvent Max Conc. mg/mL Max Conc. mM
Solubility
DMSO 37.84 100

Preparing Stock Solutions for SB 328437

The following data is based on the product molecular weight 378.38. Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Select a batch to recalculate based on the batch molecular weight:
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 2.64 mL 13.21 mL 26.43 mL
5 mM 0.53 mL 2.64 mL 5.29 mL
10 mM 0.26 mL 1.32 mL 2.64 mL
50 mM 0.05 mL 0.26 mL 0.53 mL

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Product Datasheets for SB 328437

Certificate of Analysis / Product Datasheet
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Safety Datasheet

References for SB 328437

References are publications that support the biological activity of the product.

White et al (2000) Identification of potent, selective non-peptide CC chemokine receptor-3 antagonist that inhibits eotaxin-, eotaxin-2-, and monocyte chemotactic protein-4-induced eosinophil migration. J.Biol.Chem. 275 36626 PMID: 10969084

Mori et al (2007) Selective suppression of Th2-mediated airway eosinophil infiltration by low-molecular weight CCR3 antagonists. Int.Immunol. 19 913 PMID: 17804691

Abonyo et al (2005) Autoregulation of CCL26 synthesis and secretion in A549 cells: a possible mechanism by which alveolar epithelial cells modulate airway inflammation. Am.J.Physiol.Lung Cell.Mol.Physiol. 289 L478 PMID: 15863444

If you know of a relevant reference for SB 328437, please let us know.

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Keywords: SB 328437, SB 328437 supplier, SB328437, Potent, selective, CCR3, antagonists, chemokine, receptors, Rantes, Chemokine, CC, Receptors, 3650, Tocris Bioscience

2 Citations for SB 328437

Citations are publications that use Tocris products. Selected citations for SB 328437 include:

Christoph et al (2012) Graft-versus-host disease reduces regulatory T-cell migration into the tumour tissue. Immunology 137 80-8 PMID: 22681312

Jing et al (2020) Blocking the autocrine regulatory loop of Gankyrin/STAT3/CCL24/CCR3 impairs the progression and pazopanib resistance of clear cell renal cell carcinoma. Cell Death Dis 11 117 PMID: 32051393

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Literature in this Area

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