Date published: 2026-5-4

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IL-8RB Inhibitors

IL-8RB inhibitors belong to a distinctive chemical class of compounds that target the Interleukin-8 Receptor Type B (IL-8RB), a transmembrane receptor belonging to the G protein-coupled receptor (GPCR) family. These inhibitors are designed to modulate the signaling pathways associated with IL-8RB, which plays a crucial role in mediating the effects of Interleukin-8 (IL-8), a pro-inflammatory chemokine. IL-8RB, also known as CXCR2, is predominantly expressed on the surfaces of various immune cells, including neutrophils, macrophages, and dendritic cells. The chemical structures of IL-8RB inhibitors are characterized by their diverse arrangements of aromatic and heterocyclic moieties, enabling them to interact with specific binding sites on the receptor's extracellular domain. Through competitive or allosteric interactions, these inhibitors can disrupt the binding of IL-8 to IL-8RB, thereby modulating downstream signaling cascades and attenuating immune responses. Computational and structural studies have shed light on the complex interactions between IL-8RB inhibitors and the receptor's binding pocket, elucidating the intricate network of hydrogen bonding, van der Waals interactions, and electrostatic forces that govern their binding affinity. IL-8RB inhibitors show promise as tools for unraveling the intricate pathways involved in immune response modulation. By selectively blocking IL-8RB-mediated signaling, these inhibitors provide researchers with an opportunity to dissect the roles of IL-8 in inflammation, immune cell recruitment, and various disease conditions. As researchers continue to refine their understanding of the molecular mechanisms underlying IL-8RB inhibition, novel compounds with enhanced selectivity and potency are being developed.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

SB 225002

182498-32-4sc-202803
sc-202803A
1 mg
5 mg
$36.00
$102.00
2
(1)

SB 225002 functions as a selective IL-8 receptor antagonist, exhibiting unique binding affinity that alters receptor conformation. This compound disrupts the typical ligand-receptor interaction, effectively blocking downstream signaling pathways associated with inflammation. Its kinetic behavior showcases a slow association rate, promoting sustained receptor occupancy. The molecular structure of SB 225002 enhances its specificity, allowing for targeted modulation of chemotactic responses in immune cells.

SB 265610

211096-49-0sc-361341
sc-361341A
1 mg
10 mg
$81.00
$209.00
(0)

SB 265610 acts as a potent IL-8 receptor blocker, characterized by its ability to stabilize the inactive form of the receptor. This compound exhibits a unique interaction profile, favoring specific hydrogen bonding and hydrophobic contacts that enhance its binding efficacy. Its reaction kinetics reveal a rapid dissociation rate, allowing for dynamic modulation of receptor activity. The structural features of SB 265610 facilitate selective engagement, influencing cellular migration and inflammatory responses.

Reparixin

266359-83-5sc-507446
5 mg
$78.00
(0)

A small-molecule inhibitor targeting CXCR1 and CXCR2 receptors, explored for its anti-inflammatory and anti-metastatic properties.

AZD 5069

878385-84-3sc-507447
5 mg
$230.00
(0)

An active CXCR2 antagonist under investigation for affecting conditions like chronic obstructive pulmonary disease (COPD).

BX 471

217645-70-0sc-507448
5 mg
$240.00
(0)

A CXCR2 antagonist studied in research models to inhibit neutrophil recruitment in inflammation.

MSX-122

897657-95-3sc-507328
50 mg
$690.00
(0)

A CXCR2 antagonist studied for its potential in reducing inflammation in conditions like acute lung injury.