Page last updated: 2024-10-24

interleukin-8 receptor activity

Definition

Target type: molecularfunction

Combining with interleukin-8 and transmitting the signal from one side of the membrane to the other to initiate a change in cell activity. [GOC:jl, GOC:signaling]

Interleukin-8 receptor activity is a molecular function that describes the ability of a protein to bind to interleukin-8 (IL-8), a chemokine that plays a crucial role in inflammation and immune responses. IL-8 receptors, specifically CXCR1 and CXCR2, are G protein-coupled receptors (GPCRs) expressed on the surface of various cells, including neutrophils, T cells, and endothelial cells. Upon binding to IL-8, these receptors initiate a signaling cascade that involves the activation of heterotrimeric G proteins, leading to the production of second messengers like inositol trisphosphate (IP3) and diacylglycerol (DAG). This signaling pathway ultimately results in the recruitment and activation of neutrophils, the primary effector cells in the innate immune response. The recruitment of neutrophils to the site of inflammation is crucial for the clearance of pathogens and damaged tissue. Furthermore, IL-8 receptor activation can also stimulate the release of other pro-inflammatory mediators, such as chemokines and cytokines, further amplifying the inflammatory response. The molecular function of IL-8 receptor activity is therefore essential for orchestrating the inflammatory response, a complex process that involves the coordinated action of various cells and signaling molecules.'
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Proteins (2)

ProteinDefinitionTaxonomy
C-X-C chemokine receptor type 2A C-X-C chemokine receptor type 2 that is encoded in the genome of human. [PRO:WCB, UniProtKB:P25025]Homo sapiens (human)
C-X-C chemokine receptor type 1A C-X-C chemokine receptor type 1 that is encoded in the genome of human. [PRO:WCB, UniProtKB:P25024]Homo sapiens (human)

Compounds (18)

CompoundDefinitionClassesRoles
clotrimazoleconazole antifungal drug;
imidazole antifungal drug;
imidazoles;
monochlorobenzenes
antiinfective agent;
environmental contaminant;
xenobiotic
diclofenacdiclofenac : A monocarboxylic acid consisting of phenylacetic acid having a (2,6-dichlorophenyl)amino group at the 2-position.

Diclofenac: A non-steroidal anti-inflammatory agent (NSAID) with antipyretic and analgesic actions. It is primarily available as the sodium salt.
amino acid;
aromatic amine;
dichlorobenzene;
monocarboxylic acid;
secondary amino compound
antipyretic;
drug allergen;
EC 1.14.99.1 (prostaglandin-endoperoxide synthase) inhibitor;
environmental contaminant;
non-narcotic analgesic;
non-steroidal anti-inflammatory drug;
xenobiotic
disulfiramorganic disulfide;
organosulfur acaricide
angiogenesis inhibitor;
antineoplastic agent;
apoptosis inducer;
EC 1.2.1.3 [aldehyde dehydrogenase (NAD(+))] inhibitor;
EC 3.1.1.1 (carboxylesterase) inhibitor;
EC 3.1.1.8 (cholinesterase) inhibitor;
EC 5.99.1.2 (DNA topoisomerase) inhibitor;
ferroptosis inducer;
fungicide;
NF-kappaB inhibitor
itraconazolepiperazines
dexibuprofendexibuprofen: structure in first sourceibuprofennon-narcotic analgesic;
non-steroidal anti-inflammatory drug
ibuprofen, (r)-isomeribuprofen
ketoprofen
dexketoprofendexketoprofen : A monocarboxylic acid that is (S)-hydratropic acid substituted at position 3 on the phenyl ring by a benzoyl group. A cyclooxygenase inhibitor, it is used to relieve short-term pain, such as muscular pain, dental pain and dysmenorrhoea.benzophenones;
monocarboxylic acid
cyclooxygenase 1 inhibitor;
cyclooxygenase 2 inhibitor;
non-narcotic analgesic;
non-steroidal anti-inflammatory drug
sb 225002nitrophenol
quercetin7-hydroxyflavonol;
pentahydroxyflavone
antibacterial agent;
antineoplastic agent;
antioxidant;
Aurora kinase inhibitor;
chelator;
EC 1.10.99.2 [ribosyldihydronicotinamide dehydrogenase (quinone)] inhibitor;
geroprotector;
phytoestrogen;
plant metabolite;
protein kinase inhibitor;
radical scavenger
reparixinreparixin: inhibits CXCR1 to prevent polymorphonuclear cell recruitmentmonoterpenoid
sb 265610
sch 527123
sb 656933
amd 070mavorixafor: a derivative of AMD3100; a CXCR4 blockeraminoquinoline
azd8309AZD8309: CXCR2 inhibitor
a 803467A 803467: an Nav1.8 sodium channel blocker; structure in first source
gsk1325756danirixin: structure in first source