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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Protein | Definition | Taxonomy |
---|---|---|
C-X-C chemokine receptor type 2 | A 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 1 | A C-X-C chemokine receptor type 1 that is encoded in the genome of human. [PRO:WCB, UniProtKB:P25024] | Homo sapiens (human) |
Compound | Definition | Classes | Roles |
---|---|---|---|
clotrimazole | conazole antifungal drug; imidazole antifungal drug; imidazoles; monochlorobenzenes | antiinfective agent; environmental contaminant; xenobiotic | |
diclofenac | diclofenac : 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 |
disulfiram | organic 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 | |
itraconazole | piperazines | ||
dexibuprofen | dexibuprofen: structure in first source | ibuprofen | non-narcotic analgesic; non-steroidal anti-inflammatory drug |
ibuprofen, (r)-isomer | ibuprofen | ||
ketoprofen | |||
dexketoprofen | dexketoprofen : 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 225002 | nitrophenol | ||
quercetin | 7-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 | |
reparixin | reparixin: inhibits CXCR1 to prevent polymorphonuclear cell recruitment | monoterpenoid | |
sb 265610 | |||
sch 527123 | |||
sb 656933 | |||
amd 070 | mavorixafor: a derivative of AMD3100; a CXCR4 blocker | aminoquinoline | |
azd8309 | AZD8309: CXCR2 inhibitor | ||
a 803467 | A 803467: an Nav1.8 sodium channel blocker; structure in first source | ||
gsk1325756 | danirixin: structure in first source |