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GPCR/G protein

GPCRs (G-protein coupled receptors) are a major subcategory of signaling pathways that play a crucial role in transmitting signals from outside the cell to within. These receptors are involved in a wide range of physiological processes including sensory perception, neurotransmission, hormonal regulation, and immune responses.

When a ligand binds to a GPCR, it causes a conformational change in the receptor that activates an associated G-protein. The activated G-protein then triggers a cascade of intracellular signaling events that ultimately lead to a specific cellular response.

GPCRs are a diverse family of proteins that can be classified into different subtypes based on their structure and function. Some examples of GPCR subtypes include rhodopsin-like, secretin-like, and metabotropic glutamate receptors.

Dysregulation of GPCR signaling pathways has been implicated in a variety of diseases, including cancer, cardiovascular disorders, and neurological conditions. Therefore, understanding the mechanisms underlying GPCR/G protein signaling is essential for the development of novel therapeutics targeted at these pathways.

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CRF (6-33), B5148, C141H231N41O43S, Corticotropin-releasing factor binding protein (CRFBP) inhibitor peptide
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Urocortin (rat), B5146, C206H338N62O64, Endogenous CRF agonist
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Urocortin (human), B5145, C204H337N63O64, Endogenous CRF agonist
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[(pF)Phe4]Nociceptin(1-13)NH2, B5131, C61H95F5N22O15, nociceptin/orphanin FQ receptor (OP4) agonist peptide
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[Arg14,Lys15]Nociceptin, B5136, C82H137N31O22, Highly potent and selective NOP receptor agonist
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UFP-101, B5128, C82H138N32O21, selective and competitive silent antagonist for the NOP opioid receptor
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Proglumide sodium salt, B5121, C18H25N2NaO4, Non-selective cholecystokinin (CCK) antagonist
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tcY-NH2, B5123, C40H49N7O7, Selective PAR4 antagonist peptide
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LY 288513, B5125, C22H18BrN3O2, Selective CCK2 receptor antagonist
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Ghrelin (rat), B5120, C147H245N45O42, Endogenous agonist peptide for the ghrelin receptor (GHS-R1a)

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