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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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[Leu31,Pro34]-Neuropeptide Y (porcine), B5065, C190H286N54O56, High affinity neuropeptide Y Y1 receptor agonist
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CGRP (rat) TFA, B5061, C164H263F3N50O54S2, Endogenous neuropeptide, potent vasodilator
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Pancreatic Polypeptide (human), B5060, C185H287N53O54S2, Endogenous high affinity agonist for human NPY Y4 receptor
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Bombesin, B5057, C71H110N24O18S, Neuropeptide with many biological effects
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CCK Octapeptide, non-sulfated, B5058, C49H62N10O13S2, Non-sulfated form of the C-terminal octapeptide of CCK
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Nocistatin (bovine), B5052, C82H135N21O32, endogenous peptide used to block nociceptin-induced allodynia and hyperalgesia
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NocII, B5053, C92H141N23O28S2, Orphan neuropeptide,stimulates locomotion in mice
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[Phe1Ψ(CH2-NH)Gly2]Nociceptin(1-13)NH2, B5049, C61H102N22O14, Potent agonist of the nociceptin (ORL1) receptor
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Methysergide maleate, B5046, C21H27N3O2·C4H4O4, Mixed 5-HT1/5-HT2 receptor antagonist
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RS 39604 hydrochloride, B5042, C26H36ClN3O6S·HCl, potent and selective 5-HT4 antagonist

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