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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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Tabimorelin hemifumarate, B5287, C32H40N4O3·½C4H4O4, orally active ghrelin receptor (GHS-R1a) agonist
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WRW4, B5283, C61H65N15O6, Selective antagonist of formyl peptide receptor 2 (FPR2) signaling
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Motilin (human, porcine), B5284, C120H188N34O35S, Endogenous motilin receptor ligand
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GLP-2 (human), B5281, C165H254N44O55S, intestinal epithelium-specific growth factor
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GLP-2 (rat), B5282, C166H256N44O56S, intestinal epithelium-specific growth factor
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GIP (1-39), B5280, C210H316N56O61S, Endogenous truncated form of the incretin hormone GIP
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des-His1-[Glu9]-Glucagon (1-29) amide, B5273, C148H221N41O47S, Glucagon receptor antagonist
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MRS 2279, B5265, C13H18ClN5O8P2·2NH3, Selective, high affinity competitive antagonist of the P2Y1 receptor
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MRS 2500 tetraammonium salt, B5266, C13H18N5O8P2I·4NH3, Highly potent and selective antagonist of the platelet P2Y1 receptor
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BVD 10, B5267, C58H92N16O13, NPY Y1 receptor antagonist,highly selective

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