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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.

Product Search

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Fendiline (hydrochloride), C5675, C23H25N·HCl, α2-adrenergic receptor antagonist
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AH 23848 (calcium salt), C5649, C29H34NO5·1/2Ca, dual antagonist of TP1 and EP4 receptors
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VU0483605, C5611, C20H10Cl3N3O3, elective positive allosteric modulator (PAM) of mGluR1
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Raceanisodamine, C5580, C17H23NO4, weak antagonist of α1-adrenoceptors
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Tetrahydromagnolol, C5552, C18H22O2, peripheral CB2 receptor agonist
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γ-Linolenic Acid, C5518, C18H30O2, weak LTB4 receptor antagonist
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S-1 Methanandamide, C5509, C23H39NO2, CB1 receptor ligand
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S-2 Methanandamide, C5513, C23H39NO2, potent CB1 receptor agonist
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DC260126, C5495, C16H18FNO2S, free fatty acid receptor 1 (FFAR1/GPR40) antagonist
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REV 5901, C5416, C22H25NO2, antagonist of cysteinyl-leukotriene receptors

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