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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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MRS 2211, B7041, C14H10N4O8Na2PCl, P2Y13 receptor antagonist
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JTE 013, B7038, C17H19N7OCl2, S1P receptor antagonist
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LY 320135, B7036, C24H17NO4, CB1 receptor antagonist/inverse agonist
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EMD 386088 hydrochloride, B7032, C14H15N2Cl·HCl, 5-HT6 receptor agonist
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CGH 2466 dihydrochloride, B7027, C14H9N3SCl2·2HCl, adenosine receptor antagonist
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MK-571, B7023, C26H27ClN2O3S2, leukotriene D4 receptor antagonist, orally active
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WEB 2086, B7024, C22H22N5O2SCl, platelet-activating factor (PAF) receptor antagonist
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A 80426 mesylate, B7025, C23H27NO2·CH3SO3H, α2-adrenoceptor antagonist and 5-HT uptake inhibitor
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L-168,049, B7014, C24H20BrClN2O, human glucagon receptor (hGR) antagonist
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Leukotriene B4, B7011, C20H32O4, BLT1/BLT2 receptor agonist

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