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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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Salmeterol xinafoate, A3789, C36H45NO7, β2-adrenergic receptor agonist
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RS 504393, A3779, C25H27N3O3, CCR2 chemokine receptor antagonist
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RS 504393, A3779, C25H27N3O3, CCR2 chemokine receptor antagonist
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Rotigotine, A3776, C19H25NOS, Agonist of dopamine D2/D3 receptor
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Rotigotine, A3776, C19H25NOS, Agonist of dopamine D2/D3 receptor
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Rotigotine hydrochloride, A3777, C19H26ClNOS, Agonist of dopamine D2/D3 receptor
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Rotigotine hydrochloride, A3777, C19H26ClNOS, Agonist of dopamine D2/D3 receptor
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Rimonabant hydrochloride, A3766, C22H22Cl4N4O, CB1 receptor inverse agonist
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Rimonabant hydrochloride, A3766, C22H22Cl4N4O, CB1 receptor inverse agonist
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Reparixin L-lysine salt, A3753, C20H35N3O5S, CXCR1/CXCR2 inhibitor

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