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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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Olanzapine, B2240, C17H20N4S, Antagonist of 5-HT2A and dopamine D2 receptors
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Desvenlafaxine Succinate, B2246, C16H25NO2·C4H6O4·H2O, serotonin (5-HT) transporter and norepinephrine (NE) transporter reuptake inhibitor
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BRL-54443, B2245, C14H18N2O, 5-HT1E/1F receptor agonist,potent and selective
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Eletriptan HBr, B2237, C22H27BrN2O2S, selective 5-HT1B and 5-HT1D receptor agonist
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Desvenlafaxine, B2236, C16H25NO2, serotonin (5-HT) and norepinephrine (NE) reuptake inhibitor
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Almotriptan Malate, B2243, C17H25N3O2S·C4H6O5, 5-HT1B/1D-receptor agonist
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Urapidil HCl, B2242, C20H29N5O3·HCl, α1-adrenoceptor antagonist and 5-HT1A receptor agonist
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Clomipramine HCl, B2234, C19H23ClN2·HCl, SERT/NET dopamine transporter (DAT) blocker
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Ondansetron, B2241, C18H19N3O, serotonin 5-HT3 receptor antagonist
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Olanzapine, B2240, C17H20N4S, Antagonist of 5-HT2A and dopamine D2 receptors

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