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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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BMY 7378, B2263, C22H31N3O3·2HCl, 5-HT1A partial agonist and α1D adrenoceptor antagonist
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Zolmitriptan, B2261, C16H21N3O2, Potent 5-HT1B/1D/1F agonist
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WAY-100635 maleate salt, B2260, C25H34N4O2·C4H4O4, 5-HT1A receptor antagonist
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Tropisetron Hydrochloride, B2258, C17H21ClN2O2, 5-HT3 receptor antagonist
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VUF 10166, B2259, C13H15ClN4, 5-HT3 receptor antagonist
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BRL-15572, B2265, C25H27ClN2O·ClH·ClH, 5-HT1D receptor antagonist
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Dapoxetine HCl, B2264, C21H23NO·HCl, Selective serotonin reuptake inhibitor
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SB742457, B2256, C19H19N3O2S, 5-HT6 receptor antagonist,highly selective and high affinity
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BMY 7378, B2263, C22H31N3O3·2HCl, 5-HT1A partial agonist and α1D adrenoceptor antagonist
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Agomelatine, B2262, C15H17NO2, MT1/MT2 / 5-HT2C agonist

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