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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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RS 79948 hydrochloride, B6534, C19H28N2O3S·HCl, α2-adrenoreceptor antagonist
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RS 17053 hydrochloride, B6532, C24H29N2O2Cl·HCl, α1A-adrenoceptor antagonist, novel and selective
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Imiloxan hydrochloride, B6533, C14H16N2O2·HCl, α2-adrenoceptor antagonist
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1-Phenylbiguanide hydrochloride, B6528, C8H11N5·HCl, 5-HT3 receptor agonist
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BD 1047 dihydrobromide, B6521, C13H20Cl2N2·2HBr, σ1 receptor antagonist
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Xamoterol hemifumarate, B6519, 2C16H25N3O5·0.5C4H4O4, β1-adrenoceptor partial agonist
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WB 4101 hydrochloride, B6515, C19H23NO5·HCl, α1A-adrenergic antagonist
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Zaprinast, B6516, C13H13N5O2, phosphodiesterase inhibitor and GPR35 agonist
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BRL 37344, sodium salt, B6517, C19H21NO4ClNa, β3-adrenoceptor agonist,potent and selective
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MK 212 hydrochloride, B6513, C8H11ClN4·HCl, 5-HT2C receptor agonist

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