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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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TC-G 1006, B5701, C21H16F3N3O3, sphingosine-1-phosphate receptor 1 (S1P1) agonist
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LP 20 hydrochloride, B5688, C17H20N2O·HCl, ligand of the 5-HT7 receptor
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TC LPA5 4, B5689, C23H23ClN2O3, LPA5 receptor antagonist
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PU 02, B5687, C16H12N4S, negative allosteric modulator of 5-HT3 receptors
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CYM 50358 hydrochloride, B5682, C20H18Cl2N2O2·HCl, S1P4 antagonist
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RFRP 3 (human), B5683, C45H72N14O10, NPFF1 receptor agonist
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CYM 50308, B5681, C20H21F2N3O2S, S1P4 agonist
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SB 611812, B5678, C17H16Cl3F3N2O3S, Urotensin-II (UT) antagonist
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CYM 50260, B5680, C14H11Cl3FNO2, S1P4 agonist
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SB 706375, B5677, C20H22BrF3N2O5S, urotensin-II (UT) receptor antagonist

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