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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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L-817,818, B6905, C33H36N4O3, somatostatin sst5 receptor agonist
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GR 79236, B6899, C15H21N5O5, adenosine A1 receptor agonist
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SB 258585 hydrochloride, B6900, C18H22IN3O3S·HCl, 5-HT6 receptor antagonist
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AS 19, B6902, C18H25N3, Potent 5-HT7 agonist
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Ritanserin, B6898, C27H25F2N3OS, long-acting 5-HT2 receptor antagonist
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U 46619, B6890, C21H34O4, selective agonist of prostaglandin H2 (PGH2)/thromboxane A2 (TxA2) (TP) receptor
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Alytesin, B6886, C68H106N22O17S, Amphibian bombesin-like peptide
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N-Formyl-Met-Leu-Phe, B6888, C21H31N3O5S, formyl peptide receptor 1 (FPR1) agonist
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Ro 60-0175 fumarate, B6878, C11H12ClFN2·C4H4O4, 5-HT2 receptor agonist
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EMD 66684, B6875, C28H30N8O2·HCl, angiotensin AT1 receptor antagonist

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