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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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BGC 20-761, B7366, C19H22N2O, 5-HT6 antagonist,selective and high affinity
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8-(3-Chlorostyryl)caffeine, B7355, C16H15ClN4O2, adenosine A2A receptor antagonist and MAO-B inhibitor
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SSR 146977 hydrochloride, B7350, C35H42Cl2N4O2·HCl, NK3 receptor antagonist
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SN 003, B7348, C19H25N5O2, CRF1 antagonist
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Rec 15/2615 dihydrochloride, B7343, C26H33N5O5·2HCl, α1B-adrenoceptor antagonist
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NPS ALX Compound 4a dihydrochloride, B7344, C25H25N3O2S·2HCl, 5-HT6 antagonist
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Oxprenolol hydrochloride, B7345, C15H23NO3·HCl, β-adrenergic inhibitor
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2-ThioUTP tetrasodium salt, B7340, C9H11N2Na4O14P3S, P2Y2 agonist
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UTPγS trisodium salt, B7339, C9H12N2Na3O14P3S, P2Y2 and P2Y4 receptor agonist
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SCH 221510, B7326, C28H31NO, nociceptin opioid receptor (NOP) agonist

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