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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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CS 2100, B5636, C25H23N3O4S, S1P1 agonist
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SHA 68, B5625, C26H24FN3O3, neuropeptide S receptor (NPSR) antagonist
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S 32212 hydrochloride, B5623, C25H28N4O2·HCl, inverse agonist of 5-HT2C receptors
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DV 7028 hydrochloride, B5617, C21H25FN4O3·HCl, 5-HT2A receptor antagonist
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BAY 60-6583, B5612, C19H17N5O2S, Potent A2B receptor agonist
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EMD 281014 hydrochloride, B5610, C22H21FN4O·HCl, 5-HT2A antagonist
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AT 1015, B5609, C29H33N3O2·HCl, Long-acting 5-HT2A antagonist
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YE 120, B5603, C16H9Cl2N3O, GPR35 agonist
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TC-G 1004, B5580, C22H27N7O2, adenosine A2A receptors antagonist
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5-OMe-UDP trisodium salt, B5568, C10H13N2Na3O13P2, Potent P2Y6 agonist

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