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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-MCH 7c, B5564, C24H25FN2O3, melanin-concentrating hormone receptor 1 (MCH1R) antagonist
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TC-C 14G, B5559, C24H17Cl2F2NO4, CB1 receptor inverse agonist
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PSB 0777 ammonium salt, B5557, C18H20N5O7S2·NH4, adenosine A2A receptor full agonist
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C19H20Br2N2O3, B5553, C19H20Br2N2O3, OX2 receptor antagonist
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NGD 98-2 hydrochloride, B5552, C19H24F3N3O3·HCl, corticotropin-releasing factor receptor 1 (CRF1) antagonist
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MRS 2957 triethylammonium salt, B5546, C19H28N5O20P3·3(C2H5)3N, P2Y6 agonist
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SB 297006, B5542, C18H18N2O5, CCR3 antagonist
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MS 245 oxalate, B5540, C19H22N2O3S·C2H2O4, 5-HT6 antagonist
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KW 3902, B5537, C20H28N4O2, adenosine A1 receptor antagonist
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MM-22, B5527, C36H60N4O5S, biotinylated anandamide analog acts as a probe for visualizing the accumulation and intracellular trafficking of anandamide

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