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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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BMS 193885, B7327, C33H42N4O6·C3H6O3, Competitive NPY Y1 receptor antagonist
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XAC

XAC, B7314, C21H28N6O4, Adenosine receptor antagonist
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PSB 603, B7312, C24H25ClN6O4S, Adenosine A2B receptor antagonist
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PSB 0788, B7313, C25H27ClN6O4S, adenosine A2B receptor antagonist
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SB 699551, B7308, C34H45N3O·2HCl, 5-ht5a receptor antagonist
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SB 399885 hydrochloride, B7309, C18H21Cl2N3O4S·HCl, 5-HT6 antagonist
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Talopram hydrochloride, B7287, C20H25NO·HCl, noradrenalin transporter (NET) inhibitor
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2-Chloroadenosine, B7283, C10H12ClN5O4, adenosine receptor agonist
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BAY-u 9773, B7284, C27H36O5S, Antagonist of CysLT1/CysLT2 receptors
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NE 100 hydrochloride, B7281, C23H33NO2·HCl, σ1 receptor antagonist

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