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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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TCS 1102, B1044, C27H26N4O2S, Antagonist for OX2 and OX1 receptors
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AVE 0991, B1007, C29H32N4O5S2, Agonist of angiotensin-(1-7) receptor
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Vilanterol, B1005, C24H33Cl2NO5, β2-AR agonist
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Vilanterol trifenatate, B1006, C44H49Cl2NO7, β2-AR agonist
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ICI 118,551 hydrochloride, B1004, C17H28ClNO2, Highly selective β2 adrenergic receptor antagonist
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AVE 0991, B1007, C29H32N4O5S2, Agonist of angiotensin-(1-7) receptor
Image
Vilanterol trifenatate, B1006, C44H49Cl2NO7, β2-AR agonist
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Loxapine, B1001, C18H18ClN3O, 5-HT receptor antagonist
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ICI 118,551 hydrochloride, B1004, C17H28ClNO2, Highly selective β2 adrenergic receptor antagonist
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Vilanterol, B1005, C24H33Cl2NO5, β2-AR agonist

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