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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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1H-1-ethyl Candesartan Cilexetil, C5023, C35H38N6O6, selective angiotensin II type 1 receptor (AT1) antagonist
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5(S),6(R)-7-trihydroxymethyl Heptanoate, C4837, C8H16O5, inhibits leukotriene B4 (LTB4)-induced polymorphonuclear neutrophils (PMN) chemotaxis
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Lorglumide (sodium salt), C4809, C22H31Cl2N2O4·Na, nonpeptidic antagonist of the CCK A receptor
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TY 52156, C4797, C18H19Cl2N3O, sphingosine-1-phosphate receptor 3 (SIP3) antagonist
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AVE-1625, C4753, C23H20Cl2F2N2O2S, highly potent, selective antagonist for CB1 receptor
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AM6545, C4711, C26H23Cl2N5O3S, CB1 selective neutral antagonist
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E7046, C4712, C22H18F5N3O4, antagonist of the type 4 prostaglandin E2 (PGE2) receptor EP4

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