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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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Proxyphylline, C3278, C10H14N4O3, A1 adenosine receptor antagonist
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ACS 67, C3246, C32H38O5S3, analog of latanoprost (free acid),prostaglandin (PG) analog
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AL 8810 isopropyl ester, C3240, C27H37FO4, lipid soluble, esterified prodrug form of AL 8810, a FP receptor antagonist
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XAP044, C3220, C15H9IO4, mGluR7 antagonist
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Flibanserin, C3123, C20H21F3N4O, full agonist of the serotonin 5-HT1A receptor and an antagonist of 5-HT2A.
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SR 144528, C3113, C29H34ClN3O, CB2 receptor inverse agonist
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LY171883, C3110, C16H22N4O3, leukotriene D4 receptor antagonist, orally active
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HAMI3379, C3082, C34H45NO8, CysLT2 receptor antagonist
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Losartan Carboxylic Acid, C3065, C22H21ClN6O2, AT1 antagonist
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Niguldipine (hydrochloride), C3067, C36H39N3O6·HCl, α1A-adrenoceptor antagonist

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