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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 OT 39, B7693, C32H40N8O2S, oxytocin receptor partial agonist
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N,N-Dimethylsphingosine, B7694, C20H41NO2, sphingosine kinase (SphK) inhibitor
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Tegaserod maleate, B7690, C16H23N5O·C4H4O4, Partial agonist of 5-HT4
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(±)-SLV 319, B7689, C23H20Cl2N4O2S, CB1 receptor antagonist,potent and selective
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3,5-DHBA, B7686, C7H6O4, hydroxycarboxylic acid receptor 1 (HCA1) agonist
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(+)-Fluprostenol, B7680, C23H29F3O6, Prostaglandin F2α (FP) receptor agonist
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(±)-AMG 487, B7671, C32H28F3N5O4, CXCR3 antagonist
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Calhex 231 hydrochloride, B7663, C25H27ClN2O·HCl, negative allosteric modulator of Ca2+-sensing receptor (CaSR)
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BIMU 8, B7660, C19H26N4O2·HCl, 5-HT4 agonist
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TC-SP 14, B7658, C25H20F2N2O2S, agonist of Sphingosine-1-Phosphate Receptor 1 (S1P1)

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