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GPCR/G protein

G-protein-coupled receptors (GPCRs) mediate a wide range of physiological responses to environmental stimulants, neurotransmitters, hormones cytokines and lipid signaling molecules. As a result, GPCRs play a significant role in biological processes such as vision, olfaction, the autonomic nervous system, and behavior.

All GPCRs share a common seven trans-membrane structure. GPCRs are associated with heterotrimeric G-proteins which are GTP-binding proteins made of alpha, beta, and gamma subunits. When a ligand binds to GPCR, it activates the attached G-protein, the GDP is replaced with GTP. The activated G-protein then dissociates into an alpha and a beta-gamma complex which activates downstream signaling pathways. These intracellular signaling pathways include cAMP/PKA, calcium/NFAT, phospholipase C, protein tyrosine kinases, MAP kinases, PI-3-kinase, nitric oxide/cGMP, Rho, and JAK/STAT.

GPCRs are one of the most important therapeutic targets for various diseases, over 30% of all modern medicinal drugs target this family. Aberrant GPCR functions are involved in pathological conditions such as neurological, immunological and hormonal disorders. A large number of GPCRs have been identified, but whose ligands are not known, are classified as orphan receptors.

Items 1371-1380 of 1407

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  1. Ertugliflozin L-pyroglutamic acid
    C8944 Ertugliflozin L-pyroglutamic acid
    Summary: Ertugliflozin L-pyroglutamic acid is a selective sodium-glucose cotransporter 2 inhibitor used as a reference compound in metabolic and diabetes-related biochemical research.
  2. Metoclopramide hydrochloride hydrate
    C8952 Metoclopramide hydrochloride hydrate
    Summary: Metoclopramide hydrochloride hydrate is a dopamine D2 receptor antagonist and serotonergic modulator used as a pharmacological tool in neuropharmacology and gastrointestinal motility research.
  3. Etelcalcetide HCl
    C8974 Etelcalcetide HCl
    Summary: Etelcalcetide HCl is a peptide allosteric agonist of the calcium-sensing receptor, widely utilized in parathyroid signaling and mineral metabolism research.
  4. Ganirelix acetate (Antagon)
    C8984 Ganirelix acetate (Antagon)
    Summary: Ganirelix acetate (Antagon) is a synthetic decapeptide gonadotropin-releasing hormone receptor antagonist used to investigate pituitary gonadotropin signaling in reproductive endocrinology research.
  5. Naloxegol Oxalate
    C8986 Naloxegol Oxalate
    Summary: Naloxegol Oxalate is a peripherally selective μ-opioid receptor antagonist used to investigate opioid receptor signaling and gastrointestinal motility mechanisms in pharmacological research.
  6. Norepinephrine tartrate
    C8991 Norepinephrine tartrate
    Summary: Norepinephrine tartrate is a catecholamine adrenergic receptor agonist targeting α- and β-adrenergic signaling pathways, widely utilized in neurobiology, cardiovascular physiology, and receptor pharmacology research.
  7. Dobutamine HCl
    C8994 Dobutamine HCl
    Summary: Dobutamine HCl is a synthetic catecholamine and selective β1-adrenergic receptor agonist used to investigate cardiac adrenergic signaling and myocardial contractility mechanisms.
  8. Nafadotride
    A9917 Nafadotride
    Summary: An antagonist of the dopamine D3 receptor
  9. NE 52-QQ57
    A9921 NE 52-QQ57
    Summary: A selective oral G-protein-coupled receptor 4 (GPR4) antagonist
      ≥10.2 mg/mL
  10. Methoxamine hydrochloride
    A9922 Methoxamine hydrochloride
    Summary: An α1-adrenergic receptor selective agonist
      ≥35.4 mg/mL

Items 1371-1380 of 1407

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