Histamine H1 Receptor

Histamine H1 receptors are Gα q/11-protein-coupled receptors that mediate allergic responses. These receptors are expressed in a wide variety of tissues including the gastrointestinal tract, CNS, airway and vascular smooth muscle cells and endothelial cells.

Products for Histamine H1 Receptor - Page 2

  1. Cat.No. Product Name Information/Activity
  2. BCC1262 Loratadine Loratadine (SCH-29851) is a selective inverse peripheral histamine H1-receptor agonist with an IC50 of >32 μM. Loratadine has anti-dengue-virus (DENV) activity. Loratadine chemical structure
  3. BCC6740 Mepyramine maleate Mepyramine maleate, a first generation antihistamine, is an antagonist of histamine H1 receptor, with Kds of 0.8 nM, 5200 nM and >3000 nM for H1, H2, and H3 receptor, respectively, and a pKd of 9.4 for H1 receptor. Mepyramine maleate chemical structure
  4. BCC4923 Mirtazapine Mirtazapine is a 5-HT receptor inhibitor. Mirtazapine is a potent and orally active noradrenergic and specific serotonergic antidepressant (NaSSA) agent by blocking 5-HT2 and 5-HT3 receptors. Mirtazapine chemical structure
  5. BCC4545 Olopatadine HCl Olopatadine hydrochloride (ALO4943A) is a histamine blocker used to treat allergic conjunctivitis. Olopatadine HCl chemical structure
  6. BCC3866 Terfenadine Terfenadine ((±)-Terfenadine) is a potent open-channel blocker of hERG with an IC50 of 204 nM. Terfenadine, an H1 histamine receptor antagonist, acts as a potent apoptosis inducer in melanoma cells through modulation of Ca2+ homeostasis. Terfenadine induces ROS-dependent apoptosis, simultaneously activates Caspase-4, -2, -9. Terfenadine chemical structure
  7. BCC6742 trans-Triprolidine hydrochloride 550-70-9 trans-Triprolidine hydrochloride chemical structure
  8. BCC7838 Zotepine 26615-21-4 Zotepine chemical structure

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