1. Signaling Pathways
  2. GPCR/G Protein
    Immunology/Inflammation
    Neuronal Signaling
  3. Histamine Receptor

Histamine Receptor

Histamine Receptors are a class of G protein-coupled receptors with histamine as their endogenous ligand. There are four known histamine receptors: H1 receptor, H2 receptor, H3 receptor, H4 receptor. The H1 receptor is a histamine receptor belonging to the family of Rhodopsin-like G-protein-coupled receptors. This receptor, which is activated by the biogenic amine histamine, is expressed throughout the body, to be specific, in smooth muscles, on vascular endothelial cells, in the heart, and in the central nervous system. H2 receptors are positively coupled to adenylate cyclase via Gs. It is a potent stimulant of cAMP production, which leads to activation of Protein Kinase A. Histamine H3 receptors are expressed in the central nervous system and to a lesser extent the peripheral nervous system, where they act asautoreceptors in presynaptic histaminergic neurons, and also control histamine turnover by feedback inhibition of histamine synthesis and release. The Histamine H4 receptor has been shown to be involved in mediating eosinophil shape change and mast cell chemotaxis.

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-107647AR
    (R)-(+)-Dimethindene maleate (Standard)
    Antagonist
    (R)-(+)-Dimethindene maleate (Standard) is the analytical standard of (R)-(+)-Dimethindene (maleate) (HY-107647A). This product is intended for research and analytical applications. (R)-(+)-Dimethindene maleate is an orally active H1-receptor blocker with antihistaminic properties in pigs.
    (R)-(+)-Dimethindene maleate (Standard)
  • HY-100661R
    Cetirizine Impurity D (Standard)
    Antagonist
    Cetirizine Impurity D (Standard) is the analytical standard of Cetirizine Impurity D. This product is intended for research and analytical applications. Cetirizine Impurity D is an impurity of Cetirizine. Cetirizine, a second-generation antihistamine, is a specific, orally active and long-acting histamine H1-receptor antagonist. Cetirizine marks antiallergic properties and inhibits eosinophil chemotaxis during the allergic response.
    Cetirizine Impurity D (Standard)
  • HY-B0170
    Azatadine
    Inhibitor
    Azatadine is an orally active histamine H1 receptor inhibitor, cetylcholine receptor inhibitor, and serotonin receptor inhibitor. Azatadine induces sedation and exhibits topical anesthetic properties. Azatadine can be used for the research of allergic rhinitis.
    Azatadine
  • HY-14447R
    Bilastine (Standard)
    Antagonist
    Bilastine (Standard) is the analytical standard of Bilastine. This product is intended for research and analytical applications. Bilastine is a histamine H1 receptor antagonist that can be used to treat allergic rhinoconjunctivitis and urticaria.
    Bilastine (Standard)
  • HY-101724
    ReN-1869 hydrochloride
    Antagonist
    ReN 1869 hydrochloride is a novel, selective histamine H1 receptor antagonist, which demonstrates affinity to the histamine H1 receptor (guinea pig brain) with Ki of 0.19±0.04 μM and the non-selective σ site (guinea pig brain) with Ki of 0.45 μM.
    ReN-1869 hydrochloride
  • HY-U00018
    (±)-Tazifylline
    Antagonist
    (±)-Tazifylline is a potent, selective and long-acting histamine H1 receptor antagonist.
    (±)-Tazifylline
  • HY-101635
    Proxibarbal
    Inhibitor
    Proxibarbal is a barbiturate derivative. Proxibarbal has anti-anxiety properties and is also used for the study of migraine headaches.
    Proxibarbal
  • HY-101601
    Bamirastine
    Inhibitor
    Bamirastine inhibits ligand binding to recombinant human histamine H1 receptors (rhH1R) with an IC50 value of 17.3 nM.
    Bamirastine
  • HY-101745
    Rocastine
    Antagonist
    Rocastine is a selective, nonsedating H1 antagonist, acting as an antihistamine.
    Rocastine
  • HY-B0895R
    Hydroxyzine pamoate (Standard)
    Antagonist
    Hydroxyzine (pamoate) (Standard) is the analytical standard of Hydroxyzine (pamoate). This product is intended for research and analytical applications. Hydroxyzine pamoate is a histamine receptor H1 antagonist.
    Hydroxyzine pamoate (Standard)
  • HY-12199S
    Pitolisant-d10
    Inhibitor
    Pitolisant-d10 (Tiprolisant-d10) is deuterium labeled Pitolisant. Pitolisant is a potent and selective nonimidazole inverse agonist at the recombinant human histamine H3 receptor (Ki=0.16 nM).
    Pitolisant-d<sub>10</sub>
  • HY-17043S3
    Loratadine-13C6
    Agonist
    Loratadine-13C6 (SCH 29851-13C6) is 13C labeled 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 can inhibit immunologic release of inflammatory mediators.
    Loratadine-<sup>13</sup>C<sub>6</sub>
  • HY-B1557R
    Betazole (Standard)
    Agonist
    Betazole (Standard) is the analytical standard of Betazole. This product is intended for research and analytical applications. Betazole (Ametazole), a pyrazole analogue of histamine, is an orally active histamine H2 receptor agonist. Betazole induces gastric acid secretion and causes an immediate and significant increase in common bile duct pressure. Betazole is used as a diagnostic agent known as histalog for investigating gastric acid secretory capacity.
    Betazole (Standard)
  • HY-121399
    Gizzerosine
    Agonist
    Gizzerosine is an H2 receptor agonist. It can stimulate the gastric acid secretion of broiler chickens, thus causing gizzard erosion in them. Gizzerosine has significant research value in the fields of agricultural farming and feed science.
    Gizzerosine
  • HY-167653
    FR-145715
    Antagonist
    FR-145715 is a histamine H2 receptor antagonist, with specific anti-Helicobacter pylori activities. FR-145715 can be used for the research of gastric lesions.
    FR-145715
  • HY-104003R
    S 38093 (Standard)
    Antagonist
    S 38093 (Standard) is the analytical standard of S 38093 (HY-104003). This product is intended for research and analytical applications. S 38093 is a brain-penetrant, orally active antagonist of H3 receptor, with Kis of 8.8, 1.44 and 1.2 μM for rat, mouse and human H3 receptors, respectively.
    S 38093 (Standard)
  • HY-13710AR
    Dimethindene maleate (Standard)
    Antagonist
    Dimethindene (maleate) (Standard) is the analytical standard of Dimethindene (maleate). This product is intended for research and analytical applications. Dimethindene maleate is a selective histamine H1 antagonist with antihistamine effects. Dimethindene maleate can be used for the research of hypersensitivity reactions.
    Dimethindene maleate (Standard)
  • HY-114724
    HSR-609
    HSR-609 is an orally active amphoteric antiallergic agent. HSR-609 has a high affinity for histamine H1-receptor in the guinea pig cerebral cortex. HSR-609 inhibits allergic airway hyperresponsiveness to Acetylcholine. HSR-609 shows poor ability to penetrate into the CNS in mice and guinea pigs.
    HSR-609
  • HY-100661
    Cetirizine Impurity D
    Antagonist
    Cetirizine Impurity D is an impurity of Cetirizine. Cetirizine, a second-generation antihistamine, is a specific, orally active and long-acting histamine H1-receptor antagonist. Cetirizine marks antiallergic properties and inhibits eosinophil chemotaxis during the allergic response.
    Cetirizine Impurity D
  • HY-105505
    KF-17625
    Inhibitor
    KF-17625 is an orally active bronchodilator. KF-17625 can inhibit bronchoconstriction induced by Carbachol (HY-B1208), Histamine (HY-B1204), or Leukotriene D4 (HY-113456). KF-17625 can inhibit canine tracheal phosphodiesterase (PDE) IV (IC50 = 12 μM) and Concanavalin-A (HY-P2149)-induced histamine release from rat mast cells (44% inhibition at 10 mM). KF-17625 can be used for the researches of immunology and inflammation.
    KF-17625
Cat. No. Product Name / Synonyms Application Reactivity

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