GLPBio

Histamine Receptor

Histamine receptor has 4 subtypes (H1,H2,H3 and H4) which mediates various biological fuctions, including allergic reaction, gastric acid secretion and inflammation etc.

Products Related to Histamine Receptor(243)

  • GC10127 structure
    GC10127Betahistine 2HCl
    CAS: 5579-84-0
    Purity: >99.50%

    Betahistine 2HCl is an orally active histamine H1 receptor agonist and a H3 receptor antagonist.

  • GC10306 structure
    GC10306Hydroxyzine 2HCl
    CAS: 2192-20-3
    Purity: >99.50%

    Hydroxyzine 2HCl, a benzodiazepine antihistamine agent, acts as a orally active histamineH1-receptor and serotonin antagonist.

  • GC10369 structure
    GC10369Roxatidine Acetate HCl
    CAS: 93793-83-0
    Purity: >98.00%

    Roxatidine Acetate HCl is a potent, selective, competitive and orally active histamine H2-receptor antagonist.

  • GC10400 structure
    GC10400JNJ-7777120
    CAS: 459168-41-3
    Purity: >98.00%

    JNJ-7777120 is a histamine H 4 receptor (H 4 R: K i = 4.5nM) antagonist.

  • GC10478 structure
    GC10478Mizolastine dihydrochloride
    CAS: 1056596-82-7
    Purity: >98%

    Histamine H1-receptor antagonist

  • GC10511 structure
    GC10511Olopatadine HCl
    CAS: 140462-76-6
    Purity: >99.50%

    Olopatadine HCl (ALO4943A) is a histamine blocker used to treat allergic conjunctivitis.

  • GC10806 structure
    GC10806Histamine 2HCl
    CAS: 56-92-8
    Purity: >98.00%

    Histamine 2HCl is an endogenous metabolite.

  • GC10966 structure
    GC10966Fexofenadine HCl
    CAS: 153439-40-8
    Purity: >99.50%

    Fexofenadine HCl is an orally active and nonsedative histamine H1 receptor antagonist.

  • GC11009 structure
    GC11009Cetirizine DiHCl
    CAS: 83881-52-1
    Purity: >99.00%

    Cetirizine DiHCl, a second-generation antihistamine and the carboxylated metabolite of hydroxyzine, is a specific, orally active and long-acting histamine H1-receptor antagonist.

  • GC11033 structure
    GC11033Rupatadine Fumarate
    CAS: 182349-12-8
    Purity: >99.50%

    Inhibitor of PAF and histamine (H1) receptor

  • GC12039 structure
    GC12039Cyclizine 2HCl
    CAS: 5897-18-7
    Purity: >98%

    Histamine H1 receptor antagonist

  • GC12061 structure
    GC12061Tripelennamine HCl
    CAS: 154-69-8
    Purity: >99.50%

    Tripelennamine HCl, an ethylenediamine derivative, is a potent histamine H1-receptor antagonist.

  • GC12365 structure
    GC12365Ranitidine hydrochloride
    CAS: 66357-59-3
    Purity: >98.00%

    Ranitidine hydrochloride, an inhibitor of gastric acid secretion, competitively antagonizes histamine-induced increases in contraction frequency with a pA2 value of 7.2.

  • GC12549 structure
    GC12549Mizolastine
    CAS: 108612-45-9
    Purity: >98.00%

    Histamine H1-receptor antagonist

  • GC12794 structure
    GC12794Nizatidine
    CAS: 76963-41-2
    Purity: >99.00%

    Histamine H2 receptor antagonist

  • GC12924 structure
    GC12924Ciproxifan
    CAS: 184025-18-1
    Purity: >98%

    Histamine H3-receptor antagonist

  • GC13341 structure
    GC13341Brompheniramine hydrogen maleate
    CAS: 980-71-2
    Purity: >99.50%

    Brompheniramine ((±)-Brompheniramine) maleate is a potent and orally active antihistamine of the alkylamine class.

  • GC13486 structure
    GC13486Cimetidine
    CAS: 51481-61-9
    Purity: >98.00%

    H2 receptor antagonist

  • GC14070 structure
    GC14070Azatadine
    CAS: 3964-81-6
    Purity: >98%

    Histamine and cholinergic inhibitor

  • GC14250 structure
    GC14250Bepotastine Besilate
    CAS: 190786-44-8
    Purity: >99.50%

    Non-sedating, selective antagonist of histamine 1 (H1) receptor

  • GC14726 structure
    GC14726Mianserin HCl
    CAS: 21535-47-7
    Purity: >99.50%

    Mianserin HCl (Org GB 94) is a H1 receptor inverse agonist and is a psychoactive agent of the tetracyclic antidepressant.

  • GC14892 structure
    GC14892Clemastine Fumarate
    CAS: 14976-57-9
    Purity: >99.50%

    Clemastine Fumarate, the over-the-counter antihistamine and muscarinic receptor blocker, has remyelinating potential in Multiple sclerosis (MS).

  • GC15068 structure
    GC15068Buclizine HCl
    CAS: 129-74-8
    Purity: >98.00%

    Buclizine HCl is an orally active antihistamine antiallergic compound.

  • GC15214 structure
    GC15214Levodropropizine
    CAS: 99291-25-5
    Purity: >99.50%

    Histamine receptor inhibitor,cough suppressant