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Histamine Receptor
Histamine Receptor Isoform Specific Products
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Histamine Receptor Inhibitors
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Histamine Receptor Agonists
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Histamine Receptor Antagonists
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Histamine Receptor Ligands
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Histamine Receptor Related Products (880)
Related Products (880)
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Antibodies (2)
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Histamine Receptor Isoform Comparison
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Chloropyramine hydrochloride (Standard)
0 ImagesChloropyramine hydrochloride (Standard) is the analytical standard of Chloropyramine hydrochloride. This product is intended for research and analytical applications. Chloropyramine hydrochloride is a histamine receptor H1 antagonist which can also inhibit the biochemical function of VEGFR-3 and FAK. -
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Proxyfan Oxalate
0 ImagesCat. No.: HY-107557ACAS No.: 1620017-81-3Proxyfan Oxalate is a potent histamine H3 receptor antagonist with Ki values of 2.9 nM and 2.7 nM for rat and human H3 receptor, respectively. Proxyfan Oxalate is over 1000-fold more potent at H3 receptors than other histamine receptors. -
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Hydroxyzine-d4 dihydrochloride
0 ImagesSynonyms: Vistaril-d4' dihydrochloride; Atarax-d4' dihydrochlorideHydroxyzine-d4 (dihydrochloride) is the deuterium labeled Hydroxyzine dihydrochloride. Hydroxyzine dihydrochloride, a benzodiazepine antihistamine agent, acts as a orally active histamine?H1-receptor and serotonin antagonist. Hydroxyzine dihydrochloride has anxiolytic effect and can be used forthe research of generalised anxiety disorder. -
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Pheniramine (Standard)
0 ImagesCat. No.: HY-B0971ARCAS No.: 86-21-5Synonyms: Prophenpyridamine (Standard); Tripoton (Standard); Pheniramine solution (Standard)Pheniramine (Standard) is the analytical standard of Pheniramine. This product is intended for research and analytical applications. Pheniramine (Prophenpyridamine;Tripoton) is a first-generation histamine H1 receptor antagonist, acts on the central nervous system (CNS) with sedative and hypnotic effect. Pheniramine displays antitumor effect and induces leukemia cells apoptosis. Pheniramine is also a safe and effective local agent that can suppress or relieve pain, with antipruritic effects. -
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Asenapine citrate
0 ImagesCat. No.: HY-10121BCAS No.: 1411867-74-7Synonyms: Org 5222 citrateAsenapine citrate, an atypical antipsychotic, is an antagonist of serotonin receptors (pKi: 8.4-10.5), adrenoceptors (pKi: 8.9-9.5), dopamine receptors (pKi: 8.9-9.4) and histamine receptors (pKi: 8.2-9.0). Asenapine citrate can be used in the research of schizophrenia and bipolar disorder. -
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Ebastine-d5
0 ImagesCat. No.: HY-B0674SCAS No.: 1216953-13-7 -
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SCH 79687
0 ImagesCat. No.: HY-182296CAS No.: 224585-45-9SCH 79687 is an orally active histamine H3 receptor antagonist, with a Ki of 1.9 nM in rats and 13 nM in guinea pigs. SCH 79687 acts as a competitive antagonist against (R)-α-methylhistamine. SCH 79687 attenuates the inhibitory effect of (R)-α-methylhistamine-induced sympathetic hypertensive responses in guinea pigs. When used in combination with H1 antagonists, SCH 79687 inhibits Compound 48/80 (HY-115768)-induced nasal congestion in cats. SCH 79687 can be used for the research of allergic rhinitis. -
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FUB 465
0 ImagesCat. No.: HY-124147CAS No.: 184028-93-1FUB 465 is an orally active inverse agonist at the constitutively active histamine H3 receptor with a pKi of 6.2 for H3 receptor. FUB 465 can be used in the research of central nervous system diseases. -
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Methapyrilene fumarate
0 ImagesCat. No.: HY-W707972CAS No.: 33032-12-1Methapyrilene fumarate is a histamine receptor H1 antagonist. Methapyrilene fumarate has sedative effects. Methapyrilene fumarate is being studied for its analgesic properties. -
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Olopatadine-d6 (hydrochloride)
0 ImagesCat. No.: HY-B0426AS2Synonyms: ALO4943A-d6 hydrochloride; KW4679-d6 hydrochlorideOlopatadine-d6 (ALO4943A-d6; KW4679-d6) hydrochloride is deuterium-labeled Olopatadine (hydrochloride) (HY-B0426A). Olopatadine hydrochloride (ALO4943A; KW4679) is an orally active histamine H1 receptor antagonist and mast cell stabilizer. Olopatadine hydrochloride exerts antiallergic effects by blocking histamine H1 receptor-mediated activities. Olopatadine hydrochloride inhibits exocytosis, chemokine release, F-actin polymerization, CXCL10-induced calcium influx, and T cell chemotactic activity. Olopatadine hydrochloride also reduces the expression levels of CXCR3 on the surface of CD4+ and CD8+ T cells. Olopatadine hydrochloride inhibits scratching behavior, improves dermatitis scores, and suppresses intraepidermal neurite outgrowth. Olopatadine hydrochloride simultaneously decreases the levels of inflammatory markers, growth factors, histamine, and specific IgE, while increasing the expression of ErbB3A/HER3A. Olopatadine hydrochloride can be used in research related to seasonal pollinosis, chronic rhinitis, urticaria, allergic conjunctivitis, alopecia areata, and atopic dermatitis. -
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Pheniramine
0 ImagesPheniramine (Prophenpyridamine;Tripoton) is a first-generation histamine H1 receptor antagonist, acts on the central nervous system (CNS) with sedative and hypnotic effect. Pheniramine displays antitumor effect and induces leukemia cells apoptosis. Pheniramine is also a safe and effective local agent that can suppress or relieve pain, with antipruritic effects. -
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DA 4626
0 ImagesCat. No.: HY-122148CAS No.: 83184-14-9DA 4626 is a competitive H2-histamine receptor antagonist. DA 4626 inhibits adenylate cyclase activity with a KB value of 40 nM. -
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- Dacemazine
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Ebastine-d6
0 ImagesCat. No.: HY-B0674S1Synonyms: LAS-W 090-d6; RP64305-d6 -
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Hydroxyzine dihydrochloride (Standard)
0 ImagesHydroxyzine (dihydrochloride) (Standard) is the analytical standard of Hydroxyzine (dihydrochloride). This product is intended for research and analytical applications. Hydroxyzine dihydrochloride, a benzodiazepine antihistamine agent, acts as a orally active histamine H1-receptor and serotonin antagonist. Hydroxyzine dihydrochloride has anxiolytic effect and can be used forthe research of generalised anxiety disorder. -
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Noberastine maleate
0 ImagesCat. No.: HY-167850CAS No.: 111922-05-5Synonyms: R 64947 maleateNoberastine maleate is a potent Histamine H1 antagonist. Noberastine maleate has specific peripheral antihistamine activity . -
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Carcinine
0 ImagesCat. No.: HY-107567CAS No.: 56897-53-1Synonyms: β-AlanylhistamineCarcinine (β-Alanylhistamine) is a selective and orally active histamine H3 receptor antagonist with a Ki of 0.2939 μM. Carcinine can reduce histamine content. Carcinine exhibits anti-oxidant activity and neuroprotective effects. Carcinine shows positive inotropic effect and can reduce blood sugar and blood lipid levels. Carcinine can be used for the researches of inflammation, neurological, cardiovascular and metabolic disease, such as retinal damage, seizure and diabetes. -
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Fenspiride
0 ImagesFenspiride, an orally active non-steroidal antiinflammatory agent, is an antagonist of H1-histamine receptor. Fenspiride inhibites phosphodiesterase 3 (PDE3), phosphodiesterase 4 (PDE4) and phosphodiesterase 5 (PDE5) activities with -log IC50 values of 3.44, 4.16 and approximately 3.8, respectively. Fenspiride can be used for the research of respiratory diseases. -
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Clobenpropit
0 ImagesCat. No.: HY-115447CAS No.: 145231-45-4Clobenpropit is a potent histamine H3-receptor antagonist. Clobenpropit decreases dopamine release and increases histamine levels in the hypothalamus. Clobenpropit shows antipsychotic-like activities. Clobenpropit causes a resuscitating effect in rats subjected to the hemorrhagic shock. -
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Atiprosine
0 ImagesCat. No.: HY-119854CAS No.: 89303-63-9Synonyms: AY-28228Atiprosine (AY-28228) is an orally effective selective α1-adrenergic receptor antagonist with a pA2 value of 8.11. Atiprosine exhibits antagonistic activity against α2-adrenergic receptors (α1-adrenergic receptor), 5-HT₂ receptors (5-HT₂ receptor), and H₁ receptors (H₁ receptor). The pA2 values for these receptors are 6.04, 6.87, and 7.32 respectively. Atiprosine has antihypertensive and hypotensive effects in rats, dogs, and monkeys. It can be used for research on cardiovascular and mental disorders. -
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Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
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