- Signaling Pathways
- GPCR/G Protein Immunology/Inflammation Neuronal Signaling
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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 Activators
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Histamine Receptor Ligands
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Histamine Receptor Related Products (860)
Related Products (860)
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Antibodies (2)
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Histamine Receptor Isoform Comparison
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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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- Buclizine
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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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Doxylamine-d5 succinate
0 ImagesCat. No.: HY-A0069SCAS No.: 1216840-94-6Doxylamine-d5 succinate is deuterium labeled Doxylamine succinate (HY-A0069A). Doxylamine succinate is a first-generation antihistamine and acts as a histamine H1 receptor antagonist. Doxylamine succinate is orally active, possessing analgesic and hypnotic activities. Doxylamine succinate enhances the activities of CYP2B, CYP2A, CYP3A and thyroxine-glucuronosyltransferase via promoting substrate hydroxylation and thyroxine metabolic pathways. Doxylamine succinate decreases serum thyroxine (T4) level and elevates serum thyroid-stimulating hormone (TSH) level. Doxylamine succinate induces liver enlargement and increases the activities of hepatic microsomal cytochrome P450, cytochrome b5 and NADPH-cytochrome c reductase. Doxylamine succinate can be used for the research of nausea, allergy, insomnia. -
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rel-Asenapine hydrochloride
0 ImagesCat. No.: HY-10121DCAS No.: 1261398-77-9Synonyms: rel-Org 5222 hydrochloriderel-Asenapine (rel-Org 5222) hydrochloride is a relative configuration of Asenapine hydrochloride (HY-16567). Asenapine (Org 5222) hydrochloride, 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 hydrochloride can be used in the research of schizophrenia and bipolar disorder. -
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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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(E/Z)-Chlorprothixene-d6 hydrochloride
0 ImagesCat. No.: HY-B0274CSCAS No.: 1246832-91-6(E/Z)-Chlorprothixene-d6 hydrochloride is the deuterium labeled (E/Z)-Chlorprothixene hydrochloride. -
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- Dacemazine
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Propiomazine maleate
0 ImagesCat. No.: HY-U00051BCAS No.: 3568-23-8Propiomazine maleate is an orally active antihistamine agent. Propiomazine maleate is a potent prolactin (PRL) release stimulant, whose effect depends on the antagonism of the dopaminergic system and can inhibit the secretion of luteinizing hormone (LH). Propiomazine maleate is mainly used for anesthesia assistance, mental disorders and anxiety-induced sedation, and can also be used in research related to insomnia. -
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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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H3R antagonist 5
0 ImagesCat. No.: HY-14517CAS No.: 879368-27-1H3R antagonist 5 (Compound 1b) is a selective histamine H3 receptor inverse agonist with a IC50 of 0.54 nM and the ability to cross the blood-brain barrier. H3R antagonist 5 can be used in central nervous system-related research. -
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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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Phenyl-α-D-mannopyranoside
0 ImagesCat. No.: HY-N20706CAS No.: 21797-50-2Phenyl-α-D-mannopyranoside is a Concanavalin A inhibitor. Phenyl-α-D-mannopyranoside blocks Histamine (HY-B1204) release induced by Concanavalin A (HY-P2149) . Phenyl-α-D-mannopyranoside acts as a donor in the transfer reaction catalyzed by α-D-mannosidase, forming isomeric mannosides with D-ribose as the acceptor. -
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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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D-20133
0 ImagesCat. No.: HY-106919CAS No.: 146764-26-3D-20133 is an orally active Hexadecylphosphocholine analog. D-20133 can both enhance and inhibit antigen-induced histamine release. D-20133 shows antineoplastic activity against small DMBA (HY-W011845)-induced mammary carcinomas. -
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Sorry. There is currently no product that acts on isoform Bcl-2, Bcl-W and Bim together.Please
try each isoform separately.