- Signaling Pathways
- GPCR/G Protein Immunology/Inflammation Neuronal Signaling
- Histamine Receptor
Histamine Receptor
Histamine Receptor Isoform Specific Products
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Histamine Receptor Inhibitors
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Histamine Receptor Related Products (882)
Related Products (882)
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Antibodies (2)
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Histamine Receptor Isoform Comparison
- 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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BRL 22321 free base
0 ImagesCat. No.: HY-126127CAS No.: 72364-91-1BRL 22321 free base is a stabilizer with similar mast cell stabilizing activity to Cromolyn sodium (HY-B0320A) and also has some smooth muscle relaxant activity. BRL 22321 free base is more potent than Cromolyn sodium (HY-B0320A) in inhibiting rat passive cutaneous and peritoneal anaphylaxis and antigen-induced histamine release from passively sensitized rat peritoneal cells. -
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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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Loratadine n-oxide
0 ImagesCat. No.: HY-147085CAS No.: 165739-62-8Loratadine n-oxide is a metabolite of Loratadine. Loratadine n-oxide shows antihistamine activity. -
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Methicillin sodium hydrate (Standard)
0 ImagesCat. No.: HY-121544ARCAS No.: 7246-14-2Methicillin (sodium hydrate) (Standard) is the analytical standard of Methicillin (sodium hydrate). This product is intended for research and analytical applications. Methicillin sodium hydrate is a narrow-spectrum β-lactam antibiotic, acts by inhibiting penicillin-binding proteins (PBPs). Methicillin sodium hydrate is active against Staphylococcus aureus and Staphylococcus epidermidis that are resistant to other penicillins. Methicillin sodium hydrate can be used for the research of skin infections, osteomyelitis, and endocarditis. -
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Efletirizine
0 ImagesEfletirizine (EFZ) is an orally active antihistamine with high selectivity and affinity to the H1-receptor. Efletirizine can be used for allergic disease research. -
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- Chloropyramine
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Zotepine-d6
0 ImagesCat. No.: HY-W744038CAS No.: 2512222-52-3Zotepine-d6 is the deuterium labeled Zotepine (HY-103093). Zotepine, an antipsychotic agent, is a potent antagonist of 5-HT2A, 5-HT2C, Histamine H1, α1-adrenergic and Dopamine D2 receptors, with Kds of 2.6 nM, 3.2 nM, 3.3 nM, 7.3 nM and 8 nM, respectively. Zotepine exhibits antidepressive and anxiolytic effects in vivo. -
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Lodoxamide-15N2,d2
0 ImagesCat. No.: HY-W755511CAS No.: 2733832-83-0Synonyms: U-42585E free acid-15N2,d2Lodoxamide-15N2,d2 (U-42585E (free acid)-15N2,d2) is the deuterium and 15N-labeled Lodoxamide (HY-14270). Lodoxamide (U-42585E free acid) is an antiallergic compound acting as a mast-cell stabilizer for the treatment of asthma and allergic conjunctivitis. -
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Levomequitazine
0 ImagesCat. No.: HY-14845CAS No.: 88598-74-7Synonyms: (S)-MequitazineLevomequitazine (Compound V0114) ((S)-Mequitazine), the levorotatory enantiomer of Mequitazine (HY-B2168), is an orally active, inverse H4 receptor agonist (IC50s: 94 nM (hM2), 17 nM (hM3)). Levomequitazine strongly binds to human histamine H4 receptor. Levomequitazine antagonizes the activating action induced by histamine on H4 receptor. Levomequitazine induces a powerful and statistically significant anti-inflammatory effect. Levomequitazine can be used for research on inflammatory diseases. -
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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.