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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 (882)
Related Products (882)
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Antibodies (2)
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Histamine Receptor Isoform Comparison
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Burimamide
0 ImagesCat. No.: HY-124517CAS No.: 34970-69-9Burimamide is a blocker of histamine H2-receptor. Burimamide inhibits gastric acid secretion evoked by Pentagastrin (HY-A0261) or Gastrin. Burimamide also has alpha-adrenoceptor blocking activity. Burimamide in combination with the H1-receptor antagonist Mepyramine (HY-B1281) shows anti-inflammatory activity in a rat paw edema model induced by Compound 48/80 (HY-115768). -
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SCH-44643
0 ImagesCat. No.: HY-123397CAS No.: 133330-43-5SCH-44643 is an orally active platelet activating factor (PAF) and histamine antagonist. -
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Thiethylperazine (Standard)
0 ImagesThiethylperazine (Standard) is the analytical standard of Thiethylperazine. This product is intended for research and analytical applications. Thiethylperazine, a phenothiazine derivate, is an orally active and potent dopamine D2-receptor and histamine H1-receptor antagonist. Thiethylperazine is also a selective ABCC1activator that reduces amyloid-β (Aβ) load in mice. Thiethylperazine has anti-emetic, antipsychotic and antimicrobial effects. -
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Ciproxifan maleate (Standard)
0 ImagesSynonyms: FUB 359 maleate (Standard)Ciproxifan (maleate) (Standard) is the analytical standard of Ciproxifan (maleate). This product is intended for research and analytical applications. Ciproxifan maleate (FUB 359 maleate) is a potent, selective, orally bioavailable and competitive antagonist of histamine H3-receptor, with an IC50 of 9.2 nM. Ciproxifan maleate displays low apparent affinity at other receptor subtypes. Ciproxifan maleate can be used for the research of aging disorders and Alzheimer's disease. -
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Picumast
0 ImagesCat. No.: HY-106706CAS No.: 39577-20-3Synonyms: Auteral; BM 15100Picumast (Auteral; BM 15100) is an orally active antiallergic agent with histamine receptor antagonistic activity. Picumast inhibits allergy-related cascade reactions by suppressing mediator release from tissue mast cells while exerting histamine antagonistic effects. Picumast inhibits allergic reactions in rats, guinea pigs, and cynomolgus monkeys. Picumast can be used in allergy-related research. -
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Asenapine-d3,13C
0 ImagesCat. No.: HY-10121S4CAS No.: 1217729-73-1Synonyms: Org 5222-d3,13CAsenapine-d3,13C (Org 5222-d3,13C) is deuterium and 13C labeled Asenapine. Asenapine (Org 5222), 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 can be used in the research of schizophrenia and bipolar disorder. -
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Decloxizine dihydrochloride (Standard)
0 ImagesSynonyms: UCB 1402 dihydrochloride (Standard); NSC289116 dihydrochloride (Standard)Decloxizine (UCB-1402; NSC289116) dihydrochloride (Standard) is the analytical standard of Decloxizine dihydrochloride. This product is intended for research and analytical applications. Decloxizine dihydrochloride is an orally active bronchodilator that can penetrate the blood-brain barrier. Decloxizine dihydrochloride is a piperazine-type H1 histamine receptor antagonist. Decloxizine dihydrochloride selectively blocks H1 histamine receptors, inhibiting histamine-induced capillary dilation, edema, and itching. Decloxizine dihydrochloride has some 5-HT2 receptor antagonistic activity. Decloxizine dihydrochloride can be used in studies of urticaria, allergic rhinitis, and bronchial asthma. -
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GSK334429
0 ImagesCat. No.: HY-116386CAS No.: 799557-57-6GSK334429 is a selective and orally active non-imidazole histamine H3 receptor antagonist with a pKi of 9.49 against human H3 receptor. GSK334429 can be utilized in neurological research. -
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Histamine H2 receptor antagonist-1
0 ImagesCat. No.: HY-116596CAS No.: 127966-78-3Antiulcer Agent 3 is a orally active histamine H2-receptor competitive antagonist (pA2 = 6.7). Antiulcer Agent 3 reduces gastric acid secretion. Antiulcer Agent 3 reduces gastric lesions in water-immersion stress-induced ulcer rat models. Antiulcer Agent 3 protects against HCl-ethanol-induced gastric lesions in rats. Antiulcer Agent 3 can be used for the research of peptic ulcer disease. -
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OUP-186
0 ImagesCat. No.: HY-117981CAS No.: 1480830-24-7OUP-186 is a histamine H3 receptor antagonist. -
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Oxatomide (Standard)
0 ImagesCat. No.: HY-123205RCAS No.: 60607-34-3Synonyms: KW-4354 (Standard)Oxatomide (Standard) (KW-4354 (Standard)) is the analytical standard of Oxatomide (HY-123205). This product is intended for research and analytical applications. Oxatomide (KW-4354) is an orally active dual antagonist of the H1-histamine receptor and the P2X7 receptor, as well as an inhibitor of serotonin. Oxatomide possesses antihistaminic, antiallergic and anti-inflammatory activities. Oxatomide can be used in the research of allergic diseases. -
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Promethazine (Standard)
0 ImagesPromethazine (Standard) is the analytical standard of Promethazine. This product is intended for research and analytical applications. Promethazine is an orally active histamine receptor antagonist. Promethazine is first-generation antihistamine of the phenothiazine family, shows strong sedative and weak antipsychotic effects. -
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A-304121
0 ImagesCat. No.: HY-125087CAS No.: 360551-71-9A-304121 is a selective and brain penetrating H3 receptor antagonist. A-304121 is a cognition-enhancing agent. -
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Fenspiride hydrochloride (Standard)
0 ImagesFenspiride (hydrochloride) (Standard) is the analytical standard of Fenspiride (hydrochloride). This product is intended for research and analytical applications. Fenspiride, 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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Bepotastine (Standard)
0 ImagesBepotastine (Standard) is the analytical standard of Bepotastine. This product is intended for research and analytical applications. Bepotastine is a selective and orally active second-generation histamine H1 receptor antagonist, can suppress the expression of nerve growth factor (NGF). Bepotastine has the potential for allergic rhinitis, allergic conjunctivitis and urticaria/pruritus research. -
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(R)-(-)-Chlorpheniramine maleate
0 ImagesCat. No.: HY-125137CAS No.: 23095-76-3(R)-(-)-Chlorpheniramine maleate is an enantiomer of Chlorpheniramine maleate (HY-B0286A). Chlorpheniramine maleate is a H1 antihistamines. (R)-(-)-Chlorpheniramine maleate can be used for allergic diseases such as rhinitis and urticaria research. -
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Minocromil
0 ImagesCat. No.: HY-U00258CAS No.: 85118-44-1Synonyms: FPL59360Minocromil (FPL59360) is a new Anti-asthmatic agent. -
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FRG8701
0 ImagesCat. No.: HY-U00238CAS No.: 108498-50-6FRG-8701 is a new Histamine H2-receptor antagonist with an IC50 of ranging from 0.25 to 0.43 μM. -
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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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