- 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 Related Products (880)
Related Products (880)
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Antibodies (2)
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Histamine Receptor Isoform Comparison
- Dibenamine
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Histamine-15N3
0 ImagesCat. No.: HY-B1204S4Synonyms: Ergamine-15N3Histamine-15N3 is the 15N3-labeled Histamine (HY-B1204). Histamine is the agonist for histamine receptor and a vasodilator. Histamine is an organic nitrogen compound that participates in local immune responses, regulates intestinal physiological functions, and acts as a neurotransmitter. Histamine affects p38 MAPK/Akt signaling pathway, exhibits antitumor, antioxidant and anti-inflammatory activities. Histamine can be used in the research of acute myeloid leukemia, malignant melanoma, and renal cell carcinoma. -
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Lavoltidine
0 ImagesCat. No.: HY-121450CAS No.: 76956-02-0Synonyms: Loxtidine; AH-234844Lavoltidine (Loxtidine) is an an orally active, irreversible and highly potent histamine H2-receptor antagonist. Lavoltidine strongly inhibits gastric acid secretion and also induces hypergastrinemia. -
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GSK-1004723
0 ImagesCat. No.: HY-101633CAS No.: 955359-72-5GSK-1004723 is a novel H1/H3 receptor antagonist with limited activity for the suppression of seasonal allergic rhinitis. GSK-1004723 is available as a suspension or solution for intranasal administration. -
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Diphenhydramine-d3
0 ImagesCat. No.: HY-B0303S1CAS No.: 170082-18-5Diphenhydramine-d3 is the deuterium labeled Diphenhydramine (HY-B0303). Diphenhydramine is a first-generation histamine H1-receptor antagonist with anti-cholinergic effect. Diphenhydramine hydrochloride can across the ovine blood-brain barrier (BBB). -
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Nivimedone
0 ImagesCat. No.: HY-105594CAS No.: 49561-92-4Synonyms: BRL 10833 free baseNivimedone (BRL 10833 free base) is an orally active antiallergic agent. Nivimedone inhibits IgE-mediated passive cutaneous anaphylaxis in rats. Nivimedone suppresses antigen-induced histamine release from lung tissues passively sensitized with atopic serum. Nivimedone can be used in research related to bronchial asthma. -
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Platelet aggregation-IN-3
0 ImagesCat. No.: HY-176060CAS No.: 1029802-21-8Platelet aggregation-IN-3 (Compound 5) is a ligand for H2 histamine receptors, α2(A,C)-adrenergic receptors (α2-AR), and 5-HT2(B,C) serotonin receptors. Platelet aggregation-IN-3 can inhibit platelet aggregation induced by ADP and collagen and can also modulate tumour cell-induced platelet aggregation (TCIPA). Platelet aggregation-IN-3 is promising for research of antiplatelet therapy in cardiovascular diseases and the prevention of cancer-related thrombosis and tumour metastasis. -
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Dacemazine hydrochloride
0 ImagesCat. No.: HY-119913ACAS No.: 25384-29-6Synonyms: Ahistan hydrochlorideDacemazine hydrochloride (Ahistan hydrochloride) is a phenothiazine derivative that functions as an H1 histamine antagonist and has been evaluated for its potential as an anticancer agent. -
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Chlorpheniramine-d4 maleate
0 ImagesCat. No.: HY-B0286ASCAS No.: 2747915-71-3Chlorpheniramine-d4 (maleate) is deuterium labeled Chlorpheniramine (maleate). -
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ORF 17583
0 ImagesCat. No.: HY-182427CAS No.: 78441-46-0ORF 17583 is a Ranitidine (HY-B0693) analogue and H2 receptor antagonist. ORF 17583 exhibits typical reversible competitive antagonism in the guinea pig right atria model, causing a dose-dependent rightward shift of the histamine concentration-response curve without reducing the maximum effect, and its action is fully reversible upon washing. ORF 17583 can be used for research on peptic ulcers and hyperacidity. -
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Alimemazine
0 ImagesAlimemazine is a phenothiazine derivative that is generally used as an antipruritic agent and also a hemagglutinin (HA)-receptor antagonist.Alimemazine (Trimeprazine) is also acts as a partial agonist against the histamine H1 receptor (H1R) and other GPCRs. Alimemazine displays antiserotonin, antispasmodic, and antiemetic properties. -
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Cetirizine N-oxide dihydrochloride
0 ImagesCat. No.: HY-W653762ACetirizine N-oxide dihydrochloride is an oxidative degradation product of the histamine H1 receptor antagonist Cetirizine (HY-17042). -
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4'-O-Methylnyasol
0 ImagesCat. No.: HY-N8426CAS No.: 79004-25-4Synonyms: Ellisinin A4'-O-Methylnyasol is an inhibitor of β-hexosaminidase. 4'-O-Methylnyasol inhibits β-hexosaminidase release from rat basophilic leukemia-2H3 cells with an IC50 of 52.67 μM. -
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Azelastine-13C,d3 hydrochloride
0 ImagesCat. No.: HY-B0462SAzelastine-13C,d3 (hydrochloride) is the 13C- and deuterium labeled Azelastine hydrochloride. Azelastine-13C,d3 (hydrochloride), an antihistamine, is a potent and selective histamine 1 (H1) antagonist. Azelastine-13C,d3 (hydrochloride) can be used for the research of allergic rhinitis, asthma, diabetic hyperlipidemic and SARS-CoV-2. -
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2-(5,6,7,8-Tetrahydroimidazo[1,5-a]pyridin-1-yl)ethanamine dihydrochloride
0 ImagesCat. No.: HY-184787CAS No.: 51132-15-12-(5,6,7,8-Tetrahydroimidazo[1,5-a]pyridin-1-yl) ethanamine dihydrochloride is a histamine receptor-inactive compound that serves as a negative control. -
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Desloratadine-d4 hydrobromide
0 ImagesCat. No.: HY-B0539S4Synonyms: Sch34117-d4 hydrobromideDesloratadine-d4 hydrobromide is deuterated labeled Desloratadine (HY-B0539). Desloratadine (Sch34117) is the orally active major metabolite of the nonsedating H1-antihistamine Loratadine. Desloratadine is a selective H1-receptor antagonist that has anti-allergic and anti-inflammatory activities. -
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- H3R antagonist 7
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Mepyramine-d2
0 ImagesCat. No.: HY-118807SSynonyms: Pyrilamine-d2Mepyramine-d2 (Pyrilamine-d2) is the d2-labeled Mepyramine (HY-118807). Mepyramine (Pyrilamine) is a selective histamine H1 receptor antagonist and KCNQ channel inhibitor, with an IC50 of 12.5 μM against KCNQ2/Q3. Mepyramine shows no activity against allergic asthma in mice when used alone, but modulates the effect of JNJ 7777120 (HY-13508) on allergic asthma in mice; it inhibits the development of morphine physical dependence and increases histamine levels in mouse brains. Mepyramine can be used in studies related to seizures, convulsions, allergic asthma and morphine physical dependence. -
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AY 29315
0 ImagesCat. No.: HY-167141CAS No.: 114394-28-4AY 29315 is a selective and orally active histamine H2-receptor antagonist. AY 29315 can inhibit astric acid secretion and shows antiulcer activity. AY 29315 can be used for the research of gastric ulcer. -
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Buclizine dihydrochloride (Standard)
0 ImagesCat. No.: HY-A0128ARCAS No.: 129-74-8Buclizine (dihydrochloride) (Standard) is the analytical standard of Buclizine (dihydrochloride). This product is intended for research and analytical applications. Buclizine dihydrochloride is an orally active antihistamine antiallergic compound. Buclizine dihydrochloride is a potent teratogen in the rat and shows anti-tumor activity. -
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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.