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Histamine Receptor
Histamine Receptor Isoform Specific Products
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Histamine Receptor Inhibitors
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Histamine Receptor Produits associés (860)
Produits associés (860)
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Histamine Receptor Isoform Comparison
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Adriforant
0 ImagesCat. No.: HY-19705CAS No.: 943057-12-3Synonyms: PF-3893787PF-3893787 is a novel histamine H4 receptor antagonist binding affinity (Ki=2.4 nM) and is also a functional (Ki=1.56 nM) antagonist. -
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PIPE-791
0 ImagesCat. No.: HY-184986CAS No.: 2901868-37-7PIPE-791 is an orally active, blood-brain barrier-permeable selective antagonist of LPAR1. PIPE-791 inhibits LPA-induced calcium mobilization, collagen expression, histamine release, and the activation of fibroblasts, microglia and macrophages. PIPE-791 induces oligodendrocyte precursor cell differentiation, myelination and remyelination, and increases the number of microglia in the retina of normotensive rats. PIPE-791 protects mature oligodendrocytes from cytokine-induced death, reduces the levels of pulmonary fibrosis markers and alleviates neuroinflammation in preclinical models. PIPE-791 can be used in the research of glaucoma, neuroinflammatory diseases, chronic osteoarthritis pain, idiopathic pulmonary fibrosis and multiple sclerosis. -
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Meclizine dihydrochloride monohydrate
0 ImagesCat. No.: HY-B0349BCAS No.: 31884-77-2Synonyms: Meclozine dihydrochloride monohydrateMeclizine (Meclozine) dihydrochloride monohydrate, an antihistamine, reversibly inhibits the interaction of histamine at the H1 receptors. Meclizine dihydrochloride is a member of the piperazine class of H1 antagonists. Meclizine dihydrochloride monohydrate is an effective anti-motion sickness agent. Meclizine dihydrochloride monohydrate crosses the blood-brain barrier. Meclizine dihydrochloride monohydrate is an agonist ligand for mouse constitutive androstane receptor (CAR) and an inverse agonist for Human CAR. Meclizine dihydrochloride monohydrate can be used for the research of polyQ toxicity disorders, such as Huntington's disease. -
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S 38093 hydrochloride
0 ImagesCat. No.: HY-104003ACAS No.: 1222097-72-4S 38093 hydrochloride is a brain-penetrant, orally active antagonist of H3 receptor, with Kis of 8.8, 1.44 and 1.2 µM for rat, mouse and human H3 receptors, respectively. -
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Pemirolast
0 ImagesCat. No.: HY-137863CAS No.: 69372-19-6Pemirolast is an orally active antiallergic agent. Pemirolast attenuates Paclitaxel (HY-B0015) hypersensitivity reactions. Pemirolast can be used for bronchial asthma and conjunctivitis research-. -
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Teverelix
0 ImagesCat. No.: HY-105173CAS No.: 151272-78-5Synonyms: EP 24332 -
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Desloratadine-d4
0 ImagesCat. No.: HY-B0539SCAS No.: 381727-29-3Synonyms: Sch34117-d4Desloratadine-d4 is the deuterium labeled Desloratadine. 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[1][2]. -
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Loratadine-d4
0 ImagesCat. No.: HY-17043SCAS No.: 381727-27-1Synonyms: Loratidine-d4; SCH 29851-d4Loratadine-d4 is the deuterium labeled Loratadine. Loratadine (SCH-29851) is a selective inverse peripheral histamine H1-receptor agonist with an IC50 of >32 μM. Loratadine has anti-dengue-virus (DENV) activity. Loratadine can inhibit immunologic release of inflammatory mediators. -
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Betahistine-d3 dihydrochloride
0 ImagesBetahistine-d3 (dihydrochloride) is the deuterium labeled Betahistine dihydrochloride. Betahistine dihydrochloride is an orally active histamine H1 receptor agonist and a H3 receptor antagonist. Betahistine dihydrochloride is used for the study of rheumatoid arthritis (RA). -
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Cimetidine-d3
0 ImagesCat. No.: HY-14289SCAS No.: 1185237-29-9Synonyms: SKF-92334-d3Cimetidine-d3 is the deuterium labeled Cimetidine. Cimetidine (SKF-92334) is an orally active and inverse histamine H2 receptor antagonist with a Ki of 0.6 μM. Cimetidine is an inverse agonist. Cimetidine has anti-cancer and anti-inflammatory activity. -
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Desloratadine-d9
0 ImagesCat. No.: HY-B0539S1CAS No.: 1795024-82-6Synonyms: Sch34117-d9Desloratadine-d9 is the deuterium labeled Desloratadine. 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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Levocetirizine-d4 dihydrochloride
0 ImagesCat. No.: HY-B0814SSynonyms: (R)-Cetirizine-d4 dihydrochlorideLevocetirizine-d4 (dihydrochloride) is the deuterium labeled Levocetirizine. Levocetirizine ((R)-Cetirizine) is a third-generation peripheral H1-receptor antagonist. Levocetirizine is an antihistaminic agent which is the R-enantiomer of Cetirizine. Levocetirizine has a higher affinity for the histamine H1-receptor than (S)-Cetirizine and can effectively treat allergic rhinitis and chronic idiopathic urticaria[1]. -
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Carebastine-d5 Methyl Ester
0 ImagesCat. No.: HY-121356S1CAS No.: 1190019-51-2Carebastine-d5 Methyl Ester is the deuterium labeled Carebastine. Carebastine is the active metabolite of Ebastine. Carebastine is a histamine H1 receptor antagonist. Carebastine inhibits VEGF-induced HUVEC and HPAEC proliferation, migration and angiogenesis in a dose-dependent manner. Carebastine suppresses the expression of macrophage migration inhibitory factor. -
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Chlorprothixene-d6 hydrochloride
0 ImagesCat. No.: HY-B0274ASChlorprothixene-d6 hydrochloride is the deuterium labeled Chlorprothixene hydrochloride. Chlorprothixene hydrochloride is a dopamine and histamine receptors antagonist with Kis of 18 nM, 2.96 nM, 4.56 nM, 9 nM and 3.75 nM for hD1, hD2, hD3, hD5 and hH1 receptors, respectively. Antipsychotic activity. -
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(E/Z)-Triprolidine-d8 hydrochloride
0 ImagesCat. No.: HY-B1808SCAS No.: 1795134-06-3(E/Z)-Triprolidine-d8 (hydrochloride) is the deuterium labeled (E/Z)-Triprolidine hydrochloride. -
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Promethazine-d6 hydrochloride
0 ImagesCat. No.: HY-B1296SCAS No.: 1189947-02-1Synonyms: (±)-Promethazine-d6 hydrochloridePromethazine-d6 (hydrochloride) is the deuterium labeled Promethazine hydrochloride. Promethazine hydrochloride is an orally active histamine receptor antagonist. -
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Carebastine-d5
0 ImagesCat. No.: HY-121356SCAS No.: 1189661-02-6Carebastine-d5 is the deuterium labeled Carebastine. Carebastine is the active metabolite of Ebastine. Carebastine is a histamine H1 receptor antagonist. Carebastine inhibits VEGF-induced HUVEC and HPAEC proliferation, migration and angiogenesis in a dose-dependent manner. Carebastine suppresses the expression of macrophage migration inhibitory factor. -
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(±)-Carbinoxamine-d6
0 ImagesCat. No.: HY-B1589SCAS No.: 1216872-59-1(±)-Carbinoxamine-d6 is the deuterium labeled (±)-Carbinoxamine (HY-B1589). (±)-Carbinoxamine is a blood-brain barrier-permeable histamine H1 receptor antagonist. (±)-Carbinoxamine blocks the action of histamine on H1 receptors, reducing symptoms such as sneezing, rhinitis, rhinorrhea, erythema, pruritus and urticaria. (±)-Carbinoxamine inhibits influenza virus entry into cells via endocytosis, targets the early stage of the viral life cycle, and simultaneously reduces viral replication levels in the lungs, alleviating pathological damage and inflammatory responses in lung tissues. (±)-Carbinoxamine can be used in research on allergic rhinitis, influenza, etc. -
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N-Desmethyl diphenhydramine-d3 (hydrochloride)
0 ImagesCat. No.: HY-139519SCAS No.: 1794759-12-8N-Desmethyl diphenhydramine-d3 (hydrochloride) is the deuterium labeled N-Desmethyl diphenhydramine hydrochloride. -
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Nizatidine-d3
0 ImagesNizatidine-d3 is the deuterium labeled Nizatidine. Nizatidine is a potent and orally active histamine H2 receptor antagonist, can be used for the research of stomach?and?intestines ulcers. Nizatidine works by decreasing the secretion of gastric?acid the stomach makes and prevent ulcers from coming back after they have healed in animal models. -
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