Histamine Receptor

Histamine Receptor(组胺受体)

Histamine receptor has 4 subtypes (H1,H2,H3 and H4) which mediates various biological fuctions, including allergic reaction, gastric acid secretion and inflammation etc.

Histamine Receptor 相关产品(236)

  • GC37959 structure
    GC37959Zaltidine
    CAS: 85604-00-8
    纯度: >99.00%

    Zaltidine(CP-57361)是H2受体拮抗剂,有抗分泌活性。

  • GC38450 structure
    GC38450LML134
    CAS: 1542135-76-1
    纯度: >99.50%

    LML134 (化合物 18b) 是一种具有口服活性,高选择性 H3R (组胺 3 受体) 反向激动剂,对 hH3R 的 cAMP 和 bdg 的 Kis 分别为 0.3 nM 和 12 nM。LML134 快速穿透大脑,导致高 H3R 占有率,并以快速的动力学特征使其目标脱离。LML134 用于治疗过度睡眠障碍。

  • GC38558 structure
    GC38558PF-03654746 Tosylate
    CAS: 1039399-17-1
    纯度: >99.50%

    PF-03654746 Tosylate (PF-03654746) 是一种有效的选择性组胺 H3 receptor 拮抗剂,具有脑渗透性。PF-03654746 Tosylate (PF-03654746) 可减少过敏原引起的鼻炎反应。PF-03654746 Tosylate (PF-03654746) 用于治疗人类认知障碍,改善阿尔茨海默病人 (AD) 的认知。

  • GC39378 structure
    GC39378Emedastine
    CAS: 87233-61-2
    纯度: >98.00%

    A histamine H 1 receptor antagonist

  • GC39479 structure
    GC39479Bepotastine
    CAS: 125602-71-3
    纯度: >98.00%

    Bepotastine是一种非镇静的、具有口服活性的第二代组胺H1受体(histamine H1 receptor)拮抗剂,其作用选择性高于H3受体、α1、α2和β肾上腺素能受体、多巴胺D2受体、血清素5-HT2受体、乙酰胆碱迷走神经受体以及苯二氮䓬受体。

  • GC39735 structure
    GC39735Triprolidine hydrochloride monohydrate
    CAS: 6138-79-0
    纯度: >99.50%

    Triprolidine Hydrochloride is the hydrochloride salt form of Triprolidine, which is the first generation histamine H1 antagonist used in allergic rhinitis.

  • GC41715 structure
    GC41715(R)-Cetirizine (hydrochloride)
    CAS: 130018-87-0
    纯度: >99.50%

    A selective histamine H 1 receptor antagonist

  • GC43353 structure
    GC43353Cyproheptadine (hydrochloride hydrate)
    CAS: 41354-29-4
    纯度: >99.00%

    An antihistamine with antiserotonergic and anticholinergic activities

  • GC43427 structure
    GC43427Dexchlorpheniramine (maleate)
    CAS: 2438-32-6
    纯度: >98.00%

    A histamine H 1 receptor antagonist

  • GC43598 structure
    GC43598Emedastine (fumarate)
    CAS: 87233-62-3
    纯度: >98.00%

    A histamine H 1 receptor antagonist

  • GC44360 structure
    GC44360Nedocromil (sodium salt)
    CAS: 69049-74-7
    纯度: >98.00%

    A mast cell stabilizer

  • GC46185 structure
    GC46185Nimbin
    CAS: 5945-86-8
    纯度: >98.00%

    A limonoid with diverse biological activities

  • GC48835 structure
    GC48835Diphenylpyraline
    CAS: 147-20-6
    纯度: >95.00%

    A histamine H 1 receptor antagonist

  • GC48892 structure
    GC48892NSC 19005
    CAS: 5452-87-9
    纯度: >95.00%

    A potential impurity found in commercial preparations of betahistine

  • GC50405 structure
    GC50405JNJ 39758979 dihydrochloride

    高亲和力和选择性组胺H4拮抗剂;口服生物利用度

  • GC60072 structure
    GC60072Betahistine
    CAS: 5638-76-6
    纯度: >98.00%

    A histamine H 3 receptor antagonist and histamine H 1 receptor agonist

  • GC60563 structure
    GC60563Acrivastine D7
    CAS: 172165-56-9

    AcrivastineD7(BW825CD7)是Acrivastine的一种氘代化合物。Acrivastine是一种短效的histamine1受体拮抗剂。

  • GC60641 structure
    GC60641Betahistine mesylate
    CAS: 54856-23-4
    纯度: >98.00%

    Betahistine mesylate is the mesylate salt form of Betahistine, a histamine analog and H3 receptor agonist that serves as a vasodilator.

  • GC60691 structure
    GC60691Cetirizine Impurity C
    CAS: 83881-59-8

    CetirizineImpurityC是Cetirizine的一种杂质。Cetirizine是羟嗪的羧化代谢物,是第二代抗组胺剂。Cetirizine是一种特异的、具有口服活性的H1受体(histamineH1-receptor)的长效拮抗剂。

  • GC60709 structure
    GC60709Cinnarizine D8
    CAS: 1185242-27-6

    An internal standard for the quantification of cinnarizine

  • GC60791 structure
    GC60791Doxepin D3 Hydrochloride
    CAS: 347840-07-7

    DoxepinD3Hydrochloride是DoxepinHydrochloride的氘代物。Doxepinhydrochloride是一种口服活性的三环抗抑郁药。Doxepinhydrochloride是一种有效的选择性组胺受体H1拮抗剂。Doxepinhydrochloride也是一种有效的CYP450抑制剂,并显着抑制CYP4502C19和CYP4501A2。

  • GC60924 structure
    GC60924Hydroxyzine D8
    CAS: 1189480-47-4

    An internal standard for the quantification of hydroxyzine

  • GC61256 structure
    GC61256Rupatadine D4 fumarate
    CAS: 1795153-63-7

    RupatadineD4fumarate(UR-12592D4fumarate)是Rupatadinefumarate的氘代标记物。RupatadineFumarate(UR-12592Fumarate)富马酸盐是PAF/H1受体双抑制剂,Ki值分别为0.55μM和0.1μM。

  • GC61401 structure
    GC61401Oxatomide
    CAS: 60607-34-3
    纯度: >99.00%

    Oxatomide是一种口服活性的H1受体拮抗剂(抗组胺药)。