histamine receptor 3

H3R-IN-1 Hydrochloride 是一种有效的组胺H3受体 (H3R) 的反向激动剂。

H3 receptor-MO-1 是一种有效的组胺 H3 受体 (histamine H3 receptor) 调节剂，可用于研究神经分裂和认知障碍。

PF 03654746 FA 是人组胺受体H（3）拮抗剂，可用于研究认知障碍和阿尔茨海默病。

H3 receptor antagonist 1 is used in the study of neurological diseases, histamine H3 receptor antagonist.

OUP-186 is a high affinity and human rat species-selective antagonist of histamine H3 receptor. OUP-186 suppressed the proliferation of breast cancer cells. The IC50 values at 48 hours for OUP-186 was approximately 50 μM. OUP-186 potently induced cell dea

Epinastine (WAL801) 是一种抗组胺剂和肥大细胞稳定剂。Epinastine 是一种有效的，选择性的，口服活性的组胺 H1 受体 (histamine H1 receptor) 拮抗剂。Epinastine 还抑制人嗜酸性粒细胞释放 IL-8 并具有抗过敏作用。

VUF10460 是一种非咪唑组胺 H4 受体激动剂，与大鼠H4受体结合的pKi 值为7.46。

LML134 (LML-134) 是一种可口服的高选择性组胺 H3 受体反向激动剂，有用于过度睡眠障碍的潜力，对 hH3R 的 cAMP 和 bdg 的Kis 分别为 0.3 和 12 nM。

Chloropyramine hydrochloride (Alergosan) 是一种组胺受体 H1 拮抗剂，可抑制VEGFR-3和FAK 的生化功能。

Doxepin D3 Hydrochloride is a deuterium-labeled doxepin hydrochloride.Doxepin hydrochloride is an oral active tricyclic antidepressant used as a sedative.Doxepin hydrochloride is also an effective CYP450 inhibitor, significantly inhibiting CYP450 2C19 and

H3R-IN-1 为一种高效的组胺受体 3 (H3R) 反向激动剂。

HDAC6-IN-49（Compound 3）作为HDAC的抑制剂，针对HDAC6与HDAC1的IC50值分别为0.012 μM和0.735 μM。此化合物还能够抑制MAO-B、胆碱酯酶 (ChE)、组胺受体 (H3R)以及血清素6受体 (5-HT6R)。在生物学应用方面，HDAC6-IN-49对SH-SY5Y细胞展示出神经保护效果，并在果蝇的帕金森病模型与C. elegans的阿尔茨海默病模型中改善了认知功能与运动能力。

GSK-1004723 is a novel antagonist of histamine H(1) and H(3) receptor. It represents a potential novel therapy for allergic rhinitis.

JNJ-28583867 is an inhibitor of histamine H(3) receptor antagonist and serotonin reuptake.

VUF 8328 is an agonist of histamine H(3) receptor.

A-304121 is a histamine H(3) receptor.

3-hydroxy Desloratidine is a major metabolite of desloratadine , a tricyclic antagonist of the histamine H1 receptor.

Tripelennamine 是一种乙二胺衍生物，是一种有效的组胺 H1受体拮抗剂，可减轻由组织胺引起的机体过敏反应。Tripelennamine 可用于鼻炎、结膜炎、过敏性和过敏性反应的研究。

Brompheniramine ((±)-Brompheniramine) 是具有口服活性的烷基胺类抗组胺药。Brompheniramine 是组胺 H1 受体的选择性拮抗剂 (Kd = 6.06 nM)。Brompheniramine 可用于过敏性鼻炎，它具有抗胆碱能、抗抑郁和麻醉作用。Brompheniramine 可阻断钙离子通道、钠离子通道和 hERG 通道，IC50分别为 16.12 μM, 21.26 μM 和 0.90 μM。

Izuforant (JW1601) (Compound 24) 具有有效的抗炎和止痒活性。 Izuforant 对人血清素3受体 (h5-HT3R) 具有结合亲和力，IC50值为 9.1 μM。它也是组胺 H4 受体 (H4R) 的口服活性拮抗剂，对人 H4R 的IC50值为 36 nM。

Ciproxifan (FUB-359) 是一种高效且特异性的组胺 H3 受体拮抗剂，IC50值为 9.2 nM，可用于研究衰老性疾病和阿尔兹海默症。

Abarelix acetate is a synthetic third generation gonadotropin-releasing hormone receptor (GnRHR) antagonist. It increases histamine release from rat peritoneal mast cells in vitro and from a human skin model ex vivo. In vivo, abarelix decreases plasma luteinizing hormone (LH) levels six hours post-treatment in castrated rats, with levels returning to baseline within 24 hours.3 Abarelix (2 mg kg) also transiently decreases plasma testosterone levels in intact rats, with levels returning to baseline within seven days post-treatment. Formulations containing abarelix have previously been used in the treatment of advanced prostate cancer.

Maprotiline-d3 is intended for use as an internal standard for the quantification of maprotiline by GC- or LC-MS. Maprotiline is a tricyclic antidepressant. It binds to the norepinephrine transporter (NET) and is selective for NET over the serotonin and dopamine transporters. Maprotiline also binds to the serotonin (5-HT) receptor subtype 5-HT2A, as well as histamine H1, muscarinic acetylcholine, α1-adrenergic, and dopamine D2 receptors. In vivo, maprotiline inhibits norepinephrine reuptake in rat brain and peripheral tissues. It reduces isolation-induced aggressive behavior and inhibits electrical foot-shock stimulation-induced belligerence in mice when administered at doses ranging from 3 to 10 mg kg. Maprotiline also reduces aggressive behavior in rhesus monkeys housed in groups. Formulations containing maprotiline have been used in the treatment of depression and anxiety.

Pitolisant hydrochloride (Ciproxidine) 是一种有效的、选择性的组胺 H3 受体反向激动剂，Ki 为0.16 nM。