HazMat Fee + There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.
| Type | HazMat fee for 500 gram (Estimated) |
| Excepted Quantity | USD 0.00 |
| Limited Quantity | USD 15-60 |
| Inaccessible (Haz class 6.1), Domestic | USD 80+ |
| Inaccessible (Haz class 6.1), International | USD 150+ |
| Accessible (Haz class 3, 4, 5 or 8), Domestic | USD 100+ |
| Accessible (Haz class 3, 4, 5 or 8), International | USD 200+ |


| 规格 | 价格 | 会员价 | 库存 | 数量 | |||
|---|---|---|---|---|---|---|---|
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| 产品名称 | H1 receptor ↓ ↑ | H2 receptor ↓ ↑ | H3 receptor ↓ ↑ | H4 receptor ↓ ↑ | Histamine receptor ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Hydroxyzine 2HCl | 99+% | ||||||||||||||||||
| Cyclizine | ✔ | 97% | |||||||||||||||||
| Loratadine |
+
B(0)AT2, IC50: 4 μM |
98% | |||||||||||||||||
| Desloratadine |
++
Histamine H1 receptor, IC50: 51 nM |
98% | |||||||||||||||||
| Doxylamine succinate | ✔ | 99% | |||||||||||||||||
| Ebastine | ✔ | 98% | |||||||||||||||||
| Tripelennamine HCl |
+
H1 receptor, IC50: 30 μM |
98% | |||||||||||||||||
| Meclizine 2HCl | ✔ | 98% | |||||||||||||||||
| Chlorpheniramine maleate |
+++
Histamine H1 receptor, IC50: 12 nM |
99% | |||||||||||||||||
| Diphenhydramine HCl | ✔ | 99% | |||||||||||||||||
| Alcaftadine |
++++
H1 receptor, pKi: 8.5 |
++
H2 receptor, pKi: 7.2 |
99%+ | ||||||||||||||||
| Fexofenadine HCl |
++
Histamine H1 receptor, IC50: 246 nM |
99%+ | |||||||||||||||||
| Bilastine |
+++
H1 receptor, Ki: 44.15 nM |
98% | |||||||||||||||||
| Pemirolast potassium | ✔ | 98% | |||||||||||||||||
| Bepotastine besilate |
+
Histamine H1 receptor, pIC50: 5.7 |
98% | |||||||||||||||||
| Mizolastine |
+++
Histamine H1 receptor, IC50: 47 nM |
98% | |||||||||||||||||
| Brompheniramine maleate | ✔ | 98% | |||||||||||||||||
| Carbinoxamine maleate salt | ✔ | 99+% | |||||||||||||||||
| Clemastine fumarate |
++++
Histamine H1 receptor, IC50: 3 nM |
98% | |||||||||||||||||
| Ketotifen fumarate salt | ✔ | 95% | |||||||||||||||||
| Rupatadine Fumarate |
++
Histamine H1 receptor, Ki: 102 nM |
PAFR | 98% | ||||||||||||||||
| Famotidine | ✔ | 97% | |||||||||||||||||
| Roxatidine Acetate HCl |
+
Histamine H2 receptor, IC50: 3.2 μM |
98% | |||||||||||||||||
| Lafutidine | ✔ | 99% | |||||||||||||||||
| Cimetidine | ✔ | 98% | |||||||||||||||||
| Nizatidine |
++++
Histamine H2 receptor, IC50: 0.9 nM |
AChE | 98% | ||||||||||||||||
| Ranitidine | ✔ | 96% | |||||||||||||||||
| Betahistine |
+
Histamine H3 receptor, IC50: 1.9 μM |
99% | |||||||||||||||||
| Ciproxifan maleate |
+++
Histamine H3 receptor, IC50: 9.2 nM |
99%+ | |||||||||||||||||
| S 38093 |
++
rat H3 receptor, Ki: 1.44 μM human H3 receptor, Ki: 1.2 μM |
98% | |||||||||||||||||
| JNJ-7777120 |
++++
Histamine H4 receptor, Ki: 4.5 nM |
99% | |||||||||||||||||
| Azelastine HCl | ✔ | 98% | |||||||||||||||||
| Epinastine HCl | ✔ | 99% | |||||||||||||||||
| Levodropropizine | ✔ | 97% | |||||||||||||||||
| Cyproheptadine HCl | ✔ | 98% | |||||||||||||||||
| Hesperetin | ✔ | 97% | |||||||||||||||||
| Olopatadine HCl | ✔ | 98% | |||||||||||||||||
| Mianserin HCl | ✔ | 99+% | |||||||||||||||||
| Buclizine 2HCl | ✔ | 95% | |||||||||||||||||
| Latrepirdine 2HCl | ✔ | GluR | 99% | ||||||||||||||||
| Cetirizine 2HCl | ✔ | 98% | |||||||||||||||||
| 1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 | |||||||||||||||||||
| 描述 | Histamine is an organic nitrogenous compound involved in local immune responses as well as regulating physiological function in the gut and acting as a neurotransmitter. Histamine acts via H1 and H2 receptors to produce vasodilation and increased vascular permeability; elevated levels of histamine are found in inflamed tissue[3]. Bilateral EP (experimental periodontitis) was induced for 2 weeks and histamine treatment (0.1 mg/kg subcutaneously) was started 5 days before the end of the experimental period in male rats. Histamine treatment partially reversed the methacholine-induced salivation reduction produced by EP while preventing SMG (submandibular gland) histological damage. Furthermore, histamine completely prevented enhanced EP-induced apoptosis. Histamine is able to reduce periodontitis-induced damage to SMG and bone structure[4]. Histamines play an important role as a neurotransmitter in the central nervous system and participate in several physiological functions, such as the regulation of body temperature, food intake, circadian rhythm and analgesia. Histamines facilitate memory performance in mice[5]. In HL-60 cells, histamine and 2-methylhistamine increased cytosolic Ca2+ concentration ([Ca2+]i) in a clemastine-sensitive manner. Histamine and 2-methylhistamine act as H1-receptor agonists in HL-60 cells[6]. |
| Concentration | Treated Time | Description | References | |
| human airway smooth muscle cells | 10 μM | ~127 seconds delay before shortening | Study histamine-induced cell contraction and shortening | ACS Nano. 2021 Jul 27;15(7):11585-11596 |
| HEK293T cells | 2.5 μM | 30 minutes | Identified CG1358 (HisT) as a histamine-specific transporter, whose transport activity is Na+-dependent but Cl−-independent, and highly specific to histamine | Sci Adv. 2022 Oct 28;8(43):eabq1780 |
| CINs (cholinergic interneurons) | 10 μM | To assess the effects of histamine on CIN excitability, results showed histamine significantly increased spontaneous firing frequency of CINs | Biol Psychiatry. 2023 Jun 1;93(11):1041-1052 | |
| PV-INs (parvalbumin-expressing fast-spiking interneurons) | 10 μM | To assess the effects of histamine on PV-IN excitability and resting membrane potential, results showed no significant effect of histamine on PV-IN excitability or resting membrane potential | Biol Psychiatry. 2023 Jun 1;93(11):1041-1052 | |
| human induced pluripotent stem cells (hiPSCs) | 10 μM | 3-5 days | promoted cardiac progenitor cell generation and cardiomyocyte differentiation | Stem Cell Res Ther. 2020 Mar 4;11(1):27 |
| HeLa cells | 30 μM | 1 min | The IC50 value of the inhibition of histamine (30 μM, 1 min)-induced Ca2+ rise was 951 nM for cetirizine/DBD-pz, which is equivalent to the IC50 value of cetirizine (867 nM) | Br J Pharmacol. 2012 Jan;165(1):167-82. |
[2]Maintz L, Novak N. Histamine and histamine intolerance. Am J Clin Nutr. 2007 May;85(5):1185-96.
[3]Greaves MW, Sabroe RA. Histamine: the quintessential mediator. J Dermatol. 1996 Nov;23(11):735-40
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
9.00mL 1.80mL 0.90mL |
44.99mL 9.00mL 4.50mL |
89.97mL 17.99mL 9.00mL |
|
| CAS号 | 51-45-6 |
| 分子式 | C5H9N3 |
| 分子量 | 111.14 |
| SMILES Code | NCCC1=CNC=N1 |
| MDL No. | MFCD00005210 |
| 别名 | Ergamine; NSC 33792 |
| 运输 | 蓝冰 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Keep in dark place, inert atmosphere, store in freezer, under -20°C |
| 溶解方案 |
H2O: 30 mg/mL(269.92 mM) |
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