货号:A840009
同义名:
Neprotin; Yatrorizine
Jatrorrhizine是从一些植物种类(如Enantia chlorantha)中提取的原小檗碱生物碱,能够非竞争性抑制MAO-A和MAO-B,IC50分别为4μM和62μM,同时具有抗炎、抗微生物和抗真菌活性。
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 | MAO ↓ ↑ | MAO-A ↓ ↑ | MAO-B ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Sennoside A |
++
MAO, IC50: 17 μM |
98%+ | |||||||||||||||||
| Glycyrrhizic acid |
++++
MAO, IC50: 0.16 μM |
80% HPLC | |||||||||||||||||
| Rasagiline |
++++
MAO-A, IC50: 412 nM |
++++
MAO-B, IC50: 4.43 nM |
97% | ||||||||||||||||
| Isatin |
++
MAO, IC50: 15 μM |
+
MAO-A, IC50: 58 μM |
++
MAO-B, IC50: 14 μM |
98% | |||||||||||||||
| Paeonol |
+
MAO-A, IC50: 54.6 μM |
+
MAO-B, IC50: 42.5 μM |
98% | ||||||||||||||||
| Tranylcypromine HCl |
+++
MAO-A, IC50: 11.5 μM |
+++
MAO-B, IC50: 7 μM |
97% | ||||||||||||||||
| Moclobemide |
+++
MAO-A (5-HT), IC50: 6.1 μM |
99%+ | |||||||||||||||||
| Pargyline HCl |
++
MAO-A, Ki: 13 μM |
+++
MAO-B, Ki: 0.5 μM |
99%+ | ||||||||||||||||
| Safinamide |
++++
MAO-B, IC50: 98 nM |
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。 | |||||||||||||||||||
| 靶点 |
|
| 描述 | Jatrorrhizine is an alkaloid isolated from Coptis chinensis with neuroprotective. In vitro uptake tests showed that jatrorrhizine strongly inhibited PMAT-mediated MPP+ uptake with an IC50 value of 1.05 μM and reduced 5-HT and NE uptake mediated by hOCT2, hOCT3 and hPMAT with IC50 values of 0.1-1 μM (for OCT2 and OCT3) and 1-10 μM (for PMAT)[3]. Moreover, jatrorrhizine distinctly inhibited the proliferation of MDA-MB-231, MCF-7 and 4T1 cells with IC50 values of 11.08 ± 1.19 μM, 17.11 ± 4.54 μM and 22.14 ± 2.87 μM, induced mitochondrial dysfunction and early apoptosis involving mitochondrial apoptotic pathway[4]. JAT (Jatrorrhizine) inhibited the proliferation of HCT-116 and HT-29 cells with IC50 values of 6.75±0.29 μM and 5.29±0.13 μM, respectively, for 72 hrs. In addition, JAT inhibited Wnt signaling pathway by reducing β-catenin and increasing GSK-3β expressions. In HCT-116 nude mice xenograft model, JAT inhibited tumor growth and metastasis, and induced apoptosis of tumor cells[5]. Jatrorrhizine dose-dependently (0.1, 0.3 and 1 mg/kg) offset delayed gastric emptying and intestinal transit (geometric centre and the migration of Evans blue) in postoperative ileus[6]. JAT administration could alleviate the learning and memory deficits in AD. Furthermore, JAT treatment reduced the levels of Aβ plaques in the cortex and hippocampus of APP/PS1 double-transgenic mice[7]. |
| Concentration | Treated Time | Description | References | |
| Caco-2 cells | 10 μM | 120 minutes | To evaluate the permeability and efflux capacity of Jatrorrhizine in Caco-2 cell monolayers. Results showed a net efflux value of 1.73 ± 0.42 × 10−6 cm/s for Jatrorrhizine. | Acta Pharmacol Sin. 2019 Jan;40(1):133-142 |
| HepG2 cells | 20 μM | 24 hours | To examine the effect of Jatrorrhizine on AMPK activity, results showed that Jatrorrhizine had no significant effect on AMPK activity. | J Transl Med. 2011 May 15;9:62 |
| HepG2 cells | 40 μM | 8 hours | To examine the effect of Jatrorrhizine on LDLR mRNA expression, results showed that Jatrorrhizine had no significant effect on LDLR mRNA expression. | J Transl Med. 2011 May 15;9:62 |
| HepG2 cells | 20 μM | 8 hours | To examine the effect of Jatrorrhizine on InsR mRNA expression, results showed that Jatrorrhizine increased InsR mRNA level by around 1.5 folds. | J Transl Med. 2011 May 15;9:62 |
| MNV-infected RAW264.7 macrophages | 10, 20, 40 μM | 48 hours | To evaluate the effect of Jatrorrhizine on cytotoxicity caused by MNV infection, results showed that Jatrorrhizine significantly inhibited the reduction in cell viability caused by MNV infection | Vaccines (Basel). 2023 Jan 12;11(1):164 |
| RAW264.7 macrophages | 5, 10, 20, 40, 80, 160 μM | 48 hours | To evaluate the effect of Jatrorrhizine on the viability of RAW264.7 macrophages, results showed that Jatrorrhizine had no significant effect on cell viability at concentrations of 5-160 μM | Vaccines (Basel). 2023 Jan 12;11(1):164 |
| human umbilical cord vein endothelial cells (HUVECs) | 1 μM | 48 hours | To evaluate the protective effect of Jatrorrhizine on HUVECs under high glucose conditions, results showed that JAT reversed high glucose-induced downregulation of Akt/eNOS phosphorylation, alleviated ER stress and oxidative stress, and increased NO release. | Int J Mol Sci. 2022 Oct 11;23(20):12064 |
| RBL-2H3 cells | 20 μg/ml and 40 μg/ml | 24 hours | Inhibited RBL-2H3 cell degranulation, significantly reduced β-hexosaminidase release | J Allergy Clin Immunol. 2010 Dec;126(6):1208-17. e3 |
| Human umbilical vein endothelial cells (HUVECs) | 10 μg/ml | 24 hours | To investigate the effect of Jatrorrhizine on LPS-induced inflammatory response in HUVECs, results showed that Jatrorrhizine inhibited the HMGB1/NF-κB/NLRP3 signaling pathway. | Phytomedicine. 2022 Jun;100:154083 |
| Administration | Dosage | Frequency | Description | References | ||
| C57BL/6J mice | High-fat diet-induced obese and diabetic mouse model | Oral | 50 mg/kg/day | Once daily for 5 weeks | To evaluate the protective effect of Jatrorrhizine on vascular function in diabetic and obese mice, results showed that JAT improved endothelium-dependent relaxations, reduced blood pressure, improved glucose tolerance and insulin sensitivity, reduced hepatic lipid accumulation, and improved plasma lipid profile. | Int J Mol Sci. 2022 Oct 11;23(20):12064 |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
2.96mL 0.59mL 0.30mL |
14.78mL 2.96mL 1.48mL |
29.55mL 5.91mL 2.96mL |
|
| CAS号 | 3621-38-3 |
| 分子式 | C20H20NO4 |
| 分子量 | 338.38 |
| SMILES Code | COC1=C(OC)C2=C[N+]3=C(C4=CC(OC)=C(O)C=C4CC3)C=C2C=C1 |
| MDL No. | MFCD01310242 |
| 别名 | Neprotin; Yatrorizine |
| 运输 | 蓝冰 |
| InChI Key | MXTLAHSTUOXGQF-UHFFFAOYSA-O |
| Pubchem ID | 72323 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Inert atmosphere, 2-8°C |
| 溶解方案 |
DMSO: 3 mg/mL(8.87 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO H2O: 5 mg/mL(14.78 mM),配合低频超声助溶 |
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