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- 详细信息
- 文献和实验
- 技术资料
- 英文名:
(3S,4aS,6aS,6bS,8aS,9S,9aS,12S,15aS,15bR,16aS,16bR)-3,9-Dihydroxy-9,12,16b-trimethyldocosahydrobenzo[4,5]indeno[1,2-h]pyrido[1,2-b]isoquinolin-5(15bH)-one
- 供应商:
上海安毕达生物科技有限公司
- CAS号:
18059-10-4
- 规格:
50μL/1mL/1mg/5mg/10mg
| 规格: | 50μL | 产品价格: | ¥109.0 |
|---|---|---|---|
| 规格: | 1mL | 产品价格: | ¥429.0 |
| 规格: | 1mg | 产品价格: | ¥206.0 |
| 规格: | 5mg | 产品价格: | ¥454.0 |
| 规格: | 10mg | 产品价格: | ¥706.0 |
Peiminine is an alkaloid extracted from the bulb of Fritillaria thunbergii Miq that reportedly has anticancer and anti-inflammatory effects. Peiminine downregulated the levels of specific genes and proteins in vitro and consequently suppressed OC (Osteoclasts) differentiation and function2. Peiminine inhibits lung inflammation and pulmonary fibrosis in a rat model of bleomycin-induced lung injury, by reducing circulating IFN-γ levels and inhibiting signal transduction pathways involving TGF-β, CTGF, ERK1/2, NF-κB and FasL3. Peiminine induced G0/G1-phase arrest, apoptosis, and autophagy in human osteosarcoma cells via the ROS/JNK signaling pathway both in vitro and in vivo4. Peiminine (1, 3, or 5 mg/kg) could reduce the W/D ratio and the MPO activity significantly. Furthermore, the histopathological changes and the expression of TNF-α, IL-1β, and IL-6 were inhibited after the peiminine treatment. In vitro, peiminine significantly inhibited LPS-induced IL-8 production in A549 lung epithelial cells5. Peiminine suppressed the development of CRC through inhibiting the viability, colony formation and metastasis of CRC (Colorectal cancer) cells via LINC00659/miR-760 axis6.
溶解方案(细胞实验)
DMSO 中的溶解度 : ≥ 100 mg/mL (232.75 mM; 吸湿的 DMSO 对产品的溶解度有显著影响,请使用新开封的 DMSO)|* "≥" means soluble, but saturation unknown.
溶解方案(动物实验)
"方案 一": "请依序添加每种溶剂:10% DMSO 40% PEG300 5% Tween-80 45% SalineSolubility: ≥ 2.5 mg/mL (5.82 mM); 澄清溶液 此方案可获得 ≥ 2.5 mg/mL(饱和度未知)的澄清溶液。以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中,混合均匀;再向上述体系中加入 50 μL Tween-80,混合均匀;然后再继续加入 450 μL 生理盐水 定容至 1 mL。生理盐水的配制:将 0.9 g 氯化钠,溶解于 ddH₂O 并定容至 100 mL,可以得到澄清透明的生理盐水溶液。"
"方案 二": "请依序添加每种溶剂:10% DMSO 90% (20% SBE-β-CD in Saline)Solubility: ≥ 2.5 mg/mL (5.82 mM); 澄清溶液 此方案可获得 ≥ 2.5 mg/mL(饱和度未知)的澄清溶液。以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 900 μL 20% 的 SBE-β-CD 生理盐水水溶液 中,混合均匀。2 g SBE-β-CD(磺丁基醚 β-环糊精)粉末定容于 10 mL 的生理盐水中,完全溶解至澄清透明。"
"方案 三": "请依序添加每种溶剂:10% DMSO 90% Corn OilSolubility: ≥ 2.5 mg/mL (5.82 mM); 澄清溶液 此方案可获得 ≥ 2.5 mg/mL(饱和度未知)的澄清溶液,此方案实验周期在半个月以上的动物实验酌情使用。以 1 mL 工作液为例,取 100 μL 25.0 mg/mL 的澄清 DMSO 储备液加到 900 μL玉米油中,混合均匀。"
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文献和实验Zhu M, Xu W, Jiang J, Wang Y, Guo Y, Yang R, Chang Y, Zhao B, Wang Z, Zhang J, Wang T, Shangguan L, Wang S. Peiminine Suppresses RANKL-Induced Osteoclastogenesis by Inhibiting the NFATc1, ERK, and NF-κB Signaling Pathways. Front Endocrinol (Lausanne). 2021 Sep 24;12:736863
Guo H, Ji F, Liu B, Chen X, He J, Gong J. Peiminine ameliorates bleomycin-induced acute lung injury in rats. Mol Med Rep. 2013 Apr;7(4):1103-10
Yu L, Chen Y, Yuan S, Cao Y, Bi Z. Peiminine Induces G0/G1-Phase Arrest, Apoptosis, and Autophagy via the ROS/JNK Signaling Pathway in Human Osteosarcoma Cells in Vitro and in Vivo. Front Pharmacol. 2021 Nov 12;12:770846
Du B, Cao L, Wang K, Miu J, Yao L, Xu Z, Song J. Peiminine Attenuates Acute Lung Injury Induced by LPS Through Inhibiting Lipid Rafts Formation. Inflammation. 2020 Jun;43(3):1110-1119
Li J, Qin Y, Wang W, Yang K, Zhang M. Peiminine inhibits the progression of colorectal cancer through up-regulating miR-760 via declining the expression of long noncoding RNA LINC00659. Anticancer Drugs. 2021 Feb 1;32(2):148-156
病Fusarium avenaceum、软腐病Erwinia carotovora、蛴螬等。 商品田于5月中旬采挖,洗净后分级加工,鳞茎直径3.5cm以上者,摘除心芽,分瓣的鳞片,加工品称大贝;直径3.5cm以下者,不摘心芽,加工品称珠贝。将分级后的鳞茎,撞破表皮至渗出浆液时,每100kg加贝壳灰或熟石灰3-4kg,继续撞匀,灰附着在鳞片上吸收浆液,晒干即成商品。 鳞茎含甾醇类生物碱,如贝母碱(贝母素甲Peimine Verticine)约0.1%、去氢贝母碱(贝母素乙Peiminine
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