Pexiganan
(Synonyms: MSI 78 free base) 目录号 : GC69691Pexiganan (MSI 78 free base) 是 magainin 2 的合成形式类似物。Pexiganan 是一种强效且具有口服活性的广谱抗菌肽。Pexiganan 可用于感染相关的研究,如糖尿病足溃疡感染。
Cas No.:147664-63-9
Sample solution is provided at 25 µL, 10mM.
Pexiganan (MSI 78 free base) is a synthetic analog of magainin 2. Pexiganan is a potent and orally active broad-spectrum antimicrobial peptide. Pexiganan can be used in the research of infections, such as diabetic foot ulcer infections[1].
Pexiganan (MIC: 0-128 μg/mL approximately) shows broad-spectrum antibacterial activity against 3,109 clinical isolates of gram-positive and gram-negative, anaerobic and aerobic bacteria[2].
Pexiganan (4 μg/mL) inhibits gastric ulcer strain and gastric cancer strain[3].
Pexiganan (1, 3, 10 or 30 mg/kg, p.o., daily for three consecutive days) shows H. pylori clearance efficiency in H. pylori-infected mouse[3].
Pexiganan (1 mg/kg, i.p.) shows antimicrobial activity in rat models of Gram-negative septic shock[4].
Animal Model: | H. pylori-infected mouse[3]. |
Dosage: | 1, 3, 10 or 30 mg/kg |
Administration: | Oral administration, daily for three consecutive days. |
Result: | Lowered H. pylori urease activities in mouse stomachs. |
Animal Model: | Rat models of Gram-negative septic shock (induced by E.coli ATCC 25922)[4]. |
Dosage: | 1 mg/kg |
Administration: | Intraperitoneal injection (i.p.) |
Result: | Displayed antimicrobial activities and survival rates of 67.7%. |
[1]. Lamb HM, et al. Pexiganan acetate. Drugs. 1998 Dec;56(6):1047-52; discussion 1053-4.
[2]. Ge Y, et al. In vitro antibacterial properties of pexiganan, an analog of magainin. Antimicrob Agents Chemother. 1999 Apr;43(4):782-8.
[3]. Zhang XL, et al. The synthetic antimicrobial peptide pexiganan and its nanoparticles (PNPs) exhibit the anti-helicobacter pylori activity in vitro and in vivo. Molecules. 2015 Mar 2;20(3):3972-85.
[4]. Giacometti A, et al. Effects of pexiganan alone and combined with betalactams in experimental endotoxic shock. Peptides. 2005 Feb;26(2):207-16.
Cas No. | 147664-63-9 | SDF | Download SDF |
别名 | MSI 78 free base | ||
分子式 | C122H210N32O22 | 分子量 | 2477.17 |
溶解度 | H2O : 100 mg/mL (40.37 mM; Need ultrasonic) | 储存条件 | Store at -20°C |
General tips | 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。 为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。 |
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Shipping Condition | 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。 |
制备储备液 | |||
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1 mg | 5 mg | 10 mg |
1 mM | 0.4037 mL | 2.0184 mL | 4.0369 mL |
5 mM | 0.0807 mL | 0.4037 mL | 0.8074 mL |
10 mM | 0.0404 mL | 0.2018 mL | 0.4037 mL |
第一步:请输入基本实验信息(考虑到实验过程中的损耗,建议多配一只动物的药量) | ||||||||||
给药剂量 | mg/kg | 动物平均体重 | g | 每只动物给药体积 | ul | 动物数量 | 只 | |||
第二步:请输入动物体内配方组成(配方适用于不溶于水的药物;不同批次药物配方比例不同,请联系GLPBIO为您提供正确的澄清溶液配方) | ||||||||||
% DMSO % % Tween 80 % saline | ||||||||||
计算重置 |
计算结果:
工作液浓度: mg/ml;
DMSO母液配制方法: mg 药物溶于 μL DMSO溶液(母液浓度 mg/mL,
体内配方配制方法:取 μL DMSO母液,加入 μL PEG300,混匀澄清后加入μL Tween 80,混匀澄清后加入 μL saline,混匀澄清。
1. 首先保证母液是澄清的;
2.
一定要按照顺序依次将溶剂加入,进行下一步操作之前必须保证上一步操作得到的是澄清的溶液,可采用涡旋、超声或水浴加热等物理方法助溶。
3. 以上所有助溶剂都可在 GlpBio 网站选购。
Quality Control & SDS
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- Purity: >99.00%
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