Alborixin
目录号 : GC91660Alborixin is an ionophore originally isolated from S. albus that has diverse biological activities.
Cas No.:57760-36-8
Sample solution is provided at 25 µL, 10mM.
Quality Control & SDS
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- Purity: >70.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
Alborixin is an ionophore originally isolated from S. albus that has diverse biological activities.1,2,3,4 It is active against B. cereus, B. megaterium, S. lactis, S. aureus, and C. xerosis (MIC50s = 0.4, <0.1, 0.8, 0.2, 0.8 mg/kg, respectively).[1] Alborixin decreases the proliferation of eight cancer cell lines (IC50s = 3.2 to 15.4 µM).[2] It induces apoptosis, decreases the mitochondrial membrane potential, and increases the levels of reactive oxygen species (ROS) in HCT116 colon cancer cells when used at a concentration of 5 µM. Alborixin (1 mg/kg) increases heart rate, right ventricular contractile force, systolic and diastolic arterial blood pressure, and plasma levels of glucose in the coronary sinus and hepatic veins, as well as decreases the QT interval and plasma levels of potassium and sodium, but not calcium, in the coronary sinus and hepatic, renal, and deep femoral veins in normotensive dogs.[3] It reduces the number of C. parvum oocytes in C. parvum-infected mice when administered at doses of 1.5 or 2.5 mg/kg.[4] Alborixin is toxic to mice (LD50 = 150 mg/kg).[1]
References:
[1].Delhomme, C., Kergomard, A., Kergomard, G., et al.Alborixin, a new antibiotic ionophore: Taxonomy, isolation and biological propertiesJ. Antibiot. (Tokyo)29(7)692-695(1976).
[2].Shah, A.M., Wani, A., Qazi, P.H., et al.Isolation and characterization of alborixin from Streptomyces scabrisporus: A potent cytotoxic agent against human colon (HCT-116) cancer cellsChem. Biol. Interact.256198-208(2016).
[3].Moins, N., Gachon, P., and Duchene-Marullaz, P.Effects of two monocarboxylic ionophores, grisorixin and alborixin, on cardiovascular function and plasma cation concentrations in the anesthetized dogJ. Cardiovasc. Pharmacol.1(6)659-671(1979).
[4].Blagburn, B.L., Sundermann, C.A., Lindsay, D.S., et al.Inhibition of Cryptosporidium parvum in neonatal Hsd:(ICR)BR Swiss mice by polyether ionophores and aromatic amidinesAntimicrob. Agents Chemother.35(7)1520-1523(1991).
Cas No. | 57760-36-8 | SDF | Download SDF |
分子式 | C48H84O14 | 分子量 | 885.2 |
溶解度 | Dichloromethane: Soluble,DMSO: Soluble,Ethanol: Soluble,Methanol: Soluble | 储存条件 | -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 | |||
1 mg | 5 mg | 10 mg | |
1 mM | 1.1297 mL | 5.6484 mL | 11.2969 mL |
5 mM | 0.2259 mL | 1.1297 mL | 2.2594 mL |
10 mM | 0.113 mL | 0.5648 mL | 1.1297 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 | |||
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% DMSO % % Tween 80 % saline | ||||||||||
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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。
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