1',4"-Sophorolactone 6',6"-diacetate (Synonyms:槐糖脂;Lactonic sophorolipid)
目录号 : KCM11530 CAS No. : 148409-20-5 纯度 : ≥95%
1',4"-Sophorolactone 6',6"-diacetate is a major glycolipid produced from fermentation of sugar by yeasts including C. bombicola. This lactone form of sophorolipid has found use as a biosurfactant, possessing lower surface tension compared to the acid form of sophorolipids.
规格 价格 是否有货 数量
500mg
In-stock
1g
In-stock
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生物活性

1',4"-Sophorolactone 6',6"-diacetate is an apoptosis inducer and antimicrobial surfactant with antitumor activity. Lactonic sophorolipid regulates Bax/Bcl-gene expression through caspase-3/9 and induces apoptosis in tumor cells. 1',4"-Sophorolactone 6',6"-diacetate can disrupt cell membrane permeability and exert antibacterial effects (MIC for oral pathogens is 100-400 μg/mL). 1',4"-Sophorolactone 6',6"-diacetate promotes mitochondrial membrane potential depolarization, activates the intrinsic apoptotic pathway, and can synergize with antibiotics to enhance the antibacterial effect. 1',4"-Sophorolactone 6',6"-diacetate can be used in liver cancer research and the development of oral hygiene antibacterial agents.

体外研究

1',4"-Sophorolactone 6',6"-diacetate inhibits HepG2 cell viability with an IC50 of 25 μg/mL (24 h) and induces apoptosis, accompanied by an increase in Caspase-3/9 enzyme activity and upregulation of Bax/Bcl-2 gene expression [1].

1',4"-Sophorolactone 6',6"-diacetate (2.5-160 μg/mL; 24 h) exhibits dose-dependent inhibition of proliferation in colon cancer cells such as HT29 and HCT116, and also has cytotoxic effects on normal cells [2].

1',4"-Sophorolactone 6',6"-diacetate (100-400 μg/mL; 24-48 h) showed antibacterial activity (MIC=100-400 μg/mL) against oral pathogens such as Streptococcus mutant strains and Actinobacteres naeslundii, and disrupted biofilm formation.

分子式
C34H56O14
分子量
688.8
CAS号
148409-20-5
中文名称
槐糖脂
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder -20°C 3 years
  4°C 2 years
In solvent -80°C 6 months
  -20°C 1 month
溶解性数据
In Vitro:

DMSO : 200 mg/mL (290.36 mM; Need ultrasonic)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 1.4518 mL 7.2590 mL 14.5180 mL
5 mM 0.2904 mL 1.4518 mL 2.9036 mL
10 mM 0.1452 mL 0.7259 mL 1.4518 mL
*

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, 6 months; -20°C, 1 month。-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。

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂:

——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
分比是指该溶剂在您配制终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶

  • 1.

    请依序添加每种溶剂:10% DMSO → 40% PEG300 → 5% Tween-80 → 45% saline

    Solubility: ≥ 2.08 mg/mL (3.02 mM); Clear solution

    此方案可获得 ≥ 2.08 mg/mL (3.02 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 20.8 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中,混合均匀;向上述体系中加入50 μL Tween-80,混合均匀;然后继续加入 450 μL生理盐水定容至 1 mL。

  • 2.

    请依序添加每种溶剂:10% DMSO  → 90% corn oil

    Solubility: ≥ 2.08 mg/mL (3.02 mM); Clear solution

    此方案可获得 ≥ 2.08 mg/mL (3.02 mM,饱和度未知) 的澄清溶液,此方案不适用于实验周期在半个月以上的实验。

    以 1 mL 工作液为例,取 100 μL 20.8 mg/mL 的澄清 DMSO 储备液加到 900 μL玉米油中,混合均匀。

The molarity calculator equation
Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)
The dilution calculator equation
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2