Gypenoside A(Synonyms: 七叶胆苷 A;绞股蓝皂苷 A)

天然产物 糖类和糖苷 Saccharides and Glycosides

Gypenoside A;(Synonyms: 七叶胆苷 A;绞股蓝皂苷 A)

Gypenoside A 是从绞股蓝中分离得到的天然产物。

Gypenoside A(Synonyms: 七叶胆苷 A;绞股蓝皂苷 A)

Gypenoside A Chemical Structure

CAS No. : 157752-01-7

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10 mg ¥5710 In-stock
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生物活性

Gypenoside A is a natural compound isolaated from Gynostemma pentaphyllum Makino[1].

分子量

899.07

Formula

C46H74O17

CAS 号

157752-01-7

中文名称

七叶胆苷 A;绞股蓝皂苷 A

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4deg;C, protect from light

*In solvent : -80deg;C, 6 months; -20deg;C, 1 month (protect from light)

参考文献
  • [1]. Liu G, et al. Determination on the glycosyl sequence of gypenoside A by TLC-FABMS. Zhong Yao Cai. 1997 Aug;20(8):398-400.

Gypenoside XLVI(Synonyms: 绞股蓝皂苷 XLVI)

天然产物 糖类和糖苷 Saccharides and Glycosides

Gypenoside XLVI;(Synonyms: 绞股蓝皂苷 XLVI) 纯度: 98.09%

Gypenoside XLVI 是一种来自绞股蓝 (Gynostamma pentaphallum) 的主要达玛烷型三萜皂苷之一。Gypenoside XLVI 具有四环三萜结构,并具有有效的非小细胞肺癌 A549 细胞抑制活性。

Gypenoside XLVI(Synonyms: 绞股蓝皂苷 XLVI)

Gypenoside XLVI Chemical Structure

CAS No. : 94705-70-1

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5 mg ¥2690 In-stock
10 mg ¥4570 In-stock
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生物活性

Gypenoside XLVI is one of the major dammarane-type triterpenoid saponins from Gynostamma pentaphallum[1]. Gypenoside XLVI has a tetracyclic triterpene structure and possess potent non-small cell lung carcinoma A549 cell inhibitory activity[2].

分子量

963.15

Formula

C48H82O19

CAS 号

94705-70-1

中文名称

绞股蓝皂苷 XLVI

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

-20deg;C, sealed storage, away from moisture and light

*In solvent : -80deg;C, 6 months; -20deg;C, 1 month (sealed storage, away from moisture and light)

参考文献
  • [1]. Zheng Y , et al. Gynosaponin TN-1 producing from the enzymatic conversion of gypenoside XLVI by naringinase and its cytotoxicity on hepatoma cell lines. Food Chem Toxicol. 2018 Sep;119:161-168.

    [2]. Zhang L , et al. Simultaneous determination of gypenoside LVI, gypenoside XLVI, 2α-OH-protopanaxadiol and their two metabolites in rat plasma by LC-MS/MS and its application to pharmacokinetic studies. J Chromatogr B Analyt Technol Biomed Life Sci. 2015 Nov 15;1005:9-16.

Gypenoside XIII(Synonyms: 绞股蓝皂苷 XIII)

天然产物 糖类和糖苷 Saccharides and Glycosides

Gypenoside XIII;(Synonyms: 绞股蓝皂苷 XIII)

Gypenoside XIII 属于绞股蓝总皂苷 (gypenosides) 中一种。绞股蓝总皂苷是从绞股蓝 (Gynostemma pentaphyllum) 中提取,具有多种药理学特性,可预防心血管疾病,特别是动脉粥样硬化。

Gypenoside XIII(Synonyms: 绞股蓝皂苷 XIII)

Gypenoside XIII Chemical Structure

CAS No. : 80325-22-0

规格 价格 是否有货
5 mg ¥2690 询问价格 货期
10 mg ¥4570 询问价格 货期

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生物活性

Gypenoside XIII is belonging to the gypenosides. Gypenosides, extracted from Gynostemma pentaphyllum, have various pharmacological properties and protect against cardiovascular diseases, especially atherosclerosis[1].

分子量

754.99

Formula

C41H70O12

CAS 号

80325-22-0

中文名称

绞股蓝皂苷 XIII

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

参考文献
  • [1]. Yang K, et al. Gypenoside XVII Prevents Atherosclerosis by Attenuating Endothelial Apoptosis and Oxidative Stress: Insight into the ERα-Mediated PI3K/Akt Pathway. Int J Mol Sci. 2017 Feb 9;18(2).

Gypenoside XLIX(Synonyms: 绞股蓝皂苷 XLIX)

天然产物 糖类和糖苷 Saccharides and Glycosides

Gypenoside XLIX (Synonyms: 绞股蓝皂苷 XLIX) 纯度: 99.35%

Gypenoside XLIX 是一种达玛烷型糖苷,是绞股蓝 (G. pentaphyllum) 的主要成分。Gypenoside XLIX 是一种选择性过氧化物酶体增殖物激活受体 (PPAR)-α 激活剂,可抑制细胞因子诱导的血管细胞粘附分子-1 (VCAM-1) 在人体内皮细胞中过度表达和过度活跃。

Gypenoside XLIX(Synonyms: 绞股蓝皂苷 XLIX)

Gypenoside XLIX Chemical Structure

CAS No. : 94987-08-3

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10 mg ¥1400 In-stock
20 mg ¥2300 In-stock
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生物活性

Gypenoside XLIX, a dammarane-type glycoside, is a prominent component of G. pentaphyllum. Gypenoside XLIX is a selective peroxisome proliferator-activated receptor (PPAR)-alpha activator and inhibits cytokine-induced vascular cell adhesion molecule-1 (VCAM-1) overexpression and hyperactivity in human endothelial cells[1].

IC50 & Target[1]

PPAR-α

 

分子量

1047.23

Formula

C52H86O21

CAS 号

94987-08-3

中文名称

绞股蓝皂苷 XLIX

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, protect from light

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

溶解性数据
In Vitro: 

DMSO : 125 mg/mL (119.36 mM; Need ultrasonic)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 0.9549 mL 4.7745 mL 9.5490 mL
5 mM 0.1910 mL 0.9549 mL 1.9098 mL
10 mM 0.0955 mL 0.4775 mL 0.9549 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 (protect from light)。-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: ≥ 6.25 mg/mL (5.97 mM); Clear solution

    此方案可获得 ≥ 6.25 mg/mL (5.97 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 62.5 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。

    将 0.9 g 氯化钠,完全溶解于 100 mL ddH₂O 中,得到澄清透明的生理盐水溶液

  • 2.

    请依序添加每种溶剂: 10% DMSO    90% (20% SBE-β-CD in saline)

    Solubility: ≥ 6.25 mg/mL (5.97 mM); Clear solution

    此方案可获得 ≥ 6.25 mg/mL (5.97 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 62.5 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。

    将 2 g 磺丁基醚 β-环糊精加入 5 mL 生理盐水中,再用生理盐水定容至 10 mL,完全溶解,澄清透明
  • 3.

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

    Solubility: ≥ 6.25 mg/mL (5.97 mM); Clear solution

    此方案可获得 ≥ 6.25 mg/mL (5.97 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 62.5 mg/mL 的澄清 DMSO 储备液加到 900 μL玉米油中,混合均匀。

*以上所有助溶剂都可在 MCE 网站选购。
参考文献
  • [1]. Huang TH , et al. Gypenoside XLIX, a naturally occurring PPAR-alpha activator, inhibits cytokine-induced vascular cell adhesion molecule-1 expression and activity in human endothelial cells. Eur J Pharmacol. 2007 Jun 22;565(1-3):158-65.

Gypenoside LXXV(Synonyms: 绞股蓝皂苷LXXV)

天然产物 糖类和糖苷 Saccharides and Glycosides

Gypenoside LXXV;(Synonyms: 绞股蓝皂苷LXXV) 纯度: 98.80%

Gypenoside LXXV 是从绞股蓝中分离出来的,是人参皂甙 Rb1 的去糖基化形式之一。Gypenoside LXXV 显著降低癌细胞活力并显示出有效的抗癌作用。

Gypenoside LXXV(Synonyms: 绞股蓝皂苷LXXV)

Gypenoside LXXV Chemical Structure

CAS No. : 110261-98-8

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生物活性

Gypenoside LXXV, isolated from Gynostemma pentaphyllum, is one of the deglycosylated shapes of ginsenoside Rb1. Gypenoside LXXV significantly reduces cancer cell viability and displays an anti-cancer effect[1].

体外研究
(In Vitro)

Gypenoside LXXV (1.0-100 μM; for 48 hours) reduces proliferation in a dose-dependent manner[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay[1]

Cell Line: Three cancer cell lines (HeLa (cervical cancer cell line), B16 (melanoma cell line), and MDA-MB231 (human breast cancer cell line)
Concentration: 1.0-100 μM
Incubation Time: For 48 hours
Result: Reduced proliferation in a dose-dependent manner and inhibited almost all cancer cells at 50 μM.

分子量

785.01

Formula

C42H72O13

CAS 号

110261-98-8

中文名称

绞股蓝皂苷LXXV

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4deg;C, protect from light

*In solvent : -80deg;C, 6 months; -20deg;C, 1 month (protect from light)

参考文献
  • [1]. Chang-Hao Cui, et al. Enhanced Production of Gypenoside LXXV Using a Novel Ginsenoside-Transforming β-Glucosidase from Ginseng-Cultivating Soil Bacteria and Its Anti-Cancer Property. Molecules. 2017 May 19;22(5):844.

Gypenoside L(Synonyms: 绞股蓝皂苷L)

天然产物 糖类和糖苷 Saccharides and Glycosides

Gypenoside L;(Synonyms: 绞股蓝皂苷L) 纯度: 99.42%

Gypenoside L 是一种皂苷,存在于 Gynostemma pentaphyllum 中。Gypenoside L 增加 SA-β-半乳糖苷酶活性,促进衰老相关分泌细胞因子的产生。Gypenoside L 还可以激活 p38ERK MAPK 通路和 NF-κB 通路以诱导衰老。Gypenoside L 具有抗肿瘤和抗炎活性。

Gypenoside L(Synonyms: 绞股蓝皂苷L)

Gypenoside L Chemical Structure

CAS No. : 94987-09-4

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生物活性

Gypenoside L is a saponin that can be found in Gynostemma pentaphyllum. Gypenoside L increases the SA-β-galactosidase activity, promotes the production of senescence-associated secretory cytokines. Gypenoside L also can activate p38 and ERK MAPK pathways and NF-κB pathway to induce senescence. Gypenoside L exhibits anti-tumor and anti-inflammatory activities[1][2].

体外研究
(In Vitro)

Gypenoside L (20-80 μg/mL; 24 h) increases the mRNA expression levels of SASP, such as IL-1α, IL-6, TIMP-1, CXCL-1 and CXCL-2 in HepG2 and ECA-109 cells[1].
Gypenoside L (20-80 μg/mL; 24 h) causes cell cycle arrest at S phase[1].
GPL (3.125-100 μg/mL) significantly inhibits LPS-induced NO accumulation in RAW264.7 cells[2].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

801.01

Formula

C42H72O14

CAS 号

94987-09-4

中文名称

绞股蓝皂苷L

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

-20deg;C, protect from light

*In solvent : -80deg;C, 6 months; -20deg;C, 1 month (protect from light)

溶解性数据
In Vitro:;

DMSO : 100 mg/mL (124.84 mM; Need ultrasonic)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 1.2484 mL 6.2421 mL 12.4842 mL
5 mM 0.2497 mL 1.2484 mL 2.4968 mL
10 mM 0.1248 mL 0.6242 mL 1.2484 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 (protect from light)。-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: ≥ 2.5 mg/mL (3.12 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (3.12 mM,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;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。

    将 0.9 g 氯化钠,完全溶解于 100 mL ddH₂O 中,得到澄清透明的生理盐水溶液

  • 2.

    请依序添加每种溶剂:;10% DMSO ;; 90% (20% SBE-β-CD in saline)

    Solubility: ≥ 2.5 mg/mL (3.12 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (3.12 mM,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。

    将 2 g 磺丁基醚 β-环糊精加入 5 mL 生理盐水中,再用生理盐水定容至 10 mL,完全溶解,澄清透明
  • 3.

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

    Solubility: ≥ 2.5 mg/mL (3.12 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (3.12 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 25.0 mg/mL 的澄清 DMSO 储备液加到 900 μL玉米油中,混合均匀。

*以上所有助溶剂都可在 MCE 网站选购。
参考文献
  • [1]. Ma J, et, al. Gypenoside L Inhibits Proliferation of Liver and Esophageal Cancer Cells by Inducing Senescence. Molecules. 2019 Mar 18;24(6):1054.

    [2]. Shen CY, et, al. Comparison of the Effects and Inhibitory Pathways of the Constituents from Gynostemma pentaphyllum against LPS-Induced Inflammatory Response. J Agric Food Chem. 2018 Oct 31;66(43):11337-11346.