Podophyllotoxin glucoside

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Podophyllotoxin glucoside 

Podophyllotoxin glucoside 是鬼臼毒素衍生物,具有抗肿瘤作用。

Podophyllotoxin glucoside

Podophyllotoxin glucoside Chemical Structure

CAS No. : 16481-54-2

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生物活性

Podophyllotoxin glucoside is a podophyllotoxin derivative, has anti-tumor effects[1].

分子量

576.55

Formula

C28H32O13

CAS 号

16481-54-2

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]. K R Hande, et al. Etoposide: four decades of development of a topoisomerase II inhibitor. Eur J Cancer

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Podophyllotoxin glucoside

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Podophyllotoxin glucoside 

Podophyllotoxin glucoside 是鬼臼毒素衍生物,具有抗肿瘤作用。

Podophyllotoxin glucoside

Podophyllotoxin glucoside Chemical Structure

CAS No. : 16481-54-2

规格 是否有货
100 mg   询价  
250 mg   询价  
500 mg   询价  

* Please select Quantity before adding items.

生物活性

Podophyllotoxin glucoside is a podophyllotoxin derivative, has anti-tumor effects[1].

分子量

576.55

Formula

C28H32O13

CAS 号

16481-54-2

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]. K R Hande, et al. Etoposide: four decades of development of a topoisomerase II inhibitor. Eur J Cancer

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Podophyllotoxin glucoside

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Podophyllotoxin glucoside 

Podophyllotoxin glucoside 是鬼臼毒素衍生物,具有抗肿瘤作用。

Podophyllotoxin glucoside

Podophyllotoxin glucoside Chemical Structure

CAS No. : 16481-54-2

规格 是否有货
100 mg   询价  
250 mg   询价  
500 mg   询价  

* Please select Quantity before adding items.

生物活性

Podophyllotoxin glucoside is a podophyllotoxin derivative, has anti-tumor effects[1].

分子量

576.55

Formula

C28H32O13

CAS 号

16481-54-2

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]. K R Hande, et al. Etoposide: four decades of development of a topoisomerase II inhibitor. Eur J Cancer

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Apigenin 7-glucoside(Synonyms: 芹甙元-7-葡萄糖苷; Apigenin-7-O-β-D-glucopyranoside; Cosmosiin; Apigetrin)

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Apigenin 7-glucoside (Synonyms: 芹甙元-7-葡萄糖苷; Apigenin-7-O-β-D-glucopyranoside; Cosmosiin; Apigetrin) 纯度: 98.97%

Apigenin-7-glucoside (Apigenin-7-O-β-D-glucopyranoside),ROS 清除剂,具有抗增殖,抗氧化活性。

Apigenin 7-glucoside(Synonyms: 芹甙元-7-葡萄糖苷; Apigenin-7-O-β-D-glucopyranoside;  Cosmosiin;  Apigetrin)

Apigenin 7-glucoside Chemical Structure

CAS No. : 578-74-5

规格 价格 是否有货 数量
10 mM * 1 mL in DMSO ¥1210 In-stock
5 mg ¥950 In-stock
10 mg ¥1550 In-stock
25 mg ¥3410 In-stock
50 mg ¥5760 In-stock
100 mg ¥9500 In-stock
200 mg   询价  
500 mg   询价  

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生物活性

Apigenin-7-glucoside (Apigenin-7-O-β-D-glucopyranoside) exhibits significant anti-proliferative and antioxidant activity and scavenges reactive oxygen species (ROS)[1][2].

体外研究
(In Vitro)

Apigenin 7-glucoside exhibits significant anti-proliferative activity against B16F10 melanoma cells after 24 and 48 h of incubation. Apigenin-7-glucoside provoks an increase of subG0/G1, S and G2/M phase cell proportion with a significant decrease of cell proportion in G0/G1 phases. Apigenin-7-glucoside enhances melanogenesis synthesis and tyrosinase activity of B16F10 melanoma cells[1].
Apigenin 7-glucoside specifically induces the differentiation of CD34+ cells towards the erythroid lineage and inhibited the myeloid differentiation. Apigenin 7-glucoside has strong antioxidant activity against reactive oxygen species (ROS) in vitro in a concentration-dependent manner[2].

上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

432.38

Formula

C21H20O10

CAS 号

578-74-5

中文名称

芹甙元-7-葡萄糖苷;芹菜素-7-葡萄甙;大波斯菊苷

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 : ≥ 100 mg/mL (231.28 mM)

* “≥” means soluble, but saturation unknown.

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 2.3128 mL 11.5639 mL 23.1278 mL
5 mM 0.4626 mL 2.3128 mL 4.6256 mL
10 mM 0.2313 mL 1.1564 mL 2.3128 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 (5.78 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (5.78 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 (5.78 mM); Clear solution

    此方案可获得 ≥ 2.5 mg/mL (5.78 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
*以上所有助溶剂都可在 上海金畔生物科技有限公司 网站选购。
参考文献
  • [1]. Nasr Bouzaiene N et al. Effect of apigenin-7-glucoside, genkwanin and naringenin on tyrosinase activity and melanin synthesis in B16F10 melanoma cells. Life Sci. 2016 Jan 1;144:80-5.

    [2]. Samet I et al. Olive leaf components apigenin 7-glucoside and luteolin 7-glucoside direct human hematopoietic stem cell differentiation towards erythroid lineage. Differentiation. 2015 Jun;89(5):146-55.

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Rhapontigenin 3′-O-glucoside(Synonyms: 丹叶大黄素 3′-O-葡萄糖苷)

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Rhapontigenin 3′-O-glucoside (Synonyms: 丹叶大黄素 3′-O-葡萄糖苷) 纯度: 99.74%

Rhapontigenin 3′-O-glucoside 是 Rhapontigenin 的衍生物。Rhapontigenin 是一种有效的 P450 1A1 抑制剂,可用于预防癌症。

Rhapontigenin 3

Rhapontigenin 3′-O-glucoside Chemical Structure

CAS No. : 94356-22-6

规格 价格 是否有货 数量
1 mg ¥2290 In-stock
5 mg ¥6860 In-stock
10 mg   询价  
50 mg   询价  

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生物活性

Rhapontigenin 3′-O-glucoside is a derivative of Rhapontigenin. Rhapontigenin is a potent inactivator of human P450 1A1 and is a good candidate for a cancer chemopreventive agent[1].

体外研究
(In Vitro)

Rhapontigenin exhibits a potent and selective inhibition of human P450 1A1 with an IC50 of 0.4 μM. Rhapontigenin shows 400-fold selectivity for P450 1A1 over P450 1A2 and 23-fold selectivity for P450 1A1 over P450 1B1[1].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

420.41

Formula

C21H24O9

CAS 号

94356-22-6

中文名称

丹叶大黄素 3′-O-葡萄糖苷

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)

参考文献
  • [1]. Chun YJ, et al. Mechanism-based inhibition of human cytochrome P450 1A1 by rhapontigenin. Drug Metab Dispos. 2001 Apr;29(4 Pt 1):389-93.

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Delphinidin 3-glucoside chloride(Synonyms: 氯化飞燕草素葡萄糖苷; Delphinidin 3-O-glucoside chloride; Delphinidin 3-O-β-glucoside chloride)

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Delphinidin 3-glucoside chloride (Synonyms: 氯化飞燕草素葡萄糖苷; Delphinidin 3-O-glucoside chloride; Delphinidin 3-O-β-glucoside chloride) 纯度: 99.83%

Delphinidin 3-glucoside chloride (Delphinidin 3-O-glucoside chloride) 是在欧洲越橘提取物中发现的一种活性花色苷。Delphinidin 3-glucoside chloride 诱导 B 细胞慢性淋巴细胞性白血病 (B CLL) 的促凋亡作用。Delphinidin 3-glucoside chloride 通过结合 ERβ 发挥植物雌激素活性,IC50 为 9.7 μM。Delphinidin-3-O-glucoside chloride 抑制 EGFRIC50 为 2.37 µM。

Delphinidin 3-glucoside chloride(Synonyms: 氯化飞燕草素葡萄糖苷; Delphinidin 3-O-glucoside chloride; Delphinidin 3-O-β-glucoside chloride)

Delphinidin 3-glucoside chloride Chemical Structure

CAS No. : 6906-38-3

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生物活性

Delphinidin 3-glucoside chloride (Delphinidin 3-O-glucoside chloride) is an active anthocyanin found in bilberry extract. Delphinidin 3-glucoside chloride induces a pro-apoptotic effect in B cell chronic lymphocytic leukaemia (B CLL)[1]. Delphinidin 3-glucoside chloride exerts phytoestrogen activity by binding to ERβ, with an IC50 of 9.7 μM[2]. Delphinidin-3-O-glucoside chloride inhibits EGFR with an IC50 of 2.37 µM[3].

IC50 & Target

IC50: 2.37 µM (EGFR)[3]

分子量

500.84

Formula

C21H21ClO12

CAS 号

6906-38-3

中文名称

氯化飞燕草素葡萄糖苷;氯化飞燕草素-3-O-葡萄糖苷

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

-20°C, sealed storage, away from moisture and light

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

溶解性数据
In Vitro: 

DMSO : 10 mg/mL (19.97 mM; ultrasonic and warming and heat to 60°C)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 1.9966 mL 9.9832 mL 19.9665 mL
5 mM 0.3993 mL 1.9966 mL 3.9933 mL
10 mM 0.1997 mL 0.9983 mL 1.9966 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 (sealed storage, away from moisture and 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: ≥ 0.5 mg/mL (1.00 mM); Clear solution

    此方案可获得 ≥ 0.5 mg/mL (1.00 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 5.0 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: ≥ 0.5 mg/mL (1.00 mM); Clear solution

    此方案可获得 ≥ 0.5 mg/mL (1.00 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 5.0 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
*以上所有助溶剂都可在 Shanghai Jinpan Biotech Co Ltd 网站选购。
参考文献
  • [1]. Mahmoud Alhosin, et al. Bilberry extract (Antho 50) selectively induces redox-sensitive caspase 3-related apoptosis in chronic lymphocytic leukemia cells by targeting the Bcl-2/Bad pathway. Sci Rep. 2015 Mar 11;5:8996.

    [2]. Naoki Nanashima, et al. Phytoestrogenic Activity of Blackcurrant Anthocyanins Is Partially Mediated through Estrogen Receptor Beta. Molecules. 2017 Dec 29;23(1):74.

    [3]. Candice Mazewski, et al. Comparison of the effect of chemical composition of anthocyanin-rich plant extracts on colon cancer cell proliferation and their potential mechanism of action using in vitro, in silico, and biochemical assays. Food Chem. 2018 Mar 1;242:378-388.

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Isoquercetin(Synonyms: 槲皮素-3-葡萄糖苷; Quercetin 3-glucoside)

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Isoquercetin (Synonyms: 槲皮素-3-葡萄糖苷; Quercetin 3-glucoside) 纯度: 99.61%

Isoquercetin (Quercetin 3-glucoside) 是天然存在的多酚,具有抗氧化,抗增殖和抗炎特性。Isoquercetin 通过 Nrf2/ARE 抗氧化剂信号传导途径减轻乙醇诱导的肝毒性,氧化应激和炎症反应。Isoquercetin 通过调节核因子-κB (NF-κB) 转录调节系统调节一氧化氮合酶 2 (NO2) 的表达。Isoquercetin 具有高生物利用度和低毒性,是预防糖尿病妊娠出生缺陷的有希望的候选药物。

Isoquercetin(Synonyms: 槲皮素-3-葡萄糖苷; Quercetin 3-glucoside)

Isoquercetin Chemical Structure

CAS No. : 482-35-9

规格 价格 是否有货 数量
Free Sample (0.1-0.5 mg)   Apply now  
10 mM * 1 mL in DMSO ¥550 In-stock
5 mg ¥500 In-stock
10 mg ¥800 In-stock
25 mg ¥1600 In-stock
50 mg   询价  
100 mg   询价  

* Please select Quantity before adding items.

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生物活性

Isoquercetin (Quercetin 3-glucoside) is a naturally occurring polyphenol that has antioxidant, anti-proliferative, and anti-inflammatory properties. Isoquercetin alleviates ethanol-induced hepatotoxicity, oxidative stress, and inflammatory responses via the Nrf2/ARE antioxidant signaling pathway[1]. Isoquercetin regulates the expression of nitric oxide synthase 2 (NO2) via modulating the nuclear factor-κB (NF-κB) transcription regulation system. Isoquercetin has high bioavailability and low toxicity, is a promising candidate agent to prevent birth defects in diabetic pregnancies[2].

体外研究
(In Vitro)

Isoquercetin (Quercetin 3-glucoside; 5-20 μM; 24 hours) substantially reduces ethanol-induced cytotoxicity , protects hepatic cells against ethanol-stimulated liver injury[1]. Isoquercetin (10 μM; pre-treat 1 hour) dramatically downregulates the levels of ethanol-induced iNOS protein expression in HepG2 cells[1].

上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay[1]

Cell Line: HepG2 cells
Concentration: 5 μM, 10 μM, 20 μM
Incubation Time: 24 hours
Result: Caused significantly enhanced cell viability as positive controls.

Western Blot Analysis[1]

Cell Line: HepG2 cells
Concentration: 10 μM
Incubation Time: 1 hour
Result: Decreased ethanol‐ induced iNOS protein expression.

Clinical Trial

分子量

464.38

Formula

C21H20O12

CAS 号

482-35-9

中文名称

槲皮素-3-葡萄糖苷

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 : 19.23 mg/mL (41.41 mM; Need ultrasonic)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 2.1534 mL 10.7670 mL 21.5341 mL
5 mM 0.4307 mL 2.1534 mL 4.3068 mL
10 mM 0.2153 mL 1.0767 mL 2.1534 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: ≥ 1.92 mg/mL (4.13 mM); Clear solution

    此方案可获得 ≥ 1.92 mg/mL (4.13 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 19.2 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: ≥ 1.92 mg/mL (4.13 mM); Clear solution

    此方案可获得 ≥ 1.92 mg/mL (4.13 mM,饱和度未知) 的澄清溶液。

    以 1 mL 工作液为例,取 100 μL 19.2 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: ≥ 1.92 mg/mL (4.13 mM); Clear solution

    此方案可获得 ≥ 1.92 mg/mL (4.13 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 19.2 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 上海金畔生物科技有限公司 网站选购。
参考文献
  • [1]. Lee S, et al. Relative protective activities of quercetin, quercetin-3-glucoside, and rutin in alcohol-induced liver injury. J Food Biochem. 2019 Aug 5:e13002.

    [2]. Tan C, et al. Modulation of nuclear factor-κB signaling and reduction of neural tube defects by quercetin-3-glucoside in embryos of diabetic mice. Am J Obstet Gynecol. 2018 Aug;219(2):197.e1-197.e8.

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Cynaroside(Synonyms: 木犀草苷; Luteolin 7-glucoside; Luteolin 7-O-β-D-glucoside)

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Cynaroside (Synonyms: 木犀草苷; Luteolin 7-glucoside; Luteolin 7-O-β-D-glucoside) 纯度: 98.67%

Cynaroside (Luteolin 7-glucoside) 是一个类黄酮的化合物。Cynaroside 还是一种流感依赖 RNA 的 RNA 聚合酶抑制剂,IC50 为 32 nM。

Cynaroside(Synonyms: 木犀草苷; Luteolin 7-glucoside;  Luteolin 7-O-β-D-glucoside)

Cynaroside Chemical Structure

CAS No. : 5373-11-5

规格 价格 是否有货 数量
10 mM * 1 mL in DMSO ¥1045 In-stock
5 mg ¥950 In-stock
10 mg ¥1450 In-stock
25 mg ¥2900 In-stock
50 mg ¥5000 In-stock
100 mg ¥8000 In-stock
200 mg   询价  
500 mg   询价  

* Please select Quantity before adding items.

Cynaroside 相关产品

相关化合物库:

  • Natural Product Library Plus
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  • Anti-Infection Compound Library
  • Cell Cycle/DNA Damage Compound Library
  • Natural Product Library
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  • Medicine Food Homology Compound Library
  • Phenols Library
  • Traditional Chinese Medicine Monomer Library
  • Flavonoids Library
  • Food-Sourced Compound Library

生物活性

Cynaroside (Luteolin 7-glucoside) is a flavone, a flavonoid-like chemical compound. Cynaroside is also a potent influenza RNA-dependent RNA polymerase inhibitor with an IC50 of 32 nM[1].

分子量

448.38

Formula

C21H20O11

CAS 号

5373-11-5

中文名称

木犀草苷;青兰苷

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 : 83.33 mg/mL (185.85 mM; Need ultrasonic)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 2.2303 mL 11.1513 mL 22.3025 mL
5 mM 0.4461 mL 2.2303 mL 4.4605 mL
10 mM 0.2230 mL 1.1151 mL 2.2303 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: 50% PEG300    50% saline

    Solubility: 16.67 mg/mL (37.18 mM); Suspended solution; Need ultrasonic

  • 2.

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

    Solubility: ≥ 2.08 mg/mL (4.64 mM); Clear solution

    此方案可获得 ≥ 2.08 mg/mL (4.64 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。

    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

  • 3.

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

    Solubility: ≥ 2.08 mg/mL (4.64 mM); Clear solution

    此方案可获得 ≥ 2.08 mg/mL (4.64 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 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
*以上所有助溶剂都可在 上海金畔生物科技有限公司 网站选购。
参考文献
  • [1]. Václav Zima, et al. Unraveling the Anti-Influenza Effect of Flavonoids: Experimental Validation of Luteolin and its Congeners as Potent Influenza Endonuclease Inhibitors. Eur J Med Chem. 22 August 2020, 112754.

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Chrysophanol 8-O-glucoside(Synonyms: 大黄酚-8-O-葡萄糖苷)

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Chrysophanol 8-O-glucoside (Synonyms: 大黄酚-8-O-葡萄糖苷)

Chrysophanol 8-O-glucoside 来自 Rumex acetosa 根部,具有中等的弹性蛋白酶抑制活性。

Chrysophanol 8-O-glucoside(Synonyms: 大黄酚-8-O-葡萄糖苷)

Chrysophanol 8-O-glucoside Chemical Structure

CAS No. : 13241-28-6

规格 价格 是否有货 数量
5 mg ¥5380 In-stock
10 mg ¥9140 In-stock
50 mg   询价  
100 mg   询价  

* Please select Quantity before adding items.

Chrysophanol 8-O-glucoside 相关产品

相关化合物库:

  • Natural Product Library Plus
  • Bioactive Compound Library Plus
  • Metabolism/Protease Compound Library
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  • Traditional Chinese Medicine Monomer Library
  • Food-Sourced Compound Library

生物活性

Chrysophanol 8-O-glucoside, from the roots of Rumex acetosa, shows moderate elastase inhibition activity[1].

分子量

416.38

Formula

C21H20O9

CAS 号

13241-28-6

中文名称

大黄酚-8-O-葡萄糖苷

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, sealed storage, away from moisture and light

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

参考文献
  • [1]. T. Annamalai, et al. Pulmatin from the roots of Rumex acetosa. Scholars Research Library. Der Pharmacia Lettre, 2013, 5 (5):116-119.

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Genistein 8-c-glucoside(Synonyms: 染料木素 8-C-葡萄糖苷; G8CG)

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Genistein 8-c-glucoside (Synonyms: 染料木素 8-C-葡萄糖苷; G8CG) 纯度: 99.72%

Genistein 8-c-glucoside (G8CG) 是一种葡萄糖苷。Genistein 8-c-glucoside 诱导线粒体膜去极化并诱导细胞凋亡 (apoptosis)。

Genistein 8-c-glucoside(Synonyms: 染料木素 8-C-葡萄糖苷; G8CG)

Genistein 8-c-glucoside Chemical Structure

CAS No. : 66026-80-0

规格 价格 是否有货 数量
1 mg ¥2860 In-stock
5 mg ¥8570 In-stock
10 mg   询价  
50 mg   询价  

* Please select Quantity before adding items.

Genistein 8-c-glucoside 相关产品

相关化合物库:

  • Natural Product Library Plus
  • Bioactive Compound Library Plus

生物活性

Genistein 8-c-glucoside (G8CG) is a glucoside. Genistein 8-c-glucoside induces mitochondrial membrane depolarization and induces apoptosis[1].

分子量

432.38

Formula

C21H20O10

CAS 号

66026-80-0

中文名称

染料木素 8-C-葡萄糖苷

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
参考文献
  • [1]. Antosiak A, et al. Cytotoxic activity of genistein-8-C-glucoside form Lupinus luteus L. and genistein against human SK-OV-3 ovarian carcinoma cell line. Med Chem Res. 2017;26(1):64-73.

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Emodin-8-glucoside

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Emodin-8-glucoside  纯度: 99.04%

Emodin-8-glucoside 是从芦荟中分离出的蒽醌衍生物,与 DNA 的小沟结合。

Emodin-8-glucoside

Emodin-8-glucoside Chemical Structure

CAS No. : 23313-21-5

规格 价格 是否有货 数量
5 mg ¥1600 In-stock
10 mg ¥2720 In-stock
50 mg   询价  
100 mg   询价  

* Please select Quantity before adding items.

Emodin-8-glucoside 相关产品

相关化合物库:

  • Natural Product Library Plus
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  • Natural Product Library
  • Anti-Cancer Compound Library
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  • Terpenoids Library
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  • Traditional Chinese Medicine Monomer Library
  • Food-Sourced Compound Library

生物活性

Emodin-8-glucoside is an anthraquinone derivative isolated from Aloe vera, binds to minor groove of DNA[1].

分子量

432.38

Formula

C21H20O10

CAS 号

23313-21-5

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 : 50 mg/mL (115.64 mM; ultrasonic and warming and heat to 60°C)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 2.3128 mL 11.5639 mL 23.1278 mL
5 mM 0.4626 mL 2.3128 mL 4.6256 mL
10 mM 0.2313 mL 1.1564 mL 2.3128 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: 2.08 mg/mL (4.81 mM); Suspended solution; Need ultrasonic

    此方案可获得 2.08 mg/mL (4.81 mM) 的均匀悬浊液,悬浊液可用于口服和腹腔注射。

    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。

    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: 1.67 mg/mL (3.86 mM); Suspended solution; Need ultrasonic

    此方案可获得 1.67 mg/mL (3.86 mM) 的均匀悬浊液,悬浊液可用于口服和腹腔注射。

    以 1 mL 工作液为例,取 100 μL 16.7 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
*以上所有助溶剂都可在 上海金畔生物科技有限公司 网站选购。
参考文献
  • [1]. Das A, et al. Interaction of aloe active compounds with calf thymus DNA. J Mol Recognit. 2019 Oct;32(10):e2786.

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Phloracetophenone 4′-O-glucoside

Phloracetophenone 4′-O-glucoside

  【编号】:SPR02934

  【产品名称】:Phloracetophenone 4′-O-glucoside

  【规格】:10mg

  【用途】:

  Phloracetophenone 4'-O-glucoside对照品

  编号:SPR02934
  英文名称:Phloracetophenone 4'-O-glucoside
  CAS No.:5027-30-5
  分 子 式:C14H18O9
  分 子 量:330.289
  类别:上海金畔生物科技有限公司,天然提取物
  作为标准品,对照品或者供研究用,不能直接用于人体。

Oleuropeic acid 8-O-glucoside对照品

Oleuropeic acid 8-O-glucoside对照品

  【编号】:SPR02894

  【产品名称】:Oleuropeic acid 8-O-glucoside对照品

  【规格】:10mg

  【用途】:

  Oleuropeic acid 8-O-glucoside对照品

  编号:SPR02894
  英文名称:Oleuropeic acid 8-O-glucoside
  CAS No.:865887-46-3
  分 子 式:C16H26O8
  分 子 量:346.376
  类别:上海金畔生物科技有限公司,天然提取物
  作为标准品,对照品或者供研究用,不能直接用于人体。

Norpterosin B glucoside对照品

Norpterosin B glucoside对照品

  【编号】:SPR04284

  【产品名称】:Norpterosin B glucoside对照品

  【规格】:10mg

  【用途】:

  Norpterosin B glucoside对照品

  编号:SPR04284
  英文名称:Norpterosin B glucoside
  英文别名:(2R)-12-O-beta-D-glycopyranosylnorpterosin B;(2R)-6-[(beta-D-glucopyranosyloxy)methyl]–2,3-dihydro-2,5,7-trimethyl-1H-inden-1-one
  CAS No.:1226785-88-1
  分 子 式:C19H26O7
  分 子 量:366.41
  类别:上海金畔生物科技有限公司,天然提取物
  作为标准品,对照品或者供研究用,不能直接用于人体。

Cleistanthin B(Synonyms: Diphyllin O-glucoside)

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Cleistanthin B (Synonyms: Diphyllin O-glucoside) 纯度: ≥99.0%

Cleistanthin B (Diphyllin O-glucoside) 是一种具有口服活性的芳基萘木酚素内酯糖苷。Cleistanthin B 在 Vero 细胞中表现出抗 SARS-CoV-2 作用,EC50 值为 6.51 µM。Cleistanthin B 在体内具有抗肿瘤、利尿和抗高血压的作用。

Cleistanthin B(Synonyms: Diphyllin O-glucoside)

Cleistanthin B Chemical Structure

CAS No. : 30021-77-3

规格 价格 是否有货 数量
1 mg ¥6400 In-stock
5 mg   询价  
10 mg   询价  

* Please select Quantity before adding items.

生物活性

Cleistanthin B (Diphyllin O-glucoside) is an orally active arylnaphthalene lignan lactone glycoside. Cleistanthin B exhibits anti-SARS-CoV-2 effects in Vero cells, with EC50 of 6.51 µM. Cleistanthin B also exhibits antitumor, diuretic and antihypertensive effects in vivo[1][2][3][4].

IC50 & Target

IC50: 6.51 µM (SARS-CoV-2)[1]

体外研究
(In Vitro)

Cleistanthin B exhibits anti-SARS-CoV-2 effects in Vero cells, with EC50 of 6.51 µM[1].
Cleistanthin B shows no cytotoxic to Vero cells in concentrations up to 100 µM[1].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究
(In Vivo)

Cleistanthin B (25-100 mg/kg; p.o. for 10 dys) has antitumor activity against EAC and DAL tumor mice but it is not effective against solid tumor[2].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

542.49

Formula

C27H26O12

CAS 号

30021-77-3

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)

参考文献
  • [1]. Stefanik M, et, al. Antiviral Activity of Vacuolar ATPase Blocker Diphyllin against SARS-CoV-2. Microorganisms. 2021 Feb 25;9(3):471.

    [2]. Thummar VR, et, al. Evaluation of in vivo antitumor activity of cleistanthin B in Swiss albino mice. J Tradit Complement Med. 2015 Sep 3;6(4):383-388.

    [3]. Parasuraman S, et, al. Diuretic effects of cleistanthin a and cleistanthin B from the leaves of cleistanthus collinus in wistar rats. J Young Pharm. 2012 Apr;4(2):73-7.

    [4]. Priyadharsini RP, et, al. Evaluation of the antihypertensive activity and alpha adrenergic receptor interaction of cleistanthins A and B. J Basic Clin Pharm. 2014 Sep;5(4):109-14.

所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务

Cleistanthin B(Synonyms: Diphyllin O-glucoside)

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Cleistanthin B (Synonyms: Diphyllin O-glucoside) 纯度: ≥99.0%

Cleistanthin B (Diphyllin O-glucoside) 是一种具有口服活性的芳基萘木酚素内酯糖苷。Cleistanthin B 在 Vero 细胞中表现出抗 SARS-CoV-2 作用,EC50 值为 6.51 µM。Cleistanthin B 在体内具有抗肿瘤、利尿和抗高血压的作用。

Cleistanthin B(Synonyms: Diphyllin O-glucoside)

Cleistanthin B Chemical Structure

CAS No. : 30021-77-3

规格 价格 是否有货 数量
1 mg ¥6400 In-stock
5 mg   询价  
10 mg   询价  

* Please select Quantity before adding items.

生物活性

Cleistanthin B (Diphyllin O-glucoside) is an orally active arylnaphthalene lignan lactone glycoside. Cleistanthin B exhibits anti-SARS-CoV-2 effects in Vero cells, with EC50 of 6.51 µM. Cleistanthin B also exhibits antitumor, diuretic and antihypertensive effects in vivo[1][2][3][4].

IC50 & Target

IC50: 6.51 µM (SARS-CoV-2)[1]

体外研究
(In Vitro)

Cleistanthin B exhibits anti-SARS-CoV-2 effects in Vero cells, with EC50 of 6.51 µM[1].
Cleistanthin B shows no cytotoxic to Vero cells in concentrations up to 100 µM[1].

上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究
(In Vivo)

Cleistanthin B (25-100 mg/kg; p.o. for 10 dys) has antitumor activity against EAC and DAL tumor mice but it is not effective against solid tumor[2].

上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

542.49

Formula

C27H26O12

CAS 号

30021-77-3

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)

参考文献
  • [1]. Stefanik M, et, al. Antiviral Activity of Vacuolar ATPase Blocker Diphyllin against SARS-CoV-2. Microorganisms. 2021 Feb 25;9(3):471.

    [2]. Thummar VR, et, al. Evaluation of in vivo antitumor activity of cleistanthin B in Swiss albino mice. J Tradit Complement Med. 2015 Sep 3;6(4):383-388.

    [3]. Parasuraman S, et, al. Diuretic effects of cleistanthin a and cleistanthin B from the leaves of cleistanthus collinus in wistar rats. J Young Pharm. 2012 Apr;4(2):73-7.

    [4]. Priyadharsini RP, et, al. Evaluation of the antihypertensive activity and alpha adrenergic receptor interaction of cleistanthins A and B. J Basic Clin Pharm. 2014 Sep;5(4):109-14.

所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务

Cleistanthin B(Synonyms: Diphyllin O-glucoside)

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

Cleistanthin B (Synonyms: Diphyllin O-glucoside) 纯度: ≥99.0%

Cleistanthin B (Diphyllin O-glucoside) 是一种具有口服活性的芳基萘木酚素内酯糖苷。Cleistanthin B 在 Vero 细胞中表现出抗 SARS-CoV-2 作用,EC50 值为 6.51 µM。Cleistanthin B 在体内具有抗肿瘤、利尿和抗高血压的作用。

Cleistanthin B(Synonyms: Diphyllin O-glucoside)

Cleistanthin B Chemical Structure

CAS No. : 30021-77-3

规格 价格 是否有货 数量
1 mg ¥6400 In-stock
5 mg   询价  
10 mg   询价  

* Please select Quantity before adding items.

生物活性

Cleistanthin B (Diphyllin O-glucoside) is an orally active arylnaphthalene lignan lactone glycoside. Cleistanthin B exhibits anti-SARS-CoV-2 effects in Vero cells, with EC50 of 6.51 µM. Cleistanthin B also exhibits antitumor, diuretic and antihypertensive effects in vivo[1][2][3][4].

IC50 & Target

IC50: 6.51 µM (SARS-CoV-2)[1]

体外研究
(In Vitro)

Cleistanthin B exhibits anti-SARS-CoV-2 effects in Vero cells, with EC50 of 6.51 µM[1].
Cleistanthin B shows no cytotoxic to Vero cells in concentrations up to 100 µM[1].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究
(In Vivo)

Cleistanthin B (25-100 mg/kg; p.o. for 10 dys) has antitumor activity against EAC and DAL tumor mice but it is not effective against solid tumor[2].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

542.49

Formula

C27H26O12

CAS 号

30021-77-3

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)

参考文献
  • [1]. Stefanik M, et, al. Antiviral Activity of Vacuolar ATPase Blocker Diphyllin against SARS-CoV-2. Microorganisms. 2021 Feb 25;9(3):471.

    [2]. Thummar VR, et, al. Evaluation of in vivo antitumor activity of cleistanthin B in Swiss albino mice. J Tradit Complement Med. 2015 Sep 3;6(4):383-388.

    [3]. Parasuraman S, et, al. Diuretic effects of cleistanthin a and cleistanthin B from the leaves of cleistanthus collinus in wistar rats. J Young Pharm. 2012 Apr;4(2):73-7.

    [4]. Priyadharsini RP, et, al. Evaluation of the antihypertensive activity and alpha adrenergic receptor interaction of cleistanthins A and B. J Basic Clin Pharm. 2014 Sep;5(4):109-14.

所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务

Junipediol B 8-O-glucoside对照品

Junipediol B 8-O-glucoside对照品

  【编号】:SPR02890

  【产品名称】:Junipediol B 8-O-glucoside对照品

  【规格】:10mg

  【用途】:

  Junipediol B 8-O-glucoside对照品

  编号:SPR02890
  英文名称:Junipediol B 8-O-glucoside
  CAS No.:188894-19-1
  分 子 式:C16H22O9
  分 子 量:358.343
  类别:上海金畔生物科技有限公司,天然提取物
  作为标准品,对照品或者供研究用,不能直接用于人体。

Ikshusterol 3-O-glucoside对照品

Ikshusterol 3-O-glucoside对照品

  【编号】:SPR00921

  【产品名称】:Ikshusterol 3-O-glucoside对照品

  【规格】:10mg

  【用途】:

  Ikshusterol 3-O-glucoside对照品

  编号:SPR00921
  英文名称:Ikshusterol 3-O-glucoside
  CAS No.:112137-81-2
  分 子 式:C35H60O7
  分 子 量:592.858
  类别:上海金畔生物科技有限公司,天然提取物
  作为标准品,对照品或者供研究用,不能直接用于人体。

Iriflophenone 3-C-glucoside对照品

Iriflophenone 3-C-glucoside对照品

  【编号】:SPR01493

  【产品名称】:Iriflophenone 3-C-glucoside对照品

  【规格】:10mg

  【用途】:

  Iriflophenone 3-C-glucoside对照品

  编号:SPR01493
  英文名称:Iriflophenone 3-C-glucoside
  CAS No.:104669-02-5
  分 子 式:C19H20O10
  分 子 量:408.359
  类别:上海金畔生物科技有限公司,天然提取物
  作为标准品,对照品或者供研究用,不能直接用于人体。