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Ganoderic acid E
Ganoderic acid E 是存在于灵芝中的一个三萜化合物。
Ganoderic acid E Chemical Structure
CAS No. : 98665-14-6
规格
是否有货
5 mg
询价
10 mg
询价
25 mg
询价
* Please select Quantity before adding items.
生物活性
Ganoderic acid E is a triterpenoid found in Ganoderma lucidum[1].
分子量
512.63
Formula
C30H40O7
CAS 号
98665-14-6
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]. Kikuchi T, et al. Ganoderic acid D, E, F, and H and lucidenic acid D, E, and F, new triterpenoids from Ganoderma lucidum[J]. Chem.pharm.bull, 2008, 33(6):2624-2627.
上海金畔生物科技有限公司提供天然产物萜类及其苷类Terpenoids and Glycosides。
Ganoderic acid D(Synonyms: 灵芝酸 D) 纯度: 99.18%
Ganoderic acid D 是一种高度氧化的四环三萜类化合物 (tetracyclic triterpenoid),是灵芝 (Ganoderma lucidum) 的主要活性成分。Ganoderic acid D 上调 SIRT3 的蛋白质表达并通过 SIRT3 诱导脱乙酰化的亲环蛋白 D (CypD)。Ganoderic acid D 抑制结肠癌细胞的能量重编程,包括结肠癌细胞中的葡萄糖摄取,乳酸产生,丙酮酸和乙酰辅酶的产生。Ganoderic acid D 诱导 HeLa 人宫颈癌细胞凋亡 (apoptosis)。
Ganoderic acid D Chemical Structure
CAS No. : 108340-60-9
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价格
是否有货
数量
1 mg
¥900
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5 mg
¥2300
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10 mg
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50 mg
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Ganoderic acid D 相关产品
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Anti-Aging Compound Library
Antioxidants Compound Library
Lipid Compound Library
Oxygen Sensing Compound Library
Medicine Food Homology Compound Library
Terpenoids Library
Glutamine Metabolism Compound Library
Traditional Chinese Medicine Monomer Library
Anti-Colorectal Cancer Compound Library
生物活性
Ganoderic acid D, a highly oxygenated tetracyclic triterpenoid, is the major active component of Ganoderma lucidum. Ganoderic acid D upregulates the protein expression of SIRT3 and induces the deacetylated cyclophilin D (CypD) by SIRT3. Ganoderic acid D inhibits the energy reprogramming of colon cancer cells including glucose uptake, lactate production, pyruvate and acetyl-coenzyme production in colon cancer cells[1]. Ganoderic acid D induces HeLa human cervical carcinoma apoptosis[2].
IC50 & Target[1]
SIRT3
体外研究 (In Vitro)
Ganoderic acid D can inhibit the growth of numerous cancer cell lines and it inhibits HeLa human cervical carcinoma cells with an IC50 of 17.3 mM[2]. Ganoderic acid D (1-50 μM; 24-72 hours) reduces the cell survival rate in a dose- and time-dependent manner[2]. Ganoderic acid D (10, 50 μM; 24, 48 hours) induces G2/M phase arrest[2]. Ganoderic acid D (10, 50 μM; 24, 48 hours) induces a morphological change typical of apoptosis in HeLa cells[2]. Ganoderic acid D (10 μM; 48 hours) up-regulates 14-3-3E and PRDX3[2].
Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.
Cell Viability Assay[2]
Cell Line:
HeLa human cervical carcinoma cell line (CCL-2)
Concentration:
1, 5, 10, 20, 50 μM
Incubation Time:
24, 48, 72 hours
Result:
Reduced the cell survival rate in a dose- and time-dependent manner and had an IC50 value of 17.3 μM for 48 hours treatment.
Cell Cycle Analysis[2]
Cell Line:
HeLa human cervical carcinoma cell line (CCL-2)
Concentration:
10, 50 μM
Incubation Time:
24, 48 hours
Result:
Induced G2/M phase arrest. Displayed a cell cycle profile with an elevated G2/M cell population after 24-h treatment with 10 μM.
Apoptosis Analysis[2]
Cell Line:
HeLa human cervical carcinoma cell line (CCL-2)
Concentration:
10, 50 μM
Incubation Time:
48 hours
Result:
Induced a morphological change typical of apoptosis in HeLa cells.
Western Blot Analysis[2]
Cell Line:
HeLa human cervical carcinoma cell line (CCL-2)
Concentration:
10 μM
Incubation Time:
48 hours
Result:
Up-regulated 14-3-3E and PRDX3.
分子量
514.65
Formula
C30H42O7
CAS 号
108340-60-9
中文名称
灵芝酸 D
运输条件
Room temperature in continental US; may vary elsewhere.
[1]. Liu Z, et al. Effect of ganoderic acid D on colon cancer Warburg effect: Role of SIRT3/cyclophilin D. Eur J Pharmacol. 2018 Apr 5;824:72-77.
[2]. Yue QX, et al. Proteomics characterization of the cytotoxicity mechanism of ganoderic acid D and computer-automated estimation of the possible drug target network. Mol Cell Proteomics. 2008 May;7(5):949-61.
上海金畔生物科技有限公司提供天然产物萜类及其苷类Terpenoids and Glycosides。
Ganoderic acid H(Synonyms: 灵芝酸H) 纯度: 97.14%
Ganoderic acid H 是一种从灵芝中提取的羊毛脂烷型三萜,能通过抑制转录因子AP-1 和 NF-kappaB 信号来抑制乳腺癌细胞细胞的生长和入侵。
Ganoderic acid H Chemical Structure
CAS No. : 98665-19-1
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价格
是否有货
数量
1 mg
¥3430
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5 mg
¥10290
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10 mg
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50 mg
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Ganoderic acid H 相关产品
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生物活性
Ganoderic acid H is a lanostane-type triterpene isolated from Ganoderma lucidum. Ganoderic acid H suppresses growth and invasive behavior of breast cancer cells through the inhibition of transcription factors AP-1 and NF-kappaB signaling[1].
分子量
572.69
Formula
C32H44O9
CAS 号
98665-19-1
中文名称
灵芝酸H
运输条件
Room temperature in continental US; may vary elsewhere.
[1]. Jiang J, et al. Ganoderic acids suppress growth and invasive behavior of breast cancer cells by modulating AP-1 and NF-kappaB signaling. Int J Mol Med. 2008 May;21(5):577-84.
上海金畔生物科技有限公司提供天然产物萜类及其苷类Terpenoids and Glycosides。
Ganoderic acid A(Synonyms: 灵芝酸 A) 纯度: 99.20%
Ganoderic acid A 能够抑制 JAK-STAT3 信号通路,也能抑制细胞增殖,存活率和 ROS。
Ganoderic acid A Chemical Structure
CAS No. : 81907-62-2
规格
价格
是否有货
数量
10 mM * 1 mL in DMSO
¥1380
In-stock
1 mg
¥500
In-stock
5 mg
¥1250
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10 mg
¥2000
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25 mg
¥3200
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50 mg
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100 mg
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Ganoderic acid A 相关产品
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生物活性
Ganoderic acid A can inhibit of the JAK-STAT3 signaling pathway, also inhibit proliferation, viability, ROS.
IC50 & Target
Human Endogenous Metabolite
体外研究 (In Vitro)
A lower doses of Ganoderic acid A enhance HLA class II-mediated antigen presentation and CD4+ T cell recognition of lymphoma[1]. Ganoderic acid A promots cisplatin-induced cell death by enhancing the sensitivity of HepG2 cells to cisplatin mainly via the signal transducer and activator of transcription 3 suppression[2]. Ganoderic acid Ainhibits proliferation, viability, ROS, DPPH, and analyzed the expression of SOD1, SOD2, and SOD3 by Real time PCR in a PC-3 cell in a dose-dependent manner[3]. Ganoderic acid A effectively inhibites the proliferation of human osteosarcoma HOS and MG-63 cells in a dose-dependent manner, and induced obvious cell apoptosis in both cells[4].
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)
Ganoderic acid A treatment significantly prolonged survival of EL4 challenged mice and decreased tumor metastasis to the liver[4].
Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.
分子量
516.67
Formula
C30H44O7
CAS 号
81907-62-2
中文名称
灵芝酸 A
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)
溶解性数据
In Vitro:
DMSO : 62.5 mg/mL (120.97 mM; Need ultrasonic)
配制储备液
浓度溶剂体积质量
1 mg
5 mg
10 mg
1 mM
1.9355 mL
9.6774 mL
19.3547 mL
5 mM
0.3871 mL
1.9355 mL
3.8709 mL
10 mM
0.1935 mL
0.9677 mL
1.9355 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:
[1]. Radwan FF et al. Reduction of myeloid-derived suppressor cells and lymphoma growth by a natural triterpenoid. J Cell Biochem. 2015 Jan;116(1):102-14.
[2]. Yao X et al. Inhibition of the JAK-STAT3 signaling pathway by ganoderic acid A enhances chemosensitivity of HepG2 cells to cisplatin. Planta Med. 2012 Nov;78(16):1740-8.
[3]. Gill BS et al. Evaluating anti-oxidant potential of ganoderic acid A in STAT 3 pathway in prostate cancer. Mol Biol Rep. 2016 Sep 17.
[4]. Shao J et al. [Ganoderic acid A suppresses proliferation and invasion and induces apoptosis in human osteosarcoma cells]. Nan Fang Yi Ke Da Xue Xue Bao. 2015 May;35(5):619-24.
上海金畔生物科技有限公司提供天然产物萜类及其苷类Terpenoids and Glycosides。
Ganoderic acid B(Synonyms: 灵芝酸B) 纯度: 99.31%
Ganoderic acid B 是从灵芝中分离出的一种三萜化合物。Ganoderic acid B 能作为端粒酶抑制剂抑制 Epstein-Barr 病毒 (EBV) 抗原的活化。Ganoderic acid B 是一种 HIV-1 protease 的中等强度抑制剂。
Ganoderic acid B Chemical Structure
CAS No. : 81907-61-1
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是否有货
数量
1 mg
¥1500
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5 mg
¥3750
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生物活性
Ganoderic acid B is a triterpene isolated from a mushroom Ganoderma lucidum. Ganoderic acid B inhibits the activation of Epstein-Barr virus (EBV) antigens as telomerase inhibitor. Ganoderic acid B is a moderately active inhibitor against HIV-1 protease[1][2][3].
IC50 & Target
HIV-1 protease[3]
分子量
516.67
Formula
C30H44O7
CAS 号
81907-61-1
中文名称
灵芝酸B
运输条件
Room temperature in continental US; may vary elsewhere.
[1]. Zhou S, et al. Triterpenes and Soluble Polysaccharide Changes in Lingzhi or Reishi Medicinal Mushroom, Ganoderma lucidum (Agaricomycetes), During Fruiting Growth. Int J Med Mushrooms. 2018;20(9):859-871.
[2]. Zheng DS, et al. Triterpenoids from Ganoderma lucidum inhibit the activation of EBV antigens as telomerase inhibitors. Exp Ther Med. 2017 Oct;14(4):3273-3278.
[3]. el-Mekkawy S, et al. Anti-HIV-1 and anti-HIV-1-protease substances from Ganoderma lucidum. Phytochemistry. 1998 Nov;49(6):1651-7.
上海金畔生物科技有限公司提供天然产物萜类及其苷类Terpenoids and Glycosides。
Ganoderic acid J(Synonyms: 灵芝酸 J) 纯度: 98.27%
Ganoderic acid J 是可从真菌灵芝中分离得到的天然萜类。具有抗炎活性。
Ganoderic acid J Chemical Structure
CAS No. : 100440-26-4
规格
价格
是否有货
数量
1 mg
¥5900
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5 mg
¥14800
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10 mg
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50 mg
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Ganoderic acid J 相关产品
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生物活性
Ganoderic acid J is a natural terpenoid isolated from the Fungus Ganoderma lucidum. Ganoderic acid J possesses anti-inflammatory anti-inflammatory activity[1][2].
分子量
514.65
Formula
C30H42O7
CAS 号
100440-26-4
中文名称
灵芝酸 J
运输条件
Room temperature in continental US; may vary elsewhere.
[1]. Tsuyoshi Nishitoba, et al. New Terpenoids, Ganoderic Acid J and Ganolucidic Acid C, from the Fungus Ganoderma lucidum. Agricultural and Biological Chemistry Volume 49, 1985 – Issue 12.
[2]. Hai-Guo Su, et al. Lanostane triterpenoids with anti-inflammatory activities from Ganoderma lucidum. Phytochemistry. 2020 May;173:112256.
Ganoderic acid C2 is a bioactive triterpenoid in Ganoderma lucidum. Ganoderic acid C2 possesses the potential anti-tumor bioactivity, antihistamine, anti-aging and cytotoxic effects. Ganoderic acid C2 exhibits high inhibitory activity against the rat lens aldose reductase (RLAR) with an IC50 of 3.8 µM[1][2].
IC50 & Target
IC50: 3.8 µM (RLAR)[2]
分子量
518.68
Formula
C30H46O7
CAS 号
103773-62-2
中文名称
灵芝酸C2
运输条件
Room temperature in continental US; may vary elsewhere.
[1]. Guo XY, et al. l characterization of minor metabolites and pharmacokinetics of ganoderic acid C2 in rat plasma by HPLC coupled with electrospray ionization tandem mass spectrometry. J Pharm Biomed Anal. 2013 Mar 5;75:64-73.
[2]. Fatmawati S, et al. Inhibition of aldose reductase in vitro by constituents of Ganoderma lucidum. Planta Med. 2010 Oct;76(15):1691-3.