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Ginsenoside Rg5/人参皂甙 Rg5 {[allProObj[0].p_purity_real_show]}

货号:A260602 同义名: 人参皂苷Rg5

Ginsenoside Rg5是一种从人参(Panax ginseng C. A. Mey.)根部分离和纯化的天然产物,具有抗炎作用。

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There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Ginsenoside Rg5/人参皂甙 Rg5 化学结构 CAS号:186763-78-0
Ginsenoside Rg5/人参皂甙 Rg5 化学结构
CAS号:186763-78-0
Ginsenoside Rg5/人参皂甙 Rg5 3D分子结构
CAS号:186763-78-0
Ginsenoside Rg5/人参皂甙 Rg5 化学结构 CAS号:186763-78-0
Ginsenoside Rg5/人参皂甙 Rg5 3D分子结构 CAS号:186763-78-0
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Ginsenoside Rg5/人参皂甙 Rg5 纯度/质量文件 产品仅供科研

货号:A260602 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 IGF-1R Insulin Receptor 其他靶点 纯度
BMS-536924 ++

IGF-1R, IC50: 100 nM

+++

Insulin Receptor, IC50: 73 nM

FAK,MEK 98%
GSK1904529A +++

IGF-1R, IC50: 27 nM

+++

Insulin Receptor, IC50: 25 nM

98+%
Picropodophyllin ++++

IGF-1R, IC50: 1 nM

99%+
NVP-AEW541 ++

IGF-1R, IC50: 0.15 μM

++

Insulin Receptor, IC50: 0.14 μM

FLT3 99%+
NVP-ADW742 +

IGF-1R, IC50: 0.17 μM

98%
GSK1838705A +++

IGF-1R, IC50: 2 nM

++++

Insulin Receptor, IC50: 1.6 nM

ALK 98%
BMS-754807 ++++

IGF-1R, IC50: 1.8 nM

++++

Insulin Receptor, IC50: 1.7 nM

99%+
Linsitinib +++

IGF-1R, IC50: 35 nM

++

Insulin Receptor, IC50: 75 nM

99%+
AG1024 +

IGF-1R, IC50: 7 μM

+

Insulin Receptor, IC50: 57 μM

98%
PQ401 +

IGF-1R, IC50: <1 μM

99%+
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。
产品名称 NF-κB 其他靶点 纯度
Ammonium pyrrolidine-1-carbodithioate 98%
QNZ ++++

NF-κB, IC50: 11 nM

99%+
Sodium 4-Aminosalicylate Dihydrate 98%
Sodium Salicylate 95%
Parthenolide p53 97% HPLC
JSH-23 +

NF-κB, IC50: 7.1 μM

98%
Phenethyl caffeate 98%
Andrographolide 98+%
Curcumin Nrf2,HDAC 98%
SC75741 +++

NF-κB, EC50: 200 nM

99%+
CBL0137 HCl ++

NF-κB, EC50: 0.47 μM

p53 99%+
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。
产品名称 COX COX-1 COX-2 其他靶点 纯度
Piroxicam 98%
Salicylic acid 98%
Phenacetin 98%
Etodolac 99%
Flunixin meglumine 98%
Ibuprofen L-lysine 98%
Nabumetone 98%
Acemetacin 98%
Diflunisal 98%
Pranoprofen 98%
Ampiroxicam 98%
Meloxicam 98%
Sulindac 98%
Ketoprofen 98%
Mefenamic Acid 95%
Bromfenac sodium 98%
Oxaprozin 99%
Aspirin 99%
Nepafenac 98%
Zaltoprofen 99%
Salicin 98%
Suprofen 99%+
Xanthohumol 99%
Parecoxib 98%
Tolfenamic Acid +++

COX-2, IC50: 0.2 μM

98%
Etoricoxib 99%
Niflumic Acid 98%
Valdecoxib ++++

COX-2, IC50: 5 nM

99+%
Ibuprofen +

COX-1, IC50: 13 μM

+

COX-2, IC50: 370 μM

98%
Indomethacin ++

COX1, IC50: 0.28 μM

+

COX-2, IC50: 14 μM

97%
Lornoxicam ++++

COX-1, IC50: 5 nM

++++

COX-2, IC50: 8 nM

98%
Meclofenamic acid sodium ++++

COX-1, IC50: 40 nM

+++

COX-2, IC50: 50 nM

99%
Asaraldehyde 98%
Naproxen +

COX-1, IC50: 8.7 μM

+

COX-2, IC50: 5.2 μM

98%
Diclofenac Sodium Salt +++

COX-1, IC50: 60 nM

+++

COX-2, IC50: 200 nM

98%
NS-398 ++

COX-2, IC50: 3.8 μM

95%
Amfenac Sodium Hydrate ++

COX-1, IC50: 250 nM

+++

COX-2, IC50: 150 nM

98%+
Nimesulide +

COX-2, IC50: 26 μM

98%
Lumiracoxib ++

COX-1, Ki: 3 μM

+++

COX-2, Ki: 60 nM

98%
Rutaecarpine 95%
Celecoxib ++++

COX-2, IC50: 40 nM

98%
Carprofen ++++

canine COX2, IC50: 30 nM

98%
Ketorolac ++

COX-1 (human), IC50: 1.23 μM

++

COX-2 (human), IC50: 3.50 μM

98%
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

Ginsenoside Rg5/人参皂甙 Rg5 生物活性

描述 Ginsenoside Rg5 is a natural product isolated and purified from the roots of Panax ginseng C. A. Mey. showing anti-inflammatory effect.

Ginsenoside Rg5/人参皂甙 Rg5 细胞实验

Cell Line
Concentration Treated Time Description References
HEK293T cells 300 nM 24 hours Increased interaction between MyoD and E2A J Ginseng Res. 2023 Nov;47(6):726-734
conventional type 1 dendritic cells (cDC1s) 50 μM 2 hours Enhanced efferocytosis of cDC1s from SLC7A11-WT mice J Ginseng Res. 2023 Nov;47(6):784-794
bone marrow-derived dendritic cells (BMDCs) 50 μM 48 hours Enhanced efferocytotic capability of BMDCs from db/db mice J Ginseng Res. 2023 Nov;47(6):784-794
SK-N-SH cells 10 μM 48 hours To evaluate the inhibitory effect of ginsenoside Rg5 on HSV-1-induced neuroinflammation, results showed that ginsenoside Rg5 significantly inhibited inflammatory cytokine expression. J Ginseng Res. 2024 Jul;48(4):384-394
Vero cells 10 μM 48 hours To evaluate the inhibitory effect of ginsenoside Rg5 on HSV-1 replication, results showed that ginsenoside Rg5 significantly inhibited HSV-1 replication. J Ginseng Res. 2024 Jul;48(4):384-394
primary pulmonary microvascular endothelial cells (PPMECs) 20 μM and 60 μM 6 hours Ginsenoside Rg5 pretreatment significantly reduced IR-induced oxidative stress, apoptosis, and mitochondrial dysfunction. J Ginseng Res. 2025 May;49(3):260-270
H9c2 cells 10 μM 2 hours Rg5 promoted HK-II binding to mitochondria and inhibited Drp1 activation via Akt activation, protecting mitochondrial morphological and functional integrity. Cell Death Dis. 2017 Feb 23;8(2):e2625
Neonatal rat ventricular myocytes (NRVMs) 10 μM 2 hours Rg5 prevented cellular acidification by combating fatty-acid oxidation and restoring PDH activity, thereby protecting mitochondrial HK-II binding and enhancing cardiomyocyte resistance to ischemic injury. Cell Death Dis. 2017 Feb 23;8(2):e2625
Primary myoblast cells 300 nM 72 hours Promoted primary myoblast differentiation, increased number of fused myoblasts J Ginseng Res. 2023 Nov;47(6):726-734
C2C12 myoblasts 100,300 nM 48 hours Promoted C2C12 myoblast differentiation, increased expression levels of MHC, troponin-T, and myogenin J Ginseng Res. 2023 Nov;47(6):726-734
Caco-2 cells 8 μM 2 hours To evaluate the effects of Rg5 on the function of ABCB1 transporter, results showed that Rg5 inhibited the function of ABCB1 transporter. J Ginseng Res. 2020 Mar;44(2):247-257
A549/T cells 2, 4, 8 μM 48 hours To evaluate the reversal effects of Rg5 on ABCB1-mediated multidrug resistance, results showed that Rg5 significantly increased the intracellular accumulation of ABCB1 substrates, thereby reversing drug resistance. J Ginseng Res. 2020 Mar;44(2):247-257
A2780/T cells 2, 4, 8 μM 48 hours To evaluate the reversal effects of Rg5 on ABCB1-mediated multidrug resistance, results showed that Rg5 significantly increased the intracellular accumulation of ABCB1 substrates, thereby reversing drug resistance. J Ginseng Res. 2020 Mar;44(2):247-257
NCI-H292 human pulmonary mucoepidermoid carcinoma cells 0, 10, 50, 100 μg/mL 2 hours To evaluate the effect of Rg5 on MUC5AC secretion and mRNA levels. Results showed that Rg5 significantly reduced MUC5AC secretion and mRNA levels without cytotoxicity. J Ginseng Res. 2023 Jan;47(1):97-105
HT22 cells 0 mg/mL, 20 mg/mL, 40 mg/mL 4 h pretreatment followed by 6 h thermal stress Investigate the protective effect of Rg5 against thermal stress-induced apoptosis in HT22 cells. Results showed Rg5 inhibited p21 expression and PARP cleavage, reduced NO production, and modulated HO-1/Nrf2 signaling and cognitive-associated proteins (e.g., BDNF, GSK3β). J Ginseng Res. 2018 Apr;42(2):225-228

Ginsenoside Rg5/人参皂甙 Rg5 动物实验

Species
Animal Model
Administration Dosage Frequency Description References
ICR mice Isoproterenol-induced cardiac ischemia model Oral 50 mg/kg 2 consecutive days Rg5 promoted Akt translocation to mitochondria, increased mitochondrial HK-II binding, suppressed Drp1 recruitment, and reduced cell apoptosis, thereby protecting the heart from ischemic injury. Cell Death Dis. 2017 Feb 23;8(2):e2625
Nude mice A549/T cell xenograft model Intraperitoneal injection 10, 30, 50 mg/kg Every 3 days for a total of nine injections To evaluate the reversal effects of Rg5 on ABCB1-mediated multidrug resistance in vivo, results showed that Rg5 significantly suppressed the growth of drug-resistant tumors. J Ginseng Res. 2020 Mar;44(2):247-257
Mice Db/db mice (diabetic model) Oral gavage 20 or 80 mg/kg/day Once daily for one week Promoted skin wound healing in diabetic mice and reduced apoptotic cells in wound areas J Ginseng Res. 2023 Nov;47(6):784-794
Zebrafish Zebrafish model Water bath exposure 2.54 mg/mL 24 hours To study the metabolic pathways and metabolites of ginsenoside Rg5 in zebrafish J Ginseng Res. 2017 Jan;41(1):78-84
C57BL/6 mice Radiation-induced acute lung injury model Intraperitoneal injection 30 mg/kg/day For 3 consecutive days Ginsenoside Rg5 pretreatment attenuated radiation-induced acute lung damage, preserved endothelial cell junction integrity, and maintained endothelial barrier function in vivo. J Ginseng Res. 2025 May;49(3):260-270

Ginsenoside Rg5/人参皂甙 Rg5 参考文献

[1]Cho YL, Hur SM, et al. Specific activation of insulin-like growth factor-1 receptor by ginsenoside Rg5 promotes angiogenesis and vasorelaxation. J Biol Chem. 2015 Jan 2;290(1):467-77.

[2]Kim TW, Joh EH, et al. Ginsenoside Rg5 ameliorates lung inflammation in mice by inhibiting the binding of LPS to toll-like receptor-4 on macrophages. Int Immunopharmacol. 2012 Jan;12(1):110-6.

Ginsenoside Rg5/人参皂甙 Rg5 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.30mL

0.26mL

0.13mL

6.52mL

1.30mL

0.65mL

13.04mL

2.61mL

1.30mL

Ginsenoside Rg5/人参皂甙 Rg5 技术信息

CAS号186763-78-0
分子式C42H70O12
分子量 767.0
SMILES Code C[C@@]([C@@]12C)(CC[C@@]3([H])C4(C)C)[C@@](C[C@@H](O)[C@]1([H])[C@@H](/C(C)=C/C/C=C(C)\C)CC2)([H])[C@]3(CC[C@@H]4O[C@@](O[C@H](CO)[C@@H](O)[C@@H]5O)([H])[C@@H]5O[C@]([C@@H]([C@@H](O)[C@@H]6O)O)([H])O[C@@H]6CO)C
MDL No. MFCD22200429
别名 人参皂苷Rg5
运输蓝冰
存储条件

In solvent -20°C: 3-6个月 -80°C: 12个月

Pure form Sealed in dry, store in freezer, under -20°C

溶解方案

DMSO: 50 mg/mL(65.19 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

请根据您的动物给药指南选择适当的溶解方案。
以下溶解方案都请先按照体外实验的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
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