20(S)-人参皂苷Rh2

20(S)-人参皂苷Rh2结构式
20(S)-人参皂苷Rh2结构式
品牌特惠专场
常用名 20(S)-人参皂苷Rh2 英文名 20(S)-Ginsenoside Rh2
CAS号 78214-33-2 分子量 622.873
密度 1.2±0.1 g/cm3 沸点 726.4±60.0 °C at 760 mmHg
分子式 C36H62O8 熔点 N/A
MSDS 中文版 美版 闪点 393.1±32.9 °C
符号 GHS07
GHS07
信号词 Warning

Ginsenoside Rh2 mediates changes in the microRNA expression profile of human non-small cell lung cancer A549 cells.

Oncol. Rep. 29(2) , 523-8, (2013)

Non-small cell lung cancer (NSCLC) is the most common type of lung cancer insensitive to chemotherapy. Efforts are, therefore, directed toward understanding the molecular mechanisms of chemotherapy insensitivity and the development of new anticancer drugs. Gi...

Structural modification of ginsenoside Rh(2) by fatty acid esterification and its detoxification property in antitumor.

Bioorg. Med. Chem. Lett. 22(2) , 1082-5, (2012)

Ginsenoside Rh(2), one of the most important ginsenosides with anticancer properties in red ginseng, has been developed as principal antitumor ingredient for clinical use. However, the cytotoxicity test in human hepatocyte cell line QSG-7701 (IC(50) 37.3μM) i...

A dynamic study on reversal of multidrug resistance by ginsenoside Rh₂ in adriamycin-resistant human breast cancer MCF-7 cells.

Talanta 88 , 345-51, (2012)

The quartz crystal microbalance (QCM) dynamic measurements indicate that ginsenoside Rh(2) (G-Rh(2)) could inhibit the proliferation of adriamycin-resistant human breast cancer MCF-7 cells (MCF-7/ADR) in a concentration-dependent way. The combined treatment o...

In vitro studies on the oxidative metabolism of 20(s)-ginsenoside Rh2 in human, monkey, dog, rat, and mouse liver microsomes, and human liver s9.

Drug Metab. Dispos. 40(10) , 2041-53, (2012)

20(S)-Ginsenoside Rh2 (Rh2)-containing products are widely used in Asia, Europe, and North America. However, extremely limited metabolism information greatly impedes the complete understanding of its clinical safety and effectiveness. The present study aims t...

Microbial transformation of ginsenoside Rg3 to ginsenoside Rh2 by Esteya vermicola CNU 120806.

World J. Microbiol. Biotechnol. 28(4) , 1807-11, (2012)

In the present investigation, we successfully employed a cell-free extract of Esteya vermicola CNU 120806 to convert ginsenoside Rg3 to Rh2. Three important factors including pH, temperature and substrate concentration were optimized for the preparation of Rh...

Antihyperglycemic effect of ginsenoside Rh2 by inducing islet β-cell regeneration in mice.

Horm. Metab. Res. 44(1) , 33-40, (2012)

The present study was designed to determine the antihyperglycemic function of ginsenoside Rh2 (GS-Rh2) by the regeneration of β-cells in mice that underwent 70% partial pancreatectomy (PPx), and to explore the mechanisms of GS-Rh2-induced β-cell proliferation...

Sulfated derivative of 20(S)-ginsenoside Rh2 inhibits inflammatory cytokines through MAPKs and NF-kappa B pathways in LPS-induced RAW264.7 macrophages.

Inflammation 35(5) , 1659-68, (2012)

In the previous study, we found that sulfated derivative B2 of ginsenoside Rh2 (Rh2-B2) has greater anti-inflammatory effects than 20(S)-ginsenoside Rh2. However, the anti-inflammatory mechanism of Rh2-B2 remains unclear. We therefore assessed the effects of ...

Ginsenoside Rh2(S) induces differentiation and mineralization of MC3T3-E1 cells through activation of the PKD/AMPK signaling pathways.

Int. J. Mol. Med. 28(5) , 753-9, (2011)

As part of our search for biologically active anti-osteoporotic agents that enhance differentiation and mineralization of osteoblastic MC3T3-E1 cells, we identified the ginsenoside Rh2(S). Mostly known to exhibit beneficial effects in cancer prevention and me...

Sulfated derivatives of 20(S)-ginsenoside Rh2 and their inhibitory effects on LPS-induced inflammatory cytokines and mediators.

Fitoterapia 84 , 303-7, (2013)

Ginsenoside Rh2 is one of the most important ginsenosides in ginseng with antitumor, antidiabetic, antiallergic, and anti-inflammatory effects. However, the extremely poor oral bioavailability induced by its low water solubility greatly limits the potency of ...

Cholesterol-dependent induction of dendrite formation by ginsenoside Rh2 in cultured melanoma cells.

Int. J. Mol. Med. 26(6) , 787-93, (2010)

Herbal remedies containing root extracts of Panax ginseng are commonly used for complementary or alternative therapies. Ginsenosides, the major components of root extracts, are responsible for ginseng's pharmacological and biological effects; however, their m...