نتایج جستجو برای: ginsenoside rg3

تعداد نتایج: 2325  

Journal: :Molecular pharmacology 2005
Jun-Ho Lee Sang Min Jeong Jong-Hoon Kim Byung-Hwan Lee In-Soo Yoon Joon-Hee Lee Sun-Hye Choi Dong-Hyun Kim Hyewhon Rhim Sung Soo Kim Jai-Il Kim Choon-Gon Jang Jin-Ho Song Seung-Yeol Nah

We demonstrated previously that ginsenoside Rg(3) (Rg(3)), an active ingredient of Panax ginseng, inhibits brain-type Na(+) channel activity. In this study, we sought to elucidate the molecular mechanisms underlying Rg(3)-induced Na(+) channel inhibition. We used the two-microelectrode voltage-clamp technique to investigate the effect of Rg(3) on Na(+) currents (I(Na)) in Xenopus laevis oocytes...

Journal: :Molecular pharmacology 2008
Jun-Ho Lee Byung-Hwan Lee Sun-Hye Choi In-Soo Yoon Mi Kyung Pyo Tae-Joon Shin Woo-Sung Choi Yoongho Lim Hyewhon Rhim Kwang Hee Won Yong Whan Lim Han Choe Dong-Hyun Kim Yang In Kim Seung-Yeol Nah

We have demonstrated previously that the 20(S) but not the 20(R) form of ginsenoside Rg(3) inhibited K(+) currents flowing through Kv1.4 (hKv1.4) channels expressed in Xenopus laevis oocytes, pointing to the presence of specific interaction site(s) for Rg(3) in the hKv1.4 channel. In the current study, we sought to identify this site(s). To this end, we first assessed how point mutations of var...

2016
Il-Dong Choi Ju-Hee Ryu Dong-Eun Lee Myoung-Hee Lee Jae-Joong Shim Young-Tae Ahn Jae-Hun Sim Chul-Sung Huh Wang-Seob Shim Sung-Vin Yim Eun-Kyoung Chung Kyung-Tae Lee

To evaluate the pharmacokinetics of compound K after oral administration of HYFRG and RG in humans, an open-label, randomized, single-dose, fasting, and one-period pharmacokinetic study was conducted. After oral administration of a single 3 g dose of HYFRG and RG to 24 healthy Korean males, the mean (±SD) of AUC0-t and C max of compound K from HYFRG were 1466.83 ± 295.89 ng·h/mL and 254.45 ± 51...

2013
JIAN-LI GAO GUI-YUAN LV BAI-CHENG HE BING-QIANG ZHANG HONGYU ZHANG NING WANG CHONG-ZHI WANG WEI DU CHUN-SU YUAN TONG-CHUAN HE

Plant-derived active constituents and their semi-synthetic or synthetic analogs have served as major sources of anticancer drugs. 20(S)-protopanaxadiol (PPD) is a metabolite of ginseng saponin of both American ginseng (Panax quinquefolius L.) and Asian ginseng (Panax ginseng C.A. Meyer). We previously demonstrated that ginsenoside Rg3, a glucoside precursor of PPD, exhibits anti-proliferative e...

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