Ginsenoside Rg2, a steroid glycosides, is abundant in Panax ginseng root, which has been used for prevention of illness.

人参皂苷 Rh2 (标准品) 是人参皂苷 Rh2 的参考标准，用于研究和分析应用。人参皂苷 Rh2 通过多种途径诱导癌细胞中 caspase-8 和 caspase-9 的激活及凋亡。

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

Panaxadiol, a natural product isolated and purified from the roots of Panax ginseng C.

Ginsenoside Re is a panaxatriol saponin that has diverse in vitro and in vivo effects, including vasorelaxant, antioxidant, antihyperlipidemic, and angiogenic actions.

人参皂苷Rh1（Prosapogenin A2）抑制PPAR-γ、TNF-α、IL-6和IL-1β的表达。

20(R)-Ginsenoside Rg3, a natural product isolated and purified from the roots of Panax ginseng C.

Ginsenoside Ro, a natural product isolated and purified from the root of Panax ginseng C. A. Mey., is reported to have anti-infllammtory, anti-hepatitic activities, and showed inhibitory activity against 5αR with IC(50) value of 259.4 μm

Ginsenoside Rc is a steroid glycoside, and a triterpene saponin found exclusively in the plant genus Panax (ginseng) with properties that inhibit or prevent tumors growth.

Ginsenoside Rf, extracted from the traditional Chinese herb ginseng, is a natural anticancer products known for its favorable safety and efficacy profiles.

(20S)-Protopanaxadiol is an aglycon metabolic derivative of the protopanaxadiol-type ginseng saponin and an apoptosis inducer.

Ginsenoside C-K (Standard) 是 Ginsenoside C-K 的分析标准品。Ginsenoside C-K 是一种 Ginsenoside Rb1 的细菌代谢物。Ginsenoside C-K 通过抑制诱生型一氧化氮合酶 (iNOS) 和 COX-2 来发挥抗炎作用。在人肝微粒体中，Ginsenoside C-K 抑制 CYP2C9 和 CYP2A6 活性，IC50 分别为 32.0±3.6 μM和 63.6±4.2 μM。

Ginsenoside Rg3 is a steroid glycoside derivative which affects endothelium relaxation in the aorta.

Notoginsenoside R1, the main bioactive component isolated and purified from the roots of Panax notoginseng (Burk.)F.H.Chen, is reported to have some neuronal protective, antihypertensive effects.

Pseudoginsenoside F11, a natural product isolated and purified from the roots of Panax ginseng C. A. Mey., antagonized the morphine stimulated opioid receptor signalling directly at the cellular level, and the memory dysfunction induced by scopolamine.

β-ODAP is an analog of glutamic acid present in Lathyrus sativus (grass pea) that activates AMPA receptors.

Ginsenoside Rk3 is reportedly present in the processed Radix notoginseng that is often used as a major ingredient of the compound preparation for ischemic heart diseases.

Notoginsenoside Ft1, a natural saponin isolated and purified from the roots of Panax notoginseng, may accelerate diabetic wound healing by orchestrating multiple processes, including promoting fibroblast proliferation, enhancing angiogenesis, and attenuating inflammatory response, which provided a great potential application of it in clinics for patients with diabetic foot ulcers, arrest the proliferation and elicited the apoptosis of SH-SY5Y cells possibly via p38 MAPK and ERK1/2 pathways, which indicates the potential therapeutic effect of it on human neuroblastoma, activate both glucocorticoid and estrogen receptors to induce endothelium-dependent, nitric oxide-mediated relaxations in rat mesenteric arteries, and enhance platelet aggregation by activating a signalling network mediated through P2Y12 receptors.