| Cat.No. | Name | Information |
|---|---|---|
| M9075 | Etomoxir sodium salt | Etomoxir((R)-(+)-Etomoxir) sodium salt is an irreversible inhibitor of carnitine palmitoyltransferase 1a (CPT-1a), inhibits fatty acid oxidation (FAO) through CPT-1a and inhibits palmitate β-oxidation in human, rat and guinea pig. |
| M10566 | Valepotriate | Valepotriate has anti-epileptic and anti-cancer activities, it isolated from Valeriana jatamansi Jones. |
| M4255 | Gomisin-N | Gomisin N is isolated from Schisandra chinensis and has good effects on promoting sleep and tranquillity in animal models. Gomisin N could be used for allergy studies. Gomisin N is also an anti-tumor agent with the ability to increase anti-tumor growth by inducing apoptosis of cancer cells. |
| M4250 | Schisandrin-C | Schisandrin-C is a natural product extracted from seeds, stems and other plants of Schisandra chinensis (Turcz.) Baill, which has antiviral, anti-cancer, anti-inflammatory and other activities. |
| M4226 | Liensinine-Perchlorate | Liensinine Perchlorate, a component of Nelumbo Nucifera Gaertn, has antihypertensive and anticancer activities. Liensinine Perchlorate can induce apoptosis in colorectal cancer (CRC) cells. |
| M4198 | Demethylzeylasteral | Demethylzeylasteral is a triterpene compound isolated from Tripterygium wilfordii with anti-inflammatory, immunosuppressive and anti-tumor activities. Demethylzeylasteral significantly reduces atherosclerosis (AS). Demethylzeylasteral inhibits triple negative breast cancer by blocking TGF-β signaling pathway. |
| M4153 | Genistin | Genistin (Genistine) is a kind of isoflavone of phytoestrogens, which is an effective antiadipogenic agent. Genistin inhibits breast cancer cell growth and promotes apoptotic cell death by regulating ERalpha signaling pathway. |
| M4109 | Alisol-B-23-acetate | Alisol B 23-acetate (23-acetylalismol B) is a triterpenoid compound that promotes regeneration of damaged liver by activating farnesol receptors. |
| M4104 | 20(S)-NotoginsenosideR2 | Notoginsenoside R2(Notoginsenoside R2) is a newly isolated panax Notoginsenoside R2, which showed protective effects against oxidative stress and cell apoptosis induced by 6-OHDA. |
| M4087 | Ginsenoside-F5 | Ginsenoside F5, which was obtained from Panax ginseng, significantly inhibited the growth of HL-60 cells through apoptosis pathway. |
| M4086 | Ginsenoside-F4 | Ginsenoside F4 (GF4), Ginsenoside, isolated from Panax notoginseng or red ginseng. Ginsenoside F4 (GF4) can inhibit human lymphocytic tumor JK cells by inducing apoptosis. Ginsenoside F4 (GF4) inhibited the expression of matrix metalloproteinase 13 (MMP 13) in IL-1β -treated chondrocytes, blocked cartilage damage in rabbit cartilage tissue culture, and prevented cartilage collagen matrix decomposition in pathological tissues. |
| M4084 | Ginsenoside-F2 | Ginsenoside F2, a metabolite of Ginsenoside Rb1, induces apoptosis and protective autophagy in breast cancer stem cells. |
| M4046 | Calycosin | Calycosin is a natural compound that can be isolated from Radix Astragali., with antioxidant and anti-inflammatory activities. Calycosin can be used for the research of ovarian cancer and breast cancer. |
| M4004 | Hyperoside | Hyperoside is a potent natural activator of Nur77 receptor, which can be potentially used for the research of occlusive vascular diseases. Hyperoside is also a NF-κB inhibitor. Hyperoside shows anti-tumor, antifungal, anti-inflammatory, anti-viral, and anti-oxidative activities, and can induce apoptosis. |
| M3967 | α-Hederin | α-Hederin is a triterpene saponin which affects the binding behavior, dynamics, and regulation of beta 2-adrenergic receptors. |
| M3943 | Sanguinarine | Sanguinarine, a plant alkaloid with anti-proliferative effects against cancers, is a potent and specific protein phosphatase (PP) 2C inhibitor. |
| M3425 | Mitotane | Mitotane is an isomer of DDD and a derivative of DDT that induces CYP3A4 gene expression through steroid and exogenous receptor (SXR) activation, and has anticancer activity, and may be used in studies related to adrenocortical carcinoma. |
| M3307 | 5-Aminolevulinic acid hydrochloride | 5-Aminolevulinic acid hydrochloride is an intermediate in heme biosynthesis in the body and the universal precursor of tetrapyrroles. |
| M2763 | Ibandronate sodium | Ibandronate sodium is a potent nitrogen-containing bisphosphonate that can be used in studies related to osteoporosis. |
| M2557 | Ezatiostat | Ezatiostat (TER199, TLK199) is a glutathione analog inhibitor of glutathione S-transferase (GST) P1-1. Ezatiostat leads to JNK activation by inhibiting GSTP1. Ezatiostat stimulates both lymphocyte production and bone marrow progenitor proliferation. |
| M2375 | Aloperine | Aloperine is exhibits anti-inflammatory, antibacterial, antiviral, and anti-tumor properties. |
| M1955 | 23-Hydroxybetulinic acid | 23-Hydroxybetulinic acid is a novel anticancer substance. |
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