| Cat.No. | Name | Information |
|---|---|---|
| M17888 | 1,5-Dihydroxyxanthone | 1,5-Dihydroxyxanthone |
| M17866 | Mogrol | Mogrol is a biometabolite of mogrosides, and acts via inhibition of the ERK1/2 and STAT3 pathways, or reducing CREB activation and activating AMPK signaling. |
| M17865 | Euphol | Euphol is a tetracyclic triterpene alcohol isolated from the sap of Euphorbia tirucalli with anti-mutagenic, anti-inflammatory and immunomodulatory effects, orally active. Euphol inhibits the monoacylglycerol lipase (MGL) activity via a reversible mechanism (IC50=315 nM). |
| M17862 | Lupenone | Lupenone plays a role through the PI3K/Akt/mTOR and NF-κB signaling pathways. Lupenone has anti-inflammatory, antiviral, antidiabetic and anticancer activities. |
| M17858 | Niloticin | Niloticin is a osteoclastogenesis inhibitor. Niloticin inhibits osteoclastogenesis by blocking RANKL-RANK interaction and suppressing the AKT, MAPK, and NF-κB signaling pathways. Niloticin has anti-viral, antioxidative, and mosquitocidal activities. |
| M17844 | Lanosterol | Lanosterol is an intermediate of cholesterol synthesis and use of lanosterol induces ubiquitination and degradation of a rate-controlling enzyme of cholesterol synthesis, i.e., HMG CoA reductase. Lanosterol suppresses the aggregation and cytotoxicity of misfolded proteins linked with neurodegenerative diseases. |
| M17832 | β-Amyrin | β-Amyrin |
| M17808 | Hancolupenone | Hancolupenone is a natural product for research related to life sciences. |
| M17797 | Quillaic acid | Quillaic acid is an anti-gastric cancer and anti-proliferation agent that can promote apoptosis of cancer cells. Quillaic acid also has analgesic and local anti-inflammatory activity. |
| M17793 | 16-Oxoalisol A | 16-Oxoalisol A |
| M17784 | Oleanonic acid | Oleanonic acid (3-Oxooleanolic acid) is an orally available triterpene that has anti-inflammatory and insecticidal properties. In vitro, oleanonic acid can improve oxidative stress, autophagy defects, ferroptosis, mitochondrial damage, and endoplasmic reticulum stress induced by Amyloid-β, and in vivo, it can alleviate myocardial hypertrophy in rats. |
| M17770 | Pyracrenic acid | Pyracrenic acid |
| M17765 | Ginsenoside Rk3 | Ginsenoside Rk3 significantly inhibits TNF-α-induced NF-κB transcriptional activity, with an IC50 of 14.24±1.30 μM in HepG2 cells. |
| M17752 | Karaviloside VIII | Karaviloside VIII |
| M17749 | Ganodermanontriol | Ganodermanontriol is a sterol isolated from Ganoderma lucidum, induces anti-inflammatory activity in tert-butyl hydroperoxide (t-BHP)-damaged hepatic cells through the expression of HO-1. |
| M17652 | Zeaxanthin dipalmitate | Zeaxanthin dipalmitate |
| M17651 | Tigogenin | Tigogenin |
| M17619 | 7-Oxo-β-sitosterol | 7-Oxo-β-sitosterol |
| M17603 | Cedrol | Cedrol is a potent competitive inhibitor of cytochrome P-450 (CYP) enzymes. Cedrol inhibits CYP2B6-mediated bupropion hydroxylase and CYP3A4-mediated midazolam hydroxylation with Ki of 0.9 μM and 3.4 μM, respectively. Cedrol also has weak inhibitory effect on CYP2C8, CYP2C9, and CYP2C19 enzymes. |
| M17591 | Heliangin | Heliangin |
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