Hot Products
| Catalog No. | Information |
| CFN96878 | 1-Methoxyphaseollidin 1-Methoxyphaseollidin exhibits anti-Helicobacter pylori activity against the CLAR and AMOX-resistant strain as well as four CLAR (AMOX)-sensitive strains. 1-Methoxyphaseollidin may show moderate cytotoxic activity against KB and L1210 cells. 1-Methoxyphaseollidin also shows inhibition of lysoPAF acetyltransferase activity. |
| CFN95101 | 1-Methyl-2,8-dihydroxy-3-carboxy-9,10-anthraquinone Reference standards. |
| CFN91687 | 1-Methyl-2-[(6Z,9Z)-6,9-pentadecadiene]-4(1H)-quinolone Methyl-2-[(6Z,9Z)-6,9-pentadecadienyl]-4(1H)-quinolone9 is an antagonist of angiotensin II receptor (IC50=48.2 μM). Methyl-2-[(6Z,9Z)-6,9-pentadecadienyl]-4(1H)-quinolone9 is a quinolone alkaloid from Evodia rutaecarpa.1-methyl-2-[(6Z,9Z)-6,9-pentadecadienyl]-4(1H)-quinolone is an MAO-B inhibitor.1-Methyl-2-[(6Z,9Z)-6,9-pentadecadiene]-4(1H)-quinolone exhibits potent anti-Helicobacter pylori activity with a minimum inhibitory concentration (MIC) value of 10-20 μg/ml. 1-Methyl-2-[(6Z,9Z)-6,9-pentadecadiene]-4(1H)-quinolone exhibits dose-dependent DGAT inhibition with IC 50 of 13.5 μ. |
| CFN96296 | 1-Methyl-2-undecylquinolin-4(1H)-one 1-Methyl-2-undecyl-4(1H)-quinolone, and dihydroevocarpine should also be served as the chemical markers together with evodiamine for the quality control of Evodia rutaecarpa (Juss.) Benth. 1-Methyl-2-undecyl-4(1H)-quinolone shows a selective inhibition of type B MAO (MAO-B) activity with the IC(50) value of 15.3 microM using a substrate kynuramine, but does not inhibit type A MAO (MAO-A) activity.It can mitigate high phosphate-induced human aortic valve interstitial cells (HAVICs) calcification by inhibiting phosphate cotransporter (PiT-1) gene expression. It also shows moderate antiangiogenic activity against human tumor cells. |
| CFN91719 | 1-Naphthalenol 1-Naphthalenol is an excited state proton transfer (ESPT) fluorescent molecular probe. IC50 & Target: Human Endogenous Metabolite |
| CFN90219 | 1-O-Acetyl britannilactone 1-O-Acetyl britannilactone shows antifungal, and anti-cancer activities, it suppresses angiogenesis and lung cancer cell growth possibly via regulating the VEGFR-Src-FAK signaling. 1-O-Acetyl britannilactone may be one anti-inflammatory drug which inhibits the expression of COX-2 gene by blocking NF-κB activation and thus suppresses the inflammatory response to LPS in vascular smooth muscle cells. |
| CFN89438 | 1-O-Acetylbritannilactone 1-O-Acetylbritannilactone has anticancer activity, it suppresses angiogenesis and lung cancer cell growth possibly via regulating the VEGFR-Src-FAK signaling, it also can combine with gemcitabine elicits a potent apoptosis of lung cancer cell. 1-O-Acetylbritannilactone may serve as a novel therapeutic intervention for various cardiovascular diseases, including chronic ischemia, by regulating VEGF signaling and modulating angiogenesis; it is a potent inhibitor of LPS-stimulated VSMC inflammatory responses through blockade of NF-kappaB activity and inhibition of inflammatory gene COX-2 expression. 1-O-Acetylbritannilactone may act as potent natural skin-lightening agents, it exhibits anti-melanogenic activity by suppression of tyrosinase expression via ERK and Akt signaling. |
| CFN90938 | 1-Octacosanol 1-Octacosanol is reported to possess cholesterol-lowering effects, antiaggregatory properties, cytoprotective use, and ergogenic properties, it is used as a nutritional supplement. |
| CFN95053 | 1-O-galloyl-6-O-cinnamoylglucose Reference standards. |
| CFN96731 | 1-O-Methylnataloe-emodin Reference standards. |
