| Cat.No. | Name | Information |
|---|---|---|
| M4400 | Narirutin | Narirutin is one of the active ingredients isolated from Citrus unshiu and has antioxidant and anti-inflammatory activities. Narirutin is a shikimate kinase inhibitor with anti-tuberculosis potency. |
| M4399 | Quercimeritrin | Quercimeritrin (Quercetin-7-O-β-D-glucopyranoside) is isolated from dentate wormwood leaves and has significant amylase activity. Quercimeritrin (Quercetin-7-O-beta-D-glucopyranoside) has antibacterial activity, it shows promising activity against Staphylococcus aureus. |
| M4398 | Dimethylfraxetin | Dimethylfraxetin is a Carbonic anhydrase inhibitor, with a Ki value of 0.0097 μM. |
| M4397 | Fraxin | Fraxin is a glucoside of fraxetin, an O-methylated coumarin. Fraxin shows its antioxidative effect through inhibition of cyclo AMP phosphodiesterase enzyme. Fraxin was administered orally to rats to investigate its metabolism. |
| M4396 | Fraxetin | Fraxetin is separate from Cortex Fraxini. Fraxetin has anti-tumor, antioxidant and anti-inflammatory effects. Fraxetin can induce apoptosis. |
| M4395 | Chrysin-7-O-glucoronide | Chrysin-7-O-glucoronide |
| M4394 | Wogonoside | Wogonoside is a flavonoid glycoside isolated from Scutellaria baicalensis and has anti-inflammatory effects. Wogonoside induces autophagy in breast cancer cells by regulating the MAPK-MTOR pathway. |
| M4393 | Wogonin | Wogonin is a cell-permeable and orally available flavonoid that displays anti-inflammatory and anticancer properties. |
| M4392 | Scutellarin-methylester | Scutellarin Methyl ester is a component of breviscapine, a crude extract of several flavonoids in breviscapine. |
| M4391 | Isoimperatorin | Isoimperatorin is a methanol extract from the root of Angelica dahurica. It effectively inhibits acetylcholinesterase (AChE) with IC50 of 74.6 μM. |
| M4390 | Imperatorin | Imperatorin is a potent NO synthesis inhibitor with an IC50 of 9.2 μmol and a BChE inhibitor with an IC50 of 31.4 μmol. Imperatorin is a weak agonist of TRPV1 with an EC50 of 12.6±3.2 μM. |
| M4389 | Carnosol | Carnosol is a phenolic diterpene with antioxidant and anticarcinogenic activities. |
| M4388 | Rosmarinic acid | Rosmarinic acid (RA, Rosemary acid) is a naturally occurring hydroxylated compound, it has the ability to block complement fixation, inhibit lipoxygenase and cyclooxygenase activity and inhibit the expression of CCL11 and CCR3 by suppressing the IKK-β activity in NF-κB activation signaling. |
| M4387 | Carnosic-acid | Carnosic acid inhibits oxidative stress and inflammation, inhibits cell proliferation, and has antibacterial activity. |
| M4386 | Gossypol Acetate (Gossypol Acetic Acid) | Gossypol Acetate (Gossypol Acetic Acid) was combined with Bcl-XL and Bcl-2 proteins with Ki values of 0.5-0.6 μM and 0.2-0.3 mM, respectively. |
| M4384 | Quercitrin | Quercitrin (Quercitrin) is a natural compound in bitter buckwheat, which has anti-inflammatory effects and has the potential to be used in cardiovascular disease research. |
| M4383 | Artemisinic-acid | Artemisinic acid is an amorphane sesquiterpene isolated from Artemisia annua L., possesses a variety of pharmacological activity, such as antimalarial activity, anti-tumor activity effect. |
| M4382 | Artemisinin | Artemisinin (Qinghaosu) is a kind of sesquiterpene lactone, an antimalarial drug isolated from the aboveground part of Artemisia annua L. Artemisinin inhibits AKT signaling by decreasing pAKT in a dose-dependent manner. Artemisinin can reduce the proliferation, migration, invasion, tumorigenesis and metastasis of cancer cells, and Artemisinin has neuroprotective effects. |
| M4381 | Curdione | Curdione, a sesquiterpenoid isolated from Zedoary, has high biological activity and has the effects of inhibiting platelet aggregation and preventing thrombosis. |
| M4380 | Curcumol | Curcumol ((-) -curcumol) is a bioactive sesquiterpene with many pharmacological activities, such as anti-cancer, anti-microbial, anti-fungal, antiviral and anti-inflammatory. Curcumol can effectively induce apoptosis in many cancer cells by targeting key signaling pathways such as MAPK/ERK, PI3K/Akt and NF-κB, which are often abnormally regulated in several cancers. |
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