| Cat.No. | Name | Information |
|---|---|---|
| M4481 | Mangiferin | Mangiferin is an Nrf2 activator. Mangiferin inhibits nuclear translocation of NF-κB subunit P65 and P50. Mangiferin has antioxidant, anti-diabetic, anti-hyperuricemia, antiviral, anticancer and anti-inflammatory activities. |
| M4480 | Bakuchiol | Bakuchiol is a phytoestrogens from psoralea seeds that have anti-tumor and other effects. |
| M4479 | Isopsoralen | Isopsoralen (Angelicin) is a furocoumarin naturally occurring tricyclic aromatic compound which has anti-cancer, antiviral, anti-inflammatory activity. |
| M4478 | Psoralen | Psoralen(Furocoumarin) is an active ingredient from Fructus Psoraleae; has anticancer activity. |
| M4477 | Costunlide | Costunlide |
| M4476 | Dehydrocostus-Lactone | Dehydrocostus-lactone (DHE) is a natural sesquiterpene lactone, inhibits IKKβ activity, IκBα phosphorylation and degradation, coactivators p300 recruitments and p50/p65 NF-κB nuclear translocation, and their DNA binding activity on COX-2 promoter. |
| M4475 | 7-O-ethyl-morroniside | 7-O-ethylmorroniside is a iridoid glycoside in the fruit of Cornus officinalis, which is a traditional medicine in China and is used in the study of kidney diseases, including diabetic nephropathy. |
| M4474 | Cornuside | Cornuside is a terpene glycoside isolated from the fruit of Cornus officinalis Sieb. Et Zucc. Cornus officinalis is a traditional Oriental medicine that can be used to study inflammatory diseases and promote blood circulation. |
| M4473 | Morroniside | Morroniside plays a neuroprotective role by inhibiting neuronal apoptosis and mMP9/2 expression. |
| M4472 | Verbenalin | Verbenalin is a verbenoside, which has anti-inflammatory, antifungal and antiviral activities. Verbenalin is used to study prostatitis. Verbenalin reduces cerebral ischemia-reperfusion injury. |
| M4471 | Loganin | Loganin, the main iridoid glycoside in cornus officinalis, has anti-inflammatory and anti-shock effects. |
| M4470 | 5-hydroxymethyl-2-furaldehyde | 5-hydroxymethyl-2-furaldehyde inhibits yeast growth and fermentation as stressors. |
| M4469 | Cinnamaldehyde | Cinnamaldehyde is a naturally occurring flavonoid found in the bark of Cinnamomum cinnamomi and other Cinnamomum species such as camphor and cinnamon, and can act through a variety of signaling pathways, including PPARs, AMPK, PI3K/IRS-1, RBP4-GLUT4, ERK/JNK/p38MAPK, TRPA1-ghrelin, and the Nrf2 pathways.Cinnamaldehyde also has the potential to modulate the activities of PTP1B and α-amylase with antifungal activity and antioxidant activity. |
| M4468 | Cinnamyl-alcohol | Cinnamyl Alcohol isolated from Chestnut flower showed anti-obesity activity by inhibiting the expression of PPARγ. |
| M4467 | Lathyrol | Lathyrol is a natural product with anticancer properties. |
| M4466 | Euhorbiasteroid | Euhorbiasteroid |
| M4464 | 9-methoxycamptothecine | 10-methoxycamptothecin, a natural bioactive derivative of camptothecin (CPT) isolated from Camptotheca acuminata, has been proven to have high anticancer properties. It was found that 10-methoxycamptothecin had higher cytotoxicity than 10-hydroxycamptothecin by measuring its antitumor activity against cell line 2774. |
| M4462 | Oroxin-B | Oroxin B (OB) is a flavonoid isolated from the traditional Chinese herb Oroxylum indicum (L.) Vent. Oroxin B (OB) can inhibit hepatoma cells by up-regulating PTEN, down-regulating COX-2, VEGF, PI3K and P-Akt, and induce early apoptosis. Oroxin B (OB) induces suppressive ER stress in malignant lymphoma cells. |
| M4461 | Oroxin-A | Oroxin-A is extracted from Oroxylum indicum. |
| M4460 | Oroxylin-A | Oroxylin A is an active flavonoid that inhibits the phosphorylation of MDM2 and SIRT1 through the inhibition of CDK9, thus inhibiting MDM2-mediated degradation of P53 and SIRT1-mediated deacetylation of P53, and ultimately stabilizing the P53 protein.Oroxylin A has strong anticancer activity. |
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