| Cat.No. | Name | Information |
|---|---|---|
| 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. |
| M4459 | Oroxyloside | Oroxyloside (Oroxylin A-7-O-glucuronide) is a flavonoid glucuronide isolated from the dried root of Scutellaria baicalensis, with prolyl oligopeptidase (POP) inhibitory activity. |
| M4458 | Tetrahydroberberine | Tetrahydroberberine is an isoquinoline alkaloid isolated from corydalis tuber; has micromolar affinity for dopamine D(2) (pK(i) = 6.08) and 5-HT(1A) (pK(i) = 5.38) receptors but moderate to no affinity for other relevant serotonin receptors (5-HT(1B), 5-HT(1D), 5-HT(3), and 5-HT(4); pK(i) < 5.00). |
| M4456 | Sec-O-Glucosylhamaudol | Sec-o-glucosylhamaudol is a natural product isolated from The apostrophophore, which can reduce the protein level of μ-opioid receptor and can be used for pain relief research. |
| M4455 | 5-O-Methylvisammioside | 5-O-methylvisammioside isa natural compound isolated from parsnip. |
| M4454 | 2-acetylacteoside | 2' -acetylacteoside (2' -acetylacteoside) is a kind of phenylethanol glycoside isolated from Phyllostachys chinensis, which can inhibit erythrocyte hemolysis induced by free radicals and has scavenging activity. |
| M4453 | Tubuloside-A | Tubuloside A is A phenyl ethanol glycoside with antioxidant activity and liver protection activity. |
| M4452 | Echinacoside | Echinacoside is a phenylethanol compound isolated from Cistanche salsa that effectively inhibits the Wnt/β-catenin signaling pathway. Echinacoside plays a neuroprotective role by activating Trk receptors and their downstream signaling pathways. Echinacoside also has significant anti-osteoporosis activity. |
| M4451 | Isoacteoside | Isoacteoside is a natural product that significantly inhibits the formation of glycation end products. |
| M4450 | Acteoside | Acteoside is isolated from Acanthus mollis, acts as an ATP-competitive inhibitor of PKC, with an IC50 of 25 µM, and has antitumor, anti-inflammatory and antineuropathic pain activity. |
| M4449 | Cimigenol-3-O-α-L-arabinoside | Cimiracemoside C, the active ingredient in cohosh, activates AMPK and has anti-diabetes potential. |
| M4448 | Acetylcimigenol-3-O-α-L-arabinopyranside | Acetylshengmanol -3-O-α -L-arabinose is an extract of cohosh. |
| M4447 | 3-Hydroxy-4-methoxycinnamic-acid | Isoferulic acid (3-Hydroxy-4-methoxycinnamic acid) is a kind of cinnamic acid derivative with anti - diabetes activity. Isoferulic acid (3-hydroxy-4-methoxycinnamic acid) binds and activates α 1-adrenergic receptor (IC50=1.4 μM), Enhanced β -endorphin secretion (EC50=52.2 nM) and increased in vitro glucose use. Isoferulic acid also has activity against influenza virus. |
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