Cat.No. | Name | Information |
---|---|---|
M4617 | Cucurbitacin E | Cucurbitacin E is a natural compound which from the climbing stem of Cucumic melo L, which significantly suppresses the activity of the cyclin B1/CDC2 complex. |
M4616 | Cucurbitacin B | Cucurbitacin B is a natural compound with anticancer activity. Cucurbitacin B belongs to a class of highly oxidized tetracyclic triterpenoids and is oral active. Cucurbitacin B inhibits tumor cell growth, migration and invasion and cycle arrest. |
M4615 | 2-O-beta-L-galactopyranosylorientin | 2" -o-beta-l-galactopyrano sylorientin extracted from the flower of Trollius Ledebouri. 2" -o-beta-l-galactopyrano sylorientin is involved in transporter-mediated efflux and is a substrate for multidrug-resistant protein 2 (MRP2). It has anti-inflammatory effects. |
M4613 | Betulinaldehyde | Betulinaldehyde(Betunal), a pentacyclic triterpenoid, has anti-bacterial and fungal activities such as Staphylococcus aureus. |
M4612 | Arctigenin | Arctigenin ((-) -arctigenin) is a bioactive lignan that can be used as an antitumor agent. Arctigenin has effective antioxidant, anti-inflammatory and antiviral activities. Arctigenin can be used to study metabolic disorders and central nervous system dysfunction. |
M4611 | oleanolic acid-3-O-β-D-glucopyranosyl (1→2)-α-L-arabinopyranoside | Oleanolic |
M4610 | Raddeanoside-R8 | Raddeanoside R8 is a saponin that can be isolated from the fresh roots of anemone. |
M4609 | Raddeanin-A | Raddeanin-A displays moderate inhibitory activity against histone deacetylases (HDACs) and has high antiangiogenic potency, antitumor activity. |
M4608 | Swertiamarin | Swertiamarin |
M4607 | Phloretin | Phloretin (NSC 407292; RJC 02792) is a specific, competitive and orally active inhibitor of sodium/glucose cotransporters in the intestine (SGLT1) and kidney (SGLT2). |
M4606 | Phloridzin | Phloridzin is a non-selective SGLT inhibitor with Kis of 300 and 39 nM for hSGLT1 and hSGLT2, respectively. Phlorizin is also a Na+/K+-ATPase inhibitor. |
M4605 | Aucubin | Aucubin is a iridoid glycoside that can be extracted from many traditional herbs. Aucubin has many biological activities, such as antioxidant, anti-aging, anti-inflammatory, antibacterial, anti-fibrosis, anti-cancer, liver protection, neuroprotection and bone protection. |
M4604 | Catalpol | Catalpol (Catalpinoside), is a kind of irisin found in Rehmannia glutinosa, with neuroprotective, hypoglycemic, anti-inflammatory, anti-cancer, anti-convulsive, antioxidant and anti-HBV effects. |
M4603 | D-(-)-Quinic-acid | D-(-)-Quinic-acid is a cyclohexanecarboxylic acid. |
M4602 | p-Coumaric-acid | P -Coumaric acid is an isomer of cinnamic acid, which has anti-tumor and anti-mutagenic activities. |
M4600 | Synephrine | Synephrine is an alkaloid from Citrus aurantium that is also an agonist of adrenoceptors. |
M4599 | Arbutin | Arbutin (β -arbutin) is a natural polyphenol isolated from the bear fruit plant Arctostaphylos uvaursi with antioxidant, anti-inflammatory and anti-tumor properties. It is a competitive inhibitor of tyrosinase in melanocytes, with a Kiapp value of 1.42 mM for monopholase. The value of p-diphenol enzyme Kiapp was 0.9 mM. Arbutin is also used as a bleaching agent. |
M4598 | Rhoifolin | RhoifolinRhoifolin is a flavonoid glycoside isolated from the leaves of Guanxi pomelo (Citrus Grandis). Rhoifolin is beneficial to diabetic complications by enhancing adiponectin secretion, tyrosine phosphorylation of insulin receptor-β and translocation of GLUT4. Rhoifolin ameliorates titanium-stimulated osteolysis and attenuates osteoclast formation through ranKL-induced NF-κB and MAPK pathways. |
M4597 | Silicristin | Silychristin is a flavonoid rich in milk thistle fruits, which has antioxidant effects. Silychristin is an effective inhibitor of thyroid hormone transporter MCT8 and can strongly inhibit T3 uptake with IC50 of 110 nM. |
M4596 | Silydianin | Silydianin, the active ingredient of silythistle, has anti-collagenase and anti-elastic enzyme activities. Silydianin is a natural protein tyrosine phosphatase 1B (PTP1B) inhibitor with an IC50 value of 17.38 μM. Silydianin inhibited the production and release of oxidation products in vitro. |
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