| Cat.No. | Name | Information |
|---|---|---|
| M19388 | Chicanin | Chicanine is a lignan compound of Schisandra chinesis, inhibits LPS-induced phosphorylation of p38 MAPK, ERK 1/2 and IκB-α, with anti-inflammatory activity. |
| M19383 | Aegeline | Aegeline, a main alkaloid, mimics the yeast SNARE protein Sec22p in suppressing α-synuclein and Bax toxicity in yeast. Aegeline restores growth of yeast cells suppressed by either αsyn or Bax. Antioxidant activity. |
| M19382 | Sinigrin | Sinigrin is a major glucosinolate present in plants of the Brassicaceae family, with anti-adipogenic effects. |
| M19381 | Guaiacin | Guaiacin is a arylnaphthalene type lignin isolated from the barks of Machilus thunbergii SIEB. et ZUCC (Lauraceae). Guaiacin significantly increases alkaline phosphatase activity and osteoblast differentiation. |
| M19374 | L-Rhamnose monohydrate | L-Rhamnose monohydrate is a deoxy sugar found in plants and bacteria. Rhamnose monohydrate crosses the epithelia via the transcellular pathway and acts as a marker of intestinal absorption. |
| M19371 | Handelin | Handelin is a guaianolide dimer from Chrysanthemum boreale that has potent anti-inflammatory activity by down-regulating NF-κB signaling and pro-inflammatory cytokine production. |
| M19369 | Geraniol | Geraniol, an olefinic terpene, was found to inhibit growth of Candida albicans and Saccharomyces cerevisiae strains. |
| M19368 | Osthenol | Osthenol (Ostenol) is a selective, reversible, and competitive human monoamine oxidase-A (hMAO-A) inhibitor (Ki=0.26 µM). Osthenol potently inhibits recombinant hMAO-A with an IC50 of 0.74 µM and shows a high selectivity index for hMAO-A versus hMAO-B. |
| M19366 | Karanjin | Karanjin induces GLUT4 translocation in skeletal muscle cells by increasing AMPK activity. Karanjin can induce cancer cell death through cell cycle arrest and enhance apoptosis. |
| M19363 | Parishin | Parishin is a phenolic glucoside isolated from Gastrodia elata. Parishin exhibits antiaging effects and extends the lifespan of yeast via regulation of Sir2/Uth1/TOR signaling pathway. |
| M19361 | Rosmanol | Rosmanol could inhibit the oxidation of low density lipoprotein (LPL) and significantly inhibit lipopolysaccharide induced iNOS and COX-2 expression, with anti-inflammatory effect. |
| M19358 | MONASCIN | Monascin inhibits the activation of NOR 1 (an NO donor). Monascin also exhibits anti-tumor-initiating activity and anti-inflammatory activity with oral administration. |
| M19356 | Columbin | Columbin is an orally active diterpenoid furanolactone from Calumbae radix, has anti-inflammatory and anti-trypanosomal effects. Columbin selectively inhibits COX-2 (EC50=53.1 μM) over COX-1 (EC50=327 μM). |
| M19354 | Cytosine | Cytosine is one of the four major bases found in DNA and RNA. cytosine modifications exhibit circadian oscillations associated with epigenetic diversity and aging. |
| M19353 | Fraxinol | Fraxinol is isolated from Lobelia chinensis. |
| M19351 | Catenarin | Catenarin |
| M19349 | Hinokinin | Hinokinin (Cubebinolide) is a compound isolated from the stems of Hypoestes aristate. Hinokinin exhibits moderate activity of HIV-1 protease enzyme. |
| M19347 | Nimbolide | Nimbolide induces apoptosis through inactivation of NF-κB. Nimbolide inhibits CDK4/CDK6 kinase activity. Nimbolide suppresses the NF-κB, Wnt, PI3K-Akt, MAPK and JAK-STAT signaling pathways. |
| M19344 | Charantin | Charantin |
| M19332 | Licraside | Licraside is isolated from Glycyrrhiza uralesis Fish. |
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