Products with Phytotoxic Bioactivity

Explore BioCrick products associated with Phytotoxic biological activity, including catalog numbers, product names and available bioactivity information.

Phytotoxic Bioactivity Products

Cat. No. Product Name
BCN4959 Gramine
Gramine has anti-tumor, anti-viral and anti-inflammatory properties; it can activate of antioxidants and inactivative of SOD in M. aeruginosa, it also has phytotoxicity on M. aeruginosa may be due to oxidative damage via oxidation of ROS .
BCN5238 Methyl orsellinate
1. Methyl orsellinate is a phytotoxic compound, it can cause significant inhibition of radicle growth of Amaranthus hypochondriacus and Echinochloa crus-galli, interact with bovine-brain calmodulin and inhibit the activation of the calmodulin-dependent enzyme cAMP phosphodiesterase. 2. Methyl orsellinate exhibits antifungal activity. 3. Methyl orsellinate can inhibit PTP1B activity with 50% inhibitory concentration values of 277 +/- 8.6 microM, the selective inhibition of PTP1B has been widely recognized as a potential drug target for the treatment of type 2 diabetes and obesity, methyl orsellinate may can treat the type 2 diabetes and obesity.
BCN6156 (2S,3S)-(-)-Glucodistylin
1. Highest concentrations of (2R,3R)-(+)-glucodistylin, (2S,3S)-(-)-glucodistylin and 3-O-( -d-xylopyranosyl)taxifolin occur in European beeches can strongly infest with beech scale.
BCN6217 Cinnamic acid
Cinnamic acid, a naturally occurring aromatic fatty acid of low toxicity, has anti-diabetic , anticancer and antioxidant activities. It is a cell differentiation inducer and protein isoprenylation inhibitor, shows a significant radio-protective effect by reducing the DNA damage induced by X-rays. Cinnamic acid inhibited feeding by detritivores, this inhibition occurs at concentrations found in nature and may be a major factor controlling the rate of decay of organic matter. It inhibited mushroom tyrosinase activity in reversiblywith the IC 50 value of 2.10 mM.
BCN6538 7,8-Benzoflavone
7,8-Benzoflavone is one of the most potent inhibitors of breast cancer resistance protein (BCRP).

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