Informação sobre produto
- (+)-Marmesinin
- (2R)-2-[1-(β-<span class="text-smallcaps">D</span>-Glucopyranosyloxy)-1-methylethyl]-2,3-dihydro-7H-furo[3,2-g][1]benzopyran-7-one
- (2R)-2-[2-[(2S,3R,4S,5S,6R)-3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]-2,3-dihydrofuro[3,2-g]chromen-7-one
- 1-methyl-1-(7-oxo-2,3-dihydro-7H-furo[3,2-g]chromen-3-yl)ethyl beta-D-glucopyranoside
- 2-[(2R)-7-oxo-2,3-dihydro-7H-furo[3,2-g]chromen-2-yl]propan-2-yl beta-D-glucopyranoside
- 7H-Furo[3,2-g][1]benzopyran-7-one, 2-[1-(β-<span class="text-smallcaps">D</span>-glucopyranosyloxy)-1-methylethyl]-2,3-dihydro-, (2R)-
- 7H-Furo[3,2-g][1]benzopyran-7-one, 2-[1-(β-<span class="text-smallcaps">D</span>-glucopyranosyloxy)-1-methylethyl]-2,3-dihydro-, (R)-
- Nodakenetin, β-<span class="text-smallcaps">D</span>-glucopyranoside
Nodakenin is a coumarin derivative that has shown to be a potent inhibitor of DNA polymerase. It is effective in the prevention of injury-induced DNA damage. Nodakenin has been shown to bind to nuclear DNA in vitro, with a binding constant of 10-10 M. It also inhibits the growth of bacteria that are resistant to peucedanum root or nodakenin by binding to their dna and preventing transcription and replication. Nodakenin shows anti-inflammatory effects by inhibiting prostaglandin synthesis, which may be due to its inhibition of cyclooxygenase enzymes.
Propriedades químicas
Consulta técnica sobre: 3D-FN74165 Nodakenin
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