Emodin 8-O-b-D-glucopyranoside

CAS: 23313-21-5

Ref. 3D-ME33279

Product Information

• Name: Emodin 8-O-b-D-glucopyranoside
• Synonyms: 1,6-Dihydroxy-3-Methyl-8-(Β-D-Glucopyranosyloxy)-9,10-Anthraquinone, 1-(β-<span class="text-smallcaps">D</span>-Glucopyranosyloxy)-3,8-dihydroxy-6-methyl-9,10-anthracenedione, 8-O-β-<span class="text-smallcaps">D</span>-Glucopyranosylemodin, 9,10-Anthracenedione, 1-(β-<span class="text-smallcaps">D</span>-glucopyranosyloxy)-3,8-dihydroxy-6-methyl-, Anthraglycoside B, Emodin 8-O-glucoside, Emodin 8-O-β-<span class="text-smallcaps">D</span>-glucopyranoside, Emodin 8-O-β-<span class="text-smallcaps">D</span>-glucoside, Emodin 8-O-β-glucoside, Emodin 8-β-<span class="text-smallcaps">D</span>-glucopyranoside, Emodin 8-β-<span class="text-smallcaps">D</span>-glucoside, Emodin glucoside B, Glucopyranoside, 3,8-dihydroxy-6-methyl-1-anthraquinonyl, β-<span class="text-smallcaps">D</span>-, NSC 257449

Description

Emodin is a natural product that can be extracted from the rhizome of Curcuma aromatica, a chinese herb. It has been shown to have neuroprotective effects in animal studies and has been used as an adjuvant in the treatment of cervical cancer. Emodin also inhibits the replication of human immunodeficiency virus type 1 (HIV-1) and herpes simplex virus type 1 (HSV-1). Emodin is also active against microbial infection, including bacterial infections, such as those caused by Staphylococcus aureus, and viral infections, such as influenza A virus. The main mechanism of action of emodin is its inhibition of DNA synthesis by binding to viral dna or bacterial rna polymerase. Emodin has also been found to inhibit protein synthesis by binding to ribosomes. This drug binds to urea nitrogen molecules in bacteria and disrupts their growth by inhibiting protein synthesis.

• Brand: Biosynth

Chemical properties

• Molecular weight: 432.38 g/mol
• Formula: C₂₁H₂₀O₁₀
• Purity: Min. 95%
• Color/Form: Powder