CAS 79886-49-0
:1,2,6-Tri-O-galloyl-β-D-glucose
Description:
1,2,6-Tri-O-galloyl-β-D-glucose is a chemical compound that belongs to the class of galloyl esters, which are derived from gallic acid and glucose. This compound features three galloyl groups esterified to the hydroxyl positions at the 1, 2, and 6 positions of the glucose molecule, contributing to its unique structural and functional properties. It is known for its potential antioxidant and anti-inflammatory activities, making it of interest in various fields, including pharmacology and food science. The presence of multiple hydroxyl groups enhances its solubility in polar solvents and may facilitate interactions with biological macromolecules. Additionally, its structural complexity allows for various applications in the development of functional foods and nutraceuticals. The compound's stability and reactivity can be influenced by environmental factors such as pH and temperature, which are important considerations in its practical applications. Overall, 1,2,6-Tri-O-galloyl-β-D-glucose represents a significant compound in the study of natural products and their health benefits.
Formula:C27H24O18
InChI:InChI=1S/C27H24O18/c28-11-1-8(2-12(29)18(11)34)24(39)42-7-17-21(37)22(38)23(44-25(40)9-3-13(30)19(35)14(31)4-9)27(43-17)45-26(41)10-5-15(32)20(36)16(33)6-10/h1-6,17,21-23,27-38H,7H2/t17-,21-,22+,23-,27+/m1/s1
InChI key:InChIKey=LLENXGNWVNSBQG-VFTFQOQOSA-N
SMILES:O(C(=O)C1=CC(O)=C(O)C(O)=C1)[C@H]2[C@H](OC(=O)C3=CC(O)=C(O)C(O)=C3)[C@@H](O)[C@H](O)[C@@H](COC(=O)C4=CC(O)=C(O)C(O)=C4)O2
Synonyms:- 1,2,6-Tri-O-galloyl-β-D-glucose
- β-D-Glucopyranose, 1,2,6-tris(3,4,5-trihydroxybenzoate)
- 1,2,6-Tri-galloyl-β-D-glucose
- 1,2,6-Tri-O-galloyl-β-D-glucopyranose
- 1,2,6-Tri-O-galloyl-β-D-glucoside
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Found 1 products.
1,2,6-Tri-O-galloylglucose
CAS:<p>1,2,6-Tri-O-galloylglucose is a natural compound that has been shown to have inhibitory effects on the human immunodeficiency virus (HIV) enzyme serine protease. This inhibits the viral replication process by preventing the protease from cleaving viral polyproteins. The compound also inhibits complement activation and has antioxidant properties. 1,2,6-Tri-O-galloylglucose is active against leukemia cells and has been shown to be more effective at lower pH levels. It also has an inhibitory effect on ellagitannins and anticomplement activity.</p>Formula:C27H24O18Purity:Min. 95%Molecular weight:636.47 g/mol
