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Tellimagrandin II

Product Name
Tellimagrandin II
CAS No.
81571-72-4
Chemical Name
Tellimagrandin II
Synonyms
Aids070905;Aids-070905;Tellimagrandin 2;Tellimagrandin II;Tellimagrandin II (Synonyms: Eugeniin);1-O,2-O,3-O-Trigalloyl-4-O,6-O-(2,2',3,3',4,4'-hexahydroxy[1,1'-biphenyl]-6,6'-diylbiscarbonyl)-β-D-glucopyranose;1-O,2-O,3-O-Trigalloyl-4-O,6-O-[2,2',3,3',4,4'-hexahydroxy[1,1'-biphenyl]-6,6'-diylbis(carbonyl)]-β-D-glucopyranose;4-O,6-O-[(4,4',5,5',6,6'-Hexahydroxy-1,1'-biphenyl-2,2'-diyl)bis(carbonyl)]-1-O,2-O,3-O-trigalloyl-β-D-glucopyranose;β-D-Glucopyranose, cyclic 4,6-[(1S)-4,4',5,5',6,6'-hexahydroxy[1,1'-biphenyl]-2,2'-dicarboxylate] 1,2,3-tris(3,4,5-trihydroxybenzoate);.beta.-D-Glucopyranose, cyclic 4,6-[(1S)-4,4',5,5',6,6'-hexahydroxy[1,1'-biphenyl]-2,2'-dicarboxylate] 1,2,3-tris(3,4,5-trihydroxybenzoate)
CBNumber
CB42292032
Molecular Formula
C41H30O26
Formula Weight
938.66
MOL File
81571-72-4.mol
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Tellimagrandin II Property

Boiling point:
1503.7±65.0 °C(Predicted)
Density 
2.13±0.1 g/cm3(Predicted)
storage temp. 
4°C, protect from light
pka
7.50±0.70(Predicted)
form 
Solid
color 
Off-white to light yellow
LogP
3.138 (est)
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Hazard and Precautionary Statements (GHS)

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Tellimagrandin II Chemical Properties,Usage,Production

Uses

Tellimagrandin II (Eugeniin), with oral activity, is the first intermediate of the ellagitannin series derived from 4C1-glucose. It inhibits the resistance of Staphylococcus aureus by disrupting the integrity of the cell wall, leading to the loss of cytoplasmic contents. Additionally, Tellimagrandin II exhibits anti-inflammatory effects and inhibits acetylcholinesterase (AChE) activity, improving memory impairment. Tellimagrandin II holds potential for research in the fields of antibacterial, anti-inflammatory, and neurodegenerative diseases[1][2][3][4].

Biological Activity

Tellimagrandin II (Eugeniin), the first intermediate in the 4C1-glucose derived series of ellagitannins, also inhibits antibiotic resistance of drug-resistant Staphylococcus aureus[1][2].

in vivo

Tellimagrandin II (100 and 200 mg/kg, p.o., once daily for 10 days) improved learning and memory functions in Scopolamine (HY-N0296)-induced amnesiac ICR mice[4].

Animal Model:Scopolamine (HY-N0296)-induced amnesiac ICR mouse model[4]
Dosage:100 and 200 mg/kg
Administration:Oral gavage (p.o.), once daily for 10 days
Result:Improved learning and memory functions in the passive avoidance and water maze tests.

References

[1]. Ruth Niemetz, et al. Oxidation of pentagalloylglucose to the ellagitannin, tellimagrandin II, by a phenol oxidase from Tellima grandiflora leaves. Phytochemistry. 2003 Feb;62(3):301-6. [2]. Yu-Wei Chang, et al. Tellimagrandin II, A Type of Plant Polyphenol Extracted from Trapa bispinosa Inhibits Antibiotic Resistance of Drug-Resistant Staphylococcus aureus. Int J Mol Sci. 2019 Nov 18;20(22):5790.

Tellimagrandin II Preparation Products And Raw materials

Raw materials

Preparation Products

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Tellimagrandin II Suppliers

Aladdin Scientific
Tel
Email
tp@aladdinsci.com
Country
United States
ProdList
52923
Advantage
58

81571-72-4, Tellimagrandin IIRelated Search:


  • 1-O,2-O,3-O-Trigalloyl-4-O,6-O-(2,2',3,3',4,4'-hexahydroxy[1,1'-biphenyl]-6,6'-diylbiscarbonyl)-β-D-glucopyranose
  • 1-O,2-O,3-O-Trigalloyl-4-O,6-O-[2,2',3,3',4,4'-hexahydroxy[1,1'-biphenyl]-6,6'-diylbis(carbonyl)]-β-D-glucopyranose
  • 4-O,6-O-[(4,4',5,5',6,6'-Hexahydroxy-1,1'-biphenyl-2,2'-diyl)bis(carbonyl)]-1-O,2-O,3-O-trigalloyl-β-D-glucopyranose
  • Tellimagrandin 2
  • Tellimagrandin II
  • .beta.-D-Glucopyranose, cyclic 4,6-[(1S)-4,4',5,5',6,6'-hexahydroxy[1,1'-biphenyl]-2,2'-dicarboxylate] 1,2,3-tris(3,4,5-trihydroxybenzoate)
  • Aids070905
  • Aids-070905
  • β-D-Glucopyranose, cyclic 4,6-[(1S)-4,4',5,5',6,6'-hexahydroxy[1,1'-biphenyl]-2,2'-dicarboxylate] 1,2,3-tris(3,4,5-trihydroxybenzoate)
  • Tellimagrandin II (Synonyms: Eugeniin)
  • 81571-72-4