32769-01-0

Basic information

• Product Name: 3',5'-Dimethoxytricetin 7-O-β-D-glucopypranoside
• Synonyms: 2-(4-Hydroxy-3,5-dimethoxyphenyl)-7-(β-D-glucopyranosyloxy)-5-hydroxy-4H-1-benzopyran-4-one;3',5'-Dimethoxytricetin 7-O-β-D-glucopypranoside;7-[(β-D-Glucopyranosyl)oxy]-4',5-dihydroxy-3',5'-dimethoxyflavone;Tricin 7-glucoside
• CAS NO: 32769-01-0
• Molecular Formula: C₂₃H₂₄O₁₂
• Molecular Weight: 432.379
• Mol File: 32769-01-0.mol

Chemical Properties

• Melting Point: 244-246 °C
• Boiling Point: 819.2±65.0 °C(Predicted)
• Appearance: /
• Density: 1.582±0.06 g/cm3(Predicted)
• PKA: 6.08±0.40(Predicted)
• CAS DataBase Reference: 3',5'-Dimethoxytricetin 7-O-β-D-glucopypranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 3',5'-Dimethoxytricetin 7-O-β-D-glucopypranoside(32769-01-0)
• EPA Substance Registry System: 3',5'-Dimethoxytricetin 7-O-β-D-glucopypranoside(32769-01-0)

Safety Data

• Hazardous Substances Data: 32769-01-0(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
3',5'-Dimethoxytricetin 7-O-β-D-glucopypranoside is used as an antimicrobial agent for its ability to combat various strains of bacteria, making it a valuable component in the development of new antibiotics to address the growing issue of antibiotic resistance.
Used in Cancer Treatment:
In the field of oncology, 3',5'-Dimethoxytricetin 7-O-β-D-glucopypranoside is utilized as an anticancer agent, either on its own or in combination with other therapeutic agents. Its potential to target and inhibit the growth of cancer cells, as well as its ability to enhance the effectiveness of existing cancer treatments, positions it as a promising compound in the search for novel cancer therapies.
Overall, 3',5'-Dimethoxytricetin 7-O-β-D-glucopypranoside's diverse range of applications highlights its potential as a versatile compound with significant implications for human health and well-being. Further research and development are necessary to fully harness its therapeutic potential and bring it to the forefront of modern medicine.

Upstream product

• 1365536-83-9 1-(2-(benzyloxy)-6-hydroxy-4-(methoxymethoxy)phenyl)ethan-1-one 
• 6527-32-8 4-(benzyloxy)-3,5-dimethoxybenzaldehyde 
• 133-89-1 UDP-glucose 
• 520-32-1 5,7,4'trihydroxy-3',5'-dimethoxyflavone 

Downstream Products

• 50-99-7 D-glucose 
• 520-32-1 5,7,4'trihydroxy-3',5'-dimethoxyflavone 

Relevant articles and documents

Differentially evolved glucosyltransferases determine natural variation of rice flavone accumulation and UV-tolerance

Decoration of phytochemicals contributes to the majority of metabolic diversity in nature, whereas how this process alters the biological functions of their precursor molecules remains to be investigated. Flavones, an important yet overlooked subclass of flavonoids, are most commonly conjugated with sugar moieties by UDP-dependent glycosyltransferases (UGTs). Here, we report that the natural variation of rice flavones is mainly determined by OsUGT706D1 (flavone 7-O-glucosyltransferase) and OsUGT707A2 (flavone 5-O-glucosyltransferase). UV-B exposure and transgenic evaluation demonstrate that their allelic variation contributes to UV-B tolerance in nature. Biochemical characterization of over 40 flavonoid UGTs reveals their differential evolution in angiosperms. These combined data provide biochemical insight and genetic regulation into flavone biosynthesis and additionally suggest that adoption of the positive alleles of these genes into breeding programs will likely represent a potential strategy aimed at producing stress-tolerant plants.

NEW THERAPEUTIC MOLECULES and DEVIATES FOR CRC

The chemically synthesized compound Tricin 7-O-beta -D- glucopyranoside, native to the plant Deschampsia Antarctica and present in aqueous extracts of the plant DeschampsiaAntarctica said compound having the ability to inhibit tumor growth in mammals with colorectal carcinoma.