(+)-Afzelechin (CAS 2545-00-8)
(+)-Afzelechin (CAS:
2545-00-8) has molecular formula C15H14O5 and molecular weight 274.27 g/mol. This compound has been the subject of numerous scientific investigations due to its structural features and practical utility in synthetic chemistry and industrial processes. View product details →
Product Background
This comprehensive research profile examines the scientific literature surrounding (+)-Afzelechin.
Key Research Findings
- Both free and bound phenolic fraction exhibited relatively high capacity to scavenge DPPH free radicals.
- The results revealed that after 84 days of O exposure, the malondialdehyde and proline contents in Q.
- Results showed that hard seeds had extremely low germination rates, rough seed coat surfaces, reduced hilum aperture size, and densely arranged internal palisade layers with maxi
- DFR also showed positive correlations with Afzelechin, Epiafzelechin, and Baimaside.
Detailed Literature Analysis
Below are the top-ranked research papers for (+)-Afzelechin, presented with bibliographic details and scientific abstracts.
Synthetic Chemistry
1. Nitrogen deposition mitigates ozone-induced stress in Quercus aliena: Transcriptomic and metabolomic perspectives.
Ozone (O(3)) pollution poses an increasingly serious threat to forest ecosystems. To investigate the effects of O(3) exposure on Quercus aliena and elucidate its defense mechanisms, we exposed Q. aliena to O(3) and monitored its responses using physiological, transcriptomic, and metabolomic analyses. The results revealed that after 84 days of O
🔑 Key Finding: The results revealed that after 84 days of O
2. Dual regulation of seed coat structure and flavonoids biosynthesis on seed dormancy formation of alfalfa.
The metabolic regulation of flavonoids and GAs reinforces the defensive function of the seed coat, thereby establishing and maintaining dormancy. Medicago falcata L. is an important genetic resource for stress resistance in legumes with high seed value. However, its hard seed coat causes low germination rates, uneven seedling emergence, and pro
3. Joint analysis of transcriptional metabolism for flavonoid synthesis during different developmental periods in oil palm exocarp.
To identify candidate genes for breeding oil palm varieties with high flavonoid content through molecular biotechnology, this study analyzed the metabolomes and transcriptomes of oil palm exocarp at different developmental stages using LC-MS/MS and RNA-Seq techniques. The green fruiting type (FS) oil palm exocarp at 95 days (FS1), 125 days (FS2
Biological & Pharmacological Studies
4. Differential analysis of free and bound phenolic compounds and its antioxidant activity of Ficus hirta Vahl. root cortex with different leaf morphotypes based on metabolomics.
The free and bound phenolic compounds and its antioxidant activities in the root cortext of F. hirta Vahl. were analyzed by UPLC-MS. 57 phenolic compounds were identified, among which 49 are novel and reported for the first time. Psoralen was the most common free phenolic, followed by coniferin and bergapten. Coniferin, afzelechin, naringenin,
Conclusion
The research literature on (+)-Afzelechin demonstrates sustained scientific interest, with publications continuing through 0. The compound serves as an important building block in synthetic chemistry and has been explored for various applications. Researchers and industrial users can view detailed specifications or submit an inquiry for pricing and availability.
Data Sources: PubMed/MEDLINE, CrossRef. 4 papers analyzed. Last updated: 2026-05-25. This article is automatically generated from peer-reviewed research data.