41743-41-3
Chemical Structure
Procyanidin A2
- CAS No.: 41743-41-3
- Formula:C30H24O12
- Molecular Weight:576.50
IUPAC Name: (2R,3R,8S,14R,15R)-2,8-bis(3,4-dihydroxyphenyl)-3,4-dihydro-2H,14H-8,14-methanobenzo[7,8][1,3]dioxocino[4,5-h]chromene-3,5,11,13,15-pentaol
InChIKey: NSEWTSAADLNHNH-LSBOWGMISA-N
SMILES: O[C@]1([C@]2(C3=CC(O)=C(O)C=C3)OC4=C(C5=C(C[C@@H](O)[C@@H](C6=CC(O)=C(O)C=C6)O5)C(O)=C4)[C@@]1([H])C7=C(O)C=C(O)C=C7O2)[H]
Biological Activity: Procyanidin A2 is a flavonoid found in grapes, with anti-cancer, antioxidant, antimicrobial and anti-inflammation activity[1][2].
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Procyanidin A2 | 99.80% | Procyanidin A2 is a flavonoid found in grapes, with anti-cancer, antioxidant, antimicrobial and anti-inflammation activity. | ||||||||||||||||||||
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Procyanidin A2 (Standard) | ≥98% | Procyanidin A2 (Standard) is the analytical standard of Procyanidin A2. This product is intended for research and analytical applications. Procyanidin A2 is a flavonoid found in grapes, with anti-cancer, antioxidant, antimicrobial and anti-inflammation activity. | ||||||||||||||||||||
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- [1]. LingrongWen, et al. Identification of flavonoids in litchi (Litchi chinensis Sonn.) leaf and evaluation of anticancer activities. Journal of Functional Foods. January 2014, 6, P: 555-563.
- [2]. Coleman SL, et al. Procyanidin A2 Modulates IL-4-Induced CCL26 Production in Human Alveolar Epithelial Cells. Int J Mol Sci. 2016 Nov 12;17(11). [Content Brief]