Chemistry:Pachypodol
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| Names | |
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| IUPAC name
4′,5-Dihydroxy-3,3′,7-trimethoxyflavone
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| Systematic IUPAC name
5-Hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,7-dimethoxy-4H-1-benzopyran-4-one | |
| Other names
Quercetin 3,7,3'-trimethyl ether
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| Identifiers | |
3D model (JSmol)
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| MeSH | C008751 |
PubChem CID
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| Properties | |
| C18H16O7 | |
| Molar mass | 344.319 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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| Infobox references | |
Tracking categories (test):
Pachypodol is a chemical compound classified as an O-methylated flavonol. It can be isolated from a variety of plants including Calycopteris floribunda,[1] Pogostemon cablin,[2] and Croton ciliatoglanduliferus.[3]
References
- ↑ Ali, Husne-Ara; Chowdhury, A. K. Azad; Rahman, Abul K. M.; Borkowski, Tomasz; Nahar, Lutfun; Sarker, Satyajit D. (2008). "Pachypodol, a flavonol from the leaves of Calycopteris floribunda, inhibits the growth of CaCo 2 colon cancer cell line in vitro". Phytotherapy Research 22 (12): 1684–1687. doi:10.1002/ptr.2539. PMID 18570232.
- ↑ Umar Ijaz, Muhammad; Rauf, Ayesha; Mustafa, Shama; Ahmed, Hussain; Ashraf, Asma; Al-Ghanim, Khalid; Swamy Mruthinti, Satyanarayana; Mahboob, S. (2022). "Pachypodol attenuates Perfluorooctane sulphonate-induced testicular damage by reducing oxidative stress". Saudi Journal of Biological Sciences 29 (3): 1380–1385. doi:10.1016/j.sjbs.2021.12.012. PMID 35280584.
- ↑ González-Vázquez, Raquel; King Díaz, Beatriz; Aguilar, María Isabel; Diego, Nelly; Lotina-Hennsen, Blas (2006). "Pachypodol from Croton ciliatoglanduliferus Ort. As Water-Splitting Enzyme Inhibitor on Thylakoids". Journal of Agricultural and Food Chemistry 54 (4): 1217–1221. doi:10.1021/jf051897s. PMID 16478239.
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