Pachypodol information

Pachypodol
Names
	IUPAC name 4′,5-Dihydroxy-3,3′,7-trimethoxyflavone
	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
Identifiers
CAS Number	33708-72-4 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:70007 ;
ChemSpider	4444996 ;
MeSH	C008751
PubChem CID	5281677;
UNII	8AG6B2DMP5 ;
CompTox Dashboard (EPA)	DTXSID80187388 ;
	InChI InChI=1S/C18H16O7/c1-22-10-7-12(20)15-14(8-10)25-17(18(24-3)16(15)21)9-4-5-11(19)13(6-9)23-2/h4-8,19-20H,1-3H3 Key: KQFUXLQBMQGNRT-UHFFFAOYSA-N ; InChI=1/C18H16O7/c1-22-10-7-12(20)15-14(8-10)25-17(18(24-3)16(15)21)9-4-5-11(19)13(6-9)23-2/h4-8,19-20H,1-3H3 Key: KQFUXLQBMQGNRT-UHFFFAOYAA;
	SMILES COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)OC)O;
Properties
Chemical formula	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). verify (what is ?) Infobox references

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]

^ 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. S2CID 1498024.
^ 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. PMC 8913419. 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.

[1] 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. S2CID 1498024.

[2] 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. PMC 8913419. PMID 35280584.

[3] 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.

Pachypodol information

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Pachypodol

Flavonoid

Quercetin

Agastache rugosa

Fisetin

Kaempferol

Isoquercetin

Rutin

C18H16O7

Myricetin

Troxerutin

Icariin

Flavonols

Quercitrin

Hyperoside

Rhamnetin

Astragalin

Robinin

Monoxerutin

Patuletin

Myricitrin

Avicularin

Miquelianin

Trifolin

Galangin

Afzelin