Purpurogallin

Purpurogallin
Names
	Preferred IUPAC name 1,7,8,9-Tetrahydroxy-2H-benzoannulen-2-one
	Other names Purpurogalline; 2,3,4,6-Tetrahydroxybenzocyclohepten-5-one; PPG
Identifiers
CAS Number	569-77-7 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:8647 ;
ChemSpider	4444893 ;
ECHA InfoCard	100.008.478
KEGG	C09964 ;
MeSH	C026133
PubChem CID	5281571;
UNII	L3Z7U4N28P ;
CompTox Dashboard (EPA)	DTXSID40205436 ;
	InChI InChI=1S/C11H8O5/c12-6-3-1-2-5-4-7(13)10(15)11(16)8(5)9(6)14/h1-4,13,15-16H,(H,12,14) Key: WDGFFVCWBZVLCE-UHFFFAOYSA-N ;
	SMILES C1=CC(=O)C(=C2C(=C1)C=C(C(=C2O)O)O)O;
Properties
Chemical formula	C11H8O5
Molar mass	220.180 g·mol−1
Appearance	Red crystalline solid
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). verify (what is ?) Infobox references

Purpurogallin is an aglycone natural product. It is an orange-red solid that is soluble in polar organic solvents but not in water. Its glycoside (ether-linked to sugar), called dryophantin, is found in nutgalls and oak barks. Purpurogallin can be prepared by oxidation of pyrogallol with sodium periodate.^[1]

Medicinal aspects

Purpurogallin is bioactive^[2] It can inhibit 2-hydroxy and 4-hydroxyestradiol methylation by catechol-O-methyltransferase.^[3] It potently and specifically inhibits TLR1/TLR2 activation pathway.^[4]

References

^ Kelly-Hunt, Alexandra E.; Mehan, Aman; Brooks, Sarah; Leanca, Miron A.; McKay, Jack E. D.; Mahamed, Nashad; Lambert, Daniel; Dempster, Nicola M.; Allen, Robert J.; Evans, Andrew R.; Sarker, Satyajit D.; Nahar, Lutfun; Sharples, George P.; Drew, Michael G. B.; Fielding, Alistair J.; Ismail, Fyaz M. D. (2022). "Synthesis and Analytical Characterization of Purpurogallin: A Pharmacologically Active Constituent of Oak Galls" (PDF). Journal of Chemical Education. 99 (2): 983–993. Bibcode:2022JChEd..99..983K. doi:10.1021/acs.jchemed.1c00699. S2CID 245366264.
^ Wu, Tai-Wing; Zeng, Ling-Hua; Wu, Jun; Fung, Kwok-Pui; Weisel, Richard D; Hempel, Andrew; Camerman, Norman (1996). "Molecular structure and antioxidant specificity of purpurogallin in three types of human cardiovascular cells". Biochemical Pharmacology. 52 (7): 1073–80. doi:10.1016/0006-2952(96)00447-9. PMID 8831727.
^ Lambert, Joshua D; Chen, Dapeng; Wang, Ching Y; Ai, Ni; Sang, Shengmin; Ho, Chi-Tang; Welsh, William J; Yang, Chung S (2005). "Benzotropolone inhibitors of estradiol methylation: Kinetics and in silico modeling studies". Bioorganic & Medicinal Chemistry. 13 (7): 2501–7. doi:10.1016/j.bmc.2005.01.037. PMID 15755652.
^ Cheng, Kui; Wang, Xiaohui; Zhang, Shuting; Yin, Hang (2012). "Discovery of Small-Molecule Inhibitors of the TLR1/TLR2 Complex". Angewandte Chemie International Edition. 51 (49): 12246–9. doi:10.1002/anie.201204910. PMC 3510333. PMID 22969053.

This article about an aromatic compound is a stub. You can help Wikipedia by expanding it.

Zdroj:https://en.wikipedia.org?pojem=Purpurogallin
Text je dostupný za podmienok Creative Commons Attribution/Share-Alike License 3.0 Unported; prípadne za ďalších podmienok. Podrobnejšie informácie nájdete na stránke Podmienky použitia.

[1] Kelly-Hunt, Alexandra E.; Mehan, Aman; Brooks, Sarah; Leanca, Miron A.; McKay, Jack E. D.; Mahamed, Nashad; Lambert, Daniel; Dempster, Nicola M.; Allen, Robert J.; Evans, Andrew R.; Sarker, Satyajit D.; Nahar, Lutfun; Sharples, George P.; Drew, Michael G. B.; Fielding, Alistair J.; Ismail, Fyaz M. D. (2022). "Synthesis and Analytical Characterization of Purpurogallin: A Pharmacologically Active Constituent of Oak Galls" (PDF). Journal of Chemical Education. 99 (2): 983–993. Bibcode:2022JChEd..99..983K. doi:10.1021/acs.jchemed.1c00699. S2CID 245366264.

[2] Wu, Tai-Wing; Zeng, Ling-Hua; Wu, Jun; Fung, Kwok-Pui; Weisel, Richard D; Hempel, Andrew; Camerman, Norman (1996). "Molecular structure and antioxidant specificity of purpurogallin in three types of human cardiovascular cells". Biochemical Pharmacology. 52 (7): 1073–80. doi:10.1016/0006-2952(96)00447-9. PMID 8831727.

[3] Lambert, Joshua D; Chen, Dapeng; Wang, Ching Y; Ai, Ni; Sang, Shengmin; Ho, Chi-Tang; Welsh, William J; Yang, Chung S (2005). "Benzotropolone inhibitors of estradiol methylation: Kinetics and in silico modeling studies". Bioorganic & Medicinal Chemistry. 13 (7): 2501–7. doi:10.1016/j.bmc.2005.01.037. PMID 15755652.

[4] Cheng, Kui; Wang, Xiaohui; Zhang, Shuting; Yin, Hang (2012). "Discovery of Small-Molecule Inhibitors of the TLR1/TLR2 Complex". Angewandte Chemie International Edition. 51 (49): 12246–9. doi:10.1002/anie.201204910. PMC 3510333. PMID 22969053.

[1]

[2]

[3]

[4]

Names

Preferred IUPAC name 1,7,8,9-Tetrahydroxy-2H-benzoannulen-2-one
Other names Purpurogalline 2,3,4,6-Tetrahydroxybenzocyclohepten-5-one PPG
Identifiers
CAS Number	569-77-7^Y
3D model (JSmol)	Interactive image
ChEBI	CHEBI:8647^N
ChemSpider	4444893^N
ECHA InfoCard	100.008.478
KEGG	C09964^N
MeSH	C026133
PubChem CID	5281571
UNII	L3Z7U4N28P^Y
CompTox Dashboard (EPA)	DTXSID40205436
InChI InChI=1S/C11H8O5/c12-6-3-1-2-5-4-7(13)10(15)11(16)8(5)9(6)14/h1-4,13,15-16H,(H,12,14)^N Key: WDGFFVCWBZVLCE-UHFFFAOYSA-N^N
SMILES C1=CC(=O)C(=C2C(=C1)C=C(C(=C2O)O)O)O
Properties
Chemical formula	C₁₁H₈O₅
Molar mass	220.180 g·mol⁻¹
Appearance	Red crystalline solid
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). N verify (what is ^YN ?) Infobox references