Chemistry:Cryptostictic acid

From HandWiki
Cryptostictic acid
Names
IUPAC name
13,17-Dihydroxy-4-(hydroxymethyl)-5-methoxy-7,12-dimethyl-2,10,16-trioxatetracyclo[9.7.0.03,8.014,18]octadeca-1(11),3(8),4,6,12,14(18)-hexaene-9,15-dione
Identifiers
3D model (JSmol)
ChemSpider
Properties
C19H16O9
Molar mass 388.328 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Tracking categories (test):

Cryptostictic acid is a chemical compound of the depsidone class. It has the molecular formula C
19
H
16
O
9
and is a secondary metabolite of various lichens. It was first reported in 1980 as a constituent of Lobaria oregana.[1] It has since been identified in lichens in the genera Ramalina,[2] Oxneriaria,[3] and Usnea,[4] among others.

References

  1. Shimada (Née Miyoshi), Sachiko; Saitoh, Tamotsu; Sankawa, Ushio; Shibata, Shoji (1980). "New depsidones from Lobaria oregana". Phytochemistry 19 (2): 328–330. doi:10.1016/S0031-9422(00)81987-1. Bibcode1980PChem..19..328S. 
  2. Parrot, Delphine; Jan, Saleem; Baert, Nicolas; Guyot, Sylvain; Tomasi, Sophie (2013). "Comparative metabolite profiling and chemical study of Ramalina siliquosa complex using LC–ESI-MS/MS approach". Phytochemistry 89: 114–124. doi:10.1016/j.phytochem.2013.02.002. PMID 23489575. Bibcode2013PChem..89..114P. 
  3. Zulfiqar, Rizwana; Asghar, Hafiza Simab; Habib, Kamran; Khalid, Abdul Nasir (2023). "Two new species of the genus Oxneriaria (Lichenized Ascomycota: Megasporaceae) from Pakistan". Plant Systematics and Evolution 309 (1): 2. doi:10.1007/s00606-022-01836-w. Bibcode2023PSyEv.309....2Z. 
  4. Lohézic-Le Dévéhat, Françoise; Tomasi, Sophie; Elix, John A.; Bernard, Aurélie; Rouaud, Isabelle; Uriac, Philippe; Boustie, Joël (2007). "Stictic Acid Derivatives from the Lichen Usnea articulata and Their Antioxidant Activities". Journal of Natural Products 70 (7): 1218–1220. doi:10.1021/np070145k.