AI Article Synopsis

  • This study investigates the chemical composition of extracts from two lichen samples collected in Algeria, using hexane, chloroform, and ethanol as solvents for extraction.
  • Hexane extracts were fractionated based on solubility in methanol, leading to the identification of various fatty acids and orsellinic acid derivatives via GC-MS analysis.
  • The chloroform and ethanol extracts also underwent analysis using HPLC-MS/MS, revealing characteristic substances, including chloroatranorin and stictic acid, with some variations in their chemical profiles.

Article Abstract

In this work, we carried out studies of the chemical composition of hexane, chloroform and ethanol extracts from two samples of the lichen collected in Algeria. Each sample of the lichen was collected on two different supports: and . Hexane extracts were prepared, in Soxhlet; each hexane extract was fractionated by its solubility in methanol; the products soluble in methanol were separated (cold): 1-Hexane, 2-Hexane; and the products insoluble in methanol (cold): 1-Cires, 2-Cires. A diazomethane esterified sample of 1-Hexane, 2-Hexane, 1-Cires and 2-Cires was analyzed by GC-MS, and the components were identified as methyl esters. In the 1-Hexane and 2-Hexane fractions, the methyl esters of the predominant fatty acids in the lichen were identified: palmitic acid, linoleic acid, oleic acid and stearic acid; a hydrocarbon was also identified: 13-methyl-17-norkaur-15-ene and several derivatives of orsellinic acid. In the 1-Cires and 2-Cires fractions, the previous fatty acids were no longer observed, and only the derivatives of orsellinic acid were found. The analysis of the 1-Hexane, 2-Hexane fractions by HPLC-MS/MS allows us to identify different chemical components, and the most characteristic products of the lichen were identified, such as Atranol, Chloroatranol, Atranorin and Chloroatranorin. In the fractions of 1-Cires and 2-Cires, the HPLC-MS/MS analysis reveals that they are very similar in their chemical components; the characteristic products of this lichen in this fraction are Atranorin and Chloroatranorin. In the extracts of chloroform, 1-Chloroform and 2-Chloroform, the analysis carried out by HPLC-MS/MS shows small differences in their chemical composition at the level of secondary products; among the products to be highlighted for this work, we have chloroatranorin, the stictic acid, norstictic acid and other derivatives. In the analysis of the most polar extracts carried out in ethanol: 1-Ethanol and 2-Ethanol, HPLC-MS/MS analysis shows very similar chemical compositions in these two extracts with small differences. In these extracts, the following acids were identified as characteristic compounds of this lichen: constictic acid, stictic acid, substictic acid and methylstictic acid. In the HPLC-MS/MS analysis of all these extracts, alectoronic acid was not found.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9416662PMC
http://dx.doi.org/10.3390/molecules27165229DOI Listing

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Article Synopsis
  • This study investigates the chemical composition of extracts from two lichen samples collected in Algeria, using hexane, chloroform, and ethanol as solvents for extraction.
  • Hexane extracts were fractionated based on solubility in methanol, leading to the identification of various fatty acids and orsellinic acid derivatives via GC-MS analysis.
  • The chloroform and ethanol extracts also underwent analysis using HPLC-MS/MS, revealing characteristic substances, including chloroatranorin and stictic acid, with some variations in their chemical profiles.
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Mutat Res

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New Chemicals Section, Department of National Health and Welfare, Environmental Health Centre, Ottawa, Ont., Canada.

To obtain insight into the identity of chemicals associated with the mutagenicity of United States National Institute of Standards and Technology (NIST) Standard Reference Materials SRM 1649 (urban dust) and SRM 1650 (diesel particulate), parallel mutagenicity tests and chemical analyses were performed on dichloromethane and sequential organic extracts of these samples. SRM 1649 and 1650 were sequentially extracted with five organic solvents of increasing polarity, in order to partition mutagenic components into discrete fractions. The solvents (with associated polarity index) were as follows: (1) hexane (0.

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