Miriquidic acid

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Miriquidic acid
Category Others
Catalog number BBF-05152
CAS 35578-70-2
Molecular Weight 458.5
Molecular Formula C25H30O8

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Description

Miriquidic acid is a substance isolated from Lecidea lilienstroemii and Lecidea leucophaea.

Specification

IUPAC Name 2-hydroxy-4-[2-hydroxy-4-methoxy-6-(3-oxopentyl)benzoyl]oxy-6-pentylbenzoic acid
Canonical SMILES CCCCCC1=C(C(=CC(=C1)OC(=O)C2=C(C=C(C=C2O)OC)CCC(=O)CC)O)C(=O)O
InChI InChI=1S/C25H30O8/c1-4-6-7-8-15-12-19(14-20(27)22(15)24(29)30)33-25(31)23-16(9-10-17(26)5-2)11-18(32-3)13-21(23)28/h11-14,27-28H,4-10H2,1-3H3,(H,29,30)
InChI Key UCYIOAVHQGSYLP-UHFFFAOYSA-N

Properties

Boiling Point 642.7±55.0°C (Predicted)
Density 1.245±0.06 g/cm3 (Predicted)

Reference Reading

1. Spatial mapping of lichen specialized metabolites using LDI-MSI: chemical ecology issues for Ophioparma ventosa
Pierre Le Pogam, Béatrice Legouin, Audrey Geairon, Hélène Rogniaux, Françoise Lohézic-Le Dévéhat, Walter Obermayer, Joël Boustie, Anne-Cécile Le Lamer Sci Rep. 2016 Nov 24;6:37807. doi: 10.1038/srep37807.
Imaging mass spectrometry techniques have become a powerful strategy to assess the spatial distribution of metabolites in biological systems. Based on auto-ionisability of lichen metabolites using LDI-MS, we herein image the distribution of major secondary metabolites (specialized metabolites) from the lichen Ophioparma ventosa by LDI-MSI (Mass Spectrometry Imaging). Such technologies offer tremendous opportunities to discuss the role of natural products through spatial mapping, their distribution patterns being consistent with previous chemical ecology reports. A special attention was dedicated to miriquidic acid, an unexpected molecule we first reported in Ophioparma ventosa. The analytical strategy presented herein offers new perspectives to access the sharp distribution of lichen metabolites from regular razor blade-sectioned slices.
2. In situ DART-MS as a Versatile and Rapid Dereplication Tool in Lichenology: Chemical Fingerprinting of Ophioparma ventosa
Pierre Le Pogam, Anne-Cécile Le Lamer, Béatrice Legouin, Joël Boustie, David Rondeau Phytochem Anal. 2016 Nov;27(6):354-363. doi: 10.1002/pca.2635. Epub 2016 Sep 30.
Introduction: Lichens widely occur all over the world and are known to produce unique secondary metabolites with various biological activities. Objective: To develop high-throughput screening approaches requiring little to no sample preparation to alleviate the dereplication holdup and accelerate the discovery workflow of new structures from lichens. Methodology: The extracellular distribution of lichen metabolites is incentive for in situ chemical profiling of lichens using the ambient mass spectrometry DART-MS. For this purpose, the chlorolichen Ophioparma ventosa, producing an array of lichen polyphenolics that encompass the main structural classes associated to lichen chemodiversity, represented a relevant model to assess the versatility of this platform. The feasibility of this approach was first established by analysing the pure compounds known from this species prior to being extended to different solid organs of the lichen. Results: All tested compounds could be detected in positive and negative ion modes, most often with prevalent protonated or deprotonated molecules. Only depsides underwent a significant in-source fragmentation in both ionisation modes, which should be regarded as an added value for their structural elucidation. In situ DART-MS analyses of Ophioparma ventosa provided an extensive chemical profile and noteworthy pinpointed miriquidic acid, an unusual lichen depside so far unknown within this species. At last, in situ DART-MS granted a first insight into the distribution of the metabolites within the lichen. Conclusion: DART-MS represents a versatile tool to the wide field of lichenology, facilitating accelerated and sharp analyses of lichens and bypassing costly and tedious procedures of solvent extraction. Copyright © 2016 John Wiley & Sons, Ltd.

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