Structure Database (LMSD)
Common Name
Lecanoric acid
Systematic Name
4-(2,4-dihydroxy-6-methylbenzoyl)oxy-2-hydroxy-6-methylbenzoic acid
Synonyms
- Orsellinate depside
3D model of Lecanoric acid
Please note: Where there are chiral atoms but the stereochemistry is undefined, the 3D model takes an arbitrary conformation
Classification
Category
Main Class
Sub Class
Biological Context
Lecanoric acid is a naturally occurring depside polyphenol isolated from a variety of lichens.1 It is a potent antioxidant, surpassing ascorbic acid in a 2,2-diphenyl-1-picryl-hydrazyl-hydrate (DPPH) free radical scavenging assay (IC50s = 424.51 and 6.42 μg/ml for lecanoric and ascorbic acid, respectively).2 Lecanoric acid has antibacterial and antifungal activities with minimum inhibitory concentrations ranging from 0.5 to 1 mg/ml for a panel of fifteen microorganisms. In a cell viability assay, lecanoric acid exhibits antiproliferative activity against HeLa cells (IC50 = 123.97 μg/ml). Lecanoric acid also exhibits antidiabetic and hypolipidemic properties.1,3
This information has been provided by Cayman Chemical
References
1. Thadhani, V.M., and Karunaratne, V. Potential of lichen compounds as antidiabetic agents with antioxidative properties: A review. Oxid. Med. Cell. Longev. 2017, (2017).
References
String Representations
InChiKey (Click to copy)
HEMSJKZDHNSSEW-UHFFFAOYSA-N
InChi (Click to copy)
InChI=1S/C16H14O7/c1-7-3-9(17)5-11(18)14(7)16(22)23-10-4-8(2)13(15(20)21)12(19)6-10/h3-6,17-19H,1-2H3,(H,20,21)
SMILES (Click to copy)
C1(C(O)=CC(O)=CC=1C)C(=O)OC1C=C(C(C(=O)O)=C(C)C=1)O
Other Databases
Calculated Physicochemical Properties
Heavy Atoms
23
Rings
2
Aromatic Rings
2
Rotatable Bonds
4
Van der Waals Molecular Volume
279.25
Topological Polar Surface Area
124.29
Hydrogen Bond Donors
4
Hydrogen Bond Acceptors
7
logP
2.34
Molar Refractivity
79.27
Admin
Created at
-
Updated at
4th Feb 2022