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Names | |
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IUPAC name
4-(2,4-Dihydroxy-6-pentylbenzoyl)oxy-2-hydroxy-6-pentylbenzoic acid
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Identifiers | |
3D model (
JSmol)
|
|
ChEBI | |
ChEMBL | |
ChemSpider | |
PubChem
CID
|
|
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C24H30O7 | |
Molar mass | 430.5 g/mol |
Melting point | 122 °C (252 °F; 395 K) dec |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Anziaic acid is a depside found in lichens. It gives a red reaction in the C test. The two phenolic rings have a pentyl side chain. It is an ester dimer of olivetolic acid. [1]
Anziaic acid works as an antibacterial compound by inhibiting topoisomerase. [2] [3]
Anziaic acid has been artificially produced from olivetolic acid by benzylation of the O-phenol positions, and then condensing with trifluoroacetic anhydride. [1]
Anziaic acid is colourless. It can be dissolved in ethanol, ethanol-water mixture, or cyclohexane-benzene mixture. [1]
Perlatolic acid, dihydropicrolichenic acid, 2'-O-methylanziaic acid, 2-O-methylperlatolic acid, 2'-O-methylperlatolic and planaic acid are derivatives of anziaic acid, where a methyl group replaces a hydrogen in some of the hydroxy positions on the rings. [1]
Anziaic acid is found in Parmeliaceae including Hypotrachyna, [2] Stereocaulon, [4] and Cetrelia, [5]
{{
cite journal}}
: CS1 maint: DOI inactive as of January 2024 (
link)
![]() | |
Names | |
---|---|
IUPAC name
4-(2,4-Dihydroxy-6-pentylbenzoyl)oxy-2-hydroxy-6-pentylbenzoic acid
| |
Identifiers | |
3D model (
JSmol)
|
|
ChEBI | |
ChEMBL | |
ChemSpider | |
PubChem
CID
|
|
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C24H30O7 | |
Molar mass | 430.5 g/mol |
Melting point | 122 °C (252 °F; 395 K) dec |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Anziaic acid is a depside found in lichens. It gives a red reaction in the C test. The two phenolic rings have a pentyl side chain. It is an ester dimer of olivetolic acid. [1]
Anziaic acid works as an antibacterial compound by inhibiting topoisomerase. [2] [3]
Anziaic acid has been artificially produced from olivetolic acid by benzylation of the O-phenol positions, and then condensing with trifluoroacetic anhydride. [1]
Anziaic acid is colourless. It can be dissolved in ethanol, ethanol-water mixture, or cyclohexane-benzene mixture. [1]
Perlatolic acid, dihydropicrolichenic acid, 2'-O-methylanziaic acid, 2-O-methylperlatolic acid, 2'-O-methylperlatolic and planaic acid are derivatives of anziaic acid, where a methyl group replaces a hydrogen in some of the hydroxy positions on the rings. [1]
Anziaic acid is found in Parmeliaceae including Hypotrachyna, [2] Stereocaulon, [4] and Cetrelia, [5]
{{
cite journal}}
: CS1 maint: DOI inactive as of January 2024 (
link)