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| Names | |
|---|---|
|
Preferred IUPAC name
4-({4-[(2,4-Dihydroxy-6-methylbenzoyl)oxy]-2-hydroxy-6-methylbenzoyl}oxy)-2-hydroxy-6-methylbenzoic acid | |
| Identifiers | |
3D model (
JSmol)
|
|
| ChEMBL | |
| ChemSpider | |
PubChem
CID
|
|
| UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
| Properties | |
| C24H20O10 | |
| Molar mass | 468.414 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
| |
Gyrophoric acid is a depside that can be found in the lichen Cryptothecia rubrocincta and in Xanthoparmelia pokomyi. [1] It can also be found in most of the species of the Actinogyra, Lasallia, and Umbilicaria genera. [2]
-
^ Candan Mehmet, Yilmaz Meral, Tay Thrgay, Kivanc Merih and Türk Hayrettin (2006).
"Antimicrobial activity of extracts of the lichen Xanthoparmelia pokomyi and its gyrophoric and stenosporic acid constituents". Zeitschrift für Naturforschung C. 61 (5–6): 319–323.
doi:
10.1515/znc-2006-5-603.
PMID
16869486.
S2CID
22255609.
{{ cite journal}}: CS1 maint: multiple names: authors list ( link) INIST 17912298 - ^ Casselman, Karen Leigh (1994). "Lichen Dyes: Preparation and Dyeing". Maine Naturalist. 2 (2): 105–110. doi: 10.2307/3858253. ISSN 1063-3626. JSTOR 3858253.
 | This article about an aromatic compound is a stub. You can help Wikipedia by expanding it. |
|
| |
| Names | |
|---|---|
|
Preferred IUPAC name
4-({4-[(2,4-Dihydroxy-6-methylbenzoyl)oxy]-2-hydroxy-6-methylbenzoyl}oxy)-2-hydroxy-6-methylbenzoic acid | |
| Identifiers | |
3D model (
JSmol)
|
|
| ChEMBL | |
| ChemSpider | |
PubChem
CID
|
|
| UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
| Properties | |
| C24H20O10 | |
| Molar mass | 468.414 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
| |
Gyrophoric acid is a depside that can be found in the lichen Cryptothecia rubrocincta and in Xanthoparmelia pokomyi. [1] It can also be found in most of the species of the Actinogyra, Lasallia, and Umbilicaria genera. [2]
-
^ Candan Mehmet, Yilmaz Meral, Tay Thrgay, Kivanc Merih and Türk Hayrettin (2006).
"Antimicrobial activity of extracts of the lichen Xanthoparmelia pokomyi and its gyrophoric and stenosporic acid constituents". Zeitschrift für Naturforschung C. 61 (5–6): 319–323.
doi:
10.1515/znc-2006-5-603.
PMID
16869486.
S2CID
22255609.
{{ cite journal}}: CS1 maint: multiple names: authors list ( link) INIST 17912298 - ^ Casselman, Karen Leigh (1994). "Lichen Dyes: Preparation and Dyeing". Maine Naturalist. 2 (2): 105–110. doi: 10.2307/3858253. ISSN 1063-3626. JSTOR 3858253.
|
| This article about an aromatic compound is a stub. You can help Wikipedia by expanding it. |