Names | |
---|---|
Preferred IUPAC name
2-Hydroxy-6-[4-hydroxy-2-methoxy-6-(methoxycarbonyl)phenoxy]-4-methylbenzoic acid | |
Identifiers | |
3D model (
JSmol)
|
|
ChemSpider | |
EC Number |
|
PubChem
CID
|
|
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C17H16O8 | |
Molar mass | 348.307 g·mol−1 |
Hazards | |
GHS labelling: [1] | |
Warning | |
H410 | |
P273, P391, P501 | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Asterric acid is a fungal metabolite that can inhibit endothelin binding, [2] [3] first isolated from Aspergillus terreus. [4] Its derivatives and similar phenolic fungal isolates are a subject of research on anti-angiogenic compounds. [5]
Names | |
---|---|
Preferred IUPAC name
2-Hydroxy-6-[4-hydroxy-2-methoxy-6-(methoxycarbonyl)phenoxy]-4-methylbenzoic acid | |
Identifiers | |
3D model (
JSmol)
|
|
ChemSpider | |
EC Number |
|
PubChem
CID
|
|
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C17H16O8 | |
Molar mass | 348.307 g·mol−1 |
Hazards | |
GHS labelling: [1] | |
Warning | |
H410 | |
P273, P391, P501 | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Asterric acid is a fungal metabolite that can inhibit endothelin binding, [2] [3] first isolated from Aspergillus terreus. [4] Its derivatives and similar phenolic fungal isolates are a subject of research on anti-angiogenic compounds. [5]