| |
| Names | |
|---|---|
|
Preferred IUPAC name
Methyl 2-hydroxy-4-methoxy-6-methylbenzoate | |
| Other names
Methyl 3-hydroxy-5-methoxy-2-toluate
| |
| Identifiers | |
3D model (
JSmol)
|
|
| ChemSpider | |
PubChem
CID
|
|
| UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| Properties | |
| C10H12O4 | |
| Molar mass | 196.202 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
| |
Sparassol is an antibiotic and antifungal isolated from Sparassis crispa. [1]
External links
- ^ Woodward, S.; Sultan, H. Y.; Barrett, D. K.; Pearce, R. B. (1993). "Two new antifungal metabolites produced by Sparassis crispa in culture and in decayed trees". Journal of General Microbiology. 139: 153–159. doi: 10.1099/00221287-139-1-153.
 | This antiinfective drug article is a stub. You can help Wikipedia by expanding it. |
 | This article about an organic compound is a stub. You can help Wikipedia by expanding it. |
|
| |
| Names | |
|---|---|
|
Preferred IUPAC name
Methyl 2-hydroxy-4-methoxy-6-methylbenzoate | |
| Other names
Methyl 3-hydroxy-5-methoxy-2-toluate
| |
| Identifiers | |
3D model (
JSmol)
|
|
| ChemSpider | |
PubChem
CID
|
|
| UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| Properties | |
| C10H12O4 | |
| Molar mass | 196.202 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
| |
Sparassol is an antibiotic and antifungal isolated from Sparassis crispa. [1]
External links
- ^ Woodward, S.; Sultan, H. Y.; Barrett, D. K.; Pearce, R. B. (1993). "Two new antifungal metabolites produced by Sparassis crispa in culture and in decayed trees". Journal of General Microbiology. 139: 153–159. doi: 10.1099/00221287-139-1-153.
|
| This antiinfective drug article is a stub. You can help Wikipedia by expanding it. |
|
| This article about an organic compound is a stub. You can help Wikipedia by expanding it. |