Fusaric acid
From Wikipedia, the free encyclopedia
| Fusaric a cid | |
|---|---|
 |
|
|
5-butylpyridine-2-carboxylic acid |
|
|
Other names
5-Butylpicolinic acid Fusarinic acid |
|
| Identifiers | |
| CAS number | 536-69-6 |
| PubChem | 3442 |
| Properties | |
| Molecular formula | C10H13NO2 |
| Molar mass | 179.21572 g/mol |
| Density | ? g/cm³ |
| Melting point |
? °C |
| Boiling point |
? °C |
| Acidity (pKa) | ? |
| Hazards | |
| Flash point | ?°C |
| Related compounds | |
| Related compounds | picolinic acid |
 (verify) (what is:  / ?)Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
|
| Infobox references |
Fusaric acid is a picolinic acid derivative. It is typically isolated from various Fusarium species, and has been proposed for a various therapeutic applications. However, it is primarily used as a research tool.
Its mechanism of action is not well understood. It likely inhibits Dopamine beta-hydroxylase (the enzyme that converts dopamine to norepinephrine). It may also have other actions, such as the inhibition of cell proliferation and DNA synthesis.
[edit] References
 |
This article does not cite any references or sources. Please help improve this article by adding citations to reliable sources. Unsourced material may be challenged and removed. (March 2010) |
|
