501-81-5
501-81-5
Chemical Structure
3-Pyridineacetic acid
- CAS No.: 501-81-5
- Formula:C7H7NO2
- Molecular Weight:137.14
IUPAC Name: 2-(pyridin-3-yl)acetic acid
InChIKey: WGNUNYPERJMVRM-UHFFFAOYSA-N
SMILES: C1=NC=CC=C1CC(O)=O
Biological Activity: 3-Pyridineacetic acid is an orally active nicotinic acid analog. 3-Pyridineacetic acid enhances cholesterol oxidation in rat liver mitochondria. 3-Pyridineacetic acid inhibits Triton-induced hypercholesterolemia in rats. 3-Pyridineacetic acid can be used in research related to hypercholesterolemia[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
3-Pyridineacetic acid | 99.98% | 3-Pyridineacetic acid is an orally active nicotinic acid analog. 3-Pyridineacetic acid enhances cholesterol oxidation in rat liver mitochondria. 3-Pyridineacetic acid inhibits Triton-induced hypercholesterolemia in rats. 3-Pyridineacetic acid can be used in research related to hypercholesterolemia. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
3-Pyridineacetic acid (Standard) | ≥98% | 3-Pyridineacetic acid (Standard) is an analytical standard for 3-Pyridineacetic acid (HY-W015806). This product is for research and analytical applications. 3-Pyridineacetic acid is an orally active nicotinic acid analog. 3-Pyridineacetic acid enhances cholesterol oxidation in rat liver mitochondria. 3-Pyridineacetic acid inhibits Triton-induced hypercholesterolemia in rats. 3-Pyridineacetic acid can be used in research related to hypercholesterolemia. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
References
- [1]. Kritchevsky D, et al. Influence of nicotinic, picolinic and pyridine-3-sulfonic acids on cholesterol metabolism in the rat. The Journal of Nutrition. 1964 Jan 1;82(1):157-61.
- [2]. Ginoulhiac, et al. 3-Pyridineacetic acid and nicotinic acid: blood levels, urinary elimination and excretion of nicotinic acid derivatives in man. 1962: 948-949.
