Cilostamide
From Wikipedia, the free encyclopedia
|
|
This article needs more links to other articles to help integrate it into the encyclopedia. (February 2016) |
| Names | |
|---|---|
| IUPAC name
N-Cyclohexyl-N-methyl-4-[(2-oxo-1H-quinolin-6-yl)oxy]butanamide
|
|
| Identifiers | |
| 68550-75-4 | |
| ChEMBL | ChEMBL34431 |
| ChemSpider | 2651 |
| 5167 | |
| Jmol 3D model | Interactive image |
| PubChem | 2753 |
|
|
|
|
| Properties | |
| C20H26N2O3 | |
| Molar mass | 342.44 g·mol−1 |
|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
|
| Infobox references | |
Cilostamide is a PDE3 inhibitor.[1]
References[edit]
- ^ De Jonge, HR; Tilly, BC; Hogema, BM; Pfau, DJ; Kelley, CA; Kelley, MH; Melita, AM; Morris, MT; Viola, RM; Forrest, JN (2013). "CGMP Inhibition of Type 3 Phosphodiesterase is the Major Mechanism by which C-type Natriuretic Peptide Activates CFTR in the Shark Rectal Gland". American Journal of Physiology. Cell Physiology 306: C343–C353. doi:10.1152/ajpcell.00326.2013. PMID 24259420.
| This article about an organic compound is a stub. You can help Wikipedia by expanding it. |

