Nateglinide
| Systematic (IUPAC) name | |
|---|---|
| 3-phenyl-2-[(4-propan-2-ylcyclohexanecarbonyl)amino]propanoic acid | |
| Clinical data | |
| Trade names | Starlix |
| AHFS/Drugs.com | monograph |
| MedlinePlus | a699057 |
| Licence data | EMA:Link, US FDA:link |
| Pregnancy cat. | ? |
| Legal status | POM (UK) ℞-only (US) |
| Routes | Oral |
| Pharmacokinetic data | |
| Protein binding | 98% |
| Half-life | 1.5 hours |
| Identifiers | |
| CAS number | 105816-04-4 |
| ATC code | A10BX03 |
| PubChem | CID 60026 |
| DrugBank | APRD00593 |
| ChemSpider | 10482084 |
| UNII | 41X3PWK4O2 |
| KEGG | D01111 |
| ChEMBL | CHEMBL286559 |
| Chemical data | |
| Formula | C19H27NO3 |
| Mol. mass | 317.423 g/mol |
| SMILES | eMolecules & PubChem |
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Nateglinide (INN, trade name Starlix) is a drug for the treatment of type 2 diabetes. Nateglinide was developed by Ajinomoto, a Japanese company and sold by the Swiss pharmaceutical company Novartis.
Nateglinide belongs to the meglitinide class of blood glucose-lowering drugs.
[edit] Pharmacology
Nateglinide lowers blood glucose by stimulating the release of insulin from the pancreas. It achieves this by closing ATP-dependent potassium channels in the membrane of the β cells. This depolarizes the β cells and causes voltage-gated calcium channels to open. The resulting calcium influx induces fusion of insulin-containing vesicles with the cell membrane, and insulin secretion occurs.
[edit] Dosage
Nateglinide is delivered in 60mg & 120mg tablet form.
[edit] External links
- Starlix - website of the manufacturer.
- How Nateglinide Works - website of the manufacturer.
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