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CAS RN: 21187-98-4 | Product Number: G0381
Gliclazide
Purity: >98.5%(T)(HPLC)
- 1-[3-Azabicyclo[3.3.0]oct-3-yl]-3-p-toluenesulfonylurea
Size | Unit Price | Philadelphia, PA | Portland, OR | Japan* | Quantity |
---|---|---|---|---|---|
5G |
$66.00
|
2 | 1 | 17 |
|
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Product Number | G0381 |
Purity / Analysis Method | >98.5%(T)(HPLC) |
Molecular Formula / Molecular Weight | C__1__5H__2__1N__3O__3S = 323.41 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
CAS RN | 21187-98-4 |
Reaxys Registry Number | 1657836 |
PubChem Substance ID | 135726993 |
Merck Index (14) | 4439 |
MDL Number | MFCD00409893 |
Appearance | White to Almost white powder to crystal |
Purity(HPLC) | min. 98.5 area% |
Purity(Neutralization titration) | min. 98.5 % |
Melting point | 165.0 to 169.0 °C |
Melting Point | 167 °C |
Solubility in water | Insoluble |
Solubility (soluble in) | Dimethylformamide |
Solubility (slightly sol. in) | Ethanol, Methanol |
RTECS# | YT4500000 |
HS Number | 2935.90.9500 |
References
- Gliclazide. An update of its pharmacological properties and therapeutic efficacy in non-insulin-dependent diabetes mellitus (a review)
- Sulfonylurea stimulation of insulin secretion (a review)
- Gliclazide modified release (a review)
- Improvement of water solubility and in vitro dissolution rate of gliclazide by complexation with β-cyclodextrin
- Enhancement of dissolution rate of gliclazide using solid dispersions with polyethylene glycol 6000
- Cogrinding as an approach to enhance dissolution rate of a poorly water-soluble drug (gliclazide)
- The development and validation of liquid chromatography method for the simultaneous determination of metformin and glipizide, gliclazide, glibenclamide, or glimperide in plasma
References
- The receptor for antidiabetic sulfonylureas controls the activity of the ATP-modulated potassium channel in insulin-secreting cells
- H. Schmid-Antomarchi, L. De Weille, M. Fosset, M. Lazdunski, J. Biol. Chem. 1987, 262, 15840.
- Antidiabetic sulfonylureas control action potential properties in heart cells via high affinity receptors that are linked to ATP-dependent potassium channels
- M. Fosset, J. R. De Weille, R. D. Green, H. Schmid-Antomarchi, M. Lazdunski, J. Biol. Chem. 1988, 263, 7933.
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