MDL | - |
---|---|
Molecular Weight | 564.67 |
Molecular Formula | C28H44N4O8 |
SMILES | O=C(N)C(C)(C)CNCCCOC1=CC=C(CC2=C(C(C)C)NN=C2O[C@H]3[C@@H]([C@H]([C@@H]([C@@H](CO)O3)O)O)O)C(C)=C1 |
Mizagliflozin (DSP-3235 free base) is a potent, orally active and selective SGLT1 inhibitor, with a K i of 27 nM for human SGLT1 . Mizagliflozin displays 303-fold selectivity over SGLT2 . Mizagliflozin is used as an antidiabetic drug that can modify postprandial blood glucose excursion. Mizagliflozin also exhibits potential in the amelioration of chronic constipation [1] .
Ki: 27 nM (hSGLT1), 8170 nM (hSGLT2) [1]
Mizagliflozin (DSP-3235 free base) (3-30 mg/kg; oral) exerts a laxative effect
[1]
.
Mizagliflozin administrated intravenously (0.3 mg/kg) and orally (3 mg/kg) declined with a short half-life (0.23 and 1.14 h, respectively)
[2]
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Animal Model: | Male Wistar rats (rat model of low-fiber-diet-induced constipation) [1] |
Dosage: | 3, 10, 30 mg/kg |
Administration: | Oral |
Result: | Increased fecal wet weight in a rat model of low-fiber-diet-induced constipation. |
NCT Number | Sponsor | Condition | Start Date | Phase |
---|---|---|---|---|
NCT05541939 | Vogenx, Inc. |
Postbariatric Hypoglycemia
|
September 13, 2022 | Phase 2 |
Solid
Room temperature in continental US; may vary elsewhere.
4°C, protect from light
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
H 2 O : ≥ 100 mg/mL ( 177.09 mM )
DMSO : 100 mg/mL ( 177.09 mM ; Need ultrasonic)
* "≥" means soluble, but saturation unknown.
Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
---|
1 mM | 1.7709 mL | 8.8547 mL | 17.7095 mL |
5 mM | 0.3542 mL | 1.7709 mL | 3.5419 mL |
10 mM | 0.1771 mL | 0.8855 mL | 1.7709 mL |