Mizagliflozin
- Product Name
- Mizagliflozin
- CAS No.
- 666843-10-3
- Chemical Name
- Mizagliflozin
- Synonyms
- KGA3235;KGA 3235;KGA-3235;GSK1614235;GSK-1614235;GSK 1614235;Mizagliflozin;DSP-3235 free base;KGA-3235 free base;GSK-1614235 free base
- CBNumber
- CB34919871
- Molecular Formula
- C28H44N4O8
- Formula Weight
- 564.68
- MOL File
- 666843-10-3.mol
Mizagliflozin Property
- Boiling point:
- 837.0±65.0 °C(Predicted)
- Density
- 1.274±0.06 g/cm3(Predicted)
- storage temp.
- 4°C, protect from light
- solubility
- Methanol: 250 mg/mL (442.74 mM); DMSO: 100 mg/mL (177.09 mM)
- form
- Solid
- pka
- 12.65±0.70(Predicted)
- color
- Off-white to light yellow
N-Bromosuccinimide Price
- Product number
- CS-0016832
- Product name
- Mizagliflozin
- Purity
- 99.64%
- Packaging
- 5mg
- Price
- $480
- Updated
- 2021/12/16
- Product number
- CS-0016832
- Product name
- Mizagliflozin
- Purity
- 99.64%
- Packaging
- 10mg
- Price
- $800
- Updated
- 2021/12/16
- Product number
- CS-0016832
- Product name
- Mizagliflozin
- Purity
- 99.64%
- Packaging
- 25mg
- Price
- $1600
- Updated
- 2021/12/16
- Product number
- CS-0016832
- Product name
- Mizagliflozin
- Purity
- 99.64%
- Packaging
- 50mg
- Price
- $2500
- Updated
- 2021/12/16
- Product number
- CS-0016832
- Product name
- Mizagliflozin
- Purity
- 99.64%
- Packaging
- 100mg
- Price
- $4000
- Updated
- 2021/12/16
Mizagliflozin Chemical Properties,Usage,Production
Uses
Mizagliflozin (DSP-3235 free base) is a potent, orally active and selective SGLT1 inhibitor, with a Ki of 27 nM for human SGLT1. Mizagliflozin displays 303-fold selectivity over SGLT2. Mizagliflozin is used as an antidiabetic agent that can modify postprandial blood glucose excursion. Mizagliflozin also exhibits potential in the amelioration of chronic constipation[1].
in vivo
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]
| 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. |
IC 50
SGLT1
References
[1] Inoue T, et al. Mizagliflozin, a novel selective SGLT1 inhibitor, exhibits potential in the amelioration of chronic constipation. Eur J Pharmacol. 2017 Jul 5;806:25-31. DOI:10.1016/j.ejphar.2017.04.010
[2] Ohno H, et al. Absorption, disposition, metabolism and excretion of [14C]mizagliflozin, a novel selective SGLT1 inhibitor, in rats. Xenobiotica. 2019 Apr;49(4):463-473. DOI:10.1080/00498254.2018.1449269
Mizagliflozin Preparation Products And Raw materials
Raw materials
Preparation Products
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