[CAS NO. 666843-10-3]  Mizagliflozin

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PRODUCTS SPECIFICATIONS [666843-10-3]

Catalog
HY-17638
Brand
MCE
CAS
666843-10-3

DESCRIPTION [666843-10-3]

Overview

MDL-
Molecular Weight564.67
Molecular FormulaC28H44N4O8
SMILESO=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

For research use only. We do not sell to patients.

1 Publications Citing Use of MCE


Summary

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] .


IC50 & Target

Ki: 27 nM (hSGLT1), 8170 nM (hSGLT2) [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]

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.

Clinical Trial

NCT Number Sponsor Condition Start Date Phase
NCT05541939 Vogenx, Inc.
Postbariatric Hypoglycemia
September 13, 2022 Phase 2

Appearance

Solid


Shipping

Room temperature in continental US; may vary elsewhere.


Storage

4°C, protect from light

* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)


Solvent & Solubility

In Vitro:

H 2 O : ≥ 100 mg/mL ( 177.09 mM )

DMSO : 100 mg/mL ( 177.09 mM ; Need ultrasonic)

* "≥" means soluble, but saturation unknown.

Preparing
Stock Solutions
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
* Please refer to the solubility information to select the appropriate solvent.
In Vivo:
  • 1.

    Add each solvent one by one: 10% DMSO >> 40% PEG300 >> 5% Tween-80 >> 45% saline

    Solubility: ≥ 2.5 mg/mL (4.43 mM); Clear solution

  • 2.

    Add each solvent one by one: 10% DMSO >> 90% (20% SBE-β-CD in saline)

    Solubility: ≥ 2.5 mg/mL (4.43 mM); Clear solution

  • 3.

    Add each solvent one by one: 10% DMSO >> 90% corn oil

    Solubility: ≥ 2.5 mg/mL (4.43 mM); Clear solution

* All of the co-solvents are available by MCE.