Mizagliflozin

Mizagliflozin Suppliers list
Company Name: Shanghai Beckham Medical Technology Co., Ltd  
Tel: 13816613772
Email: huahero21@sina.com
Company Name: Twochem Co.Ltd  
Tel: 021-021-58111628 15800915896
Email: sales@twochem.com
Company Name: Shanghai YuanYe Biotechnology Co., Ltd.  
Tel: 15026964105
Email: 2881489226@qq.com
Company Name: ShangHai Biochempartner Co.,Ltd  
Tel: 177-54423994 17754423994
Email: 2853530910@QQ.com
Company Name: Tianjin heowns Biochemical Technology Co., Ltd.  
Tel: 400-6387771-6039 18920764717
Email: sales@heowns.com

Mizagliflozin manufacturers

  • Mizagliflozin
  • Mizagliflozin pictures
  • $61.00
  • 2026-07-31
  • CAS:666843-10-3
  • Purity: 99.60%
  • Supply Ability: 10g
Mizagliflozin Basic information
Product Name:Mizagliflozin
Synonyms:Mizagliflozin;DSP-3235 free base;GSK-1614235 free base;KGA-3235 free base;Propanamide, 3-[[3-[4-[[3-(β-D-glucopyranosyloxy)-5-(1-methylethyl)-1H-pyrazol-4-yl]methyl]-3-methylphenoxy]propyl]amino]-2,2-dimethyl-;GSK1614235,Chronic,KGA 3235,DSP-3235,selective,Sodium-dependent glucose cotransporters,KGA-3235,constipation,Mizagliflozin,antidiabetic,disorder,SGLT,gastrointestinal,DSP 3235,inhibit,GSK 1614235,Inhibitor,KGA3235,GSK-1614235,DSP3235;Mizagliflozin (KWA 0711);GSK 1614235
CAS:666843-10-3
MF:C28H44N4O8
MW:564.68
EINECS:
Product Categories:
Mol File:666843-10-3.mol
Mizagliflozin Structure
Mizagliflozin Chemical Properties
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
pka12.65±0.70(Predicted)
color Off-white to light yellow
Safety Information
MSDS Information
Mizagliflozin Usage And Synthesis
UsesMizagliflozin (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 50SGLT1
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
Tag:Mizagliflozin(666843-10-3) Related Product Information
KGA2727 Mizagliflozin 4-[[4-[(1E)-4-(2,9-Diazaspiro[5.5]undec-2-yl)-1-buten-1-yl]-2-methylphenyl]methyl]-5-(1-methylethyl)-1H-pyrazol-3-yl β-D-glucopyranoside Canagliflozin Ipragliflozin Phlorizin