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Miglitol(BAY1099 Glyset)
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Miglitol(BAY1099 Glyset)图片
CAS NO:72432-03-2
规格:≥98%
包装与价格:
包装价格(元)
250mg电议
500mg电议
1g电议
2g电议
5g电议
10g电议

产品介绍
理化性质和储存条件
Molecular Weight (MW)207.22
FormulaC8H17NO5
CAS No.72432-03-2
Storage-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)DMSO: 3 mg/mL (14.5 mM)
Water: <1 mg/mL
Ethanol: <1 mg/mL
Other infoIUPAC/Chemical Name: (2R,3R,4R,5S)-1-(2-hydroxyethyl)-2-(hydroxymethyl)piperidine-3,4,5-triol
InChi Key: IBAQFPQHRJAVAV-ULAWRXDQSA-N
InChi Code: InChI=1S/C8H17NO5/c10-2-1-9-3-6(12)8(14)7(13)5(9)4-11/h5-8,10-14H,1-4H2/t5-,6+,7-,8-/m1/s1
SMILES Code: O[C@H]1[C@@H]([C@H](CN([C@@H]1CO)CCO)O)O
SynonymsBAY-M-1099; BAY-M 1099; BAY M-1099; BAY-1099; BAY 1099; BAY1099; Seibule; Diastabol; Glyset; Miglitol.
实验参考方法
In Vitro

In vitro activity: Miglitol is an oral anti-diabetic drug that acts by inhibiting the ability of the patient to breakdown complex carbohydrates into glucose.


Kinase Assay: Miglitol is an oral anti-diabetic drug that acts by inhibiting the ability of the patient to breakdown complex carbohydrates into glucose. It is primarily used in diabetes mellitus type 2 for establishing greater glycemic control by preventing the digestion of carbohydrates (such as disaccharides, oligosaccharides, and polysaccharides) into monosaccharides which can be absorbed by the body.


Cell Assay: Miglitol inhibits glycoside hydrolase enzymes called alpha-glucosidases. Since miglitol works by preventing digestion of carbohydrates, it lowers the degree of postprandial hyperglycemia. It must be taken at the start of main meals to have maximal effect. Its effect will depend on the amount of non-monosaccharide carbohydrates in a person's diet. Dietary supplementation with miglitol from pre-onset stage in OLETF rats delays the onset and development of diabetes and preserves the insulin secretory function of pancreatic islets

In VivoMiglitol was orally administered at 40 mg/100 g of high-fat diet containing 45% kcal as fat to 12-week-old rats for 29 days, and age-matched rats without the agent were used as the respective controls
Animal model rats
Formulation & Dosage 40 mg/100 g; oral
References Eur J Pharmacol, 2009. 624(1-3): p. 51-7.; Horm Metab Res, 2009. 41(3): p. 213-20.