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72432-03-2

72432-03-2 structure
72432-03-2 structure
  • Name: Miglitol
  • Chemical Name: Miglitol
  • CAS Number: 72432-03-2
  • Molecular Formula: C8H17NO5
  • Molecular Weight: 207.224
  • Catalog: API Hormone and endocrine-regulating drugs Pancreatic hormones and other blood sugar regulating drugs
  • Create Date: 2018-09-01 11:54:59
  • Modify Date: 2024-01-02 10:11:41
  • Miglitol is an oral anti-diabetic drug that acts by inhibiting the ability of the patient to breakdown complex carbohydrates into glucose.Target: OthersMiglitol 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. 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 [1]. Miglitol 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 [2].

Name Miglitol
Synonyms BAY m 1099
Miglitol
(2R,3R,4R,5S)-1-(2-Hydroxyethyl)-2-(hydroxymethyl)piperidin-3,4,5-triol
Diastabol
(2R,3R,4R,5S)-1-(2-Hydroxyethyl)-2-(hydroxymethyl)-3,4,5-piperidinetriol
EINECS 276-661-6
MFCD00867240
GLYSET
Plumarol
BAY-m-1099
Seibule
(2R,3R,4R,5S)-1-(2-hydroxyethyl)-2-(hydroxymethyl)piperidine-3,4,5-triol
N-(2-Hydroxyethyl)moranoline
3,4,5-Piperidinetriol, 1-(2-hydroxyethyl)-2-(hydroxymethyl)-, (2R,3R,4R,5S)-
BAY 1099
(2R,3R,4R,5S)-1-(2-hydroxyéthyl)-2-(hydroxyméthyl)pipéridine-3,4,5-triol
Description Miglitol is an oral anti-diabetic drug that acts by inhibiting the ability of the patient to breakdown complex carbohydrates into glucose.Target: OthersMiglitol 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. 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 [1]. Miglitol 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 [2].
Related Catalog
References

[1]. Fukaya, N., et al., The alpha-glucosidase inhibitor miglitol delays the development of diabetes and dysfunctional insulin secretion in pancreatic beta-cells in OLETF rats. Eur J Pharmacol, 2009. 624(1-3): p. 51-7.

[2]. Hirata, A., et al., Effect of miglitol, an alpha-glucosidase inhibitor, on atherogenic outcomes in balloon-injured diabetic rats. Horm Metab Res, 2009. 41(3): p. 213-20.

Density 1.5±0.1 g/cm3
Boiling Point 453.7±45.0 °C at 760 mmHg
Melting Point 114ºC
Molecular Formula C8H17NO5
Molecular Weight 207.224
Flash Point 284.3±27.4 °C
Exact Mass 207.110672
PSA 104.39000
LogP -1.40
Vapour Pressure 0.0±2.5 mmHg at 25°C
Index of Refraction 1.598
Storage condition -20°C Freezer
Water Solubility Soluble
RIDADR NONH for all modes of transport

~95%

72432-03-2 structure

72432-03-2

Literature: Wennekes, Tom; Meijer, Alfred J.; Groen, Albert K.; Boot, Rolf G.; Groener, Johanna E.; Van Eijk, Marco; Ottenhoff, Roelof; Bijl, Nora; Ghauharali, Karen; Song, Hang; O'Shea, Tom J.; Liu, Hanlan; Yew, Nelson; Copeland, Diane; Van Den Berg, Richard J.; Van Der Marel, Gijsbert A.; Overkleeft, Herman S.; Aerts, Johannes M. Journal of Medicinal Chemistry, 2010 , vol. 53, # 2 p. 689 - 698

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72432-03-2 structure

72432-03-2

Literature: Tetrahedron Letters, , vol. 52, # 29 p. 3802 - 3804

~65%

72432-03-2 structure

72432-03-2

Literature: Concia, Alda Lisa; Lozano, Caries; Castillo, Jose A.; Parella, Teodor; Joglar, Jesus; Clapes, Pere Chemistry - A European Journal, 2009 , vol. 15, # 15 p. 3808 - 3816

~99%

72432-03-2 structure

72432-03-2

Literature: Fouace; Therisod Tetrahedron Letters, 2000 , vol. 41, # 38 p. 7313 - 7315

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72432-03-2 structure

72432-03-2

Literature: Journal of Natural Products, , vol. 65, # 2 p. 198 - 202

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72432-03-2 structure

72432-03-2

Literature: Tetrahedron Letters, , vol. 52, # 29 p. 3802 - 3804

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72432-03-2 structure

72432-03-2

Literature: Tetrahedron Letters, , vol. 52, # 29 p. 3802 - 3804

~%

72432-03-2 structure

72432-03-2

Literature: Tetrahedron Letters, , vol. 52, # 29 p. 3802 - 3804

~%

72432-03-2 structure

72432-03-2

Literature: Tetrahedron Letters, , vol. 41, # 38 p. 7313 - 7315