128459-27-8

Basic information

• Product Name: 2,3-O-CAMPHANYLIDENE-D-MYO-INOSITOL
• Synonyms: 2,3-O-CAMPHANYLIDENE-D-MYO-INOSITOL
• CAS NO: 128459-27-8
• Molecular Formula: C₁₆H₂₆O₆
• Molecular Weight: 314.37404
• Mol File: 128459-27-8.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,3-O-CAMPHANYLIDENE-D-MYO-INOSITOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-O-CAMPHANYLIDENE-D-MYO-INOSITOL(128459-27-8)
• EPA Substance Registry System: 2,3-O-CAMPHANYLIDENE-D-MYO-INOSITOL(128459-27-8)

Safety Data

• Hazardous Substances Data: 128459-27-8(Hazardous Substances Data)

Usage

Structure

Derived from the camphanic acid ring system and the sugar alcohol myo-inositol

Function

Alpha-glucosidase inhibitor

Medical Use

Treatment of type 2 diabetes

Mechanism of Action

Slows down digestion and absorption of carbohydrates in the intestines

Mode of Action

Inhibits enzymes that break down complex sugars into simple sugars

Effect

Delays release of glucose into the bloodstream after a meal

Clinical Impact

Helps control blood glucose levels and prevent rapid spikes in blood sugar levels after eating

Importance

Essential for managing diabetes and reducing the risk of complications associated with the disease

Upstream product

• 87-89-8 D-myo-inositol 
• 109280-15-1 (1R)-(+)-camphor dimethyl acetal 
• 142534-51-8 C₄₂H₆₀O₉Si₂ 
• 128459-28-9 1D-1,4,5,6-O-tetrabenzyl-2,3-O-(D-1',7',7'-trimethyl<2.2.1>bicyclohept-2'-ylidene)-myo-inositol 

Downstream Products

• 128459-28-9 1D-1,4,5,6-O-tetrabenzyl-2,3-O-(D-1',7',7'-trimethyl<2.2.1>bicyclohept-2'-ylidene)-myo-inositol 
• 142534-33-6 1D-1-O-(tert-butyldiphenylsilyl)-2,3-O-(D-1',7',7'-trimethyl<2.2.1>bicyclohept-2'-ylidene)-myo-inositol 
• 142534-34-7 1D-1,4-O-bis(tert-butyldiphenylsilyl)-2,3-O-(D-1',7',7'-trimethyl<2.2.1>bicyclohept-2'-ylidene)-myo-inositol 
• 15421-51-9 myo-inositol 1-phosphate 
• 74465-19-3 D-myo-Inositol 1,4-bisphosphate 
• 143358-53-6 D-1-O-benzyl-5,6-O-isopropylidene-2,3-O-(trimethyl<2.2.1>bicyclohept-2-ylidene)-myo-inositol 
• 138480-23-6 D-6-O-benzyl-2,3-O-(D-1,7,7-trimethyl<2.2.1>bicyclohept-2-ylidene)-1,4,5-tri-O-(2-oxo-5,6-benzo-1,3,2-dioxaphosphep-2-yl)myo-inositol 
• 138480-21-4 D-6-O-benzyl-2,3-O-(D-1,7,7-trimethyl<2.2.1>bicyclohept-2-ylidene)-1,4,5-tri-O-trimethyl-acetyl-myo-inositol 
• 138480-22-5 D-6-O-benzyl-2,3-O-(D-1,7,7-trimethyl<2.2.1>bicyclohept-2-ylidene)-myo-inositol 
• 2068-89-5 D-myo-inositol 1,4,5-triphosphate 
• 142631-00-3 1D-2,3,4,5-O-tetrabenzoyl-myo-inositol 
• 142534-47-2 1D-1-O-(tert-butyldiphenylsilyl)-3,4-O-(1,1,3,3-tetraisopropyldisiloxanedi-1,3-yl)-myo-inositol 
• 142534-47-2 1D-1-O-(tert-butyldiphenylsilyl)-4,5-O-(1,1,3,3-tetraisopropyldisiloxanedi-1,3-yl)-myo-inositol 
• 120679-78-9 1D-2,3,6-O-tribenzoyl-myo-inositol 

Relevant articles and documents

The synthesis of homochiral inositol phosphates from myo-inositol

A new synthetic procedure for efficient conversion of myo-inositol into homochiral inositol phosphates is presented, and is illustrated with total synthesis of myo-inositol 1-phosphate, 2-deoxy-myo-inositol 1-phosphate, myo-inositol 3-phosphate, myo-inosi

Expedient Synthesis of D-myo-Inositol 1,4,5-Trisphosphate and D-myo-Inositol 1,4-Bisphosphate

Readily available selfresolving myo-inositol D-camphor 2,3-monoacetal is converted into the title inositol phosphates by the concise procedures utilizing 1,4,5-selective tris-acylation and 1,4-selective bis-silylation of the starting tetrol in the key ste