165874-23-7

Usage

Uses

Used in Pharmaceutical Applications:
.beta.-D-Allopyranose, 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-3-O-(phenylmethyl)-4,6-O-(phenylmethylene)is used as a potential pharmaceutical agent for [application reason]. The complex structure and multiple functional groups of .beta.-D-Allopyranose, 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-3-O-(phenylmethyl)-4,6-O-(phenylmethylene)- may offer unique interactions with biological targets, making it a candidate for the development of new drugs or therapies.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, .beta.-D-Allopyranose, 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-3-O-(phenylmethyl)-4,6-O-(phenylmethylene)is used as a starting material or a structural motif for the design and synthesis of novel bioactive molecules. Its unique features may inspire the creation of new compounds with specific biological activities or improved pharmacological properties.
Used in Drug Delivery Systems:
.beta.-D-Allopyranose, 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-3-O-(phenylmethyl)-4,6-O-(phenylmethylene)may also be utilized in the development of drug delivery systems. Its structural characteristics could be exploited to enhance the solubility, stability, or targeted delivery of therapeutic agents, potentially improving their efficacy and reducing side effects.

Upstream product

• 65947-37-7 allyl 2-deoxy-2-acetamido-4,6-O-benzylidene-β-D-glucopyranoside 
• 165874-26-0 allyl 4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-allopyranoside 
• 165874-21-5 allyl 2-acetamido-4,6-O-benzylidene-2-deoxy-β-D-allopyranoside 
• 165874-20-4 allyl 4,6-O-benzylidene-2-deoxy-2-phthalimido-3-O-trifluoromethanesulfonyl-β-D-glucopyranoside 
• 165874-25-9 allyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-allopyranoside 
• 165874-19-1 allyl 2-acetamido-4,6-O-benzylidene-2-deoxy-3-O-methanesulfonyl-β-D-glucopyranoside 
• 165874-22-6 allyl 2-acetamido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-β-D-allopyranoside 
• 114853-35-9 allyl 4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 100-39-0 benzyl bromide 
• 85-44-9 phthalic anhydride 
• 165375-32-6 prop-1-enyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-2-phthalimido-β-D-allopyranoside 

Downstream Products

• 165874-29-3 C₅₈H₅₀Cl₃N₃O₁₃ 
• 165874-27-1 allyl 3,6-di-O-benzyl-4-O-(3-O-benzyl-4,6-benzylidene-2-deoxy-2-phthalimido-β-D-allopyranosyl)-2-deoxy-2-phthalimido-β-D-allopyranoside 
• 165874-28-2 3,6-di-O-benzyl-4-O-(3-O-benzyl-4,6-benzylidene-2-deoxy-2-phthalimido-β-D-allopyranosyl)-2-deoxy-2-phthalimido-β-D-allopyranose 
• 158528-74-6 (1S,5S)-3-dimethylamino-8-exo-hydroxymethyl-7-endo-hydroxy-2-oxa-4-azabicyclo<3.3.0>oct-3-en-6-endo-yl 2-acetamido-4-O-(2-acetamido-2-deoxy-β-D-allopyranosyl)-2-deoxy-β-D-allopyranoside 
• 165874-24-8 2,2,2-Trichloro-acetimidic acid (4aR,6S,7R,8S,8aS)-8-benzyloxy-7-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yl ester 

Relevant academic research and scientific papers

Syntheses of the Fungicide/Insecticide Allosamidin and a Structural Isomer

A synthesis of the naturally occurring inhibitor of chitin metabolism, allosamidin 1, involves, as the key step, condensation between the allosamizoline derivative 39, prepared following oxyamination of the cyclopentene 19, and the disaccharide glycosylating agent 54 which was synthesised from 2-acetamido-2-deoxy-D-glucose.The structural isomer 59 of allosamidin is also reported.Brief biological test results obtained using isomers 1 and 59 are recorded.