711017-85-5

Usage

Uses

Used in Medicinal Chemistry:
BOC-(2S)-GLY-4-PYRANOYL is used as a key intermediate in the synthesis of various pharmaceutical compounds due to its unique stereochemistry and pyran ring structure. It aids in the development of new drugs with improved efficacy and selectivity.
Used in Pharmaceutical Research:
In pharmaceutical research, BOC-(2S)-GLY-4-PYRANOYL serves as a valuable tool for studying the structure-activity relationships of drug candidates. Its incorporation into molecules can provide insights into the binding interactions with biological targets, leading to the optimization of drug candidates.
Used in Drug Development:
BOC-(2S)-GLY-4-PYRANOYL is utilized in the design and synthesis of novel drug candidates, particularly in the areas of oncology, neurodegenerative diseases, and infectious diseases. Its unique structural features can enhance the potency, selectivity, and pharmacokinetic properties of drug molecules, contributing to the development of more effective therapeutic agents.
Used in Chemical Research:
BOC-(2S)-GLY-4-PYRANOYL is employed as a versatile building block in organic synthesis, enabling the creation of diverse chemical libraries. Its reactivity and functional group compatibility make it suitable for various synthetic routes, facilitating the exploration of new chemical space and the discovery of novel bioactive compounds.
Used in Biological Research:
In biological research, BOC-(2S)-GLY-4-PYRANOYL can be used to probe the interactions between small molecules and biological macromolecules, such as proteins and nucleic acids. Its incorporation into molecular probes can help elucidate the mechanisms of biological processes and identify potential therapeutic targets.
Overall, BOC-(2S)-GLY-4-PYRANOYL is a valuable compound with a wide range of applications in various fields, including medicinal chemistry, pharmaceutical research, drug development, chemical research, and biological research. Its unique structural features and versatility make it an essential component in the advancement of scientific knowledge and the development of innovative therapeutic agents.

Downstream Products

• 1251951-46-8 C₁₃H₂₄N₂O₄ 
• 1595279-97-2 (S)-ethyl 1-((S)-2-amino-2-(tetrahydro-2H-pyran-4-yl)acetyl)-2,3-dihydro-1H-pyrrolo[2,3-b]pyridine-2-carboxylate 
• 1595279-98-3 (S)-ethyl 1-((S)-2-((S)-2-(tert-butoxycarbonyl(methyl)amino)propanamido)-2-(tetrahydro-2H-pyran-4-yl)acetyl)-2,3-dihydro-1H-pyrrolo[2,3-b]pyridine-2-carboxylate 
• 1595279-99-4 (S)-1-((S)-2-((S)-2-(tert-butoxycarbonyl(methyl)amino)propanamido)-2-(tetrahydro-2H-pyran-4-yl)acetyl)-2,3-dihydro-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid 
• 1595280-00-4 tert-butyl (S)-1-((S)-2-((S)-2-(2-fluoro-6-methylphenylcarbamoyl)-2,3-dihydro-1H-pyrrolo[2,3-b]pyridin-1-yl)-2-oxo-1-(tetrahydro-2H-pyran-4-yl)ethylamino)-1-oxopropan-2-yl(methyl)carbamate 
• 1595279-29-0 (S)-1-[(S)-2-((S)-2-methylaminopropionylamino)-2-(tetrahydropyran-4-yl)acetyl]-2,3-dihydro-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid (2-fluoro-6-methylphenyl)amide 
• 1595279-96-1 (S)-ethyl 1-((S)-2-(tert-butoxycarbonylamino)-2-(tetrahydro-2H-pyran-4-yl)acetyl)-2,3-dihydro-1H-pyrrolo[2,3-b]pyridine-2-carboxylate 

Relevant academic research and scientific papers

Protected amino hydroxy adamantane carboxylic acid and process for its preparation

Dipeptidyl peptidase IV (DP 4) inhibiting compounds are provided. The provided compounds can be used for treating diabetes and related diseases, especially Type II diabetes, and other diseases as set out herein, employing such DP 4 inhibitor or a combination of such DP 4 inhibitor and one or more of another antidiabetic agent such as metformin, glyburide, troglitazone, pioglitazone, rosiglitazone and/or insulin and/or one or more of a hypolipidemic agent and/or anti-obesity agent and/or other therapeutic agent.