57682-64-1

Usage

Uses

Used in Medicinal Chemistry:
(13R,16aR)-13-[(1R,2S)-1,2-dihydroxyheptyl]-1,4,5,6,7,8,9,10,11,13,16,16a-dodecahydropyrido[2,1-d][1,5,9]triazacyclotridecin-2(3H)-one is used as a potential pharmaceutical candidate for the development of new drugs. Its unique molecular structure and functional groups may provide novel mechanisms of action and therapeutic benefits in treating various diseases and conditions.
Used in Biochemistry:
In the field of biochemistry, (13R,16aR)-13-[(1R,2S)-1,2-dihydroxyheptyl]-1,4,5,6,7,8,9,10,11,13,16,16a-dodecahydropyrido[2,1-d][1,5,9]triazacyclotridecin-2(3H)-one can be employed as a research tool to study the interactions between biomolecules and macromolecules. Its heptyl and dihydroxy functional groups may enable it to bind and modulate the activity of specific proteins or enzymes, providing insights into their function and regulation.
Used in Chemical Research:
(13R,16aR)-13-[(1R,2S)-1,2-dihydroxyheptyl]-1,4,5,6,7,8,9,10,11,13,16,16a-dodecahydropyrido[2,1-d][1,5,9]triazacyclotridecin-2(3H)-one may also be utilized in chemical research to explore its synthesis, properties, and potential applications in various chemical processes. Its complex structure and functional groups can serve as a basis for the development of new synthetic methods, catalysts, or materials with unique properties and applications.

Upstream product

• 91377-19-4 (2R,3S,6S)-3-Benzoyloxy-6-(2,2-diethoxy-ethyl)-2-((1S,2R)-1,2-dihydroxy-heptyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid benzyl ester 
• 91377-22-9 N-{4-[{3-[(2S,6R)-6-((1R,2S)-1,2-Bis-methoxymethoxy-heptyl)-2-(2,2-diethoxy-ethyl)-3,6-dihydro-2H-pyridin-1-yl]-propyl}-(toluene-4-sulfonyl)-amino]-butyl}-2,2,2-trifluoro-acetamide 
• 91377-26-3 [(2R,6R)-6-((1R,2S)-1,2-Bis-methoxymethoxy-heptyl)-1-(3-{(toluene-4-sulfonyl)-[4-(2,2,2-trifluoro-acetylamino)-butyl]-amino}-propyl)-1,2,3,6-tetrahydro-pyridin-2-yl]-acetic acid methyl ester 
• 98262-79-4 6-{(Z)-3-[(2S,3S)-3-((S)-1-Acetoxy-hexyl)-oxiranyl]-allyl}-8-oxo-1,5,9-triaza-cyclotridecane-1,5-dicarboxylic acid 1-tert-butyl ester 5-(2,2,2-trichloro-ethyl) ester 
• 91387-41-6 (2S,3R,6S)-2-((1R,2S)-1,2-Bis-methoxymethoxy-heptyl)-6-(2,2-diethoxy-ethyl)-3-methanesulfonyloxy-piperidine-1-carboxylic acid benzyl ester 
• 91377-21-8 N-{3-[(2S,6R)-6-((1R,2S)-1,2-Bis-methoxymethoxy-heptyl)-2-(2,2-diethoxy-ethyl)-3,6-dihydro-2H-pyridin-1-yl]-propyl}-4-methyl-benzenesulfonamide 
• 91377-23-0 (2R,3S,6S)-3-Benzoyloxy-6-(2,2-diethoxy-ethyl)-2-((Z)-hept-1-enyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid benzyl ester 
• 91377-20-7 (2S,6R)-6-((1R,2S)-1,2-Bis-methoxymethoxy-heptyl)-2-(2,2-diethoxy-ethyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid benzyl ester 
• 98262-80-7 (4R,15aR)-4-((1R,2S)-2-Acetoxy-1-hydroxy-heptyl)-14-oxo-1,4,6,7,9,10,11,12,13,14,15,15a-dodecahydro-5H-4a,8,13-triaza-benzocyclotridecene-8-carboxylic acid tert-butyl ester 
• 91377-18-3 (4R,15aR)-4-((1R,2S)-1,2-Dihydroxy-heptyl)-8-(toluene-4-sulfonyl)-1,4,6,7,8,9,10,11,12,13,15,15a-dodecahydro-5H-4a,8,13-triaza-benzocyclotridecen-14-one 

Relevant academic research and scientific papers

A TOTAL SYNTHESIS OF (+/-)-CANNABISATIVINE

A synthesis of racemic cannabisativine is reported.Intramolecular opening of an erythro-acetoxy epoxide by a secondary amino group provided the side chain containing the desired stereochemistry.