844637-85-0

Usage

Uses

Used in Pharmaceutical Industry:
(-)-(7R,7''R,8S,8''S,7'E)-4''-hydroxy-3,3'',5,5'-tetramethoxy-4',7-epoxy-8,3'-sesquineolign-7'-en-7'',9,9',9''-tetraol is used as a potential pharmaceutical candidate for various applications due to its complex structure and the presence of multiple functional groups. Its biological properties may contribute to the development of new drugs or therapeutic agents.
Used in Nutraceutical Industry:
In the nutraceutical industry, (-)-(7R,7''R,8S,8''S,7'E)-4''-hydroxy-3,3'',5,5'-tetramethoxy-4',7-epoxy-8,3'-sesquineolign-7'-en-7'',9,9',9''-tetraol may be utilized for its potential health benefits. (-)-(7R,7''R,8S,8''S,7'E)-4''-hydroxy-3,3'',5,5'-tetramethoxy-4',7-epoxy-8,3'-sesquineolign-7'-en-7'',9,9',9''-tetraol's unique structure and functional groups could offer advantages in the development of dietary supplements or functional foods.
Used in Cosmetic Industry:
(-)-(7R,7''R,8S,8''S,7'E)-4''-hydroxy-3,3'',5,5'-tetramethoxy-4',7-epoxy-8,3'-sesquineolign-7'-en-7'',9,9',9''-tetraol may also find applications in the cosmetic industry, where its complex structure and functional groups could be leveraged for the development of skincare products or other beauty formulations.
Note: The specific applications and industries mentioned above are hypothetical and provided as examples based on the general properties of sesquineolign compounds. Further research and development would be necessary to determine the actual uses and benefits of (-)-(7R,7''R,8S,8''S,7'E)-4''-hydroxy-3,3'',5,5'-tetramethoxy-4',7-epoxy-8,3'-sesquineolign-7'-en-7'',9,9',9''-tetraol in these industries.

Upstream product

• 97399-78-5 buddlenol A 
• 458-35-5 coniferol 
• 20675-96-1 Syringenin 

Relevant academic research and scientific papers

Enantiomeric neolignans and sesquineolignans from Jatropha integerrima and their absolute configurations

Two pairs of new sesquineolignan enantiomers, (±)-jatrointelignans A and B (1a/1b and 2a/2b), one pair of new neolignan enantiomers, (±)-jatrointelignan D (4a/4b), and two new neolignans, (+)-jatrointelignan C (3a), and (+)-schisphenlignan I (5a) together

Arabidopsis peroxidase-catalyzed copolymerization of coniferyl and sinapyl alcohols: Kinetics of an endwise process

In order to determine the mechanism of the earlier copolymerization steps of two main lignin precursors, sinapyl (S) alcohol and coniferyl (G) alcohol, microscale in vitro oxidations were carried out with a PRX34 Arabidopsis thaliana peroxidase in the presence of H2O2. This plant peroxidase was found to have an in vitro polymerization activity similar to the commonly used horseradish peroxidase. The selected polymerization conditions lead to a bulk polymerization mechanism when G alcohol was the only phenolic substrate available. In the same conditions, the presence of S alcohol at a 50/50 S/G molar ratio turned this bulk mechanism into an endwise one. A kinetics monitoring (size-exclusion chromatography and liquid chromatography-mass spectrometry) of the different species formed during the first 24 h oxidation of the S/G mixture allowed sequencing the bondings responsible for oligomerization. Whereas G homodimers and GS heterodimers exhibit low reactivity, the SS pinoresinol structure act as a nucleating site of the polymerization through an endwise process. This study is particularly relevant to understand the impact of S units on lignin structure in plants and to identify the key step at which this structure is programmed.