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Modified Terpenic Acids from Boswellia serrata : Biological Activity
(Englisch)
Anti-inflammatory, Anti-arthritic and Anti-cancer Activity
Suvarna Shenvi & G. Chandrasekara Reddy

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Autor/Autorin: Shenvi Suvarna

Suvarna Shenvi did Ph.D in Organic Chemistry from Univ. of Mysore, India, and currently working as a Research Scientist. Her research interests are in the area of natural products: isolation, characterization and synthetic modification of terpenic acids having anticancer, anti-inflammatory and anti-arthritic activity.
Isolation and identification of naturally occurring pentacyclic triterpinoid (Boswellic acids), tetra cyclic triterpnoids (Tirucallic acids) from Boswellia serrata. Synthesized novel hybrid molecules using boswellic acids with NSAIDs and studied their anti-inflammatory, anti-arthritic activity on in vivo models. Enhancement of biologically potent molecule from naturally occurring mixture of boswellic acids by converting them into one by allylic oxidation using various oxidizing agents and optimized the best one. Boswellic acid nanoparticles were prepared and analysed using SEM technique. Naturally occurring boswellic acids which are anti-inflammatory agents are lipophylic in nature and thus become a limiting factor in terms of their bioavailability. Hence for first time succefully prepared water soluble glycosides of 11-keto-?-boswellic acids. Synthesized novel A-ring modified via second order Beckmann rearrangement compounds from 3-oxo-tircallic acid evaluated for their anticancer activity against human cancer cell lines and discovered that the A-ring modified compounds were showed the improved anticancer activity specially on prostate caner cell line.
Isolation and identification of naturally occurring pentacyclic triterpinoid (Boswellic acids), tetra cyclic triterpnoids (Tirucallic acids) from Boswellia serrata. Synthesized novel hybrid molecules using boswellic acids with NSAIDs and studied their anti-inflammatory, anti-arthritic activity on in vivo models. Enhancement of biologically potent molecule from naturally occurring mixture of boswellic acids by converting them into one by allylic oxidation using various oxidizing agents and optimized the best one. Boswellic acid nanoparticles were prepared and analysed using SEM technique. Naturally occurring boswellic acids which are anti-inflammatory agents are lipophylic in nature and thus become a limiting factor in terms of their bioavailability. Hence for first time succefully prepared water soluble glycosides of 11-keto-beta-boswellic acids. Synthesized novel A-ring modified via second order Beckmann rearrangement compounds from 3-oxo-tircallic acid evaluated for their anticancer activity against human cancer cell lines and discovered that the A-ring modified compounds were showed the improved anticancer activity specially on prostate caner cell line.


Über den Autor

Suvarna Shenvi did Ph.D in Organic Chemistry from Univ. of Mysore, India, and currently working as a Research Scientist. Her research interests are in the area of natural products: isolation, characterization and synthetic modification of terpenic acids having anticancer, anti-inflammatory and anti-arthritic activity.


Klappentext

Isolation and identification of naturally occurring pentacyclic triterpinoid (Boswellic acids), tetra cyclic triterpnoids (Tirucallic acids) from Boswellia serrata. Synthesized novel hybrid molecules using boswellic acids with NSAIDs and studied their anti-inflammatory, anti-arthritic activity on in vivo models. Enhancement of biologically potent molecule from naturally occurring mixture of boswellic acids by converting them into one by allylic oxidation using various oxidizing agents and optimized the best one. Boswellic acid nanoparticles were prepared and analysed using SEM technique. Naturally occurring boswellic acids which are anti-inflammatory agents are lipophylic in nature and thus become a limiting factor in terms of their bioavailability. Hence for first time succefully prepared water soluble glycosides of 11-keto-¿-boswellic acids. Synthesized novel A-ring modified via second order Beckmann rearrangement compounds from 3-oxo-tircallic acid evaluated for their anticancer activity against human cancer cell lines and discovered that the A-ring modified compounds were showed the improved anticancer activity specially on prostate caner cell line.



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