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Psiguanol, a novel α-pyrone derivative from Psidium guajava leaves and vasorelaxant activity in rat aorta cells through intracellular cGMP-dependent opening of calcium-activated potassium channels

The phytochemical investigation of leaves led to the isolation of total nineteen compounds which belongs to meroterpenoids, flavonoid, phenolics, and triterpenoids. The compounds were isolated using extensive chromatography techniques and identified as psiguanol ( ), as new compound along with guaja...

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Published in:Natural product research 2024-01, p.1-14
Main Authors: Srivastava, Shraddha, Mishra, Divya, Bisht, Rohit, Savita, Kumari, Singh, Kishan, Rani, Poonam, Chanda, Debabrata, Dev, Kapil
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creator Srivastava, Shraddha
Mishra, Divya
Bisht, Rohit
Savita, Kumari
Singh, Kishan
Rani, Poonam
Chanda, Debabrata
Dev, Kapil
description The phytochemical investigation of leaves led to the isolation of total nineteen compounds which belongs to meroterpenoids, flavonoid, phenolics, and triterpenoids. The compounds were isolated using extensive chromatography techniques and identified as psiguanol ( ), as new compound along with guajadial ( ), psidial A ( ), -caryophyllene ( ), quercetin ( ), avicularin ( ), guaijaverin ( ), hyperin ( ), rutin ( ), ursolic acid ( ), corosolic acid ( ), asiatic acid ( ), -sitosterol ( ), -sitosterol-D-glucoside ( ), ellagic acid ( ), 3,3',4'-trimethylellagic acid 4-O-glucoside ( ), protocatechuic acid ( ), gallic acid ( ), and tricosanoic acid ( ) as known molecules. The compound was isolated for the first time from this plant. The isolated compounds were evaluated for vasorelaxation activity in rat aorta cells and it was observed that compound exhibited the most potent vasorelaxation response in the model in isolated rat aorta cells. Mechanistically, the vasorelaxation activity of was mediated through cGMP-dependent BK channel opening.
doi_str_mv 10.1080/14786419.2023.2294477
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title Psiguanol, a novel α-pyrone derivative from Psidium guajava leaves and vasorelaxant activity in rat aorta cells through intracellular cGMP-dependent opening of calcium-activated potassium channels
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