Previously undescribed antioxidative O-heterocyclic angiotensin converting enzyme inhibitors from the intertidal seaweed Sargassum wightii as potential antihypertensives

Anusree, M and Chakraborty, Kajal (2018) Previously undescribed antioxidative O-heterocyclic angiotensin converting enzyme inhibitors from the intertidal seaweed Sargassum wightii as potential antihypertensives. Food Research International, 113. pp. 474-486. ISSN 0963-9969

Text Kajal Chakraborty_2018_Food Research International_Previously undescribed antioxidative O-heterocyclic angiotensin converting enzyme inhibitors from seaweed.pdf Restricted to Registered users only Download (1MB) | Please mail the copy request to cmfrilibrary@gmail.com

Abstract

Four previously undescribed antioxidative O-heterocyclic analogues, characterized as 3″-isopropyl-3c-{3b-[(2- oxo-3,4-dihydro-2H-chromen-3-yl) methyl] butyl}-2″-butenyl-3′-hydroxy-2′-(2′b-methoxy-2′-oxoethyl)-3′, 4′- dihydro-2H-pyran-4′-carboxylate (1), 2c-methylbutyl-6-[6c-(benzoyloxy)propyl]-6-methyl-tetrahydro-2Hpyran- 2-carboxylate (2), 6-{6b-[3′-(5′a-methyl propyl)-3′, 4′-dihydro-2H-pyran-6′-yl] ethyl}-tetrahydro-2Hpyran- 2-one (3) and 7-(7c-methylpentyl)-hexahydro-2H-chromen-2-one (4) were isolated from the ethylacetate: methanol fraction of the brown seaweed Sargassum wightii. Nuclear magnetic resonance and mass spectroscopic experiments unambiguously attributed their structural identities. Antihypertensive activities of the studied compounds were determined in terms of their angiotensin converting enzyme (ACE) inhibitory potential. The 2H-pyranylcarboxylate derivative (1) displayed comparable activity (IC50 0.08 mg/mL) with standard antihypertensive agent captopril (IC50 0.07 mg/mL). The O-heterocyclic derivatives bearing 2H-pyran-4′-carboxylate (1) and 2H-pyran-2-carboxylate (2) frameworks showed significantly greater (p < 0.05) 1, 1-diphenyl-2- picryl-hydrazil radical quenching potential {IC50 (1) 0.34 and IC50 (2) 0.45 mg/mL} compared to the standard antioxidant α-tocopherol (IC50 0.63 mg/mL). Structure-activity relationship analyses demonstrated that the electronic and lipophilic descriptors might significantly contribute towards the target bioactivities of 2H-pyranylcarboxylates (1 and 2). Molecular docking simulations were carried out for ACE inhibition, and the binding energy obtained for the compounds (~7.04–8.48 kcal/mol) demonstrated their potential enzyme-ligand interactions. The potential of hitherto undescribed O-heterocyclic derivatives as natural antioxidant and antihypertensive functional food supplements and their utilization as therapeutic leads in the antihypertensive management were described in the present study.

Item Type:	Article
Uncontrolled Keywords:	Sargassum wightii; Sargassaceae; Brown seaweed O-heterocyclic analogues; 2H-pyranylcarboxylate; Antioxidant activity; Angiotensin converting enzyme inhibitory; activity; Molecular docking simulations
Subjects:	Fish Biotechnology > Bioactive compound Algae > Seaweed
Divisions:	CMFRI-Kochi > Marine Biotechnology, Fish Nutrition and Health Division Subject Area > CMFRI > CMFRI-Kochi > Marine Biotechnology, Fish Nutrition and Health Division CMFRI-Kochi > Marine Biotechnology, Fish Nutrition and Health Division Subject Area > CMFRI-Kochi > Marine Biotechnology, Fish Nutrition and Health Division
Depositing User:	Arun Surendran
Date Deposited:	13 Aug 2018 06:23
Last Modified:	13 Aug 2018 06:23
URI:	http://eprints.cmfri.org.in/id/eprint/12991

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