Isolation and synthesis of pinocembrin and pinostrobin from Artocarpus odoratissimus [Pemencilan dan sintesis pinocembrin dan pinostrobin dari Artocarpus odoratissimus]

Artocarpus odoratissimus is native to Borneo and Mindanao Island. In Sarawak, it is locally known as Terap. Previous studies showed Artocarpus species are rich in phenolic compounds, including flavonoids, stilbenoids and arylbenzofurons. The chemical profile of the indigenous plants from Sarawak, su...

Full description

Bibliographic Details
Main Authors: Nyokat, Nyotia, Yen, Khongheng, Hamzah, A. S., Lim, Isabel Fong, Saaidin, Aimi Suhaili
Format: Article
Language:English
Published: Malaysian Society of Analytical Sciences 2017
Subjects:
Online Access:http://ir.unimas.my/id/eprint/18939/
http://ir.unimas.my/id/eprint/18939/2/ISOLATION.pdf
_version_ 1848838614191964160
author Nyokat, Nyotia
Yen, Khongheng
Hamzah, A. S.
Lim, Isabel Fong
Saaidin, Aimi Suhaili
author_facet Nyokat, Nyotia
Yen, Khongheng
Hamzah, A. S.
Lim, Isabel Fong
Saaidin, Aimi Suhaili
author_sort Nyokat, Nyotia
building UNIMAS Institutional Repository
collection Online Access
description Artocarpus odoratissimus is native to Borneo and Mindanao Island. In Sarawak, it is locally known as Terap. Previous studies showed Artocarpus species are rich in phenolic compounds, including flavonoids, stilbenoids and arylbenzofurons. The chemical profile of the indigenous plants from Sarawak, such as A. odoratissimus has not been studied intensively and the analyses of medicinal properties have not been explored. Thus, a phytochemical study is carried out on the root extracts of A. odoratissimus using various chromatographic methods and it has led to the isolation of two known flavonoids, namely pinocembrin (1) and pinostrobin (2). The structures are identified by comparison of their 1H and 13C NMR data with those reported in the literature. Flavonoid molecule incorporated as multifunctional in the pharmaceutical industry. It has a vast range of pharmacological activities, such as antimicrobial, anti-inflammatory, antioxidant, and anticancer activities. Pinocembrin and pinostrobin which are successfully synthesized with 2-hydroxy,4,6-methoxyacetphenone and benzaldehyde as starting materials were discussed.
first_indexed 2025-11-15T06:58:21Z
format Article
id unimas-18939
institution Universiti Malaysia Sarawak
institution_category Local University
language English
last_indexed 2025-11-15T06:58:21Z
publishDate 2017
publisher Malaysian Society of Analytical Sciences
recordtype eprints
repository_type Digital Repository
spelling unimas-189392022-06-23T01:55:55Z http://ir.unimas.my/id/eprint/18939/ Isolation and synthesis of pinocembrin and pinostrobin from Artocarpus odoratissimus [Pemencilan dan sintesis pinocembrin dan pinostrobin dari Artocarpus odoratissimus] Nyokat, Nyotia Yen, Khongheng Hamzah, A. S. Lim, Isabel Fong Saaidin, Aimi Suhaili QD Chemistry Artocarpus odoratissimus is native to Borneo and Mindanao Island. In Sarawak, it is locally known as Terap. Previous studies showed Artocarpus species are rich in phenolic compounds, including flavonoids, stilbenoids and arylbenzofurons. The chemical profile of the indigenous plants from Sarawak, such as A. odoratissimus has not been studied intensively and the analyses of medicinal properties have not been explored. Thus, a phytochemical study is carried out on the root extracts of A. odoratissimus using various chromatographic methods and it has led to the isolation of two known flavonoids, namely pinocembrin (1) and pinostrobin (2). The structures are identified by comparison of their 1H and 13C NMR data with those reported in the literature. Flavonoid molecule incorporated as multifunctional in the pharmaceutical industry. It has a vast range of pharmacological activities, such as antimicrobial, anti-inflammatory, antioxidant, and anticancer activities. Pinocembrin and pinostrobin which are successfully synthesized with 2-hydroxy,4,6-methoxyacetphenone and benzaldehyde as starting materials were discussed. Malaysian Society of Analytical Sciences 2017-10 Article PeerReviewed text en http://ir.unimas.my/id/eprint/18939/2/ISOLATION.pdf Nyokat, Nyotia and Yen, Khongheng and Hamzah, A. S. and Lim, Isabel Fong and Saaidin, Aimi Suhaili (2017) Isolation and synthesis of pinocembrin and pinostrobin from Artocarpus odoratissimus [Pemencilan dan sintesis pinocembrin dan pinostrobin dari Artocarpus odoratissimus]. Malaysian Journal of Analytical Sciences, 21 (5). pp. 1156-1161. ISSN 1394-2506 http://www.ukm.my/mjas/mjas2018/ DOI: 10.17576/mjas-2017-2105-19
spellingShingle QD Chemistry
Nyokat, Nyotia
Yen, Khongheng
Hamzah, A. S.
Lim, Isabel Fong
Saaidin, Aimi Suhaili
Isolation and synthesis of pinocembrin and pinostrobin from Artocarpus odoratissimus [Pemencilan dan sintesis pinocembrin dan pinostrobin dari Artocarpus odoratissimus]
title Isolation and synthesis of pinocembrin and pinostrobin from Artocarpus odoratissimus [Pemencilan dan sintesis pinocembrin dan pinostrobin dari Artocarpus odoratissimus]
title_full Isolation and synthesis of pinocembrin and pinostrobin from Artocarpus odoratissimus [Pemencilan dan sintesis pinocembrin dan pinostrobin dari Artocarpus odoratissimus]
title_fullStr Isolation and synthesis of pinocembrin and pinostrobin from Artocarpus odoratissimus [Pemencilan dan sintesis pinocembrin dan pinostrobin dari Artocarpus odoratissimus]
title_full_unstemmed Isolation and synthesis of pinocembrin and pinostrobin from Artocarpus odoratissimus [Pemencilan dan sintesis pinocembrin dan pinostrobin dari Artocarpus odoratissimus]
title_short Isolation and synthesis of pinocembrin and pinostrobin from Artocarpus odoratissimus [Pemencilan dan sintesis pinocembrin dan pinostrobin dari Artocarpus odoratissimus]
title_sort isolation and synthesis of pinocembrin and pinostrobin from artocarpus odoratissimus [pemencilan dan sintesis pinocembrin dan pinostrobin dari artocarpus odoratissimus]
topic QD Chemistry
url http://ir.unimas.my/id/eprint/18939/
http://ir.unimas.my/id/eprint/18939/
http://ir.unimas.my/id/eprint/18939/
http://ir.unimas.my/id/eprint/18939/2/ISOLATION.pdf