Phytochemical study of flavonoids from the leaves of muntingia calabura, synthesis of flavonoid mannich base derivatives and their anticancer activity against breast carcinoma cell lines

Due to the continuous evolution of multi-drug resistant tumors, the development of new drugs with enhanced efficacy is essential. Hence, there is a growing interest in making chemical modifications to the natural flavonoids to improve the bioactivity. The aim of this study is to extract, isolate and...

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Main Author: Chang, Chew Cheen
Format: Final Year Project / Dissertation / Thesis
Published: 2023
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Online Access:http://eprints.utar.edu.my/5734/1/the_SIA_2023_CCC.pdf
http://eprints.utar.edu.my/5734/
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author Chang, Chew Cheen
author_facet Chang, Chew Cheen
author_sort Chang, Chew Cheen
building UTAR Library
collection Institutional Repository
content_provider Universiti Tunku Abdul Rahman
content_source UTAR Institutional Repository
continent Asia
country Malaysia
description Due to the continuous evolution of multi-drug resistant tumors, the development of new drugs with enhanced efficacy is essential. Hence, there is a growing interest in making chemical modifications to the natural flavonoids to improve the bioactivity. The aim of this study is to extract, isolate and characterize the chemical constituents from the leaves of Muntingia calabura, synthesize and characterize flavonoid Mannich base derivatives and evaluate their cytotoxic activity. Initially, dried leaves of Muntingia calabura were extracted with 95% ethanol, followed by 1:1 water/ethyl acetate (EA) partition. The EA crude extract was then subjected to continuous column chromatography over silica gel to obtain pure compounds. The pure compounds were characterized by spectroscopic techniques. Subsequently, the isolated flavonoids were subjected to Mannich reaction. The synthesized compounds were characterized by spectroscopic techniques. Cytototoxic activity of the parent compounds and synthesized compounds were evaluated against two breast cancer cell lines i.e., MCF-7, MDA-MB-231, and one normal breast cell line, MCF-10A via MTT assay. A total of eighteen flavonoids were isolated from the leaves of Muntingia iii calabura. Among them, 3,5-dihydroxy-7-methoxyflavanone (M1), 7,8- dihydroxyflavanone (M17), and 2’,3’,4’-trihydroxychalcone (M6) were isolated from the leaves of Muntingia calabura for the first time. For Mannich bases, a total of twenty flavonoid Mannich bases were synthesized. Cytotoxic activity against MDA-MB-231 cancer cell line showed that flavonoid Mannich bases exhibited greater activity than parent compounds. 5,7-dihydroxy-8-(4- methoxybenzylamine)-2-phenyl-4H-chromen-4-one (M14f) showed the highest cytotoxic activity against MDA-MB-231 cell with IC50 of 5.75±0.82 µM. For MCF-7 cell line, the parent compounds and Mannich bases showed moderate activity with the IC50 range of 9.17-68.5 µM. For cytotoxic activity against MCF-10A cell line, parent compounds, 5,7-dihydroxyflavone (M14) showed highest toxicity against MCF-10A with IC50 of 10.55±1.05 µM. The results suggest that synthetic modifications have produced the compounds with improved anticancer activity and selectivity against breast cancer cells.
format Final Year Project / Dissertation / Thesis
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publishDate 2023
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spelling my-utar-eprints.57342023-09-18T13:41:05Z Phytochemical study of flavonoids from the leaves of muntingia calabura, synthesis of flavonoid mannich base derivatives and their anticancer activity against breast carcinoma cell lines Chang, Chew Cheen Q Science (General) QM Human anatomy QR180 Immunology QR355 Virology RD Surgery Due to the continuous evolution of multi-drug resistant tumors, the development of new drugs with enhanced efficacy is essential. Hence, there is a growing interest in making chemical modifications to the natural flavonoids to improve the bioactivity. The aim of this study is to extract, isolate and characterize the chemical constituents from the leaves of Muntingia calabura, synthesize and characterize flavonoid Mannich base derivatives and evaluate their cytotoxic activity. Initially, dried leaves of Muntingia calabura were extracted with 95% ethanol, followed by 1:1 water/ethyl acetate (EA) partition. The EA crude extract was then subjected to continuous column chromatography over silica gel to obtain pure compounds. The pure compounds were characterized by spectroscopic techniques. Subsequently, the isolated flavonoids were subjected to Mannich reaction. The synthesized compounds were characterized by spectroscopic techniques. Cytototoxic activity of the parent compounds and synthesized compounds were evaluated against two breast cancer cell lines i.e., MCF-7, MDA-MB-231, and one normal breast cell line, MCF-10A via MTT assay. A total of eighteen flavonoids were isolated from the leaves of Muntingia iii calabura. Among them, 3,5-dihydroxy-7-methoxyflavanone (M1), 7,8- dihydroxyflavanone (M17), and 2’,3’,4’-trihydroxychalcone (M6) were isolated from the leaves of Muntingia calabura for the first time. For Mannich bases, a total of twenty flavonoid Mannich bases were synthesized. Cytotoxic activity against MDA-MB-231 cancer cell line showed that flavonoid Mannich bases exhibited greater activity than parent compounds. 5,7-dihydroxy-8-(4- methoxybenzylamine)-2-phenyl-4H-chromen-4-one (M14f) showed the highest cytotoxic activity against MDA-MB-231 cell with IC50 of 5.75±0.82 µM. For MCF-7 cell line, the parent compounds and Mannich bases showed moderate activity with the IC50 range of 9.17-68.5 µM. For cytotoxic activity against MCF-10A cell line, parent compounds, 5,7-dihydroxyflavone (M14) showed highest toxicity against MCF-10A with IC50 of 10.55±1.05 µM. The results suggest that synthetic modifications have produced the compounds with improved anticancer activity and selectivity against breast cancer cells. 2023-05 Final Year Project / Dissertation / Thesis NonPeerReviewed application/pdf http://eprints.utar.edu.my/5734/1/the_SIA_2023_CCC.pdf Chang, Chew Cheen (2023) Phytochemical study of flavonoids from the leaves of muntingia calabura, synthesis of flavonoid mannich base derivatives and their anticancer activity against breast carcinoma cell lines. Master dissertation/thesis, UTAR. http://eprints.utar.edu.my/5734/
spellingShingle Q Science (General)
QM Human anatomy
QR180 Immunology
QR355 Virology
RD Surgery
Chang, Chew Cheen
Phytochemical study of flavonoids from the leaves of muntingia calabura, synthesis of flavonoid mannich base derivatives and their anticancer activity against breast carcinoma cell lines
title Phytochemical study of flavonoids from the leaves of muntingia calabura, synthesis of flavonoid mannich base derivatives and their anticancer activity against breast carcinoma cell lines
title_full Phytochemical study of flavonoids from the leaves of muntingia calabura, synthesis of flavonoid mannich base derivatives and their anticancer activity against breast carcinoma cell lines
title_fullStr Phytochemical study of flavonoids from the leaves of muntingia calabura, synthesis of flavonoid mannich base derivatives and their anticancer activity against breast carcinoma cell lines
title_full_unstemmed Phytochemical study of flavonoids from the leaves of muntingia calabura, synthesis of flavonoid mannich base derivatives and their anticancer activity against breast carcinoma cell lines
title_short Phytochemical study of flavonoids from the leaves of muntingia calabura, synthesis of flavonoid mannich base derivatives and their anticancer activity against breast carcinoma cell lines
title_sort phytochemical study of flavonoids from the leaves of muntingia calabura, synthesis of flavonoid mannich base derivatives and their anticancer activity against breast carcinoma cell lines
topic Q Science (General)
QM Human anatomy
QR180 Immunology
QR355 Virology
RD Surgery
url http://eprints.utar.edu.my/5734/1/the_SIA_2023_CCC.pdf
http://eprints.utar.edu.my/5734/
url_provider http://eprints.utar.edu.my