Synthesis, characterization, in-vitro and in-silico therapeutic studies of cinnamaldehyde derivatives

Cinnamomum verum (cinnamon) is a versatile spice belonging to the family Lauraceae. The plant is widely used for its various therapeutic potential viz. antimicrobial, antioxidant, anti-inflammatory, anti-diabetic, anticancer, etc. Its phytocompounds render these therapeutic efficacies of cinnamon. C...

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Published in:JOURNAL OF MOLECULAR STRUCTURE
Main Authors: Singh, Neetu; Yadav, Surender Singh; Kumar, Sanjiv; Narasihman, Balasubramanian; Ramasamy, Kalavathy; Lim, Siong Meng; Shah, Syed Adnan Ali
Format: Article
Language:English
Published: ELSEVIER 2025
Subjects:
Online Access:https://www-webofscience-com.uitm.idm.oclc.org/wos/woscc/full-record/WOS:001328017200001
author Singh
Neetu; Yadav
Surender Singh; Kumar
Sanjiv; Narasihman
Balasubramanian; Ramasamy
Kalavathy; Lim
Siong Meng; Shah
Syed Adnan Ali
spellingShingle Singh
Neetu; Yadav
Surender Singh; Kumar
Sanjiv; Narasihman
Balasubramanian; Ramasamy
Kalavathy; Lim
Siong Meng; Shah
Syed Adnan Ali
Synthesis, characterization, in-vitro and in-silico therapeutic studies of cinnamaldehyde derivatives
Chemistry
author_facet Singh
Neetu; Yadav
Surender Singh; Kumar
Sanjiv; Narasihman
Balasubramanian; Ramasamy
Kalavathy; Lim
Siong Meng; Shah
Syed Adnan Ali
author_sort Singh
spelling Singh, Neetu; Yadav, Surender Singh; Kumar, Sanjiv; Narasihman, Balasubramanian; Ramasamy, Kalavathy; Lim, Siong Meng; Shah, Syed Adnan Ali
Synthesis, characterization, in-vitro and in-silico therapeutic studies of cinnamaldehyde derivatives
JOURNAL OF MOLECULAR STRUCTURE
English
Article
Cinnamomum verum (cinnamon) is a versatile spice belonging to the family Lauraceae. The plant is widely used for its various therapeutic potential viz. antimicrobial, antioxidant, anti-inflammatory, anti-diabetic, anticancer, etc. Its phytocompounds render these therapeutic efficacies of cinnamon. Cinnamaldehyde is the main active compound of cinnamon. Owing to the numerous pharmacology of cinnamaldehyde, cinnamaldehyde was procured from Himedia. Cinnamaldehyde Schiff bases were synthesized by refluxing (40-60 degrees C) cinnamaldehyde with different primary amines for 4-6 h. Glacial acetic acid was used as a catalyst. The product confirmation was done based on thin-layer chromatography. The derivatives were characterized and investigated for antimicrobial (disc-diffusion and broth-dilution methods), antioxidant (DPPH and ABTS assays), and cytotoxicity activities (SRB assay). Higher antibacterial activities were noticed with compounds, NS-6A (ZI(sa) = 13.7 +/- 2.05 mm) and E.O.A (MICec, pa = 6.25 mg/mL) whereas the maximum antifungal results were observed with E.O.A (ZI(fo) = 13.1 +/- 0.14 mm), MCA (MICao = 6.25 mg/mL) by. Compounds MCA (% RSA(DPPH) = 85.35, % RSA(ABTS) = 92.26), E.O.A (% RSA(DPPH) = 83.81, % RSA(ABTS) = 90.54) and NS-9A (% RSA(DPPH) = 83.42, % RSA(ABTS) = 90.32) showed highest antioxidant activity. The highest cytotoxicity against the HCT-116 cell line was observed in compounds MCA (IC50 = 0.27 mu g/mL), and E.O.A (IC50 = 0.38 mu g/mL). Compound NS-4A was observed with the highest docking score (-8.527). Conclusively, E.O.A, MCA, and NS-9A were the most potent compounds and need further in-depth exploration.
ELSEVIER
0022-2860
1872-8014
2025
1321

10.1016/j.molstruc.2024.140165
Chemistry

WOS:001328017200001
https://www-webofscience-com.uitm.idm.oclc.org/wos/woscc/full-record/WOS:001328017200001
title Synthesis, characterization, in-vitro and in-silico therapeutic studies of cinnamaldehyde derivatives
title_short Synthesis, characterization, in-vitro and in-silico therapeutic studies of cinnamaldehyde derivatives
title_full Synthesis, characterization, in-vitro and in-silico therapeutic studies of cinnamaldehyde derivatives
title_fullStr Synthesis, characterization, in-vitro and in-silico therapeutic studies of cinnamaldehyde derivatives
title_full_unstemmed Synthesis, characterization, in-vitro and in-silico therapeutic studies of cinnamaldehyde derivatives
title_sort Synthesis, characterization, in-vitro and in-silico therapeutic studies of cinnamaldehyde derivatives
container_title JOURNAL OF MOLECULAR STRUCTURE
language English
format Article
description Cinnamomum verum (cinnamon) is a versatile spice belonging to the family Lauraceae. The plant is widely used for its various therapeutic potential viz. antimicrobial, antioxidant, anti-inflammatory, anti-diabetic, anticancer, etc. Its phytocompounds render these therapeutic efficacies of cinnamon. Cinnamaldehyde is the main active compound of cinnamon. Owing to the numerous pharmacology of cinnamaldehyde, cinnamaldehyde was procured from Himedia. Cinnamaldehyde Schiff bases were synthesized by refluxing (40-60 degrees C) cinnamaldehyde with different primary amines for 4-6 h. Glacial acetic acid was used as a catalyst. The product confirmation was done based on thin-layer chromatography. The derivatives were characterized and investigated for antimicrobial (disc-diffusion and broth-dilution methods), antioxidant (DPPH and ABTS assays), and cytotoxicity activities (SRB assay). Higher antibacterial activities were noticed with compounds, NS-6A (ZI(sa) = 13.7 +/- 2.05 mm) and E.O.A (MICec, pa = 6.25 mg/mL) whereas the maximum antifungal results were observed with E.O.A (ZI(fo) = 13.1 +/- 0.14 mm), MCA (MICao = 6.25 mg/mL) by. Compounds MCA (% RSA(DPPH) = 85.35, % RSA(ABTS) = 92.26), E.O.A (% RSA(DPPH) = 83.81, % RSA(ABTS) = 90.54) and NS-9A (% RSA(DPPH) = 83.42, % RSA(ABTS) = 90.32) showed highest antioxidant activity. The highest cytotoxicity against the HCT-116 cell line was observed in compounds MCA (IC50 = 0.27 mu g/mL), and E.O.A (IC50 = 0.38 mu g/mL). Compound NS-4A was observed with the highest docking score (-8.527). Conclusively, E.O.A, MCA, and NS-9A were the most potent compounds and need further in-depth exploration.
publisher ELSEVIER
issn 0022-2860
1872-8014
publishDate 2025
container_volume 1321
container_issue
doi_str_mv 10.1016/j.molstruc.2024.140165
topic Chemistry
topic_facet Chemistry
accesstype
id WOS:001328017200001
url https://www-webofscience-com.uitm.idm.oclc.org/wos/woscc/full-record/WOS:001328017200001
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