Anti-inflammatory Activity of 1-Substituted Glyoxal β- Carboline Derivatives
The anti-inflammatory properties of R-carbolines have been widely studied, highlighting their potential in treating inflammatory disorders. This research investigates the antiinflammatory activity of selected 1-substituted glyoxal R-carboline derivatives, achieved through a one-step conversion of 5-...
Published in: | MALAYSIAN JOURNAL OF FUNDAMENTAL AND APPLIED SCIENCES |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
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PENERBIT UTM PRESS
2024
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Online Access: | https://www-webofscience-com.uitm.idm.oclc.org/wos/woscc/full-record/WOS:001338878300018 |
author |
Zulkifli Siti Zafirah; Asha'ari Nur Ain Nabilah; Aziz Ahmad Fawwaz Aiman; Pungot Noor Hidayah |
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Zulkifli Siti Zafirah; Asha'ari Nur Ain Nabilah; Aziz Ahmad Fawwaz Aiman; Pungot Noor Hidayah Anti-inflammatory Activity of 1-Substituted Glyoxal β- Carboline Derivatives Science & Technology - Other Topics |
author_facet |
Zulkifli Siti Zafirah; Asha'ari Nur Ain Nabilah; Aziz Ahmad Fawwaz Aiman; Pungot Noor Hidayah |
author_sort |
Zulkifli |
spelling |
Zulkifli, Siti Zafirah; Asha'ari, Nur Ain Nabilah; Aziz, Ahmad Fawwaz Aiman; Pungot, Noor Hidayah Anti-inflammatory Activity of 1-Substituted Glyoxal β- Carboline Derivatives MALAYSIAN JOURNAL OF FUNDAMENTAL AND APPLIED SCIENCES English Article The anti-inflammatory properties of R-carbolines have been widely studied, highlighting their potential in treating inflammatory disorders. This research investigates the antiinflammatory activity of selected 1-substituted glyoxal R-carboline derivatives, achieved through a one-step conversion of 5-hydroxy-L-tryptophan with activated glyoxal, without forming tetrahydroR-carboline (THRC) intermediates. These derivatives (4e 4e-g ) were synthesized successfully without requiring expensive metal catalysts, prolonged reaction times, or stringent reaction conditions, and yielded moderate amounts. Our findings indicate that all the derivatives significantly inhibit xanthine oxidase (XO) activity, leading to a reduction in reactive oxygen species (ROS) and free radicals. This inhibition disrupts the inflammatory cascade and attenuates the inflammatory response. PENERBIT UTM PRESS 2289-5981 2289-599X 2024 20 5 10.11113/mjfas.v20n5.3630 Science & Technology - Other Topics gold WOS:001338878300018 https://www-webofscience-com.uitm.idm.oclc.org/wos/woscc/full-record/WOS:001338878300018 |
title |
Anti-inflammatory Activity of 1-Substituted Glyoxal β- Carboline Derivatives |
title_short |
Anti-inflammatory Activity of 1-Substituted Glyoxal β- Carboline Derivatives |
title_full |
Anti-inflammatory Activity of 1-Substituted Glyoxal β- Carboline Derivatives |
title_fullStr |
Anti-inflammatory Activity of 1-Substituted Glyoxal β- Carboline Derivatives |
title_full_unstemmed |
Anti-inflammatory Activity of 1-Substituted Glyoxal β- Carboline Derivatives |
title_sort |
Anti-inflammatory Activity of 1-Substituted Glyoxal β- Carboline Derivatives |
container_title |
MALAYSIAN JOURNAL OF FUNDAMENTAL AND APPLIED SCIENCES |
language |
English |
format |
Article |
description |
The anti-inflammatory properties of R-carbolines have been widely studied, highlighting their potential in treating inflammatory disorders. This research investigates the antiinflammatory activity of selected 1-substituted glyoxal R-carboline derivatives, achieved through a one-step conversion of 5-hydroxy-L-tryptophan with activated glyoxal, without forming tetrahydroR-carboline (THRC) intermediates. These derivatives (4e 4e-g ) were synthesized successfully without requiring expensive metal catalysts, prolonged reaction times, or stringent reaction conditions, and yielded moderate amounts. Our findings indicate that all the derivatives significantly inhibit xanthine oxidase (XO) activity, leading to a reduction in reactive oxygen species (ROS) and free radicals. This inhibition disrupts the inflammatory cascade and attenuates the inflammatory response. |
publisher |
PENERBIT UTM PRESS |
issn |
2289-5981 2289-599X |
publishDate |
2024 |
container_volume |
20 |
container_issue |
5 |
doi_str_mv |
10.11113/mjfas.v20n5.3630 |
topic |
Science & Technology - Other Topics |
topic_facet |
Science & Technology - Other Topics |
accesstype |
gold |
id |
WOS:001338878300018 |
url |
https://www-webofscience-com.uitm.idm.oclc.org/wos/woscc/full-record/WOS:001338878300018 |
record_format |
wos |
collection |
Web of Science (WoS) |
_version_ |
1818940498034819072 |