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Synthesis, anti-angiogenic activity and prediction toxicity of (E)-3-(3-methoxyphenyl) propenoic acid

BACKGROUND: Anti-angiogenic medications, one of cancer chemo preventive mechanism were permitted for different cancers. Nevertheless, major primary and secondary resistance obstruct efficacy in several tumor types. Moreover, the improvement of safe and effective NSAIDs for angiogenesis inhibition is...

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Autores principales: Ekowati, Juni, Nofianti, Kholis Amalia, Yunita, Maya Nurwartanti, Hamid, Iwan Sahrial, Dwiningrum, Fitria, Ramadhan, Darwin Ryan, Ananda, Ghinalya Chalbi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications, Pavia, Italy 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10365650/
https://www.ncbi.nlm.nih.gov/pubmed/37492539
http://dx.doi.org/10.4081/jphia.2022.2534
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author Ekowati, Juni
Nofianti, Kholis Amalia
Yunita, Maya Nurwartanti
Hamid, Iwan Sahrial
Dwiningrum, Fitria
Ramadhan, Darwin Ryan
Ananda, Ghinalya Chalbi
author_facet Ekowati, Juni
Nofianti, Kholis Amalia
Yunita, Maya Nurwartanti
Hamid, Iwan Sahrial
Dwiningrum, Fitria
Ramadhan, Darwin Ryan
Ananda, Ghinalya Chalbi
author_sort Ekowati, Juni
collection PubMed
description BACKGROUND: Anti-angiogenic medications, one of cancer chemo preventive mechanism were permitted for different cancers. Nevertheless, major primary and secondary resistance obstruct efficacy in several tumor types. Moreover, the improvement of safe and effective NSAIDs for angiogenesis inhibition is complicated, because of their serious toxicity. So, we require improving clinically appropriate strategies to boost efficacy of anti-angiogenic drugs with low risk of toxicity. OBJECTIVES: The present study aimed to synthesize the (E)-3- (3-methoxyphenyl)propenoic acid (3MPCA), to determine the anti-angiogenic activity and predict its toxicity. METHODS: 3MPCA was obtained by Knoevenagel reaction using microwave irradiation at 400 Watt. The anti-angiogenesis experimental was performed using chorioallantois membrane of embryonated chicken eggs induced by b-FGF. The potency of 3MPCA was verified at dosage 30 and 60 ng and compared with celecoxib 60 ng. Toxicity prediction of 3MPCA was performed by ProTox II online program. RESULTS: The results showed that 3MPCA was achieved in good yield (89%). Anti angogenic activity was showed by endothelial cells growth in neovascular capillaries of new blood vessel of chorioallantois membrane of embryonated chicken eggs. The endothelial cells growth decreased until 41.7-83%. The prediction LD50 was 1772mg/kg. CONCLUSION: (E)-3-(3-methoxyphenyl)propenoic acid can be obtained through Knovenagel reaction using microwave irradiation and it has potential as anti-angiogenesis inhibitor with low toxicity.
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spelling pubmed-103656502023-07-25 Synthesis, anti-angiogenic activity and prediction toxicity of (E)-3-(3-methoxyphenyl) propenoic acid Ekowati, Juni Nofianti, Kholis Amalia Yunita, Maya Nurwartanti Hamid, Iwan Sahrial Dwiningrum, Fitria Ramadhan, Darwin Ryan Ananda, Ghinalya Chalbi J Public Health Afr Article BACKGROUND: Anti-angiogenic medications, one of cancer chemo preventive mechanism were permitted for different cancers. Nevertheless, major primary and secondary resistance obstruct efficacy in several tumor types. Moreover, the improvement of safe and effective NSAIDs for angiogenesis inhibition is complicated, because of their serious toxicity. So, we require improving clinically appropriate strategies to boost efficacy of anti-angiogenic drugs with low risk of toxicity. OBJECTIVES: The present study aimed to synthesize the (E)-3- (3-methoxyphenyl)propenoic acid (3MPCA), to determine the anti-angiogenic activity and predict its toxicity. METHODS: 3MPCA was obtained by Knoevenagel reaction using microwave irradiation at 400 Watt. The anti-angiogenesis experimental was performed using chorioallantois membrane of embryonated chicken eggs induced by b-FGF. The potency of 3MPCA was verified at dosage 30 and 60 ng and compared with celecoxib 60 ng. Toxicity prediction of 3MPCA was performed by ProTox II online program. RESULTS: The results showed that 3MPCA was achieved in good yield (89%). Anti angogenic activity was showed by endothelial cells growth in neovascular capillaries of new blood vessel of chorioallantois membrane of embryonated chicken eggs. The endothelial cells growth decreased until 41.7-83%. The prediction LD50 was 1772mg/kg. CONCLUSION: (E)-3-(3-methoxyphenyl)propenoic acid can be obtained through Knovenagel reaction using microwave irradiation and it has potential as anti-angiogenesis inhibitor with low toxicity. PAGEPress Publications, Pavia, Italy 2023-03-16 /pmc/articles/PMC10365650/ /pubmed/37492539 http://dx.doi.org/10.4081/jphia.2022.2534 Text en ©Copyright: the Author(s) https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution Noncommercial License (by-nc 4.0) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Article
Ekowati, Juni
Nofianti, Kholis Amalia
Yunita, Maya Nurwartanti
Hamid, Iwan Sahrial
Dwiningrum, Fitria
Ramadhan, Darwin Ryan
Ananda, Ghinalya Chalbi
Synthesis, anti-angiogenic activity and prediction toxicity of (E)-3-(3-methoxyphenyl) propenoic acid
title Synthesis, anti-angiogenic activity and prediction toxicity of (E)-3-(3-methoxyphenyl) propenoic acid
title_full Synthesis, anti-angiogenic activity and prediction toxicity of (E)-3-(3-methoxyphenyl) propenoic acid
title_fullStr Synthesis, anti-angiogenic activity and prediction toxicity of (E)-3-(3-methoxyphenyl) propenoic acid
title_full_unstemmed Synthesis, anti-angiogenic activity and prediction toxicity of (E)-3-(3-methoxyphenyl) propenoic acid
title_short Synthesis, anti-angiogenic activity and prediction toxicity of (E)-3-(3-methoxyphenyl) propenoic acid
title_sort synthesis, anti-angiogenic activity and prediction toxicity of (e)-3-(3-methoxyphenyl) propenoic acid
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10365650/
https://www.ncbi.nlm.nih.gov/pubmed/37492539
http://dx.doi.org/10.4081/jphia.2022.2534
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