TY - JOUR
T1 - Synthesis, anti-angiogenic activity and prediction toxicity of (E)-3-(3-methoxyphenyl) propenoic acid
AU - Ekowati, Juni
AU - Nofianti, Kholis Amalia
AU - Yunita, Maya Nurwartanti
AU - Hamid, Iwan Sahrial
AU - Dwiningrum, Fitria
AU - Ramadhan, Darwin Ryan
AU - Ananda, Ghinalya Chalbi
N1 - Publisher Copyright:
© the Author(s), 2023.
PY - 2023
Y1 - 2023
N2 - 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 compli-cated, because of their serious toxicity. So, we require improving clinically appropriate strategies to boost efficacy of anti-angio-genic 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.
AB - 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 compli-cated, because of their serious toxicity. So, we require improving clinically appropriate strategies to boost efficacy of anti-angio-genic 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.
KW - (E)-3-(3-methoxyphenyl) propenoic acid
KW - Anti-angiogenesis
KW - Good health and well-being
KW - m-methoxy cinnamic acid
UR - http://www.scopus.com/inward/record.url?scp=85153246324&partnerID=8YFLogxK
U2 - 10.4081/jphia.2023.2534
DO - 10.4081/jphia.2023.2534
M3 - Article
AN - SCOPUS:85153246324
SN - 2038-9922
VL - 14
JO - Journal of Public Health in Africa
JF - Journal of Public Health in Africa
IS - S1
M1 - 2534
ER -