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Antidiabetic, antioxidant, molecular docking and HPTLC analysis of miquelianin isolated from Euphorbia schimperi C. Presl

The present study demonstrates the miquelianin or quercetin 3-O-glucuronide (compound 1) isolated from aerial parts of Euphorbia schimperi exhibited significant results for antioxidant and antidiabetic potential. The compound 1 along with kaempferol 3-O-glucuronide (compound 2) and quercetin 3-O-rha...

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Autores principales: Ahmed, Sarfaraz, Al-Rehaily, Adnan J., Alam, Perwez, Alqahtani, Ali S., Hidayatullah, Syed, Rehman, Md. Tabish, Mothana, Ramzi A., Abbas, Syed Sadiq, Khan, M.U., Khalid, Jamal M., Siddiqui, Nasir A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6598219/
https://www.ncbi.nlm.nih.gov/pubmed/31297020
http://dx.doi.org/10.1016/j.jsps.2019.03.008
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author Ahmed, Sarfaraz
Al-Rehaily, Adnan J.
Alam, Perwez
Alqahtani, Ali S.
Hidayatullah, Syed
Rehman, Md. Tabish
Mothana, Ramzi A.
Abbas, Syed Sadiq
Khan, M.U.
Khalid, Jamal M.
Siddiqui, Nasir A.
author_facet Ahmed, Sarfaraz
Al-Rehaily, Adnan J.
Alam, Perwez
Alqahtani, Ali S.
Hidayatullah, Syed
Rehman, Md. Tabish
Mothana, Ramzi A.
Abbas, Syed Sadiq
Khan, M.U.
Khalid, Jamal M.
Siddiqui, Nasir A.
author_sort Ahmed, Sarfaraz
collection PubMed
description The present study demonstrates the miquelianin or quercetin 3-O-glucuronide (compound 1) isolated from aerial parts of Euphorbia schimperi exhibited significant results for antioxidant and antidiabetic potential. The compound 1 along with kaempferol 3-O-glucuronide (compound 2) and quercetin 3-O-rhamnoside (compound 3) isolated from the same source were quantified by validated HPTLC method. Antioxidant activity was determined by chemical means in terms of ABTS radical cation and DPPH radical scavenging activity. Compound 1 showed significant scavenging activity in both ABTS and DPPH assays as compared to standard BHA. In ABTS method IC(50) values of compound 1 and standard BHA is found to be 58.90 ± 3.40 µg/mL and 28.70 ± 5.20 µg/mL respectively while in DPPH assay IC(50) values of Compound 1 and standard BHA is 47.20 ± 4.90 µg/mL and 34.50 ± 6.20 µg/mL respectively. Antidiabetic effect was studied through α-amylase and α-glucosidase inhibitory activity. The mechanistic approach through molecular modelling also support the strong binding sites of compound 1 which showed significant α-amylase and α-glucosidase inhibitory activities with IC(50) values 128.34 ± 12.30 and 89.20 ± 9.20 µg/mL respectively as compared to acarbose 64.20 ± 5.60 and 52.40 ± 4.60 µg/mL respectively. The results of validated RP-HPTLC analyses revealed the concentration of compound 1 found to be 16.39 µg/mg and for compound 2 and compound 3 as 3.92 and 14.98 µg/mg of dried extract, respectively.
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spelling pubmed-65982192019-07-11 Antidiabetic, antioxidant, molecular docking and HPTLC analysis of miquelianin isolated from Euphorbia schimperi C. Presl Ahmed, Sarfaraz Al-Rehaily, Adnan J. Alam, Perwez Alqahtani, Ali S. Hidayatullah, Syed Rehman, Md. Tabish Mothana, Ramzi A. Abbas, Syed Sadiq Khan, M.U. Khalid, Jamal M. Siddiqui, Nasir A. Saudi Pharm J Article The present study demonstrates the miquelianin or quercetin 3-O-glucuronide (compound 1) isolated from aerial parts of Euphorbia schimperi exhibited significant results for antioxidant and antidiabetic potential. The compound 1 along with kaempferol 3-O-glucuronide (compound 2) and quercetin 3-O-rhamnoside (compound 3) isolated from the same source were quantified by validated HPTLC method. Antioxidant activity was determined by chemical means in terms of ABTS radical cation and DPPH radical scavenging activity. Compound 1 showed significant scavenging activity in both ABTS and DPPH assays as compared to standard BHA. In ABTS method IC(50) values of compound 1 and standard BHA is found to be 58.90 ± 3.40 µg/mL and 28.70 ± 5.20 µg/mL respectively while in DPPH assay IC(50) values of Compound 1 and standard BHA is 47.20 ± 4.90 µg/mL and 34.50 ± 6.20 µg/mL respectively. Antidiabetic effect was studied through α-amylase and α-glucosidase inhibitory activity. The mechanistic approach through molecular modelling also support the strong binding sites of compound 1 which showed significant α-amylase and α-glucosidase inhibitory activities with IC(50) values 128.34 ± 12.30 and 89.20 ± 9.20 µg/mL respectively as compared to acarbose 64.20 ± 5.60 and 52.40 ± 4.60 µg/mL respectively. The results of validated RP-HPTLC analyses revealed the concentration of compound 1 found to be 16.39 µg/mg and for compound 2 and compound 3 as 3.92 and 14.98 µg/mg of dried extract, respectively. Elsevier 2019-07 2019-03-19 /pmc/articles/PMC6598219/ /pubmed/31297020 http://dx.doi.org/10.1016/j.jsps.2019.03.008 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Ahmed, Sarfaraz
Al-Rehaily, Adnan J.
Alam, Perwez
Alqahtani, Ali S.
Hidayatullah, Syed
Rehman, Md. Tabish
Mothana, Ramzi A.
Abbas, Syed Sadiq
Khan, M.U.
Khalid, Jamal M.
Siddiqui, Nasir A.
Antidiabetic, antioxidant, molecular docking and HPTLC analysis of miquelianin isolated from Euphorbia schimperi C. Presl
title Antidiabetic, antioxidant, molecular docking and HPTLC analysis of miquelianin isolated from Euphorbia schimperi C. Presl
title_full Antidiabetic, antioxidant, molecular docking and HPTLC analysis of miquelianin isolated from Euphorbia schimperi C. Presl
title_fullStr Antidiabetic, antioxidant, molecular docking and HPTLC analysis of miquelianin isolated from Euphorbia schimperi C. Presl
title_full_unstemmed Antidiabetic, antioxidant, molecular docking and HPTLC analysis of miquelianin isolated from Euphorbia schimperi C. Presl
title_short Antidiabetic, antioxidant, molecular docking and HPTLC analysis of miquelianin isolated from Euphorbia schimperi C. Presl
title_sort antidiabetic, antioxidant, molecular docking and hptlc analysis of miquelianin isolated from euphorbia schimperi c. presl
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6598219/
https://www.ncbi.nlm.nih.gov/pubmed/31297020
http://dx.doi.org/10.1016/j.jsps.2019.03.008
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