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Accurate Identification of Bioactive Meliaceae Limonoids by UHPLC–MS/MS Based Structure–Fragment Relationships (SFRs)

[Image: see text] Limonoids are bioactive plant specialized metabolites found in the Meliaceae family. The basic limonoids, i.e., azadiradione, epoxyazadiradione, and gedunin have been exploited for various bioactivities and therefore are the potential drug leads for tomorrow. However, their low abu...

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Autores principales: Mulani, Fayaj A., Nandikol, Sharvani S., Haldar, Saikat, Thulasiram, Hirekodathakallu V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8515590/
https://www.ncbi.nlm.nih.gov/pubmed/34661002
http://dx.doi.org/10.1021/acsomega.1c03697
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author Mulani, Fayaj A.
Nandikol, Sharvani S.
Haldar, Saikat
Thulasiram, Hirekodathakallu V.
author_facet Mulani, Fayaj A.
Nandikol, Sharvani S.
Haldar, Saikat
Thulasiram, Hirekodathakallu V.
author_sort Mulani, Fayaj A.
collection PubMed
description [Image: see text] Limonoids are bioactive plant specialized metabolites found in the Meliaceae family. The basic limonoids, i.e., azadiradione, epoxyazadiradione, and gedunin have been exploited for various bioactivities and therefore are the potential drug leads for tomorrow. However, their low abundance, structural similarity, and lack of adequate mass fragmentation data have hampered their accurate identification and quantification from various sources. In the present study, basic limonoids such as azadirone, azadiradione, epoxyazadiradione, and gedunin isolated from Neem were utilized for the synthesis of their derivatives and isotopologs. A total of 30 one compounds were used in this study among which five were isolated, two were biotransformed, and 24 were synthesized. Among the synthesized compounds nine are novel compounds including six deuterated analogs/isotopologs which are (1,3-(2)H)-1,2-dihydro-3β-hydroxyazadiradione (9), (1,3,16-(2)H)-1,2-dihydro-3β-16β-dihydroxyazadiradione (10), 3β-hydroxyazadiradione (11), 3β-16β-dihydroxyazadiradione (12), (3-(2)H)-3β-hydroxyazadiradione (13), (3,16-(2)H)-3β-16β-dihydroxyazadiradione (14), (1,3,7-(2)H)-1,2-dihydro-3β-hydroxy-7-deacetylazadiradione (15), 1,2,20,21,22,23-hexahydroazadiradione (17), and (1,3-(2)H)-1,2-dihydro-3β-hydroxygedunin (29). These limonoids along with their semisynthesized derivatives were subjected to ultra high performance liquid chromatography mass spectrometry (UHPLC–MS/MS) and the fragmentation pathway was established based on structure–fragment relationships (SFRs), utilizing high resolution MS/MS data. We have developed a most reliable and easily reproducible protocol describing in depth analysis of SFRs based on the structural modifications and synthesis of isotopologs. Also, the MS/MS fragment library of these basic limonoids generated in this study acts as a fingerprint for accurate identification and quantification of limonoids by MS/MS analysis in various plant tissue extracts, phytopharmaceutical formulations and biological samples.
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spelling pubmed-85155902021-10-15 Accurate Identification of Bioactive Meliaceae Limonoids by UHPLC–MS/MS Based Structure–Fragment Relationships (SFRs) Mulani, Fayaj A. Nandikol, Sharvani S. Haldar, Saikat Thulasiram, Hirekodathakallu V. ACS Omega [Image: see text] Limonoids are bioactive plant specialized metabolites found in the Meliaceae family. The basic limonoids, i.e., azadiradione, epoxyazadiradione, and gedunin have been exploited for various bioactivities and therefore are the potential drug leads for tomorrow. However, their low abundance, structural similarity, and lack of adequate mass fragmentation data have hampered their accurate identification and quantification from various sources. In the present study, basic limonoids such as azadirone, azadiradione, epoxyazadiradione, and gedunin isolated from Neem were utilized for the synthesis of their derivatives and isotopologs. A total of 30 one compounds were used in this study among which five were isolated, two were biotransformed, and 24 were synthesized. Among the synthesized compounds nine are novel compounds including six deuterated analogs/isotopologs which are (1,3-(2)H)-1,2-dihydro-3β-hydroxyazadiradione (9), (1,3,16-(2)H)-1,2-dihydro-3β-16β-dihydroxyazadiradione (10), 3β-hydroxyazadiradione (11), 3β-16β-dihydroxyazadiradione (12), (3-(2)H)-3β-hydroxyazadiradione (13), (3,16-(2)H)-3β-16β-dihydroxyazadiradione (14), (1,3,7-(2)H)-1,2-dihydro-3β-hydroxy-7-deacetylazadiradione (15), 1,2,20,21,22,23-hexahydroazadiradione (17), and (1,3-(2)H)-1,2-dihydro-3β-hydroxygedunin (29). These limonoids along with their semisynthesized derivatives were subjected to ultra high performance liquid chromatography mass spectrometry (UHPLC–MS/MS) and the fragmentation pathway was established based on structure–fragment relationships (SFRs), utilizing high resolution MS/MS data. We have developed a most reliable and easily reproducible protocol describing in depth analysis of SFRs based on the structural modifications and synthesis of isotopologs. Also, the MS/MS fragment library of these basic limonoids generated in this study acts as a fingerprint for accurate identification and quantification of limonoids by MS/MS analysis in various plant tissue extracts, phytopharmaceutical formulations and biological samples. American Chemical Society 2021-10-01 /pmc/articles/PMC8515590/ /pubmed/34661002 http://dx.doi.org/10.1021/acsomega.1c03697 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Mulani, Fayaj A.
Nandikol, Sharvani S.
Haldar, Saikat
Thulasiram, Hirekodathakallu V.
Accurate Identification of Bioactive Meliaceae Limonoids by UHPLC–MS/MS Based Structure–Fragment Relationships (SFRs)
title Accurate Identification of Bioactive Meliaceae Limonoids by UHPLC–MS/MS Based Structure–Fragment Relationships (SFRs)
title_full Accurate Identification of Bioactive Meliaceae Limonoids by UHPLC–MS/MS Based Structure–Fragment Relationships (SFRs)
title_fullStr Accurate Identification of Bioactive Meliaceae Limonoids by UHPLC–MS/MS Based Structure–Fragment Relationships (SFRs)
title_full_unstemmed Accurate Identification of Bioactive Meliaceae Limonoids by UHPLC–MS/MS Based Structure–Fragment Relationships (SFRs)
title_short Accurate Identification of Bioactive Meliaceae Limonoids by UHPLC–MS/MS Based Structure–Fragment Relationships (SFRs)
title_sort accurate identification of bioactive meliaceae limonoids by uhplc–ms/ms based structure–fragment relationships (sfrs)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8515590/
https://www.ncbi.nlm.nih.gov/pubmed/34661002
http://dx.doi.org/10.1021/acsomega.1c03697
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