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Alkaloids from the Leaves of Annona crassiflora and Their Cytotoxic Activity
Aporphines are a class of alkaloids mostly reported in Magnoliids. The genus Annona , Annonaceae, presents great structural diversity of these compounds. Chemical investigation of leaves from Annona crassiflora Mart. resulted in the identification of an undescribed aporphine alkaloid, which was name...
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Published in: | Revista brasileira de farmacognosia 2021-04, Vol.31 (2), p.244-248 |
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creator | Peña-Hidalgo, Miguel Furtado, Luciana Costa Costa-Lotufo, Letícia V. Ferreira, Marcelo J. P. Santos, Déborah Y. A. C. |
description | Aporphines are a class of alkaloids mostly reported in Magnoliids. The genus
Annona
, Annonaceae, presents great structural diversity of these compounds. Chemical investigation of leaves from
Annona crassiflora
Mart. resulted in the identification of an undescribed aporphine alkaloid, which was named as crassiflorine, in addition to six known analogues: anonaine, annoretine, xylopine, tetrahydropalmatrubine, litseglutine B, and stephalagine. The structure of crassiflorine was established through 1D and 2D NMR data in combination with HREIMS and IR analyses. The cytotoxic activity for all tested compounds was marginal (IC
50
> 30 μM) against breast carcinoma (MCF-7) and colorectal carcinoma (HCT-116) cell lines.
Graphical abstract |
doi_str_mv | 10.1007/s43450-021-00147-4 |
format | article |
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Annona
, Annonaceae, presents great structural diversity of these compounds. Chemical investigation of leaves from
Annona crassiflora
Mart. resulted in the identification of an undescribed aporphine alkaloid, which was named as crassiflorine, in addition to six known analogues: anonaine, annoretine, xylopine, tetrahydropalmatrubine, litseglutine B, and stephalagine. The structure of crassiflorine was established through 1D and 2D NMR data in combination with HREIMS and IR analyses. The cytotoxic activity for all tested compounds was marginal (IC
50
> 30 μM) against breast carcinoma (MCF-7) and colorectal carcinoma (HCT-116) cell lines.
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Annona
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Annona crassiflora
Mart. resulted in the identification of an undescribed aporphine alkaloid, which was named as crassiflorine, in addition to six known analogues: anonaine, annoretine, xylopine, tetrahydropalmatrubine, litseglutine B, and stephalagine. The structure of crassiflorine was established through 1D and 2D NMR data in combination with HREIMS and IR analyses. The cytotoxic activity for all tested compounds was marginal (IC
50
> 30 μM) against breast carcinoma (MCF-7) and colorectal carcinoma (HCT-116) cell lines.
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Annona
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Annona crassiflora
Mart. resulted in the identification of an undescribed aporphine alkaloid, which was named as crassiflorine, in addition to six known analogues: anonaine, annoretine, xylopine, tetrahydropalmatrubine, litseglutine B, and stephalagine. The structure of crassiflorine was established through 1D and 2D NMR data in combination with HREIMS and IR analyses. The cytotoxic activity for all tested compounds was marginal (IC
50
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ispartof | Revista brasileira de farmacognosia, 2021-04, Vol.31 (2), p.244-248 |
issn | 1981-528X 1981-528X |
language | eng |
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source | Springer Nature |
subjects | Medicine Pharmacy Short Communication |
title | Alkaloids from the Leaves of Annona crassiflora and Their Cytotoxic Activity |
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