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  5. The phytochemical investigation of five African Croton species: Croton oligandrus, Croton megalocarpus, Croton menyharthii, Croton rivularis and Croton megalobotrys.

The phytochemical investigation of five African Croton species: Croton oligandrus, Croton megalocarpus, Croton menyharthii, Croton rivularis and Croton megalobotrys.

Resource type
Journal article
Creator (person)
Langat, Moses K.
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Djuidje, Elvire F.K.
Ndunda, Beth M.
Isyaka, Sani M.
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Dolan, Nathalie S.
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Ettridge, Gareth D.
Whitmore, Hannah
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Lopez, Isabel
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Alqahtani, Alaa M.
Atiku, Ibrahim
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Lobe, Jules S.
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Mas-Claret, Eduard
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Crouch, Neil R.
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Midiwo, Jacob O.
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Mulholland, Dulcie A.
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Kamdem, Alain F. W.
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Date published
December 2020
Abstract
The chemistry of five African Croton taxa, Croton oligandrus Pierre ex Hutch., Croton megalocarpus Hutch., Croton menyharthii Pax, Croton rivularis Mull.Arg. and Croton megalobotrys Mull.Arg. is described. The undescribed ent-19-hydroxyisopimara-8(9),15-dien-7-one and ent-isopimara-7(8),15-dien-16,19-diol were isolated from the fruits of C. oligandrus, ent-isopimara-7(8),15-dien-19-yl octadecanoate was obtained from both the fruits and leaves, and ent-19-hydroxyisopimara-8(9),15-dien-7-one was isolated from the leaves of this species. The undescribed 3,4,15,16-diepoxy-8α-hydroxycleroda-13(16),14-dien-12S,17-olide and (5S,9R,10S)-7,13-ent-abietadien-2-one were isolated from the leaves and roots of C. megalocarpus respectively. Compounds isolated from C. menyharthii, C. rivularis and C. megalobotrys have been reported from other sources. The structures of the compounds were determined using NMR, IR and MS experiments. The absolute configurations of the ent-isopimarane, ent-abietane and ent-clerodane diterpenoids isolated were confirmed by comparing calculated and experimental electronic circular dichroism (ECD) spectra. DP4+ probability calculations were used to assign the configuration at C-8 for 3,4,15,16-diepoxy-8α-hydroxycleroda-13(16),14-dien-12S,17-olide. Epoxy-ent-clerodadiene, 3β,4β:15,16-diepoxy-13(16),14-ent-clerodadien-17,12S-olide, 3β,4β:15,16-diepoxy-8α-hydroxy-ent-cleroda-13(16),14-dien-12,17-olide, 7,13-abietadien-2-ol, (5S,9R,10S)-7,13-ent-abietadien-2-one, crotonolide E, furocrotinsulolide A, epoxychiromodine, 3β,4β:15,16-diepoxy-13(16),14-ent-clerodadiene and crotohalimaneic acid were selected for screening based on their ability to add diversity to the NCI small molecule compound collection, and were evaluated against the NCI60 panel of human tumour cell lines at 10μM level, but found inactive.
Funder
Funder nameAwards
University of KwaZulu Natal, South Africa
University of Surrey, United Kingdom
National Research Foundation, South Africa
Royal Society, United Kingdom
Postdoctoral Fellowship
University of Nairobi, Kenya
International Foundation of Sciences
International Science Program, Sweden
Organisation for the Prohibition of Chemical Weapons, Netherlands
Natural Products Research Network for East and Central Africa
Journal title
Phytochemistry Letters
Volume
40
Publisher
Elsevier BV
Place of publication
Amsterdam, Netherlands
ISSN
1874-3900
Date accepted
September 24, 2020
Official URL
http://dx.doi.org/10.1016/j.phytol.2020.09.020
Rights statement
In Copyright
DOI
10.1016/j.phytol.2020.09.020
Keywords
Croton oligandrus
Croton rivularis
Croton megalobotrys
Croton megalocarpus
Croton menyharthii
ent-Diterpenoids
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