- Title
- Cordidepsine is A Potential New Anti-HIV Depsidone from Cordia millenii
- Creator
- Zeukang, Rostanie D
- Creator
- Siwe-Noundou, Xavier
- Creator
- Fotsing, Maurice T
- Creator
- Mbafor, Joseph T
- Creator
- Krause, Rui W M
- Creator
- Choudhary, Muhammad I
- Creator
- Atchade, Alex de Theodore
- Subject
- To be catalogued
- Date Issued
- 2019
- Date
- 2019
- Type
- text
- Type
- article
- Identifier
- http://hdl.handle.net/10962/193988
- Identifier
- vital:45413
- Identifier
- xlink:href="https://doi.org/10.3390/molecules24173202"
- Description
- Chemical investigation of Cordia millenii, Baker resulted in the isolation of a new depsidone, cordidepsine (1), along with twelve known compounds including cyclooctasulfur (2), lup-20(29)-en-3-triacontanoate (3), 1-(26-hydroxyhexacosanoyl)glycerol (4), glyceryl-1-hexacosanoate (5) betulinic acid (6), lupenone (7), β-amyrone (8), lupeol (9), β-amyrin (10), allantoin (11), 2′-(4-hydroxyphenyl)ethylpropanoate (12) and stigmasterol glycoside (13). Hemi-synthetic reactions were carried out on two isolated compounds (5 and 6) to afford two new derivatives, that is, cordicerol A (14) and cordicerol B (15), respectively. The chemical structures of all the compounds were established based on analysis and interpretation of spectroscopic data such as electron ionization mass spectrometry (EI–MS), high resolution electrospray ionization mass spectrometry (HR-ESI–MS), fast atom bombardment mass spectrometry (FAB–MS), one dimension and two dimension nuclear magnetic resonance (1D and 2D-NMR) spectral data as well as X-ray crystallography (XRC). Lupeol ester derivatives [Lup-20(29)-en-3-triacontanoate (3)], monoglycerol derivatives [1-(26-hydroxyhexacosanoyl)glycerol (4) and glyceryl-1 hexacosanoate (5)] were isolated for the first time from Cordia genus while sulfur allotrope [cyclooctasulfur (2)] was isolated for the first time from plant origin. Biological assays cordidepsine (1) exhibited significant anti-HIV integrase activity with IC50 = 4.65 μM; EtOAc extract of stem barks, EtOAc fraction of roots and leaves were not toxic against 3T3 cells.
- Format
- computer
- Format
- online resource
- Format
- application/pdf
- Format
- 1 online resource (14 pages)
- Format
- Publisher
- MDPI
- Language
- English
- Relation
- Molecules
- Relation
- Dongmo Zeukang, R., Siwe-Noundou, X., Tagatsing Fotsing, M., Tabopda Kuiate, T., Mbafor, J.T., Krause, R.W., Choudhary, M.I. and Atchadé, A.D.T., 2019. Cordidepsine is A Potential New Anti-HIV Depsidone from Cordia millenii, Baker. Molecules, 24(17), p.3202
- Relation
- Molecules volume 24 number 17 p. 3202 2019 1420-3049
- Rights
- Publisher
- Rights
- Use of this resource is governed by the terms and conditions of the MDPI Open Access Statement (https://www.int-res.com/journals/terms-of-use/)
- Rights
- Open Access
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Collections
Krause, Rui Werner Maçedo (Prof)
RU Department of Chemistry
SDG 03. Good Health and Well-Being
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|---|---|---|---|---|---|---|---|
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