Steroids from Dysoxylum grande (Meliaceae) leaves

Seven new 23-oxo-cholestane derivatives named as grandol A (1), B (2), C (3), D (4), E (5), F (6), and G (7) were isolated from Dysoxylum grande leaves alongside with a new 3,4-secodammar-4(28)-en-3-oic acid derivative (8). The structures of the compounds were elucidated based on the interpretation...

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Main Authors: Low, Kok Wah, Abas, Faridah, Cordell, Geoffrey A., Ito, Hideyuki, Ismail, Intan Safinar
Format: Article
Language:English
English
Published: Elsevier 2013
Online Access:http://psasir.upm.edu.my/id/eprint/30301/
http://psasir.upm.edu.my/id/eprint/30301/1/Steroids%20from%20Dysoxylum%20grande.pdf
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author Low, Kok Wah
Abas, Faridah
Cordell, Geoffrey A.
Ito, Hideyuki
Ismail, Intan Safinar
author_facet Low, Kok Wah
Abas, Faridah
Cordell, Geoffrey A.
Ito, Hideyuki
Ismail, Intan Safinar
author_sort Low, Kok Wah
building UPM Institutional Repository
collection Online Access
description Seven new 23-oxo-cholestane derivatives named as grandol A (1), B (2), C (3), D (4), E (5), F (6), and G (7) were isolated from Dysoxylum grande leaves alongside with a new 3,4-secodammar-4(28)-en-3-oic acid derivative (8). The structures of the compounds were elucidated based on the interpretation of spectroscopic data, and their relative configurations were established by NOESY 2D NMR data. All of the isolates were tested for anti-acetylcholinesterase activity using thin layer chromatography (TLC)-bioautography with fast blue B salt. Only grandol A (1) and B (2) showed positive results, with clear discoloration at a concentration of 12.5 ppm. However, the obtained IC50 values for grandol A and B, when using Ellman’s method, were not significant (>200 μg/ml).
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institution Universiti Putra Malaysia
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language English
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publishDate 2013
publisher Elsevier
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spelling upm-303012015-10-01T07:30:43Z http://psasir.upm.edu.my/id/eprint/30301/ Steroids from Dysoxylum grande (Meliaceae) leaves Low, Kok Wah Abas, Faridah Cordell, Geoffrey A. Ito, Hideyuki Ismail, Intan Safinar Seven new 23-oxo-cholestane derivatives named as grandol A (1), B (2), C (3), D (4), E (5), F (6), and G (7) were isolated from Dysoxylum grande leaves alongside with a new 3,4-secodammar-4(28)-en-3-oic acid derivative (8). The structures of the compounds were elucidated based on the interpretation of spectroscopic data, and their relative configurations were established by NOESY 2D NMR data. All of the isolates were tested for anti-acetylcholinesterase activity using thin layer chromatography (TLC)-bioautography with fast blue B salt. Only grandol A (1) and B (2) showed positive results, with clear discoloration at a concentration of 12.5 ppm. However, the obtained IC50 values for grandol A and B, when using Ellman’s method, were not significant (>200 μg/ml). Elsevier 2013-02 Article PeerReviewed application/pdf en http://psasir.upm.edu.my/id/eprint/30301/1/Steroids%20from%20Dysoxylum%20grande.pdf Low, Kok Wah and Abas, Faridah and Cordell, Geoffrey A. and Ito, Hideyuki and Ismail, Intan Safinar (2013) Steroids from Dysoxylum grande (Meliaceae) leaves. Steroids, 78 (2). pp. 210-219. ISSN 0039-128X; ESSN: 1878-5867 10.1016/j.steroids.2012.09.011 English
spellingShingle Low, Kok Wah
Abas, Faridah
Cordell, Geoffrey A.
Ito, Hideyuki
Ismail, Intan Safinar
Steroids from Dysoxylum grande (Meliaceae) leaves
title Steroids from Dysoxylum grande (Meliaceae) leaves
title_full Steroids from Dysoxylum grande (Meliaceae) leaves
title_fullStr Steroids from Dysoxylum grande (Meliaceae) leaves
title_full_unstemmed Steroids from Dysoxylum grande (Meliaceae) leaves
title_short Steroids from Dysoxylum grande (Meliaceae) leaves
title_sort steroids from dysoxylum grande (meliaceae) leaves
url http://psasir.upm.edu.my/id/eprint/30301/
http://psasir.upm.edu.my/id/eprint/30301/
http://psasir.upm.edu.my/id/eprint/30301/1/Steroids%20from%20Dysoxylum%20grande.pdf