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Antiproliferative Compounds from Cleistanthus boivinianus from the Madagascar Dry Forest1

[Image: see text] The two new lignans 3α-O-(β-d-glucopyranosyl)desoxypodophyllotoxin (1) and 4-O-(β-d-glucopyranosyl)dehydropodophyllotoxin (2) were isolated from Cleistanthus boivinianus, together with the known lignans deoxypicropodophyllotoxin (3), (±)-β-apopicropodophyllin (4), (−)-desoxypodophy...

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Autores principales: Liu, Yixi, Young, Kelly, Rakotondraibe, L. Harinantenaina, Brodie, Peggy J., Wiley, Jessica D., Cassera, Maria B., Callmander, Martin W., Rakotondrajaona, R., Rakotobe, Etienne, Rasamison, Vincent E., TenDyke, Karen, Shen, Yongchun, Kingston, David G. I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society and American Society of Pharmacognosy 2015
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4517784/
https://www.ncbi.nlm.nih.gov/pubmed/26091020
http://dx.doi.org/10.1021/np501020m
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author Liu, Yixi
Young, Kelly
Rakotondraibe, L. Harinantenaina
Brodie, Peggy J.
Wiley, Jessica D.
Cassera, Maria B.
Callmander, Martin W.
Rakotondrajaona, R.
Rakotobe, Etienne
Rasamison, Vincent E.
TenDyke, Karen
Shen, Yongchun
Kingston, David G. I.
author_facet Liu, Yixi
Young, Kelly
Rakotondraibe, L. Harinantenaina
Brodie, Peggy J.
Wiley, Jessica D.
Cassera, Maria B.
Callmander, Martin W.
Rakotondrajaona, R.
Rakotobe, Etienne
Rasamison, Vincent E.
TenDyke, Karen
Shen, Yongchun
Kingston, David G. I.
author_sort Liu, Yixi
collection PubMed
description [Image: see text] The two new lignans 3α-O-(β-d-glucopyranosyl)desoxypodophyllotoxin (1) and 4-O-(β-d-glucopyranosyl)dehydropodophyllotoxin (2) were isolated from Cleistanthus boivinianus, together with the known lignans deoxypicropodophyllotoxin (3), (±)-β-apopicropodophyllin (4), (−)-desoxypodophyllotoxin (5), (−)-yatein (6), and β-peltatin-5-O-β-d-glucopyranoside (7). The structures of all compounds were characterized by spectroscopic techniques. Compounds 1, 4, and 5 showed potent antiproliferative activities against the A2780 ovarian cancer cell line, with IC(50) values of 33.0 ± 3.6, 63.1 ± 6.7, and 230 ± 1 nM, respectively. Compounds 2 and 7 showed only modest A2780 activities, with IC(50) values of 2.1 ± 0.3 and 4.9 ± 0.1 μM, respectively, while compounds 3 and 6 had IC(50) values of >10 μM. Compound 1 also had potent antiproliferative activity against the HCT-116 human colon carcinoma cell line, with an IC(50) value of 20.5 nM, and compound 4 exhibited modest antiproliferative activity against the A2058 human caucasian metastatic melanoma and MES-SA human uterine sarcoma cell lines, with IC(50) values of 4.6 and 4.0 μM, respectively.
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spelling pubmed-45177842016-06-19 Antiproliferative Compounds from Cleistanthus boivinianus from the Madagascar Dry Forest1 Liu, Yixi Young, Kelly Rakotondraibe, L. Harinantenaina Brodie, Peggy J. Wiley, Jessica D. Cassera, Maria B. Callmander, Martin W. Rakotondrajaona, R. Rakotobe, Etienne Rasamison, Vincent E. TenDyke, Karen Shen, Yongchun Kingston, David G. I. J Nat Prod [Image: see text] The two new lignans 3α-O-(β-d-glucopyranosyl)desoxypodophyllotoxin (1) and 4-O-(β-d-glucopyranosyl)dehydropodophyllotoxin (2) were isolated from Cleistanthus boivinianus, together with the known lignans deoxypicropodophyllotoxin (3), (±)-β-apopicropodophyllin (4), (−)-desoxypodophyllotoxin (5), (−)-yatein (6), and β-peltatin-5-O-β-d-glucopyranoside (7). The structures of all compounds were characterized by spectroscopic techniques. Compounds 1, 4, and 5 showed potent antiproliferative activities against the A2780 ovarian cancer cell line, with IC(50) values of 33.0 ± 3.6, 63.1 ± 6.7, and 230 ± 1 nM, respectively. Compounds 2 and 7 showed only modest A2780 activities, with IC(50) values of 2.1 ± 0.3 and 4.9 ± 0.1 μM, respectively, while compounds 3 and 6 had IC(50) values of >10 μM. Compound 1 also had potent antiproliferative activity against the HCT-116 human colon carcinoma cell line, with an IC(50) value of 20.5 nM, and compound 4 exhibited modest antiproliferative activity against the A2058 human caucasian metastatic melanoma and MES-SA human uterine sarcoma cell lines, with IC(50) values of 4.6 and 4.0 μM, respectively. American Chemical Society and American Society of Pharmacognosy 2015-06-19 2015-07-24 /pmc/articles/PMC4517784/ /pubmed/26091020 http://dx.doi.org/10.1021/np501020m Text en Copyright © 2015 American Chemical Society and American Society of Pharmacognosy This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Liu, Yixi
Young, Kelly
Rakotondraibe, L. Harinantenaina
Brodie, Peggy J.
Wiley, Jessica D.
Cassera, Maria B.
Callmander, Martin W.
Rakotondrajaona, R.
Rakotobe, Etienne
Rasamison, Vincent E.
TenDyke, Karen
Shen, Yongchun
Kingston, David G. I.
Antiproliferative Compounds from Cleistanthus boivinianus from the Madagascar Dry Forest1
title Antiproliferative Compounds from Cleistanthus boivinianus from the Madagascar Dry Forest1
title_full Antiproliferative Compounds from Cleistanthus boivinianus from the Madagascar Dry Forest1
title_fullStr Antiproliferative Compounds from Cleistanthus boivinianus from the Madagascar Dry Forest1
title_full_unstemmed Antiproliferative Compounds from Cleistanthus boivinianus from the Madagascar Dry Forest1
title_short Antiproliferative Compounds from Cleistanthus boivinianus from the Madagascar Dry Forest1
title_sort antiproliferative compounds from cleistanthus boivinianus from the madagascar dry forest1
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4517784/
https://www.ncbi.nlm.nih.gov/pubmed/26091020
http://dx.doi.org/10.1021/np501020m
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