Evidence map›Paper›PMID 26091020›Full record

ArticleJournal of natural products2015

Antiproliferative Compounds from Cleistanthus boivinianus from the Madagascar Dry Forest.

Yixi Liu, Kelly Young, L Harinantenaina Rakotondraibe, Peggy J Brodie, Jessica D Wiley, Maria B Cassera, Martin W Callmander, R Rakotondrajaona, Etienne Rakotobe, Vincent E Rasamison and 3 more

Open access · greenAbstract read
In one paragraph

Article in Journal of natural products, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Antiproliferative Compounds fromTetrahedron letters · 2015
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 2 countries.

Yixi Liu
Kelly Young
L Harinantenaina Rakotondraibe
Peggy J Brodie
Jessica D Wiley
Maria B Cassera
Martin W Callmander§Missouri Botanical Garden, P.O. Box 299, St. Louis, Missouri 63166, United States.
R Rakotondrajaona⊥Centre National d'Application des Recherches Pharmaceutiques, B.P. 702, Antananarivo 101, Madagascar.
Etienne Rakotobe⊥Centre National d'Application des Recherches Pharmaceutiques, B.P. 702, Antananarivo 101, Madagascar.
Vincent E Rasamison⊥Centre National d'Application des Recherches Pharmaceutiques, B.P. 702, Antananarivo 101, Madagascar.
Karen TenDyke∥Eisai Inc., 4 Corporate Drive, Andover, Massachusetts 01810, United States.
Yongchun Shen∥Eisai Inc., 4 Corporate Drive, Andover, Massachusetts 01810, United States.
David G I Kingston
Virginia Tech · USNational Application Center for Pharmaceutical Research · MGEisai (United States) · USMissouri Botanical Garden · US

Funding

BIODIVERSITY UTILIZATION IN MADAGASCAR AND SURINAMEU01TW000313 · FIC · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI KINGSTON, DAVID GEORGE IAN · 1993 to 2013
$9.5M
Discovery and Mechanism of Antimalarial Natural ProductsR01AT008088 · NCCIH · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI CASSERA, MARIA BELEN, CLEMENT, JASON ANDERSON · 2014 to 2018
$2.0M
FIC NIH HHS U01 TW000313FIC NIH HHS U01 TW00313NCCIH NIH HHS R01 AT008088
6 · The paper itself

Abstract

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 IC50 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 IC50 values of 2.1 ± 0.3 and 4.9 ± 0.1 μM, respectively, while compounds 3 and 6 had IC50 values of >10 μM. Compound 1 also had potent antiproliferative activity against the HCT-116 human colon carcinoma cell line, with an IC50 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 IC50 values of 4.6 and 4.0 μM, respectively.

Indexed as

4-ButyrolactoneAntineoplastic Agents, PhytogenicCell ProliferationDioxolesDrug Screening Assays, AntitumorForestsHCT116 CellsHumansInhibitory Concentration 50LignansMadagascarMalpighiaceaeMolecular StructureNuclear Magnetic Resonance, BiomolecularPlant LeavesPlasmodium falciparum3alpha-O-(beta-D-glucopyranosyl)desoxypodophyllotoxin4-Butyrolactone4-O-(beta-D-glucopyranosyl)dehydropodophyllotoxinAntineoplastic Agents, PhytogenicDioxolesLignansyatein

Identifiers

PMID26091020
PMCPMC4517784
OpenAlexW2329496607

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.