Evidence map›Paper›PMID 26784163›Full record

ArticleMolecules (Basel, Switzerland)2016

Synthesis of Canthardin Sulfanilamides and Their Acid Anhydride Analogues via a Ring-Opening Reaction of Activated Aziridines and Their Associated Pharmacological Effects.

Ling-Ling Chiang, Ing-Jy Tseng, Pen-Yuan Lin, Shiow-Yunn Sheu, Ching-Tung Lin, Yun-Han Hsieh, Yi-Jing Lin, Hsiao-Ling Chen, Mei-Hsiang Lin

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 36% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. Drug Design and Discovery: Principles and Applications.Molecules (Basel, Switzerland) · 2017
    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

9 authors at 2 institutions in 1 country.

Ling-Ling ChiangSchool of Respiratory Therapy, Taipei Medical University, Taipei 11031, Taiwan. llchiang@tmu.edu.tw.
Ing-Jy TsengGerontology Health Management, College of Nursing, Taipei Medical University, Taipei 11031, Taiwan. Ingjy@tmu.edu.tw.
Pen-Yuan LinDepartment of Pharmaceutical Sciences, School of Pharmacy, Taipei Medical University, Taipei 11031, Taiwan. lpy0620@tmu.edu.tw.
Shiow-Yunn SheuDepartment of Pharmaceutical Sciences, School of Pharmacy, Taipei Medical University, Taipei 11031, Taiwan. amel@tmu.edu.tw.
Ching-Tung LinDepartment of Chemistry, Tam-Kang University, Danshui 25137, New Taipei City, Taiwan. rocketqueenohya@hotmail.com.
Yun-Han HsiehDepartment of Pharmaceutical Sciences, School of Pharmacy, Taipei Medical University, Taipei 11031, Taiwan. jay4273803@hotmail.com.
Yi-Jing LinDepartment of Pharmaceutical Sciences, School of Pharmacy, Taipei Medical University, Taipei 11031, Taiwan. m301101003@tmu.edu.tw.
Hsiao-Ling ChenDepartment of Pharmaceutical Sciences, School of Pharmacy, Taipei Medical University, Taipei 11031, Taiwan. m301101001@tmu.edu.tw.
Mei-Hsiang LinDepartment of Pharmaceutical Sciences, School of Pharmacy, Taipei Medical University, Taipei 11031, Taiwan. mhl00001@tmu.edu.tw.
Taipei Medical University · TWTamkang University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cantharidinimide derivatives, 5a-h, including sulfanilamides containing pyrimidyl, pyrazinyl, hydrogen, thiazolyl, and oxazolyl groups were synthesized. Modification of cantharidinimide by means of the reaction of activated aziridine ring opening led to the discovery of a novel class of antitumor compounds. The analogues 10i-k, 11l-n, 12o-p, and 16q-s were obtained from treating cantharidinimide 6 and analogues (7, 8, and 13) with activated aziridines, which produced a series of ring-opened products including normal and abnormal types. Some of these compounds showed cytotoxic effects in vitro against HL-60, Hep3B, MCF7, and MDA-MB-231 cancer cells. The most potent cytostatic compound, N-cantharidinimido-sulfamethazine (5a), exhibited anti-HL-60 and anti-Hep3B cell activities. Two compounds 5g and 5h displayed slight effects on the Hep3B cell line, while the other compounds produced no response in these four cell lines.

Indexed as

AnhydridesAntineoplastic AgentsAziridinesCantharidinCell Line, TumorCell SurvivalHL-60 CellsHumansInhibitory Concentration 50MCF-7 CellsOxazolesPyrazolesPyrimidinesStructure-Activity RelationshipSulfanilamidesThiazolesAnhydridesAntineoplastic AgentsAziridinesCantharidinOxazolesPyrazolesPyrimidinesSulfanilamidesThiazolescantharidincantharidinimidemethylsulfanylaziridine

Identifiers

PMID26784163
PMCPMC6273973
OpenAlexW2245223179

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.