Evidence map›Paper›PMID 29037996›Full record

ArticleEuropean journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences2018

Synthesis, anti-cancer screening and tyrosyl-DNA phosphodiesterase 1 (Tdp1) inhibition activity of novel piperidinyl sulfamides.

Jung Ho Jun, Vineet Kumar, Thomas S Dexheimer, Iwona Wedlich, Marc C Nicklaus, Yves Pommier, Sanjay V Malhotra

Abstract read
In one paragraph

Article in European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Synthesis, Spectroscopic Characterization, andMolecules (Basel, Switzerland) · 2018
    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

7 authors.

Jung Ho JunDepartment of Chemistry, University of Kansas, KS 66045, USA.
Vineet KumarDepartment of Radiation Oncology, Stanford University, 3165 Porter Drive, Palo Alto, CA 94304, USA.
Thomas S DexheimerLaboratory of Molecular Pharmacology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, 20892, USA.
Iwona WedlichChemical Biology Laboratory, Frederick National Laboratory for Cancer Research, 376 Boyles Street, Frederick, MD 21702, USA.
Marc C NicklausChemical Biology Laboratory, Frederick National Laboratory for Cancer Research, 376 Boyles Street, Frederick, MD 21702, USA.
Yves PommierLaboratory of Molecular Pharmacology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, 20892, USA.
Sanjay V MalhotraDepartment of Radiation Oncology, Stanford University, 3165 Porter Drive, Palo Alto, CA 94304, USA. Electronic address: smalhotra@stanford.edu.

Funding

DNA Repair, Cell Cycle Checkpoints and Apoptosis as Targets for Anticancer DrugsZIABC006150 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI POMMIER, YVES · 2009 to 2025
$23.0M
In Silico Screening for Cancer TargetsZICBC010639 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI NICKLAUS, MARC · 2009 to 2024
$4.2M
DNA TOPOISOMERASES AS TARGET OF ACTION OF ANTICANCER DRUGSZ01BC006161 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI POMMIER, YVES · 1996 to 2008
$1.5M
The Open NCI Database - Drug Development ToolZ01BC010517 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI NICKLAUS, MARC · 2003 to 2008
$692k
CCR NIH HHS HHSN261200800001CIntramural NIH HHS Z01 BC006161Intramural NIH HHS Z01 BC010517NCI NIH HHS HHSN261200800001E
6 · The paper itself

Abstract

Novel piperidinyl-based sulfamide derivatives were designed and synthesized through various synthetic routes. Anticancer activities of these sulfamides were evaluated by phenotypic screening on National Cancer Institute's 60 human tumor cell lines (NCI-60). Preliminary screening at 10μM concentration showed that piperidinyl sulfamide aminoester 26 (NSC 749204) was sensitive to most of the cell lines in the panel. Further dose-response studies showed that 26 was highly selective for inhibition of colon cancer cell lines with minimum GI

Indexed as

Antineoplastic AgentsBinding SitesCell Line, TumorHumansModels, MolecularMolecular StructurePhosphodiesterase InhibitorsPhosphoric Diester HydrolasesProtein ConformationStructure-Activity RelationshipAntineoplastic AgentsPhosphodiesterase InhibitorsPhosphoric Diester Hydrolasestyrosyl-DNA phosphodiesteraseAnti-cancerBiological activityPiperidinyl sulfamidesSynthesisTyrosyl-DNA phosphodiesterase 1 (Tdp1)

Identifiers

PMID29037996
PMCPMC8087116

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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.