Evidence map›Paper›PMID 33603966›Full record

ArticleACS medicinal chemistry letters2021

Investigation on the Anticancer Activity of Symmetric and Unsymmetric Cyclic Sulfamides.

Jaden Jungho Jun, Divya Duscharla, Ramesh Ummanni, Paul R Hanson, Sanjay V Malhotra

Open access · greenAbstract read
In one paragraph

Article in ACS medicinal chemistry letters, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

2 citing papers in PubMed, 12 citations in OpenAlex.

  1. RSC advances · 2023
    Article
  2. 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

5 authors at 4 institutions in 2 countries.

Jaden Jungho JunDepartment of Pharmaceutical Sciences and Computational Chemical Genomics Screening Center, National Institutes of Health (NIH) National Center of Excellence for Computational Drug Abuse Research, Drug Discovery Institute, School of Pharmacy, University of Pittsburgh, Pittsburgh, Pennsylvania 15261, United States.
Divya DuscharlaDepartment of Applied Biology, CSIR-Indian Institute of Chemical Technology, Hyderabad 500007, India.
Ramesh UmmanniDepartment of Applied Biology, CSIR-Indian Institute of Chemical Technology, Hyderabad 500007, India.
Paul R HansonDepartment of Chemistry, University of Kansas, 1567 Irving Hill Road, Lawrence, Kansas 66045-7582, United States.
Sanjay V MalhotraDepartment of Cell, Development and Cancer Biology, Oregon Health & Science University, Portland, Oregon 97201, United States.
Indian Institute of Chemical Technology · INNational Institutes of Health · USOregon Health & Science University · USUniversity of Kansas · US

Funding

Mentoring CoreP20GM103418 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI SUSAN J. BROWN · 2012 to 2026
$63.0M
NOVEL DESYMMETRIZATION METHODS ON A PHOSPHORUS TEMPLATER01GM058103 · NIGMS · UNIVERSITY OF KANSAS LAWRENCE · PI HANSON, PAUL R. · 1998 to 2002
$574k
Avance II 500 High Performance Digital NMR Spectrometer SystemS10RR024664 · NCRR · UNIVERSITY OF KANSAS LAWRENCE · PI VANDERVELDE, DAVID G · 2007 to 2007
$468k
AVIII HD 400 NMR spectrometer to replace existing DRX 400S10OD016360 · OD · UNIVERSITY OF KANSAS LAWRENCE · PI DOUGLAS, JUSTIN TRIGALET · 2014 to 2014
$297k
NCRR NIH HHS S10 RR024664NIGMS NIH HHS P20 GM103418NIGMS NIH HHS R01 GM058103NIH HHS S10 OD016360
6 · The paper itself

Abstract

The sulfamide functional group has been extensively employed in organic synthesis to discover probes and drugs in various applications such as cancer, human immunodeficiency virus (HIV), virus, and diabetes. Herein, we describe the synthesis of 7-membered symmetric and unsymmetric sulfamide compounds and their biological evaluation through the National Cancer Institute (NCI) panel of 60 human tumor cell lines (NCI-60) and the mechanism of action study. The results of a study from the NCI-60 cell line exhibited that many synthesized cyclic sulfamide compounds inhibited breast cancer (MDA-MB-468). The mechanism of action study of a representative compound

Identifiers

PMID33603966
PMCPMC7883376
OpenAlexW3122815025

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.