Evidence map›Paper›PMID 22830497›Full record

ArticleMedicinal chemistry (Shariqah (United Arab Emirates))2012

New cathepsin D inhibitor library utilizing hydroxyethyl isosteres with cyclic tertiary amines.

Rose M McConnell, Kalyani Inapudi, Naveen Kadasala, Karthika Yarlagadda, Priya Velusamy, Matthew S McConnell, Adam Green, Carol Trana, Kelley Sayyar, James S McConnell

Open access · greenAbstract read
In one paragraph

Article in Medicinal chemistry (Shariqah (United Arab Emirates)), 2012. 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
–field-weighted citation impact, top 86% 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, 4 citations in OpenAlex.

  1. Review
  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

10 authors at 1 institution in 1 country.

Rose M McConnellDepartment of Chemistry, Western Illinois University, Macomb, IL 61455, USA. RM-McConnell@wiu.edu
Kalyani Inapudi
Naveen Kadasala
Karthika Yarlagadda
Priya Velusamy
Matthew S McConnell
Adam Green
Carol Trana
Kelley Sayyar
James S McConnell
Western Illinois University · US

Funding

SYNTHESIS AND EVALUATION OF NEW CATHEPSIN D INHIBITORSR15CA086933 · NCI · WESTERN ILLINOIS UNIVERSITY · PI MCCONNELL, ROSE M · 2000 to 2009
$550k
NCI NIH HHS 3R15 CA086933-04NCI NIH HHS 3R15CA086933-04A2S1NCI NIH HHS R15 CA086933
6 · The paper itself

Abstract

The design and synthesis of hydroxyethylamine isosteres as inhibitors of cathepsin D based on SAR data have been accomplished. A library of 96 of these hydroxyethylamine isosteres are described and many have proven to be very potent inhibitors of human cathepsin D activity as measured using a fluorometric assay technique, via peptide substrate Ac-Glu-Glu(Edans)-Lys-Pro-Ile-Cys-Phe-Phe-Arg-Leu-Gly-Lys(Methyl Red)-Glu-NH(2). Compounds showing strongest inhibition of cathepsin D activity were those that contain a hydroxyethyl-N'-2- or N'-(4-chlorophenyl)piperazine moiety (IC(50) values range from 0.55 to 8.5 nM), with N'-(2-pyrimidyl)piperizine (IC(50) values range from 0.5 to 21.6 nM), with N-N'- L-piperazinocolinamide (IC(50) values range from 0.001 - 0.25 nM), or N-N'-L-piperazinocolin-N-methylamide (IC(50) values range from 0.015 - 7.3 nM).

Indexed as

AminesCathepsin DHumansInhibitory Concentration 50LiverProtease InhibitorsSmall Molecule LibrariesAminesCathepsin DProtease InhibitorsSmall Molecule Libraries

Identifiers

PMID22830497
PMCPMC3535272
OpenAlexW2166242793

What OpenQuestion holds

Textmetadata
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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.