Evidence map›Paper›PMID 31307240›Full record

ArticleJournal of enzyme inhibition and medicinal chemistry2019

Synthesis of substituted 15β-alkoxy estrone derivatives and their cofactor-dependent inhibitory effect on 17β-HSD1.

Bianka Edina Herman, Anita Kiss, János Wölfling, Erzsébet Mernyák, Mihály Szécsi, Gyula Schneider

Abstract read
In one paragraph

Article in Journal of enzyme inhibition and medicinal chemistry, 2019. 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
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.

  1. Article
  2. Review
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

6 authors.

Bianka Edina Hermana First Department of Medicine , University of Szeged , Szeged , Hungary.
Anita Kissb Department of Organic Chemistry , University of Szeged , Szeged , Hungary.
János Wölflingb Department of Organic Chemistry , University of Szeged , Szeged , Hungary.
Erzsébet Mernyákb Department of Organic Chemistry , University of Szeged , Szeged , Hungary.
Mihály Szécsia First Department of Medicine , University of Szeged , Szeged , Hungary.
Gyula Schneiderb Department of Organic Chemistry , University of Szeged , Szeged , Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

17β-Hydroxysteroid dehydrogenase type 1 (17β-HSD1) is a key enzyme in the biosynthesis of 17β-estradiol. Novel estrone-based compounds bearing various 15β-oxa-linked substituents and hydroxy, methoxy, benzyloxy, and sulfamate groups in position C3 as potential 17β-HSD1 inhibitors have been synthesized. In addition,

Indexed as

17-Hydroxysteroid DehydrogenasesDose-Response Relationship, DrugEnzyme InhibitorsEstroneHumansMolecular ConformationStructure-Activity Relationship17-Hydroxysteroid Dehydrogenases3 (or 17)-beta-hydroxysteroid dehydrogenaseEnzyme InhibitorsEstrone17β-HSD1estrogen biosynthesisMichael additionNADPH and NADHsubstituted 15β-alkoxy-estrone derivatives

Identifiers

PMID31307240
PMCPMC6691805

What OpenQuestion holds

Textmetadata
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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.