Evidence map›Paper›PMID 41103099›Full record

ArticleArchiv der Pharmazie2025

Synthesis and Biological Evaluation of Novel 2-(Piperidin-4-yl)-1,2,3,4-tetrahydroisoquinoline and 2-(Piperidin-4-yl)decahydroisoquinoline Antimycotics.

Marie-Christin Hain, Monika Klimt, Franz Bracher, Ulrike Binder, Jürgen Krauß

Abstract read
In one paragraph

Article in Archiv der Pharmazie, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Marie-Christin HainDepartment of Pharmacy, Center of Drug Research, Ludwig-Maximilians University Munich, Munich, Germany.
Monika KlimtDepartment of Pharmacy, Center of Drug Research, Ludwig-Maximilians University Munich, Munich, Germany.
Franz BracherDepartment of Pharmacy, Center of Drug Research, Ludwig-Maximilians University Munich, Munich, Germany.ORCID https://orcid.org/0000-0003-0009-8629
Ulrike BinderInstitute of Hygiene and Medical Microbiology, Department of Hygiene, Microbiology and Virology, Medical University Innsbruck, Innsbruck, Austria.ORCID https://orcid.org/0000-0002-2160-2903
Jürgen KraußDepartment of Pharmacy, Center of Drug Research, Ludwig-Maximilians University Munich, Munich, Germany.ORCID https://orcid.org/0000-0002-2464-2011

Funding

The authors received no specific funding for this study.
6 · The paper itself

Abstract

Piperidine antimycotics like fenpropidin are well established in agrochemistry. On the other hand, numerous isoquinoline derivatives show remarkable antimycotic effects. Here we present a series of 13 hybrid molecules of both lead structures, which were prepared using reductive amination as key reaction step. Pre-screening against Yarrowia lipolytica resulted in a batch of promising candidates whose antifungal efficacy was further evaluated against clinically relevant species. In these assays, complete growth inhibition was seen for five or six compounds against C. albicans or C. krusei, respectively, and in two against C. glabrata, whereas no antifungal activity was observed against mold isolates, with the exception of 6i, which led to complete growth inhibition of aspergilli, and two compounds (6k and 6 l) that were able to inhibit Rhizopus arrhizus.

Indexed as

Antifungal AgentsCandidaIsoquinolinesPiperidinesTetrahydroisoquinolinesDose-Response Relationship, DrugMicrobial Sensitivity TestsMolecular StructureStructure-Activity RelationshipYarrowiaAntifungal AgentsIsoquinolinesPiperidinesTetrahydroisoquinolines4‐aminopiperidineantifungalsCandida spp.reductive aminationyeasts

Identifiers

PMID41103099
PMCPMC12531613

What OpenQuestion holds

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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.