Evidence map›Paper›PMID 42755039›Full record

ArticleChemical biology & drug design2026

Synthesis, Structural Characterization, and Investigation of Biological Effects of Novel Benzothiazole-Triazole Derivatives Designed as AKT Kinase Inhibitors.

Bilge Çiftçi, Zeynep Gülenç, Büşra Korkut Çelikateş, Derya Osmaniye

Abstract read
In one paragraph

Article in Chemical biology & drug design, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Bilge ÇiftçiInstitute of Graduate Education, Anadolu University, Eskişehir, Turkey.ORCID https://orcid.org/0000-0002-4153-1209
Zeynep GülençInstitute of Graduate Education, Anadolu University, Eskişehir, Turkey.ORCID https://orcid.org/0009-0003-0368-0291
Büşra Korkut ÇelikateşDepartment of Pharmaceutical Toxicology, Faculty of Pharmacy, Anadolu University, Eskişehir, Turkey.ORCID https://orcid.org/0000-0003-0149-3065
Derya OsmaniyeDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, Anadolu University, Eskişehir, Turkey.ORCID https://orcid.org/0000-0002-0499-436X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer (BC) is one of the most common cancers in women worldwide, and the need for new, more effective treatment options remains. The PI3K/Akt signaling pathway and the aromatase enzyme are among the molecular targets that play a critical role in the development and progression of BC. In this study, novel benzothiazole-triazole derivatives were synthesized, and their structures were confirmed using NMR and HRMS analyses. The cytotoxic activities of the eight synthesized compounds in the MCF-7 BC cell line were evaluated using the MTT method, with NIH/3T3 cells used as a healthy cell model. The IC

Indexed as

Antineoplastic AgentsBenzothiazolesProtein Kinase InhibitorsProto-Oncogene Proteins c-aktTriazolesAnimalsApoptosisAromataseDrug DesignFemaleHumansMCF-7 CellsMiceMolecular Docking SimulationNIH 3T3 CellsPhosphatidylinositol 3-KinasesAntineoplastic AgentsAromataseBenzothiazolesPhosphatidylinositol 3-KinasesProtein Kinase InhibitorsProto-Oncogene Proteins c-aktTriazolesAKTapoptosisbenzothiazolebreast cancerPI3K

Identifiers

PMID42755039
PMCPMC13586420

What OpenQuestion holds

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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.