Evidence map›Paper›PMID 42823835›Full record

ArticleChemistryOpen2026

Synthesis and Cytotoxic Activity of 1,3-Selenazole-2-Amine Derivatives With Computational ADMET Profiling.

Gulay Dilek, Senem Akkoc

Abstract read
In one paragraph

Article in ChemistryOpen, 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

2 authors.

Gulay DilekFaculty of Pharmacy, Department of Basic Pharmaceutical Sciences, Zonguldak Bulent Ecevit University, Zonguldak, Türkiye.ORCID https://orcid.org/0000-0001-6562-2554
Senem AkkocFaculty of Pharmacy, Department of Basic Pharmaceutical Sciences, Suleyman Demirel University, Isparta, Türkiye.ORCID https://orcid.org/0000-0002-1260-9425

Funding

Süleyman Demirel Üniversitesi TSG-2024-9516
6 · The paper itself

Abstract

A set of newly developed 1,3-selenazole-2-amine derivatives (1-4) was prepared via a modified Hantzsch-type cyclization of appropriately substituted α-bromoacetophenones with selenourea under reflux conditions. The synthesized compounds were tested for cytotoxic activity in HT-29 (colon cancer), MCF-7 (breast cancer), and L929 (mouse fibroblast) cell lines using the MTT assay. The compounds induced weak to moderate cytotoxicity in MCF-7 cells. Among them, compound 4 showed cytotoxic activity with IC

Indexed as

AminesAntineoplastic AgentsAzolesOrganoselenium CompoundsAnimalsDrug Screening Assays, AntitumorHT29 CellsHumansMCF-7 CellsMiceMolecular StructureStructure-Activity RelationshipAminesAntineoplastic AgentsAzolesOrganoselenium Compounds1,3‐selenazoleantitumor agentscytotoxicityHantzsch‐type cyclizationselenium

Identifiers

PMID42823835
PMCPMC13631558

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.