Evidence map›Paper›PMID 42074168›Full record

ArticleInternational journal of molecular sciences2026

Picolinamides with β-Thiophosphorylated Amine Residues as a Useful Scaffold to Generate Biologically Active Pd(II) Pincer Complexes.

Diana V Aleksanyan, Aleksandra A Kalashnikova, Anna Yu Katranova, Ekaterina Yu Rybalkina, Nikolay N Kalitin, Yulia L Volodina, Yana V Ryzhmanova, Yulia V Nelyubina, Oleg I Artyushin, Zinaida S Klemenkova and 1 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 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

11 authors.

Diana V AleksanyanA. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, ul. Vavilova 28, Str. 1, Moscow 119334, Russia.
Aleksandra A KalashnikovaA. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, ul. Vavilova 28, Str. 1, Moscow 119334, Russia.ORCID 0000-0001-6362-0096
Anna Yu KatranovaA. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, ul. Vavilova 28, Str. 1, Moscow 119334, Russia.
Ekaterina Yu RybalkinaN. N. Blokhin National Medical Research Center of Oncology of the Ministry of Health of the Russian Federation, Kashirskoe Shosse 23, Moscow 115478, Russia.
Nikolay N KalitinN. N. Blokhin National Medical Research Center of Oncology of the Ministry of Health of the Russian Federation, Kashirskoe Shosse 23, Moscow 115478, Russia.ORCID 0000-0002-3177-7766
Yulia L VolodinaN. N. Blokhin National Medical Research Center of Oncology of the Ministry of Health of the Russian Federation, Kashirskoe Shosse 23, Moscow 115478, Russia.
Yana V RyzhmanovaInstitute of Biochemistry and Physiology of Microorganisms, Federal Research Center "Pushchino Scientific Center of Biological Research of the Russian Academy of Sciences", pr. Nauki 5, Pushchino 142292, Russia.ORCID 0000-0003-2987-5604
Yulia V NelyubinaAdvanced Engineering School, ITMO University, ul. Lomonosova 9, St. Petersburg 191002, Russia.
Oleg I ArtyushinA. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, ul. Vavilova 28, Str. 1, Moscow 119334, Russia.
Zinaida S KlemenkovaA. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, ul. Vavilova 28, Str. 1, Moscow 119334, Russia.
Vladimir A KozlovA. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, ul. Vavilova 28, Str. 1, Moscow 119334, Russia.

Funding

Russian Science Foundation 22-73-10044-P
6 · The paper itself

Abstract

The creation of new potential metal-based therapeutics largely relies on the development of useful ligand scaffolds. In recent years, our research group has introduced thiophosphoryl-functionalized carboxamides as a convenient framework for obtaining biologically active cyclopalladated derivatives. In continuation of these studies, β-(aminoalkyl)phosphine sulfides bearing additional substituents in the ethylene backbone were synthesized for the first time and reacted with picolinic acid to afford a series of new functionalized amide ligands. The latter readily underwent direct cyclopalladation under the action of PdCl

Indexed as

AminesAntineoplastic AgentsCoordination ComplexesPalladiumPicolinic AcidsAnti-Bacterial AgentsApoptosisCell Line, TumorHumansLigandsAminesAnti-Bacterial AgentsAntineoplastic AgentsCoordination ComplexesLigandsPalladiumpicolinamidePicolinic Acidsantibacterial activitycarboxamidescytotoxicitypalladiumpincer complexesthiophosphorylated amines

Identifiers

PMID42074168
PMCPMC13115956

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Registered trials

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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.