Evidence map›Paper›PMID 36768608›Full record

ArticleInternational journal of molecular sciences2023

Conjugates of Tacrine and Salicylic Acid Derivatives as New Promising Multitarget Agents for Alzheimer's Disease.

Galina F Makhaeva, Nadezhda V Kovaleva, Elena V Rudakova, Natalia P Boltneva, Maria V Grishchenko, Sofya V Lushchekina, Tatiana Y Astakhova, Olga G Serebryakova, Elena N Timokhina, Ekaterina F Zhilina and 8 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
8.0field-weighted citation impact, top 2% of its field
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

14 citing papers in PubMed, 33 citations in OpenAlex.

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  11. Alzheimer's Disease: A Suitable Case for Treatment with Precision Medicine?Medical principles and practice : international journal of the Kuwait University, Health Science Centre · 2024
    Review
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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

18 authors at 6 institutions in 2 countries.

Galina F MakhaevaInstitute of Physiologically Active Compounds at Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, Chernogolovka 142432, Russia.ORCID 0000-0002-8136-6906
Nadezhda V KovalevaInstitute of Physiologically Active Compounds at Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, Chernogolovka 142432, Russia.ORCID 0000-0002-4990-5068
Elena V RudakovaInstitute of Physiologically Active Compounds at Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, Chernogolovka 142432, Russia.
Natalia P BoltnevaInstitute of Physiologically Active Compounds at Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, Chernogolovka 142432, Russia.ORCID 0000-0002-7171-8832
Maria V GrishchenkoPostovsky Institute of Organic Synthesis, Urals Branch of Russian Academy of Sciences, Yekaterinburg 620990, Russia.
Sofya V LushchekinaInstitute of Physiologically Active Compounds at Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, Chernogolovka 142432, Russia.ORCID 0000-0002-6922-020X
Tatiana Y AstakhovaEmanuel Institute of Biochemical Physics Russian Academy of Sciences, Moscow 119334, Russia.
Olga G SerebryakovaInstitute of Physiologically Active Compounds at Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, Chernogolovka 142432, Russia.
Elena N TimokhinaEmanuel Institute of Biochemical Physics Russian Academy of Sciences, Moscow 119334, Russia.
Ekaterina F ZhilinaPostovsky Institute of Organic Synthesis, Urals Branch of Russian Academy of Sciences, Yekaterinburg 620990, Russia.
Evgeny V ShchegolkovPostovsky Institute of Organic Synthesis, Urals Branch of Russian Academy of Sciences, Yekaterinburg 620990, Russia.ORCID 0000-0001-6611-2855
Mariya V UlitkoInstitute of Natural Sciences and Mathematics of the Ural Federal University Named after the First President of Russia B. N. Yeltsin, Ekaterinburg 620083, Russia.
Eugene V RadchenkoInstitute of Physiologically Active Compounds at Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, Chernogolovka 142432, Russia.ORCID 0000-0002-2091-7022
Vladimir A PalyulinInstitute of Physiologically Active Compounds at Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, Chernogolovka 142432, Russia.ORCID 0000-0001-8792-8386
Yanina V BurgartPostovsky Institute of Organic Synthesis, Urals Branch of Russian Academy of Sciences, Yekaterinburg 620990, Russia.
Victor I SaloutinPostovsky Institute of Organic Synthesis, Urals Branch of Russian Academy of Sciences, Yekaterinburg 620990, Russia.ORCID 0000-0003-1976-7861
Sergey O BachurinInstitute of Physiologically Active Compounds at Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, Chernogolovka 142432, Russia.ORCID 0000-0003-3637-818X
Rudy J RichardsonDepartment of Environmental Health Sciences, University of Michigan, Ann Arbor, MI 48109, USA.ORCID 0000-0002-2028-5723
Institute of Physiologically Active Compounds · RUInstitute of Organic Synthesis · RUInstitute of Biochemical Physics NM Emanuel · RULomonosov Moscow State University · RUUniversity of Michigan · USUral Federal University · RU

Funding

Alternatives Research & Development Foundation N/AMinistry of Science and Higher Education of the Russian Federation 22041400110-4.Ministry of Science and Higher Education of the Russian Federation AAAA-A19-119011790134-1Russian Foundation for Basic Research FFSN-2021-0005University of Michigan: Mcubed Grant N/A
6 · The paper itself

Abstract

A series of previously synthesized conjugates of tacrine and salicylamide was extended by varying the structure of the salicylamide fragment and using salicylic aldehyde to synthesize salicylimine derivatives. The hybrids exhibited broad-spectrum biological activity. All new conjugates were potent inhibitors of acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) with selectivity toward BChE. The structure of the salicylamide moiety exerted little effect on anticholinesterase activity, but AChE inhibition increased with spacer elongation. The most active conjugates were salicylimine derivatives: IC

Indexed as

Alzheimer DiseaseTacrineAcetylcholinesteraseAmyloid beta-PeptidesAnimalsAntioxidantsButyrylcholinesteraseCholinesterase InhibitorsMiceMolecular Docking SimulationSalicylamidesSalicylic AcidStructure-Activity RelationshipAcetylcholinesteraseAmyloid beta-PeptidesAntioxidantsButyrylcholinesteraseCholinesterase InhibitorssalicylamideSalicylamidesSalicylic AcidTacrineacetylcholinesteraseADMET predictionAlzheimer’s diseaseantioxidant activityAβ42 self-aggregationbutyrylcholinesterasemetal chelationpropidium displacementsalicylic acid derivativestacrine conjugates

Identifiers

PMID36768608
PMCPMC9916969
OpenAlexW4317930302

What OpenQuestion holds

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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.