Evidence map›Paper›PMID 25313319›Full record

ArticleACS medicinal chemistry letters2014

Discovery of 3-Arylcoumarin-tetracyclic Tacrine Hybrids as Multifunctional Agents against Parkinson's Disease.

Koneni V Sashidhara, Ram K Modukuri, Pooja Jadiya, K Bhaskara Rao, Tanuj Sharma, Rizwanul Haque, Deependra Kumar Singh, Dibyendu Banerjee, Mohammad Imran Siddiqi, Aamir Nazir

Open access · bronzeAbstract read
In one paragraph

Article in ACS medicinal chemistry letters, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

12 citing papers in PubMed, 43 citations in OpenAlex.

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  6. Natural source, bioactivity and synthesis of 3-Arylcoumarin derivatives.Journal of enzyme inhibition and medicinal chemistry · 2022
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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

10 authors at 1 institution in 1 country.

Koneni V SashidharaMedicinal and Process Chemistry Division, Laboratory of Functional Genomics and Molecular Toxicology, and Division of Molecular and Structural Biology, CSIR-Central Drug Research Institute, (CSIR-CDRI) , BS-10/1, Sector 10, Jankipuram Extension, Sitapur Road, Lucknow 226031, India.
Ram K ModukuriMedicinal and Process Chemistry Division, Laboratory of Functional Genomics and Molecular Toxicology, and Division of Molecular and Structural Biology, CSIR-Central Drug Research Institute, (CSIR-CDRI) , BS-10/1, Sector 10, Jankipuram Extension, Sitapur Road, Lucknow 226031, India.
Pooja JadiyaMedicinal and Process Chemistry Division, Laboratory of Functional Genomics and Molecular Toxicology, and Division of Molecular and Structural Biology, CSIR-Central Drug Research Institute, (CSIR-CDRI) , BS-10/1, Sector 10, Jankipuram Extension, Sitapur Road, Lucknow 226031, India.
K Bhaskara RaoMedicinal and Process Chemistry Division, Laboratory of Functional Genomics and Molecular Toxicology, and Division of Molecular and Structural Biology, CSIR-Central Drug Research Institute, (CSIR-CDRI) , BS-10/1, Sector 10, Jankipuram Extension, Sitapur Road, Lucknow 226031, India.
Tanuj SharmaMedicinal and Process Chemistry Division, Laboratory of Functional Genomics and Molecular Toxicology, and Division of Molecular and Structural Biology, CSIR-Central Drug Research Institute, (CSIR-CDRI) , BS-10/1, Sector 10, Jankipuram Extension, Sitapur Road, Lucknow 226031, India.
Rizwanul HaqueMedicinal and Process Chemistry Division, Laboratory of Functional Genomics and Molecular Toxicology, and Division of Molecular and Structural Biology, CSIR-Central Drug Research Institute, (CSIR-CDRI) , BS-10/1, Sector 10, Jankipuram Extension, Sitapur Road, Lucknow 226031, India.
Deependra Kumar SinghMedicinal and Process Chemistry Division, Laboratory of Functional Genomics and Molecular Toxicology, and Division of Molecular and Structural Biology, CSIR-Central Drug Research Institute, (CSIR-CDRI) , BS-10/1, Sector 10, Jankipuram Extension, Sitapur Road, Lucknow 226031, India.
Dibyendu BanerjeeMedicinal and Process Chemistry Division, Laboratory of Functional Genomics and Molecular Toxicology, and Division of Molecular and Structural Biology, CSIR-Central Drug Research Institute, (CSIR-CDRI) , BS-10/1, Sector 10, Jankipuram Extension, Sitapur Road, Lucknow 226031, India.
Mohammad Imran SiddiqiMedicinal and Process Chemistry Division, Laboratory of Functional Genomics and Molecular Toxicology, and Division of Molecular and Structural Biology, CSIR-Central Drug Research Institute, (CSIR-CDRI) , BS-10/1, Sector 10, Jankipuram Extension, Sitapur Road, Lucknow 226031, India.
Aamir NazirMedicinal and Process Chemistry Division, Laboratory of Functional Genomics and Molecular Toxicology, and Division of Molecular and Structural Biology, CSIR-Central Drug Research Institute, (CSIR-CDRI) , BS-10/1, Sector 10, Jankipuram Extension, Sitapur Road, Lucknow 226031, India.
Central Drug Research Institute · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A series of multifunctional directed 3-arylcoumarin-tetracyclic tacrine derivatives was designed and synthesized for the treatment of Parkinson's disease (PD). A number of derivatives (18, 19, 20, 21, and 24) demonstrated significant reduction of aggregation of "human" alpha-synuclein (α-synuclein) protein, expressing on transgenic Caenorhabditis elegans (C. elegans) model NL5901. Moreover, compounds 16, 18, and 24 also exhibited good antioxidant properties and significantly increased the dopamine (DA) content in N2 and NL5901 strains of C. elegans. Interestingly, the protective efficacy of these hybrids seems to be mediated via activation of longevity promoting transcription factor DAF-16. In addition, molecular modeling studies have evidenced the exquisite interaction of most active compounds 18 and 24 with α-synuclein protein. Taken together, the data indicate that the derivatives may be useful leads against aging and age associated PD.

Indexed as

3-ArylcoumarinC. elegansParkinson’s diseasereactive oxygen speciestetracyclic tacrineα-synuclein

Identifiers

PMID25313319
PMCPMC4190629
OpenAlexW2321058114

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.