Evidence map›Paper›PMID 36214960›Full record

ArticleMolecular diversity2023

Design, synthesis, and pharmacological evaluation of [1, 3] dioxolo-chromeno[2,3-b]pyridines as anti-seizure agents.

Visarapu Malathi, Nissi Sharon, Pannala Padmaja, Deepak Lokwani, Saurabh Khadse, Prashant Chaudhari, Atul A Shirkhedkar, Pedavenkatagari Narayana Reddy, Vinod G Ugale

Abstract read
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In one paragraph

Article in Molecular diversity, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.7field-weighted citation impact, top 36% 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

1 citing paper in PubMed, 6 citations in OpenAlex.

  1. Article
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

9 authors at 4 institutions in 1 country.

Visarapu MalathiDepartment of Chemistry, School of Science, Gitam Deemed to be University, Hyderabad, TS, India.
Nissi SharonDepartment of Chemistry, School of Science, Gitam Deemed to be University, Hyderabad, TS, India.
Pannala PadmajaCentre for Semio Chemicals, CSIR-Indian Institute of Chemical Technology, Hyderabad, India.
Deepak LokwaniRajarshi Shahu College of Pharmacy, Buldana, Maharashtra, India.
Saurabh KhadseDepartment of Pharmaceutical Chemistry, R. C. Patel Institute of Pharmaceutical Education and Research, Shirpur, Maharashtra, 425405, India.
Prashant ChaudhariDepartment of Pharmaceutical Chemistry, R. C. Patel Institute of Pharmaceutical Education and Research, Shirpur, Maharashtra, 425405, India.
Atul A ShirkhedkarDepartment of Pharmaceutical Chemistry, R. C. Patel Institute of Pharmaceutical Education and Research, Shirpur, Maharashtra, 425405, India.
Pedavenkatagari Narayana ReddyDepartment of Chemistry, School of Science, Gitam Deemed to be University, Hyderabad, TS, India. npedaven@gitam.edu.
Vinod G UgaleDepartment of Pharmaceutical Chemistry, R. C. Patel Institute of Pharmaceutical Education and Research, Shirpur, Maharashtra, 425405, India. vinod.ugale@rediffmail.com.ORCID http://orcid.org/0000-0002-6157-6295
GITAM University · INShri Vile Parle Kelavani Mandal · INAgharkar Research Institute · INIndian Institute of Chemical Technology · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An efficient one-pot three-component reaction for the synthesis of [1,3]dioxolo[4',5':6,7]chromeno[2,3-b]pyridines 4(a-i) has been developed. Synthesis was achieved by reacting sesamol (1), aromatic aldehydes 2(a-i), and 2-aminopropene-1,1,3-tricarbonitrile (3) in the presence of triethylamine at 100 °C under neat reaction condition. Simple operational procedure, broad substrate scope, column chromatography free separations, and high yield of products make it an efficient and largely acceptable synthetic strategy. Synthesized compounds 4(a-i) were further screened for preliminary anticonvulsant activity using MES and scPTZ tests. These analogs were also checked for neurotoxicity and hepatotoxicity. Selected active compounds have been then screened quantitatively to determine ED

Indexed as

AnticonvulsantsPyridinesDrug DesignMolecular Dynamics SimulationMolecular StructureReceptors, GABA-AStructure-Activity RelationshipAnticonvulsantsPyridinesReceptors, GABA-A[1,3]Dioxolochromeno[2,3-b]pyridinesAnticonvulsantsDesignMolecular dockingSynthesis

Identifiers

PMID36214960
OpenAlexW4304080534

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.