Evidence map›Paper›PMID 28376844›Full record

ArticleDaru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences2017

Carboxylate derivatives of tributyltin (IV) complexes as anticancer and antileishmanial agents.

Durdana Waseem, Arshad Farooq Butt, Ihsan-Ul Haq, Moazzam Hussain Bhatti, Gul Majid Khan

Open access · hybridAbstract read
In one paragraph

Article in Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

15 citing papers in PubMed, 37 citations in OpenAlex.

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  6. Molecular docking andHeliyon · 2022
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  7. Phytochemical analysis and comprehensive evaluation of pharmacological potential ofSaudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2022
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  8. Anti-Inflammatory Potential of Daturaolone fromPharmaceuticals (Basel, Switzerland) · 2021
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  9. Withametelin: a biologically active withanolide in cancer, inflammation, pain and depression.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2020
    Article
  10. Article
  11. 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

5 authors at 2 institutions in 1 country.

Durdana WaseemDepartment of Pharmacy, Quaid-i-Azam University, Islamabad, 45320, Pakistan.
Arshad Farooq ButtDepartment of Chemistry, Allama Iqbal Open University, H-8, Islamabad, 44000, Pakistan.
Ihsan-Ul HaqDepartment of Pharmacy, Quaid-i-Azam University, Islamabad, 45320, Pakistan.
Moazzam Hussain BhattiDepartment of Chemistry, Allama Iqbal Open University, H-8, Islamabad, 44000, Pakistan.
Gul Majid KhanDepartment of Pharmacy, Quaid-i-Azam University, Islamabad, 45320, Pakistan. gmkhan@qau.edu.pk.
Quaid-i-Azam University · PKAllama Iqbal Open University · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTributyltin (IV) compounds are promising candidates for drug development. In the current study, we evaluated in-vitro and in-silico profile of carboxylate derivatives of tributyltin (IV) complexes.

methodsADMET and drug-likeliness properties were predicted using MetaPrint2D React, preADMET, SwissADME and Molsoft tools. SwissTargetPrediction predicted molecular targets for compounds. In-vitro bioactivity was evaluated by quantifying cytotoxicity against HepG2, THP-1 cell lines, isolated lymphocytes and leishmania promastigotes as well as measuring protein kinase (PK) inhibition activity.

resultsResults indicate partial compliance of compounds with drug-likeliness rules. Ch-409 complies with WDI and Lipinski rules. ADMET profile prediction shows strong plasma protein binding except for Ch-409, low to high GI absorption and BBB penetration (C

conclusionsSelected carboxylate derivatives of tributyltin (IV) complexes possess significant antileishmanial and cytotoxic potential. These are promising compounds for the development of antileishmanial and anticancer drugs. Graphical Abstract Carboxylate derivatives of tributyltin (IV) complexes as anticancer and antileishmanial agents.

Indexed as

Antineoplastic AgentsAntiprotozoal AgentsCaco-2 CellsCell LineCell ProliferationCell SurvivalComputer SimulationDose-Response Relationship, DrugHep G2 CellsHumansLeishmaniaProtein Kinase InhibitorsStructure-Activity RelationshipTrialkyltin CompoundsAntineoplastic AgentsAntiprotozoal AgentsProtein Kinase InhibitorsTrialkyltin CompoundsADMETAnticancerAntileishmanialOrganotin (IV)Protein kinase inhibition

Identifiers

PMID28376844
PMCPMC5381078
OpenAlexW2604232123

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.