Evidence map›Paper›PMID 33833504›Full record

ArticleDrug design, development and therapy2021

Amino Acid Conjugates of Aminothiazole and Aminopyridine as Potential Anticancer Agents: Synthesis, Molecular Docking and in vitro Evaluation.

Shagufta Naz, Fawad Ali Shah, Humaira Nadeem, Sadia Sarwar, Zhen Tan, Muhammad Imran, Tahir Ali, Jing Bo Li, Shupeng Li

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 45% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
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 2 countries.

Shagufta NazRiphah Institute of Pharmaceutical Sciences, Riphah International University, Islamabad, 44000, Pakistan.
Fawad Ali ShahRiphah Institute of Pharmaceutical Sciences, Riphah International University, Islamabad, 44000, Pakistan.ORCID 0000-0002-5415-2179
Humaira NadeemRiphah Institute of Pharmaceutical Sciences, Riphah International University, Islamabad, 44000, Pakistan.
Sadia SarwarRiphah Institute of Pharmaceutical Sciences, Riphah International University, Islamabad, 44000, Pakistan.ORCID 0000-0002-2514-8306
Zhen TanHospital of Chengdu University of Traditional Chinese Medicine, Chengdu, People's Republic of China.
Muhammad ImranRiphah Institute of Pharmaceutical Sciences, Riphah International University, Islamabad, 44000, Pakistan.ORCID 0000-0002-0915-3527
Tahir AliShenzhen University Clinical Research Center for Neurological Diseases, Health Management Center, Shenzhen University General Hospital, Shenzhen University Clinical Medical Academy, Shenzhen University, Shenzhen, People's Republic of China.ORCID 0000-0002-2138-1303
Jing Bo LiShenzhen University Clinical Research Center for Neurological Diseases, Health Management Center, Shenzhen University General Hospital, Shenzhen University Clinical Medical Academy, Shenzhen University, Shenzhen, People's Republic of China.
Shupeng LiState Key Laboratory of Oncogenomics, School of Chemical Biology and Biotechnology, Shenzhen Graduate School, Peking University, Shenzhen, People's Republic of China.
Riphah International University · PKShenzhen University · CNChengdu University of Traditional Chinese Medicine · CNPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe development of resistance to available anticancer drugs is increasingly becoming a major challenge and new chemical entities could be unveiled to compensate this therapeutic failure. The current study demonstrated the synthesis of 2-aminothiazole [

methodsBiological assays were performed to investigate the antioxidant and anticancer potential of synthesized compounds. Redox imbalance and oxidative stress are hallmarks of cancer, therefore, synthesized compounds were preliminarily screened for their antioxidant activity using DPPH assay, and further five derivatives

resultsResults revealed that

conclusionAnticancer activities of compounds

Indexed as

Molecular Docking SimulationAmino AcidsAminopyridinesAntineoplastic AgentsAntioxidantsBiphenyl CompoundsCell ProliferationDose-Response Relationship, DrugDrug Screening Assays, AntitumorHumansMolecular StructurePicratesThiazolesTumor Cells, Cultured1,1-diphenyl-2-picrylhydrazylAmino AcidsAminopyridinesAntineoplastic AgentsAntioxidantsBiphenyl CompoundsPicratesThiazolesanticancer activityantioxidant activitymolecular dockingpyridinethiazole

Identifiers

PMID33833504
PMCPMC8021256
OpenAlexW3147815484

What OpenQuestion holds

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LicenceCC BY-NC
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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.