Evidence map›Paper›PMID 37218207›Full record

ArticleCurrent organic synthesis2024

Novel Penicillin Derivatives Against Selected Multiple-drug Resistant Bacterial Strains: Design, Synthesis, Structural Analysis,

Narmin Hamaamin Hussen, Shokhan Jamal Hamid, Mohammed Nawzad Sabir, Aso Hameed Hasan, Sewara Jalal Mohammed, Aras Ahmed Kamal Shali

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Article in Current organic synthesis, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

7 citing papers in PubMed, 17 citations in OpenAlex.

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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

6 authors at 2 institutions in 1 country.

Narmin Hamaamin HussenDepartment of Pharmacognosy and Pharmaceutical Chemistry, College of Pharmacy, University of Sulaimaniyah, Sulaimani, 46001, Kurdistan Region-Iraq, Iraq.
Shokhan Jamal HamidDepartment of Pharmacognosy and Pharmaceutical Chemistry, College of Pharmacy, University of Sulaimaniyah, Sulaimani, 46001, Kurdistan Region-Iraq, Iraq.
Mohammed Nawzad SabirDepartment of Pharmacognosy and Pharmaceutical Chemistry, College of Pharmacy, University of Sulaimaniyah, Sulaimani, 46001, Kurdistan Region-Iraq, Iraq.
Aso Hameed HasanDepartment of Chemistry, College of Science, University of Garmian, Kalar, 46021, Kurdistan Region-Iraq, Iraq.
Sewara Jalal MohammedDepartment of Chemistry, College of Science, University of Sulaimaniyah, Qlyasan Street, Sulaimani, 46001, Kurdistan Regional-Iraq, Iraq.
Aras Ahmed Kamal ShaliDepartment of Biology, College of Science, University of Sulaimaniyah, Qlyasan Street, Sulaimani, 46001, Kurdistan Regional-Iraq, Iraq.
Kurdistan Regional Government · IQUniversity of Sulaimani · IQ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe rising numbers of multiple drug-resistant (MDR) pathogens and the consequent antibacterial therapy failure that resulted in severe medical conditions push to illustrate new molecules with extended activity against the resistant strains. In this manner, chemical derivatization of known antibiotics is proposed to save efforts in drug discovery, and penicillins serve as an ideal in this regard.

methodsSeven synthesized 6-aminopenicillanic acid-imine derivatives (2a-g) were structure elucidated using FT-IR, 1H NMR,

resultsThe MIC values were 8 to 32 μg/mL with more potency than ampicillin, explained by better membrane penetration and more ligand-protein binding capacity. The 2g entity was active against

conclusionThe products showed antibacterial activity against selected MDR species and good PHK, PHD properties, and low predicted toxicity, offering them as future candidates that require further preclinical assays.

Indexed as

Anti-Bacterial AgentsDrug DesignDrug Resistance, Multiple, BacterialMicrobial Sensitivity TestsMolecular Docking SimulationPenicillinsEscherichia coliMolecular StructurePseudomonas aeruginosaStaphylococcus aureusStructure-Activity RelationshipAnti-Bacterial AgentsPenicillinsADMET.antibacterial assaychemical derivatizationcomputational modellingiminePenicillins

Identifiers

PMID37218207
OpenAlexW4376140633

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.