Evidence map›Paper›PMID 36770652›Full record

ArticleMolecules (Basel, Switzerland)2023

Rhamnopyranoside-Based Fatty Acid Esters as Antimicrobials: Synthesis, Spectral Characterization, PASS, Antimicrobial, and Molecular Docking Studies.

Abul Fazal Muhammad Sanaullah, Puja Devi, Takbir Hossain, Sulaiman Bin Sultan, Mohammad Mohib Ullah Badhon, Md Emdad Hossain, Jamal Uddin, Md Abdul Majed Patwary, Mohsin Kazi, Mohammed Mahbubul Matin

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2023. 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
–field-weighted citation impact
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.

  1. Review
  2. Article
  3. 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

10 authors.

Abul Fazal Muhammad SanaullahBioorganic and Medicinal Chemistry Laboratory, Department of Chemistry, Faculty of Science, University of Chittagong, Chittagong 4331, Bangladesh.ORCID 0000-0002-4653-2059
Puja DeviBioorganic and Medicinal Chemistry Laboratory, Department of Chemistry, Faculty of Science, University of Chittagong, Chittagong 4331, Bangladesh.
Takbir HossainBioorganic and Medicinal Chemistry Laboratory, Department of Chemistry, Faculty of Science, University of Chittagong, Chittagong 4331, Bangladesh.ORCID 0000-0002-6871-3686
Sulaiman Bin SultanBioorganic and Medicinal Chemistry Laboratory, Department of Chemistry, Faculty of Science, University of Chittagong, Chittagong 4331, Bangladesh.ORCID 0000-0001-5962-8001
Mohammad Mohib Ullah BadhonBioorganic and Medicinal Chemistry Laboratory, Department of Chemistry, Faculty of Science, University of Chittagong, Chittagong 4331, Bangladesh.
Md Emdad HossainWazed Miah Science Research Centre (WMSRC), Jahangirnagar University, Savar, Dhaka 1342, Bangladesh.ORCID 0000-0003-1398-2851
Jamal UddinCenter for Nanotechnology, Department of Natural Sciences, Coppin State University, Baltimore, MD 21216, USA.ORCID 0000-0002-6714-9286
Md Abdul Majed PatwaryDepartment of Chemistry, Comilla University, Cumilla 3506, Bangladesh.ORCID 0000-0003-4680-957X
Mohsin KaziDepartment of Pharmaceutics, College of Pharmacy, King Saud University, P.O. Box 2457, Riyadh 11451, Saudi Arabia.ORCID 0000-0002-5611-0378
Mohammed Mahbubul MatinBioorganic and Medicinal Chemistry Laboratory, Department of Chemistry, Faculty of Science, University of Chittagong, Chittagong 4331, Bangladesh.ORCID 0000-0003-4965-2280

Funding

Ministry of Science and Technology, Bangladesh Grant number SRG-226639 (2022-2023)Researchers Supporting Project, King Saud University, Riyadh, Saudi Arabia RSP-2023R301
6 · The paper itself

Abstract

The most widely used and accessible monosaccharides have a number of stereogenic centers that have been hydroxylated and are challenging to chemically separate. As a result, the task of regioselective derivatization of such structures is particularly difficult. Considering this fact and to get novel rhamnopyranoside-based esters, DMAP-catalyzed di-

Indexed as

Antifungal AgentsAnti-Infective AgentsFluconazoleMolecular Docking SimulationMolecular StructureRhamnoseSpectroscopy, Fourier Transform InfraredStearatesAntifungal AgentsAnti-Infective AgentsFluconazoleRhamnoseStearatesdi-O-stearatein vitro testmethyl α-l-rhamnopyranosidemolecular dockingregioselective acylationstructure-activity relationshipsugar esters

Identifiers

PMID36770652
PMCPMC9919056

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.