Evidence map›Paper›PMID 35424949›Full record

ArticleRSC advances2022

Synthesis, biological and computational studies of flavonoid acetamide derivatives.

Daniel K Isika, Fatma Nur Özkömeç, Mustafa Çeşme, Omowunmi A Sadik

Open access · goldAbstract read
In one paragraph

Article in RSC advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

11 citing papers in PubMed, 36 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

4 authors at 2 institutions in 2 countries.

Daniel K IsikaDepartment of Chemistry and Environmental Science, BioSensor Materials for Advanced Research & Technology (BioSMART Center), New Jersey Institute of Technology, University Heights 161 Warren Street Newark NJ 07102 USA dki3@njit.edu sadik@njit.edu.ORCID https://orcid.org/0000-0003-2874-1903
Fatma Nur ÖzkömeçDepartment of Biology, Faculty of Art and Sciences, Kahramanmaras Sutcu Imam University 46040 Kahramanmaras Turkey fatmanurozkomec9@gmail.com.ORCID https://orcid.org/0000-0002-7789-735X
Mustafa ÇeşmeDepartment of Chemistry, Faculty of Art and Sciences, Kahramanmaras Sutcu Imam University 46040 Kahramanmaras Turkey mustafacesme@msn.com.ORCID https://orcid.org/0000-0002-2020-5965
Omowunmi A SadikDepartment of Chemistry and Environmental Science, BioSensor Materials for Advanced Research & Technology (BioSMART Center), New Jersey Institute of Technology, University Heights 161 Warren Street Newark NJ 07102 USA dki3@njit.edu sadik@njit.edu.ORCID https://orcid.org/0000-0001-8514-0608
Kahramanmaraş Sütçü İmam University · TRNew Jersey Institute of Technology · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study reports the synthesis and characterization of a novel class of flavonoid acetamide derivatives (FA) of quercetin, apigenin, fisetin, kaempferol, and luteolin. Flavonoids display numerous biological properties but are limited by aqueous insolubility, enzymatic degradation, instability, and low bioavailability. FAs were synthesized, with 80-82% yields, through the sequential modification of the flavonoid hydroxyl groups into the acetamide moieties. Bioavailability, antioxidant, and ADMET are structure-activity-dependent properties that vary across different classes of flavonoids and dictate the prevalent biological applications of the flavonoids. Thus, the FAs were evaluated for their bioavailability, antioxidant, and ADMET toxicity properties

Identifiers

PMID35424949
PMCPMC8966662
OpenAlexW4224013729

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.