Evidence map›Paper›PMID 40649366›Full record

ReviewMolecules (Basel, Switzerland)2025

Hydrazides as Powerful Tools in Medicinal Chemistry: Synthesis, Reactivity, and Biological Applications.

Sofia Teixeira, Elisabete M S Castanheira, M Alice Carvalho

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2025. 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
–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

7 citing papers in PubMed.

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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

3 authors.

Sofia TeixeiraCentre of Chemistry of University of Minho (CQ-UM), Campus de Gualtar, 4710-057 Braga, Portugal.ORCID 0000-0002-4086-0975
Elisabete M S CastanheiraCentre of Physics of Minho and Porto Universities (CF-UM-UP), University of Minho, Campus de Gualtar, 4710-057 Braga, Portugal.ORCID 0000-0002-5829-6081
M Alice CarvalhoCentre of Chemistry of University of Minho (CQ-UM), Campus de Gualtar, 4710-057 Braga, Portugal.ORCID 0000-0002-8666-0362

Funding

FEDER/FCT PTDC/MED-ONC/31354/2017FEDER/FCT PTDC/SAU-PAR/2766/2021Fundação para a Ciência e a Tecnologia (FCT - Portugal) Strategic Funding of CF-UM-UP (UIDB/04650/2020)Fundação para a Ciência e a Tecnologia (FCT - Portugal) Strategic Funding of CQUM (UIDB/00686/2020)Fundação para a Ciência e a Tecnologia (FCT - Portugal), FSE (Fundo Social Europeu) through "Programa Operacional Regional Norte" 2020.04975.BD
6 · The paper itself

Abstract

The increase in drug resistance and the high toxicity of current drugs have inspired the scientific community to develop new drugs for various diseases. Hydrazides have become an attractive functional group to easily obtain a plethora of novel compounds with a broad range of biological activities. This review, which contains studies in the literature from the previous five years, focuses on the synthesis methods and biological applications of hydrazides and their derivatives. Here, the details of the experimental reaction conditions used for the synthesis of hydrazides and their derivatives (hydrazide-hydrazones and heterocycle derivatives) are presented, as well as the purification methods and the biological activity of the synthesized compounds.

Indexed as

Chemistry, PharmaceuticalHydrazinesHumansHydrazonesMolecular StructureHydrazinesHydrazonesbioactive hydrazide derivativeshydrazide derivativeshydrazidessynthesis

Identifiers

PMID40649366
PMCPMC12251600

What OpenQuestion holds

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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.