Vinícius R. Campos

ORCID: 0000-0003-3676-5964
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Crystallization and Solubility Studies
  • X-ray Diffraction in Crystallography
  • Bioactive Compounds and Antitumor Agents
  • Synthesis and biological activity
  • Synthesis and Biological Evaluation
  • Cancer therapeutics and mechanisms
  • Synthesis and Characterization of Heterocyclic Compounds
  • Click Chemistry and Applications
  • Multicomponent Synthesis of Heterocycles
  • Quinazolinone synthesis and applications
  • Tuberculosis Research and Epidemiology
  • Crystallography and molecular interactions
  • Porphyrin and Phthalocyanine Chemistry
  • Carbohydrate Chemistry and Synthesis
  • Concrete Corrosion and Durability
  • Enzyme Catalysis and Immobilization
  • Sesquiterpenes and Asteraceae Studies
  • Cyclopropane Reaction Mechanisms
  • Free Radicals and Antioxidants
  • Pneumocystis jirovecii pneumonia detection and treatment
  • Natural product bioactivities and synthesis
  • Venomous Animal Envenomation and Studies
  • Rabies epidemiology and control
  • Biological Activity of Diterpenoids and Biflavonoids
  • Chronic Myeloid Leukemia Treatments

Universidade Federal de Sergipe
2025

Universidade Federal Fluminense
2015-2024

Hospital Israelita Albert Einstein
2022-2024

Rede de Química e Tecnologia
2022

Hospital Municipal São José
2022

Fundação Oswaldo Cruz
2021

Discovery Air (Canada)
2020

Brazilian National Association of Graduate Programs in Communication
2015-2017

University of Aveiro
2017

Universidade Federal do Rio de Janeiro
2017

Tuberculosis treatment remains a challenge that requires new antitubercular agents due to the emergence of multidrug-resistant Mycobacterium strains. This paper describes synthesis, activity and theoretical analysis N-substituted-phenylamino-5-methyl-1H-1,2,3-triazole-4-carbohydrazides (8a–b, 8e–f, 8i–j 8n–o) analogues (8c–d, 8g–h, 8l–m 8p–q). These derivatives were synthesized in good yields some them showed promising profile. Interestingly N-acylhydrazone (NAH) 8n was most potent against...

10.1016/j.bmc.2011.07.035 article EN publisher-specific-oa Bioorganic & Medicinal Chemistry 2011-07-26

Genetically improved farmed tilapia (GIFT) is a strain of Nile ( Oreochromis niloticus ) developed for production and commercial parameters. Skin color, one the characteristics distinguishing varieties, an important phenotypic trait associated with qualitative productive performance. This study aimed to assess fillet skin in GIFT black red phenotypes. For this, 24 from same spawning stock were divided into two groups based on namely variety (dark skin) (reddish skin). There no significant...

10.1371/journal.pone.0314928 article EN cc-by PLoS ONE 2025-02-21

The current treatment used against envenomation by Lachesis muta venom still presents several side effects. This paper describes the synthesis, pharmacological and theoretical evaluations of new 1-arylsulfonylamino-5-methyl-1H-[1,2,3]-triazole-4-carboxylic acid ethyl esters (8a–f) tested hemolytic profile L. snake venom. Their structures were elucidated one- two-dimensional NMR techniques (1H, APT, HETCOR 1JCH nJCH, n = 2, 3) high-resolution electrospray ionization mass spectrometry. series...

10.1016/j.bmc.2009.09.031 article EN publisher-specific-oa Bioorganic & Medicinal Chemistry 2009-09-25

This review discusses the development and applications of bioconjugates derived from natural hydroxycinnamic acids (HCA), such as coumaric, sinapic, ferulic, caffeic acids, combined with various biomaterials. These offer a range benefits including antioxidant properties, UV protection, customized hydrophilic–lipophilic balance, improved safety, solubility, emolliency, biocompatibility, biodegradability, targeted delivery for biomedical, cosmetic, food applications. The increasing demand...

10.3390/compounds4040037 article EN cc-by Compounds 2024-10-10

A novel series of carbohydrate-based 1,2-naphthoquinones 13a–c and their substituted phenylhydrazono derivatives 14a–l were synthesized evaluated for cytotoxicity against HL-60, MDA-MB435, HCT-116 SF-295 cancer cell lines. The compounds 9a–c showed the best profile (IC50 below 2 μM) HL-60 MDA-MB 435 human cells, while hydrazone derivative 14i 1.65 was selective leukemia when compared to reference drug doxorubicin. None exhibited lytic effects mouse erythrocytes. Characterization all...

10.1039/c2ra21514d article EN RSC Advances 2012-01-01

In this work a microwave-assisted Knoevenagel/Michael/cyclization multicomponent domino methodology, using ethanol as solvent and the ionic liquid 1-methylimidazolium chloride catalyst was developed for synthesis of spiro compounds. The reaction conditions considered ideal were determined from methodological study varying solvent, catalyst, amount temperature, heating mode. Finally, generality methodology evaluated by exploring scope reaction, starting materials (isatin, malononitrile,...

10.3390/molecules27228051 article EN cc-by Molecules 2022-11-19

Starting from 2-hydroxy-1,4-naphthoquinone (lawsone), we synthesized eight new 6H-dibenzo[b,h]xanthene derivatives selectively under solvent-free conditions. Spectroscopic investigations confirmed that only the isomer was obtained in all cases. Computational studies provide a rationalization for selective appearance of these isomers having as an intermediate addition product.

10.1021/acs.joc.6b00864 article EN The Journal of Organic Chemistry 2016-06-09

(1) Background: The pandemic led to significant healthcare disruptions, resulting in postponed surgeries and extended waiting times for non-urgent treatments, including hysteroscopies essential diagnosing endometrial cancer. This study aims formulate a risk stratification model enhance the prioritization of hysteroscopy procedures Brazil; (2) Methods: A case-control was conducted at Vila Santa Catarina Hospital São Paulo, analyzing medical records 2103 women who underwent between March 2019...

10.3390/jcm13041145 article EN Journal of Clinical Medicine 2024-02-18

Natural alkylated hydroxy cinnamates (AHCs) isolated from medicinal plants and the thereby designed synthesized cinnamides are derivatives of cinnamic acids such as p-coumaric, sinapic, ferulic, caffeic acids, which naturally derived human dietary sources. The pharmacological properties displayed by AHCs based on their inherent structure range include antioxidant, antimicrobial, antiplasmodial, anti-tyrosinase, Alzheimer’s Parkinson’s disease therapy, anticancer metabolic biopesticides, have...

10.3390/compounds4040044 article EN cc-by Compounds 2024-12-04

A new and efficient method for the synthesis of hexahydropyrimidine-fused 1,4-naphthoquinones in one step with high yields from reaction lawsone 1,3,5-triazinanes was developed.

10.3762/bjoc.11.137 article EN cc-by Beilstein Journal of Organic Chemistry 2015-07-22

This work describes the first determination of absolute configuration (AC) (-)-cubebin by means electronic circular dichroism (ECD), supported quantum chemical calculations.The comparison experimental ECD with corresponding prediction for proper diastereoisomer resulted in definitive assignment AC naturally occurring as (8R,8aR,9S).The challenging relative (RC) cubebin based only on nuclear magnetic resonance (NMR) methods is stressed.Computation 13 C and 1 H NMR shifts all possible...

10.21577/0103-5053.20200103 article EN cc-by Journal of the Brazilian Chemical Society 2020-01-01
Coming Soon ...