Ionic liquid-assisted synthesis of dihydropyrimidin(thi)one Biginelli adducts and investigation of their mechanism of urease inhibition-Reference-Cited by-同舟云学术

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Ionic liquid-assisted synthesis of dihydropyrimidin(thi)one Biginelli adducts and investigation of their mechanism of urease inhibition

Published:2019 Issue:38 Volume:43 Page:15187-15200
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Braga Taniris Cafiero¹²³⁴⁵,Silva Thamara Ferreira⁶⁷⁸³⁴,Maciel Thamilla Maria Silva⁹¹⁰¹¹¹²⁵,da Silva Edjan Carlos Dantas¹³¹⁰¹¹¹²⁵,da Silva-Júnior Edeildo Ferreira¹³¹⁰¹¹¹²⁵,Modolo Luzia Valentina⁶⁷⁸³⁴^ORCID,Figueiredo Isis Martins⁹¹⁰¹¹¹²⁵,Santos Josué Carinhanha Caldas⁹¹⁰¹¹¹²⁵^ORCID,de Aquino Thiago Mendonça¹³¹⁰¹¹¹²⁵,de Fátima Ângelo¹²³⁴⁵^ORCID

Affiliation:

1. Grupo de Estudos em Química Orgânica e Biológica (GEQOB)

2. Departamento de Química

3. Universidade Federal de Minas Gerais

4. Belo Horizonte

5. Brazil

6. Grupo de Estudos em Bioquímica de Plantas (GEBioPlan)

7. Departamento de Botânica

8. Instituto de Ciências Biológicas

9. Laboratório de Instrumentação e Desenvolvimento em Química Analítica (LINQA)

10. Instituto de Química e Biotecnologia

11. Universidade Federal de Alagoas

12. Maceió

13. Núcleo de Análises e Pesquisa em Ressonância Magnética Nuclear (NAPRMN)

Abstract

Three out of twenty-six synthesized Biginelli adducts were identified as potent competitive urease inhibitors.

Funder

Fundação de Amparo à Pesquisa do Estado de Minas Gerais

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2019/NJ/C9NJ03556G

Reference78 articles.

1. THE ISOLATION AND CRYSTALLIZATION OF THE ENZYME UREASE

2. Ureases: Historical aspects, catalytic, and non-catalytic properties – A review

3. An overview on the potential of natural products as ureases inhibitors: A review

4. Recent advances in design of new urease inhibitors: A review

5. The Burden Borne by Urease

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