Literature DB >> 30343191

Quinoline and quinolone dimers and their biological activities: An overview.

Xue-Mei Chu1, Cong Wang2, Wen Liu1, Li-Li Liang1, Kai-Kai Gong3, Cheng-Ying Zhao4, Kun-Lai Sun5.   

Abstract

Quinoline and quinolone motifs which act as structural subunits of more complex natural products are ubiquitous in nature, and they are useful pharmacophores which play a pivotal role in drug development. Compared with the corresponding monomeric compounds, the dimers usually exhibited some unique properties, so dimers have caused great interests in recent years. Quinline and quinolone dimers possess various biological properties such as antibacterial, anticancer, antimalarial and antitubercular activities, and some of them which are exemplified by piperaquine have already used in clinical practice. Numerous quinline and quinolone dimers have been synthesized and screened for their in vitro and in vivo biological activities, and some of them exhibited promising potency. Therefore, quinline and quinolone dimers have the potential for clinical deployment in the control and eradication of various diseases. This review covers the recent advances of quinline and quinolone dimers as bioactive substances. The structure-activity relationship was also discussed to provide an insight for rational designs of more active quinline and quinolone dimers.
Copyright © 2018 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  Antibacterial; Anticancer; Antimalarial; Antitubercular; Dimer; Quinoline; Quinolone; Structure-activity relationship

Mesh:

Substances:

Year:  2018        PMID: 30343191     DOI: 10.1016/j.ejmech.2018.10.035

Source DB:  PubMed          Journal:  Eur J Med Chem        ISSN: 0223-5234            Impact factor:   6.514


  15 in total

1.  Close the ring to break the cycle: tandem quinolone-alkyne-cyclisation gives access to tricyclic pyrrolo[1,2-a]quinolin-5-ones with potent anti-protozoal activity.

Authors:  Dávid Szamosvári; Kayla Sylvester; Philipp Schmid; Kuan-Yi Lu; Emily R Derbyshire; Thomas Böttcher
Journal:  Chem Commun (Camb)       Date:  2019-06-13       Impact factor: 6.222

2.  Synthesis and evaluation of the in vitro and in vivo antitrypanosomal activity of 2-styrylquinolines.

Authors:  Roger Espinosa; Sara Robledo; Camilo Guzmán; Natalia Arbeláez; Lina Yepes; Gílmar Santafé; Alex Sáez
Journal:  Heliyon       Date:  2021-05-12

Review 3.  Molecular targets and anticancer activity of quinoline-chalcone hybrids: literature review.

Authors:  Mamdouh F A Mohamed; Gamal El-Din A Abuo-Rahma
Journal:  RSC Adv       Date:  2020-08-21       Impact factor: 4.036

4.  An efficient 3-acylquinoline synthesis from acetophenones and anthranil via C(sp3)-H bond activation mediated by Selectfluor.

Authors:  Yejun Gao; Robert C Hider; Yongmin Ma
Journal:  RSC Adv       Date:  2019-04-02       Impact factor: 3.361

5.  Efficacy of the 7-chloro-4-(3-hydroxy-benzilidenehydrazo)quinoline derivative against infection caused by Leishmania amazonensis.

Authors:  Luciana Maria Ribeiro Antinarelli; Marcus Vinicius Nora de Souza; Eduardo Antonio Ferraz Coelho; Wallace Pacienza Lima; Elaine Soares Coimbra
Journal:  Rev Soc Bras Med Trop       Date:  2020-06-22       Impact factor: 1.581

Review 6.  A Review on Recent Advances in Nitrogen-Containing Molecules and Their Biological Applications.

Authors:  Nagaraju Kerru; Lalitha Gummidi; Suresh Maddila; Kranthi Kumar Gangu; Sreekantha B Jonnalagadda
Journal:  Molecules       Date:  2020-04-20       Impact factor: 4.411

7.  Crystal structure and Hirshfeld surface analysis of hexyl 1-hexyl-2-oxo-1,2-di-hydro-quinoline-4-carboxyl-ate.

Authors:  Younos Bouzian; Sevgi Kansiz; Lhassane Mahi; Noureddine Hamou Ahabchane; Joel T Mague; Necmi Dege; Khalid Karrouchi; El Mokhtar Essassi
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2020-04-09

8.  Synthesis and biological evaluation of novel 3-(quinolin-4-ylamino)benzenesulfonamidesAQ3 as carbonic anhydrase isoforms I and II inhibitors.

Authors:  Mohammad M Al-Sanea; Ahmed Elkamhawy; Sora Paik; Silvia Bua; So Ha Lee; Mohamed A Abdelgawad; Eun Joo Roh; Wagdy M Eldehna; Claudiu T Supuran
Journal:  J Enzyme Inhib Med Chem       Date:  2019-12       Impact factor: 5.051

9.  Crystal structure, DFT study and Hirshfeld surface analysis of ethyl 6-chloro-2-eth-oxy-quinoline-4-carboxyl-ate.

Authors:  Younos Bouzian; Khalid Karrouchi; El Hassane Anouar; Rachid Bouhfid; Suhana Arshad; El Mokhtar Essassi
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2019-05-31

10.  Intestinal cestodes of chicken are effectively killed by quinoline-rich extract of Spilanthes acmella.

Authors:  Pawi Bawitlung Lalthanpuii; Kholhring Lalchhandama
Journal:  Vet World       Date:  2020-04-30
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.