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11 Results Found

  • Article
  • Open Access
8 Citations
6,497 Views
16 Pages

Role of Quinone Reductase 2 in the Antimalarial Properties of Indolone-Type Derivatives

  • Laure-Estelle Cassagnes,
  • Nambinina Rakotoarivelo,
  • Serena Sirigu,
  • Pierre Pério and ,
  • Ennaji Najahi,
  • Léonard M. G. Chavas,
  • Andrew Thompson,
  • Régis Gayon,
  • Gilles Ferry and
  • Françoise Nepveu
  • + 8 authors+ 3 authors

30 January 2017

Indolone-N-oxides have antiplasmodial properties against Plasmodium falciparum at the erythrocytic stage, with IC50 values in the nanomolar range. The mechanism of action of indolone derivatives involves the production of free radicals, which follows...

  • Article
  • Open Access
5 Citations
2,960 Views
16 Pages

Synthesis and Antimicrobial Activity of 3-Alkylidene-2-Indolone Derivatives

  • He Huang,
  • Yating Zhang,
  • Qiu Du,
  • Changji Zheng and ,
  • Chenghua Jin and
  • Siqi Li
  • + 1 author+ 0 author

15 November 2024

The escalating threat of antibiotic-resistant bacteria and fungi underscores an urgent need for new antimicrobial agents. This study aimed to synthesize and evaluate the antimicrobial activities of two series of 3-alkylidene-2-indolone derivatives. W...

(This article belongs to the Section Organic Chemistry)
  • Article
  • Open Access
8 Citations
3,121 Views
16 Pages

Synthesis and Biological Evaluation of Novel Synthetic Indolone Derivatives as Anti-Tumor Agents Targeting p53-MDM2 and p53-MDMX

  • Yali Wang,
  • Bo Ji,
  • Zhongshui Cheng,
  • Lianghui Zhang and ,
  • Yingying Cheng,
  • Yingying Li,
  • Jin Ren,
  • Wenbo Liu and
  • Yuanyuan Ma
  • + 4 authors+ 0 author

A series of novel indolone derivatives were synthesized and evaluated for their binding affinities toward MDM2 and MDMX. Some compounds showed potent MDM2 and moderate MDMX activities. Among them, compound A13 exhibited the most potent affinity towar...

(This article belongs to the Special Issue Anticancer Agents: Design, Synthesis and Evaluation III)
  • Article
  • Open Access
8 Citations
4,284 Views
11 Pages

Australindolones, New Aminopyrimidine Substituted Indolone Alkaloids from an Antarctic Tunicate Synoicum sp.

  • Sofia Kokkaliari,
  • Kim Pham,
  • Nargess Shahbazi,
  • Laurent Calcul and ,
  • Lukasz Wojtas,
  • Nerida G. Wilson,
  • Alexander D. Crawford and
  • Bill J. Baker
  • + 3 authors+ 0 author

8 March 2022

Five new alkaloids have been isolated from the lipophilic extract of the Antarctic tunicate Synoicum sp. Deep-sea specimens of Synoicum sp. were collected during a 2011 cruise of the R/V Nathanial B. Palmer to the southern Scotia Arc, Antarctica. Cru...

  • Article
  • Open Access
7 Citations
4,582 Views
18 Pages

Integrating Molecular Network and Culture Media Variation to Explore the Production of Bioactive Metabolites by Vibrio diabolicus A1SM3

  • Natalia Conde-Martínez,
  • Anelize Bauermeister,
  • Alan Cesar Pilon,
  • Norberto Peporine Lopes and
  • Edisson Tello

27 March 2019

Vibrio diabolicus A1SM3 strain was isolated from a sediment sample from Manaure Solar Saltern in La Guajira and the produced crude extracts have shown antibacterial activity against methicillin-resistant Staphylococcus aureus and cytotoxic activity a...

(This article belongs to the Special Issue Bioprospecting of Marine Microorganisms)
  • Review
  • Open Access
7 Citations
5,889 Views
28 Pages

29 July 2021

This review focuses on the synthesis of polyheterocyclic structures with a variety of medicinal and optoelectronic applications, starting from readily available 4,5,6,7-tetrahydroindol-4-one analogs. First, routes toward the 4,5,6,7-tetrahydroindol-4...

(This article belongs to the Collection Heterocyclic Compounds)
  • Short Note
  • Open Access
2,936 Views
5 Pages

3,6-Dihydro-5H-pyrazolo [4′,3′:5,6]pyrano[3,4-b]indol-5-one

  • Amalia D. Kalampaliki,
  • Sofia Kanellopoulou and
  • Ioannis K. Kostakis

20 July 2022

Pyrano [3,4-b]indol-1(9H)-ones and indolo [2,3-c]coumarins are important classes of heterocyclic compounds with versatile biological activities. Herein, we describe a straightforward and scalable synthesis of 3,6-dihydro-5H-pyrazolo [4′,3&prime...

(This article belongs to the Section Organic Synthesis and Biosynthesis)
  • Article
  • Open Access
13 Citations
3,547 Views
11 Pages

Antimalarial Properties of Dunnione Derivatives as NQO2 Substrates

  • Monivan Chhour,
  • Agnès Aubouy,
  • Sandra Bourgeade-Delmas,
  • Pierre Pério and ,
  • Hélène Ternet-Fontebasso,
  • Mahamane Haidara,
  • Gilles Ferry,
  • Françoise Nepveu,
  • Jean A. Boutin and
  • Karine Reybier
  • + 5 authors+ 0 author

15 October 2019

Dunnione, a natural product isolated from the leaves of Streptocarpus dunnii (Gesneriaceae), acts as a substrate for quinone-reductases that may be associated with its antimalarial properties. Following our exploration of reactive oxygen species-prod...

(This article belongs to the Section Medicinal Chemistry)
  • Article
  • Open Access
5 Citations
6,027 Views
13 Pages

31 March 2019

The present work describes the synthesis of a new copper (II) complex with bidentate ligands based on oxindole (indolin-2-one) derivatives, namely: 1H,1′H,1″H-[2,3′:2′,3″-terbenzo[b]pyrrol]-2″(3″H)-one (L1) and [sodium diethyldithiocarbamate (DTC)] (...

(This article belongs to the Special Issue Advance Electrode Materials for Perovskite Solar Cells and Electrochemical Supercapacitor)
  • Review
  • Open Access
3 Citations
3,095 Views
30 Pages

Medicinally Significant Enantiopure Compounds from Garcinia Acid Isolated from Garcinia gummi-gutta

  • Simimole Haleema,
  • Chithra Gopinath,
  • Zabeera Kallingathodi,
  • Grace Thomas and
  • Prasad L. Polavarapu

9 October 2024

Garcinia gummi-gutta, commonly known as Garcinia cambogia (syn.), is a popular traditional herbal medicine known for its role in treating obesity, and has been incorporated into several nutraceuticals globally for this purpose. The fruit rind is also...

(This article belongs to the Special Issue Chemistry: Symmetry/Asymmetry—Feature Papers and Reviews)
  • Article
  • Open Access
174 Views
27 Pages

29 October 2026

Objective: Toll-like receptor 7 (TLR7) is an important pattern recognition receptor. It mainly participates in the recognition of single-stranded RNA and is closely related to various disease processes. In humans, the enormous potential of TLR7 antag...

(This article belongs to the Section Medicinal Chemistry)