Artemisinin and its derivatives: a novel class of anti-malarial and anti-cancer agents. - Wikidata - awgldk - TriplyDB

Artemisinin and its derivatives: a novel class of anti-malarial and anti-cancer agents.

Artemisinin and its derivatives: a novel class of anti-malarial and anti-cancer agents.

http://www.wikidata.org/entity/Q37683458

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Rearrangements of organic peroxides and related processes Convergence and divergence of bitterness biosynthesis and regulation in Cucurbitaceae Simultaneous isolation of artemisinin and its precursors from Artemisia annua L. by preparative RP-HPLC.Dihydroartemisinin exerts its anticancer activity through depleting cellular iron via transferrin receptor-1.Design, synthesis, and study of a mycobactin-artemisinin conjugate that has selective and potent activity against tuberculosis and malaria pH-responsive artemisinin derivatives and lipid nanoparticle formulations inhibit growth of breast cancer cells in vitro and induce down-regulation of HER family members.Human p38 mitogen-activated protein kinase inhibitor drugs inhibit Plasmodium falciparum replication Enhancement of cytotoxicity of artemisinin toward cancer cells by transferrin-mediated carbon nanotubes nanoparticles.Affordable and rapid HPTLC method for the simultaneous analysis of artemisinin and its metabolite artemisinic acid in Artemisia annua L.Dihydroartemisinin induces apoptosis preferentially via a Bim-mediated intrinsic pathway in hepatocarcinoma cells.Disruption of spermatogenesis in the liver fluke, Fasciola hepatica by two artemisinin derivatives, artemether and artesunate.Therapeutic effects of dihydroartemisinin and transferrin against glioblastoma.A randomized trial of the efficacy of artesunate and three quinine regimens in the treatment of severe malaria in children at the Ebolowa Regional Hospital, Cameroon.Application of the Triazolization Reaction to Afford Dihydroartemisinin Derivatives with Anti-HIV Activity.Controlled oxidation of remote sp3 C-H bonds in artemisinin via P450 catalysts with fine-tuned regio- and stereoselectivity Endoperoxide formation by an α-ketoglutarate-dependent mononuclear non-haem iron enzyme Artemisinin-derived dimer phosphate esters as potent anti-cytomegalovirus (anti-CMV) and anti-cancer agents: a structure-activity study.Development of Anticancer Agents from Plant-Derived Sesquiterpene Lactones.A structural and functional study on the 2-C-methyl-d-erythritol-4-phosphate cytidyltransferase (IspD) from Bacillus subtilis.A Novel Tumor-Activated Prodrug Strategy Targeting Ferrous Iron Is Effective in Multiple Preclinical Cancer Models The molecular and cellular action properties of artemisinins: what has yeast told us?Artemisinin derivatives: a patent review (2006 - present).Terpenoids: natural products for cancer therapy.New uses for old drugs: the tale of artemisinin derivatives in the elimination of schistosomiasis japonica in China.Conformational analysis of δ-lactones by DFT calculations: the parent compound and its monomethyl and selected dimethyl derivatives.Dimeric Sesquiterpenoids.Erythrophagocytosis enhances heme-dependent cytotoxicity of antimalarial drugs in canine histiocytic sarcoma cell line DH82.Design, Synthesis and Cytotoxicity of Novel Dihydroartemisinin-Coumarin Hybrids via Click Chemistry.The road to avibactam: the first clinically useful non-β-lactam working somewhat like a β-lactam.Artemisinin and its derivatives in treating protozoan infections beyond malaria.Artemisinin rewires the protein interaction network in cancer cells: network analysis, pathway identification, and target prediction.Anti-cancer activity of DHA on gastric cancer--an in vitro and in vivo study.Synthesis and cytotoxicity of novel 10-substituted dihydroartemisinin derivatives containing N-arylphenyl-ethenesulfonamide groups.An asymmetric synthesis of 1,2,4-trioxane anticancer agents via desymmetrization of peroxyquinols through a Brønsted acid catalysis cascade.Bioinformatic and experimental fishing for artemisinin-interacting proteins from human nasopharyngeal cancer cells.Synthesis and antimalarial activity of 3,3-spiroanellated 5,6-disubstituted 1,2,4-trioxanes.Four-step synthesis of the antimalarial cardamom peroxide via an oxygen stitching strategy.Concise photochemical synthesis of the antimalarial indole alkaloid decursivine.β-Cyclodextrin polymer nanoparticles as carriers for doxorubicin and artemisinin: a spectroscopic and photophysical study.AaMYB1 and its orthologue AtMYB61 affect terpene metabolism and trichome development in Artemisia annua and Arabidopsis thaliana.

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P2860

Artemisinin and its derivatives: a novel class of anti-malarial and anti-cancer agents.

http://www.wikidata.org/entity/Q37683458

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

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bilimsel makale

@tr

scientific article published on 24 August 2009

@en

vedecký článok

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vetenskaplig artikel

@sv

videnskabelig artikel

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vědecký článek

@cs

name

Artemisinin and its derivatives: a novel class of anti-malarial and anti-cancer agents.

@en

Artemisinin and its derivatives: a novel class of anti-malarial and anti-cancer agents.

@nl

type

label

Artemisinin and its derivatives: a novel class of anti-malarial and anti-cancer agents.

@en

Artemisinin and its derivatives: a novel class of anti-malarial and anti-cancer agents.

@nl

prefLabel

Artemisinin and its derivatives: a novel class of anti-malarial and anti-cancer agents.

@en

Artemisinin and its derivatives: a novel class of anti-malarial and anti-cancer agents.

@nl

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Chemical Society Reviews

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Artemisinin and its derivatives: a novel class of anti-malarial and anti-cancer agents.

@en

P2093

Abhishek Goswami

http://www.w3.org/2001/XMLSchema#string

Devdutt Chaturvedi

http://www.w3.org/2001/XMLSchema#string

Nabin C Barua

http://www.w3.org/2001/XMLSchema#string

Partha Pratim Saikia

http://www.w3.org/2001/XMLSchema#string

Paruchuri G Rao

http://www.w3.org/2001/XMLSchema#string

P2860

Malaria in 2002

The economic and social burden of malaria

Knowledge of the proposed chemical mechanism of action and cytochrome p450 metabolism of antimalarial trioxanes like artemisinin allows rational design of new antimalarial peroxides

Novel, potent, semisynthetic antimalarial carba analogues of the first-generation 1,2,4-trioxane artemether

Novel antitumor artemisinin derivatives targeting G1 phase of the cell cycle.

Chemotherapy for falciparum malaria: the armoury, the problems and the prospects.

Medical need, scientific opportunity and the drive for antimalarial drugs.

Malaria-infected mice are cured by a single dose of novel artemisinin derivatives.

Treatment of malaria--1990.

Second generation, orally active, antimalarial, artemisinin-derived trioxane dimers with high stability, efficacy, and anticancer activity.

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435-454

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scholarly article

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10.1039/B816679J

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2

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39

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2009-08-24T00:00:00Z

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41175047

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20111769

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