» Articles » PMID: 11741486

C-16 Artemisinin Derivatives and Their Antimalarial and Cytotoxic Activities: Syntheses of Artemisinin Monomers, Dimers, Trimers, and Tetramers by Nucleophilic Additions to Artemisitene

Overview
Journal J Med Chem
Specialty Chemistry
Date 2001 Dec 14
PMID 11741486
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Nucleophilic additions of lithium keto and ester enolates and mono- and bifunctional Grignard reagents to artemisitene provided C-16-derived artemisinin monomers, dimers, trimers, and tetramers whose antimalarial and cytotoxic activities have been evaluated.

Citing Articles

Optical Properties of Artemisinin and Its Derivatives.

Ma J, Qiao W, Mu X, Dong J, Quan J, Tian C ACS Omega. 2020; 5(48):30849-30857.

PMID: 33324794 PMC: 7726762. DOI: 10.1021/acsomega.0c03361.


Potent antiviral activity of topoisomerase I and II inhibitors against Kaposi's sarcoma-associated herpesvirus.

Gonzalez-Molleda L, Wang Y, Yuan Y Antimicrob Agents Chemother. 2011; 56(2):893-902.

PMID: 22106228 PMC: 3264263. DOI: 10.1128/AAC.05274-11.


Glycyrrhiza glabra (Linn.) and Lavandula officinalis (L.) cell suspension cultures-based biotransformation of β-artemether.

Patel S, Gaur R, Upadhyaya M, Mathur A, Mathur A, Bhakuni R J Nat Med. 2011; 65(3-4):646-50.

PMID: 21544685 DOI: 10.1007/s11418-011-0539-5.


Dinitroaliphatics as linkers: application in the synthesis of novel artemisinin carba-dimer.

Goswami A, Saikia P, Saikia B, Barua N Mol Divers. 2011; 15(3):707-12.

PMID: 21203838 DOI: 10.1007/s11030-010-9296-8.


Malaria-infected mice are cured by a single oral dose of new dimeric trioxane sulfones which are also selectively and powerfully cytotoxic to cancer cells.

Rosenthal A, Chen X, Liu J, West D, Hergenrother P, Shapiro T J Med Chem. 2009; 52(4):1198-203.

PMID: 19186946 PMC: 2698029. DOI: 10.1021/jm801484v.