Dihydroartemisinin (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Dihydroartemisinin" in English language version.

refsWebsite

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13nih.gov

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10doi.org

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1harvard.edu

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doi.org

Woo SH, Parker MH, Ploypradith P, Northrop J, Posner GH (1998). "Direct conversion of pyranose anomeric OH→F→R in the artemisinin family of antimalarial trioxanes". Tetrahedron Letters. 39 (12): 1533–6. doi:10.1016/S0040-4039(98)00132-4.
Arinaitwe E, Sandison TG, Wanzira H, Kakuru A, Homsy J, Kalamya J, et al. (December 2009). "Artemether-lumefantrine versus dihydroartemisinin-piperaquine for falciparum malaria: a longitudinal, randomized trial in young Ugandan children". Clinical Infectious Diseases. 49 (11): 1629–1637. doi:10.1086/647946. PMID 19877969.
Tilley L, Straimer J, Gnädig NF, Ralph SA, Fidock DA (September 2016). "Artemisinin Action and Resistance in Plasmodium falciparum". Trends in Parasitology. 32 (9): 682–696. doi:10.1016/j.pt.2016.05.010. PMC 5007624. PMID 27289273.
Zani B, Gathu M, Donegan S, Olliaro PL, Sinclair D (January 2014). "Dihydroartemisinin-piperaquine for treating uncomplicated Plasmodium falciparum malaria". The Cochrane Database of Systematic Reviews. 2014 (1): CD010927. doi:10.1002/14651858.CD010927. PMC 4470355. PMID 24443033.
Cumming JN, Ploypradith P, Posner GH (1996). Antimalarial activity of artemisinin (Qinghaosu) and related trioxanes: Mechanism(s) of action. Advances in Pharmacology. Vol. 37. pp. 253–297. doi:10.1016/S1054-3589(08)60952-7. ISBN 9780120329380. PMID 8891104.
Posner GH, O'Neill PM (June 2004). "Knowledge of the proposed chemical mechanism of action and cytochrome p450 metabolism of antimalarial trioxanes like artemisinin allows rational design of new antimalarial peroxides". Accounts of Chemical Research. 37 (6): 397–404. doi:10.1021/ar020227u. PMID 15196049.
Zhou Y, Li W, Xiao Y (April 2016). "Profiling of Multiple Targets of Artemisinin Activated by Hemin in Cancer Cell Proteome". ACS Chemical Biology. 11 (4): 882–888. doi:10.1021/acschembio.5b01043. PMID 26854499.
Liu K, Dai L, Li C, Liu J, Wang L, Lei J (July 2016). "Self-assembled targeted nanoparticles based on transferrin-modified eight-arm-polyethylene glycol-dihydroartemisinin conjugate". Scientific Reports. 6: 29461. Bibcode:2016NatSR...629461L. doi:10.1038/srep29461. PMC 4932499. PMID 27377918.
Efferth T (April 2006). "Molecular pharmacology and pharmacogenomics of artemisinin and its derivatives in cancer cells". Current Drug Targets. 7 (4): 407–421. doi:10.2174/138945006776359412. PMID 16611029.
Cabello CM, Lamore SD, Bair WB, Qiao S, Azimian S, Lesson JL, et al. (August 2012). "The redox antimalarial dihydroartemisinin targets human metastatic melanoma cells but not primary melanocytes with induction of NOXA-dependent apoptosis". Investigational New Drugs. 30 (4): 1289–1301. doi:10.1007/s10637-011-9676-7. PMC 3203350. PMID 21547369.

harvard.edu

ui.adsabs.harvard.edu

Liu K, Dai L, Li C, Liu J, Wang L, Lei J (July 2016). "Self-assembled targeted nanoparticles based on transferrin-modified eight-arm-polyethylene glycol-dihydroartemisinin conjugate". Scientific Reports. 6: 29461. Bibcode:2016NatSR...629461L. doi:10.1038/srep29461. PMC 4932499. PMID 27377918.

nih.gov

pubmed.ncbi.nlm.nih.gov

Arinaitwe E, Sandison TG, Wanzira H, Kakuru A, Homsy J, Kalamya J, et al. (December 2009). "Artemether-lumefantrine versus dihydroartemisinin-piperaquine for falciparum malaria: a longitudinal, randomized trial in young Ugandan children". Clinical Infectious Diseases. 49 (11): 1629–1637. doi:10.1086/647946. PMID 19877969.
Tilley L, Straimer J, Gnädig NF, Ralph SA, Fidock DA (September 2016). "Artemisinin Action and Resistance in Plasmodium falciparum". Trends in Parasitology. 32 (9): 682–696. doi:10.1016/j.pt.2016.05.010. PMC 5007624. PMID 27289273.
Zani B, Gathu M, Donegan S, Olliaro PL, Sinclair D (January 2014). "Dihydroartemisinin-piperaquine for treating uncomplicated Plasmodium falciparum malaria". The Cochrane Database of Systematic Reviews. 2014 (1): CD010927. doi:10.1002/14651858.CD010927. PMC 4470355. PMID 24443033.
Cumming JN, Ploypradith P, Posner GH (1996). Antimalarial activity of artemisinin (Qinghaosu) and related trioxanes: Mechanism(s) of action. Advances in Pharmacology. Vol. 37. pp. 253–297. doi:10.1016/S1054-3589(08)60952-7. ISBN 9780120329380. PMID 8891104.
Posner GH, O'Neill PM (June 2004). "Knowledge of the proposed chemical mechanism of action and cytochrome p450 metabolism of antimalarial trioxanes like artemisinin allows rational design of new antimalarial peroxides". Accounts of Chemical Research. 37 (6): 397–404. doi:10.1021/ar020227u. PMID 15196049.
Zhou Y, Li W, Xiao Y (April 2016). "Profiling of Multiple Targets of Artemisinin Activated by Hemin in Cancer Cell Proteome". ACS Chemical Biology. 11 (4): 882–888. doi:10.1021/acschembio.5b01043. PMID 26854499.
Liu K, Dai L, Li C, Liu J, Wang L, Lei J (July 2016). "Self-assembled targeted nanoparticles based on transferrin-modified eight-arm-polyethylene glycol-dihydroartemisinin conjugate". Scientific Reports. 6: 29461. Bibcode:2016NatSR...629461L. doi:10.1038/srep29461. PMC 4932499. PMID 27377918.
Efferth T (April 2006). "Molecular pharmacology and pharmacogenomics of artemisinin and its derivatives in cancer cells". Current Drug Targets. 7 (4): 407–421. doi:10.2174/138945006776359412. PMID 16611029.
Cabello CM, Lamore SD, Bair WB, Qiao S, Azimian S, Lesson JL, et al. (August 2012). "The redox antimalarial dihydroartemisinin targets human metastatic melanoma cells but not primary melanocytes with induction of NOXA-dependent apoptosis". Investigational New Drugs. 30 (4): 1289–1301. doi:10.1007/s10637-011-9676-7. PMC 3203350. PMID 21547369.

ncbi.nlm.nih.gov

Tilley L, Straimer J, Gnädig NF, Ralph SA, Fidock DA (September 2016). "Artemisinin Action and Resistance in Plasmodium falciparum". Trends in Parasitology. 32 (9): 682–696. doi:10.1016/j.pt.2016.05.010. PMC 5007624. PMID 27289273.
Zani B, Gathu M, Donegan S, Olliaro PL, Sinclair D (January 2014). "Dihydroartemisinin-piperaquine for treating uncomplicated Plasmodium falciparum malaria". The Cochrane Database of Systematic Reviews. 2014 (1): CD010927. doi:10.1002/14651858.CD010927. PMC 4470355. PMID 24443033.
Liu K, Dai L, Li C, Liu J, Wang L, Lei J (July 2016). "Self-assembled targeted nanoparticles based on transferrin-modified eight-arm-polyethylene glycol-dihydroartemisinin conjugate". Scientific Reports. 6: 29461. Bibcode:2016NatSR...629461L. doi:10.1038/srep29461. PMC 4932499. PMID 27377918.
Cabello CM, Lamore SD, Bair WB, Qiao S, Azimian S, Lesson JL, et al. (August 2012). "The redox antimalarial dihydroartemisinin targets human metastatic melanoma cells but not primary melanocytes with induction of NOXA-dependent apoptosis". Investigational New Drugs. 30 (4): 1289–1301. doi:10.1007/s10637-011-9676-7. PMC 3203350. PMID 21547369.