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News from the WHO Division of Control of Tropical Diseases
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TDR News (News from the WHO Division of Control of Tropical Diseases) 1994, 46, 5.
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TDR News
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2
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0031080653
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Quinoline antimalarials: Mechanisms of action and resistance
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Foley, M.; Tilley, L. Quinoline Antimalarials: Mechanisms of Action and Resistance. Int. J. Parasitol. 1997, 27, 213-240.
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Int. J. Parasitol.
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Foley, M.1
Tilley, L.2
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3
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0029006420
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The toxicity of artemisinin and related-compounds on neuronal and glial-cells in culture
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Fishwick, J.; McClean, W. G.; Edwards, G.; Ward, S. A. The Toxicity of Artemisinin and Related-Compounds on Neuronal and Glial-Cells in Culture. Chem. Biol. Interact. 1995, 96, 263-271.
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Chem. Biol. Interact.
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Fishwick, J.1
McClean, W.G.2
Edwards, G.3
Ward, S.A.4
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4
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0031953576
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Metabolism of beta-arteether to dihydroqinghaosu by human liver microsomes and recombinant cytochrome P450
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Grace, J. M.; Aguilar, A. J.; Trotman, K. M.; Brewer, T. G. Metabolism of Beta-Arteether to Dihydroqinghaosu by Human Liver Microsomes and Recombinant Cytochrome P450. Drug Metab. Dispos. 1998, 26, 313-317.
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Drug Metab. Dispos.
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Grace, J.M.1
Aguilar, A.J.2
Trotman, K.M.3
Brewer, T.G.4
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5
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0001357958
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A concise synthesis of novel aromatic analogues of artemisinin
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Jung, M.; Lee, S. A Concise Synthesis of Novel Aromatic Analogues of Artemisinin. Heterocycles 1997, 45, 1055-1058.
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Heterocycles
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Jung, M.1
Lee, S.2
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6
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84928945683
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Efficient preparation of novel qinghaosu (artemisinin) derivatives-conversion of qinghao (artemisinic) acid into deoxoqinghaosu derivatives and 5-carba-4-deoxoartesunic acid
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Haynes, R. K.; Vonwiller, S. C. Efficient Preparation of Novel Qinghaosu (Artemisinin) Derivatives-Conversion of Qinghao (Artemisinic) Acid into Deoxoqinghaosu Derivatives and 5-Carba-4-deoxoartesunic acid. Synlett 1992, 481-482.
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(1992)
Synlett
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Haynes, R.K.1
Vonwiller, S.C.2
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7
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0032546313
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Direct conversion of pyranose anomeric OH - F - R in the artemisinin family of antimalarial trioxanes
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Woo, S. H.; Parker, M. P.; Ploypradith, P.; Northrop, J.; Posner, G. H. Direct conversion of Pyranose anomeric OH - F - R in the Artemisinin Family of Antimalarial Trioxanes. Tetrahedron Lett. 1998, 39, 1533-1536.
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Tetrahedron Lett.
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Woo, S.H.1
Parker, M.P.2
Ploypradith, P.3
Northrop, J.4
Posner, G.H.5
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8
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0030938872
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Synthesis and cytotoxicity of novel artemisinin analogues
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Jung, M. Synthesis and Cytotoxicity of Novel Artemisinin Analogues. Bioorg. Med. Chem. Lett. 1997, 7, 1091-1094.
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Bioorg. Med. Chem. Lett.
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Jung, M.1
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9
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0028788118
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Synthesis and antimalarial activities of several fluorinated artemisinin derivatives
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(a) Pu, Y. M.; Torok, D. S.; Ziffer, H.; Pan, X. Q.; Meshnick, S. R. Synthesis and Antimalarial Activities of Several Fluorinated Artemisinin Derivatives. J. Med. Chem. 1995, 38, 4120-4124.
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Pu, Y.M.1
Torok, D.S.2
Ziffer, H.3
Pan, X.Q.4
Meshnick, S.R.5
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10
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0032497703
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Synthesis and antimalarial activities of fluoroalkyl derivatives of dihydroartemisinin
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(b) Nga, T. T. T.; Menage, C.; Begue, J. P.; Bonnet Delpon, D.; Gantier, J. C. Synthesis and Antimalarial Activities of Fluoroalkyl Derivatives of Dihydroartemisinin. J. Med. Chem. 1998, 41, 4101.
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Nga, T.T.T.1
Menage, C.2
Begue, J.P.3
Bonnet Delpon, D.4
Gantier, J.C.5
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11
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0029061802
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Structure-activity relationships of lactone ring-opened analogues of the antimalarial 1,2,4-trioxane artemisinin
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Posner, G. H.; McGarvey, D. J.; Oh, C. H.; Kumar, N.; Meshnick, S. R.; Asawamahasadka, W. Structure-Activity Relationships of Lactone Ring-Opened Analogues of the Antimalarial 1,2,4-Trioxane Artemisinin. J. Med Chem. 1995, 38, 607-612.
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Posner, G.H.1
McGarvey, D.J.2
Oh, C.H.3
Kumar, N.4
Meshnick, S.R.5
Asawamahasadka, W.6
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12
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0029044697
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Synthesis and antimalarial activities of 12-beta-allyldeoxoartemisinin and its derivatives
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Pu, Y.-M.; Ziffer, H. Synthesis and Antimalarial Activities of 12-Beta-Allyldeoxoartemisinin and its Derivatives. J. Med. Chem. 1995, 38, 613-616.
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Pu, Y.-M.1
Ziffer, H.2
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13
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0018606732
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Quantitative assessment of antimalarial activity in vitro by a semi-automated microdilution technique
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Desjardins, R. E.; Canfield, J.; Haynes, D.; Chulay, D. J. Quantitative Assessment of Antimalarial Activity In Vitro by a Semi-automated Microdilution Technique. Antimicrob. Agents Chemother. 1979, 16, 710-718.
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Desjardins, R.E.1
Canfield, J.2
Haynes, D.3
Chulay, D.J.4
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0028305219
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Mechanism-based design, synthesis and in vitro antimalarial testing of new 4-methylated trioxanes structurally related to artemisinin
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For a report of a carbon-centered radical intermediate in iron(II)-promoted reductive cleavage of an antimalarial trioxane, see: Posner, G. H.; Oh, C. H.; Wang, D.; Gerena, L.; Milhous, W. K.; Meshnick, S. R.; Asawamahasakada, W. Mechanism-Based Design, Synthesis and in Vitro Antimalarial Testing of New 4-Methylated Trioxanes structurally Related to Artemisinin. J. Med. Chem. 1994, 37, 1256-1258.
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Posner, G.H.1
Oh, C.H.2
Wang, D.3
Gerena, L.4
Milhous, W.K.5
Meshnick, S.R.6
Asawamahasakada, W.7
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15
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0032514426
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A carbonyl oxide route to antimalarial yingzhaosu a analogues: Synthesis and antimalarial activity
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O'Neill, P. M.; Searle, N. L.; Maggs, J. L.; Raynes, K. J.; Ward, S. A.; Maggs, J. L.; Park, B. K.; Posner, G. H. A Carbonyl Oxide Route to Antimalarial Yingzhaosu A Analogues: Synthesis and Antimalarial Activity. Tetrahedron Lett. 1998, 39, 6085-6088.
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O'Neill, P.M.1
Searle, N.L.2
Maggs, J.L.3
Raynes, K.J.4
Ward, S.A.5
Maggs, J.L.6
Park, B.K.7
Posner, G.H.8
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16
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0030976258
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The biomimetic iron-mediated degradation of arteflene (Ro-42-1611), an endoperoxide antimalarial: Implications for the mechanism of antimalarial activity
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O'Neill, P. M.; Bishop, L. P.; Searle, N. L.; Maggs, J. L.; Bray, P. G.; Ward, S. A.; Park, B. K. The Biomimetic Iron-Mediated Degradation of Arteflene (Ro-42-1611), An Endoperoxide Antimalarial: Implications for the Mechanism of Antimalarial Activity. Tetrahedron Lett. 1997, 38, 4263-4266.
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Tetrahedron Lett.
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O'Neill, P.M.1
Bishop, L.P.2
Searle, N.L.3
Maggs, J.L.4
Bray, P.G.5
Ward, S.A.6
Park, B.K.7
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17
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0029886413
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Structure-activity relationships of the antimalarial agent artemisinin. 3. Total synthesis of (+)-13-carbaartemisinin and related tetra- and tricyclic structures
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For a discussion of the Fe(II)-mediated decomposition of C-10-deoxoartemisinin, see: Avery, M. A.; Fan, P.-C.; Karle, J. M.; Bonk, J. D.; Miller, R.; Goins, D. K. Structure-Activity Relationships of the Antimalarial Agent Artemisinin. 3. Total Synthesis of (+)-13-Carbaartemisinin and Related Tetra- and Tricyclic Structures. J. Med. Chem. 1996, 39, 1885-1897.
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Avery, M.A.1
Fan, P.-C.2
Karle, J.M.3
Bonk, J.D.4
Miller, R.5
Goins, D.K.6
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18
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0032522115
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Unified mechanistic framework for the Fe(II) induced cleavage of quinghaosu and derivatives/analogues. The first spin trapping for the previously postulated secondary C-4 radical
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Wu, W. M.; Wu, Y. K.; Wu, Y. L.; Yao, Z. J.; Zhou, C. M.; Li, Y.; Shan, F. Unified Mechanistic Framework for the Fe(II) Induced Cleavage of Quinghaosu and Derivatives/Analogues. The First Spin Trapping for the Previously Postulated Secondary C-4 Radical. J. Am. Chem. Soc. 1998, 120, 3325-3325.
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Wu, W.M.1
Wu, Y.K.2
Wu, Y.L.3
Yao, Z.J.4
Zhou, C.M.5
Li, Y.6
Shan, F.7
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19
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0032510451
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Orally active antimalarial 3-substituted trioxanes: New synthetic methodology and biological evaluation
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Posner, G. H.; Cumming, J. N.; Woo, S.-H.; Ploypradith, P.; Xie, S.; Shapiro, T. A. Orally active antimalarial 3-substituted trioxanes: New synthetic methodology and biological evaluation. J. Med. Chem. 1998, 41, 940.
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J. Med. Chem.
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Posner, G.H.1
Cumming, J.N.2
Woo, S.-H.3
Ploypradith, P.4
Xie, S.5
Shapiro, T.A.6
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20
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0032510380
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Design, synthesis, derivatization, and structure-activity relationships of simplified, tricyclic, 1,2,4-trioxane alcohol analogues of the antimalarial artemisinin
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Cumming, J. N.; Wang, D.; Park, S. B.; Shapiro, T. A.; Posner, G. H. Design, Synthesis, Derivatization, and Structure-Activity Relationships of Simplified, Tricyclic, 1,2,4-Trioxane Alcohol Analogues of the Antimalarial Artemisinin. J. Med. Chem. 1998, 41, 952-964.
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J. Med. Chem.
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Cumming, J.N.1
Wang, D.2
Park, S.B.3
Shapiro, T.A.4
Posner, G.H.5
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21
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0031722604
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Safety assessment of peroxide antimalarials: Clinical and chemical perspectives
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Park, B. K.; O'Neill, P. M.; Maggs, J. L.; Pirmohamed, M. Safety Assessment of Peroxide Antimalarials: Clinical and Chemical Perspectives. Br. J. Clin. Pharmacol. 1998, 46, 521.
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Park, B.K.1
O'Neill, P.M.2
Maggs, J.L.3
Pirmohamed, M.4
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22
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0017751397
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Plasmodium falciparum in culture; use of outdated erythrocytes and description of the candle jar methodology
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