-
1
-
-
33947520442
-
2-C-Methylerythritol phosphate pathway of isoprenoid biosynthesis as a target in identifying new antibiotics, herbicides, and immunomodulators: A review
-
Ershov, Y. V. 2-C-Methylerythritol phosphate pathway of isoprenoid biosynthesis as a target in identifying new antibiotics, herbicides, and immunomodulators: a review Appl. Biochem. Microbiol. 2007, 43, 115-138
-
(2007)
Appl. Biochem. Microbiol.
, vol.43
, pp. 115-138
-
-
Ershov, Y.V.1
-
2
-
-
84856679687
-
Global malaria mortality between 1980 and 2010: A systematic analysis
-
Murray, C. J. L.; Rosenfeld, L. C.; Lim, S. S.; Andrews, K. G.; Foreman, K. J.; Haring, D.; Fullman, N.; Naghavi, M.; Lozano, R.; Lopez, A. D. Global malaria mortality between 1980 and 2010: a systematic analysis Lancet 2012, 379, 413-431
-
(2012)
Lancet
, vol.379
, pp. 413-431
-
-
Murray, C.J.L.1
Rosenfeld, L.C.2
Lim, S.S.3
Andrews, K.G.4
Foreman, K.J.5
Haring, D.6
Fullman, N.7
Naghavi, M.8
Lozano, R.9
Lopez, A.D.10
-
3
-
-
33646168046
-
Malarial parasites vs antimalarials: Never-ending rumble in the jungle
-
Mordmüller, B.; Kremsner, P. G. Malarial parasites vs. antimalarials: never-ending rumble in the jungle Curr. Mol. Med. 2006, 6, 247-251
-
(2006)
Curr. Mol. Med.
, vol.6
, pp. 247-251
-
-
Mordmüller, B.1
Kremsner, P.G.2
-
4
-
-
77956637142
-
When is enough enough? The need for a robust pipeline of high-quality antimalarials
-
Wells, T. N.; Poll, E. M. When is enough enough? The need for a robust pipeline of high-quality antimalarials Discovery Med. 2010, 9, 389-398
-
(2010)
Discovery Med.
, vol.9
, pp. 389-398
-
-
Wells, T.N.1
Poll, E.M.2
-
5
-
-
0019252768
-
Studies on new phosphonic acid antibiotics. 3. Isolation and characterization of FR-31564, FR-32863 and FR-33289
-
Okuhara, M.; Kuroda, Y.; Goto, T.; Okamoto, M.; Terano, H.; Kohsaka, M.; Aoki, H.; Imanaka, H. Studies on new phosphonic acid antibiotics. 3. Isolation and characterization of FR-31564, FR-32863 and FR-33289 J. Antibiot. 1980, 33, 24-28
-
(1980)
J. Antibiot.
, vol.33
, pp. 24-28
-
-
Okuhara, M.1
Kuroda, Y.2
Goto, T.3
Okamoto, M.4
Terano, H.5
Kohsaka, M.6
Aoki, H.7
Imanaka, H.8
-
6
-
-
0019257873
-
Studies on new phosphonic acid antibiotics. 4. Structure determination of FR-33289, FR-31564 and FR-32863
-
Kuroda, Y.; Okuhara, M.; Goto, T.; Okamoto, M.; Terano, H.; Kohsaka, M.; Aoki, H.; Imanaka, H. Studies on new phosphonic acid antibiotics. 4. Structure determination of FR-33289, FR-31564 and FR-32863 J. Antibiot. 1980, 33, 29-35
-
(1980)
J. Antibiot.
, vol.33
, pp. 29-35
-
-
Kuroda, Y.1
Okuhara, M.2
Goto, T.3
Okamoto, M.4
Terano, H.5
Kohsaka, M.6
Aoki, H.7
Imanaka, H.8
-
7
-
-
0033520336
-
Inhibitors of the nonmevalonate pathway of isoprenoid biosynthesis as antimalarial drugs
-
Jomaa, H.; Wiesner, J.; Sanderbrand, S.; Altincicek, B.; Weidemeyer, C.; Hintz, M.; Turbachova, I.; Eberl, M.; Zeidler, J.; Lichtenthaler, H. K.; Soldati, D.; Beck, E. Inhibitors of the nonmevalonate pathway of isoprenoid biosynthesis as antimalarial drugs Science 1999, 285, 1573-1576
-
(1999)
Science
, vol.285
, pp. 1573-1576
-
-
Jomaa, H.1
Wiesner, J.2
Sanderbrand, S.3
Altincicek, B.4
Weidemeyer, C.5
Hintz, M.6
Turbachova, I.7
Eberl, M.8
Zeidler, J.9
Lichtenthaler, H.K.10
Soldati, D.11
Beck, E.12
-
8
-
-
34248596742
-
Targeting the methyl erythritol phosphate (MEP) pathway for novel antimalarial, antibacterial and herbicidal drug discovery: Inhibition of 1-deoxy- d -xylulose-5-phosphate reductoisomerase (DXR) enzyme
-
Singh, N.; Cheve, G.; Avery, M. A.; McCurdy, C. R. Targeting the methyl erythritol phosphate (MEP) pathway for novel antimalarial, antibacterial and herbicidal drug discovery: inhibition of 1-deoxy- d -xylulose-5-phosphate reductoisomerase (DXR) enzyme Curr. Pharm. Des. 2007, 13, 1161-1177
-
(2007)
Curr. Pharm. Des.
, vol.13
, pp. 1161-1177
-
-
Singh, N.1
Cheve, G.2
Avery, M.A.3
McCurdy, C.R.4
-
9
-
-
3042761500
-
Isoprenoid biosynthesis as a novel target for antibacterial and antiparasitic drugs
-
Rohmer, M.; Grosdemange-Billiard, C.; Seemann, M.; Tritsch, D. Isoprenoid biosynthesis as a novel target for antibacterial and antiparasitic drugs Curr. Opin. Invest. Drugs 2004, 5, 154-162
-
(2004)
Curr. Opin. Invest. Drugs
, vol.5
, pp. 154-162
-
-
Rohmer, M.1
Grosdemange-Billiard, C.2
Seemann, M.3
Tritsch, D.4
-
10
-
-
23844526860
-
Isoprenoid biosynthetic pathways as anti-infective drug targets
-
Rohdich, F.; Bacher, A.; Eisenreich, W. Isoprenoid biosynthetic pathways as anti-infective drug targets Biochem. Soc. Trans. 2005, 33, 785-791
-
(2005)
Biochem. Soc. Trans.
, vol.33
, pp. 785-791
-
-
Rohdich, F.1
Bacher, A.2
Eisenreich, W.3
-
11
-
-
0035953022
-
Diaryl ester prodrugs of FR900098 with improved in vivo antimalarial activity
-
Reichenberg, A.; Wiesner, J.; Weidemeyer, C.; Dreiseidler, E.; Sanderbrand, S.; Altincicek, B.; Beck, E.; Schlitzer, M.; Jomaa, H. Diaryl ester prodrugs of FR900098 with improved in vivo antimalarial activity Bioorg. Med. Chem. Lett. 2001, 11, 833-835
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 833-835
-
-
Reichenberg, A.1
Wiesner, J.2
Weidemeyer, C.3
Dreiseidler, E.4
Sanderbrand, S.5
Altincicek, B.6
Beck, E.7
Schlitzer, M.8
Jomaa, H.9
-
12
-
-
22544446490
-
Alkoxycarbonyloxyethyl ester prodrugs of FR900098 with improved in vivo antimalarial activity
-
Ortmann, R.; Wiesner, J.; Reichenberg, A.; Henschker, D.; Beck, E.; Jomaa, H.; Schlitzer, M. Alkoxycarbonyloxyethyl ester prodrugs of FR900098 with improved in vivo antimalarial activity Arch. Pharm. 2005, 338, 305-314
-
(2005)
Arch. Pharm.
, vol.338
, pp. 305-314
-
-
Ortmann, R.1
Wiesner, J.2
Reichenberg, A.3
Henschker, D.4
Beck, E.5
Jomaa, H.6
Schlitzer, M.7
-
13
-
-
84886468343
-
-
International Patent Application DE/10356410-A1, WO/2005048715-A2, and WO/2005048715-A3, Bioagency AG.
-
Kurz, T.; Geffken, D.; Kaula, U.; Herbicidal/Pharmaceutical Composition Contains New and Known alpha-Substituted Organophosphorus Compound, Useful for Treating e.g. Viral, Bacterial or Protozoal Infections. International Patent Application DE/10356410-A1, WO/2005048715-A2, and WO/2005048715-A3, 2005; Bioagency AG.
-
(2005)
Herbicidal/Pharmaceutical Composition Contains New and Known Alpha-Substituted Organophosphorus Compound, Useful for Treating Eg Viral, Bacterial or Protozoal Infections
-
-
Kurz, T.1
Geffken, D.2
Kaula, U.3
-
14
-
-
14244257854
-
Isoprenoid biosynthesis as a target for antibacterial and antiparasitic drugs: Phosphonohydroxamic acids as inhibitors of deoxyxylulose phosphate reducto-isomerase
-
Kuntz, L.; Tritsch, D.; Grosdemange-Billiard, C.; Hemmerlin, A.; Willem, A.; Bacht, T. J.; Rohmer, M. Isoprenoid biosynthesis as a target for antibacterial and antiparasitic drugs: phosphonohydroxamic acids as inhibitors of deoxyxylulose phosphate reducto-isomerase Biochem. J. 2005, 386, 127-135
-
(2005)
Biochem. J.
, vol.386
, pp. 127-135
-
-
Kuntz, L.1
Tritsch, D.2
Grosdemange-Billiard, C.3
Hemmerlin, A.4
Willem, A.5
Bacht, T.J.6
Rohmer, M.7
-
15
-
-
33745178164
-
Synthesis and antimalarial activity of chain substituted pivaloyloxymethyl ester analogues of fosmidomycin and FR900098
-
Kurz, T.; Schlüter, K.; Kaula, U.; Bergmann, B.; Walter, R. D.; Geffken, D. Synthesis and antimalarial activity of chain substituted pivaloyloxymethyl ester analogues of fosmidomycin and FR900098 Bioorg. Med. Chem. 2006, 14, 5121-5135
-
(2006)
Bioorg. Med. Chem.
, vol.14
, pp. 5121-5135
-
-
Kurz, T.1
Schlüter, K.2
Kaula, U.3
Bergmann, B.4
Walter, R.D.5
Geffken, D.6
-
16
-
-
33144477580
-
Synthesis of α-substituted fosmidomycin analogues as highly potent Plasmodium falciparum growth inhibitors
-
Haemers, T.; Wiesner, J.; Van Poecke, S.; Goeman, J.; Henschker, D.; Beck, E.; Jomaa, H.; Van Calenbergh, S. Synthesis of α-substituted fosmidomycin analogues as highly potent Plasmodium falciparum growth inhibitors Bioorg. Med. Chem. Lett. 2006, 16, 1888-1891
-
(2006)
Bioorg. Med. Chem. Lett.
, vol.16
, pp. 1888-1891
-
-
Haemers, T.1
Wiesner, J.2
Van Poecke, S.3
Goeman, J.4
Henschker, D.5
Beck, E.6
Jomaa, H.7
Van Calenbergh, S.8
-
17
-
-
33845286167
-
Arylmethyl substituted derivatives of fosmidomycin: Synthesis and antimalarial activity
-
Schlüter, K.; Walter, R. D.; Bergmann, B.; Kurz, T. Arylmethyl substituted derivatives of fosmidomycin: synthesis and antimalarial activity Eur. J. Med. Chem. 2006, 41, 1385-1397
-
(2006)
Eur. J. Med. Chem.
, vol.41
, pp. 1385-1397
-
-
Schlüter, K.1
Walter, R.D.2
Bergmann, B.3
Kurz, T.4
-
18
-
-
40949137369
-
Synthesis of beta- and gamma-oxa isosteres of fosmidomycin and FR900098 as antimalarial candidates
-
Haemers, T.; Wiesner, J.; Giessmann, D.; Verbrugghen, T.; Hillaert, U.; Ortmann, R.; Jomaa, H.; Link, A.; Schlitzer, M.; Van Calenbergh, S. Synthesis of beta- and gamma-oxa isosteres of fosmidomycin and FR900098 as antimalarial candidates Bioorg. Med. Chem. 2008, 16, 3361-3371
-
(2008)
Bioorg. Med. Chem.
, vol.16
, pp. 3361-3371
-
-
Haemers, T.1
Wiesner, J.2
Giessmann, D.3
Verbrugghen, T.4
Hillaert, U.5
Ortmann, R.6
Jomaa, H.7
Link, A.8
Schlitzer, M.9
Van Calenbergh, S.10
-
19
-
-
77954734834
-
Synthesis and evaluation of α-halogenated analogues of 3-(acetylhydroxyamino)propylphosphonic acid (FR900098) as antimalarials
-
Verbrugghen, T.; Cos, P.; Maes, L.; Van Calenbergh, S. Synthesis and evaluation of α-halogenated analogues of 3-(acetylhydroxyamino) propylphosphonic acid (FR900098) as antimalarials J. Med. Chem. 2010, 53, 5342-5346
-
(2010)
J. Med. Chem.
, vol.53
, pp. 5342-5346
-
-
Verbrugghen, T.1
Cos, P.2
Maes, L.3
Van Calenbergh, S.4
-
20
-
-
77957653130
-
Synthesis and antiplasmodial activity of highly active reverse analogues of the antimalarial drug candidate fosmidomycin
-
Behrendt, C. T.; Kunfermann, A.; Illarionova, V.; Matheeussen, A.; Gräwert, T.; Groll, M.; Rohdich, F.; Bacher, A.; Eisenreich, W.; Fischer, M.; Maes, L.; Kurz, T. Synthesis and antiplasmodial activity of highly active reverse analogues of the antimalarial drug candidate fosmidomycin ChemMedChem 2010, 5, 1673-1676
-
(2010)
ChemMedChem
, vol.5
, pp. 1673-1676
-
-
Behrendt, C.T.1
Kunfermann, A.2
Illarionova, V.3
Matheeussen, A.4
Gräwert, T.5
Groll, M.6
Rohdich, F.7
Bacher, A.8
Eisenreich, W.9
Fischer, M.10
Maes, L.11
Kurz, T.12
-
21
-
-
80053909858
-
Reverse fosmidomycin derivatives against the antimalarial drug target IspC (Dxr)
-
Behrendt, C. T.; Kunfermann, A.; Illarionova, V.; Matheeussen, A.; Pein, M. K.; Gräwert, T.; Kaiser, J.; Bacher, A.; Eisenreich, W.; Illarionov, B.; Fischer, M.; Maes, L.; Groll, M.; Kurz, T. Reverse fosmidomycin derivatives against the antimalarial drug target IspC (Dxr) J. Med. Chem. 2011, 54, 6796-6802
-
(2011)
J. Med. Chem.
, vol.54
, pp. 6796-6802
-
-
Behrendt, C.T.1
Kunfermann, A.2
Illarionova, V.3
Matheeussen, A.4
Pein, M.K.5
Gräwert, T.6
Kaiser, J.7
Bacher, A.8
Eisenreich, W.9
Illarionov, B.10
Fischer, M.11
Maes, L.12
Groll, M.13
Kurz, T.14
-
22
-
-
79960652249
-
Design, synthesis, and X-ray crystallographic studies of α-aryl substituted fosmidomycin analogues as inhibitors of Mycobacterium tuberculosis 1-deoxy- d -xylulose 5-phosphate reductoisomerase
-
Andaloussi, M.; Henriksson, L. M.; Wieckowska, A.; Lindh, M.; Bjorkelid, C.; Larsson, A. M.; Suresh, S.; Iyer, H.; Srinivasa, B. R.; Bergfors, T.; Unge, T.; Mowbray, S. L.; Larhed, M.; Jones, T. A.; Karlén, A. Design, synthesis, and X-ray crystallographic studies of α-aryl substituted fosmidomycin analogues as inhibitors of Mycobacterium tuberculosis 1-deoxy- d -xylulose 5-phosphate reductoisomerase J. Med. Chem. 2011, 54, 4964-4976
-
(2011)
J. Med. Chem.
, vol.54
, pp. 4964-4976
-
-
Andaloussi, M.1
Henriksson, L.M.2
Wieckowska, A.3
Lindh, M.4
Bjorkelid, C.5
Larsson, A.M.6
Suresh, S.7
Iyer, H.8
Srinivasa, B.R.9
Bergfors, T.10
Unge, T.11
Mowbray, S.L.12
Larhed, M.13
Jones, T.A.14
Karlén, A.15
-
23
-
-
34047118490
-
α-Phenylethyl substituted bis(pivaloyloxymethyl) ester analogues of fosmidomycin and FR900098
-
Kurz, T.; Behrendt, C.; Kaula, U.; Bergmann, B.; Walter, R. D. α-Phenylethyl substituted bis(pivaloyloxymethyl) ester analogues of fosmidomycin and FR900098 Aust. J. Chem. 2007, 60, 154-158
-
(2007)
Aust. J. Chem.
, vol.60
, pp. 154-158
-
-
Kurz, T.1
Behrendt, C.2
Kaula, U.3
Bergmann, B.4
Walter, R.D.5
-
26
-
-
0020068460
-
Pharmakokinetics of fosmidomycin, a new phosphonic acid antibiotic
-
Murakawa, T.; Sakamoto, H.; Fukada, S.; Konishi, T.; Nishida, M. Pharmakokinetics of fosmidomycin, a new phosphonic acid antibiotic Antimicrob. Agents Chemother. 1982, 21, 224-230
-
(1982)
Antimicrob. Agents Chemother.
, vol.21
, pp. 224-230
-
-
Murakawa, T.1
Sakamoto, H.2
Fukada, S.3
Konishi, T.4
Nishida, M.5
-
27
-
-
0023159833
-
Pharmakokinetic evaluation of fosmidomycin, a new phosphonic acid antibiotic
-
Kuemmerle, H. P.; Murakawa, T.; Desantis, F. Pharmakokinetic evaluation of fosmidomycin, a new phosphonic acid antibiotic Chemioterapia 1987, 6, 113-119
-
(1987)
Chemioterapia
, vol.6
, pp. 113-119
-
-
Kuemmerle, H.P.1
Murakawa, T.2
Desantis, F.3
-
28
-
-
6944247618
-
Fosmidomycin-clindamycin for the treatment of Plasmodium falciparum malaria
-
Borrmann, S.; Issifou, S.; Esser, G.; Adegnika, A. A.; Ramharter, M.; Matsiegui, P. B.; Oyakhirome, S.; Mawili-Mboumba, D. P.; Missinou, M. A.; Kun, J. F. J.; Jomaa, H.; Kremsner, P. G. Fosmidomycin-clindamycin for the treatment of Plasmodium falciparum malaria J. Infect. Dis. 2004, 190, 1534-1540
-
(2004)
J. Infect. Dis.
, vol.190
, pp. 1534-1540
-
-
Borrmann, S.1
Issifou, S.2
Esser, G.3
Adegnika, A.A.4
Ramharter, M.5
Matsiegui, P.B.6
Oyakhirome, S.7
Mawili-Mboumba, D.P.8
Missinou, M.A.9
Kun, J.F.J.10
Jomaa, H.11
Kremsner, P.G.12
-
29
-
-
77952382039
-
That was then but this is now: Malaria research in the time of an eradication agenda
-
Kappe, S. H. I.; Vaughan, A. M.; Boddey, J. A.; Cowman, A. F. That was then but this is now: malaria research in the time of an eradication agenda Science 2010, 328, 862-866
-
(2010)
Science
, vol.328
, pp. 862-866
-
-
Kappe, S.H.I.1
Vaughan, A.M.2
Boddey, J.A.3
Cowman, A.F.4
-
30
-
-
0001180669
-
A facile preparation of N -(isopropoxyalkyl) amides by generation and trapping of N -acyliminium ions from ionization-rearrangement reactions of N -triflyloxy amides
-
Hoffman, R. V.; Nayyar, N. K. A facile preparation of N -(isopropoxyalkyl) amides by generation and trapping of N -acyliminium ions from ionization-rearrangement reactions of N -triflyloxy amides J. Org. Chem. 1994, 59, 3530-3539
-
(1994)
J. Org. Chem.
, vol.59
, pp. 3530-3539
-
-
Hoffman, R.V.1
Nayyar, N.K.2
-
31
-
-
37049070589
-
Electrochemical studies on haloamides. 3. Haloacetamides and haloacetohydroxamates
-
Casadei, M. A.; Dirienzo, B.; Inesi, A.; Moracci, F. M. Electrochemical studies on haloamides. 3. Haloacetamides and haloacetohydroxamates J. Chem. Soc., Perkin Trans. 1 1992, 375-378
-
(1992)
J. Chem. Soc., Perkin Trans. 1
, pp. 375-378
-
-
Casadei, M.A.1
Dirienzo, B.2
Inesi, A.3
Moracci, F.M.4
-
32
-
-
0007188245
-
Organosulfur compounds. 23. Addition of elemental sulfur to phosphonate carbanions and its application for synthesis of α-phosphoryl organosulfur compounds: Synthesis of aromatic ketones
-
Mikolajczyk, M.; Grzejszczak, S.; Chefczynska, A.; Zatorski, A. Organosulfur compounds. 23. Addition of elemental sulfur to phosphonate carbanions and its application for synthesis of α-phosphoryl organosulfur compounds: synthesis of aromatic ketones J. Org. Chem. 1979, 44, 2967-2972
-
(1979)
J. Org. Chem.
, vol.44
, pp. 2967-2972
-
-
Mikolajczyk, M.1
Grzejszczak, S.2
Chefczynska, A.3
Zatorski, A.4
-
33
-
-
15144356086
-
Facile dealkylation of phosphonic acid dialkyl esters by bromotrimethylsilane
-
McKenna, C. E.; Higa, M. T.; Cheung, N. H.; McKenna, M. C. Facile dealkylation of phosphonic acid dialkyl esters by bromotrimethylsilane Tetrahedron Lett. 1977, 155-158
-
(1977)
Tetrahedron Lett.
, pp. 155-158
-
-
McKenna, C.E.1
Higa, M.T.2
Cheung, N.H.3
McKenna, M.C.4
-
34
-
-
84861017386
-
Methyl effects on protein-ligand binding
-
Leung, C. S.; Leung, S. S. F.; Tirado-Rives, J.; Jorgensen, W. L. Methyl effects on protein-ligand binding J. Med. Chem. 2012, 55, 4489-4500
-
(2012)
J. Med. Chem.
, vol.55
, pp. 4489-4500
-
-
Leung, C.S.1
Leung, S.S.F.2
Tirado-Rives, J.3
Jorgensen, W.L.4
-
35
-
-
84864197038
-
α-Substituted β-oxa isosteres of fosmidomycin: Synthesis and biological evaluation
-
Brücher, K.; Illarionov, B.; Held, J.; Tschan, S.; Kunfermann, A.; Pein, M. K.; Bacher, A.; Gräwert, T.; Maes, L.; Mordmueller, B.; Fischer, M.; Kurz, T. α-Substituted β-oxa isosteres of fosmidomycin: synthesis and biological evaluation J. Med. Chem. 2012, 55, 6566-6575
-
(2012)
J. Med. Chem.
, vol.55
, pp. 6566-6575
-
-
Brücher, K.1
Illarionov, B.2
Held, J.3
Tschan, S.4
Kunfermann, A.5
Pein, M.K.6
Bacher, A.7
Gräwert, T.8
Maes, L.9
Mordmueller, B.10
Fischer, M.11
Kurz, T.12
-
36
-
-
0029902679
-
Program DYNAFIT for the analysis of enzyme kinetic data: Application to HIV proteinase
-
Kuzmic, P. Program DYNAFIT for the analysis of enzyme kinetic data: application to HIV proteinase Anal. Biochem. 1996, 237, 260-273
-
(1996)
Anal. Biochem.
, vol.237
, pp. 260-273
-
-
Kuzmic, P.1
-
37
-
-
0003474751
-
-
3 rd ed. Cambridge University Press: New York.
-
Press, W. H.; Teukolsky, S. A.; Vetterling, W. T.; Flannery, B. P. Numerical Recipes: The Art of Scientific Computing, 3 rd ed.; Cambridge University Press: New York, 2007.
-
(2007)
Numerical Recipes: The Art of Scientific Computing
-
-
Press, W.H.1
Teukolsky, S.A.2
Vetterling, W.T.3
Flannery, B.P.4
-
38
-
-
84858198467
-
Plasmodium falciparum apicoplast drugs: Targets or off-targets?
-
Botte, C. Y.; Dubar, F.; McFadden, G. I.; Marechal, E.; Biot, C. Plasmodium falciparum apicoplast drugs: targets or off-targets? Chem. Rev. 2012, 112, 1269-1283
-
(2012)
Chem. Rev.
, vol.112
, pp. 1269-1283
-
-
Botte, C.Y.1
Dubar, F.2
McFadden, G.I.3
Marechal, E.4
Biot, C.5
-
39
-
-
84856430758
-
Molecular basis of fosmidomycin's action on the human malaria parasite Plasmodium falciparum
-
Umeda, T.; Tanaka, N.; Kusakabe, Y.; Nakanishi, M.; Kitade, Y.; Nakamura, K. T. Molecular basis of fosmidomycin's action on the human malaria parasite Plasmodium falciparum Sci. Rep. 2011, 1-8
-
(2011)
Sci. Rep.
, pp. 1-8
-
-
Umeda, T.1
Tanaka, N.2
Kusakabe, Y.3
Nakanishi, M.4
Kitade, Y.5
Nakamura, K.T.6
-
40
-
-
0038043258
-
Structural basis of fosmidomycin action revealed by the complex with 2-C-methyl- d -erythritol 4-phosphate synthase (IspC). Implications for the catalytic mechanism and anti-malaria drug development
-
Steinbacher, S.; Kaiser, J.; Eisenreich, W.; Huber, R.; Bacher, A.; Rohdich, F. Structural basis of fosmidomycin action revealed by the complex with 2-C-methyl- d -erythritol 4-phosphate synthase (IspC). Implications for the catalytic mechanism and anti-malaria drug development J. Biol. Chem. 2003, 278, 18401-18407
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 18401-18407
-
-
Steinbacher, S.1
Kaiser, J.2
Eisenreich, W.3
Huber, R.4
Bacher, A.5
Rohdich, F.6
-
41
-
-
79960155208
-
Inhibition of 1-deoxy- d -xylulose-5-phosphate reductoisomerase by lipophilic phosphonates: SAR, QSAR, and crystallographic studies
-
Deng, L.; Diao, J.; Chen, P.; Pujari, V.; Yao, Y.; Cheng, G.; Crick, D. C.; Prasad, B. V. V; Song, Y. Inhibition of 1-deoxy- d -xylulose-5-phosphate reductoisomerase by lipophilic phosphonates: SAR, QSAR, and crystallographic studies J. Med. Chem. 2011, 54, 4721-4734
-
(2011)
J. Med. Chem.
, vol.54
, pp. 4721-4734
-
-
Deng, L.1
Diao, J.2
Chen, P.3
Pujari, V.4
Yao, Y.5
Cheng, G.6
Crick, D.C.7
Prasad, B.V.V.8
Song, Y.9
-
42
-
-
0002744982
-
The nature of cationic intermediates derived from α-thiophosphoryl and α-thiocarbonyl mesylates - Neighboring thiophosphoryl and thiocarbonyl participation
-
Creary, X.; Mehrsheikhmohammadi, M. E. The nature of cationic intermediates derived from α-thiophosphoryl and α-thiocarbonyl mesylates-neighboring thiophosphoryl and thiocarbonyl participation J. Org. Chem. 1986, 51, 7-15
-
(1986)
J. Org. Chem.
, vol.51
, pp. 7-15
-
-
Creary, X.1
Mehrsheikhmohammadi, M.E.2
-
43
-
-
0017311840
-
Human malaria parasites in continous culture
-
Trager, W.; Jensen, J. B. Human malaria parasites in continous culture Science 1976, 193, 673-675
-
(1976)
Science
, vol.193
, pp. 673-675
-
-
Trager, W.1
Jensen, J.B.2
-
44
-
-
0018704491
-
Synchronization of Plasmodium-falciparum erythrocytic stages in culture
-
Lambros, C.; Vanderberg, J. P. Synchronization of Plasmodium-falciparum erythrocytic stages in culture J. Parasitol. 1979, 65, 418-420
-
(1979)
J. Parasitol.
, vol.65
, pp. 418-420
-
-
Lambros, C.1
Vanderberg, J.P.2
-
45
-
-
23044496331
-
Simple histidine-rich protein 2 double-site sandwich enzyme-linked immunosorbent assay for use in malaria drug sensitivity testing
-
Noedl, H.; Bronnert, J.; Yingyuen, K.; Herwig, B. A.; Attlmayr, B.; Kollaritsch, H.; Fukuda, M. Simple histidine-rich protein 2 double-site sandwich enzyme-linked immunosorbent assay for use in malaria drug sensitivity testing Antimicrob. Agents Chemother. 2005, 49, 3575-3577
-
(2005)
Antimicrob. Agents Chemother.
, vol.49
, pp. 3575-3577
-
-
Noedl, H.1
Bronnert, J.2
Yingyuen, K.3
Herwig, B.A.4
Attlmayr, B.5
Kollaritsch, H.6
Fukuda, M.7
-
46
-
-
70149113077
-
-
R Development Core Team. R Foundation for Statistical Computing: Vienna, Austria.
-
R Development Core Team. R: A Language and Environment for Statistical Computing; R Foundation for Statistical Computing: Vienna, Austria, 2009.
-
(2009)
R: A Language and Environment for Statistical Computing
-
-
-
47
-
-
0027879008
-
Automatic processing of rotation diffraction data from crystals of initially unknown symmetry and cell constants
-
Kabsch, W. Automatic processing of rotation diffraction data from crystals of initially unknown symmetry and cell constants J. Appl. Crystallogr. 1993, 26, 795-800
-
(1993)
J. Appl. Crystallogr.
, vol.26
, pp. 795-800
-
-
Kabsch, W.1
-
48
-
-
0030924992
-
Refinement of macromolecular structures by the maximum-likelihood method
-
Murshudov, G. N.; Vagin, A. A.; Dodson, E. J. Refinement of macromolecular structures by the maximum-likelihood method Acta Crystallogr., Sect. D: Biol. Crystallogr. 1997, 53, 240-255
-
(1997)
Acta Crystallogr., Sect. D: Biol. Crystallogr.
, vol.53
, pp. 240-255
-
-
Murshudov, G.N.1
Vagin, A.A.2
Dodson, E.J.3
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