-
1
-
-
33751547539
-
How many drug targets are there?
-
Overington, J. P.; Al-Lazikani, B.; Hopkins, A. L. How many drug targets are there? Nature Rev. Drug Discovery 2006, 5, 993-996
-
(2006)
Nature Rev. Drug Discovery
, vol.5
, pp. 993-996
-
-
Overington, J.P.1
Al-Lazikani, B.2
Hopkins, A.L.3
-
2
-
-
79959790904
-
Development of novel drugs for human African trypanosomiasis
-
Brun, R.; Don, R.; Jacobs, R. T.; Wang, M. Z.; Barrett, M. P. Development of novel drugs for human African trypanosomiasis Future Microbiol. 2011, 6, 677-691
-
(2011)
Future Microbiol.
, vol.6
, pp. 677-691
-
-
Brun, R.1
Don, R.2
Jacobs, R.T.3
Wang, M.Z.4
Barrett, M.P.5
-
3
-
-
84856955769
-
High-throughput decoding of antitrypanosomal drug efficacy and resistance
-
Alsford, S.; Eckert, S.; Baker, N.; Glover, L.; Sanchez-Flores, A.; Leung, K. F.; Turner, D. J.; Field, M. C.; Berriman, M.; Horn, D. High-throughput decoding of antitrypanosomal drug efficacy and resistance Nature 2012, 482, 232-236
-
(2012)
Nature
, vol.482
, pp. 232-236
-
-
Alsford, S.1
Eckert, S.2
Baker, N.3
Glover, L.4
Sanchez-Flores, A.5
Leung, K.F.6
Turner, D.J.7
Field, M.C.8
Berriman, M.9
Horn, D.10
-
4
-
-
33750507750
-
Targeting of toxic compounds to the trypanosome's interior
-
Barrett, M. P.; Gilbert, I. H. Targeting of toxic compounds to the trypanosome's interior Adv. Parasitol. 2006, 63, 125-183
-
(2006)
Adv. Parasitol.
, vol.63
, pp. 125-183
-
-
Barrett, M.P.1
Gilbert, I.H.2
-
5
-
-
62249111310
-
Targeting of Toxic Compounds to the Trypanosomes
-
Barrett, M. P.; Gilbert, I. H. Targeting of Toxic Compounds to the Trypanosomes Adv. Parasitol. 2006, 63, 126-183
-
(2006)
Adv. Parasitol.
, vol.63
, pp. 126-183
-
-
Barrett, M.P.1
Gilbert, I.H.2
-
6
-
-
42449155428
-
A mechanism for cross-resistance to nifurtimox and benznidazole in trypanosomes
-
Wilkinson, S. R.; Taylor, M. C.; Horn, D.; Kelly, J. M.; Cheeseman, I. A mechanism for cross-resistance to nifurtimox and benznidazole in trypanosomes Proc. Natl. Acad. Sci. U. S. A. 2008, 105, 5022-5027
-
(2008)
Proc. Natl. Acad. Sci. U. S. A.
, vol.105
, pp. 5022-5027
-
-
Wilkinson, S.R.1
Taylor, M.C.2
Horn, D.3
Kelly, J.M.4
Cheeseman, I.5
-
7
-
-
77953760001
-
Cross-resistance to nitro drugs and implications for treatment of human African trypanosomiasis
-
Sokolova, A. Y.; Wyllie, S.; Patterson, S.; Oza, S. L.; Read, K. D.; Fairlamb, A. H. Cross-resistance to nitro drugs and implications for treatment of human African trypanosomiasis Antimicrob. Agents Chemother. 2010, 54, 2893-2900
-
(2010)
Antimicrob. Agents Chemother.
, vol.54
, pp. 2893-2900
-
-
Sokolova, A.Y.1
Wyllie, S.2
Patterson, S.3
Oza, S.L.4
Read, K.D.5
Fairlamb, A.H.6
-
8
-
-
79953882988
-
Nifurtimox activation by trypanosomal type i nitroreductases generates cytotoxic nitrile metabolites
-
Hall, B. S.; Bot, C.; Wilkinson, S. R. Nifurtimox activation by trypanosomal type I nitroreductases generates cytotoxic nitrile metabolites J. Biol. Chem. 2011, 286, 13088-13095
-
(2011)
J. Biol. Chem.
, vol.286
, pp. 13088-13095
-
-
Hall, B.S.1
Bot, C.2
Wilkinson, S.R.3
-
9
-
-
33847377170
-
Mode of action of natural and synthetic drugs against Trypanosoma cruzi and their interaction with the mammalian host
-
Maya, J.; Cassels, B.; Iturriaga Vasquez, P.; Ferreira, J.; Faundez, M.; Iturriaga Vásquez, P.; Faúndez, M.; Galanti, N.; Ferreira, A.; Morello, A. Mode of action of natural and synthetic drugs against Trypanosoma cruzi and their interaction with the mammalian host Comp. Biochem. Physiol., Part A: Mol. Integr. Physiol. 2007, 146, 601-620
-
(2007)
Comp. Biochem. Physiol., Part A: Mol. Integr. Physiol.
, vol.146
, pp. 601-620
-
-
Maya, J.1
Cassels, B.2
Iturriaga Vasquez, P.3
Ferreira, J.4
Faundez, M.5
Iturriaga Vásquez, P.6
Faúndez, M.7
Galanti, N.8
Ferreira, A.9
Morello, A.10
-
10
-
-
84867610036
-
Miltefosine: A review of its pharmacology and therapeutic efficacy in the treatment of leishmaniasis
-
Dorlo, T. P. C.; Balasegaram, M.; Beijnen, J. H.; de Vries, P. J. Miltefosine: a review of its pharmacology and therapeutic efficacy in the treatment of leishmaniasis J. Antimicrob. Chemother. 2012, 67, 2576-2597
-
(2012)
J. Antimicrob. Chemother.
, vol.67
, pp. 2576-2597
-
-
Dorlo, T.P.C.1
Balasegaram, M.2
Beijnen, J.H.3
De Vries, P.J.4
-
11
-
-
0142258171
-
Leishmaniasis - Current chemotherapy and recent advances in the search for novel drugs
-
Croft, S. L.; Coombs, G. H. Leishmaniasis-current chemotherapy and recent advances in the search for novel drugs Trends Parasitol. 2003, 19, 502-508
-
(2003)
Trends Parasitol.
, vol.19
, pp. 502-508
-
-
Croft, S.L.1
Coombs, G.H.2
-
12
-
-
36349030128
-
Target assessment for antiparasitic drug discovery
-
Frearson, J. A.; Wyatt, P. G.; Gilbert, I. H.; Fairlamb, A. H. Target assessment for antiparasitic drug discovery Trends Parasitol. 2007, 23, 589-595
-
(2007)
Trends Parasitol.
, vol.23
, pp. 589-595
-
-
Frearson, J.A.1
Wyatt, P.G.2
Gilbert, I.H.3
Fairlamb, A.H.4
-
13
-
-
79960021792
-
Target Validation: Linking Target and Chemical Properties to Desired Product Profile
-
Wyatt, P. G.; Gilbert, I. H.; Read, K. D.; Fairlamb, A. H. Target Validation: Linking Target and Chemical Properties to Desired Product Profile Curr. Top. Med. Chem. 2011, 11, 1275-1283
-
(2011)
Curr. Top. Med. Chem.
, vol.11
, pp. 1275-1283
-
-
Wyatt, P.G.1
Gilbert, I.H.2
Read, K.D.3
Fairlamb, A.H.4
-
14
-
-
0031552096
-
Replacements for lysine in l -seryl- l -lysyl dipeptide amide inhibitors of Candida albicans myristoyl-CoA: Protein N -myristoyltransferase
-
Brown, D. L.; Devadas, B.; Lu, H. F.; Nagarajan, S.; Zupec, M. E.; Freeman, S. K.; McWherter, C. A.; Getman, D. P.; Sikorski, J. A. Replacements for lysine in l -seryl- l -lysyl dipeptide amide inhibitors of Candida albicans myristoyl-CoA: Protein N -myristoyltransferase Bioorg. Med. Chem. Lett. 1997, 7, 379-382
-
(1997)
Bioorg. Med. Chem. Lett.
, vol.7
, pp. 379-382
-
-
Brown, D.L.1
Devadas, B.2
Lu, H.F.3
Nagarajan, S.4
Zupec, M.E.5
Freeman, S.K.6
McWherter, C.A.7
Getman, D.P.8
Sikorski, J.A.9
-
15
-
-
15144352323
-
Conformationally constrained [ p -(omega-aminoalkyl)phenacetyl]- l -seryl- l -lysyl dipeptide amides as potent peptidomimetic inhibitors of Candida albicans and human myristoyl-CoA: Protein N -myristoyltransferase
-
Nagarajan, S. R.; Devadas, B.; Zupec, M. E.; Freeman, S. K.; Brown, D. L.; Lu, H. F.; Mehta, P. P.; Kishore, N. S.; McWherter, C. A.; Getman, D. P.; Gordon, J. I.; Sikorski, J. A. Conformationally constrained [ p -(omega-aminoalkyl)phenacetyl]- l -seryl- l -lysyl dipeptide amides as potent peptidomimetic inhibitors of Candida albicans and human myristoyl-CoA: Protein N -myristoyltransferase J. Med. Chem. 1997, 40, 1422-1438
-
(1997)
J. Med. Chem.
, vol.40
, pp. 1422-1438
-
-
Nagarajan, S.R.1
Devadas, B.2
Zupec, M.E.3
Freeman, S.K.4
Brown, D.L.5
Lu, H.F.6
Mehta, P.P.7
Kishore, N.S.8
McWherter, C.A.9
Getman, D.P.10
Gordon, J.I.11
Sikorski, J.A.12
-
16
-
-
0030612443
-
Selective peptidic and peptidomimetic inhibitors of Candida albicans myristoylCoA: Protein N -myristoyltransferase: A new approach to antifungal therapy
-
Sikorski, J. A.; Devadas, B.; Zupec, M. E.; Freeman, S. K.; Brown, D. L.; Lu, H. F.; Nagarajan, S.; Mehta, P. P.; Wade, A. C.; Kishore, N. S.; Bryant, M. L.; Getman, D. P.; McWherter, C. A.; Gordon, J. I. Selective peptidic and peptidomimetic inhibitors of Candida albicans myristoylCoA: Protein N -myristoyltransferase: a new approach to antifungal therapy Biopolymers 1997, 43, 43-71
-
(1997)
Biopolymers
, vol.43
, pp. 43-71
-
-
Sikorski, J.A.1
Devadas, B.2
Zupec, M.E.3
Freeman, S.K.4
Brown, D.L.5
Lu, H.F.6
Nagarajan, S.7
Mehta, P.P.8
Wade, A.C.9
Kishore, N.S.10
Bryant, M.L.11
Getman, D.P.12
McWherter, C.A.13
Gordon, J.I.14
-
17
-
-
0032510384
-
Novel biologically active nonpeptidic inhibitors of myristoylCoA: Protein N -myristoyltransferase
-
Devadas, B.; Freeman, S. K.; McWherter, C. A.; Kishore, N. S.; Lodge, J. K.; Jackson-Machelski, E.; Gordon, J. I.; Sikorski, J. A. Novel biologically active nonpeptidic inhibitors of myristoylCoA: Protein N -myristoyltransferase J. Med. Chem. 1998, 41, 996-1000
-
(1998)
J. Med. Chem.
, vol.41
, pp. 996-1000
-
-
Devadas, B.1
Freeman, S.K.2
McWherter, C.A.3
Kishore, N.S.4
Lodge, J.K.5
Jackson-Machelski, E.6
Gordon, J.I.7
Sikorski, J.A.8
-
18
-
-
0030594977
-
A chiral recognition element with an unusual size constraint affects the potency and selectivity for peptidomimetic inhibitors of Candida albicans myristoyl-CoA: Protein N -myristoyltransferase
-
Devadas, B.; Freeman, S. K.; McWherter, C. A.; Kuneman, D. W.; Vinjamoori, D. V.; Sikorski, J. A. A chiral recognition element with an unusual size constraint affects the potency and selectivity for peptidomimetic inhibitors of Candida albicans myristoyl-CoA: Protein N -myristoyltransferase Bioorg. Med. Chem. Lett. 1996, 6, 1977-1982
-
(1996)
Bioorg. Med. Chem. Lett.
, vol.6
, pp. 1977-1982
-
-
Devadas, B.1
Freeman, S.K.2
McWherter, C.A.3
Kuneman, D.W.4
Vinjamoori, D.V.5
Sikorski, J.A.6
-
19
-
-
15144355281
-
Design and synthesis of novel imidazole-substituted dipeptide amides as potent and selective inhibitors of Candida albicans myristoylCoA: Protein N -myristoyltransferase and identification of related tripeptide inhibitors with mechanism-based antifungal activity
-
Devadas, B.; Freeman, S. K.; Zupec, M. E.; Lu, H. F.; Nagarajan, S. R.; Kishore, N. S.; Lodge, J. K.; Kuneman, D. W.; McWherter, C. A.; Vinjamoori, D. V.; Getman, D. P.; Gordon, J. I.; Sikorski, J. A. Design and synthesis of novel imidazole-substituted dipeptide amides as potent and selective inhibitors of Candida albicans myristoylCoA: Protein N -myristoyltransferase and identification of related tripeptide inhibitors with mechanism-based antifungal activity J. Med. Chem. 1997, 40, 2609-2625
-
(1997)
J. Med. Chem.
, vol.40
, pp. 2609-2625
-
-
Devadas, B.1
Freeman, S.K.2
Zupec, M.E.3
Lu, H.F.4
Nagarajan, S.R.5
Kishore, N.S.6
Lodge, J.K.7
Kuneman, D.W.8
McWherter, C.A.9
Vinjamoori, D.V.10
Getman, D.P.11
Gordon, J.I.12
Sikorski, J.A.13
-
20
-
-
0029071405
-
Design and Syntheses of Potent and Selective Dipeptide Inhibitors of Candida Albicans Myristoyl-CoA-Protein N -Myristoyltransferase
-
Devadas, B.; Zupec, M. E.; Freeman, S. K.; Brown, D. L.; Nagarajan, S.; Sikorski, J. A.; McWherter, C. A.; Getman, D. P.; Gordon, J. I. Design and Syntheses of Potent and Selective Dipeptide Inhibitors of Candida Albicans Myristoyl-CoA-Protein N -Myristoyltransferase J. Med. Chem. 1995, 38, 1837-1840
-
(1995)
J. Med. Chem.
, vol.38
, pp. 1837-1840
-
-
Devadas, B.1
Zupec, M.E.2
Freeman, S.K.3
Brown, D.L.4
Nagarajan, S.5
Sikorski, J.A.6
McWherter, C.A.7
Getman, D.P.8
Gordon, J.I.9
-
21
-
-
17344386481
-
Design and synthesis of novel benzofurans as a new class of antifungal agents targeting fungal N -myristoyltransferase. Part 2
-
Ebiike, H.; Masubuchi, M.; Liu, P. L.; Kawasaki, K.; Morikami, K.; Sogabe, S.; Hayase, M.; Fujii, T.; Sakata, K.; Shindoh, H.; Shiratori, Y.; Aoki, Y.; Ohtsuka, T.; Shimma, N. Design and synthesis of novel benzofurans as a new class of antifungal agents targeting fungal N -myristoyltransferase. Part 2 Bioorg. Med. Chem. Lett. 2002, 12, 607-610
-
(2002)
Bioorg. Med. Chem. Lett.
, vol.12
, pp. 607-610
-
-
Ebiike, H.1
Masubuchi, M.2
Liu, P.L.3
Kawasaki, K.4
Morikami, K.5
Sogabe, S.6
Hayase, M.7
Fujii, T.8
Sakata, K.9
Shindoh, H.10
Shiratori, Y.11
Aoki, Y.12
Ohtsuka, T.13
Shimma, N.14
-
22
-
-
17944387642
-
Design and synthesis of novel benzofurans as a new class of antifungal agents targeting fungal N -myristoyltransferase. Part 3
-
Kawasaki, K.; Masubuchi, M.; Morikami, K.; Sogabe, S.; Aoyama, T.; Ebiike, H.; Niizuma, S.; Hayase, M.; Fujii, T.; Sakata, K.; Shindoh, H.; Shiratori, Y.; Aoki, Y.; Ohtsuka, T.; Shimma, N. Design and synthesis of novel benzofurans as a new class of antifungal agents targeting fungal N -myristoyltransferase. Part 3 Bioorg. Med. Chem. Lett. 2003, 13, 87-91
-
(2003)
Bioorg. Med. Chem. Lett.
, vol.13
, pp. 87-91
-
-
Kawasaki, K.1
Masubuchi, M.2
Morikami, K.3
Sogabe, S.4
Aoyama, T.5
Ebiike, H.6
Niizuma, S.7
Hayase, M.8
Fujii, T.9
Sakata, K.10
Shindoh, H.11
Shiratori, Y.12
Aoki, Y.13
Ohtsuka, T.14
Shimma, N.15
-
23
-
-
12444338848
-
Synthesis and biological activities of benzofuran antifungal agents targeting fungal N -myristoyltransferase
-
Masubuchi, M.; Ebiike, H.; Kawasaki, E.; Sogabe, S.; Morikami, K.; Shiratori, Y.; Tsujii, S.; Fujii, T.; Sakata, K.; Hayase, M.; Shindoh, H.; Aoki, Y.; Ohtsuka, T.; Shimma, N. Synthesis and biological activities of benzofuran antifungal agents targeting fungal N -myristoyltransferase Bioorg. Med. Chem. 2003, 11, 4463-4478
-
(2003)
Bioorg. Med. Chem.
, vol.11
, pp. 4463-4478
-
-
Masubuchi, M.1
Ebiike, H.2
Kawasaki, E.3
Sogabe, S.4
Morikami, K.5
Shiratori, Y.6
Tsujii, S.7
Fujii, T.8
Sakata, K.9
Hayase, M.10
Shindoh, H.11
Aoki, Y.12
Ohtsuka, T.13
Shimma, N.14
-
24
-
-
0035939423
-
Design and synthesis of novel benzofurans as a new class of antifungal agents targeting fungal N -myristoyltransferase. Part 1
-
Masubuchi, M.; Kawasaki, K.; Ebiike, H.; Ikeda, Y.; Tsujii, S.; Sogabe, S.; Fujii, T.; Sakata, K.; Shiratori, Y.; Aoki, Y.; Ohtsuka, T.; Shimma, N. Design and synthesis of novel benzofurans as a new class of antifungal agents targeting fungal N -myristoyltransferase. Part 1 Bioorg. Med. Chem. Lett. 2001, 11, 1833-1837
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 1833-1837
-
-
Masubuchi, M.1
Kawasaki, K.2
Ebiike, H.3
Ikeda, Y.4
Tsujii, S.5
Sogabe, S.6
Fujii, T.7
Sakata, K.8
Shiratori, Y.9
Aoki, Y.10
Ohtsuka, T.11
Shimma, N.12
-
25
-
-
21144440432
-
FTR1335 is a novel synthetic inhibitor of Candida albicans N -myristoyltransferase with fungicidal activity
-
Ebara, S.; Naito, H.; Nakazawa, K.; Ishii, F.; Nakamura, M. FTR1335 is a novel synthetic inhibitor of Candida albicans N -myristoyltransferase with fungicidal activity Biol. Pharm. Bull. 2005, 28, 591-595
-
(2005)
Biol. Pharm. Bull.
, vol.28
, pp. 591-595
-
-
Ebara, S.1
Naito, H.2
Nakazawa, K.3
Ishii, F.4
Nakamura, M.5
-
26
-
-
14844322778
-
Synthesis of potent and selective inhibitors of Candida albicans N -myristoyltransferase based on the benzothiazole structure
-
Yamazaki, K.; Kaneko, Y.; Suwa, K.; Ebara, S.; Nakazawa, K.; Yasuno, K. Synthesis of potent and selective inhibitors of Candida albicans N -myristoyltransferase based on the benzothiazole structure Bioorg. Med. Chem. 2005, 13, 2509-2522
-
(2005)
Bioorg. Med. Chem.
, vol.13
, pp. 2509-2522
-
-
Yamazaki, K.1
Kaneko, Y.2
Suwa, K.3
Ebara, S.4
Nakazawa, K.5
Yasuno, K.6
-
27
-
-
0037470198
-
Myristoyl-CoA: Protein N -myristoyltransferase, an essential enzyme and potential drug target in kinetoplastid parasites
-
Price, H. P.; Menon, M. R.; Panethymitaki, C.; Goulding, D.; McKean, P. G.; Smith, D. F. Myristoyl-CoA: Protein N -myristoyltransferase, an essential enzyme and potential drug target in kinetoplastid parasites J. Biol. Chem. 2003, 278, 7206-7214
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 7206-7214
-
-
Price, H.P.1
Menon, M.R.2
Panethymitaki, C.3
Goulding, D.4
McKean, P.G.5
Smith, D.F.6
-
28
-
-
33744806630
-
Characterization and selective inhibition of myristoyl-CoA: Protein N -myristoyltransferase from Trypanosoma brucei and Leishmania major
-
Panethymitaki, C.; Bowyer, P. W.; Price, H. P.; Leatherbarrow, R. J.; Brown, K. A.; Smith, D. F. Characterization and selective inhibition of myristoyl-CoA: Protein N -myristoyltransferase from Trypanosoma brucei and Leishmania major Biochem. J. 2006, 396, 277-85
-
(2006)
Biochem. J.
, vol.396
, pp. 277-285
-
-
Panethymitaki, C.1
Bowyer, P.W.2
Price, H.P.3
Leatherbarrow, R.J.4
Brown, K.A.5
Smith, D.F.6
-
29
-
-
71549117083
-
Myristoyl-CoA: Protein N -myristoyltransferase depletion in trypanosomes causes avirulence and endocytic defects
-
Price, H. P.; Guther, M. L. S.; Ferguson, M. A. J.; Smith, D. F. Myristoyl-CoA: Protein N -myristoyltransferase depletion in trypanosomes causes avirulence and endocytic defects Mol. Biochem. Parasitol. 2010, 169, 55-58
-
(2010)
Mol. Biochem. Parasitol.
, vol.169
, pp. 55-58
-
-
Price, H.P.1
Guther, M.L.S.2
Ferguson, M.A.J.3
Smith, D.F.4
-
30
-
-
84855848964
-
Discovery of a novel class of orally active trypanocidal N -myristoyltransferase inhibitors
-
Brand, S.; Cleghorn, L. A.; McElroy, S. P.; Robinson, D. A.; Smith, V. C.; Hallyburton, I.; Harrison, J. R.; Norcross, N. R.; Spinks, D.; Bayliss, T.; Norval, S.; Stojanovski, L.; Torrie, L. S.; Frearson, J. A.; Brenk, R.; Fairlamb, A. H.; Ferguson, M. A.; Read, K. D.; Wyatt, P. G.; Gilbert, I. H. Discovery of a novel class of orally active trypanocidal N -myristoyltransferase inhibitors J. Med. Chem. 2012, 55, 140-152
-
(2012)
J. Med. Chem.
, vol.55
, pp. 140-152
-
-
Brand, S.1
Cleghorn, L.A.2
McElroy, S.P.3
Robinson, D.A.4
Smith, V.C.5
Hallyburton, I.6
Harrison, J.R.7
Norcross, N.R.8
Spinks, D.9
Bayliss, T.10
Norval, S.11
Stojanovski, L.12
Torrie, L.S.13
Frearson, J.A.14
Brenk, R.15
Fairlamb, A.H.16
Ferguson, M.A.17
Read, K.D.18
Wyatt, P.G.19
Gilbert, I.H.20
more..
-
31
-
-
48049086591
-
Lessons learnt from assembling screening libraries for drug discovery for neglected diseases
-
Brenk, R.; Schipani, A.; James, D.; Krasowski, A.; Gilbert, I. H.; Frearson, J. A.; Wyatt, P. G. Lessons learnt from assembling screening libraries for drug discovery for neglected diseases ChemMedChem 2008, 3, 435-444
-
(2008)
ChemMedChem
, vol.3
, pp. 435-444
-
-
Brenk, R.1
Schipani, A.2
James, D.3
Krasowski, A.4
Gilbert, I.H.5
Frearson, J.A.6
Wyatt, P.G.7
-
32
-
-
77950406212
-
N -Myristoyltransferase inhibitors as new leads to treat sleeping sickness
-
Frearson, J. A.; Brand, S.; McElroy, S. P.; Cleghorn, L. A. T.; Smid, O.; Stojanovski, L.; Price, H. P.; Guther, M. L. S.; Torrie, L. S.; Robinson, D. A.; Hallyburton, I.; Mpamhanga, C. P.; Brannigan, J. A.; Wilkinson, A. J.; Hodgkinson, M.; Hui, R.; Qiu, W.; Raimi, O. G.; Van Aalten, D. M. F.; Brenk, R.; Gilbert, I. H.; Read, K. D.; Fairlamb, A. H.; Ferguson, M. A. J.; Smith, D. F.; Wyatt, P. G. N -Myristoyltransferase inhibitors as new leads to treat sleeping sickness Nature 2010, 464, 728-732
-
(2010)
Nature
, vol.464
, pp. 728-732
-
-
Frearson, J.A.1
Brand, S.2
McElroy, S.P.3
Cleghorn, L.A.T.4
Smid, O.5
Stojanovski, L.6
Price, H.P.7
Guther, M.L.S.8
Torrie, L.S.9
Robinson, D.A.10
Hallyburton, I.11
Mpamhanga, C.P.12
Brannigan, J.A.13
Wilkinson, A.J.14
Hodgkinson, M.15
Hui, R.16
Qiu, W.17
Raimi, O.G.18
Van Aalten, D.M.F.19
Brenk, R.20
Gilbert, I.H.21
Read, K.D.22
Fairlamb, A.H.23
Ferguson, M.A.J.24
Smith, D.F.25
Wyatt, P.G.26
more..
-
33
-
-
84886573221
-
-
BIO Ventures for Global Health: Washington, DC.
-
Chagas Disease; BIO Ventures for Global Health: Washington, DC, 2011; http://www.bvgh.org/Biopharmaceutical-Solutions/Global-Health-Primer/Diseases/ cid/ViewDetails/ItemID/1.aspx.
-
(2011)
Chagas Disease
-
-
-
34
-
-
70350778454
-
New medicines to improve control and contribute to the eradication of malaria
-
Wells, T. N.; Alonso, P. L.; Gutteridge, W. E. New medicines to improve control and contribute to the eradication of malaria Nature Rev. Drug Discovery 2009, 8, 879-891
-
(2009)
Nature Rev. Drug Discovery
, vol.8
, pp. 879-891
-
-
Wells, T.N.1
Alonso, P.L.2
Gutteridge, W.E.3
-
35
-
-
79961223551
-
Structure-guided lead optimization of triazolopyrimidine-ring substituents identifies potent Plasmodium falciparum dihydroorotate dehydrogenase inhibitors with clinical candidate potential
-
Coteron, J. M.; Marco, M.; Esquivias, J.; Deng, X.; White, K. L.; White, J.; Koltun, M.; El Mazouni, F.; Kokkonda, S.; Katneni, K.; Bhamidipati, R.; Shackleford, D. M.; Angulo-Barturen, I.; Ferrer, S. B.; Jimenez-Diaz, M. B.; Gamo, F. J.; Goldsmith, E. J.; Charman, W. N.; Bathurst, I.; Floyd, D.; Matthews, D.; Burrows, J. N.; Rathod, P. K.; Charman, S. A.; Phillips, M. A. Structure-guided lead optimization of triazolopyrimidine-ring substituents identifies potent Plasmodium falciparum dihydroorotate dehydrogenase inhibitors with clinical candidate potential J. Med. Chem. 2011, 54, 5540-5561
-
(2011)
J. Med. Chem.
, vol.54
, pp. 5540-5561
-
-
Coteron, J.M.1
Marco, M.2
Esquivias, J.3
Deng, X.4
White, K.L.5
White, J.6
Koltun, M.7
El Mazouni, F.8
Kokkonda, S.9
Katneni, K.10
Bhamidipati, R.11
Shackleford, D.M.12
Angulo-Barturen, I.13
Ferrer, S.B.14
Jimenez-Diaz, M.B.15
Gamo, F.J.16
Goldsmith, E.J.17
Charman, W.N.18
Bathurst, I.19
Floyd, D.20
Matthews, D.21
Burrows, J.N.22
Rathod, P.K.23
Charman, S.A.24
Phillips, M.A.25
more..
-
36
-
-
77953773127
-
Plasmodium dihydroorotate dehydrogenase: A promising target for novel anti-malarial chemotherapy
-
Phillips, M. A.; Rathod, P. K. Plasmodium dihydroorotate dehydrogenase: a promising target for novel anti-malarial chemotherapy Infect. Disord. Drug Targets 2010, 10, 226-239
-
(2010)
Infect. Disord. Drug Targets
, vol.10
, pp. 226-239
-
-
Phillips, M.A.1
Rathod, P.K.2
-
37
-
-
77954837542
-
Trypanosoma brucei pteridine reductase 1 is essential for survival in vitro and for virulence in mice
-
Sienkiewicz, N.; Ong, H. B.; Fairlamb, A. H. Trypanosoma brucei pteridine reductase 1 is essential for survival in vitro and for virulence in mice Mol. Microbiol. 2010, 77, 658-671
-
(2010)
Mol. Microbiol.
, vol.77
, pp. 658-671
-
-
Sienkiewicz, N.1
Ong, H.B.2
Fairlamb, A.H.3
-
38
-
-
67650754042
-
One Scaffold, Three Binding Modes: Novel and Selective Pteridine Reductase 1 Inhibitors Derived from Fragment Hits Discovered by Virtual Screening
-
Mpamhanga, C. P.; Spinks, D.; Tulloch, L. B.; Shanks, E. J.; Robinson, D. A.; Collie, I. T.; Fairlamb, A. H.; Wyatt, P. G.; Frearson, J. A.; Hunter, W. N.; Gilbert, I. H.; Brenk, R. One Scaffold, Three Binding Modes: Novel and Selective Pteridine Reductase 1 Inhibitors Derived from Fragment Hits Discovered by Virtual Screening J. Med. Chem. 2009, 52, 4454-4465
-
(2009)
J. Med. Chem.
, vol.52
, pp. 4454-4465
-
-
Mpamhanga, C.P.1
Spinks, D.2
Tulloch, L.B.3
Shanks, E.J.4
Robinson, D.A.5
Collie, I.T.6
Fairlamb, A.H.7
Wyatt, P.G.8
Frearson, J.A.9
Hunter, W.N.10
Gilbert, I.H.11
Brenk, R.12
-
39
-
-
79251643791
-
Design, Synthesis and Biological Evaluation of Novel Inhibitors of Trypanosoma brucei Pteridine Reductase 1
-
Spinks, D.; Ong, H. B.; Mpamhanga, C. P.; Shanks, E. J.; Robinson, D. A.; Collie, I. T.; Read, K. D.; Frearson, J. A.; Wyatt, P. G.; Brenk, R.; Fairlamb, A. H.; Gilbert, I. H. Design, Synthesis and Biological Evaluation of Novel Inhibitors of Trypanosoma brucei Pteridine Reductase 1 ChemMedChem 2011, 6, 302-308
-
(2011)
ChemMedChem
, vol.6
, pp. 302-308
-
-
Spinks, D.1
Ong, H.B.2
Mpamhanga, C.P.3
Shanks, E.J.4
Robinson, D.A.5
Collie, I.T.6
Read, K.D.7
Frearson, J.A.8
Wyatt, P.G.9
Brenk, R.10
Fairlamb, A.H.11
Gilbert, I.H.12
-
40
-
-
47249120852
-
Chemical and genetic validation of dihydrofolate reductase-thymidylate synthase as a drug target in African trypanosomes
-
Sienkiewicz, N.; Jarosławski, S.; Wyllie, S.; Fairlamb, A. H. Chemical and genetic validation of dihydrofolate reductase-thymidylate synthase as a drug target in African trypanosomes Mol. Microbiol. 2008, 69, 520-533
-
(2008)
Mol. Microbiol.
, vol.69
, pp. 520-533
-
-
Sienkiewicz, N.1
Jarosławski, S.2
Wyllie, S.3
Fairlamb, A.H.4
-
41
-
-
70350381791
-
Dissecting the essentiality of the bifunctional trypanothione synthetase-amidase in Trypanosoma brucei using chemical and genetic methods
-
Wyllie, S.; Oza, S. L.; Patterson, S.; Spinks, D.; Thompson, S.; Fairlamb, A. H. Dissecting the essentiality of the bifunctional trypanothione synthetase-amidase in Trypanosoma brucei using chemical and genetic methods Mol. Microbiol. 2009, 74, 529-540
-
(2009)
Mol. Microbiol.
, vol.74
, pp. 529-540
-
-
Wyllie, S.1
Oza, S.L.2
Patterson, S.3
Spinks, D.4
Thompson, S.5
Fairlamb, A.H.6
-
42
-
-
84555188469
-
Design, synthesis and biological evaluation of Trypanosoma brucei trypanothione synthetase inhibitors
-
Spinks, D.; Torrie, L. S.; Thompson, S.; Harrison, J. R.; Frearson, J. A.; Read, K. D.; Fairlamb, A. H.; Wyatt, P. G.; Gilbert, I. H. Design, synthesis and biological evaluation of Trypanosoma brucei trypanothione synthetase inhibitors ChemMedChem 2012, 7, 95-106
-
(2012)
ChemMedChem
, vol.7
, pp. 95-106
-
-
Spinks, D.1
Torrie, L.S.2
Thompson, S.3
Harrison, J.R.4
Frearson, J.A.5
Read, K.D.6
Fairlamb, A.H.7
Wyatt, P.G.8
Gilbert, I.H.9
-
43
-
-
73649125297
-
Chemical Validation of Trypanothione Synthetase
-
Torrie, L. S.; Wyllie, S.; Spinks, D.; Oza, S. L.; Thompson, S.; Harrison, J. R.; Gilbert, I. H.; Wyatt, P. G.; Fairlamb, A. H.; Frearson, J. A. Chemical Validation of Trypanothione Synthetase J. Biol. Chem. 2009, 284, 36137-36145
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 36137-36145
-
-
Torrie, L.S.1
Wyllie, S.2
Spinks, D.3
Oza, S.L.4
Thompson, S.5
Harrison, J.R.6
Gilbert, I.H.7
Wyatt, P.G.8
Fairlamb, A.H.9
Frearson, J.A.10
-
44
-
-
1542298986
-
Protein kinases as targets for anti-parasitic chemotherapy
-
Doerig, C. Protein kinases as targets for anti-parasitic chemotherapy Biochim. Biophys. Acta: Proteins Proteomics 2004, 1697, 155-168
-
(2004)
Biochim. Biophys. Acta: Proteins Proteomics
, vol.1697
, pp. 155-168
-
-
Doerig, C.1
-
45
-
-
0035815349
-
The CRK3 protein kinase is essential for cell cycle progression of Leishmania mexicana
-
Hassan, P.; Fergusson, D.; Grant, K. M.; Mottram, J. C. The CRK3 protein kinase is essential for cell cycle progression of Leishmania mexicana Mol. Biochem. Parasitol. 2001, 113, 189-198
-
(2001)
Mol. Biochem. Parasitol.
, vol.113
, pp. 189-198
-
-
Hassan, P.1
Fergusson, D.2
Grant, K.M.3
Mottram, J.C.4
-
46
-
-
3342936476
-
Inhibitors of Leishmania mexicana CRK3 cyclin-dependent kinase: Chemical library screen and antileishmanial activity
-
Grant, K. M.; Dunion, M. H.; Yardley, V.; Skaltsounis, A. L.; Marko, D.; Eisenbrand, G.; Croft, S. L.; Meijer, L.; Mottram, J. C. Inhibitors of Leishmania mexicana CRK3 cyclin-dependent kinase: chemical library screen and antileishmanial activity Antimicrob. Agents Chemother. 2004, 48, 3033-3042
-
(2004)
Antimicrob. Agents Chemother.
, vol.48
, pp. 3033-3042
-
-
Grant, K.M.1
Dunion, M.H.2
Yardley, V.3
Skaltsounis, A.L.4
Marko, D.5
Eisenbrand, G.6
Croft, S.L.7
Meijer, L.8
Mottram, J.C.9
-
48
-
-
54249155522
-
Network Pharmacology: The next paradigm in drug discovery
-
Hopkins, A. L. Network Pharmacology: the next paradigm in drug discovery Nature Chem. Biol. 2008, 4, 682-690
-
(2008)
Nature Chem. Biol.
, vol.4
, pp. 682
-
-
Hopkins, A.L.1
|