-
1
-
-
84861057617
-
Terpene biosynthesis: Modularity rules
-
Oldfield, E.; Lin, F.-Y. Terpene biosynthesis: modularity rules Angew. Chem., Int. Ed. 2011, 50, 2-16
-
(2011)
Angew. Chem., Int. Ed.
, vol.50
, pp. 2-16
-
-
Oldfield, E.1
Lin, F.-Y.2
-
2
-
-
78349277280
-
Statins enhance formation of phagocyte extracellular traps
-
Chow, O. A.; von Kockritz-Blickwede, M.; Bright, A. T.; Hensler, M. E.; Zinkernagel, A. S.; Cogen, A. L.; Gallo, R. L.; Monestier, M.; Wang, Y.; Glass, C. K.; Nizet, V. Statins enhance formation of phagocyte extracellular traps Cell Host Microbe 2010, 8, 445-454
-
(2010)
Cell Host Microbe
, vol.8
, pp. 445-454
-
-
Chow, O.A.1
Von Kockritz-Blickwede, M.2
Bright, A.T.3
Hensler, M.E.4
Zinkernagel, A.S.5
Cogen, A.L.6
Gallo, R.L.7
Monestier, M.8
Wang, Y.9
Glass, C.K.10
Nizet, V.11
-
3
-
-
77956292192
-
Functional microdomains in bacterial membranes
-
Lopez, D.; Kolter, R. Functional microdomains in bacterial membranes Genes Dev. 2010, 24, 1893-1902
-
(2010)
Genes Dev.
, vol.24
, pp. 1893-1902
-
-
Lopez, D.1
Kolter, R.2
-
4
-
-
40449088993
-
A cholesterol biosynthesis inhibitor blocks Staphylococcus aureus virulence
-
DOI 10.1126/science.1153018
-
Liu, C. I.; Liu, G. Y.; Song, Y.; Yin, F.; Hensler, M. E.; Jeng, W. Y.; Nizet, V.; Wang, A. H.; Oldfield, E. A cholesterol biosynthesis inhibitor blocks Staphylococcus aureus virulence Science 2008, 319, 1391-1394 (Pubitemid 351354874)
-
(2008)
Science
, vol.319
, Issue.5868
, pp. 1391-1394
-
-
Liu, C.-I.1
Liu, G.Y.2
Song, Y.3
Yin, F.4
Hensler, M.E.5
Jeng, W.-Y.6
Nizet, V.7
Wang, A.H.-J.8
Oldfield, E.9
-
5
-
-
55849131057
-
In vitro activities of ER-119884 and E5700, two potent squalene synthase inhibitors, against Leishmania amazonensis: Antiproliferative, biochemical, and ultrastructural effects
-
Fernandes Rodrigues, J. C.; Concepcion, J. L.; Rodrigues, C.; Caldera, A.; Urbina, J. A.; de Souza, W. In vitro activities of ER-119884 and E5700, two potent squalene synthase inhibitors, against Leishmania amazonensis: antiproliferative, biochemical, and ultrastructural effects Antimicrob. Agents Chemother. 2008, 52, 4098-4114
-
(2008)
Antimicrob. Agents Chemother.
, vol.52
, pp. 4098-4114
-
-
Fernandes Rodrigues, J.C.1
Concepcion, J.L.2
Rodrigues, C.3
Caldera, A.4
Urbina, J.A.5
De Souza, W.6
-
6
-
-
34250162861
-
Kinetic characterization of squalene synthase from Trypanosoma cruzi: Selective inhibition by quinuclidine derivatives
-
DOI 10.1128/AAC.01454-06
-
Sealey-Cardona, M.; Cammerer, S.; Jones, S.; Ruiz-Perez, L. M.; Brun, R.; Gilbert, I. H.; Urbina, J. A.; Gonzalez-Pacanowska, D. Kinetic characterization of squalene synthase from Trypanosoma cruzi: selective inhibition by quinuclidine derivatives Antimicrob. Agents Chemother. 2007, 51, 2123-2129 (Pubitemid 46903104)
-
(2007)
Antimicrobial Agents and Chemotherapy
, vol.51
, Issue.6
, pp. 2123-2129
-
-
Sealey-Cardona, M.1
Cammerer, S.2
Jones, S.3
Ruiz-Perez, L.M.4
Brun, R.5
Gilbert, I.H.6
Urbina, J.A.7
Gonzalez-Pacanowska, D.8
-
7
-
-
3042570789
-
In vitro and in vivo activities of E5700 and ER-119884, two novel orally active squalene synthase inhibitors, against Trypanosoma cruzi
-
DOI 10.1128/AAC.48.7.2379-2387.2004
-
Urbina, J. A.; Concepcion, J. L.; Caldera, A.; Payares, G.; Sanoja, C.; Otomo, T.; Hiyoshi, H. In vitro and in vivo activities of E5700 and ER-119884, two novel orally active squalene synthase inhibitors, against Trypanosoma cruzi Antimicrob. Agents Chemother. 2004, 48, 2379-2387 (Pubitemid 38823400)
-
(2004)
Antimicrobial Agents and Chemotherapy
, vol.48
, Issue.7
, pp. 2379-2387
-
-
Urbina, J.A.1
Concepcion, J.L.2
Caldera, A.3
Payares, G.4
Sanoja, C.5
Otomo, T.6
Hiyoshi, H.7
-
8
-
-
78650722294
-
Mechanism of action and inhibition of dehydrosqualene synthase
-
Lin, F. Y.; Liu, C. I.; Liu, Y. L.; Zhang, Y.; Wang, K.; Jeng, W. Y.; Ko, T. P.; Cao, R.; Wang, A. H.; Oldfield, E. Mechanism of action and inhibition of dehydrosqualene synthase Proc. Natl. Acad. Sci. U.S.A. 2010, 107, 21337-42
-
(2010)
Proc. Natl. Acad. Sci. U.S.A.
, vol.107
, pp. 21337-21342
-
-
Lin, F.Y.1
Liu, C.I.2
Liu, Y.L.3
Zhang, Y.4
Wang, K.5
Jeng, W.Y.6
Ko, T.P.7
Cao, R.8
Wang, A.H.9
Oldfield, E.10
-
9
-
-
33646367241
-
Structural basis for the exceptional in vivo efficacy of bisphosphonate drugs
-
DOI 10.1002/cmdc.200500059
-
Rondeau, J. M.; Bitsch, F.; Bourgier, E.; Geiser, M.; Hemmig, R.; Kroemer, M.; Lehmann, S.; Ramage, P.; Rieffel, S.; Strauss, A.; Green, J. R.; Jahnke, W. Structural basis for the exceptional in vivo efficacy of bisphosphonate drugs ChemMedChem 2006, 1, 267-273 (Pubitemid 43700307)
-
(2006)
ChemMedChem
, vol.1
, Issue.2
, pp. 267-273
-
-
Rondeau, J.-M.1
Bitsch, F.2
Bourgier, E.3
Geiser, M.4
Hemmig, R.5
Kroemer, M.6
Lehmann, S.7
Ramage, P.8
Rieffel, S.9
Strauss, A.10
Green, J.R.11
Jahnke, W.12
-
10
-
-
77749265076
-
Structure of epi-isozizaene synthase from Streptomyces coelicolor A3(2), a platform for new terpenoid cyclization templates
-
Aaron, J. A.; Lin, X.; Cane, D. E.; Christianson, D. W. Structure of epi-isozizaene synthase from Streptomyces coelicolor A3(2), a platform for new terpenoid cyclization templates Biochemistry (Moscow) 2010, 49, 1787-1797
-
(2010)
Biochemistry (Moscow)
, vol.49
, pp. 1787-1797
-
-
Aaron, J.A.1
Lin, X.2
Cane, D.E.3
Christianson, D.W.4
-
11
-
-
0032524330
-
Function-structure studies and identification of three enzyme domains involved in the catalytic activity in rat hepatic squalene synthase
-
DOI 10.1074/jbc.273.20.12515
-
Gu, P.; Ishii, Y.; Spencer, T. A.; Shechter, I. Function-structure studies and identification of three enzyme domains involved in the catalytic activity in rat hepatic squalene synthase J. Biol. Chem. 1998, 273, 12515-12525 (Pubitemid 28240626)
-
(1998)
Journal of Biological Chemistry
, vol.273
, Issue.20
, pp. 12515-12525
-
-
Gu, P.1
Ishii, Y.2
Spencer, T.A.3
Shechter, I.4
-
13
-
-
0038778632
-
Mechanism of action of 4-phenoxyphenoxyethyl thiocyanate (WC-9) against Trypanosoma cruzi, the causative agent of Chagas' disease
-
DOI 10.1128/AAC.47.6.2047-2050.2003
-
Urbina, J. A.; Concepcion, J. L.; Montalvetti, A.; Rodriguez, J. B.; Docampo, R. Mechanism of action of 4-phenoxyphenoxyethyl thiocyanate (WC-9) against Trypanosoma cruzi, the causative agent of Chagas' disease Antimicrob. Agents Chemother. 2003, 47, 2047-2050 (Pubitemid 36637844)
-
(2003)
Antimicrobial Agents and Chemotherapy
, vol.47
, Issue.6
, pp. 2047-2050
-
-
Urbina, J.A.1
Concepcion, J.L.2
Montalvetti, A.3
Rodriguez, J.B.4
Docampo, R.5
-
14
-
-
0032560138
-
Structure-activity relationship of new growth inhibitors of Trypanosoma cruzi
-
DOI 10.1021/jm970860z
-
Cinque, G. M.; Szajnman, S. H.; Zhong, L.; Docampo, R.; Schvartzapel, A. J.; Rodriguez, J. B.; Gros, E. G. Structure-activity relationship of new growth inhibitors of Trypanosoma cruzi J. Med. Chem. 1998, 41, 1540-1554 (Pubitemid 28198983)
-
(1998)
Journal of Medicinal Chemistry
, vol.41
, Issue.9
, pp. 1540-1554
-
-
Cinque, G.M.1
Szajnman, S.H.2
Zhong, L.3
Docampo, R.4
Schvartzapel, A.J.5
Rodriguez, J.B.6
Gros, E.G.7
-
15
-
-
0037194642
-
Design, synthesis, and biological evaluation of aryloxyethyl thiocyanate derivatives against Trypanosoma cruzi
-
DOI 10.1021/jm0201518
-
Elhalem, E.; Bailey, B. N.; Docampo, R.; Ujvary, I.; Szajnman, S. H.; Rodriguez, J. B. Design, synthesis, and biological evaluation of aryloxyethyl thiocyanate derivatives against Trypanosoma cruzi J. Med. Chem. 2002, 45, 3984-3999 (Pubitemid 35024300)
-
(2002)
Journal of Medicinal Chemistry
, vol.45
, Issue.18
, pp. 3984-3999
-
-
Elhalem, E.1
Bailey, B.N.2
Docampo, R.3
Ujvary, I.4
Szajnman, S.H.5
Rodriguez, J.B.6
-
16
-
-
49849121725
-
Hydrogen bonding between phenol and alkyl thiocyanates
-
Igarashi, K.; Watari, F.; Aida, K. Hydrogen bonding between phenol and alkyl thiocyanates Spectrochim. Acta. A 1969, 25, 1743
-
(1969)
Spectrochim. Acta. A
, vol.25
, pp. 1743
-
-
Igarashi, K.1
Watari, F.2
Aida, K.3
-
17
-
-
55849142244
-
New anti-tuberculosis drugs in clinical trials with novel mechanisms of action
-
Rivers, E. C.; Mancera, R. L. New anti-tuberculosis drugs in clinical trials with novel mechanisms of action Drug Discovery Today 2008, 13, 1090-1098
-
(2008)
Drug Discovery Today
, vol.13
, pp. 1090-1098
-
-
Rivers, E.C.1
Mancera, R.L.2
-
18
-
-
35948991176
-
Quinuclidine derivatives as potential antiparasitics
-
DOI 10.1128/AAC.00205-07
-
Cammerer, S. B.; Jimenez, C.; Jones, S.; Gros, L.; Lorente, S. O.; Rodrigues, C.; Rodrigues, J. C.; Caldera, A.; Ruiz Perez, L. M.; da Souza, W.; Kaiser, M.; Brun, R.; Urbina, J. A.; Gonzalez Pacanowska, D.; Gilbert, I. H. Quinuclidine derivatives as potential antiparasitics Antimicrob. Agents Chemother. 2007, 51, 4049-4061 (Pubitemid 350063999)
-
(2007)
Antimicrobial Agents and Chemotherapy
, vol.51
, Issue.11
, pp. 4049-4061
-
-
Cammerer, S.B.1
Jimenez, C.2
Jones, S.3
Gros, L.4
Lorente, S.O.5
Rodrigues, C.6
Rodrigues, J.C.F.7
Caldera, A.8
Perez, L.M.R.9
Da Souza, W.10
Kaiser, M.11
Brun, R.12
Urbina, J.A.13
Pacanowska, D.G.14
Gilbert, I.H.15
-
19
-
-
20244386998
-
Biphenylquinuclidines as inhibitors of squalene synthase and growth of parasitic protozoa
-
DOI 10.1016/j.bmc.2005.02.060
-
Orenes Lorente, S.; Gomez, R.; Jimenez, C.; Cammerer, S.; Yardley, V.; de Luca-Fradley, K.; Croft, S. L.; Ruiz Perez, L. M.; Urbina, J.; Gonzalez Pacanowska, D.; Gilbert, I. H. Biphenylquinuclidines as inhibitors of squalene synthase and growth of parasitic protozoa Bioorg. Med. Chem. 2005, 13, 3519-3529 (Pubitemid 40545807)
-
(2005)
Bioorganic and Medicinal Chemistry
, vol.13
, Issue.10
, pp. 3519-3529
-
-
Orenes Lorente, S.1
Gomez, R.2
Jimenez, C.3
Cammerer, S.4
Yardley, V.5
De Luca-Fradley, K.6
Croft, S.L.7
Ruiz Perez, L.M.8
Urbina, J.9
Pacanowska, D.G.10
Gilbert, I.H.11
-
20
-
-
77949488600
-
Synthesis and evaluation of SQ109 analogues as potential anti-tuberculosis candidates
-
Onajole, O. K.; Govender, P.; van Helden, P. D.; Kruger, H. G.; Maguire, G. E.; Wiid, I.; Govender, T. Synthesis and evaluation of SQ109 analogues as potential anti-tuberculosis candidates Eur. J. Med. Chem. 2010, 45, 2075-2079
-
(2010)
Eur. J. Med. Chem.
, vol.45
, pp. 2075-2079
-
-
Onajole, O.K.1
Govender, P.2
Van Helden, P.D.3
Kruger, H.G.4
Maguire, G.E.5
Wiid, I.6
Govender, T.7
-
21
-
-
78449264099
-
-
version 1.3; Schrödinger, LLC: Portland, OR.
-
The PyMOL Molecular Graphic System, version 1.3; Schrödinger, LLC: Portland, OR.
-
The PyMOL Molecular Graphic System
-
-
-
22
-
-
84855757480
-
-
version 2009.10; Chemical Computing Group, Inc: Montreal, Canada.
-
Molecular Operating Environment (MOE), version 2009.10; Chemical Computing Group, Inc: Montreal, Canada.
-
Molecular Operating Environment (MOE)
-
-
|