-
1
-
-
85038452096
-
-
World Health Organization, Stop TB Partnership. Tuberculosis Global Facts 2010, Accessed March 3
-
World Health Organization, Stop TB Partnership. Tuberculosis Global Facts 2010. http://www.who.int/tb (Accessed March 3, 2011)
-
(2011)
-
-
-
2
-
-
33847681052
-
Antituberculosis drugs: Ten years of research
-
DOI 10.1016/j.bmc.2007.01.030, PII S0968089607000442
-
Janin, Y.L. Antituberculosis drugs: Ten years of research. Bioorg. Med. Chem. 2007, 15, 2479-2513 (Pubitemid 46367698)
-
(2007)
Bioorganic and Medicinal Chemistry
, vol.15
, Issue.7
, pp. 2479-2513
-
-
Janin, Y.L.1
-
3
-
-
17044387299
-
New drugs for tuberculosis: Current status and future prospect
-
Brien, R.J.O.; Spiegelman, M. New drugs for tuberculosis: current status and future prospect. Clin. Chest. Med. 2005, 26, 327-340
-
(2005)
Clin. Chest. Med.
, vol.26
, pp. 327-340
-
-
Brien, R.J.O.1
Spiegelman, M.2
-
4
-
-
19544390716
-
New small-molecules synthetic antimycobacterials
-
Ballell, L.; Field, R. A.; Duncan, K.; Young, R.J. New small-molecules synthetic antimycobacterials. Antimicrob. Agents Chemother. 2005, 49, 2153-2163
-
(2005)
Antimicrob. Agents Chemother.
, vol.49
, pp. 2153-2163
-
-
Ballell, L.1
Field, R.A.2
Duncan, K.3
Young, R.J.4
-
5
-
-
0004255158
-
-
Thieme Verlag Stuttgart
-
Kleemann, A.; Engel, J.; Kutscher, B.; Reichert, D. Pharmaceutical Substances, Thieme Verlag Stuttgart, 1999
-
(1999)
Pharmaceutical Substances
-
-
Kleemann, A.1
Engel, J.2
Kutscher, B.3
Reichert, D.4
-
6
-
-
0000986415
-
Synthesis and anti-microbial activity of 2-alkylthio-6- aminobenzothiazoles
-
Sidóova, E.; Odlerová, A.; Volná, F.; Blöckinger, G. Synthesis and anti-microbial activity of 2-alkylthio-6-aminobenzothiazoles. Chem Zvesti, 1979, 33, 830-836.
-
(1979)
Chem Zvesti
, vol.33
, pp. 830-836
-
-
Sidóova, E.1
Odlerová, A.2
Volná, F.3
Blöckinger, G.4
-
7
-
-
4244120772
-
Synthesis and biological activity of 2-alkylthio-6-(bicyclo[2.2.1]hept- 5en-2,3-dicarboximido)-benzothiazoles
-
Sidóova, E.; Odlerová, A.; Perjéssy, A.; Blöckinger, G. Synthesis and biological activity of 2-alkylthio-6- (bicyclo[2.2.1]hept-5en-2,3-dicarboximido)-benzothiazoles. Chem Zvesti, 1980, 34, 269-277.
-
(1980)
Chem Zvesti
, vol.34
, pp. 269-277
-
-
Sidóova, E.1
Odlerová, A.2
Perjéssy, A.3
Blöckinger, G.4
-
8
-
-
85038455875
-
Vztahy mezi chemickou strukturou látek a jejich antimykobakterialní aktivitou vi atypickm kmenm. I. 2-alkylthio-6- aminobenzothiazoly. (Relationships between the chemical structure of substances and their antimycobacterial aktivity to atypical strains I. 2-alkylthio-6- aminobenzothiazoles)
-
Sidóova, E.; Odlerová, A.; Waisser, K. Vztahy mezi chemickou strukturou látek a jejich antimykobakterialní aktivitou vi atypickm kmenm. I. 2-alkylthio-6-aminobenzothiazoly. (Relationships between the chemical structure of substances and their antimycobacterial aktivity to atypical strains I. 2-alkylthio-6-aminobenzothiazoles). Ceskoslov. Farm. 1985, 34, 7-9
-
(1985)
Ceskoslov. Farm.
, vol.34
, pp. 7-9
-
-
Sidóova, E.1
Odlerová, A.2
Waisser, K.3
-
9
-
-
70349638300
-
Synthesis and biological evaluation of 2-mercapto-1,3-benzothiazole derivatives with potential antimicrobial aktivity
-
Franchini, C.; Muraglia, M.; Corbo, F.; Florio, M.A.; DiMola, A.; Rosato, A.; Matucci, R.; Nesi, M.; van Bambeke, F.; Vitali, C. Synthesis and biological evaluation of 2-mercapto-1,3-benzothiazole derivatives with potential antimicrobial aktivity. Arch. Pharm. Chem. Life Sci. 2009, 342, 605-613
-
(2009)
Arch. Pharm. Chem. Life Sci.
, vol.342
, pp. 605-613
-
-
Franchini, C.1
Muraglia, M.2
Corbo, F.3
Florio, M.A.4
Dimola, A.5
Rosato, A.6
Matucci, R.7
Nesi, M.8
Van Bambeke, F.9
Vitali, C.10
-
10
-
-
17844410934
-
Facile synthesis of 2-(substitutedbenzylsulfanyl)-benzothiazoles and their antimicrobial activity screening
-
Kumar, R.V.; Seshu Kumar, K.V.S.R.; Gopal, K.R. Facile synthesis of 2-(substitutedbenzylsulfanyl)-benzothiatoles and their antimicrobial activity screening. J. Heterocyclic. Chem. 2005, 42, 153-156 (Pubitemid 40591026)
-
(2005)
Journal of Heterocyclic Chemistry
, vol.42
, Issue.1
, pp. 153-156
-
-
Kumar, R.V.1
Kumar, K.V.S.R.S.2
Gopal, K.R.3
-
11
-
-
0036241881
-
Synthesis and preliminary evaluation of benzimidazole derivatives as antimicrobial agents
-
Klimeová, V.; Koí, J.; Pour, M.; Stachel, J.; Waisser, K.; Kaustová, J. Synthesis and preliminary evaluation of benzimidazole derivatives as antimicrobial agents. Eur. J. Med. Chem. 2002, 37, 409-418
-
(2002)
Eur. J. Med. Chem.
, vol.37
, pp. 409-418
-
-
Klimecová, V.1
Kocí, J.2
Pour, M.3
Stachel, J.4
Waisser, K.5
Kaustová, J.6
-
12
-
-
0036534079
-
New benzimidazole derivatives as antimycobacterial agents
-
Klimeová, V.; Koí, J.; Waisser, K.; Kaustová, J. New benzimidazole derivatives as antimycobacterial agents. Farmaco, 2002, 57, 259-265
-
(2002)
Farmaco
, vol.57
, pp. 259-265
-
-
Klimecová, V.1
Kocí, J.2
Waisser, K.3
Kaustová, J.4
-
13
-
-
62749177464
-
Preparation and in vitro evaluation of benzylsulfanyl benzoxazole derivatives as potential antituberculosis agents
-
Klimeová, V.; Koí, J.; Waisser, K.; Kaustová, J.; Möllmann, U. Preparation and in vitro evaluation of benzylsulfanyl benzoxazole derivatives as potential antituberculosis agents. Eur. J. Med. Chem. 2009, 44, 2286-2293
-
(2009)
Eur. J. Med. Chem.
, vol.44
, pp. 2286-2293
-
-
Klimecová, V.1
Kocí, J.2
Waisser, K.3
Kaustová, J.4
Möllmann, U.5
-
14
-
-
0037131751
-
Heterocyclic benzazole derivatives with antimycobacterial in vitro activity
-
DOI 10.1016/S0960-894X(02)00697-2, PII S0960894X02006972
-
Koí; J.; Klimeová, V.; Waisser, K.; Kaustová, J.; Dahse, H.M.; Möllmann, U. Heterocyclic Benzazole Derivatives with Antimycobacterial In Vitro Activity. Bioorg. Med. Chem. Lett. 2002, 12, 3275-3278 (Pubitemid 35248230)
-
(2002)
Bioorganic and Medicinal Chemistry Letters
, vol.12
, Issue.22
, pp. 3275-3278
-
-
Koci, J.1
Klimesova, V.2
Waisser, K.3
Kaustova, J.4
Dahse, H.-M.5
Mollmann, U.6
-
15
-
-
67349287483
-
Synthetic EthR inhibitors boots antituberculous activity of ethionamide
-
Willand, N.; Dirie, B.; Carette, X.; Bifani, P.; Singhal, A. Desroses, M.; Leroux, F.; Willery, E.; Mathys, V.; Deprez-Poulain, R.; Delcroix, G.; Frenois, F.; Aumercier, M.; Locht, C.; Villeret V.; Deprez, B.; Baulard, A.R. synthetic EthR inhibitors boots antituberculous activity of ethionamide. Nat. Med. 2009, 15, 537-544
-
(2009)
Nat. Med.
, vol.15
, pp. 537-544
-
-
Willand, N.1
Dirie, B.2
Carette, X.3
Bifani, P.4
Singhal, A.M.5
Leroux, F.6
Willery, E.7
Mathys, V.8
Deprez-Poulain, R.9
Delcroix, G.10
Frenois, F.11
Aumercier, M.12
Locht, C.13
Villeret, V.14
Deprez, B.15
Baulard, A.R.16
-
16
-
-
0036020524
-
Drugs that inhibit mycolic acid biosynthesis in Mycobacterium tuberculosis
-
DOI 10.2174/1389201023378328
-
Schroder, E.K.; de Souza, O.N.; Santos, D.S.; Blanchard, J.S.; Basso, L.A. Drugs that inhibit mycolic acid biosythesis in Mycobacterium tuberculosis. Curr. Pharm. Biotechnol. 2002, 3, 197-225 (Pubitemid 34823018)
-
(2002)
Current Pharmaceutical Biotechnology
, vol.3
, Issue.3
, pp. 197-225
-
-
Schroeder, E.K.1
De Souza, O.N.2
Santos, D.S.3
Blanchard, J.S.4
Basso, L.A.5
-
17
-
-
0037066702
-
The antituberculosis drug ethionamide is activated by a flavoprotein monooxygenase
-
DOI 10.1074/jbc.M110751200
-
Vannelli, T.A.; Dykman, A.; Ortiz de Montellano, P.R. The antituberculosis drug ethionamide is activated by a flavoprotein monooxygenase. J. Biol. Chem. 2002, 277, 12824-12829 (Pubitemid 34952646)
-
(2002)
Journal of Biological Chemistry
, vol.277
, Issue.15
, pp. 12824-12829
-
-
Vannelli, T.A.1
Dykman, A.2
Ortiz De Montellano, P.R.3
-
18
-
-
57149099588
-
Bicyclic nitroimidazoles act as intracellular NO donors and kill non-replicating Mycobacterium tuberculosis
-
Singh, R.; Manjunatha, U.; Boshoff, H.I. M.; Ha, Y.H.; Niyomrattanakit, P.; Ledwidge, R.; Dowd, C.S.; Lee, I.Y.; Kim, P.; Zhang, L.; Kang, S.; Keller, T.H.; Jiricek, J. Barry, C.E. 3rd. Bicyclic nitroimidazoles act as intracellular NO donors and kill non-replicating Mycobacterium tuberculosis. Science 2008, 322, 1392-1395
-
(2008)
Science
, vol.322
, pp. 1392-1395
-
-
Singh, R.1
Manjunatha, U.2
Boshoff, H.I.M.3
Ha, Y.H.4
Niyomrattanakit, P.5
Ledwidge, R.6
Dowd, C.S.7
Lee, I.Y.8
Kim, P.9
Zhang, L.10
Kang, S.11
Keller, T.H.12
Jiricek Barry, J.C.E.13
-
19
-
-
33845323336
-
OPC-67683, and nitro-dihydro-imidazooxazole derivative with promising action against tuberculosis in vitro and in mice
-
Matsumoto, M.; Hashizume, H.; Tomishige, T.; Kawasaki, M.; Tsubouchi, H.; Sasaki, H.; Shimokawa, Y.; Komatsu, M. OPC-67683, and nitro-dihydro- imidazooxazole derivative with promising action against tuberculosis in vitro and in mice. PLoS Med. 2006, 3, 2131-2143
-
(2006)
PLoS Med.
, vol.3
, pp. 2131-2143
-
-
Matsumoto, M.1
Hashizume, H.2
Tomishige, T.3
Kawasaki, M.4
Tsubouchi, H.5
Sasaki, H.6
Shimokawa, Y.7
Komatsu, M.8
-
20
-
-
65649096556
-
Benzothiazinones kill Mycobacterium tuberculosis by blocking arabinan synthesis
-
Makarov, V.; Manina, G.; Mikusova, K.; Möllmann, U.; Ryabova, O.; Saint-Joanis, B.; Dhar, N.; Pasca, M.R.; Buroni, S.; Lucarelli, A.P.; Milano, A.; De Rossi, E.; Belanova, M.; Bobovska, A.; Dianiskova, P.; Kordulakova, J.; Sala, C.; Fullnm, E.; Schneder, P.; McKinney, J.D.; Brodin, P.; Christophe, T.; Waddell, S.; Butcher, P.; Albrethesen, J.; Rosenkrands, I.; Brosch, R.; Nandi, V.; Bharath, S.; Gaonkar, S.; Shandil, R.K.; Balasubramanian, V.; Balganesh, T.; Tyagi, S.; Grosset, J.; Riccardi, G.; Cole, S.T. Benzothiazinones kill Mycobacterium tuberculosis by blocking arabinan synthesis. Science 2009, 324, 801-804
-
(2009)
Science
, vol.324
, pp. 801-804
-
-
Makarov, V.1
Manina, G.2
Mikusova, K.3
Möllmann, U.4
Ryabova, O.5
Saint-Joanis, B.6
Dhar, N.7
Pasca, M.R.8
Buroni, S.9
Lucarelli, A.P.10
Milano, A.11
De Rossi, E.12
Belanova, M.13
Bobovska, A.14
Dianiskova, P.15
Kordulakova, J.16
Sala, C.17
Fullnm, E.18
Schneder, P.19
McKinney, J.D.20
Brodin, P.21
Christophe, T.22
Waddell, S.23
Butcher, P.24
Albrethesen, J.25
Rosenkrands, I.26
Brosch, R.27
Nandi, V.28
Bharath, S.29
Gaonkar, S.30
Shandil, R.K.31
Balasubramanian, V.32
Balganesh, T.33
Tyagi, S.34
Grosset, J.35
Riccardi, G.36
Cole, S.T.37
more..
-
21
-
-
73649143180
-
High content screening identifies decaprenyl-phosphoribose 2epimerase as a target for intracellular antimycobacterial inhibitors
-
Christophe, T.; Jackson, M.; Jeon, H.K.; Fenistein, D.; Contreras-Dominguez, M.; Kim, J.; Genovesio, A.; Carralot, J.P.; Ewann, F.; Kim, E.H.; Lee, S.Y.; Kang, S.; Seo, M.S.; Park, E.J.; Akovierová, H.; Pham, H.; Riccardi, G.; Nam, J.Y.; Marsollier, L.; Kempf, M.; Joly-Guillou, M.L.; Oh, T.; Shin, W.K.; No, Z.; Nehrbass, U.; Brosch, R.; Cole, S.T.; Brodin, P. High content screening identifies decaprenyl-phosphoribose 2epimerase as a target for intracellular antimycobacterial inhibitors. PLoS Pathog. 2009, 5, 1-10
-
(2009)
PLoS Pathog.
, vol.5
, pp. 1-10
-
-
Christophe, T.1
Jackson, M.2
Jeon, H.K.3
Fenistein, D.4
Contreras-Dominguez, M.5
Kim, J.6
Genovesio, A.7
Carralot, J.P.8
Ewann, F.9
Kim, E.H.10
Lee, S.Y.11
Kang, S.12
Seo, M.S.13
Park, E.J.14
Akovierová, H.15
Pham, H.16
Riccardi, G.17
Nam, J.Y.18
Marsollier, L.19
Kempf, M.20
Joly-Guillou, M.L.21
Oh, T.22
Shin, W.K.23
No, Z.24
Nehrbass, U.25
Brosch, R.26
Cole, S.T.27
Brodin, P.28
more..
-
22
-
-
84984081900
-
Toxicity of organic sulfides to the eggs and larvae of the twospotted spider mite
-
Cranham, J.E.; Cummings, W.A.W.; Johston, A.M.; Stevenson, H.A. Toxicity of organic sulfides to the eggs and larvae of the twospotted spider mite. J. Sci. Food Agric. 1958, 9, 143-147
-
(1958)
J. Sci. Food Agric.
, vol.9
, pp. 143-147
-
-
Cranham, J.E.1
Cummings, W.A.W.2
Johston, A.M.3
Stevenson, H.A.4
-
23
-
-
0011112761
-
Activation of bivalent sulfur-compounds with cupric chloride and zinc chloride -benzylation and acylation of aromatic-compounds with sulfides and thiols esters
-
Maekawa, K.; Narasaka, K.; Mukaiyama, T. Activation of bivalent sulfur-compounds with cupric chloride and zinc chloride -benzylation and acylation of aromatic-compounds with sulfides and thiols esters. Bull. Chem. Soc. Jpn. 1973, 46, 3478-3482
-
(1973)
Bull. Chem. Soc. Jpn.
, vol.46
, pp. 3478-3482
-
-
Maekawa, K.1
Narasaka, K.2
Mukaiyama, T.3
-
24
-
-
0000355152
-
Stereochemistry of direct olefin formation from carbonylcompounds and lithiated heterocyclic sulfones
-
Baudin, J.B.; Hareau, G.; Julia, S.A.; Lorne, R.; Ruel, O. Stereochemistry of direct olefin formation from carbonylcompounds and lithiated heterocyclic sulfones. Bull. Soc. Chim. Fr. 1993, 130, 856-878
-
(1993)
Bull. Soc. Chim. Fr.
, vol.130
, pp. 856-878
-
-
Baudin, J.B.1
Hareau, G.2
Julia, S.A.3
Lorne, R.4
Ruel, O.5
-
25
-
-
0002352172
-
Benzothiazole compounds XI. synthesis and antimicribial aktivity of 2-and 2,6-substituted benzothiazoles
-
Sutoris, V.; Foltínová, P.; Blaeckinger, G. Benzothiazole compounds . XI. Synthesis and antimicribial aktivity of 2-and 2,6-substituted benzothiazoles. Chem. Zvesti 1977, 31, 92-97
-
(1977)
Chem. Zvesti
, vol.31
, pp. 92-97
-
-
Sutoris, V.1
Foltínová, P.2
Blaeckinger, G.3
-
26
-
-
0017880337
-
SYNTHESE ET ETUDE DES ACTIVITES ANTIPARASITAIRES ET MOLLUSCICIDES DE DERIVES POLYCYCLIQUES DE LA PYRIDINE. I. COMPARAISON DES DERIVES SUBSTITUES EN 2 DE LA THAIZOLO [5,4-b] PYRIDINE ET DU BENZOTHIAZOLE
-
Gayral, P.; Bourdais, J.; Lorre, A.; Abenhaim, D.; Dusset, F.; Pommies, M.; Fouret, G. Synthesis and anti-parasitic and mollusccidal activities of polycyclic derivatives of pyridine. 1. Comparison of 2-substituted thiazolo[5,4-B]pyridine and benzothiazole derivatives. Eur. J. Med. Chem. 1978, 13, 171-175 (Pubitemid 8323368)
-
(1978)
European Journal of Medicinal Chemistry
, vol.13
, Issue.2
, pp. 171-175
-
-
Gayral, P.1
Bourdais, J.2
Lorre, A.3
-
27
-
-
0034962109
-
Differentiation between inducers of apoptosis and nonspecific cytotoxic drugs by means of cell analyzer and immunoassay
-
Dahse, H.M.; Schlegel, B.; Gräfe, U. Differentiation between inducers of apoptosis and nonspecific cytotoxin drugs by means of cell analyzer and immunoassay. Pharmazie 2001, 56, 489-491 (Pubitemid 32591646)
-
(2001)
Pharmazie
, vol.56
, Issue.6
, pp. 489-491
-
-
Dahse, H.-M.1
Schlegel, B.2
Grafe, U.3
-
28
-
-
84911792416
-
Atomic physicochemical parameters for three dimensional structure directed quantitative structure-activity relationships III
-
Ghose, A.K.; Pritchett, A.; Crippen, G.M. Atomic physicochemical parameters for three dimensional structure directed quantitative structure-activity relationships III. Modeling hydrophobic interactions. J. Comput. Chem. 1988, 9, 80-90
-
(1988)
Modeling Hydrophobic Interactions. J. Comput. Chem.
, vol.9
, pp. 80-90
-
-
Ghose, A.K.1
Pritchett, A.2
Crippen, G.M.3
-
29
-
-
0024716284
-
Atomic physicochemical parameters for threedimensional structure directed quantitative structure-activity relationships 4 Additional parameters for hydrophobic and dispersive interactions and their application for an automated superposition of certain naturally oc-curring nucleoside antibiotics
-
Viswanadhan, V.N.; Ghose, A.K.; Revankar, G.R.; Robins, R.K. Atomic physicochemical parameters for threedimensional structure directed quantitative structure-activity relationships. 4. Additional parameters for hydrophobic and dispersive interactions and their application for an automated superposition of certain naturally oc-curring nucleoside antibiotics. J. Chem. Inf. Comput. Sci. 1989, 29, 163-172
-
(1989)
J. Chem. Inf. Comput. Sci.
, vol.29
, pp. 163-172
-
-
Viswanadhan, V.N.1
Ghose, A.K.2
Revankar, G.R.3
Robins, R.K.4
-
30
-
-
0023289451
-
Atomic physicochemical parameters for three-dimensional-structure- directed quantitative structure- activity relationships 2 Modeling dispersive and hydrophobic interactions
-
Ghose, A.K.; Crippen, G.M. Atomic physicochemical parameters for three-dimensional-structure-directed quantitative structure- activity relationships. 2. Modeling dispersive and hydrophobic interactions. J. Chem. Inf. Comput. Sci. 1987, 27, 21-35.
-
(1987)
J. Chem. Inf. Comput. Sci.
, vol.27
, pp. 21-35
-
-
Ghose, A.K.1
Crippen, G.M.2
|