-
1
-
-
4644349770
-
Identification and validation of novel drug targets in tuberculosis
-
DOI 10.2174/1381612043383223
-
Duncan K., (2004) Identification and validation of novel drug targets in tuberculosis. Curr Pharm Des; 10: 3185-3194. (Pubitemid 39276608)
-
(2004)
Current Pharmaceutical Design
, vol.10
, Issue.26
, pp. 3185-3194
-
-
Duncan, K.1
-
2
-
-
33645047892
-
1.6 A crystal structure of the secreted chorismate mutase from Mycobacterium tuberculosis: Novel fold topology revealed
-
Okvist M., Dey R., Sasso S., Grahn E., Kast P., Krengel U., (2006) 1.6 A crystal structure of the secreted chorismate mutase from Mycobacterium tuberculosis: novel fold topology revealed. J Mol Biol; 357: 1483-1499.
-
(2006)
J Mol Biol
, vol.357
, pp. 1483-1499
-
-
Okvist, M.1
Dey, R.2
Sasso, S.3
Grahn, E.4
Kast, P.5
Krengel, U.6
-
3
-
-
67650529714
-
Evolutionary cycles for pericyclic reactions - Or why we keep mutating mutases
-
Roderer K., Kast P., (2009) Evolutionary cycles for pericyclic reactions-or why we keep mutating mutases. Chimia; 63: 313-317.
-
(2009)
Chimia
, vol.63
, pp. 313-317
-
-
Roderer, K.1
Kast, P.2
-
4
-
-
12544259906
-
Characterization of the secreted chorismate mutase from the pathogen Mycobacterium tuberculosis
-
Sasso S., Ramakrishnan C., Gamper M., Hilvert D., Kast P., (2005) Characterization of the secreted chorismate mutase from the pathogen Mycobacterium tuberculosis. FEBS J; 272: 375-389.
-
(2005)
FEBS J
, vol.272
, pp. 375-389
-
-
Sasso, S.1
Ramakrishnan, C.2
Gamper, M.3
Hilvert, D.4
Kast, P.5
-
5
-
-
33845393571
-
v: An AroQ enzyme not regulated by the aromatic amino acids
-
DOI 10.1128/JB.00441-06
-
Kim S.K., Reddy S.K., Nelson B.C., Vasquez G.B., Davis A., Howard A.J., Patterson S., Gilliland G.L., Ladner J.E., Reddy P.T., (2006) Biochemical and structural characterization of the secreted chorismate mutase (Rv1885c) from Mycobacterium tuberculosis H37Rv: an AroQ enzyme not regulated by the aromatic amino acids. J Bacteriol; 24: 8638-8648. (Pubitemid 44894065)
-
(2006)
Journal of Bacteriology
, vol.188
, Issue.24
, pp. 8638-8648
-
-
Kim, S.-K.1
Reddy, S.K.2
Nelson, B.C.3
Vasquez, G.B.4
Davis, A.5
Howard, A.J.6
Patterson, S.7
Gilliland, G.L.8
Ladner, J.E.9
Reddy, P.T.10
-
6
-
-
67651147947
-
Structure and function of a complex between chorismate mutase and DAHP synthase: Efficiency boost for the junior partner
-
Sasso S., Okvist M., Roderer K., Gamper M., Codoni G., Krengel U., Kast P., (2009) Structure and function of a complex between chorismate mutase and DAHP synthase: efficiency boost for the junior partner. EMBO J; 28: 2128-2142.
-
(2009)
EMBO J
, vol.28
, pp. 2128-2142
-
-
Sasso, S.1
Okvist, M.2
Roderer, K.3
Gamper, M.4
Codoni, G.5
Krengel, U.6
Kast, P.7
-
7
-
-
80055018408
-
Metabolic priming by a secreted fungal effector
-
Djamei A., Schipper K., Rabe F., Ghosh A., Vincon V., Kahnt J., Osorio S., et al,. (2011) Metabolic priming by a secreted fungal effector. Nature; 478: 395.
-
(2011)
Nature
, vol.478
, pp. 395
-
-
Djamei, A.1
Schipper, K.2
Rabe, F.3
Ghosh, A.4
Vincon, V.5
Kahnt, J.6
Osorio, S.7
-
8
-
-
84869808070
-
When inhibitors do not inhibit: Critical evaluation of rational drug design targeting chorismate mutase from Mycobacterium tuberculosis
-
Munack S., Leroux V., Roderer K., Okvist M., van Eerde A., Gundersen L.L., Krengel U., Kast P., (2012) When inhibitors do not inhibit: critical evaluation of rational drug design targeting chorismate mutase from Mycobacterium tuberculosis. Chem Biodivers; 11: 2507-2527.
-
(2012)
Chem Biodivers
, vol.11
, pp. 2507-2527
-
-
Munack, S.1
Leroux, V.2
Roderer, K.3
Okvist, M.4
Van Eerde, A.5
Gundersen, L.L.6
Krengel, U.7
Kast, P.8
-
9
-
-
34247842959
-
Ligand based virtual screening and biological evaluation of inhibitors of chorismate mutase (Rv1885c) from Mycobacterium tuberculosis H37Rv
-
DOI 10.1016/j.bmcl.2007.03.053, PII S0960894X07003447
-
Agrawal H., Kumar A., Bal N.C., Siddiqi M.I., Arora A., (2007) Ligand based virtual screening and biological evaluation of inhibitors of chorismate mutase (Rv1885c) from Mycobacterium tuberculosis H37Rv. Bioorg Med Chem Lett; 17: 3053-3058. (Pubitemid 46702633)
-
(2007)
Bioorganic and Medicinal Chemistry Letters
, vol.17
, Issue.11
, pp. 3053-3058
-
-
Agrawal, H.1
Kumar, A.2
Bal, N.C.3
Siddiqi, M.I.4
Arora, A.5
-
10
-
-
84899018013
-
-
Ph.D. thesis, Aston University, UK.
-
Sikdar S.,. Ph.D. thesis, Aston University, UK, 2010.
-
(2010)
-
-
Sikdar, S.1
-
11
-
-
84864974738
-
C-N bond formation under Cu-catalysis: Synthesis and in vitro evaluation of N-aryl substituted thieno[2,3-d]pyrimidin-4(3H)-ones against chorismate mutase
-
Adepu R., Kumar K.S., Sandra S., Rambabu D., Rama Krishna G., Reddy C.M., Kandale A., Misra P., Pal M., (2012) C-N bond formation under Cu-catalysis: Synthesis and in vitro evaluation of N-aryl substituted thieno[2,3-d]pyrimidin- 4(3H)-ones against chorismate mutase. Bioorg Med Chem; 20: 5127-5138.
-
(2012)
Bioorg Med Chem
, vol.20
, pp. 5127-5138
-
-
Adepu, R.1
Kumar, K.S.2
Sandra, S.3
Rambabu, D.4
Rama Krishna, G.5
Reddy, C.M.6
Kandale, A.7
Misra, P.8
Pal, M.9
-
12
-
-
84857369422
-
3 induced (hetero)arylation of 2,3-dichloroquinoxaline: A one-pot synthesis of mono/disubstituted quinoxalines as potential antitubercular agents
-
3 induced (hetero)arylation of 2,3-dichloroquinoxaline: a one-pot synthesis of mono/disubstituted quinoxalines as potential antitubercular agents. Bioorg Med Chem; 20: 1711-1722.
-
(2012)
Bioorg Med Chem
, vol.20
, pp. 1711-1722
-
-
Kumar, K.S.1
Rambabu, D.2
Sandra, S.3
Kapavarapua, R.4
Krishna, G.R.5
Basaveswara Rao, M.V.6
Chatti, K.7
Reddy, C.M.8
Misra, P.9
Pal, M.10
-
13
-
-
84855645319
-
Cu-mediated N-arylation of 1,2,3-triazin-4-ones: Synthesis of fused triazinone derivatives as potential inhibitors of chorismate mutase
-
Shiva Kumar K., Adepu R., Sandra S., Rambabu D., Rama Krishna G., Malla Reddy C., Misra P., Pal M., (2012) Cu-mediated N-arylation of 1,2,3-triazin-4-ones: synthesis of fused triazinone derivatives as potential inhibitors of chorismate mutase. Bioorg Med Chem Lett; 22: 1146-1150.
-
(2012)
Bioorg Med Chem Lett
, vol.22
, pp. 1146-1150
-
-
Shiva Kumar, K.1
Adepu, R.2
Sandra, S.3
Rambabu, D.4
Rama Krishna, G.5
Malla Reddy, C.6
Misra, P.7
Pal, M.8
-
14
-
-
80054781347
-
A Pd-mediated new strategy to functionalized 2-aminochromenes: Their in vitro evaluation as potential anti tuberculosis agents
-
Ram Reddy T., Srinivasula Reddy L., Rajeshwar Reddy G., Nuthalapatia V.S., Lingappa Y., Sandra S., Kapavarapua R., Misra P., Pal M., (2011) A Pd-mediated new strategy to functionalized 2-aminochromenes: their in vitro evaluation as potential anti tuberculosis agents. Bioorg Med Chem Lett; 21: 6433-6439.
-
(2011)
Bioorg Med Chem Lett
, vol.21
, pp. 6433-6439
-
-
Ram Reddy, T.1
Srinivasula Reddy, L.2
Rajeshwar Reddy, G.3
Nuthalapatia, V.S.4
Lingappa, Y.5
Sandra, S.6
Kapavarapua, R.7
Misra, P.8
Pal, M.9
-
15
-
-
33845377155
-
An inhibitor of chorismate mutase resembling the transition-state conformation
-
Bartlett P.A., Johnson C.R., (1985) An inhibitor of chorismate mutase resembling the transition-state conformation. J Am Chem Soc; 107: 7792-7793.
-
(1985)
J Am Chem Soc
, vol.107
, pp. 7792-7793
-
-
Bartlett, P.A.1
Johnson, C.R.2
-
16
-
-
0000267583
-
Stereochemistry of the rearrangement of chorismate to prephenate: Chorismate mutase involves a chair transition state
-
Sogo S.G., Widlanski T.S., Hoare J.H., Grimshaw C.E., Berchtold G.A., Knowles J.R., (1984) Stereochemistry of the rearrangement of chorismate to prephenate: chorismate mutase involves a chair transition state. J Am Chem Soc; 106: 2701-2703.
-
(1984)
J Am Chem Soc
, vol.106
, pp. 2701-2703
-
-
Sogo, S.G.1
Widlanski, T.S.2
Hoare, J.H.3
Grimshaw, C.E.4
Berchtold, G.A.5
Knowles, J.R.6
-
17
-
-
0031955595
-
A convenient methodology for the N-alkylation of isatin compounds
-
Garden S.J., Torres J.C., da Silva L.E., Pinto A.C., (1998) A convenient methodology for the N-Alkylation of isatin compounds. Syn Comm; 28: 1679-1689. (Pubitemid 28216203)
-
(1998)
Synthetic Communications
, vol.28
, Issue.9
, pp. 1679-1689
-
-
Garden, S.J.1
Torres, J.C.2
Da Silva, L.E.3
Pinto, A.C.4
-
18
-
-
84857766536
-
Rhodanine carboxylic acids as novel inhibitors of histone acetyltransferases
-
Silviya D.F., Suhaib S., Srinivasaraghava K., Wolfgang S., Manfred J., (2012) Rhodanine carboxylic acids as novel inhibitors of histone acetyltransferases. Med Chem Commun; 3: 305-311.
-
(2012)
Med Chem Commun
, vol.3
, pp. 305-311
-
-
Silviya, D.F.1
Suhaib, S.2
Srinivasaraghava, K.3
Wolfgang, S.4
Manfred, J.5
-
19
-
-
0032492942
-
New N- and O-arylations with phenylboronic acids and cupric acetate
-
DOI 10.1016/S0040-4039(98)00503-6, PII S0040403998005036
-
Chan D.M.T., Monaco K.L., Wang R.P., Winter M.P., (1998) New N- and O-arylations with phenylboronic acids and cupric acetate. Tetrahedron Lett; 39: 2933-2936. (Pubitemid 28184063)
-
(1998)
Tetrahedron Letters
, vol.39
, Issue.19
, pp. 2933-2936
-
-
Chan, D.M.T.1
Monaco, K.L.2
Wang, R.-P.3
Winters, M.P.4
-
20
-
-
0032493017
-
New aryl/heteroaryl C-N bond cross-coupling reactions via arylboronic acid/cupric acetate arylation
-
DOI 10.1016/S0040-4039(98)00504-8, PII S0040403998005048
-
Lam P.Y.S., Clark C.G., Saubern S., Adams J., Winters M.P., Chan D.M.T., Combs A., (1998) New aryl/Heteroaryl C-N bond cross-coupling reactions via arylboronic acid/cupric acetate arylation. Tetrahedron Lett; 39: 2941-2944. (Pubitemid 28184065)
-
(1998)
Tetrahedron Letters
, vol.39
, Issue.19
, pp. 2941-2944
-
-
Lam, P.Y.S.1
Clark, C.G.2
Saubern, S.3
Adams, J.4
Winters, M.P.5
Chan, D.M.T.6
Combs, A.7
-
21
-
-
1842683580
-
2-Hydroxycinchoninic acid
-
Jacobs T.L., Winstein S., Linden G.B., Robson J.H., Levy F.E., Seymour D., (1955) 2-Hydroxycinchoninic acid. Org Synth; 3: 456.
-
(1955)
Org Synth
, vol.3
, pp. 456
-
-
Jacobs, T.L.1
Winstein, S.2
Linden, G.B.3
Robson, J.H.4
Levy, F.E.5
Seymour, D.6
-
22
-
-
0141627969
-
Synthesis and evaluation of isatins and thiosemicarbazone derivatives against cruzain, falcipain-2 and rhodesain
-
DOI 10.1016/S0960-894X(03)00756-X
-
Chiyanzu I., Hansell E., Gut J., Rosenthal P.J., McKerrow J.H., Chibale K., (2003) Synthesis and evaluation of isatins and thiosemicarbazone derivatives against cruzain, falcipain-2 and rhodesain. Bioorg Med Chem Lett; 13: 3527-3530. (Pubitemid 37141422)
-
(2003)
Bioorganic and Medicinal Chemistry Letters
, vol.13
, Issue.20
, pp. 3527-3530
-
-
Chiyanzu, I.1
Hansell, E.2
Gut, J.3
Rosenthal, P.J.4
McKerrow, J.H.5
Chibale, K.6
-
23
-
-
24344485653
-
Synthesis and evaluation of anti-HIV activity of isatin β-thiosemicarbazone derivatives
-
DOI 10.1016/j.bmcl.2005.07.046, PII S0960894X05009297
-
Bal T.R., Balasubramani A., Yogeeswari P., Sriram D., (2005) Synthesis and evaluation of anti-HIV activity of isatin beta-thiosemicarbazone derivatives. Bioorg Med Chem Lett; 15: 4451-4455. (Pubitemid 41253873)
-
(2005)
Bioorganic and Medicinal Chemistry Letters
, vol.15
, Issue.20
, pp. 4451-4455
-
-
Bal, T.R.1
Anand, B.2
Yogeeswari, P.3
Sriram, D.4
-
24
-
-
0027455788
-
Isatin oxamines - A novel series of bioavailable non-NMDA antagonists
-
DOI 10.1016/S0960-894X(00)80101-8
-
Frank W., Elsebet O.N., Jergen D., Jensen L.H., (1993) Isatin oximes-A novel series of bioavailable non-NMDA antagonists. Bioorg Med Chem Lett; 3: 105-106. (Pubitemid 23028334)
-
(1993)
Bioorganic and Medicinal Chemistry Letters
, vol.3
, Issue.1
, pp. 105-106
-
-
Watjen, F.1
Nielsen, E.O.2
Drejer, J.3
Jensen, L.H.4
-
25
-
-
1942488330
-
Anticonvulsant activity of Schiff bases of isatin derivatives
-
Verma M., Pandeya S.N., Singh K.N., Stables J.P., (2004) Anticonvulsant activity of Schiff bases of isatin derivatives. Acta Pharm; 54: 49.
-
(2004)
Acta Pharm
, vol.54
, pp. 49
-
-
Verma, M.1
Pandeya, S.N.2
Singh, K.N.3
Stables, J.P.4
-
26
-
-
0025554325
-
New isatin derivatives: Synthesis and reactions
-
Martinez F., Naarmann H., (1990) New isatin derivatives: synthesis and reactions. Synth Met; 39: 195-203.
-
(1990)
Synth Met
, vol.39
, pp. 195-203
-
-
Martinez, F.1
Naarmann, H.2
-
27
-
-
1842740801
-
Palladium-Catalyzed Amination of Aryl Halides: Mechanism and Rational Catalyst Design
-
Hartwig J.F., (1997) Palladium-catalyzed amination of aryl halides: mechanism and rational catalyst design. Synlett; 4: 329-340. (Pubitemid 127498130)
-
(1997)
Synlett
, vol.1997
, Issue.4
, pp. 329-340
-
-
Hartwig, J.F.1
-
28
-
-
0038579438
-
Expanding Pd-catalyzed C-N bond-forming processes: The first amidation of aryl sulfonates, aqueous amination, and complementarity with Cu-catalyzed reactions
-
DOI 10.1021/ja035483w
-
Huang X., Anderson K.W., Zim D., Jiang L., Klapars A., Buchwald S.L., (2003) Expanding Pd-catalyzed C-N bond-forming processes: the first amidation of aryl sulfonates, aqueous amination, and complementarity with Cu-catalyzed reactions. J Am Chem Soc; 125: 6653-6655. (Pubitemid 36667448)
-
(2003)
Journal of the American Chemical Society
, vol.125
, Issue.22
, pp. 6653-6655
-
-
Huang, X.1
Anderson, K.W.2
Zim, D.3
Jiang, L.4
Klapars, A.5
Buchwald, S.L.6
-
29
-
-
0242582867
-
Insights into the Origin of High Activity and Stability of Catalysts Derived from Bulky, Electron-Rich Monophosphinobiaryl Ligands in the Pd-Catalyzed C-N Bond Formation
-
DOI 10.1021/ja037932y
-
Strieter E.R., Blackmond D.G., Buchwald S.L., (2003) Insights into the origin of high activity and stability of catalysts derived from bulky, electron-rich monophosphinobiaryl ligands in the Pd-catalyzed C-N bond formation. J Am Chem Soc; 125: 13978-13980. (Pubitemid 37420901)
-
(2003)
Journal of the American Chemical Society
, vol.125
, Issue.46
, pp. 13978-13980
-
-
Strieter, E.R.1
Blackmond, D.G.2
Buchwald, S.L.3
-
30
-
-
0037140736
-
Pd-catalyzed intermolecular amidation of aryl halides: The discovery that xantphos can be trans-chelating in a palladium complex
-
DOI 10.1021/ja012610k
-
Yin J., Buchwald S.L., (2002) Pd-catalyzed intermolecular amidation of aryl halides: the discovery that xantphos can be trans-chelating in a palladium complex. J Am Chem Soc; 124: 6043-6048. (Pubitemid 34552849)
-
(2002)
Journal of the American Chemical Society
, vol.124
, Issue.21
, pp. 6043-6048
-
-
Yin, J.1
Buchwald, S.L.2
-
31
-
-
0000699370
-
Stereocontrolled total synthesis of (±)-gelsemine
-
Fukuyamaa T., Liu G., (1997) Stereocontrolled total synthesis of (±)-gelsemine. Pure Appl Chem; 69: 501-505.
-
(1997)
Pure Appl Chem
, vol.69
, pp. 501-505
-
-
Fukuyamaa, T.1
Liu, G.2
-
32
-
-
0000841474
-
The chemistry of oxindole
-
Sumpter W.C., (1945) The chemistry of oxindole. Chem Rev; 37: 443-479.
-
(1945)
Chem Rev
, vol.37
, pp. 443-479
-
-
Sumpter, W.C.1
-
33
-
-
0028035237
-
A new efficient and mild synthesis of 2-oxindoles by one-pot Wolff-Kishner like reduction of isatin derivatives
-
Crestini C., Saladino R., (1994) A new efficient and mild synthesis of 2-oxindoles by one-pot Wolff-Kishner like reduction of isatin derivatives. Synth Commun; 24: 2835-2841. (Pubitemid 24329988)
-
(1994)
Synthetic Communications
, vol.24
, Issue.20
, pp. 2835-2841
-
-
Crestini, C.1
Saladino, R.2
-
34
-
-
21744448193
-
c-Src receptor tyrosine kinase with the application of receptor docking studies
-
DOI 10.1016/j.farmac.2005.01.015, PII S0014827X05000893
-
Olgen S., Akaho E., Nebioglu D., (2005) Synthesis and anti-tyrosine kinase activity of 3-(substituted-benzylidene)-1, 3-dihydro-indolin derivatives: investigation of their role against p60c-Src receptor tyrosine kinase with the application of receptor docking studies. Farmaco; 60: 497-506. (Pubitemid 40943388)
-
(2005)
Farmaco
, vol.60
, Issue.6-7
, pp. 497-506
-
-
Olgen, S.1
Akaho, E.2
Nebioglu, D.3
-
35
-
-
0031985277
-
Rapid, low-technology MIC determination with clinical Mycobacterium tuberculosis isolates by using the microplate Alamar Blue assay
-
Franzbalu G.S., Witzig S.R., McLaughlin C.J., Torres P., Madico G., Hernandez A., Degnan T.M., Cook B.M., Quenzer K.V., Ferguson M.R., Gilman H.R., (1998) Rapid, low-technology MIC determination with clinical Mycobacterium tuberculosis isolates by using the microplate Alamar Blue assay. J Clin Microbiol; 36: 362-366. (Pubitemid 28060296)
-
(1998)
Journal of Clinical Microbiology
, vol.36
, Issue.2
, pp. 362-366
-
-
Franzblau, S.G.1
Witzig, R.S.2
Mclaughlin, J.C.3
Torres, P.4
Madico, G.5
Hernandez, A.6
Degnan, M.T.7
Cook, M.B.8
Quenzer, V.K.9
Ferguson, R.M.10
Gilman, R.H.11
-
36
-
-
79952018068
-
A cellular viability assay to monitor drug toxicity
-
Hansen J., Bross P., (2010) A cellular viability assay to monitor drug toxicity. Methods Mol Biol; 648: 303-311.
-
(2010)
Methods Mol Biol
, vol.648
, pp. 303-311
-
-
Hansen, J.1
Bross, P.2
|