-
1
-
-
64849083163
-
Demonstration of Genetic Exchange during Cyclical Development of Leishmania in the Sand Fly Vector
-
Akopyants, N. S.; Kimblin, N.; Secundino, N.; Patrick, R.; Peters, N.; Lawyer, P.; Dobson, D. E.; Beverley, S. M.; Sacks, D. L. Demonstration of Genetic Exchange During Cyclical Development of Leishmania in the Sand Fly Vector Science 2009, 324, 265-268
-
(2009)
Science
, vol.324
, pp. 265-268
-
-
Akopyants, N.S.1
Kimblin, N.2
Secundino, N.3
Patrick, R.4
Peters, N.5
Lawyer, P.6
Dobson, D.E.7
Beverley, S.M.8
Sacks, D.L.9
-
4
-
-
0026615360
-
Stage-specific adhesion of Leishmania promastigotes to the sandfly midgut
-
Pimenta, P. F.; Turco, S. J.; McConville, M. J.; Lawyer, P. G.; Perkins, P. V.; Sacks, D. L. Stage-specific adhesion of Leishmania promastigotes to the sandfly midgut Science 1992, 256, 1812-1815
-
(1992)
Science
, vol.256
, pp. 1812-1815
-
-
Pimenta, P.F.1
Turco, S.J.2
McConville, M.J.3
Lawyer, P.G.4
Perkins, P.V.5
Sacks, D.L.6
-
5
-
-
35548987998
-
Visceral leishmaniasis: What are the needs for diagnosis, treatment and control?
-
Chappuis, F.; Sundar, S.; Hailu, A.; Ghalib, H.; Alvar, J.; Boelaer, M. Visceral leishmaniasis: what are the needs for diagnosis, treatment and control? Nature Rev. Microbiol. 2007, 5, 873-885
-
(2007)
Nature Rev. Microbiol.
, vol.5
, pp. 873-885
-
-
Chappuis, F.1
Sundar, S.2
Hailu, A.3
Ghalib, H.4
Alvar, J.5
Boelaer, M.6
-
6
-
-
0030950966
-
Leishmania and human immunodeficiency virus coinfection: The first 10 years
-
Alvar, J.; Canavate, C.; Gutierrez- Solar, B.; Jimenez, M.; Lagnon, F.; Lopez-Velet, R.; Molina, R.; Moreno, J. Leishmania and human immunodeficiency virus coinfection: the first 10 years Clin. Microbiol. Rev. 1997, 10, 298-319 (Pubitemid 27196673)
-
(1997)
Clinical Microbiology Reviews
, vol.10
, Issue.2
, pp. 298-319
-
-
Alvar, J.1
Canavate, C.2
Gutierrez-Solar, B.3
Jimenez, M.4
Laguna, F.5
Lopez-Velez, R.6
Molina, R.7
Moreno, J.8
-
8
-
-
0029761631
-
Invasion, control and persistence of Leishmania parasites
-
DOI 10.1016/S0952-7915(96)80040-9
-
Bogdon, C.; Gessner, A.; Solbach, W.; Rollinghoff, M. Invasion, control and persistence of Leishmania parasites Curr. Opin. Immunol. 1996, 8, 517-525 (Pubitemid 26280781)
-
(1996)
Current Opinion in Immunology
, vol.8
, Issue.4
, pp. 517-525
-
-
Bogdan, C.1
Gessner, A.2
Werner, S.3
Martin, R.4
-
10
-
-
26044468809
-
Opportunities and challenges in antiparasitic drug discovery
-
DOI 10.1038/nrd1824, PII N1824
-
Pink, R.; Hudson, A.; Mouriès, M. A.; Bendig, M. Opportunities and challenges in antiparasitic drug discovery Nature Rev. Drug Discovery 2005, 4, 727-740 (Pubitemid 43090494)
-
(2005)
Nature Reviews Drug Discovery
, vol.4
, Issue.9
, pp. 727-740
-
-
Pink, R.1
Hudson, A.2
Mouries, M.-A.3
Bendig, M.4
-
11
-
-
66149141810
-
ABLE: A New and Improved Amphotericin B for Visceral Leishmaniasis?
-
Berman, J. ABLE: A New and Improved Amphotericin B for Visceral Leishmaniasis? Am. J. Trop. Med. Hyg. 2009, 8, 689-690
-
(2009)
Am. J. Trop. Med. Hyg.
, vol.8
, pp. 689-690
-
-
Berman, J.1
-
12
-
-
0036319712
-
Visceral leishmaniasis: Current status of control, diagnosis, and treatment, and a proposed research and development agenda
-
DOI 10.1016/S1473-3099(02)00347-X
-
Guerin, P. J.; Olliaro, P.; Sundar, S.; Boelaert, M.; Croft, S. L.; Desjeux, P.; Wasunna, K.; Bryceson, A. D. M. Visceral leishmaniasis: current status of control, diagnosis, and treatment, and a proposed research and development agenda Lancet Infect. Dis. 2002, 2, 494-501 (Pubitemid 34826855)
-
(2002)
Lancet Infectious Diseases
, vol.2
, Issue.8
, pp. 494-501
-
-
Guerin, P.J.1
Olliaro, P.2
Sundar, S.3
Boelaert, M.4
Croft, S.L.5
Desjeux, P.6
Wasunna, M.K.7
Bryceson, A.D.M.8
-
13
-
-
0141518142
-
Characterization of pentamidine excretion in the isolated perfused rat kidney
-
DOI 10.1093/jac/dkg341
-
Poola, N. R.; Kalis, M.; Plakogiannis, F. M.; Taft, D. R. Characterization of pentamidine excretion in the isolated perfused rat kidney J. Antimicrob. Chemother. 2003, 52, 397-404 (Pubitemid 37120718)
-
(2003)
Journal of Antimicrobial Chemotherapy
, vol.52
, Issue.3
, pp. 397-404
-
-
Poola, N.R.1
Kalis, M.2
Plakogiannis, F.M.3
Taft, D.R.4
-
14
-
-
48749114756
-
Pharmacokinetics of Miltefosine in Old World Cutaneous Leishmaniasis Patients
-
Dorlo, T. P. C.; Van Thiel, P. A. M.; Huitema, A. D. R.; Keizer, R. J.; De Vries, H. J. C.; Beijnen, J. H.; De Vries, P. J. Pharmacokinetics of Miltefosine in Old World Cutaneous Leishmaniasis Patients Antimicrob. Agents Chemother. 2008, 52, 2855-2860
-
(2008)
Antimicrob. Agents Chemother.
, vol.52
, pp. 2855-2860
-
-
Dorlo, T.P.C.1
Van Thiel, P.A.M.2
Huitema, A.D.R.3
Keizer, R.J.4
De Vries, H.J.C.5
Beijnen, J.H.6
De Vries, P.J.7
-
15
-
-
33749338420
-
Development of miltefosine as an oral treatment for leishmaniasis
-
Sindermann, H.; Engel, J. Development of miltefosine as an oral treatment for leishmaniasis Trans. R. Soc. Trop. Med. Hyg. 2006, 100 (Suppl 1) S17-S20
-
(2006)
Trans. R. Soc. Trop. Med. Hyg.
, vol.100
, Issue.SUPPL. 1
-
-
Sindermann, H.1
Engel, J.2
-
16
-
-
31544439919
-
Drug resistance in leishmaniasis
-
DOI 10.1128/CMR.19.1.111-126.2006
-
Croft, S. L.; Sundar, S.; Fairlam, A. H. Drug Resistance in Leishmaniasis Clin. Microbiol. Rev. 2006, 111-126 (Pubitemid 43157649)
-
(2006)
Clinical Microbiology Reviews
, vol.19
, Issue.1
, pp. 111-126
-
-
Croft, S.L.1
Sundar, S.2
Fairlamb, A.H.3
-
17
-
-
0034780949
-
Drug resistance in Indian visceral leishmaniasis
-
DOI 10.1046/j.1365-3156.2001.00778.x
-
Sundar, S. Drug resistance in Indian visceral leishmaniasis Trop. Med. Int. Health 2001, 6, 849-854 (Pubitemid 33010870)
-
(2001)
Tropical Medicine and International Health
, vol.6
, Issue.11
, pp. 849-854
-
-
Sundar, S.1
-
18
-
-
72249097281
-
Neglected tropical diseases: Multitarget-directed ligands in the search for novel lead candidates against Trypanosomia and Leishmania
-
Cavalli, A.; Bolognesi, M. L. Neglected tropical diseases: multitarget-directed ligands in the search for novel lead candidates against Trypanosomia and Leishmania J. Med. Chem. 2009, 52, 7339-7359
-
(2009)
J. Med. Chem.
, vol.52
, pp. 7339-7359
-
-
Cavalli, A.1
Bolognesi, M.L.2
-
19
-
-
38949125112
-
Hybrid molecules with a dual mode of action: Dream or reality?
-
Meunier, B. Hybrid molecules with a dual mode of action: dream or reality? Acc. Chem. Res. 2008, 41, 69-77
-
(2008)
Acc. Chem. Res.
, vol.41
, pp. 69-77
-
-
Meunier, B.1
-
20
-
-
46849089254
-
Recent developments in fragment-based drug discovery
-
DOI 10.1021/jm8000373
-
Congreve, M.; Chessari, G.; Tisi, D.; Woodhead, A. J. Recent developments in fragment-based drug discovery J. Med. Chem. 2008, 51, 3661-3680 (Pubitemid 351956496)
-
(2008)
Journal of Medicinal Chemistry
, vol.51
, Issue.13
, pp. 3661-3680
-
-
Congreve, M.1
Chessari, G.2
Tisi, D.3
Woodhead, A.J.4
-
21
-
-
42949160050
-
Natural products as leads to potential drugs: An old process or the new hope for drug discovery?
-
DOI 10.1021/jm0704090
-
Newman, D. J. Natural Products as Leads to Potential Drugs: An Old Process or the New Hope for Drug Discovery? J. Med. Chem. 2008, 51, 2589-2599 (Pubitemid 351620778)
-
(2008)
Journal of Medicinal Chemistry
, vol.51
, Issue.9
, pp. 2589-2599
-
-
Newman, D.J.1
-
22
-
-
0037119336
-
From protein domains to drug candidates - Natural products as guiding principles in the design and synthesis of compound libraries
-
DOI 10.1002/1521-3773(20020816)41: 16<2878::AID-ANIE2878>3.0.CO;2-B
-
Breinbauer, R.; Vetter, I. R.; Waldmann, H. From protein domains to drug candidates-natural products as guiding principles in the design and synthesis of compound libraries Angew. Chem., Int. Ed. 2002, 41, 2878-2890 (Pubitemid 34966550)
-
(2002)
Angewandte Chemie - International Edition
, vol.41
, Issue.16
, pp. 2878-2890
-
-
Breinbauer, R.1
Vetter, I.R.2
Waldmann, H.3
-
23
-
-
79955568244
-
Biology-oriented synthesis of a natural-product inspired oxepane collection yields a small molecule activator of the Wnt-pathway
-
Basu, S.; Ellinger, B.; Rizzo, S.; Deraeve, C.; Schürmann, M.; Preut, H.; Arndt, H.-D.; Waldmann, H. Biology-oriented synthesis of a natural-product inspired oxepane collection yields a small molecule activator of the Wnt-pathway Proc. Natl. Acad. Sci. U. S. A. 2011, 108, 6805-6810
-
(2011)
Proc. Natl. Acad. Sci. U. S. A.
, vol.108
, pp. 6805-6810
-
-
Basu, S.1
Ellinger, B.2
Rizzo, S.3
Deraeve, C.4
Schürmann, M.5
Preut, H.6
Arndt, H.-D.7
Waldmann, H.8
-
24
-
-
0141427680
-
Natural product hybrids as new leads for drug discovery
-
DOI 10.1002/anie.200200553
-
Tietze, L. F.; Bell, H. P.; Chandrasekhar, S. Natural Product Hybrids as New Leads for Drug Discovery Angew. Chem., Int. Ed. 2003, 42, 3996-4028 (Pubitemid 37128010)
-
(2003)
Angewandte Chemie - International Edition
, vol.42
, Issue.34
, pp. 3996-4028
-
-
Tietze, L.F.1
Bell, H.P.2
Chandrasekhar, S.3
-
25
-
-
33750464876
-
Small molecule natural products in the discovery of therapeutic agents: The synthesis connection
-
DOI 10.1021/jo0610053
-
Wilson, R. M.; Danishefsky, S. J. Small molecule natural products in the discovery of therapeutic agents: the synthesis connection J. Org. Chem. 2006, 71, 8329-8351 (Pubitemid 44656020)
-
(2006)
Journal of Organic Chemistry
, vol.71
, Issue.22
, pp. 8329-8351
-
-
Wilson, R.M.1
Danishefsky, S.J.2
-
26
-
-
33748602640
-
The chemistry of recently isolated naturally occurring quinazolinone alkaloids
-
DOI 10.1016/j.tet.2006.07.098, PII S0040402006012373
-
Mhaske, S. B.; Argade, N. P. The chemistry of recently isolated naturally occurring quinazolinone alkaloids Tetrahedron 2006, 62, 9787-9826 (Pubitemid 44376561)
-
(2006)
Tetrahedron
, vol.62
, Issue.42
, pp. 9787-9826
-
-
Mhaske, S.B.1
Argade, N.P.2
-
27
-
-
0142216387
-
Quinoline, quinazoline and acridone alkaloids
-
DOI 10.1039/b208140g
-
Michael, J. P. Quinoline, quinazoline and acridone alkaloids Nat. Prod. Rep. 2003, 20, 476-493 (Pubitemid 37298577)
-
(2003)
Natural Product Reports
, vol.20
, Issue.5
, pp. 476-493
-
-
Michael, J.P.1
-
28
-
-
77952016019
-
Antimicrobial Activity of Tryptanthrins in Escherichia coli
-
Bandekar, P. P.; Roopnarine, K. A.; Parekh, V. J.; Mitchell, T. R.; Novak, M. J.; Sinden, R. R. Antimicrobial Activity of Tryptanthrins in Escherichia coli J. Med. Chem. 2010, 53, 3558-3565
-
(2010)
J. Med. Chem.
, vol.53
, pp. 3558-3565
-
-
Bandekar, P.P.1
Roopnarine, K.A.2
Parekh, V.J.3
Mitchell, T.R.4
Novak, M.J.5
Sinden, R.R.6
-
29
-
-
0036009898
-
Analysis of stereoelectronic properties, mechanism of action and pharmacophore of synthetic indolo[2,1-b]quinazoline-6,12-dione derivatives in relation to antileishmanial activity using quantum chemical, cyclic voltammetry and 3-D-QSAR CATALYST procedures
-
DOI 10.1016/S0968-0896(02)00013-5, PII S0968089602000135
-
Bhattacharjee, A. K.; Skanchy, D. J.; Jennings, B.; Hudson, T. H.; Brendle, J. J.; Werbovetz, K. A. Analysis of stereoelectronic properties, mechanism of action and pharmacophore of synthetic indolo[2,1- b ]quinazoline-6,12-dione derivatives in relation to antileishmanial activity using quantum chemical, cyclic voltammetry and 3-D-QSAR CATALYST procedures Bioorg. Med. Chem. 2002, 10, 1979-1989 (Pubitemid 34286392)
-
(2002)
Bioorganic and Medicinal Chemistry
, vol.10
, Issue.6
, pp. 1979-1989
-
-
Bhattacharjee, A.K.1
Skanchy, D.J.2
Jennings, B.3
Hudson, T.H.4
Brendle, J.J.5
Werbovetz, K.A.6
-
30
-
-
0030002917
-
Comparative study on the vasodilatory effects of three quinazoline alkaloids isolated from Evodia rutaecarpa
-
DOI 10.1021/np960161+
-
Chiou, W.; Liao, J.; Chen, C. Comparative Study on the Vasodilatory Effects of Three Quinazoline Alkaloids Isolated from Evodia rutaecarpa J. Nat. Prod. 1996, 59, 374-378 (Pubitemid 26134394)
-
(1996)
Journal of Natural Products
, vol.59
, Issue.4
, pp. 374-378
-
-
Chiou, W.-F.1
Liao, J.-F.2
Chen, C.-F.3
-
31
-
-
79959613489
-
Recent Advances in the Studies on Luotonins
-
Liang, J. L.; Cha, H. C.; Jahng, Y. Recent Advances in the Studies on Luotonins Molecules 2011, 16, 4861-4883
-
(2011)
Molecules
, vol.16
, pp. 4861-4883
-
-
Liang, J.L.1
Cha, H.C.2
Jahng, Y.3
-
32
-
-
49449111557
-
Brown Asymmetric Synthesis of 2,3-Dihydro-2-arylquinazolin-4-ones: Methodology. Application to a Potent Fluorescent Tubulin Inhibitor with Anticancer Activity
-
Chinigo, G. M.; Paige, M.; Grindrod, S.; Hamel, E.; Dakshanamurthy, S.; Chruszcz, M.; Minor, W.; Brown, M. L. Brown Asymmetric Synthesis of 2,3-Dihydro-2-arylquinazolin-4-ones: Methodology. Application to a Potent Fluorescent Tubulin Inhibitor with Anticancer Activity J. Med. Chem. 2008, 51, 4620-4631
-
(2008)
J. Med. Chem.
, vol.51
, pp. 4620-4631
-
-
Chinigo, G.M.1
Paige, M.2
Grindrod, S.3
Hamel, E.4
Dakshanamurthy, S.5
Chruszcz, M.6
Minor, W.7
Brown, M.L.8
-
33
-
-
84857356050
-
Design and synthesis of novel 7-aminoquinazoline derivatives: Antitumor and anticonvulsant activities
-
El-Azab, A. S.; ElTahir, K. E. H. Design and synthesis of novel 7-aminoquinazoline derivatives: antitumor and anticonvulsant activities Bioorg. Med. Chem. Lett. 2012, 22, 1879-1885
-
(2012)
Bioorg. Med. Chem. Lett.
, vol.22
, pp. 1879-1885
-
-
El-Azab, A.S.1
Eltahir, K.E.H.2
-
34
-
-
84859847666
-
Design, synthesis and anticonvulsant activities of novel 1-(substituted/unsubstituted benzylidene)-4-(4-(6,8-dibromo-2-(methyl/phenyl)-4- oxoquinazolin-3(4 H)-yl)phenyl) semicarbazide derivatives
-
Saravanan, G.; Alagarsamy, V.; Prakash, C. R. Design, synthesis and anticonvulsant activities of novel 1-(substituted/unsubstituted benzylidene)-4-(4-(6,8-dibromo-2-(methyl/phenyl)-4-oxoquinazolin-3(4 H)-yl)phenyl) semicarbazide derivatives Bioorg. Med. Chem. Lett. 2012, 22, 3072-3078
-
(2012)
Bioorg. Med. Chem. Lett.
, vol.22
, pp. 3072-3078
-
-
Saravanan, G.1
Alagarsamy, V.2
Prakash, C.R.3
-
35
-
-
84861602512
-
Design, synthesis and antiviral activity of novel quinazolinones
-
Wang, Z.; Wang, M.; Yao, X.; Li, Y.; Tan, J.; Wang, L.; Qiao, W.; Geng, Y.; Liu, Y.; Wang, Q. Design, synthesis and antiviral activity of novel quinazolinones Eur. J. Med. Chem. 2012, 53, 275-282
-
(2012)
Eur. J. Med. Chem.
, vol.53
, pp. 275-282
-
-
Wang, Z.1
Wang, M.2
Yao, X.3
Li, Y.4
Tan, J.5
Wang, L.6
Qiao, W.7
Geng, Y.8
Liu, Y.9
Wang, Q.10
-
36
-
-
84861583388
-
New quinazolinone-pyrimidine hybrids: Synthesis, anti-inflammatory, and ulcerogenicity studies
-
Abbas, S. E.; Awadallah, F. M.; Ibrahin, N. A.; Said, E. G.; Kamel, G. M. New quinazolinone-pyrimidine hybrids: synthesis, anti-inflammatory, and ulcerogenicity studies Eur. J. Med. Chem. 2012, 53, 141-149
-
(2012)
Eur. J. Med. Chem.
, vol.53
, pp. 141-149
-
-
Abbas, S.E.1
Awadallah, F.M.2
Ibrahin, N.A.3
Said, E.G.4
Kamel, G.M.5
-
37
-
-
77950857463
-
Synthesis, biological evaluation and molecular docking of novel series of spiro[(2 H,3 H)quinazoline-2,10-cyclohexan]-4(1 H)- one derivatives as anti-inflammatory and analgesic agents
-
Amin, K. M.; Kamel, M. M.; Anwar, M. M.; Khedr, M.; Syam, Y. M. Synthesis, biological evaluation and molecular docking of novel series of spiro[(2 H,3 H)quinazoline-2,10-cyclohexan]-4(1 H)- one derivatives as anti-inflammatory and analgesic agents Eur. J. Med. Chem. 2010, 45, 2117-2131
-
(2010)
Eur. J. Med. Chem.
, vol.45
, pp. 2117-2131
-
-
Amin, K.M.1
Kamel, M.M.2
Anwar, M.M.3
Khedr, M.4
Syam, Y.M.5
-
38
-
-
77950520478
-
Non-classical antifolates. Part 2: Synthesis, biological evaluation, and molecular modeling study of some new 2,6-substituted-quinazolin-4-ones
-
Al-Omary, F. A. M.; Abou-zeid, L. A.; Nagi, M. N.; Habib, E. E.; Abdel-Aziz, A. M.; El-Azab, A. S.; Abdel-Hamide, S. G.; Al-Omar, M. A.; Al-Obaid, A. M.; El-Subbagh, H. I. Non-classical antifolates. Part 2: Synthesis, biological evaluation, and molecular modeling study of some new 2,6-substituted-quinazolin-4-ones Bioorg. Med. Chem. Lett. 2010, 18, 2849-2863
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 2849-2863
-
-
Al-Omary, F.A.M.1
Abou-Zeid, L.A.2
Nagi, M.N.3
Habib, E.E.4
Abdel-Aziz, A.M.5
El-Azab, A.S.6
Abdel-Hamide, S.G.7
Al-Omar, M.A.8
Al-Obaid, A.M.9
El-Subbagh, H.I.10
-
39
-
-
79955627409
-
Urea/thiourea derivatives of quinazolinone lysine conjugates: Synthesis and structure-activity relationships of a new series of antimicrobials
-
Suresha, G. P.; Suhas, R.; Kapfo, W.; Gowda, D. C. Urea/thiourea derivatives of quinazolinone lysine conjugates: synthesis and structure-activity relationships of a new series of antimicrobials Eur. J. Med. Chem. 2011, 46, 2530-2540
-
(2011)
Eur. J. Med. Chem.
, vol.46
, pp. 2530-2540
-
-
Suresha, G.P.1
Suhas, R.2
Kapfo, W.3
Gowda, D.C.4
-
40
-
-
77954311987
-
Novel 6,8-dibromo-4(3 H)quinazolinone derivatives of anti-bacterial and anti-fungal activities
-
Mohameda, M. S.; Kamel, M. M.; Kassem, E. M. M.; Abotaleb, N.; AbdEl-moez, S. I.; Ahmeda, M. F. Novel 6,8-dibromo-4(3 H)quinazolinone derivatives of anti-bacterial and anti-fungal activities Eur. J. Med. Chem. 2010, 45, 3311-3319
-
(2010)
Eur. J. Med. Chem.
, vol.45
, pp. 3311-3319
-
-
Mohameda, M.S.1
Kamel, M.M.2
Kassem, E.M.M.3
Abotaleb, N.4
Abdel-Moez, S.I.5
Ahmeda, M.F.6
-
41
-
-
84870986351
-
Mimicking the Intramolecular Hydrogen Bond: Synthesis, Biological Evaluation, and Molecular Modeling of Benzoxazines and Quinazolines as Potential Antimalarial Agents
-
Gemma, S.; Camodeca, C.; Brindisi, M.; Brogi, S.; Kukreja, G.; Kunjir, S.; Gabellieri, E.; Lucantoni, L.; Habluetzel, A.; Taramelli, D.; Basilico, N.; Gualdani, R.; Tadini-Buoninsegni, F.; Bartolommei, G.; Moncelli, M. R.; Martin, R. E.; Summers, R. L.; Lamponi, S.; Savini, L.; Fiorini, I.; Valoti, M.; Novellino, E.; Campiani, G.; Butini, S. Mimicking the Intramolecular Hydrogen Bond: Synthesis, Biological Evaluation, and Molecular Modeling of Benzoxazines and Quinazolines as Potential Antimalarial Agents J. Med. Chem. 2012, 55, 10387-10404
-
(2012)
J. Med. Chem.
, vol.55
, pp. 10387-10404
-
-
Gemma, S.1
Camodeca, C.2
Brindisi, M.3
Brogi, S.4
Kukreja, G.5
Kunjir, S.6
Gabellieri, E.7
Lucantoni, L.8
Habluetzel, A.9
Taramelli, D.10
Basilico, N.11
Gualdani, R.12
Tadini-Buoninsegni, F.13
Bartolommei, G.14
Moncelli, M.R.15
Martin, R.E.16
Summers, R.L.17
Lamponi, S.18
Savini, L.19
Fiorini, I.20
Valoti, M.21
Novellino, E.22
Campiani, G.23
Butini, S.24
more..
-
42
-
-
35348825010
-
Quinazolinone derivatives as orally available ghrelin receptor antagonists for the treatment of diabetes and obesity
-
DOI 10.1021/jm070071+
-
Rudolph, J.; Esler, W. P.; O'Connor, S.; Coish, P. D. G.; Wickens, P. L.; Brands, M.; Bierer, D. E.; Bloomquist, B. T.; Bondar, G.; Chen, L.; Chuang, C.; Claus, T. H.; Fathi, Z.; Fu, W.; Khire, U. R.; Kristie, J. A.; Liu, X.; Lowe, D. B.; McClure, A. C.; Michels, M.; Ortiz, A.; Ramsden, P. D.; Schoenleber, R. W.; Shelekhin, T. E.; Vakalopoulos, A.; Wang, L.; Yi, L.; Gardell, S. J.; Livingston, J. N.; Sweet, L. J.; Bullock, W.; Quinazolinone, H. Derivatives as Orally Available Ghrelin Receptor Antagonists for the Treatment of Diabetes and Obesity J. Med. Chem. 2007, 50, 5202-5216 (Pubitemid 47585718)
-
(2007)
Journal of Medicinal Chemistry
, vol.50
, Issue.21
, pp. 5202-5216
-
-
Rudolph, J.1
Esler, W.P.2
O'Connor, S.3
Coish, P.D.G.4
Wickens, P.L.5
Brands, M.6
Bierer, D.E.7
Bloomquist, B.T.8
Bondar, G.9
Chen, L.10
Chuang, C.-Y.11
Claus, T.H.12
Fathi, Z.13
Fu, W.14
Khire, U.R.15
Kristie, J.A.16
Liu, X.-G.17
Lowe, D.B.18
McClure, A.C.19
Michels, M.20
Ortiz, A.A.21
Ramsden, P.D.22
Schoenleber, R.W.23
Shelekhin, T.E.24
Vakalopoulos, A.25
Tang, W.26
Wang, L.27
Yi, L.28
Gardell, S.J.29
Livingston, J.N.30
Sweet, L.J.31
Bullock, W.H.32
more..
-
43
-
-
80052923470
-
Synthesis and cytotoxicity of 2-phenylquinazolin-4(3 H)-one derivatives
-
Rhee, H.; Yoo, J. H.; Lee, E.; Kwon, Y. J.; Seo, H.; Lee, Y.; Choo, H. P. Synthesis and cytotoxicity of 2-phenylquinazolin-4(3 H)-one derivatives Eur. J. Med. Chem. 2011, 46, 3900-3908
-
(2011)
Eur. J. Med. Chem.
, vol.46
, pp. 3900-3908
-
-
Rhee, H.1
Yoo, J.H.2
Lee, E.3
Kwon, Y.J.4
Seo, H.5
Lee, Y.6
Choo, H.P.7
-
44
-
-
33644856439
-
1 receptor antagonists
-
DOI 10.1021/jm050232e
-
Ismail, M. A. H.; Barker, S.; Abou El Ella, D. A.; Abouzid, K. A. M.; Toubar, R. A.; Todd, M. H. Design and Synthesis of New Tetrazolyl- and Carboxy-biphenylylmethyl-quinazolin-4-one Derivatives as Angiotensin II AT1 Receptor Antagonists J. Med. Chem. 2006, 49, 1526-1535 (Pubitemid 43376500)
-
(2006)
Journal of Medicinal Chemistry
, vol.49
, Issue.5
, pp. 1526-1535
-
-
Ismail, M.A.H.1
Barker, S.2
Abou El Ella, D.A.3
Abouzid, K.A.M.4
Toubar, R.A.5
Todd, M.H.6
-
45
-
-
84856078594
-
Cyanuric chloride catalyzed mild protocol for synthesis of biologically active dihydro/spiro quinazolinones and quinazolinone-glycoconjugates
-
Sharma, M.; Pandey, S.; Chauhan, K.; Sharma, D.; Kumar, B.; Chauhan, P. M. S. Cyanuric chloride catalyzed mild protocol for synthesis of biologically active dihydro/spiro quinazolinones and quinazolinone-glycoconjugates J. Org. Chem. 2012, 77, 929-937
-
(2012)
J. Org. Chem.
, vol.77
, pp. 929-937
-
-
Sharma, M.1
Pandey, S.2
Chauhan, K.3
Sharma, D.4
Kumar, B.5
Chauhan, P.M.S.6
-
46
-
-
33644929014
-
A Pyrimidine-β-carboline and Other Alkaloids from Annona foetida with Antileishmanial Activity
-
Costa, E. V.; Pinheiro, M. L. B.; Xavier, C. M.; Silva, J. R. A.; Amaral, A. F.; Souza, A. D. L.; Barison, A.; Campos, F. R.; Ferreira, A. G.; Machado, G. M. C.; Leon, L. P. L. A Pyrimidine-β-carboline and Other Alkaloids from Annona foetida with Antileishmanial Activity J. Nat. Prod. 2006, 69, 292-294
-
(2006)
J. Nat. Prod.
, vol.69
, pp. 292-294
-
-
Costa, E.V.1
Pinheiro, M.L.B.2
Xavier, C.M.3
Silva, J.R.A.4
Amaral, A.F.5
Souza, A.D.L.6
Barison, A.7
Campos, F.R.8
Ferreira, A.G.9
Machado, G.M.C.10
Leon, L.P.L.11
-
47
-
-
66449124044
-
Synthesis and biological activities of aminopyrimidyl-indoles structurally related to meridianins
-
Akue-Gedu, R.; Debiton, E.; Ferandin, Y.; Meijer, L.; Prudhomme, M.; Anizon, F.; Moreau, P. Synthesis and biological activities of aminopyrimidyl-indoles structurally related to meridianins Bioorg. Med. Chem. 2009, 17, 4420-4424
-
(2009)
Bioorg. Med. Chem.
, vol.17
, pp. 4420-4424
-
-
Akue-Gedu, R.1
Debiton, E.2
Ferandin, Y.3
Meijer, L.4
Prudhomme, M.5
Anizon, F.6
Moreau, P.7
-
48
-
-
77952698314
-
Discovery and Development of a New Class of Leishmaniasis Lead Compounds
-
Sanchez, L. M.; Lopez, D.; Vesely, B. A.; Togna, G. D.; Gerwick, W. H.; Kyle, D. E.; Linington, R. G.; Almiramides, A-C Discovery and Development of a New Class of Leishmaniasis Lead Compounds J. Med. Chem. 2010, 53, 4187-4197
-
(2010)
J. Med. Chem.
, vol.53
, pp. 4187-4197
-
-
Sanchez, L.M.1
Lopez, D.2
Vesely, B.A.3
Togna, G.D.4
Gerwick, W.H.5
Kyle, D.E.6
Linington, R.G.7
Almiramides, A.-C.8
-
49
-
-
60749084392
-
Effectiveness of melarsoprol and eflornithine as first-line regimens for gambiense sleeping sickness in nine Médecins Sans Frontières programmes
-
Balasegaram, M.; Young, H.; Chappuis, F.; Priotto, G.; Raguenaud, M. E.; Checchi, F. Effectiveness of melarsoprol and eflornithine as first-line regimens for gambiense sleeping sickness in nine Médecins Sans Frontières programmes Trans R. Soc. Trop. Med. Hyg. 2009, 103, 280-290
-
(2009)
Trans R. Soc. Trop. Med. Hyg.
, vol.103
, pp. 280-290
-
-
Balasegaram, M.1
Young, H.2
Chappuis, F.3
Priotto, G.4
Raguenaud, M.E.5
Checchi, F.6
-
50
-
-
33750582503
-
Novel Pseudomonas aeruginosa quorum-sensing inhibitors identified in an ultra-high-throughput screen
-
DOI 10.1128/AAC.00665-06
-
Muh, U.; Schuster, M.; Heim, R.; Singh, A.; Olson, E. R.; Greenberg, E. P. Novel Pseudomonas aeruginosa Quorum-Sensing Inhibitors Identified in an Ultra-High-Throughput Screen Antimicrob. Agents Chemother. 2006, 50, 3674-3679 (Pubitemid 44684880)
-
(2006)
Antimicrobial Agents and Chemotherapy
, vol.50
, Issue.11
, pp. 3674-3679
-
-
Muh, U.1
Schuster, M.2
Heim, R.3
Singh, A.4
Olson, E.R.5
Greenberg, E.P.6
-
51
-
-
26944449731
-
Metabolic effect of telmisartan and losartan in hypertensive patients with metabolic syndrome
-
Vitale, C.; Mercuro, G.; Castiglioni, C.; Cornoldi, A.; Tulli, A.; Fini, M.; Volterrani, M.; Rosano, G. M. C. Metabolic effect of telmisartan and losartan in hypertensive patients with metabolic syndrome Cardiovasc. Diabetol. 2005, 4, 6-13
-
(2005)
Cardiovasc. Diabetol.
, vol.4
, pp. 6-13
-
-
Vitale, C.1
Mercuro, G.2
Castiglioni, C.3
Cornoldi, A.4
Tulli, A.5
Fini, M.6
Volterrani, M.7
Rosano, G.M.C.8
-
52
-
-
68149137312
-
Structure-Activity Relationship and Comparative Docking Studies for Cycloguanil Analogs as Pf DHFR-TS Inhibitors
-
Sivaprakasam, P.; Tosso, P. N.; Doerksen, R. J. Structure-Activity Relationship and Comparative Docking Studies for Cycloguanil Analogs as Pf DHFR-TS Inhibitors J. Chem. Inf. Model. 2009, 49, 1787-1796
-
(2009)
J. Chem. Inf. Model.
, vol.49
, pp. 1787-1796
-
-
Sivaprakasam, P.1
Tosso, P.N.2
Doerksen, R.J.3
-
53
-
-
0034074798
-
Interaction of pyrimethamine, cycloguanil, WR99210 and their analogues with Plasmodium falciparum dihydrofolate reductase: Structural basis of antifolate resistance
-
DOI 10.1016/S0968-0896(00)00022-5, PII S0968089600000225
-
Rastelli, G.; Sirawaraporn, W.; Sompornpisut, P.; Vilaivan, T.; Kamchonwongpaisan, S.; Quarrell, R.; Lowe, G.; Thebtaranonth, Y.; Yuthavong, Y. Interactions of pyrimethamine, cycloguanil and WR99210 and their analogues with Plasmodium falciparum dihydrofolate reductase: structural basis for antifolate resistance Bioorg. Med. Chem. 2000, 8, 1117-1128 (Pubitemid 30336406)
-
(2000)
Bioorganic and Medicinal Chemistry
, vol.8
, Issue.5
, pp. 1117-1128
-
-
Rastelli, G.1
Sirawaraporn, W.2
Sompornpisut, P.3
Vilaivan, T.4
Kamchonwongpaisan, S.5
Quarrell, R.6
Lowe, G.7
Thebtaranonth, Y.8
Yuthavong, Y.9
-
54
-
-
33747336783
-
Structurally diverse 5-substituted pyrimidine nucleosides as inhibitors of Leishmania donovani promastigotes in vitro
-
DOI 10.1016/j.bmcl.2006.07.042, PII S0960894X0600816X
-
Torrence, P. F.; Fan, X.; Zhanga, X.; Loiseau, P. M. Structurally diverse 5-substituted pyrimidine nucleosides as inhibitors of Leishmania donovani promastigotes in vitro Bioorg. Med. Chem. Lett. 2006, 16, 5047-5051 (Pubitemid 44247709)
-
(2006)
Bioorganic and Medicinal Chemistry Letters
, vol.16
, Issue.19
, pp. 5047-5051
-
-
Torrence, P.F.1
Fan, X.2
Zhang, X.3
Loiseau, P.M.4
-
55
-
-
57749083122
-
Synthesis and evaluation of 2-pyridyl pyrimidines with in vitro antiplasmodial and antileishmanial activity
-
Musonda, C. C.; Whitlock, G. A.; Witty, M. J.; Brun, R.; Kaiser, M. Synthesis and evaluation of 2-pyridyl pyrimidines with in vitro antiplasmodial and antileishmanial activity Bioorg. Med. Chem. Lett. 2009, 19, 401-405
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 401-405
-
-
Musonda, C.C.1
Whitlock, G.A.2
Witty, M.J.3
Brun, R.4
Kaiser, M.5
-
56
-
-
84861613367
-
2-Anilino-4-(benzimidazol-2-yl)pyrimidines A multikinase inhibitor scaffold with antiproliferative activity toward cancer cell lines
-
Determann, R.; Dreher, J.; Baumann, K.; Preu, L.; Jones, P. G.; Totzke, F.; Schachtele, C.; Kubbutat, M. H. G.; Kunick, C. 2-Anilino-4-(benzimidazol-2- yl)pyrimidines A multikinase inhibitor scaffold with antiproliferative activity toward cancer cell lines Eur. J. Med. Chem. 2012, 53, 254-263
-
(2012)
Eur. J. Med. Chem.
, vol.53
, pp. 254-263
-
-
Determann, R.1
Dreher, J.2
Baumann, K.3
Preu, L.4
Jones, P.G.5
Totzke, F.6
Schachtele, C.7
Kubbutat, M.H.G.8
Kunick, C.9
-
57
-
-
84862294945
-
Structure-Based Design of a Novel Series of Potent, Selective Inhibitors of the Class i Phosphatidylinositol 3-Kinases
-
Smith, A. L.; D'Angelo, N. D.; Bo, Y. Y.; Booker, S. K.; Cee, V. J.; Herberich, B.; Hong, F.; Jackson, C. L. M.; Lanman, B. A.; Liu, L.; Nishimura, N.; Pettus, L. H.; Reed, A. B.; Tadesse, S.; Tamayo, N. A.; Wurz, R. P.; Yang, K.; Andrews, K. L.; Whittington, D. A.; McCarter, J. D.; Miguel, T. S.; Zalameda, L.; Jiang, J.; Subramanian, R.; Mullady, E. L.; Caenepeel, S.; Freeman, D. J.; Wang, L.; Zhang, N.; Wu, T.; Hughes, P. E.; Norman, M. H. Structure-Based Design of a Novel Series of Potent, Selective Inhibitors of the Class I Phosphatidylinositol 3-Kinases J. Med. Chem. 2012, 55, 5188-5219
-
(2012)
J. Med. Chem.
, vol.55
, pp. 5188-5219
-
-
Smith, A.L.1
D'Angelo, N.D.2
Bo, Y.Y.3
Booker, S.K.4
Cee, V.J.5
Herberich, B.6
Hong, F.7
Jackson, C.L.M.8
Lanman, B.A.9
Liu, L.10
Nishimura, N.11
Pettus, L.H.12
Reed, A.B.13
Tadesse, S.14
Tamayo, N.A.15
Wurz, R.P.16
Yang, K.17
Andrews, K.L.18
Whittington, D.A.19
McCarter, J.D.20
Miguel, T.S.21
Zalameda, L.22
Jiang, J.23
Subramanian, R.24
Mullady, E.L.25
Caenepeel, S.26
Freeman, D.J.27
Wang, L.28
Zhang, N.29
Wu, T.30
Hughes, P.E.31
Norman, M.H.32
more..
-
58
-
-
4444288821
-
In vitro cytotoxic activities of 2-alkyl-4,6-diheteroalkyl-1,3,5- triazines: New molecules in anticancer research
-
DOI 10.1021/jm0495374
-
Menicagli, R.; Samaritani, S.; Signore, G.; Vaglini, F.; Via, L. D. In Vitro Cytotoxic Activities of 2-Alkyl-4,6-diheteroalkyl-1,3,5-triazines: New Molecules in Anticancer Research J. Med. Chem. 2004, 47, 4649-4652 (Pubitemid 39195555)
-
(2004)
Journal of Medicinal Chemistry
, vol.47
, Issue.19
, pp. 4649-4652
-
-
Menicagli, R.1
Samaritani, S.2
Signore, G.3
Vaglini, F.4
Dalla Via, L.5
-
59
-
-
79955583128
-
6-disubstituted 1,2-dihydro-1,3,5-triazine-4,6-diamines as potential antimalarials
-
6-disubstituted 1,2-dihydro-1,3,5-triazine-4,6-diamines as potential antimalarials Eur. J. Med. Chem. 2011, 46, 2022-2030
-
(2011)
Eur. J. Med. Chem.
, vol.46
, pp. 2022-2030
-
-
Gravestock, D.1
Rousseau, A.L.2
Lourens, A.C.U.3
Moleele, S.S.4
Zyl, R.L.V.5
Steenkamp, P.A.6
-
60
-
-
80455140518
-
Triazine-Based Vanilloid 1 Receptor Open Channel Blockers: Design, Synthesis, Evaluation, and SAR Analysis
-
Vidal-Mosquera, M.; Fernandez-Carvajal, A.; Moure, A.; Valente, P.; Planells-Cases, R.; Gonzalez-Ros, J. M.; Bujons, J.; Ferrer-Montiel, A.; Messeguer, A. Triazine-Based Vanilloid 1 Receptor Open Channel Blockers: Design, Synthesis, Evaluation, and SAR Analysis J. Med. Chem. 2011, 54, 7441-7452
-
(2011)
J. Med. Chem.
, vol.54
, pp. 7441-7452
-
-
Vidal-Mosquera, M.1
Fernandez-Carvajal, A.2
Moure, A.3
Valente, P.4
Planells-Cases, R.5
Gonzalez-Ros, J.M.6
Bujons, J.7
Ferrer-Montiel, A.8
Messeguer, A.9
-
61
-
-
82255183072
-
Synthesis and evaluation of inhibitors of bacterial drug efflux pumps of the major facilitator superfamily
-
Okandeji, B. O.; Greenwald, D. M.; Wroten, J.; Sello, J. K. Synthesis and evaluation of inhibitors of bacterial drug efflux pumps of the major facilitator superfamily Bioorg. Med. Chem. 2011, 19, 7679-7689
-
(2011)
Bioorg. Med. Chem.
, vol.19
, pp. 7679-7689
-
-
Okandeji, B.O.1
Greenwald, D.M.2
Wroten, J.3
Sello, J.K.4
-
62
-
-
33746047675
-
Discovery of protein phosphatase inhibitor classes by biology-oriented synthesis
-
DOI 10.1073/pnas.0601490103
-
Noren-Muller, A.; Reis-Correa, I., Jr.; Prinz, H.; Rosenbaum, C.; Saxena, K.; Schwalbe, H. J.; Vestweber, D.; Cagna, G.; Schunk, S.; Schwarz, O.; Schiewe, H.; Waldmann, H. Discovery of protein phosphatase inhibitor classes by biology-oriented synthesis Proc. Natl. Acad. Sci. U. S. A. 2006, 103, 10606-10611 (Pubitemid 44078024)
-
(2006)
Proceedings of the National Academy of Sciences of the United States of America
, vol.103
, Issue.28
, pp. 10606-10611
-
-
Noren-Muller, A.1
Reis-Correa Jr., I.2
Prinz, H.3
Rosenbaum, C.4
Saxena, K.5
Schwalbe, H.J.6
Vestweber, D.7
Cagna, G.8
Schunk, S.9
Schwarz, O.10
Schiewe, H.11
Waldmann, H.12
-
63
-
-
77249095085
-
Synthesis and structure-activity relationships of antitubercular 2-nitroimidazooxazines bearing heterocyclic side chains
-
Sutherland, H. S.; Blaser, A.; Kmentova, I.; Franzblau, S. G.; Wan, B.; Wang, Y.; Ma, Z.; Palmer, B. D.; Denny, W. A.; Thompson, A. M. Synthesis and structure-activity relationships of antitubercular 2-nitroimidazooxazines bearing heterocyclic side chains J. Med. Chem. 2010, 53, 855-866
-
(2010)
J. Med. Chem.
, vol.53
, pp. 855-866
-
-
Sutherland, H.S.1
Blaser, A.2
Kmentova, I.3
Franzblau, S.G.4
Wan, B.5
Wang, Y.6
Ma, Z.7
Palmer, B.D.8
Denny, W.A.9
Thompson, A.M.10
-
64
-
-
50249112614
-
3-(1 H -Tetrazol-5-yl)-1,4,5,6-tetrahydro-cyclopentapyrazole (MK-0354): A Partial Agonist of the Nicotinic Acid Receptor, G-Protein Coupled Receptor 109a, with Antilipolytic but No Vasodilatory Activity in Mice
-
Semple, G.; Skinner, P. J.; Gharbaoui, T.; Shin, Y.; Jung, J.; Cherrier, M. C.; Webb, P. J.; Tamura, S. Y.; Boatman, P. D.; Sage, C. R.; Schrader, T. O.; Chen, R.; Colletti, S. L.; Tata, J. R.; Waters, M.; Cheng, K.; Taggart, A. K.; Cai, T.; Carballo-Jane, E.; Behan, D. P.; Connolly, D. T.; Richman, J. G. 3-(1 H -Tetrazol-5-yl)-1,4,5,6-tetrahydro-cyclopentapyrazole (MK-0354): A Partial Agonist of the Nicotinic Acid Receptor, G-Protein Coupled Receptor 109a, with Antilipolytic but No Vasodilatory Activity in Mice J. Med. Chem. 2008, 51, 5101-5108
-
(2008)
J. Med. Chem.
, vol.51
, pp. 5101-5108
-
-
Semple, G.1
Skinner, P.J.2
Gharbaoui, T.3
Shin, Y.4
Jung, J.5
Cherrier, M.C.6
Webb, P.J.7
Tamura, S.Y.8
Boatman, P.D.9
Sage, C.R.10
Schrader, T.O.11
Chen, R.12
Colletti, S.L.13
Tata, J.R.14
Waters, M.15
Cheng, K.16
Taggart, A.K.17
Cai, T.18
Carballo-Jane, E.19
Behan, D.P.20
Connolly, D.T.21
Richman, J.G.22
more..
-
65
-
-
8644263983
-
5-Substituted tetrazoles as bioisosteres of carboxylic acids. Bioisosterism and mechanistic studies on glutathione reductase inhibitors as antimalarials
-
DOI 10.1021/jm0497545
-
Biot, C.; Bauer, H.; Schirmer, R. H.; Davioud-Charvet, E. 5-Substituted Tetrazoles as Bioisosteres of Carboxylic Acids. Bioisosterism and Mechanistic Studies on Glutathione Reductase Inhibitors as Antimalarials J. Med. Chem. 2004, 47, 5972-5983 (Pubitemid 39507339)
-
(2004)
Journal of Medicinal Chemistry
, vol.47
, Issue.24
, pp. 5972-5983
-
-
Biot, C.1
Bauer, H.2
Schirmer, R.H.3
Davioud-Charvet, E.4
-
66
-
-
33847690743
-
The Ugi reaction in the generation of new nucleosides as potential antiviral and antileishmanial agents
-
DOI 10.1016/j.bioorg.2006.08.004, PII S0045206806000629
-
Fan, X.; Zhang, X.; Bories, C.; Loiseau, P. M.; Torrence, P. F. The Ugi reaction in the generation of new nucleosides as potential antiviral and antileishmanial agents Bioorg. Chem. 2007, 35, 121-136 (Pubitemid 46365828)
-
(2007)
Bioorganic Chemistry
, vol.35
, Issue.2
, pp. 121-136
-
-
Fan, X.1
Zhang, X.2
Bories, C.3
Loiseau, P.M.4
Torrence, P.F.5
-
67
-
-
33750090397
-
Synthesis of 2,4,6-trisubstituted pyrimidine and triazine heterocycles as antileishmanial agents
-
DOI 10.1016/j.bmc.2006.08.009, PII S0968089606006559
-
Sunduru, N.; Agarwal, A.; Katiyar, S. B.; Shakya, N.; Goyal, N.; Gupta, S.; Chauhan, P. M. S. Synthesis of 2,4,6 trisubstituted pyrimidine and triazine heterocycles as antileishmanial agents Bioorg. Med. Chem. 2006, 14, 7706-7715 (Pubitemid 44584725)
-
(2006)
Bioorganic and Medicinal Chemistry
, vol.14
, Issue.23
, pp. 7706-7715
-
-
Sunduru, N.1
Agarwal, A.2
Katiyar, S.B.3
Nishi, A.4
Goyal, N.5
Gupta, S.6
Chauhan, P.M.S.7
-
68
-
-
33244494634
-
Syntheses of new substituted triazino tetrahydroisoquinolines and β-carbolines as novel antileishmanial agents
-
DOI 10.1016/j.ejmech.2005.09.007, PII S0223523405002692
-
Kumar, A.; Katiyar, S. B.; Gupta, S.; Chauhan, P. M. S. Syntheses of new substituted triazino tetrahydroisoquinolines and β-carbolines as novel antileishmanial agents Eur. J. Med. Chem. 2006, 41, 106-113 (Pubitemid 43276065)
-
(2006)
European Journal of Medicinal Chemistry
, vol.41
, Issue.1
, pp. 106-113
-
-
Kumar, A.1
Katiyar, S.B.2
Gupta, S.3
Chauhan, P.M.S.4
-
69
-
-
64249139717
-
Synthesis and antileishmanial activity of novel 2,4,6-trisubstituted pyrimidines 1,3,5-triazines
-
Sunduru, N.; Palne, S.; Chauhan, P. M. S.; Gupta, S. Synthesis and antileishmanial activity of novel 2,4,6-trisubstituted pyrimidines 1,3,5-triazines Eur. J. Med. Chem. 2009, 44, 2473-2481
-
(2009)
Eur. J. Med. Chem.
, vol.44
, pp. 2473-2481
-
-
Sunduru, N.1
Palne, S.2
Chauhan, P.M.S.3
Gupta, S.4
-
70
-
-
77950860253
-
Synthesis and biological evaluation of new [1,2,4]triazino[5,6- b ]indol-3-ylthio-1,3,5-triazines and [1,2,4]triazino[5,6- b ]indol-3-ylthio- pyrimidines against Leishmania donovani
-
Gupta, L.; Sunduru, N.; Verma, A.; Srivastava, S.; Gupta, S.; Goyal, N.; Chauhan, P. M. S. Synthesis and biological evaluation of new [1,2,4]triazino[5,6- b ]indol-3-ylthio-1,3,5-triazines and [1,2,4]triazino[5,6- b ]indol-3-ylthio-pyrimidines against Leishmania donovani Eur. J. Med. Chem. 2010, 45, 2359-2365
-
(2010)
Eur. J. Med. Chem.
, vol.45
, pp. 2359-2365
-
-
Gupta, L.1
Sunduru, N.2
Verma, A.3
Srivastava, S.4
Gupta, S.5
Goyal, N.6
Chauhan, P.M.S.7
-
71
-
-
70349643110
-
Discovery of Novel Antileishmanial Agents in an Attempt to Synthesize Pentamidine-Aplysinopsin Hybrid Molecule
-
Porwal, S.; Chauhan, S. S.; Chauhan, P. M. S.; Shakya, N.; Verma, A.; Gupta, S. Discovery of Novel Antileishmanial Agents in an Attempt to Synthesize Pentamidine-Aplysinopsin Hybrid Molecule J. Med. Chem. 2009, 19, 5793-5802
-
(2009)
J. Med. Chem.
, vol.19
, pp. 5793-5802
-
-
Porwal, S.1
Chauhan, S.S.2
Chauhan, P.M.S.3
Shakya, N.4
Verma, A.5
Gupta, S.6
-
72
-
-
84862924718
-
Synthesis of hybrid 4-anilinoquinoline triazines as potent antimalarial agents, their in silico modeling and bioevaluation as Plasmodium falciparum transketolase and β-hematin inhibitors
-
Sharma, M.; Chauhan, K.; Chauhan, S. S.; Kumar, A.; Singh, S. V.; Saxena, J. K.; Agarwal, P.; Srivastava, K.; Kumar, S. R.; Puri, S. K.; Shah, P.; Siddiqi, M. I.; Chauhan, P. M. S. Synthesis of hybrid 4-anilinoquinoline triazines as potent antimalarial agents, their in silico modeling and bioevaluation as Plasmodium falciparum transketolase and β-hematin inhibitors Med. Chem. Commun. 2012, 3, 71-79
-
(2012)
Med. Chem. Commun.
, vol.3
, pp. 71-79
-
-
Sharma, M.1
Chauhan, K.2
Chauhan, S.S.3
Kumar, A.4
Singh, S.V.5
Saxena, J.K.6
Agarwal, P.7
Srivastava, K.8
Kumar, S.R.9
Puri, S.K.10
Shah, P.11
Siddiqi, M.I.12
Chauhan, P.M.S.13
-
73
-
-
62549125426
-
Substituted quinolinyl chalcones and quinolinyl pyrimidines as a new class of anti-infective agents
-
Sharma, M.; Chaturvedi, V.; Manju, Y. K.; Bhatnagar, S.; Srivastava, K.; Puri, S. K.; Chauhan, P. M. S. Substituted quinolinyl chalcones and quinolinyl pyrimidines as a new class of anti-infective agents Eur. J. Med. Chem. 2009, 44, 2081-2091
-
(2009)
Eur. J. Med. Chem.
, vol.44
, pp. 2081-2091
-
-
Sharma, M.1
Chaturvedi, V.2
Manju, Y.K.3
Bhatnagar, S.4
Srivastava, K.5
Puri, S.K.6
Chauhan, P.M.S.7
-
74
-
-
68649086911
-
Synthesis of oxalamide and triazine derivatives as a novel class of hybrid 4-aminoquinoline with potent antiplasmodial activity
-
Sunduru, N.; Sharma, M.; Srivastava, K.; Kumar, S. R.; Puri, S. K.; Saxena, J. K.; Chauhan, P. M. S. Synthesis of oxalamide and triazine derivatives as a novel class of hybrid 4-aminoquinoline with potent antiplasmodial activity Bioorg. Med. Chem. 2009, 17, 6451-6462
-
(2009)
Bioorg. Med. Chem.
, vol.17
, pp. 6451-6462
-
-
Sunduru, N.1
Sharma, M.2
Srivastava, K.3
Kumar, S.R.4
Puri, S.K.5
Saxena, J.K.6
Chauhan, P.M.S.7
-
75
-
-
25844500311
-
Synthesis of 2-[3,5-substituted pyrazol-1-yl]-4,6-trisubstituted triazine derivatives as antimalarial agents
-
DOI 10.1016/j.bmcl.2005.08.023, PII S0960894X05010462
-
Katiyar, S. B.; Srivastava, K.; Puri, S. K.; Chauhan, P. M. S. Synthesis of 2-[3,5-substituted pyrazol-1-yl]-4,6-trisubstituted triazine derivatives as antimalarial agents Bioorg. Med. Chem. Lett. 2005, 15, 4957-4960 (Pubitemid 41400164)
-
(2005)
Bioorganic and Medicinal Chemistry Letters
, vol.15
, Issue.22
, pp. 4957-4960
-
-
Katiyar, S.B.1
Srivastava, K.2
Puri, S.K.3
Chauhan, P.M.S.4
-
76
-
-
56249130079
-
Synthesis and bioevaluation of hybrid 4-aminoquinoline triazines as a new class of antimalarial agents
-
Kumar, A.; Srivastava, K.; Kumar, S. R.; Puri, S. K.; Chauhan, P. M. S. Synthesis and bioevaluation of hybrid 4-aminoquinoline triazines as a new class of antimalarial agents Bioorg. Med. Chem. Lett. 2008, 18, 6530-6533
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 6530-6533
-
-
Kumar, A.1
Srivastava, K.2
Kumar, S.R.3
Puri, S.K.4
Chauhan, P.M.S.5
-
77
-
-
84871022132
-
A natural product inspired hybrid approach towards the synthesis of novel pentamidine based scaffolds as potential anti-parasitic agents
-
Tyagi, V.; Khan, S.; Shivahare, R.; Srivastava, K.; Gupta, S.; Kidwai, S.; Srivastava, K.; Puri, S. K.; Chauhan, P. M. S. A natural product inspired hybrid approach towards the synthesis of novel pentamidine based scaffolds as potential anti-parasitic agents Bioorg. Med. Chem. Lett. 2013, 23, 291-296
-
(2013)
Bioorg. Med. Chem. Lett.
, vol.23
, pp. 291-296
-
-
Tyagi, V.1
Khan, S.2
Shivahare, R.3
Srivastava, K.4
Gupta, S.5
Kidwai, S.6
Srivastava, K.7
Puri, S.K.8
Chauhan, P.M.S.9
-
78
-
-
0034602966
-
Five recombinant fragments of human serum albumin - Tools for the characterization of the warfarin binding site
-
Dockal, M.; Carter, D. C.; Ruker, F. Five recombinant fragments of human serum albumin-tools for the characterization of the warfarin binding site J. Biol. Chem. 2000, 275, 3042-3050
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 3042-3050
-
-
Dockal, M.1
Carter, D.C.2
Ruker, F.3
-
79
-
-
0642309823
-
Fluorescence Studies on the Interactions of Barbaloin with Bovine Serum Albumin
-
Tian, J. N.; Liu, J. Q.; Zhang, J. Y.; Hu, Z. D.; Chen, X. G. Fluorescence Studies on the Interactions of Barbaloin with Bovine Serum Albumin Chem. Pharm. Bull. 2003, 51, 579-582
-
(2003)
Chem. Pharm. Bull.
, vol.51
, pp. 579-582
-
-
Tian, J.N.1
Liu, J.Q.2
Zhang, J.Y.3
Hu, Z.D.4
Chen, X.G.5
-
80
-
-
35948946042
-
Study on the interaction between florasulam and bovine serum albumin
-
DOI 10.1007/s10895-007-0226-9
-
Ran, D. H.; Wu, X.; Zheng, J. H.; Yang, J. H.; Zhou, H. P.; Zhang, M. F.; Tang, Y. J. Study on the interaction between florasulam and bovine serum albumin J. Fluoresc. 2007, 17, 721-726 (Pubitemid 350075691)
-
(2007)
Journal of Fluorescence
, vol.17
, Issue.6
, pp. 721-726
-
-
Ran, D.1
Wu, X.2
Zheng, J.3
Yang, J.4
Zhou, H.5
Zhang, M.6
Tang, Y.7
-
81
-
-
77952951123
-
Hydrophobization of bovine serum albumin with cationic surfactants with different hydrophobic chain length
-
Kun, R.; Kis, L.; Dekany, I. Hydrophobization of bovine serum albumin with cationic surfactants with different hydrophobic chain length Colloids Surf., B 2010, 79, 61-68
-
(2010)
Colloids Surf., B
, vol.79
, pp. 61-68
-
-
Kun, R.1
Kis, L.2
Dekany, I.3
-
82
-
-
77949490963
-
Spectroscopic studies on the interaction and sonodynamic damage of neutral red (NR) to bovine serum albumin (BSA)
-
Liu, B.; Guo, Y.; Wang, J.; Xu, R.; Wang, X.; Wang, D.; Zhang, L. Q.; Xu, Y. N. Spectroscopic studies on the interaction and sonodynamic damage of neutral red (NR) to bovine serum albumin (BSA) J. Lumin. 2010, 130, 1036-1043
-
(2010)
J. Lumin.
, vol.130
, pp. 1036-1043
-
-
Liu, B.1
Guo, Y.2
Wang, J.3
Xu, R.4
Wang, X.5
Wang, D.6
Zhang, L.Q.7
Xu, Y.N.8
-
83
-
-
34548152571
-
Nitroaniline isomers interaction with bovine serum albumin and toxicological implications
-
Xiang, G. H.; Tong, C. L.; Lin, H. Z. Nitroaniline isomers interaction with bovine serum albumin and toxicological implications J. Fluoresc. 2007, 17, 512-521
-
(2007)
J. Fluoresc.
, vol.17
, pp. 512-521
-
-
Xiang, G.H.1
Tong, C.L.2
Lin, H.Z.3
-
84
-
-
84993884851
-
An improved procedure for the preparation of chalcones and related enones
-
Wattanasin, S.; Murphy, W. S. An improved procedure for the preparation of chalcones and related enones Synthesis 1980, 8, 647-650
-
(1980)
Synthesis
, vol.8
, pp. 647-650
-
-
Wattanasin, S.1
Murphy, W.S.2
-
85
-
-
84862175237
-
Chemistry and Biology of Multicomponent Reactions
-
Domling, A.; Wang, W.; Wang, K. Chemistry and Biology of Multicomponent Reactions Chem. Rev. 2012, 112, 3083-3135
-
(2012)
Chem. Rev.
, vol.112
, pp. 3083-3135
-
-
Domling, A.1
Wang, W.2
Wang, K.3
-
86
-
-
33646514430
-
1-Isocyanomethylbenzotriazole and 2,2,4,4-tetramethylbutylisocyanide- cleavable isocyanides useful for the preparation of α-aminomethyl tetrazoles
-
Domling, A.; Beck, B.; Magnin-Lachaux, M. 1-Isocyanomethylbenzotriazole and 2,2,4,4-tetramethylbutylisocyanide-cleavable isocyanides useful for the preparation of α-aminomethyl tetrazoles Tetrahedron Lett. 2006, 47, 4289-4291
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 4289-4291
-
-
Domling, A.1
Beck, B.2
Magnin-Lachaux, M.3
-
87
-
-
34250304234
-
Synthesis of marine alkaloid: 8,9-Dihydrocoscinamide B and its analogues as Novel class of antileishmanial agents
-
DOI 10.1016/j.bmcl.2007.04.035, PII S0960894X07004556
-
Gupta, L.; Talwar, A.; Shakya, N.; Palne, S.; Gupta, S.; Chauhan, P. M. S. Synthesis of marine alkaloid: 8,9-dihydrocoscinamide B and its analogues as novel class of antileishmanial agents Bioorg. Med. Chem. Lett. 2007, 17, 4075-4079 (Pubitemid 46920912)
-
(2007)
Bioorganic and Medicinal Chemistry Letters
, vol.17
, Issue.14
, pp. 4075-4079
-
-
Gupta, L.1
Talwar, A.2
Palne, S.3
Gupta, S.4
Chauhan, P.M.S.5
-
88
-
-
0021061819
-
Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
-
Mosmann, T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays J. Immunol. Methods 1983, 65, 55-63 (Pubitemid 14203433)
-
(1983)
Journal of Immunological Methods
, vol.65
, Issue.1-2
, pp. 55-63
-
-
Mosmann, T.1
-
89
-
-
0023158779
-
Evaluation of a tetrazolium-based semiautomated colorimetric assay: Assessment of radiosensitivity
-
Carmichael, J.; DeGraff, W. G.; Gazdar, A. F.; Minna, J. D.; Mitchel, J. B. Evaluation of a tetrazolium-based semiautomated colorimetrie assay: assessment of radiosensitivity Cancer Res. 1987, 47, 943-946 (Pubitemid 17027906)
-
(1987)
Cancer Research
, vol.47
, Issue.4
, pp. 943-946
-
-
Carmichael, J.1
DeGraff, W.G.2
Gazdar, A.F.3
-
90
-
-
15944401368
-
Efficacy of picroliv in combination with miltefosine, an orally effective antileishmanial drug against experimental visceral leishmaniasis
-
DOI 10.1016/j.actatropica.2004.11.009
-
Gupta, S.; Ramesh; Sharma, S. C.; Srivastava, V. M. L. Efficacy of picroliv combination with miltefosine, an orally effective antileishmanial drug against experimental visceral leishmaniasis Acta Trop. 2005, 94, 41-47 (Pubitemid 40445378)
-
(2005)
Acta Tropica
, vol.94
, Issue.1
, pp. 41-47
-
-
Gupta, S.1
Ramesh2
Sharma, S.C.3
Srivastava, V.M.L.4
-
91
-
-
77952497781
-
Study of the Effect Induced by the Substituents on the Ring-Chain Tautomerism of Schiff Bases Derived from Norephedrine
-
Talancon, D.; Bosque, R.; Lopez, C. Study of the Effect Induced by the Substituents on the Ring-Chain Tautomerism of Schiff Bases Derived from Norephedrine J. Org. Chem. 2010, 75, 3294-3300
-
(2010)
J. Org. Chem.
, vol.75
, pp. 3294-3300
-
-
Talancon, D.1
Bosque, R.2
Lopez, C.3
-
92
-
-
73249120807
-
Enhancement of the Antimalarial Activity of Ciprofloxacin Using a Double Prodrug/Bioorganometallic Approach
-
Dubar, F.; Anquetin, G.; Pradines, B.; Dive, D.; Khalife, J.; Biot, C. Enhancement of the Antimalarial Activity of Ciprofloxacin Using a Double Prodrug/Bioorganometallic Approach J. Med. Chem. 2009, 52, 7954-7957
-
(2009)
J. Med. Chem.
, vol.52
, pp. 7954-7957
-
-
Dubar, F.1
Anquetin, G.2
Pradines, B.3
Dive, D.4
Khalife, J.5
Biot, C.6
-
93
-
-
77952698982
-
Trioxaferroquines as New Hybrid Antimalarial Drugs
-
Bellot, F.; Cosledan, F.; Vendier, L.; Brocard, J.; Meunier, B.; Robert, A. Trioxaferroquines as New Hybrid Antimalarial Drugs J. Med. Chem. 2010, 53, 4103-4109
-
(2010)
J. Med. Chem.
, vol.53
, pp. 4103-4109
-
-
Bellot, F.1
Cosledan, F.2
Vendier, L.3
Brocard, J.4
Meunier, B.5
Robert, A.6
-
95
-
-
0015907980
-
Quenching of fluorescence by oxygen, a probe for structural fluctuations in macromolecules
-
Lakowicz, J. R.; Weber, G. Quenching of fluorescence by oxygen, a probe for structural fluctuations in macromolecules Biochemistry 1973, 12, 4161-4170
-
(1973)
Biochemistry
, vol.12
, pp. 4161-4170
-
-
Lakowicz, J.R.1
Weber, G.2
-
96
-
-
0019593952
-
Fluorescence quenching studies with proteins
-
Maurice, R. E.; Camillo, A. G. Fluorescence quenching studies with proteins Anal. Biochem. 1981, 114, 199-212
-
(1981)
Anal. Biochem.
, vol.114
, pp. 199-212
-
-
Maurice, R.E.1
Camillo, A.G.2
-
97
-
-
84868706832
-
Fluorescence investigation of the interaction of 2-(4-fluorophenyl)-1- phenyl-1 H -phenanthro[9,10- d ]imidazole with bovine serum albumin
-
Jayabharathi, J.; Thanikachalam, V.; Sathishkumar, R.; Jayamoorthy, K. Fluorescence investigation of the interaction of 2-(4-fluorophenyl)-1-phenyl-1 H -phenanthro[9,10- d ]imidazole with bovine serum albumin J. Photochem. Photobiol., B: Biol. 2012, 117, 222-228
-
(2012)
J. Photochem. Photobiol., B: Biol.
, vol.117
, pp. 222-228
-
-
Jayabharathi, J.1
Thanikachalam, V.2
Sathishkumar, R.3
Jayamoorthy, K.4
-
98
-
-
0015230409
-
Solute perturbation of protein fluorescence. the quenching of the tryptophyl fluorescence of model compounds and of lysozyme by iodide ion
-
Lehrer, S. S. Solute perturbation of protein fluorescence. The quenching of the tryptophyl fluorescence of model compounds and of lysozyme by iodide ion Biochemistry 1971, 10, 3254-3263
-
(1971)
Biochemistry
, vol.10
, pp. 3254-3263
-
-
Lehrer, S.S.1
-
99
-
-
34548490073
-
A fluorescence spectroscopic study of the interaction between epristeride and bovin serum albumine and its analytical application
-
DOI 10.1016/j.talanta.2007.04.041, PII S0039914007003153
-
Gong, A.; Zhu, X.; Hu, Y.; Yu, S. A fluorescence spectroscopic study of the interaction between epristeride and bovin serum albumine and its analytical application Talanta 2007, 73, 668-673 (Pubitemid 47379757)
-
(2007)
Talanta
, vol.73
, Issue.4
, pp. 668-673
-
-
Gong, A.1
Zhu, X.2
Hu, Y.3
Yu, S.4
-
100
-
-
0018091195
-
Application of a Akaike's information criterion (AIC) in the evaluation of linear pharmacokinetic equations
-
Yamaoka, K.; Nakagawa, T.; Uno, T. Application of a Akaike's information criterion (AIC) in the evaluation of linear pharmacokinetic equations J. Pharmacokinet. Biopharm. 1978, 6, 65-175
-
(1978)
J. Pharmacokinet. Biopharm.
, vol.6
, pp. 65-175
-
-
Yamaoka, K.1
Nakagawa, T.2
Uno, T.3
-
101
-
-
0027275566
-
Physiological parameters in laboratory animals and humans
-
DOI 10.1023/A:1018943613122
-
Davies, B.; Morris, T. Physiological parameters in laboratory animals and humans Pharm. Res. 1993, 10, 1093-1095 (Pubitemid 23211439)
-
(1993)
Pharmaceutical Research
, vol.10
, Issue.7
, pp. 1093-1095
-
-
Davies, B.1
Morris, T.2
-
102
-
-
24144453551
-
Use of Leishmania donovani field isolates expressing the luciferase reporter gene in in vitro drug screening
-
DOI 10.1128/AAC.49.9.3776-3783.2005
-
Gupta, A. S. R.; Sundar, S.; Goyal, N. Use of Leishmania donovani Field Isolates Expressing the Luciferase Reporter Gene in in Vitro Drug Screening Antimicrob. Agents Chemother. 2005, 49, 3776-3783 (Pubitemid 41233031)
-
(2005)
Antimicrobial Agents and Chemotherapy
, vol.49
, Issue.9
, pp. 3776-3783
-
-
Ashutosh1
Gupta, S.2
Ramesh3
Sundar, S.4
Goyal, N.5
-
103
-
-
0027753162
-
50 in studies of drug resistance of malaria parasites
-
50 in studies of drug resistance of malaria parasites Acta Trop. 1993, 55, 257-261
-
(1993)
Acta Trop.
, vol.55
, pp. 257-261
-
-
Huber, W.1
Koella, J.C.A.2
-
104
-
-
79951521220
-
Fucoidan cures infection with both antimony-susceptible and -resistant strains of Leishmania donovani through Th1 response and macrophage-derived oxidants
-
Kar, S.; Sharma, G.; Das, P. K. Fucoidan cures infection with both antimony-susceptible and -resistant strains of Leishmania donovani through Th1 response and macrophage-derived oxidants J. Antimicrob. Chemother. 2011, 66, 618-625
-
(2011)
J. Antimicrob. Chemother.
, vol.66
, pp. 618
-
-
Kar, S.1
Sharma, G.2
Das, P.K.3
|