-
1
-
-
84860494689
-
Synthesis, biological evaluation and X-ray crystallographic studies of imidazo[ 1,2-a]pyridine-based Mycobacterium tuberculosis glutamine synthetase inhibitors
-
Nordqvist, A.; Nilsson, M.T.; Lagerlund, O.; Muthas, D.; Gising, J.; Yahiaoui, S.; Odell, L.R.; Srinivasa, B.R.; Larhed, M.; Mowbray, S.L.; et al. Synthesis, biological evaluation and X-ray crystallographic studies of imidazo[1,2-a]pyridine-based Mycobacterium tuberculosis glutamine synthetase inhibitors. Med. Chem. Commun. 2012, 3, 620-626.
-
(2012)
Med. Chem. Commun.
, vol.3
, pp. 620-626
-
-
Nordqvist, A.1
Nilsson, M.T.2
Lagerlund, O.3
Muthas, D.4
Gising, J.5
Yahiaoui, S.6
Odell, L.R.7
Srinivasa, B.R.8
Larhed, M.9
Mowbray, S.L.10
-
2
-
-
79960004985
-
Imidazo[ 1,2-a]pyridin-3-amines as potential HIV-1 non-nucleoside reverse transcriptase inhibitors
-
Bode, M.L.; Gravestock, D.; Moleele, S.S.; van der Westhuyzen, C.W.; Pelly, S.C.; Steenkamp, P.A.; Hoppe, H.C.; Khan, T.; Nkabinde, L.A. Imidazo[1,2-a]pyridin-3-amines as potential HIV-1 non-nucleoside reverse transcriptase inhibitors. Bioorg. Med. Chem. 2011, 19, 4227-4237.
-
(2011)
Bioorg. Med. Chem.
, vol.19
, pp. 4227-4237
-
-
Bode, M.L.1
Gravestock, D.2
Moleele, S.S.3
Van Der Westhuyzen, C.W.4
Pelly, S.C.5
Steenkamp, P.A.6
Hoppe, H.C.7
Khan, T.8
Nkabinde, L.A.9
-
3
-
-
84857361838
-
SAR-study on a new class of imidazo[ 1,2-a]pyridinebased inhibitors of 5-lipoxygenase
-
Hieke, M.; Rödl, C.B.; Wisniewska, J.M.; la Buscato, E.; Stark, H.; Schubert-Zsilavecz, M.; Steinhilber, D.; Hofmann, B.; Proschak, E. SAR-study on a new class of imidazo[1,2-a]pyridinebased inhibitors of 5-lipoxygenase. Bioorg. Med. Chem. Lett. 2012, 22, 1969-1975.
-
(2012)
Bioorg. Med. Chem. Lett.
, vol.22
, pp. 1969-1975
-
-
Hieke, M.1
Rödl, C.B.2
Wisniewska, J.M.3
La Buscato, E.4
Stark, H.5
Schubert-Zsilavecz, M.6
Steinhilber, D.7
Hofmann, B.8
Proschak, E.9
-
4
-
-
80052951745
-
6-Substituted imidazo[ 1,2-a]pyridines: Synthesis and biological activity against colon cancer cell lines HT-29 and Caco-2
-
Dahan-Farkas, N.; Langley, C.; Rousseau, A.L.; Yadav, D.B.; Davids, H.; de Koning, C.B. 6-Substituted imidazo[1,2-a]pyridines: Synthesis and biological activity against colon cancer cell lines HT-29 and Caco-2. Eur. J. Med. Chem. 2011, 46, 4573-4583.
-
(2011)
Eur. J. Med. Chem.
, vol.46
, pp. 4573-4583
-
-
Dahan-Farkas, N.1
Langley, C.2
Rousseau, A.L.3
Yadav, D.B.4
Davids, H.5
De Koning, C.B.6
-
5
-
-
80051689495
-
Pd-catalyzed regiocontrolled Sonogashira and Suzuki cross-coupling reaction of 3,6-dihalogenoimidazo[1,2-a]pyridines: One-pot double-coupling approach
-
El Akkaoui, A.; Bassoude, I.; Koubachi, J.; Berteina-Raboin, S.; Mouaddib, A.; Guillaumet, G. Pd-catalyzed regiocontrolled Sonogashira and Suzuki cross-coupling reaction of 3,6-dihalogenoimidazo[1,2-a]pyridines: One-pot double-coupling approach. Tetrahedron 2011, 67, 7128-7138.
-
(2011)
Tetrahedron
, vol.67
, pp. 7128-7138
-
-
El Akkaoui, A.1
Bassoude, I.2
Koubachi, J.3
Berteina-Raboin, S.4
Mouaddib, A.5
Guillaumet, G.6
-
6
-
-
38349085981
-
Microwave assisted double Suzuki-Miyaura cross-coupling in the 6, 8-dibromoimidazo[ 1,2-a]pyridine series
-
Szabo, R.; Crozet, M.D.; Vanelle, P. Microwave assisted double Suzuki-Miyaura cross-coupling in the 6,8-dibromoimidazo[1,2-a]pyridine series. Synthesis 2008, 1, 127-135.
-
(2008)
Synthesis
, vol.1
, pp. 127-135
-
-
Szabo, R.1
Crozet, M.D.2
Vanelle, P.3
-
7
-
-
84856876627
-
Diverse heterocyclic scaffolds as allosteric inhibitors of akt
-
Kettle, J.G.; Brown, S.; Crafter, C.; Davies, B.R.; Dudley, P.; Fairley, G.; Faulder, P.; Fillery, S.; Greenwood, H.; Hawkins, J.; et al. Diverse Heterocyclic Scaffolds as Allosteric Inhibitors of AKT. J. Med. Chem. 2012, 55, 1261-1273.
-
(2012)
J. Med. Chem.
, vol.55
, pp. 1261-1273
-
-
Kettle, J.G.1
Brown, S.2
Crafter, C.3
Davies, B.R.4
Dudley, P.5
Fairley, G.6
Faulder, P.7
Fillery, S.8
Greenwood, H.9
Hawkins, J.10
-
8
-
-
84858735001
-
Imidazo[ 1,2-a]pyridines: Orally active positive allosteric modulators of the metabotropic glutamate 2 receptor
-
Trabanco, A.A.; Tresadern, G.; Macdonald, G.J.; Vega, J.A.; de Lucas, A.I.; Matesanz, E.; Garcia, A.; Linares, M.L.; Alonso de Diego, S.A.; Alonso, J.M.; et al. Imidazo[1,2-a]pyridines: Orally Active Positive Allosteric Modulators of the Metabotropic Glutamate 2 Receptor. J. Med. Chem. 2012, 55, 2688-2701.
-
(2012)
J. Med. Chem.
, vol.55
, pp. 2688-2701
-
-
Trabanco, A.A.1
Tresadern, G.2
MacDonald, G.J.3
Vega, J.A.4
De Lucas, A.I.5
Matesanz, E.6
Garcia, A.7
Linares, M.L.8
Alonso De Diego, S.A.9
Alonso, J.M.10
-
9
-
-
72149094340
-
Scaffold hopping from pyridones to imidazo[ 1,2-a]pyridines. New positive allosteric modulators of metabotropic glutamate 2 receptor
-
Tresadern, G.; Cid, J.M.; Macdonald, G.J.; Vega, J.A.; de Lucas, A.I.; Garcia, A.; Matesanz, E.; Linares, M.L.; Oehlrich, D.; Lavreysen, H.; et al. Scaffold hopping from pyridones to imidazo[1,2-a]pyridines. New positive allosteric modulators of metabotropic glutamate 2 receptor. Bioorg. Med. Chem. Lett. 2010, 20, 175-179.
-
(2010)
Bioorg. Med. Chem. Lett.
, vol.20
, pp. 175-179
-
-
Tresadern, G.1
Cid, J.M.2
MacDonald, G.J.3
Vega, J.A.4
De Lucas, A.I.5
Garcia, A.6
Matesanz, E.7
Linares, M.L.8
Oehlrich, D.9
Lavreysen, H.10
-
12
-
-
0034613119
-
Reactivity of 3-iodoimidazo[ 1,2-a]pyridines using a Suzuki-Type cross-coupling reaction
-
Enguehard, C.; Renou, J.-L.; Collot, V.; Hervet, M.; Rault, S.; Gueiffier, A. Reactivity of 3-iodoimidazo[1,2-a]pyridines using a Suzuki-Type cross-coupling reaction. J. Org. Chem. 2000, 65, 6572-6575.
-
(2000)
J. Org. Chem.
, vol.65
, pp. 6572-6575
-
-
Enguehard, C.1
Renou, J.-L.2
Collot, V.3
Hervet, M.4
Rault, S.5
Gueiffier, A.6
-
13
-
-
0035695091
-
(Hetero)arylation of 6-helogenoimidazo[12-a]pyridines differently substituted at C2): Influence of the 2-substituent on the Suzuki cross-coupling reaction
-
Enguehard, C.; Hervet, M.; Théry, I.; Renou, J.-L.; Fauvelle, F.; Gueiffier, A. (Hetero)arylation of 6-helogenoimidazo[1,2-a]pyridines differently substituted at C(2): Influence of the 2-substituent on the Suzuki cross-coupling reaction. Helv. Chim. Acta 2001, 84, 3610-3615.
-
(2001)
Helv. Chim. Acta
, Issue.84
, pp. 3610-3615
-
-
Enguehard, C.1
Hervet, M.2
Théry, I.3
Renou, J.-L.4
Fauvelle, F.5
Gueiffier, A.6
-
14
-
-
84866886801
-
Imidazopyrimidine and imidazopyridine derivatives as inhibitors of the pi3k/akt pathway and their preparation and use for the treatment of diseases
-
Ince, S.; Haegebarth, A.; Politz, O.; Neuhaus, R.; Bömer, U.; Scott, W. Imidazopyrimidine and Imidazopyridine Derivatives As Inhibitors of the PI3K/Akt Pathway and Their Preparation and Use for the Treatment of Diseases. PCT Int. Appl. WO 2012007345, 2012.
-
(2012)
PCT Int. Appl. WO 2012007345
-
-
Ince, S.1
Haegebarth, A.2
Politz, O.3
Neuhaus, R.4
Bömer, U.5
Scott, W.6
-
15
-
-
81255173173
-
Deprotonative metalation of chloroand bromopyridines using amido-based bimetallic species and regioselectivity-computed CH acidity relationships
-
Snégaroff, K.; Nguyen, T.T.; Marquise, N.; Halauko, Y.S.; Harford, P.J.; Roisnel, T.; Matulis, V.E.; Ivashkevich, O.A.; Chevallier, F.; Wheatley, A.E.H.; et al. Deprotonative metalation of chloroand bromopyridines using amido-based bimetallic species and regioselectivity-computed CH acidity relationships. Chem. Eur. J. 2011, 17, 13284-13297.
-
(2011)
Chem. Eur. J.
, vol.17
, pp. 13284-13297
-
-
Snégaroff, K.1
Nguyen, T.T.2
Marquise, N.3
Halauko, Y.S.4
Harford, P.J.5
Roisnel, T.6
Matulis, V.E.7
Ivashkevich, O.A.8
Chevallier, F.9
Wheatley, A.E.H.10
-
16
-
-
77951143988
-
Discovery of novel 6,6-heterocycles as transient receptor potential vanilloid (TRPV1) antagonists
-
Blum, C.A.; Caldwell, T.; Zheng, X.; Bakthavatchalam, R.; Capistoti, S.; Brielmann, H.; de Lombaert, S.; Kershaw, M.T.; Matson, D.; Krause, J.E.; et al. Discovery of novel 6,6-heterocycles as transient receptor potential vanilloid (TRPV1) antagonists. J. Med. Chem. 2010, 53, 3330-3348.
-
(2010)
J. Med. Chem.
, vol.53
, pp. 3330-3348
-
-
Blum, C.A.1
Caldwell, T.2
Zheng, X.3
Bakthavatchalam, R.4
Capistoti, S.5
Brielmann, H.6
De Lombaert, S.7
Kershaw, M.T.8
Matson, D.9
Krause, J.E.10
-
17
-
-
64349106088
-
Discovery of N-(4-(2-amino-3-chloropyridin-4- yloxy)-3-fluorophenyl)-4- ethoxy-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxamide (BMS-777607), a selective and orally efficacious inhibitor of the Met Kinase Superfamily
-
Schroeder, G.M.; An, Y.; Cai, Z.-W.; Chen, X.-T.; Clark, C.; Cornelius, L.A.M.; Dai, J.; Gullo-Brown, J.; Gupta, A.; Henley, B.; et al. Discovery of N-(4-(2-amino-3-chloropyridin-4- yloxy)-3-fluorophenyl)-4-ethoxy-1-(4- fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxamide (BMS-777607), a selective and orally efficacious inhibitor of the Met Kinase Superfamily. J. Med. Chem. 2009, 52, 1251-1254.
-
(2009)
J. Med. Chem.
, vol.52
, pp. 1251-1254
-
-
Schroeder, G.M.1
An, Y.2
Cai, Z.-W.3
Chen, X.-T.4
Clark, C.5
Cornelius, L.A.M.6
Dai, J.7
Gullo-Brown, J.8
Gupta, A.9
Henley, B.10
|