-
1
-
-
79953315208
-
Recent advances in the discovery of d -amino acid oxidase inhibitors and their therapeutic utility in schizophrenia
-
Ferraris, D. V.; Tsukamoto, T. Recent advances in the discovery of d -amino acid oxidase inhibitors and their therapeutic utility in schizophrenia Curr. Pharm. Des. 2011, 17, 103-11
-
(2011)
Curr. Pharm. Des.
, vol.17
, pp. 103-111
-
-
Ferraris, D.V.1
Tsukamoto, T.2
-
2
-
-
84877723597
-
D -Amino acid oxidase inhibitors as a novel class of drugs for schizophrenia therapy
-
Sacchi, S.; Rosini, E.; Pollegioni, L.; Molla, G. d -Amino acid oxidase inhibitors as a novel class of drugs for schizophrenia therapy Curr. Pharm. Des 2013, 19, 2499-511
-
(2013)
Curr. Pharm. des
, vol.19
, pp. 2499-2511
-
-
Sacchi, S.1
Rosini, E.2
Pollegioni, L.3
Molla, G.4
-
3
-
-
38149040091
-
In vitro and in vivo pharmacological profile of AS057278, a selective d -amino acid oxidase inhibitor with potential anti-psychotic properties
-
Adage, T.; Trillat, A. C.; Quattropani, A.; Perrin, D.; Cavarec, L.; Shaw, J.; Guerassimenko, O.; Giachetti, C.; Greco, B.; Chumakov, I.; Halazy, S.; Roach, A.; Zaratin, P. In vitro and in vivo pharmacological profile of AS057278, a selective d -amino acid oxidase inhibitor with potential anti-psychotic properties Eur. Neuropsychopharmacol. 2008, 18, 200-14
-
(2008)
Eur. Neuropsychopharmacol.
, vol.18
, pp. 200-214
-
-
Adage, T.1
Trillat, A.C.2
Quattropani, A.3
Perrin, D.4
Cavarec, L.5
Shaw, J.6
Guerassimenko, O.7
Giachetti, C.8
Greco, B.9
Chumakov, I.10
Halazy, S.11
Roach, A.12
Zaratin, P.13
-
5
-
-
44149123806
-
The discovery of fused pyrrole carboxylic acids as novel, potent d -amino acid oxidase (DAO) inhibitors
-
Sparey, T.; Abeywickrema, P.; Almond, S.; Brandon, N.; Byrne, N.; Campbell, A.; Hutson, P. H.; Jacobson, M.; Jones, B.; Munshi, S.; Pascarella, D.; Pike, A.; Prasad, G. S.; Sachs, N.; Sakatis, M.; Sardana, V.; Venkatraman, S.; Young, M. B. The discovery of fused pyrrole carboxylic acids as novel, potent d -amino acid oxidase (DAO) inhibitors Bioorg. Med. Chem. Lett. 2008, 18, 3386-91
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 3386-3391
-
-
Sparey, T.1
Abeywickrema, P.2
Almond, S.3
Brandon, N.4
Byrne, N.5
Campbell, A.6
Hutson, P.H.7
Jacobson, M.8
Jones, B.9
Munshi, S.10
Pascarella, D.11
Pike, A.12
Prasad, G.S.13
Sachs, N.14
Sakatis, M.15
Sardana, V.16
Venkatraman, S.17
Young, M.B.18
-
6
-
-
45749091007
-
Synthesis and biological evaluation of d -amino acid oxidase inhibitors
-
Ferraris, D.; Duvall, B.; Ko, Y. S.; Thomas, A. G.; Rojas, C.; Majer, P.; Hashimoto, K.; Tsukamoto, T. Synthesis and biological evaluation of d -amino acid oxidase inhibitors J. Med. Chem. 2008, 51, 3357-9
-
(2008)
J. Med. Chem.
, vol.51
, pp. 3357-3359
-
-
Ferraris, D.1
Duvall, B.2
Ko, Y.S.3
Thomas, A.G.4
Rojas, C.5
Majer, P.6
Hashimoto, K.7
Tsukamoto, T.8
-
7
-
-
66749135202
-
Discovery, SAR, and pharmacokinetics of a novel 3-hydroxyquinolin-2(1 H)-one series of potent d -amino acid oxidase (DAAO) inhibitors
-
Duplantier, A. J.; Becker, S. L.; Bohanon, M. J.; Borzilleri, K. A.; Chrunyk, B. A.; Downs, J. T.; Hu, L. Y.; El-Kattan, A.; James, L. C.; Liu, S.; Lu, J.; Maklad, N.; Mansour, M. N.; Mente, S.; Piotrowski, M. A.; Sakya, S. M.; Sheehan, S.; Steyn, S. J.; Strick, C. A.; Williams, V. A.; Zhang, L. Discovery, SAR, and pharmacokinetics of a novel 3-hydroxyquinolin-2(1 H)-one series of potent d -amino acid oxidase (DAAO) inhibitors J. Med. Chem. 2009, 52, 3576-85
-
(2009)
J. Med. Chem.
, vol.52
, pp. 3576-3585
-
-
Duplantier, A.J.1
Becker, S.L.2
Bohanon, M.J.3
Borzilleri, K.A.4
Chrunyk, B.A.5
Downs, J.T.6
Hu, L.Y.7
El-Kattan, A.8
James, L.C.9
Liu, S.10
Lu, J.11
Maklad, N.12
Mansour, M.N.13
Mente, S.14
Piotrowski, M.A.15
Sakya, S.M.16
Sheehan, S.17
Steyn, S.J.18
Strick, C.A.19
Williams, V.A.20
Zhang, L.21
more..
-
8
-
-
84867364338
-
Synthesis and SAR of 1-hydroxy-1 H -benzo[ d ]imidazol-2(3 H)-ones as inhibitors of d -amino acid oxidase
-
Berry, J. F.; Ferraris, D. V.; Duvall, B.; Hin, N.; Rais, R.; Alt, J.; Thomas, A. G.; Rojas, C.; Hashimoto, K.; Slusher, B. S.; Tsukamoto, T. Synthesis and SAR of 1-hydroxy-1 H -benzo[ d ]imidazol-2(3 H)-ones as inhibitors of d -amino acid oxidase ACS Med. Chem. Lett. 2012, 3, 839-843
-
(2012)
ACS Med. Chem. Lett.
, vol.3
, pp. 839-843
-
-
Berry, J.F.1
Ferraris, D.V.2
Duvall, B.3
Hin, N.4
Rais, R.5
Alt, J.6
Thomas, A.G.7
Rojas, C.8
Hashimoto, K.9
Slusher, B.S.10
Tsukamoto, T.11
-
9
-
-
84875168268
-
Identification of novel d -amino acid oxidase inhibitors by in silico screening and their functional characterization in vitro
-
Katane, M.; Osaka, N.; Matsuda, S.; Maeda, K.; Kawata, T.; Saitoh, Y.; Sekine, M.; Furuchi, T.; Doi, I.; Hirono, S.; Homma, H. Identification of novel d -amino acid oxidase inhibitors by in silico screening and their functional characterization in vitro J. Med. Chem. 2013, 56, 1894-190
-
(2013)
J. Med. Chem.
, vol.56
, pp. 1894-2190
-
-
Katane, M.1
Osaka, N.2
Matsuda, S.3
Maeda, K.4
Kawata, T.5
Saitoh, Y.6
Sekine, M.7
Furuchi, T.8
Doi, I.9
Hirono, S.10
Homma, H.11
-
10
-
-
84878824151
-
Synthesis of kojic acid derivatives as secondary binding site probes of d -amino acid oxidase
-
Raje, M.; Hin, N.; Duvall, B.; Ferraris, D. V.; Berry, J. F.; Thomas, A. G.; Alt, J.; Rojas, C.; Slusher, B. S.; Tsukamoto, T. Synthesis of kojic acid derivatives as secondary binding site probes of d -amino acid oxidase Bioorg. Med. Chem. Lett. 2013, 23, 3910-3913
-
(2013)
Bioorg. Med. Chem. Lett.
, vol.23
, pp. 3910-3913
-
-
Raje, M.1
Hin, N.2
Duvall, B.3
Ferraris, D.V.4
Berry, J.F.5
Thomas, A.G.6
Alt, J.7
Rojas, C.8
Slusher, B.S.9
Tsukamoto, T.10
-
11
-
-
84877704487
-
4-Hydroxypyridazin-3(2 H)-one derivatives as novel d -amino acid oxidase inhibitors
-
Hondo, T.; Warizaya, M.; Niimi, T.; Namatame, I.; Yamaguchi, T.; Nakanishi, K.; Hamajima, T.; Harada, K.; Sakashita, H.; Matsumoto, Y.; Orita, M.; Takeuchi, M. 4-Hydroxypyridazin-3(2 H)-one derivatives as novel d -amino acid oxidase inhibitors J. Med. Chem. 2013, 56, 3582-92
-
(2013)
J. Med. Chem.
, vol.56
, pp. 3582-3592
-
-
Hondo, T.1
Warizaya, M.2
Niimi, T.3
Namatame, I.4
Yamaguchi, T.5
Nakanishi, K.6
Hamajima, T.7
Harada, K.8
Sakashita, H.9
Matsumoto, Y.10
Orita, M.11
Takeuchi, M.12
-
12
-
-
84877711069
-
Structural, kinetic, and pharmacodynamic mechanisms of d -amino acid oxidase inhibition by small molecules
-
Hopkins, S. C.; Heffernan, M. L.; Saraswat, L. D.; Bowen, C. A.; Melnick, L.; Hardy, L. W.; Orsini, M. A.; Allen, M. S.; Koch, P.; Spear, K. L.; Foglesong, R. J.; Soukri, M.; Chytil, M.; Fang, Q. K.; Jones, S. W.; Varney, M. A.; Panatier, A.; Oliet, S. H.; Pollegioni, L.; Piubelli, L.; Molla, G.; Nardini, M.; Large, T. H. Structural, kinetic, and pharmacodynamic mechanisms of d -amino acid oxidase inhibition by small molecules J. Med. Chem. 2013, 56, 3710-24
-
(2013)
J. Med. Chem.
, vol.56
, pp. 3710-3724
-
-
Hopkins, S.C.1
Heffernan, M.L.2
Saraswat, L.D.3
Bowen, C.A.4
Melnick, L.5
Hardy, L.W.6
Orsini, M.A.7
Allen, M.S.8
Koch, P.9
Spear, K.L.10
Foglesong, R.J.11
Soukri, M.12
Chytil, M.13
Fang, Q.K.14
Jones, S.W.15
Varney, M.A.16
Panatier, A.17
Oliet, S.H.18
Pollegioni, L.19
Piubelli, L.20
Molla, G.21
Nardini, M.22
Large, T.H.23
more..
-
13
-
-
80053201454
-
Biophysical and physicochemical methods differentiate highly ligan d -efficient human d -amino acid oxidase inhibitors
-
Lange, J. H.; Venhorst, J.; van Dongen, M. J.; Frankena, J.; Bassissi, F.; de Bruin, N. M.; Besten, C.; de Beer, S. B.; Oostenbrink, C.; Markova, N.; Kruse, C. G. Biophysical and physicochemical methods differentiate highly ligan d -efficient human d -amino acid oxidase inhibitors Eur. J. Med. Chem. 2011, 46, 4808-19
-
(2011)
Eur. J. Med. Chem.
, vol.46
, pp. 4808-4819
-
-
Lange, J.H.1
Venhorst, J.2
Van Dongen, M.J.3
Frankena, J.4
Bassissi, F.5
De Bruin, N.M.6
Besten, C.7
De Beer, S.B.8
Oostenbrink, C.9
Markova, N.10
Kruse, C.G.11
-
14
-
-
84867373455
-
Pharmacokinetics of oral d -serine in d -amino acid oxidase knockout mice
-
Rais, R.; Thomas, A. G.; Wozniak, K.; Wu, Y.; Jaaro-Peled, H.; Sawa, A.; Strick, C. A.; Engle, S. J.; Brandon, N. J.; Rojas, C.; Slusher, B. S.; Tsukamoto, T. Pharmacokinetics of oral d -serine in d -amino acid oxidase knockout mice Drug Metab. Dispos. 2012, 40, 2067-2073
-
(2012)
Drug Metab. Dispos.
, vol.40
, pp. 2067-2073
-
-
Rais, R.1
Thomas, A.G.2
Wozniak, K.3
Wu, Y.4
Jaaro-Peled, H.5
Sawa, A.6
Strick, C.A.7
Engle, S.J.8
Brandon, N.J.9
Rojas, C.10
Slusher, B.S.11
Tsukamoto, T.12
-
15
-
-
84904040568
-
Strategies for the modulation of phase II metabolism in a series of PKCepsilon inhibitors
-
Clemens, J. J.; Coon, T.; Busch, B. B.; Asgian, J. L.; Hudson, S.; Termin, A.; Flores, T. B.; Tran, D.; Chiang, P.; Sperry, S.; Gross, R.; Abt, J.; Heim, R.; Lechner, S.; Twin, H.; Studley, J.; Brenchley, G.; Collier, P. N.; Pierard, F.; Miller, A.; Mak, C.; Dvornikovs, V.; Jimenez, J. M.; Stamos, D. Strategies for the modulation of phase II metabolism in a series of PKCepsilon inhibitors Bioorg. Med. Chem. Lett. 2014, 24, 3398-402
-
(2014)
Bioorg. Med. Chem. Lett.
, vol.24
, pp. 3398-3402
-
-
Clemens, J.J.1
Coon, T.2
Busch, B.B.3
Asgian, J.L.4
Hudson, S.5
Termin, A.6
Flores, T.B.7
Tran, D.8
Chiang, P.9
Sperry, S.10
Gross, R.11
Abt, J.12
Heim, R.13
Lechner, S.14
Twin, H.15
Studley, J.16
Brenchley, G.17
Collier, P.N.18
Pierard, F.19
Miller, A.20
Mak, C.21
Dvornikovs, V.22
Jimenez, J.M.23
Stamos, D.24
more..
-
16
-
-
84927606596
-
-
Compound 10 was dosed either intravenously (10 mg/kg) or orally (30 mg/kg) to male CD1 mice (6-8 weeks old), and blood samples were obtained via cardiac puncture at 0.08, 0.25, 0.5, 1, 2, 3 (p.o. only), 4 (i.v. only), and 6 h (p.o. only) post dose (n = 3 per time point). Plasma samples were analyzed for levels of compound 10 by LC/MS/MS. The pharmacokinetic parameters were determined using, version 5.0.1; Pharsight Inc. Mountain View, CA
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Compound 10 was dosed either intravenously (10 mg/kg) or orally (30 mg/kg) to male CD1 mice (6-8 weeks old), and blood samples were obtained via cardiac puncture at 0.08, 0.25, 0.5, 1, 2, 3 (p.o. only), 4 (i.v. only), and 6 h (p.o. only) post dose (n = 3 per time point). Plasma samples were analyzed for levels of compound 10 by LC/MS/MS. The pharmacokinetic parameters were determined using WinNonlin, version 5.0.1; Pharsight Inc.: Mountain View, CA.
-
WinNonlin
-
-
-
17
-
-
0030727396
-
Glucuronidation of entacapone, nitecapone, tolcapone, and some other nitrocatechols by rat liver microsomes
-
Lautala, P.; Kivimaa, M.; Salomies, H.; Elovaara, E.; Taskinen, J. Glucuronidation of entacapone, nitecapone, tolcapone, and some other nitrocatechols by rat liver microsomes Pharm. Res. 1997, 14, 1444-8
-
(1997)
Pharm. Res.
, vol.14
, pp. 1444-1448
-
-
Lautala, P.1
Kivimaa, M.2
Salomies, H.3
Elovaara, E.4
Taskinen, J.5
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