-
1
-
-
0042433479
-
The cholinergic hypothesis of age and Alzheimer's disease-related cognitive deficits: Recent challenges and their implications for novel drug development
-
A.V. Terry, J.J. Buccafusco, The cholinergic hypothesis of age and Alzheimer's disease-related cognitive deficits: recent challenges and their implications for novel drug development, J. Pharmacol. Exp. Ther. 306 (2003) 821-827.
-
(2003)
J. Pharmacol. Exp. Ther.
, vol.306
, pp. 821-827
-
-
Terry, A.V.1
Buccafusco, J.J.2
-
2
-
-
79954582437
-
Revisiting the cholinergic hypothesis in the development of Alzheimer's disease
-
L.A. Craig, N.S. Hong, R.J. McDonald, Revisiting the cholinergic hypothesis in the development of Alzheimer's disease, Neurosci. Biobehav. Rev. 35 (2011) 1397-1409.
-
(2011)
Neurosci. Biobehav. Rev.
, vol.35
, pp. 1397-1409
-
-
Craig, L.A.1
Hong, N.S.2
McDonald, R.J.3
-
3
-
-
84858195896
-
New pharmacological strategies for treatment of Alzheimer's disease: Focus on disease modifying drugs
-
S. Salomone, F. Caraci, G.M. Leggio, J. Fedotova, F. Drago, New pharmacological strategies for treatment of Alzheimer's disease: focus on disease modifying drugs, Br. J. Clin. Pharmacol. 73 (2012) 504-517.
-
(2012)
Br. J. Clin. Pharmacol.
, vol.73
, pp. 504-517
-
-
Salomone, S.1
Caraci, F.2
Leggio, G.M.3
Fedotova, J.4
Drago, F.5
-
4
-
-
79959370222
-
Disease-modifying treatments for Alzheimer's disease
-
D. Galimberti, E. Scarpini, Disease-modifying treatments for Alzheimer's disease, Ther. Adv. Neurol. Disord. 4 (2011) 203-216.
-
(2011)
Ther. Adv. Neurol. Disord.
, vol.4
, pp. 203-216
-
-
Galimberti, D.1
Scarpini, E.2
-
5
-
-
77951776829
-
Alzheimer's disease: Strategies for disease modification
-
M. Citron, Alzheimer's disease: strategies for disease modification, Nat. Rev. Drug Discov. 9 (2010) 387-398.
-
(2010)
Nat. Rev. Drug Discov.
, vol.9
, pp. 387-398
-
-
Citron, M.1
-
6
-
-
25844505550
-
One-compound-multiple-targets strategy to combat Alzheimer's disease
-
H.Y. Zhang, One-compound-multiple-targets strategy to combat Alzheimer's disease, FEBS Lett. 579 (2005) 5260-5264.
-
(2005)
FEBS Lett.
, vol.579
, pp. 5260-5264
-
-
Zhang, H.Y.1
-
7
-
-
12344328416
-
Rational approach to discover multipotent anti-Alzheimer drugs
-
M. Rosini, V. Andrisano, M. Bartolini, M.L. Bolognesi, P. Hrelia, A. Minarini, A. Tarozzi, C. Melchiorre, Rational approach to discover multipotent anti-Alzheimer drugs, J. Med. Chem. 48 (2005) 360-363.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 360-363
-
-
Rosini, M.1
Andrisano, V.2
Bartolini, M.3
Bolognesi, M.L.4
Hrelia, P.5
Minarini, A.6
Tarozzi, A.7
Melchiorre, C.8
-
8
-
-
84908375105
-
Multitarget drug design strategy: QuinoneeTacrine hybrids designed to block amyloid-b aggregation and to exert anticholinesterase and antioxidant effects
-
E. Nepovimova, E. Uliassi, J. Korabecny, L.E. Peña-Altamira, S. Samez, A. Pesaresi, G.E. Garcia, M. Bartolini, V. Andrisano, et al., Multitarget drug design strategy: QuinoneeTacrine hybrids designed to block amyloid-b aggregation and to exert anticholinesterase and antioxidant effects, J. Med. Chem. 57 (2014) 8576-8589.
-
(2014)
J. Med. Chem.
, vol.57
, pp. 8576-8589
-
-
Nepovimova, E.1
Uliassi, E.2
Korabecny, J.3
Peña-Altamira, L.E.4
Samez, S.5
Pesaresi, A.6
Garcia, G.E.7
Bartolini, M.8
Andrisano, V.9
-
9
-
-
80054848108
-
Multi-target-directed ligands in Alzheimer's disease treatment
-
M. Bajda, N. Guzior, M. Ignasik, B. Malawska, Multi-target-directed ligands in Alzheimer's disease treatment, Curr. Med. Chem. 18 (2011) 4949-4975.
-
(2011)
Curr. Med. Chem.
, vol.18
, pp. 4949-4975
-
-
Bajda, M.1
Guzior, N.2
Ignasik, M.3
Malawska, B.4
-
10
-
-
0035808249
-
Enzymatic formation of aurones in the extracts of yellow snapdragon flowers
-
T. Sato, T. Nakayama, S. Kikuchi, Y. Fukui, K. Yonekura-Sakakibara, T. Ueda, T. Nishino, Y. Tanaka, T. Kusumi, Enzymatic formation of aurones in the extracts of yellow snapdragon flowers, Plant Sci. 160 (2001) 229-236.
-
(2001)
Plant Sci.
, vol.160
, pp. 229-236
-
-
Sato, T.1
Nakayama, T.2
Kikuchi, S.3
Fukui, Y.4
Yonekura-Sakakibara, K.5
Ueda, T.6
Nishino, T.7
Tanaka, Y.8
Kusumi, T.9
-
11
-
-
79961245561
-
Discovery of naturally occurring aurones that are potent allosteric inhibitors of Hepatitis C virus RNA-dependent RNA polymerase
-
R. Haudecoeur, A. Ahamed-Belcem, Y. Wei, A. Fortuné, R. Brillet, C. Belle, E. Nicolle, C. Pallier, J.-M. Pawlotsky, A. Boumendjel, Discovery of naturally occurring aurones that are potent allosteric inhibitors of Hepatitis C virus RNA-dependent RNA polymerase, J. Med. Chem. 54 (2011) 5395-5402.
-
(2011)
J. Med. Chem.
, vol.54
, pp. 5395-5402
-
-
Haudecoeur, R.1
Ahamed-Belcem, A.2
Wei, Y.3
Fortuné, A.4
Brillet, R.5
Belle, C.6
Nicolle, E.7
Pallier, C.8
Pawlotsky, J.-M.9
Boumendjel, A.10
-
12
-
-
77954349448
-
Functionalized aurones as inducers of NAD(P)H: Quinone oxidoreductase1 that activate AhR/XRE and Nrf2/ARE signaling pathways: Synthesis, evaluation and SAR
-
C.Y. Lee, E.H. Chew, M.L. Go, Functionalized aurones as inducers of NAD(P)H: quinone oxidoreductase1 that activate AhR/XRE and Nrf2/ARE signaling pathways: synthesis, evaluation and SAR, Euro. J. Med. Chem. 45 (2010) 2957-2971.
-
(2010)
Euro. J. Med. Chem.
, vol.45
, pp. 2957-2971
-
-
Lee, C.Y.1
Chew, E.H.2
Go, M.L.3
-
13
-
-
79953058073
-
Aurones as modulators of ABCG2 and ABCB1: Synthesis and structure-activity relationships
-
H.M. Sim, K.Y. Loh, W.K. Yeo, C.Y. Lee, M.L. Go, Aurones as modulators of ABCG2 and ABCB1: synthesis and structure-activity relationships, Chem-Med Chem 6 (2011) 713-724.
-
(2011)
Chem-Med Chem
, vol.6
, pp. 713-724
-
-
Sim, H.M.1
Loh, K.Y.2
Yeo, W.K.3
Lee, C.Y.4
Go, M.L.5
-
14
-
-
77955983855
-
Design, synthesis and anticholinesterase activity of a novel series of 1-benzyl-4-((6-alkoxy-3-oxobenzofuran- 2(3H)-ylidene) methyl) pyridinium derivatives
-
H. Nadri, M. Pirali-Hamedani, M. Shekarchi, M. Abdollahi, V. Sheibani, M. Amanlou, A. Shafiee, A. Foroumadi, Design, synthesis and anticholinesterase activity of a novel series of 1-benzyl-4-((6-alkoxy-3-oxobenzofuran- 2(3H)-ylidene) methyl) pyridinium derivatives, Bioorg. Med. Chem. 18 (2010) 6360-6366.
-
(2010)
Bioorg. Med. Chem.
, vol.18
, pp. 6360-6366
-
-
Nadri, H.1
Pirali-Hamedani, M.2
Shekarchi, M.3
Abdollahi, M.4
Sheibani, V.5
Amanlou, M.6
Shafiee, A.7
Foroumadi, A.8
-
16
-
-
61849132762
-
Novel radioiodinated aurones as probes for Permeability of controls in the PAMPABBB assay imaging of beta-amyloid plaques in the brain
-
Y. Maya, M. Ono, H. Watanabe, M. Haratake, H. Saiji, M. Nkayama, Novel radioiodinated aurones as probes for Permeability of controls in the PAMPABBB assay imaging of beta-amyloid plaques in the brain, Bioconjugate Chem. 20 (2009) 95-101.
-
(2009)
Bioconjugate Chem.
, vol.20
, pp. 95-101
-
-
Maya, Y.1
Ono, M.2
Watanabe, H.3
Haratake, M.4
Saiji, H.5
Nkayama, M.6
-
18
-
-
0037523454
-
Profiling drug-like properties in discovery research
-
L. Di, E.H. Kerns, Profiling drug-like properties in discovery research, Curr. Opin. Chem. Biol. 7 (2003) 402-408.
-
(2003)
Curr. Opin. Chem. Biol.
, vol.7
, pp. 402-408
-
-
Di, L.1
Kerns, E.H.2
-
19
-
-
70749152806
-
Blood-brain barrier
-
Academic Press, London
-
E.H. Kerns, L. Di, Blood-brain barrier, in: Drug-like Properties: Concepts, Structure Design and Methods, Academic Press, London, p, 2008, pp. 122-136.
-
(2008)
Drug-like Properties: Concepts, Structure Design and Methods
, pp. 122-136
-
-
Kerns, E.H.1
Di, L.2
-
20
-
-
1242338756
-
Flavonoid permeability across an in situ model of the bloodebrain barrier
-
K.A. Youdim, M.Z. Qaiser, D.J. Bagley, C.C. Rice-Evans, N.J. Abbott, Flavonoid permeability across an in situ model of the bloodebrain barrier, Free Rad. Biol. Med. 36 (2003) 592-604.
-
(2003)
Free Rad. Biol. Med.
, vol.36
, pp. 592-604
-
-
Youdim, K.A.1
Qaiser, M.Z.2
Bagley, D.J.3
Rice-Evans, C.C.4
Abbott, N.J.5
-
21
-
-
77954577365
-
Flavonoid transport across RBE4 cells: A blood-brain barrier model
-
A. Faria, D. Pestana, D. Teixeira, J. Azevedo, V. De Freitas, N. Mateus, C. Calhau, Flavonoid transport across RBE4 cells: a blood-brain barrier model, Cell. Mol. Biol. Lett. 15 (2010) 234-241.
-
(2010)
Cell. Mol. Biol. Lett.
, vol.15
, pp. 234-241
-
-
Faria, A.1
Pestana, D.2
Teixeira, D.3
Azevedo, J.4
De Freitas, V.5
Mateus, N.6
Calhau, C.7
-
22
-
-
67650033008
-
Characteristics of compounds that cross the blood-brain barrier
-
W.A. Banks, Characteristics of compounds that cross the blood-brain barrier, BMC Neurol. 9 (Suppl. 1) (2009) S3.
-
(2009)
BMC Neurol.
, vol.9
, pp. S3
-
-
Banks, W.A.1
-
23
-
-
84868573143
-
Drug transport across the blood-brian barrier
-
W.M. Pardridge, Drug transport across the blood-brian barrier, J. Cereb. Blood Flow Metab. 32 (2012) 1959-1972.
-
(2012)
J. Cereb. Blood Flow Metab.
, vol.32
, pp. 1959-1972
-
-
Pardridge, W.M.1
-
24
-
-
84862825057
-
Design, synthesis and evaluation of isaindigotone derivatives as dual inhibitors for acetylcholinesterase and amyloid beta aggregation
-
J.-W. Yan, Y.-P. Li, W.-J. Ye, S.-B. Chen, J.-Q. Hou, J.-H. Tan, T.-M. Ou, D. Li, L.- Q. Gu, Z.-S. Huang, Design, synthesis and evaluation of isaindigotone derivatives as dual inhibitors for acetylcholinesterase and amyloid beta aggregation, Bioorg Med. Chem. 20 (2012) 2529-2534.
-
(2012)
Bioorg Med. Chem.
, vol.20
, pp. 2529-2534
-
-
Yan, J.-W.1
Li, Y.-P.2
Ye, W.-J.3
Chen, S.-B.4
Hou, J.-Q.5
Tan, J.-H.6
Ou, T.-M.7
Li, D.8
Gu, L.-Q.9
Huang, Z.-S.10
-
25
-
-
84899456647
-
Multitarget-directed resveratrol derivatives: Anti-cholinesterases, anti-b-amyloid aggregation and monoamine oxidase inhibition properties against Alzheimer's disease
-
L.-F. Pan, X.-B. Wang, S.-S. Xie, S.-Y. Li, L.-Y. Kong, Multitarget-directed resveratrol derivatives: anti-cholinesterases, anti-b-amyloid aggregation and monoamine oxidase inhibition properties against Alzheimer's disease, Med-Chem Comm 5 (2014) 609-616.
-
(2014)
Med-Chem Comm
, vol.5
, pp. 609-616
-
-
Pan, L.-F.1
Wang, X.-B.2
Xie, S.-S.3
Li, S.-Y.4
Kong, L.-Y.5
-
26
-
-
0035829439
-
Acetylcholinesterase inhibitors: SAR and kinetic studies on omega-[N-methyl-N-(3-alkylcarbamoyloxyphenyl) methyl]aminoalkoxyaryl derivatives
-
A. Rampa, L. Piazzi, F. Belluti, S. Gobbi, A. Bisi, M. Bartolini, V. Andrisano, V. Cavrini, A. Cavalli, M. Recanatini, P. Valenti, Acetylcholinesterase inhibitors: SAR and kinetic studies on omega-[N-methyl-N-(3-alkylcarbamoyloxyphenyl) methyl]aminoalkoxyaryl derivatives, J. Med. Chem. 44 (2001) 3810-3820.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 3810-3820
-
-
Rampa, A.1
Piazzi, L.2
Belluti, F.3
Gobbi, S.4
Bisi, A.5
Bartolini, M.6
Andrisano, V.7
Cavrini, V.8
Cavalli, A.9
Recanatini, M.10
Valenti, P.11
-
27
-
-
21244442338
-
Cholinesterase inhibitors: Xanthostigmine derivatives blocking the acetylcholinesterase-induced beta-amyloid aggregation
-
F. Belluti, A. Rampa, L. Piazzi, A. Bisi, S. Gobbi, M. Bartolini, V. Andrisano, A. Cavalli, M. Recanatini, P. Valenti, Cholinesterase inhibitors: xanthostigmine derivatives blocking the acetylcholinesterase-induced beta-amyloid aggregation, J. Med. Chem. 48 (2005) 4444-4456.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 4444-4456
-
-
Belluti, F.1
Rampa, A.2
Piazzi, L.3
Bisi, A.4
Gobbi, S.5
Bartolini, M.6
Andrisano, V.7
Cavalli, A.8
Recanatini, M.9
Valenti, P.10
-
28
-
-
30444441800
-
Discovery of benzylidenebenzofuran-3(2H)-one (aurones) as inhibitors of tyrosinase derived from human melanocytes
-
S. Okombi, D. Rival, S. Bonnet, A.M. Mariotte, E. Perrier, A. Boumendjel, Discovery of benzylidenebenzofuran-3(2H)-one (aurones) as inhibitors of tyrosinase derived from human melanocytes, J. Med. Chem. 49 (2006) 329-333.
-
(2006)
J. Med. Chem.
, vol.49
, pp. 329-333
-
-
Okombi, S.1
Rival, D.2
Bonnet, S.3
Mariotte, A.M.4
Perrier, E.5
Boumendjel, A.6
-
29
-
-
0028823072
-
Synthesis and structureactivity relationships of acetylcholinesterase inhibitors: 1-Benzyl-4-[(5,6-dimethoxy-1-oxoindan-2-yl)methyl]piperidine hydrochloride and related compounds
-
H. Sugimoto, Y. Iimura, Y. Yamnishi, K. Yamatsu, Synthesis and structureactivity relationships of acetylcholinesterase inhibitors: 1-Benzyl-4-[(5,6-dimethoxy-1-oxoindan-2-yl)methyl]piperidine hydrochloride and related compounds, J. Med. Chem. 38 (1995) 4821-4829
-
(1995)
J. Med. Chem.
, vol.38
, pp. 4821-4829
-
-
Sugimoto, H.1
Iimura, Y.2
Yamnishi, Y.3
Yamatsu, K.4
-
30
-
-
84885091255
-
Synthesis, characterization, and molecular docking of novel benzimidazole derivatives as cholinesterase inhibitors
-
Y.K. Yeung, M.A. Ali, C.W. Ang, S.C. Tan, K.-Y. Khaw, M. Vikneswaran, O. Hasnah, Synthesis, characterization, and molecular docking of novel benzimidazole derivatives as cholinesterase inhibitors, Bioorg. Chem. 49 (2013) 33-39.
-
(2013)
Bioorg. Chem.
, vol.49
, pp. 33-39
-
-
Yeung, Y.K.1
Ali, M.A.2
Ang, C.W.3
Tan, S.C.4
Khaw, K.-Y.5
Vikneswaran, M.6
Hasnah, O.7
-
31
-
-
84862159765
-
Design, synthesis, and evaluation of indanone derivatives as acetylcholinesterase inhibitors and metal-chelating agents
-
F.-C. Meng, F. Mao, W.-J. Shan, F. Qin, L. Huang, X.-S. Li, Design, synthesis, and evaluation of indanone derivatives as acetylcholinesterase inhibitors and metal-chelating agents, Bioorg. Med. Chem. Lett. 22 (2012) 4462-4466.
-
(2012)
Bioorg. Med. Chem. Lett.
, vol.22
, pp. 4462-4466
-
-
Meng, F.-C.1
Mao, F.2
Shan, W.-J.3
Qin, F.4
Huang, L.5
Li, X.-S.6
-
32
-
-
0033103478
-
Structure of acetylcholinesterase complexed with E2020 (Aricept®): Implications for the design of new anti-Alzheimer drugs
-
G. Kryger, I. Silman, J.L. Sussman, Structure of acetylcholinesterase complexed with E2020 (Aricept®): implications for the design of new anti-Alzheimer drugs, Structure 7 (1999) 297-307.
-
(1999)
Structure
, vol.7
, pp. 297-307
-
-
Kryger, G.1
Silman, I.2
Sussman, J.L.3
-
33
-
-
11644261806
-
Automated docking using a Lamarckian genetic algorithm and an empirical binding free energy function
-
G.M. Morris, D.S. Goodsell, R.S. Halliday, R. Huey, W.E. Hart, R.K. Belew, A.J. Olson, Automated docking using a Lamarckian genetic algorithm and an empirical binding free energy function, J. Comput. Chem. 19 (1998) 1639-1662.
-
(1998)
J. Comput. Chem.
, vol.19
, pp. 1639-1662
-
-
Morris, G.M.1
Goodsell, D.S.2
Halliday, R.S.3
Huey, R.4
Hart, W.E.5
Belew, R.K.6
Olson, A.J.7
-
34
-
-
46449112342
-
Cl-p interactions in protein-ligand complexes
-
Y.N. Imai, Y. Inoue, I. Nakanishi, K. Kitaura, Cl-p interactions in protein-ligand complexes, Protein Sci. 17 (2008) 1129-1137.
-
(2008)
Protein Sci.
, vol.17
, pp. 1129-1137
-
-
Imai, Y.N.1
Inoue, Y.2
Nakanishi, I.3
Kitaura, K.4
-
35
-
-
70349786321
-
Evidence for C-Cl/C-Br⋯pi interactions as an important contribution to protein-ligand binding affinity
-
H. Matter, M. Nazaré, S. Güssregen, D.W. Will, H. Scheuder, A. Bauer, M. Urmann, K. Ritter, M. Wagner, V. Wehner, Evidence for C-Cl/C-Br⋯pi interactions as an important contribution to protein-ligand binding affinity, Angew. Chem. Int. Ed. Engl. 48 (2009) 2911-2916.
-
(2009)
Angew. Chem. Int. Ed. Engl.
, vol.48
, pp. 2911-2916
-
-
Matter, H.1
Nazaré, M.2
Güssregen, S.3
Will, D.W.4
Scheuder, H.5
Bauer, A.6
Urmann, M.7
Ritter, K.8
Wagner, M.9
Wehner, V.10
-
36
-
-
84874046410
-
Halogen bonding (X-bonding): A biological perspective
-
M.R. Scholfield, C.M. Zanden, M. Carter, P.S. Ho, Halogen bonding (X-bonding): a biological perspective, Protein Sci. 22 (2013) 139-152.
-
(2013)
Protein Sci.
, vol.22
, pp. 139-152
-
-
Scholfield, M.R.1
Zanden, C.M.2
Carter, M.3
Ho, P.S.4
-
37
-
-
65649095907
-
Halogen bonding - A novel interaction for rational drug design?
-
Y. Lu, T. Shi, Y. Wang, H. Yang, X. Yan, X. Luo, H. Jiang, W. Zhu, Halogen bonding - a novel interaction for rational drug design? J. Med. Chem. 52 (2009) 2852-2862.
-
(2009)
J. Med. Chem.
, vol.52
, pp. 2852-2862
-
-
Lu, Y.1
Shi, T.2
Wang, Y.3
Yang, H.4
Yan, X.5
Luo, X.6
Jiang, H.7
Zhu, W.8
-
38
-
-
77951793408
-
Nonbonding interactions of organic halogens in biological systems: Implications for drug discovery and biomolecular design
-
Y. Lu, Y. Wang, W. Zhu, Nonbonding interactions of organic halogens in biological systems: implications for drug discovery and biomolecular design, Phys. Chem. Chem. Phys. 12 (2010) 4543-4551.
-
(2010)
Phys. Chem. Chem. Phys.
, vol.12
, pp. 4543-4551
-
-
Lu, Y.1
Wang, Y.2
Zhu, W.3
-
39
-
-
22244460783
-
Probing the subpockets of factor Xa reveals two binding modes for inhibitors based on a 2-carboxyindole scaffold: A study combining structureeactivity relationship and X-ray crystallography
-
M. Nazare, D.W. Will, H. Matter, H. Schreuder, K. Ritter, M. Urmann, M. Essrich, A. Bauer, M. Wagner, J. Czech, et al., Probing the subpockets of factor Xa reveals two binding modes for inhibitors based on a 2-carboxyindole scaffold: a study combining structureeactivity relationship and X-ray crystallography, J. Med. Chem. 48 (2005) 4511-4525.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 4511-4525
-
-
Nazare, M.1
Will, D.W.2
Matter, H.3
Schreuder, H.4
Ritter, K.5
Urmann, M.6
Essrich, M.7
Bauer, A.8
Wagner, M.9
Czech, J.10
-
40
-
-
34548821001
-
The role of halogen bonding in inhibitor recognition binding by protein kinases
-
A.R. Voth, P.S. Ho, The role of halogen bonding in inhibitor recognition binding by protein kinases, Curr. Top. Med. Chem. 7 (2007) 1336-1348.
-
(2007)
Curr. Top. Med. Chem.
, vol.7
, pp. 1336-1348
-
-
Voth, A.R.1
Ho, P.S.2
-
41
-
-
1642579680
-
Development of a computational approach to predict blood-brain barrier permeability
-
X. Liu, M. Tu, R.S. Kelly, C. Chen, B.J. Smith, Development of a computational approach to predict blood-brain barrier permeability, Drug Metab. Dispos. 32 (2004) 132-139.
-
(2004)
Drug Metab. Dispos.
, vol.32
, pp. 132-139
-
-
Liu, X.1
Tu, M.2
Kelly, R.S.3
Chen, C.4
Smith, B.J.5
-
42
-
-
84962359573
-
High throughput artificial membrane permeability assay for blood-brain barrier
-
L. Di, E.H. Kerns, K. Fan, O.J. McConnell, G.T. Carter, High throughput artificial membrane permeability assay for blood-brain barrier, Euro J. Med. Chem. 38 (2003) 223-232.
-
(2003)
Euro J. Med. Chem.
, vol.38
, pp. 223-232
-
-
Di, L.1
Kerns, E.H.2
Fan, K.3
McConnell, O.J.4
Carter, G.T.5
-
43
-
-
67049114278
-
Comparison of blood-brain barrier permeability assays: In situ brain perfusion, MDR1-MDCKII and PAMPA-BBB
-
L. Di, E.H. Kerns, I.F. Bezar, S.L. Petusky, Y.P. Huang, Comparison of blood-brain barrier permeability assays: in situ brain perfusion, MDR1-MDCKII and PAMPA-BBB, J. Pharm. Sci. 98 (2009) 1980-1991.
-
(2009)
J. Pharm. Sci.
, vol.98
, pp. 1980-1991
-
-
Di, L.1
Kerns, E.H.2
Bezar, I.F.3
Petusky, S.L.4
Huang, Y.P.5
-
44
-
-
0028596605
-
Lipophilicity and hydrogen-bonding capacity of H1-histaminic agents in relation to their central sedative side effects
-
A.M. ter Laak, R.S. Tsai, G.M. Donne-Op den Kelder, P.-A. Carrupt, B. Testa, H. Timmerman, Lipophilicity and hydrogen-bonding capacity of H1-Histaminic agents in relation to their central sedative side effects, Euro. J. Pharm. Sci. 2 (1994) 373-384.
-
(1994)
Euro. J. Pharm. Sci.
, vol.2
, pp. 373-384
-
-
Ter Laak, A.M.1
Tsai, R.S.2
Donne-Op Den Kelder, G.M.3
Carrupt, P.-A.4
Testa, B.5
Timmerman, H.6
-
45
-
-
13244293644
-
High-throughput measurement of log D and pKa
-
H. van de Waterbeemd, H. Lenneras, P. Artursson (Eds.), Wiley, Weinheim, Germany
-
J.E.A. Corner, High-throughput measurement of log D and pKa, in: H. van de Waterbeemd, H. Lenneras, P. Artursson (Eds.), Drug Bioavailability, Wiley, Weinheim, Germany, 2004.
-
(2004)
Drug Bioavailability
-
-
Corner, J.E.A.1
-
46
-
-
0032733974
-
Prediction of human clearance of twenty-nine drugs from hepatic microsomal intrinsic clearance data: Examination of in vitro half-life approach and nonspecific binding to microsomes
-
R.S. Obach, Prediction of human clearance of twenty-nine drugs from hepatic microsomal intrinsic clearance data: examination of in vitro half-life approach and nonspecific binding to microsomes, Drug Metab. Dispos. 27 (1999) 1350-1359.
-
(1999)
Drug Metab. Dispos.
, vol.27
, pp. 1350-1359
-
-
Obach, R.S.1
-
47
-
-
0034652244
-
Quantification and rapid metabolite identification in drug discovery using API time-of-flight LC/MS
-
N. Zhang, S.T. Fountain, H. Bi, D.T. Rossi, Quantification and rapid metabolite identification in drug discovery using API time-of-flight LC/MS, Anal. Chem. 72 (2000) 800-806.
-
(2000)
Anal. Chem.
, vol.72
, pp. 800-806
-
-
Zhang, N.1
Fountain, S.T.2
Bi, H.3
Rossi, D.T.4
-
48
-
-
2642513322
-
Experimental design on single-time-Point-high-throughput microsomal stability assay
-
L. Di, E.H. Kerns, N. Gao, S.Q. Li, Y.P. Huang, J.L. Bourassa, D.M. Huryn, Experimental design on single-time-Point-high-throughput microsomal stability assay, J. Pharm. Sci. 93 (2004) 1537-1544.
-
(2004)
J. Pharm. Sci.
, vol.93
, pp. 1537-1544
-
-
Di, L.1
Kerns, E.H.2
Gao, N.3
Li, S.Q.4
Huang, Y.P.5
Bourassa, J.L.6
Huryn, D.M.7
-
49
-
-
33644811612
-
A new rapid colorimetric determination of acetylcholinesterase activity
-
G.L. Ellman, D. Gourtney, V. Andres, R.M. Featherstone, A new rapid colorimetric determination of acetylcholinesterase activity, Biochem. Pharmacol. 7 (1961) 88-95.
-
(1961)
Biochem. Pharmacol.
, vol.7
, pp. 88-95
-
-
Ellman, G.L.1
Gourtney, D.2
Andres, V.3
Featherstone, R.M.4
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