-
1
-
-
0028802726
-
Cyclic nucleotide phosphodiesterases: Functional implications of multiple isoforms
-
Beavo, J. A. Cyclic nucleotide phosphodiesterases: Functional implications of multiple isoforms Physiol. Rev. 1995, 75, 725-748
-
(1995)
Physiol. Rev.
, vol.75
, pp. 725-748
-
-
Beavo, J.A.1
-
2
-
-
0032605044
-
The molecular biology of cyclic nucleotide phosphodiesterases
-
Conti, M.; Jin, S. L. The molecular biology of cyclic nucleotide phosphodiesterases Prog. Nucleic Acid Res. Mol. Biol. 1999, 63, 1-38
-
(1999)
Prog. Nucleic Acid Res. Mol. Biol.
, vol.63
, pp. 1-38
-
-
Conti, M.1
Jin, S.L.2
-
3
-
-
0032044238
-
Adaptation in cyclic AMP signalling processes: A central role for cyclic AMP phosphodiesterases
-
Houslay, M. D. Adaptation in cyclic AMP signalling processes: A central role for cyclic AMP phosphodiesterases Semin. Cell Dev. Biol. 1998, 9, 161-167 (Pubitemid 128352267)
-
(1998)
Seminars in Cell and Developmental Biology
, vol.9
, Issue.2
, pp. 161-167
-
-
Houslay, M.D.1
-
4
-
-
84857080656
-
Cyclic nucleotide phosphodiesterase (PDE) isozymes as targets of the intracellular signalling network: Benefits of PDE inhibitors in various diseases and perspectives for future therapeutic developments
-
Keravis, T.; Lugnier, C. Cyclic nucleotide phosphodiesterase (PDE) isozymes as targets of the intracellular signalling network: Benefits of PDE inhibitors in various diseases and perspectives for future therapeutic developments Br. J. Pharmacol. 2012, 165, 1288-1305
-
(2012)
Br. J. Pharmacol.
, vol.165
, pp. 1288-1305
-
-
Keravis, T.1
Lugnier, C.2
-
5
-
-
0035193364
-
Cyclic nucleotide phosphodiesterases: Relating structure and function
-
Francis, S. H.; Turko, I. V.; Corbin, J. D. Cyclic nucleotide phosphodiesterases: Relating structure and function Nucleic Acid Res. Mol. Biol. 2000, 65, 1-52
-
(2000)
Nucleic Acid Res. Mol. Biol.
, vol.65
, pp. 1-52
-
-
Francis, S.H.1
Turko, I.V.2
Corbin, J.D.3
-
6
-
-
18644376713
-
The next generation of phosphodiesterase inhibitors: Structural clues to ligand and substrate selectivity of phosphodiesterases
-
DOI 10.1021/jm040217u
-
Manallack, D.; Hughes, R.; Thompson, P. The next generation of phosphodiesterase inhibitors: Structural clues to ligand and substrate selectivity of phosphodiesterases J. Med. Chem. 2005, 48, 3449-3462 (Pubitemid 40664094)
-
(2005)
Journal of Medicinal Chemistry
, vol.48
, Issue.10
, pp. 3449-3462
-
-
Manallack, D.T.1
Hughes, R.A.2
Thompson, P.E.3
-
7
-
-
31144433061
-
Cyclic nucleotide phosphodiesterase (PDE) superfamily: A new target for the development of specific therapeutic agents
-
DOI 10.1016/j.pharmthera.2005.07.003, PII S0163725805001580
-
Lugnier, C. Cyclic nucleotide phosphodiesterase (PDE) superfamily: A new target for the development of specific therapeutic agents Pharmacol. Ther. 2006, 109, 366-398 (Pubitemid 43132818)
-
(2006)
Pharmacology and Therapeutics
, vol.109
, Issue.3
, pp. 366-398
-
-
Lugnier, C.1
-
8
-
-
33746629480
-
Phosphodiesterases in the CNS: Targets for drug development
-
DOI 10.1038/nrd2058, PII NRD2058
-
Menniti, F. S.; Faraci, W. S.; Schmidt, C. J. Phosphodiesterases in the CNS: Targets for drug development Nat. Rev. Drug Discovery 2006, 5, 660-670 (Pubitemid 44151604)
-
(2006)
Nature Reviews Drug Discovery
, vol.5
, Issue.8
, pp. 660-670
-
-
Menniti, F.S.1
Faraci, W.S.2
Schmidt, C.J.3
-
9
-
-
27344449614
-
Keynote review: Phosphodiesterase-4 as a therapeutic target
-
DOI 10.1016/S1359-6446(05)03622-6, PII S1359644605036226
-
Houslay, M. D.; Schafer, P.; Zhang, K. Y. J. Keynote review: Phosphodiesterase-4 as a therapeutic target Drug Discovery Today 2005, 10, 1503-1519 (Pubitemid 41527193)
-
(2005)
Drug Discovery Today
, vol.10
, Issue.22
, pp. 1503-1519
-
-
Houslay, M.D.1
Schafer, P.2
Zhang, K.Y.J.3
-
10
-
-
12444317667
-
Cloning and characterization of novel PDE4D isoforms PDE4D6 and PDE4D7
-
DOI 10.1016/S0898-6568(03)00042-1
-
Wang, D. G; Deng, C. J.; Bugaj-Gaweda, B.; Kwan, M.; Gunwaldsen, C.; Leonard, C.; Xin, X. N.; Hu, Y. H.; Unterbeck, A.; De Vivo, M. Cloning and characterization of novel PDE4D isoforms PDE4D6 and PDE4D7 Cell. Signalling 2003, 15, 883-891 (Pubitemid 36776662)
-
(2003)
Cellular Signalling
, vol.15
, Issue.9
, pp. 883-891
-
-
Wang, D.1
Deng, C.2
Bugaj-Gaweda, B.3
Kwan, M.4
Gunwaldsen, C.5
Leonard, C.6
Xin, X.7
Hu, Y.8
Unterbeck, A.9
De Vivo, M.10
-
11
-
-
14544272401
-
Cyclic nucleotide phosphodiesterases and their role in immunomodulatory responses: Advances in the development of specific phosphodiesterase inhibitors
-
DOI 10.1002/med.20020
-
Castro, A.; Jerez, M. J.; Gil, C.; Martinez, A. Cyclic nucleotide phosphodiesterases and their role in immunomodulatory responses: Advances in the development of specific phosphodiesterases inhibitors Med. Res. Rev. 2005, 25, 229-244 (Pubitemid 40299847)
-
(2005)
Medicinal Research Reviews
, vol.25
, Issue.2
, pp. 229-244
-
-
Castro, A.1
Jerez, M.J.2
Gil, C.3
Martinez, A.4
-
12
-
-
3242804420
-
PDE4 inhibition: A novel approach for the treatment of inflammatory bowel disease
-
DOI 10.1016/j.tips.2004.06.008, PII S0165614704001774
-
Banner, K. H.; Trevethick, M. A. PDE4 inhibition: A novel approach for the treatment of inflammatory bowel disease Trends Pharmacol. Sci. 2004, 25, 430-436 (Pubitemid 38981559)
-
(2004)
Trends in Pharmacological Sciences
, vol.25
, Issue.8
, pp. 430-436
-
-
Banner, K.H.1
Trevethick, M.A.2
-
13
-
-
1242268903
-
Anti-Inflammatory Potential of the Selective Phosphodiesterase 4 Inhibitor N-(3,5-Dichloro-pyrid-4-yl)-[1-(4-fluorobenzyl)-5-hydroxy-indole-3-yl] -glyoxylic Acid Amide (AWD 12-281), in Human Cell Preparations
-
DOI 10.1124/jpet.103.059097
-
Draheim, R.; Egerland, U.; Rundfeldt, C. Anti-inflammatory potential of the selective phosphodiesterase 4 inhibitor N -(3,5-dichloro-pyrid-4-yl)-[1-(4- fluorobenzyl)-5-hydroxy-indole-3-yl]-glyoxylic acid amide (AWD 12-281), in human cell preparations J. Pharmacol. Exp. Ther. 2004, 308, 555-563 (Pubitemid 38134217)
-
(2004)
Journal of Pharmacology and Experimental Therapeutics
, vol.308
, Issue.2
, pp. 555-563
-
-
Draheim, R.1
Egerland, U.2
Rundfeldt, C.3
-
14
-
-
10644253750
-
Phosphodiesterase 4-selective inhibition: Novel therapy for the inflammation of COPD
-
DOI 10.1016/j.pupt.2004.09.027, PII S1094553904000938
-
Jeffery, P. Phosphodiesterase 4-selective inhibition: Novel therapy for the inflammation of COPD Pulm. Pharmacol. Ther. 2005, 18, 9-17 (Pubitemid 39647748)
-
(2005)
Pulmonary Pharmacology and Therapeutics
, vol.18
, Issue.1
, pp. 9-17
-
-
Jeffery, P.1
-
15
-
-
1342264246
-
Antidepressant effects of inhibitors of cAMP phosphodiesterase (PDE4)
-
DOI 10.1016/j.tips.2004.01.003
-
O'Donnell, J. M.; Zhang, H. Antidepressant effects of inhibitors of cAMP phosphodiesterase (PDE4) Trends Pharmacol. Sci. 2004, 25, 158-163 (Pubitemid 38264507)
-
(2004)
Trends in Pharmacological Sciences
, vol.25
, Issue.3
, pp. 158-163
-
-
O'Donnell, J.M.1
Zhang, H.-T.2
-
16
-
-
4444330207
-
The potential of PDE4 inhibitors in respiratory disease
-
DOI 10.2174/1568010043343822
-
Spina, D. The potential of PDE4 inhibitors in respiratory disease Curr. Drug Targets: Inflammation Allergy 2004, 3, 231-236 (Pubitemid 39206651)
-
(2004)
Current Drug Targets: Inflammation and Allergy
, vol.3
, Issue.3
, pp. 231-236
-
-
Spina, D.1
-
17
-
-
69149095164
-
Phosphodiesterase-4 inhibition in COPD
-
O'Byrne, P. M.; Gauvreau, G. Phosphodiesterase-4 inhibition in COPD Lancet 2009, 374, 665-667
-
(2009)
Lancet
, vol.374
, pp. 665-667
-
-
O'Byrne, P.M.1
Gauvreau, G.2
-
18
-
-
74949133079
-
PDE4 inhibitors: A review of current developments (2005-2009)
-
Pages, L.; Gavalda, A.; Lehner, M. D. PDE4 inhibitors: A review of current developments (2005-2009) Expert Opin. Ther. Pat. 2009, 19, 1501-1519
-
(2009)
Expert Opin. Ther. Pat.
, vol.19
, pp. 1501-1519
-
-
Pages, L.1
Gavalda, A.2
Lehner, M.D.3
-
19
-
-
84862290893
-
Selective PDE inhibitors as novel treatments for respiratory diseases
-
Page, C. P.; Spina, D. Selective PDE inhibitors as novel treatments for respiratory diseases Curr. Opin. Pharmacol. 2012, 12, 1-12
-
(2012)
Curr. Opin. Pharmacol.
, vol.12
, pp. 1-12
-
-
Page, C.P.1
Spina, D.2
-
20
-
-
52449115420
-
Recent advances on phosphodiesterase 4 inhibitors for the treatment of asthma and chronic obstructive pulmonary disease
-
Kodimuthali, A.; Jabaris, S. S. L.; Pal, M. Recent advances on phosphodiesterase 4 inhibitors for the treatment of asthma and chronic obstructive pulmonary disease J. Med. Chem. 2008, 51, 5471-5489
-
(2008)
J. Med. Chem.
, vol.51
, pp. 5471-5489
-
-
Kodimuthali, A.1
Jabaris, S.S.L.2
Pal, M.3
-
22
-
-
69149098943
-
Roflumilast in moderate-to-severe chronic obstructive pulmonary disease treated with longacting bronchodilators: Two randomised clinical trials
-
Fabbri, L. M.; Calverley, P. M. A.; Izquierdo-Alonso, J. L.; Bundschuh, D. S.; Brose, M.; Martinez, F. J.; Rabe, K. F. Roflumilast in moderate-to-severe chronic obstructive pulmonary disease treated with longacting bronchodilators: Two randomised clinical trials Lancet 2009, 374, 695-703
-
(2009)
Lancet
, vol.374
, pp. 695-703
-
-
Fabbri, L.M.1
Calverley, P.M.A.2
Izquierdo-Alonso, J.L.3
Bundschuh, D.S.4
Brose, M.5
Martinez, F.J.6
Rabe, K.F.7
-
23
-
-
77953105482
-
The preclinical pharmacology of roflumilast - A selective, oral phosphodiesterase 4 inhibitor in development for chronic obstructive pulmonary disease
-
Hatzelmann, A.; Morcillo, E. J.; Lungarella, G.; Adnot, S.; Sanjar, S.; Beume, R.; Schudt, C.; Tenor, H. The preclinical pharmacology of roflumilast-A selective, oral phosphodiesterase 4 inhibitor in development for chronic obstructive pulmonary disease Pulm. Pharmacol. Ther. 2010, 23, 235-256
-
(2010)
Pulm. Pharmacol. Ther.
, vol.23
, pp. 235-256
-
-
Hatzelmann, A.1
Morcillo, E.J.2
Lungarella, G.3
Adnot, S.4
Sanjar, S.5
Beume, R.6
Schudt, C.7
Tenor, H.8
-
24
-
-
69149103642
-
Roflumilast in symptomatic chronic obstructive pulmonary disease: Two randomised clinical trials
-
Calverley, P. M. A.; Rabe, K. F.; Goehring, U. M.; Kristiansen, S.; Fabbri, L. M.; Martinez, F. J. Roflumilast in symptomatic chronic obstructive pulmonary disease: Two randomised clinical trials Lancet 2009, 374, 685-694
-
(2009)
Lancet
, vol.374
, pp. 685-694
-
-
Calverley, P.M.A.1
Rabe, K.F.2
Goehring, U.M.3
Kristiansen, S.4
Fabbri, L.M.5
Martinez, F.J.6
-
25
-
-
33846455467
-
SAR of a series of 5,6-dihydro-(9H)-pyrazolo[3,4-c]-1,2,4-triazolo[4,3- α]pyridines as potent inhibitors of human eosinophil phosphodiesterase
-
DOI 10.1021/jm060904g
-
Duplantier, A. J.; Bachert, E.; Cheng, J.; Cohan, V.; Jenkinson, T.; Kraus, K.; McKechney, M.; Pillar, J.; Watson, J. SAR of a series of 5,6-dihydro-(9 H)-pyrazolo[3,4- c ]-1,2,4-triazolo[4,3-α]pyridines as potent inhibitors of human eosinophil phosphodiesterase J. Med. Chem. 2007, 50, 344-349 (Pubitemid 46147713)
-
(2007)
Journal of Medicinal Chemistry
, vol.50
, Issue.2
, pp. 344-349
-
-
Duplantier, A.J.1
Bachert, E.L.2
Cheng, J.B.3
Cohan, V.L.4
Jenkinson, T.H.5
Kraus, K.G.6
McKechney, M.W.7
Pillar, J.D.8
Watson, J.W.9
-
26
-
-
0036790480
-
Deletion of phosphodiesterase 4D in mice shortens alpha2-adrenoceptor- mediated anesthesia, a behavioural correlate of emesis
-
Robichaud, A.; Stamatiou, P. B.; Jin, C.; Lachance, N.; MacDonald, D.; Laliberté, F.; Liu, S.; Huang, Z.; Conti, M.; Chan, C. C. Deletion of phosphodiesterase 4D in mice shortens alpha2-adrenoceptor-mediated anesthesia, a behavioural correlate of emesis J. Clin. Invest. 2002, 110, 1045-1052
-
(2002)
J. Clin. Invest.
, vol.110
, pp. 1045-1052
-
-
Robichaud, A.1
Stamatiou, P.B.2
Jin, C.3
Lachance, N.4
MacDonald, D.5
Laliberté, F.6
Liu, S.7
Huang, Z.8
Conti, M.9
Chan, C.C.10
-
27
-
-
0000203434
-
Phosphodiesterase 4 inhibitors, structurally unrelated to Rolipram, as promising agents for the treatment of asthma and other pathologies
-
DOI 10.1016/S0223-5234(00)00179-3
-
Dal Piaz, V.; Giovannoni, M. P. Phosphodiesterase 4 inhibitors, structurally unrelated to rolipram, as promising agents for the treatment of asthma and other pathologies Eur. J. Med. Chem. 2000, 35, 463-480 (Pubitemid 30395096)
-
(2000)
European Journal of Medicinal Chemistry
, vol.35
, Issue.5
, pp. 463-480
-
-
Dal Piaz, V.1
Giovannoni, M.P.2
-
28
-
-
74049101069
-
Putting the lid on phosphodiesterase 4
-
Houslay, M. D.; Adams, D. R. Putting the lid on phosphodiesterase 4 Nat. Biotechnol. 2010, 28, 38-40
-
(2010)
Nat. Biotechnol.
, vol.28
, pp. 38-40
-
-
Houslay, M.D.1
Adams, D.R.2
-
29
-
-
0036891154
-
4D or not 4D - The emetogenic basis of PDE4 inhibitors uncovered?
-
Giembycz, M. A. 4D or not 4D - the emetogenic basis of PDE4 inhibitors uncovered? Trends Pharmacol. Sci. 2002, 23, 548 (Pubitemid 35375796)
-
(2002)
Trends in Pharmacological Sciences
, vol.23
, Issue.12
, pp. 548
-
-
Giembycz, M.A.1
-
30
-
-
79851471591
-
Roflumilast: The first in class phosphodiesterase 4 inhibitor approved for the treatment of COPD
-
Giembycz, M. A.; Field, S. K. Roflumilast: The first in class phosphodiesterase 4 inhibitor approved for the treatment of COPD Drug Des., Dev. Ther. 2010, 4, 147-158
-
(2010)
Drug Des., Dev. Ther.
, vol.4
, pp. 147-158
-
-
Giembycz, M.A.1
Field, S.K.2
-
31
-
-
33645469506
-
Medicinal chemistry of N -acylhydrazones: New lead-compounds of analgesic, antiinflammatory and antithrombotic drugs
-
Fraga, C. A. M.; Barreiro, E. J. Medicinal chemistry of N -acylhydrazones: New lead-compounds of analgesic, antiinflammatory and antithrombotic drugs Curr. Med. Chem. 2006, 13, 167-198
-
(2006)
Curr. Med. Chem.
, vol.13
, pp. 167-198
-
-
Fraga, C.A.M.1
Barreiro, E.J.2
-
32
-
-
36749018204
-
Privileged structures: A useful concept for the rational design of new lead drug candidates
-
DOI 10.2174/138955707782331722
-
Duarte, C. D.; Barreiro, E. J.; Fraga, C. A. M. Privileged structures: A useful concept for the rational design of new lead drugs candidates Mini-Rev. Med. Chem. 2007, 7, 1108-1119 (Pubitemid 350200217)
-
(2007)
Mini-Reviews in Medicinal Chemistry
, vol.7
, Issue.11
, pp. 1108-1119
-
-
Duarte, C.D.1
Barreiro, E.J.2
Fraga, C.A.M.3
-
33
-
-
0005486004
-
Cardiotônicos: Histórico e perspectivas de uma antiga e importante classe de agentes terapêuticos
-
Fraga, C. A. M.; Barreiro, E. J. Cardiotônicos: Histórico e perspectivas de uma antiga e importante classe de agentes terapêuticos Quim. Nova 1996, 19, 182-189
-
(1996)
Quim. Nova
, vol.19
, pp. 182-189
-
-
Fraga, C.A.M.1
Barreiro, E.J.2
-
34
-
-
17444420892
-
Estratégia de simplificação molecular no planejamento racional de fármacos: A descoberta de novo agente cardioativo
-
Barreiro, E. J. Estratégia de simplificação molecular no planejamento racional de fármacos: A descoberta de novo agente cardioativo Quim. Nova 2002, 25, 1172-1180
-
(2002)
Quim. Nova
, vol.25
, pp. 1172-1180
-
-
Barreiro, E.J.1
-
35
-
-
0034780105
-
LASSBio 294, a novel cardionotropic agent, increases the calcium content in the sarcoplasmatic reticulum of saponin-skinned cardiac fibres
-
Sudo, R. T.; Zapata-Sudo, G.; Barreiro, E. J. LASSBio 294, a novel cardionotropic agent, increases the calcium content in the sarcoplasmatic reticulum of saponin-skinned cardiac fibres Br. J. Pharmacol. 2001, 134, 603-613
-
(2001)
Br. J. Pharmacol.
, vol.134
, pp. 603-613
-
-
Sudo, R.T.1
Zapata-Sudo, G.2
Barreiro, E.J.3
-
36
-
-
0036152766
-
Cyclic GMP-dependent vasodilatory properties of LASSBio 294 in rat aorta
-
Silva, C. L. M.; Noel, F.; Barreiro, E. J. Vasodilatory properties of LASSBio 294 and its dependence on cGMP increase Br. J. Pharmacol. 2002, 135, 293-298 (Pubitemid 34102124)
-
(2002)
British Journal of Pharmacology
, vol.135
, Issue.1
, pp. 293-298
-
-
Silva, C.L.M.1
Noel, F.2
Barreiro, E.J.3
-
37
-
-
0000369246
-
Heterocyclic-fused 3(2 H)-pyridazinones as potent and selective PDE IV inhibitors: Further structure-activity relationships and molecular modelling studies
-
Dal Piaz, V.; Giovannoni, M.; Castellana, C.; Palacios, J.; Beleta, J.; Domenech, T.; Segarra, V. Heterocyclic-fused 3(2 H)-pyridazinones as potent and selective PDE IV inhibitors: Further structure-activity relationships and molecular modelling studies J. Med. Chem. 1997, 40, 1417-1421
-
(1997)
J. Med. Chem.
, vol.40
, pp. 1417-1421
-
-
Dal Piaz, V.1
Giovannoni, M.2
Castellana, C.3
Palacios, J.4
Beleta, J.5
Domenech, T.6
Segarra, V.7
-
38
-
-
11844255399
-
Bioisosterism: A useful strategy for molecular modification and drug design
-
Lima, L. M.; Barreiro, E. J. Bioisosterism, an useful strategy for molecular modification and drug design Curr. Med. Chem. 2005, 12, 23-49 (Pubitemid 40089827)
-
(2005)
Current Medicinal Chemistry
, vol.12
, Issue.1
, pp. 23-49
-
-
Lima, L.M.1
Barreiro, E.J.2
-
39
-
-
67651165022
-
Studies towards the identification of putative bioactive conformation of potent vasodilator arylidene N -acylhydrazone derivatives
-
Kümmerle, A. E.; Raimundo, J. M.; Leal, C. M.; da Silva, G. S.; Balliano, T. L.; Pereira, M. A.; de Simone, C. A.; Sudo, R. T.; Zapata-Sudo, G.; Fraga, C. A.; Barreiro, E. J. Studies towards the identification of putative bioactive conformation of potent vasodilator arylidene N -acylhydrazone derivatives Eur. J. Med. Chem. 2009, 44, 4004-4009
-
(2009)
Eur. J. Med. Chem.
, vol.44
, pp. 4004-4009
-
-
Kümmerle, A.E.1
Raimundo, J.M.2
Leal, C.M.3
Da Silva, G.S.4
Balliano, T.L.5
Pereira, M.A.6
De Simone, C.A.7
Sudo, R.T.8
Zapata-Sudo, G.9
Fraga, C.A.10
Barreiro, E.J.11
-
40
-
-
17444420766
-
Synthesis and vasodilatory activity of new N-acylhydrazone derivatives, designed as LASSBio-294 analogues
-
DOI 10.1016/j.bmc.2005.03.003
-
Silva, A. G.; Zapata-Sudo, G.; Kummerle, A. E.; Fraga, C. A. M.; Barreiro, E. J.; Sudo, R. T. Synthesis and vasodilatory activity of new N -acylhydrazone derivatives, designed as LASSBio-294 analogues Bioorg. Med. Chem. 2005, 13, 3431-3437 (Pubitemid 40545797)
-
(2005)
Bioorganic and Medicinal Chemistry
, vol.13
, Issue.10
, pp. 3431-3437
-
-
Silva, A.G.1
Zapata-Sudo, G.2
Kummerle, A.E.3
Fraga, C.A.M.4
Barreiro, E.J.5
Sudo, R.T.6
-
41
-
-
0026763993
-
Mild oxidation of aldehydes to the corresponding carboxylic acids and esters: Alkaline iodine oxidation revisited
-
Yamada, S.; Morizono, D.; Yamamoto, K. Mild oxidation of aldehydes to the corresponding carboxylic acids and esters: Alkaline iodine oxidation revisited Tetrahedron Lett. 1992, 33, 4329-4332
-
(1992)
Tetrahedron Lett.
, vol.33
, pp. 4329-4332
-
-
Yamada, S.1
Morizono, D.2
Yamamoto, K.3
-
42
-
-
0034064517
-
Synthesis and analgesic activity of novel N-acylarylhydrazones and isosters, derived from natural safrole
-
DOI 10.1016/S0223-5234(00)00120-3
-
Lima, P. C.; Lima, L. M.; da Silva, K. C. M.; Léda, P. H. O.; de Miranda, A. L. P.; Fraga, C. A. M.; Barreiro, E. J. Synthesis and analgesic activity of novel N -acylhydrazones and isosters, derived from natural safrole Eur. J. Med. Chem. 2000, 35, 187-203 (Pubitemid 30165683)
-
(2000)
European Journal of Medicinal Chemistry
, vol.35
, Issue.2
, pp. 187-203
-
-
Lima, P.C.1
Lima, L.M.2
Da Silva, K.C.M.3
Leda, P.H.O.4
De Miranda, A.L.P.5
Fraga, C.A.M.6
Barreiro, E.J.7
-
43
-
-
0030951446
-
A simplified procedure for the efficient conversion of aromatic aldehydes into esters
-
Lai, G.; Anderson, W. K. A simplified procedure for the efficient conversion of aromatic aldehydes into esters Synth. Commun. 1997, 27, 1281-1283 (Pubitemid 27186703)
-
(1997)
Synthetic Communications
, vol.27
, Issue.7
, pp. 1281-1283
-
-
Lai, G.1
Anderson, W.K.2
-
44
-
-
0021893477
-
Antiulcer agents. I. Gastric antisecretory and cytoprotective properties of substituted imidazo[1,2-a]pyridines
-
DOI 10.1021/jm00145a006
-
Kaminski, J. J.; Bristol, J. A.; Puchalski, C.; Lovey, R. G.; Elliott, A. J.; Guzik, H.; Solomon, D. M.; Conn, D. J.; Domalski, M. S. Antiulcer agents. 1. Gastric antisecretory and cytoprotective properties of substituted imidazo[1,2- a ]pyridines J. Med. Chem. 1985, 28, 876-892 (Pubitemid 15012494)
-
(1985)
Journal of Medicinal Chemistry
, vol.28
, Issue.7
, pp. 876-892
-
-
Kaminski, J.J.1
Bristol, J.A.2
Puchalski, C.3
-
45
-
-
0032033406
-
Synthesis and antinociceptive properties of new structurally planned imidazo[1,2-a]pyridine 3-acylarylhydrazone derivatives
-
DOI 10.1016/S0223-5234(98)80012-3
-
Ribeiro, I. G.; da Silva, K. C. M.; Parrini, S. C.; de Miranda, A. L. P.; Fraga, C. A. M.; Barreiro, E. J. Synthesis and antinociceptive properties of new structurally planned imidazo[1, 2- a ]pyridine 3-acylarylhydrazone derivatives Eur. J. Med. Chem. 1998, 33, 225-235 (Pubitemid 28188259)
-
(1998)
European Journal of Medicinal Chemistry
, vol.33
, Issue.3
, pp. 225-235
-
-
Ribeiro, I.G.1
Da Silva, K.C.M.2
Parrini, S.C.3
De Miranda, A.L.P.4
Fraga, C.A.M.5
Barreiro, E.J.6
-
46
-
-
0022284298
-
Studies on antitubercular agents. Preparation of 1-(4-methoxybenzoyl)-2- benzalhydrazine and 2-aryl-3-(4-methoxybenzamido)-5-carboxymethyl-4-thiazolidino ne
-
Patel, J. M.; Dave, M. P.; Langalia, N. A.; Thaker, K. A. Studies on antitubercular agents preparation of 1-(4-methoxybenzoyl)-2-benzalhydrazine and 2-aryl-3-(4-methoxybenzamido)-5-carboxymethyl-4-thiazolidinone J. Indian Chem. Soc. 1985, 62, 254-255 (Pubitemid 17169771)
-
(1985)
Journal of the Indian Chemical Society
, vol.62
, Issue.3
, pp. 254-255
-
-
Patel, J.M.1
Dave, M.P.2
Langalia, N.A.3
Thaker, K.A.4
-
47
-
-
62549139640
-
Hansch analysis of substituted benzoic acid benzylidene/furan-2-yl- methylene hydrazides as antimicrobial agents
-
Kumar, P.; Narasimhan, B.; Sharma, D.; Judge, V.; Narang, R. Hansch analysis of substituted benzoic acid benzylidene/furan-2-yl-methylene hydrazides as antimicrobial agents Eur. J. Med. Chem. 2009, 44, 1853-1863
-
(2009)
Eur. J. Med. Chem.
, vol.44
, pp. 1853-1863
-
-
Kumar, P.1
Narasimhan, B.2
Sharma, D.3
Judge, V.4
Narang, R.5
-
48
-
-
84861914936
-
Antimicrobial evaluation of 4-methylsulfanyl benzylidene/3-hydroxy benzylidene hydrazides and QSAR studies
-
Kumar, D.; Narang, R.; Judge, V.; Kumar, D.; Narasimhan, B. Antimicrobial evaluation of 4-methylsulfanyl benzylidene/3-hydroxy benzylidene hydrazides and QSAR studies Med. Chem. Res. 2012, 21, 382-394
-
(2012)
Med. Chem. Res.
, vol.21
, pp. 382-394
-
-
Kumar, D.1
Narang, R.2
Judge, V.3
Kumar, D.4
Narasimhan, B.5
-
49
-
-
33947484962
-
Structural studies by nuclear magnetic resonance. V. Phenylhydrazones
-
Karabatsos, G. J.; Taller, R. A. Structural studies by nuclear magnetic resonance. V. Phenylhydrazones J. Am. Chem. Soc. 1963, 85, 3624-3629
-
(1963)
J. Am. Chem. Soc.
, vol.85
, pp. 3624-3629
-
-
Karabatsos, G.J.1
Taller, R.A.2
-
50
-
-
0000544558
-
Conformational behaviour and e / Z isomerization of N -acyl and N -aroylhydrazones
-
Palla, G.; Predieri, G.; Domiano, P.; Vignali, C.; Turner, W. Conformational behaviour and E / Z isomerization of N -acyl and N -aroylhydrazones Tetrahedron 1986, 42, 3649-3654
-
(1986)
Tetrahedron
, vol.42
, pp. 3649-3654
-
-
Palla, G.1
Predieri, G.2
Domiano, P.3
Vignali, C.4
Turner, W.5
-
51
-
-
0001477513
-
Conformational study on N -acylhydrazones of aromatic-aldehydes by NMR-spectroscopy
-
Palla, G.; Pelizzi, C.; Predieri, G.; Vignali, C. Conformational study on N -acylhydrazones of aromatic-aldehydes by NMR-spectroscopy Gazz. Chim. Ital. 1982, 112, 339-341
-
(1982)
Gazz. Chim. Ital.
, vol.112
, pp. 339-341
-
-
Palla, G.1
Pelizzi, C.2
Predieri, G.3
Vignali, C.4
-
52
-
-
84992032450
-
A facile alkylation of ethyl 2-oxocyclopentanecarboxylate
-
Barco, A.; Benetti, S.; Pollini, G. P. A facile alkylation of ethyl 2-oxocyclopentanecarboxylate Synthesis 1973, 316
-
(1973)
Synthesis
, pp. 316
-
-
Barco, A.1
Benetti, S.2
Pollini, G.P.3
-
53
-
-
21544475013
-
An efficient synthesis of substituted hydrazides
-
DOI 10.1055/s-2005-869858, D03305ST
-
Benstead, D. J.; Hulme, A. N.; McNab, H.; Wight, P. An efficient synthesis of substituted hydrazides Synlett 2005, 1571-1574 (Pubitemid 40922530)
-
(2005)
Synlett
, Issue.10
, pp. 1571-1574
-
-
Benstead, D.J.1
Hulme, A.N.2
McNab, H.3
Wight, P.4
-
54
-
-
0037424569
-
Solid-phase synthesis of an A-B loop mimetic of the Cε3 domain of human IgE: Macrocyclization by Sonogashira coupling
-
DOI 10.1021/jo026693e
-
Spivey, A. C.; McKendrick, J.; Srikaran, R.; Helm, B. A. Solid-phase synthesis of an A-B loop mimetic of the C epsilon 3 domain of human IgE: Macrocyclization by Sonogashira coupling J. Org. Chem. 2003, 68, 1843-1851 (Pubitemid 36511333)
-
(2003)
Journal of Organic Chemistry
, vol.68
, Issue.5
, pp. 1843-1851
-
-
Spivey, A.C.1
McKendrick, J.2
Srikaran, R.3
Helm, B.A.4
-
55
-
-
36549016526
-
6-endo-dig Cyclization of heteroarylesters to alkynes promoted by Lewis acid catalyst in the presence of Brønsted acid
-
DOI 10.1016/j.tetlet.2007.11.020, PII S004040390702196X
-
Hellal, M.; Bourguignon, J.; Bihel, F. J. 6- endo-dig Cyclization of heteroarylesters to alkynes promoted by Lewis acid catalyst in the presence of Brönsted acid Tetrahedron Lett. 2008, 49, 62-65 (Pubitemid 350191886)
-
(2008)
Tetrahedron Letters
, vol.49
, Issue.1
, pp. 62-65
-
-
Hellal, M.1
Bourguignon, J.-J.2
Bihel, F.J.-J.3
-
56
-
-
0022548645
-
Selective inhibition of cyclic nucleotide phosphodiesterases of human, bovine and rat aorta
-
DOI 10.1016/0006-2952(86)90333-3
-
Lugnier, C.; Schoeffter, P.; Le Bec, A.; Strouthou, E.; Stoclet, J. C. Selective inhibition of cyclic nucleotide phosphodiesterases of human, bovine and rat aorta Biochem. Pharmacol. 1986, 35, 1743-1751 (Pubitemid 16067796)
-
(1986)
Biochemical Pharmacology
, vol.35
, Issue.10
, pp. 1743-1751
-
-
Lugnier, C.1
Schoeffter, P.2
Le Bec, A.3
-
57
-
-
0035919801
-
Molecular organization of bovine rod cGMP-Phosphodiesterase 6
-
DOI 10.1006/jmbi.2001.4813
-
Tcheudji, J. F. K.; Lebeau, L.; Virmaux, N.; Maftei, C. G.; Cote, R. H.; Lugnier, C.; Schultz, P. Molecular organization of bovine rod cGMP-phosphodiesterase 6 J. Mol. Biol. 2001, 310, 781-791 (Pubitemid 32695695)
-
(2001)
Journal of Molecular Biology
, vol.310
, Issue.4
, pp. 781-791
-
-
Tcheudji, J.F.K.1
Lebeau, L.2
Virmaux, N.3
Maftei, C.G.4
Cote, R.H.5
Lugnier, C.6
Schultz, P.7
-
58
-
-
0019305529
-
Cyclic nucleotide phosphodiesterase activities from pig coronary arteries. Lack of interconvertibility of major forms
-
Keravis, T. M.; Wells, J. N.; Hardman, J. G. Cyclic nucleotide phosphodiesterase activities from pig coronary arteries. Lack of interconvertibility of major forms Biochim. Biophys. Acta 1980, 613, 116-129 (Pubitemid 10041368)
-
(1980)
Biochimica et Biophysica Acta
, vol.613
, Issue.1
, pp. 116-129
-
-
Keravis, T.M.1
Wells, J.N.2
Hardman, J.G.3
-
59
-
-
80052791467
-
The methylation effect in medicinal chemistry
-
Barreiro, E. J.; Kümmerle, A. E.; Fraga, C. A. M. The methylation effect in medicinal chemistry Chem. Rev. 2011, 111, 5215-5246
-
(2011)
Chem. Rev.
, vol.111
, pp. 5215-5246
-
-
Barreiro, E.J.1
Kümmerle, A.E.2
Fraga, C.A.M.3
-
60
-
-
18844426222
-
Selective PDE4 inhibitors as potent anti-inflammatory drugs for the treatment of airway diseases
-
Lagente, V.; Martin-Chouly, C.; Boichot, E.; Martins, M. A.; Silva, P. M. Selective PDE4 inhibitors as potent anti-inflammatory drugs for the treatment of airway diseases Mem. Inst. Oswaldo Cruz 2005, 100 (Suppl 1) 131-136 (Pubitemid 40685453)
-
(2005)
Memorias do Instituto Oswaldo Cruz
, vol.100
, Issue.SUPPL. 1
, pp. 131-136
-
-
Lagente, V.1
Martin-Chouly, C.2
Boichot, E.3
Martins, M.A.4
Silva, P.M.R.5
-
61
-
-
0035216330
-
PDE4 inhibitors induce emesis in ferrets via a noradrenergic pathway
-
Robichaud, A.; Savoie, C.; Stamatiou, P. B.; Tattersall, F. D.; Chan, C. C. PDE4 inhibitors induce emesis in ferrets via a noradrenergic pathway Neuropharmacology 2001, 40, 262-269
-
(2001)
Neuropharmacology
, vol.40
, pp. 262-269
-
-
Robichaud, A.1
Savoie, C.2
Stamatiou, P.B.3
Tattersall, F.D.4
Chan, C.C.5
-
62
-
-
0036152721
-
Assessing the emetic potential of PDE4 inhibitors in rats
-
Robichaud, A.; Savoie, C.; Stamatiou, P. B.; Lachance, N.; Jolicoeur, P.; Rasori, R.; Chan, C. C. Assessing the emetic potential of PDE4 inhibitors in rats Br. J. Pharmacol. 2002, 135, 113-118 (Pubitemid 34102104)
-
(2002)
British Journal of Pharmacology
, vol.135
, Issue.1
, pp. 113-118
-
-
Robichaud, A.1
Savoie, C.2
Stamatiou, P.B.3
Lachance, N.4
Jolicoeur, P.5
Rasori, R.6
Chan, C.C.7
-
63
-
-
0026644298
-
Anti-tumor necrosis factor ameliorates joint disease in murine collagen-induced arthritis
-
Williams, R. O.; Feldmann, M.; Maini, R. N. Anti-tumor necrosis factor ameliorates joint disease in murine collagen-induced arthritis Proc. Natl. Acad. Sci. U.S.A. 1992, 89, 9784-9788
-
(1992)
Proc. Natl. Acad. Sci. U.S.A.
, vol.89
, pp. 9784-9788
-
-
Williams, R.O.1
Feldmann, M.2
Maini, R.N.3
-
64
-
-
0028143099
-
Cytokines as mediators of chronic asthma
-
Barnes, P. J. Cytokines as mediators of chronic asthma Am. J. Respir. Crit. Care Med. 1994, 150, 542-549
-
(1994)
Am. J. Respir. Crit. Care Med.
, vol.150
, pp. 542-549
-
-
Barnes, P.J.1
-
65
-
-
0030434267
-
Pharmacological evidence for tumor necrosis factor as a mediator of allergic inflammation in the airways
-
Renzetti, L. M.; Paciorek, P. M.; Tannu, S. A.; Rinaldi, N. C.; Tocker, J. E.; Wasserman, M. A.; Gater, P. R. Pharmacological evidence for tumor necrosis factor as a mediator of allergic inflammation in the airways J. Pharmacol. Exp. Ther. 1996, 278, 847-853 (Pubitemid 27167054)
-
(1996)
Journal of Pharmacology and Experimental Therapeutics
, vol.278
, Issue.2
, pp. 847-853
-
-
Renzetti, L.M.1
Paciorek, P.M.2
Tannu, S.A.3
Rinaldi, N.C.4
Tocker, J.E.5
Wasserman, M.A.6
Gater, P.R.7
-
67
-
-
0029129429
-
The effects of antiinflammatory and antiallergic drugs on cytokine release after stimulation of human whole blood by lipopolysaccharide and zymosan A
-
Hartman, D. A.; Ochalski, S. J.; Carlson, R. P. The effects of antiinflammatory and antiallergic drugs on cytokine release after stimulation of human whole blood by lipopolysaccharide and zymosan A Inflamm. Res. 1995, 44, 269-274
-
(1995)
Inflamm. Res.
, vol.44
, pp. 269-274
-
-
Hartman, D.A.1
Ochalski, S.J.2
Carlson, R.P.3
-
68
-
-
0028882027
-
Emetic, central nervous system and pulmonary activities of rolipram in the dog
-
Heaslip, R. J.; Evans, D. Y. Emetic, central nervous system and pulmonary activities of rolipram in the dog Eur. J. Pharmacol. 1995, 286, 281-290
-
(1995)
Eur. J. Pharmacol.
, vol.286
, pp. 281-290
-
-
Heaslip, R.J.1
Evans, D.Y.2
-
69
-
-
18844426222
-
Selective PDE4 inhibitors as potent anti-inflammatory drugs for the treatment of airway diseases
-
Lagente, V.; Martin-Chouly, C.; Boichot, E.; Martins, M. A.; Silva, P. M. R. Selective PDE4 inhibitors as potent anti-inflammatory drugs for the treatment of airway diseases Mem. Inst. Oswaldo Cruz 2005, 100, 131-136 (Pubitemid 40685453)
-
(2005)
Memorias do Instituto Oswaldo Cruz
, vol.100
, Issue.SUPPL. 1
, pp. 131-136
-
-
Lagente, V.1
Martin-Chouly, C.2
Boichot, E.3
Martins, M.A.4
Silva, P.M.R.5
-
70
-
-
0023805577
-
Role of alveolar macrophages in lipopolysaccharide-induced neutrophil accumulation
-
Harmsen, A. Role of alveolar macrophages in lipopolysaccharide-induced neutrophil accumulation Infect. Immun. 1988, 56, 1858-1863
-
(1988)
Infect. Immun.
, vol.56
, pp. 1858-1863
-
-
Harmsen, A.1
-
71
-
-
0014349272
-
Fragmentation of granulocytes in pulmonary capillaries during development of the generalized Shwartzman reaction
-
Horn, R. G.; Collins, R. D. Fragmentation of granulocytes in pulmonary capillaries during development of the generalized Shwartzman reaction Lab. Invest. 1968, 19, 451-459
-
(1968)
Lab. Invest.
, vol.19
, pp. 451-459
-
-
Horn, R.G.1
Collins, R.D.2
-
72
-
-
0031743867
-
Comparison of acute endotoxin-induced lesions in A/J and C57BL/6J mice
-
O'Malley, J.; Matesic, L. E.; Zink, M. C.; Strandberg, J. D.; Mooney, M. L.; De Maio, A.; Reeves, R. H. Comparison of acute endotoxin-induced lesions in A/J and C57BL/6J mice J. Hered. 1998, 89, 525-530 (Pubitemid 28560083)
-
(1998)
Journal of Heredity
, vol.89
, Issue.6
, pp. 525-530
-
-
O'Malley, J.1
Matesic, L.E.2
Zink, M.C.3
Strandberg, J.D.4
Mooney, M.L.5
De Maio, A.6
Reeves, R.H.7
-
73
-
-
0000809670
-
Effect of cyclo-oxygenase inhibitors and modulators of cyclic AMP formation on lipopolysaccharide-induced neutrophil infiltration in mouse lung
-
Gonçalves de Moraes, V. L.; Vargaftig, B. B.; Lefort, J.; Meager, A.; Chignard, M. Effect of cyclo-oxygenase inhibitors and modulators of cyclic AMP formation on lipopolysaccharide-induced neutrophil infiltration in mouse lung Br. J. Pharmacol. 1996, 117, 1792-1796 (Pubitemid 26121627)
-
(1996)
British Journal of Pharmacology
, vol.117
, Issue.8
, pp. 1792-1796
-
-
Goncalves De Moraes, V.L.1
Vargaftig, B.B.2
Lefort, J.3
Meager, A.4
Chignard, M.5
-
74
-
-
0013981270
-
An electron microscope study of the effects of bacterial endotoxin on the blood-vascular system
-
McKay, D. G.; Margaretten, W.; Csavossy, I. An electron microscope study of the effects of bacterial endotoxin on the blood-vascular system Lab. Invest. 1966, 15, 1815-1829
-
(1966)
Lab. Invest.
, vol.15
, pp. 1815-1829
-
-
McKay, D.G.1
Margaretten, W.2
Csavossy, I.3
-
75
-
-
0019447265
-
Role of pulmonary edema in the acute pulmonary response to sepsis
-
McCaffree, D. R.; Gray, B. A.; Pennock, B. E. Role of pulmonary edema in the acute pulmonary response to sepsis J. Appl. Physiol. 1981, 50, 1198-1205 (Pubitemid 11078934)
-
(1981)
Journal of Applied Physiology Respiratory Environmental and Exercise Physiology
, vol.50
, Issue.6
, pp. 1198-1205
-
-
McCaffree, D.R.1
Gray, B.A.2
Pennock, B.E.3
-
76
-
-
0021880478
-
Effect of polyethylene glycol-superoxide dismutase and catalase on endotoxemia in pigs
-
Olson, N.; Brown, T., Jr.; Anderson, D. Effect of polyethylene glycol-superoxide dismutase and catalase on endotoxemia in pigs J. Appl. Physiol. 1985, 58, 274-284
-
(1985)
J. Appl. Physiol.
, vol.58
, pp. 274-284
-
-
Olson, N.1
Brown, Jr.T.2
Anderson, D.3
-
77
-
-
0020570257
-
Acute effects of Escherichia coli endotoxin on the pulmonary microcirculation of anesthetized sheep. Structure: Function relationships
-
Meyrick, B.; Brigham, K. L. Acute effects of E. coli endotoxin on the pulmonary microcirculation of anesthetized sheep Lab. Invest. 1983, 48, 458-470 (Pubitemid 13119069)
-
(1983)
Laboratory Investigation
, vol.48
, Issue.4
, pp. 458-470
-
-
Meyrick, B.1
Brighan, K.L.2
-
78
-
-
0014739494
-
The pulmonary ultrastructure in septic shock
-
Coalson, J. J.; Hinshaw, L. B.; Guenter, C. A. The pulmonary ultrastructure in septic shock Exp. Mol. Pathol. 1970, 12, 84-103
-
(1970)
Exp. Mol. Pathol.
, vol.12
, pp. 84-103
-
-
Coalson, J.J.1
Hinshaw, L.B.2
Guenter, C.A.3
-
79
-
-
0027263797
-
Mice treated with a leumedin or antibody to Mac-1 to inhibit leukocyte sequestration survive endotoxin challenge
-
Burch, R. M.; Noronha-Blob, L.; Bator, J. M.; Lowe, V. C.; Sullivan, J. P. Mice treated with a leumedin or antibody to Mac-1 to inhibit leukocyte sequestration survive endotoxin challenge J. Immunol. 1993, 150, 3397-3403 (Pubitemid 23129718)
-
(1993)
Journal of Immunology
, vol.150
, Issue.8
, pp. 3397-3403
-
-
Burch, R.M.1
Noronha-Blob, L.2
Bator, J.M.3
Lowe, V.C.4
Sullivan, J.P.5
-
80
-
-
34447117597
-
Cathelicidin LL-37: LPS-neutralizing, pleiotropic peptide
-
Golec, M. Cathelicidin LL-37: LPS-neutralizing, pleiotropic peptide Ann. Agric. Environ. Med. 2007, 14, 1-4 (Pubitemid 47035650)
-
(2007)
Annals of Agricultural and Environmental Medicine
, vol.14
, Issue.1
, pp. 1-4
-
-
Golec, M.1
-
81
-
-
79953022070
-
GSK256066, an exceptionally high-affinity and selective inhibitor of phosphodiesterase 4 suitable for administration by inhalation: In vitro, kinetic, and in vivo characterization
-
Tralau-Stewart, C. J.; Williamson, R. A.; Nials, A. T.; Gascoigne, M.; Dawson, J.; Hart, G. J.; Angell, A. D. R.; Solanke, Y. E.; Lucas, F. S.; Wiseman, J.; Ward, P.; Ranshaw, L. E.; Knowles, R. G. GSK256066, an exceptionally high-affinity and selective inhibitor of phosphodiesterase 4 suitable for administration by inhalation: in vitro, kinetic, and in vivo characterization J. Pharmacol. Exp. Ther. 2011, 337, 145-154
-
(2011)
J. Pharmacol. Exp. Ther.
, vol.337
, pp. 145-154
-
-
Tralau-Stewart, C.J.1
Williamson, R.A.2
Nials, A.T.3
Gascoigne, M.4
Dawson, J.5
Hart, G.J.6
Angell, A.D.R.7
Solanke, Y.E.8
Lucas, F.S.9
Wiseman, J.10
Ward, P.11
Ranshaw, L.E.12
Knowles, R.G.13
-
82
-
-
0034976397
-
Comparison of PDE 4 inhibitors, rolipram and SB 207499 (Ariflo™, in a rat model of pulmonary neutrophilia
-
DOI 10.1006/pupt.2001.0291
-
TM), in a rat model of pulmonary neutrophilia Pulm. Pharmacol. Ther. 2001, 14, 157-164 (Pubitemid 32553621)
-
(2001)
Pulmonary Pharmacology and Therapeutics
, vol.14
, Issue.2
, pp. 157-164
-
-
Spond, J.1
Chapman, R.2
Fine, J.3
Jones, H.4
Kreutner, W.5
Kung, T.T.6
Minnicozzi, M.7
-
83
-
-
0031858996
-
Systemic administration of endotoxin induces bronchopulmonary hyperreactivity dissociated from TNf-α formation and neutrophil sequestration into the murine lungs
-
Lefort, J.; Singer, M.; Leduc, D.; Renesto, P.; Nahori, M. A.; Huerre, M.; Créminon, C.; Chignard, M.; Vargaftig, B. B. Systemic administration of endotoxin induces bronchopulmonary hyperreactivity dissociated from TNF-alpha formation and neutrophil sequestration into the murine lungs J. Immunol. 1998, 161, 474-480 (Pubitemid 28285557)
-
(1998)
Journal of Immunology
, vol.161
, Issue.1
, pp. 474-480
-
-
Lefort, J.1
Singer, M.2
Leduc, D.3
Renesto, P.4
Nahori, M.A.5
Huerre, M.6
Creminon, C.7
Chignard, M.8
Vargaftig, B.B.9
-
84
-
-
0347123444
-
Ligand-Supported Homology Modeling of G-Protein-Coupled Receptor Sites: Models Sufficient for Successful Virtual Screening
-
DOI 10.1002/anie.200352776
-
Evers, A.; Klebe, G. Ligand-supported homology modeling of G-protein-coupled receptor sites: models sufficient for successful virtual screening Angew. Chem., Int. Ed. 2004, 43, 248-251 (Pubitemid 38082116)
-
(2004)
Angewandte Chemie - International Edition
, vol.43
, Issue.2
, pp. 248-251
-
-
Evers, A.1
Klebe, G.2
-
85
-
-
20844442458
-
Structural basis for the activity of drugs that inhibit phosphodiesterases
-
DOI 10.1016/j.str.2004.10.004, PII S0969212604003727
-
Card, G. L.; England, B. P.; Suzuki, Y.; Fong, D.; Powell, B.; Lee, B.; Luu, C.; Tabrizizad, M.; Gillette, S.; Ibrahim, P. N.; Artis, D. R.; Bollag, G.; Milburn, M. V.; Kim, S. H.; Schlessinger, J.; Zhang, K. Y. Structural basis for the activity of drugs that inhibit phosphodiesterases Structure 2004, 12, 2233-2247 (Pubitemid 39593200)
-
(2004)
Structure
, vol.12
, Issue.12
, pp. 2233-2247
-
-
Card, G.L.1
England, B.P.2
Suzuki, Y.3
Fong, D.4
Powell, B.5
Lee, B.6
Luu, C.7
Tabrizizad, M.8
Gillette, S.9
Ibrahim, P.N.10
Artis, D.R.11
Bollag, G.12
Milburn, M.V.13
Kim, S.-H.14
Schlessinger, J.15
Zhang, K.Y.J.16
-
86
-
-
23444454552
-
The Amber biomolecular simulation programs
-
DOI 10.1002/jcc.20290
-
Case, D. A.; Cheatham, T. E., III; Darden, T.; Gohlke, H.; Luo, R.; Merz, K. M., Jr.; Onufriev, A.; Simmerling, C.; Wang, B.; Woods, R. The Amber biomolecular simulation programs J. Comput. Chem. 2005, 26, 1668-1688 (Pubitemid 43076180)
-
(2005)
Journal of Computational Chemistry
, vol.26
, Issue.16
, pp. 1668-1688
-
-
Case, D.A.1
Cheatham III, T.E.2
Darden, T.3
Gohlke, H.4
Luo, R.5
Merz Jr., K.M.6
Onufriev, A.7
Simmerling, C.8
Wang, B.9
Woods, R.J.10
-
87
-
-
0024439087
-
Retinobenzoic acids. 4. Conformation of aromatic amides with retinoidal activity. Importance of trans-amide stucture for the activity
-
Kagechika, H.; Himi, T.; Kawachi, E.; Shudo, K. Retinobenzoic acids. 4. Conformation of aromatic amides with retinoidal activity. Importance of trans -amide structure for the activity J. Med. Chem. 1989, 32, 2292-2296 (Pubitemid 19245889)
-
(1989)
Journal of Medicinal Chemistry
, vol.32
, Issue.10
, pp. 2292-2296
-
-
Kagechika, H.1
Himi, T.2
Kawachi, E.3
Shudo, K.4
-
88
-
-
68349146235
-
Design, synthesis and analgesic properties of novel conformationally- restricted N -acylhydrazones (NAH)
-
Kümmerle, A. E.; Vieira, M. M.; Schmitt, M.; Miranda, A. L.; Fraga, C. A.; Bourguignon, J.; Barreiro, E. J. Design, synthesis and analgesic properties of novel conformationally-restricted N -acylhydrazones (NAH) Bioorg. Med. Chem. Lett. 2009, 19, 4963-4966
-
(2009)
Bioorg. Med. Chem. Lett.
, vol.19
, pp. 4963-4966
-
-
Kümmerle, A.E.1
Vieira, M.M.2
Schmitt, M.3
Miranda, A.L.4
Fraga, C.A.5
Bourguignon, J.6
Barreiro, E.J.7
-
89
-
-
0037295377
-
Discovery of quinazolines as a novel structural class of potent inhibitors of NF-κB activation
-
DOI 10.1016/S0968-0896(02)00440-6, PII S0968089602004406
-
Tobe, M.; Isobe, Y.; Tomizawa, H.; Nagasaki, T.; Takahashi, H.; Fukazawa, T.; Hayashi, H. Discovery of quinazolines as a novel structural class of potent inhibitors of NF-[kappa]B activation Bioorg. Med. Chem. 2003, 11, 383-391 (Pubitemid 36051028)
-
(2003)
Bioorganic and Medicinal Chemistry
, vol.11
, Issue.3
, pp. 383-391
-
-
Tobe, M.1
Isobe, Y.2
Tomizawa, H.3
Nagasaki, T.4
Takahashi, H.5
Fukazawa, T.6
Hayashi, H.7
-
90
-
-
0025302360
-
Mesoionic 1,2,4-triazolo[4,3-c]quinazolines
-
Gineinah, M. M.; Ismaiel, A. E. M.; El-Kerdawy, M. M.; Glennon, R. A. Mesoionic 1,2,4-triazolo[4,3-c]quinazolines J. Heterocycl. Chem. 1990, 27, 723-726 (Pubitemid 20193018)
-
(1990)
Journal of Heterocyclic Chemistry
, vol.27
, Issue.3
, pp. 723-726
-
-
Gineinah, M.M.1
Ismaiel, A.E.-K.M.2
El-Kerdawy, M.M.3
Glennon, R.A.4
-
91
-
-
0033612127
-
Suzuki-type cross-coupling reaction of 3-iodoindazoles with aryl boronic acids: A general and flexible route to 3-arylindazoles
-
DOI 10.1016/S0040-4020(99)00324-5, PII S0040402099003245
-
Collot, V.; Dallemagne, P.; Bovy, P. R.; Rault, S. Suzuki-type cross-coupling reaction of 3-iodoindazoles with aryl boronic acids: A general and flexible route to 3-arylindazoles Tetrahedron 1999, 55, 6917-6922 (Pubitemid 29236675)
-
(1999)
Tetrahedron
, vol.55
, Issue.22
, pp. 6917-6922
-
-
Collot, V.1
Dallemagne, P.2
Bovy, P.R.3
Rault, S.4
-
92
-
-
0014385564
-
Isolation of mononuclear cells and granulocytes from human blood. Isolation of monuclear cells by one centrifugation, and of granulocytes by combining centrifugation and sedimentation at 1 g
-
Böyum, A. Isolation of mononuclear cells and granulocytes from human blood. Isolation of monuclear cells by one centrifugation, and of granulocytes by combining centrifugation and sedimentation at 1 g Scand. J. Clin. Lab. Invest. Suppl. 1968, 97, 77-89
-
(1968)
Scand. J. Clin. Lab. Invest. Suppl.
, vol.97
, pp. 77-89
-
-
Böyum, A.1
-
93
-
-
0030451949
-
Increased production of tumour necrosis factor-α, interleukin-1β, and interleukin-6 by morphologically normal intestinal biopsies from patients with Crohn's disease
-
Reimund, J. M.; Wittersheim, C.; Dumont, S.; Muller, C. D.; Kenney, J. S.; Baumann, R.; Poindron, P.; Duclos, B. Increased production of tumour necrosis factor-alpha interleukin-1 beta, and interleukin-6 by morphologically normal intestinal biopsies from patients with Crohn's disease Gut 1996, 39, 684-689 (Pubitemid 26426469)
-
(1996)
Gut
, vol.39
, Issue.5
, pp. 684-689
-
-
Reimund, J.-M.1
Wittersheim, C.2
Dumont, S.3
Muller, C.D.4
Kenney, J.S.5
Baumann, R.6
Poindron, P.7
Duclos, B.8
-
94
-
-
84866333313
-
-
Version 7.3. Tripos Associates: St. Louis, MO
-
Sybyl, Version 7.3. Tripos Associates: St. Louis, MO, 2007.
-
(2007)
Sybyl
-
-
-
95
-
-
0011134241
-
Merck molecular force field. II. MMFF94 van der Waals and electrostatic parameters for intermolecular interactions
-
Halgren, T. A. Merck molecular force field. II. MMFF94 van der Waals and electrostatic parameters for intermolecular interactions J. Comput. Chem. 1996, 17, 520-552 (Pubitemid 126567068)
-
(1996)
Journal of Computational Chemistry
, vol.17
, Issue.5-6
, pp. 520-552
-
-
Halgren, T.A.1
-
96
-
-
0842341771
-
Development and use of quantum mechanical molecular models. 76. AM1: A new general purpose quantum mechanical molecular model
-
Dewar, M. J. S.; Zoebisch, E. G.; Healy, E. F.; Stewart, J. J. P. Development and use of quantum mechanical molecular models. 76. AM1: a new general purpose quantum mechanical molecular model J. Am. Chem. Soc. 1985, 107, 3902-3909
-
(1985)
J. Am. Chem. Soc.
, vol.107
, pp. 3902-3909
-
-
Dewar, M.J.S.1
Zoebisch, E.G.2
Healy, E.F.3
Stewart, J.J.P.4
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