-
1
-
-
0035413618
-
-
Chen, Z.; Gibson, T. B.; Robinson, F.; Silvestro, L.; Pearson, G.; Xu, B.; Wright, A.; Vanderbilt, C.; Cobb, M. H. MAP kinases. Chem. Rev. 2001, 101, 2449-2476.
-
Chen, Z.; Gibson, T. B.; Robinson, F.; Silvestro, L.; Pearson, G.; Xu, B.; Wright, A.; Vanderbilt, C.; Cobb, M. H. MAP kinases. Chem. Rev. 2001, 101, 2449-2476.
-
-
-
-
2
-
-
0142026209
-
p38 MAP kinases: Key signalling molecules as therapeutic targets for inflammatory diseases
-
Kumar, S.; Boehm, J.; Lee, J. C. p38 MAP kinases: Key signalling molecules as therapeutic targets for inflammatory diseases. Nat. Rev. Drug Discovery 2003, 2, 717-726.
-
(2003)
Nat. Rev. Drug Discovery
, vol.2
, pp. 717-726
-
-
Kumar, S.1
Boehm, J.2
Lee, J.C.3
-
3
-
-
29144511607
-
MAPK signalling pathways as molecular targets for anti-inflammatory therapy: From molecular mechanisms to therapeutic benefits
-
Kaminska, B. MAPK signalling pathways as molecular targets for anti-inflammatory therapy: From molecular mechanisms to therapeutic benefits. Biochim. Biophys. Acta 2005, 1754, 253-262.
-
(2005)
Biochim. Biophys. Acta
, vol.1754
, pp. 253-262
-
-
Kaminska, B.1
-
4
-
-
52449118840
-
Targeting the ribose and phosphate binding site of p38 mitogen-activated protein (MAP) kinase: Synthesis and biological testing of 2-alkylsulfanyl-, 4(5)-aryl-, 5(4)-heteroaryl- substituted imidazoles
-
Koch, P.; Baeuerlein, C.; Jank, H.; Laufer, S. Targeting the ribose and phosphate binding site of p38 mitogen-activated protein (MAP) kinase: Synthesis and biological testing of 2-alkylsulfanyl-, 4(5)-aryl-, 5(4)-heteroaryl- substituted imidazoles. J. Med. Chem. 2008, 51, 5630-5640.
-
(2008)
J. Med. Chem
, vol.51
, pp. 5630-5640
-
-
Koch, P.1
Baeuerlein, C.2
Jank, H.3
Laufer, S.4
-
5
-
-
38549166647
-
Towards the improvement of the synthesis of novel 4(5)-aryl-5(4)-heteroaryl-2-thio-substituted imidazoles and their p38MAPkinase inhibitory activity
-
Laufer, S.; Koch, P. Towards the improvement of the synthesis of novel 4(5)-aryl-5(4)-heteroaryl-2-thio-substituted imidazoles and their p38MAPkinase inhibitory activity. Org. Biomol. Chem. 2008, 6, 437-439.
-
(2008)
Org. Biomol. Chem
, vol.6
, pp. 437-439
-
-
Laufer, S.1
Koch, P.2
-
6
-
-
33644873660
-
Small molecular anti-cykotine agents
-
Wagner, G.; Laufer, S. Small molecular anti-cykotine agents. Med. Res. Rev. 2006, 26, 1-62.
-
(2006)
Med. Res. Rev
, vol.26
, pp. 1-62
-
-
Wagner, G.1
Laufer, S.2
-
7
-
-
33947626488
-
From five- to six-membered rings: 3,4-Diarylquinolinone as lead for novelp38MAPkinase inhibitors
-
Peifer, C.; Kinkel, K.; Abadleh, M.; Schollmeyer, D.; Laufer, S. From five- to six-membered rings: 3,4-Diarylquinolinone as lead for novelp38MAPkinase inhibitors. J. Med. Chem. 2007, 50, 1213-1221.
-
(2007)
J. Med. Chem
, vol.50
, pp. 1213-1221
-
-
Peifer, C.1
Kinkel, K.2
Abadleh, M.3
Schollmeyer, D.4
Laufer, S.5
-
8
-
-
0000096835
-
Click chemistry: Diverse chemical function from a few good reactions
-
Kolb, H. C.; Finn, M. G.; Sharpless, K. B. Click chemistry: Diverse chemical function from a few good reactions. Angew. Chem., Int. Ed. 2001, 40, 2004-2021.
-
(2001)
Angew. Chem., Int. Ed
, vol.40
, pp. 2004-2021
-
-
Kolb, H.C.1
Finn, M.G.2
Sharpless, K.B.3
-
9
-
-
38949106966
-
Room temperature facile synthesis of quinoxalines catalyzed by amidosulfonic acid
-
Li, Z.; Li, W.; Sun, Y.; Huang, H.; Ouyang, P. Room temperature facile synthesis of quinoxalines catalyzed by amidosulfonic acid. J. Heterocycl. Chem. 2008, 45, 285-288.
-
(2008)
J. Heterocycl. Chem
, vol.45
, pp. 285-288
-
-
Li, Z.1
Li, W.2
Sun, Y.3
Huang, H.4
Ouyang, P.5
-
10
-
-
23744463590
-
Molecular iodine. A powerful catalyst for the easy and efficient synthesis of quinoxalines
-
More, S. V.; Sastry, M. N. V.; Wang, C. C.; Yao, C. F. Molecular iodine. A powerful catalyst for the easy and efficient synthesis of quinoxalines. Tetrahedron Lett. 2005, 46, 6345-6348.
-
(2005)
Tetrahedron Lett
, vol.46
, pp. 6345-6348
-
-
More, S.V.1
Sastry, M.N.V.2
Wang, C.C.3
Yao, C.F.4
-
11
-
-
33645404779
-
Cerium(IV) ammonium nitrate (CAN) as a catalyst in tap water: A simple, efficient and green approach to the synthesis of quinoxalines
-
More, S. V.; Sastry, M. N. V.; Yao, C. F. Cerium(IV) ammonium nitrate (CAN) as a catalyst in tap water: A simple, efficient and green approach to the synthesis of quinoxalines. Green Chem. 2006, 8, 91-95.
-
(2006)
Green Chem
, vol.8
, pp. 91-95
-
-
More, S.V.1
Sastry, M.N.V.2
Yao, C.F.3
-
12
-
-
2942519827
-
General microwave-assisted protocols for the expedient synthesis of quinoxalines and heterocyclic pyrazines
-
Zhao, Z.; Wisnoski, D. D.; Wolkenberg, S. E.; Leister, W. H.; Wang, Y.; Lindsley, C. W. General microwave-assisted protocols for the expedient synthesis of quinoxalines and heterocyclic pyrazines. Tetrahedron Lett. 2004, 45, 4873-4876.
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 4873-4876
-
-
Zhao, Z.1
Wisnoski, D.D.2
Wolkenberg, S.E.3
Leister, W.H.4
Wang, Y.5
Lindsley, C.W.6
-
13
-
-
67650816016
-
3-(4-Fluorophenyl)-6- methoxy-2-(4-pyridyl)quinoxaline
-
Jahns, H.; Koch, P.; Schollmeyer, D.; Laufer, S. 3-(4-Fluorophenyl)-6- methoxy-2-(4-pyridyl)quinoxaline. Acta Crystallogr. 2009, E65, o1626.
-
(2009)
Acta Crystallogr
, vol.E65
-
-
Jahns, H.1
Koch, P.2
Schollmeyer, D.3
Laufer, S.4
-
14
-
-
0001038733
-
Rational development of practical catalysts for aromatic carbon-nitrogen bond formation
-
Wolfe, J. P.; Wagaw, S.; Marcoux, J. F.; Buchwald, S. L. Rational development of practical catalysts for aromatic carbon-nitrogen bond formation. Acc. Chem. Res. 1998, 31, 805-818.
-
(1998)
Acc. Chem. Res
, vol.31
, pp. 805-818
-
-
Wolfe, J.P.1
Wagaw, S.2
Marcoux, J.F.3
Buchwald, S.L.4
-
15
-
-
70349758388
-
3-(4-Fluorophenyl)-2-(4-pyridyl) pyrido[2,3-b]pyrazine
-
Koch, P.; Schollmeyer, D.; Laufer, S. 3-(4-Fluorophenyl)-2-(4-pyridyl) pyrido[2,3-b]pyrazine. Acta Crystallogr. 2009, E65, o2546.
-
(2009)
Acta Crystallogr
, vol.E65
-
-
Koch, P.1
Schollmeyer, D.2
Laufer, S.3
-
16
-
-
70349778753
-
2-(4-Fluorophenyl)-3-(4-pyridyl) pyrido[2,3-b]pyrazine
-
Koch, P.; Schollmeyer, D.; Laufer, S. 2-(4-Fluorophenyl)-3-(4-pyridyl) pyrido[2,3-b]pyrazine. Acta Crystallogr. 2009, E65, o2512.
-
(2009)
Acta Crystallogr
, vol.E65
-
-
Koch, P.1
Schollmeyer, D.2
Laufer, S.3
-
17
-
-
67649836759
-
4-[3-(4-Fluorophenyl)quinoxalin-2- yl]-N-isopropylpyridin-2-amine
-
Koch, P.; Schollmeyer, D.; Laufer, S. 4-[3-(4-Fluorophenyl)quinoxalin-2- yl]-N-isopropylpyridin-2-amine. Acta Crystallogr. 2009, E65, o1344.
-
(2009)
Acta Crystallogr
, vol.E65
-
-
Koch, P.1
Schollmeyer, D.2
Laufer, S.3
-
18
-
-
27644589566
-
An immunosorbent, nonradioactive p38 MAP kinase assay comparable to standard radioactive liquid-phase assays
-
Laufer, S.; Thuma, S.; Peifer, C.; Greim, C.; Herweh, Y.; Albrecht, A.; Dehner, F. An immunosorbent, nonradioactive p38 MAP kinase assay comparable to standard radioactive liquid-phase assays. Anal. Biochem. 2005, 344, 135-137.
-
(2005)
Anal. Biochem
, vol.344
, pp. 135-137
-
-
Laufer, S.1
Thuma, S.2
Peifer, C.3
Greim, C.4
Herweh, Y.5
Albrecht, A.6
Dehner, F.7
-
19
-
-
33748276903
-
Development and optimization of a non-radioactive JNK3 assay
-
Peifer, C.; Luik, S.; Thuma, S.; Herweh, Y.; Laufer, S. Development and optimization of a non-radioactive JNK3 assay. Comb. Chem. High Throughput Screening 2006, 9, 613-618.
-
(2006)
Comb. Chem. High Throughput Screening
, vol.9
, pp. 613-618
-
-
Peifer, C.1
Luik, S.2
Thuma, S.3
Herweh, Y.4
Laufer, S.5
-
20
-
-
77249154091
-
-
Jaguar, version 7.5; Schroedinger, LLC: New York, 2008
-
Jaguar, version 7.5; Schroedinger, LLC: New York, 2008.
-
-
-
-
21
-
-
77249086649
-
-
Schroedinger Suite 2008, Induced Fit Docking Protocol. Glide, version 5.0; Schroedinger, LLC: New York, 2005
-
Schroedinger Suite 2008, Induced Fit Docking Protocol. Glide, version 5.0; Schroedinger, LLC: New York, 2005.
-
-
-
-
22
-
-
20244384146
-
The development of monocyclic pyrazolone based cytokine synthesis inhibitors
-
Golebiowski, A.; Townes, J. A.; Laufersweiler, M. J.; Brugel, T. A.; Clark, M. P.; Clark, C. M.; Djung, J. F.; Laughlin, S. K.; Sabat, M. P.; Bookland, R. G.; VanRens, J. C.; De, B.; Hsieh, L. C.; Janusz, M. J.; Walter, R. L.; Webster, M. E.; Mekel, M. J. The development of monocyclic pyrazolone based cytokine synthesis inhibitors. Bioorg. Med. Chem. Lett. 2005, 15, 2285-2289.
-
(2005)
Bioorg. Med. Chem. Lett
, vol.15
, pp. 2285-2289
-
-
Golebiowski, A.1
Townes, J.A.2
Laufersweiler, M.J.3
Brugel, T.A.4
Clark, M.P.5
Clark, C.M.6
Djung, J.F.7
Laughlin, S.K.8
Sabat, M.P.9
Bookland, R.G.10
VanRens, J.C.11
De, B.12
Hsieh, L.C.13
Janusz, M.J.14
Walter, R.L.15
Webster, M.E.16
Mekel, M.J.17
|