-
1
-
-
0037928769
-
The role of dipeptidyl peptidase IV in the cleavage of glucagon family peptides
-
Zhu, L.; Tamvakopoulos, C.; Xie, D.; Dragovic, J.; Shen, X.; Fenyk-Melody, J.E.; Schmidt, K.; Bagchi, A.; Griffin, P.R.; Thornberry, N.A.; Roy, R. S. The role of dipeptidyl peptidase IV in the cleavage of glucagon family peptides. J. Biol. Chem. 2003, 278, 22418-22423.
-
(2003)
J. Biol. Chem
, vol.278
, pp. 22418-22423
-
-
Zhu, L.1
Tamvakopoulos, C.2
Xie, D.3
Dragovic, J.4
Shen, X.5
Fenyk-Melody, J.E.6
Schmidt, K.7
Bagchi, A.8
Griffin, P.R.9
Thornberry, N.A.10
Roy, R.S.11
-
2
-
-
0036869408
-
Therapy of type 2 diabetes mellitus based on the actions of glucagon-like peptide-1
-
Holst, J.J. Therapy of type 2 diabetes mellitus based on the actions of glucagon-like peptide-1. Diabetes Metab. Res. Rev. 2002, 18, 430-441.
-
(2002)
Diabetes Metab. Res. Rev
, vol.18
, pp. 430-441
-
-
Holst, J.J.1
-
3
-
-
0037045845
-
Effect of 6-week course of glucagon-like peptide 1 on glycaemic control, insulin sensitivity, and β-cell function in type 2 diabetes: A parallel-group study
-
Zander, M.; Madsbad, S.; Madsen, J.L.; Holst, J.J. Effect of 6-week course of glucagon-like peptide 1 on glycaemic control, insulin sensitivity, and β-cell function in type 2 diabetes: a parallel-group study. Lancet 2002, 359, 824-830.
-
(2002)
Lancet
, vol.359
, pp. 824-830
-
-
Zander, M.1
Madsbad, S.2
Madsen, J.L.3
Holst, J.J.4
-
4
-
-
2642519637
-
Treatment of type two diabetes mellitus with agonists of the GLP-1 receptor or DPP-IV inhibitors
-
Holst, J.J. Treatment of type two diabetes mellitus with agonists of the GLP-1 receptor or DPP-IV inhibitors. Exp. Opin. Emerg. Drugs 2004, 9, 155-166.
-
(2004)
Exp. Opin. Emerg. Drugs
, vol.9
, pp. 155-166
-
-
Holst, J.J.1
-
5
-
-
12744269699
-
Therapeutic assessment of glucagon-like peptide-1 agonists compared with dipeptidyl peptidase IV inhibitors as potential antidiabetic drugs
-
Mentlein, R. Therapeutic assessment of glucagon-like peptide-1 agonists compared with dipeptidyl peptidase IV inhibitors as potential antidiabetic drugs. Exp. Opin. Investig. Drugs 2005, 14, 57-64.
-
(2005)
Exp. Opin. Investig. Drugs
, vol.14
, pp. 57-64
-
-
Mentlein, R.1
-
6
-
-
17144374877
-
Glucagon-like peptide 1 receptor agonists and dipeptidyl peptidase IV inhbitors: New therapeutic agents for the treatment of type 2 diabetes
-
Sinclair, E.M.; Drucker, D.J. Glucagon-like peptide 1 receptor agonists and dipeptidyl peptidase IV inhbitors: new therapeutic agents for the treatment of type 2 diabetes. Curr. Opin. Endocrinol. Diabet., 2005, 12, 146-151.
-
(2005)
Curr. Opin. Endocrinol. Diabet
, vol.12
, pp. 146-151
-
-
Sinclair, E.M.1
Drucker, D.J.2
-
7
-
-
14044264798
-
Glucagon-like peptide 1 and inhibitors of dipeptidyl peptidase IV in the treatment of type 2 diabetes mellitus
-
Holst, J.J.; Deacon, C.F. Glucagon-like peptide 1 and inhibitors of dipeptidyl peptidase IV in the treatment of type 2 diabetes mellitus. Curr. Opin. Pharmacol. 2004, 4, 589-596.
-
(2004)
Curr. Opin. Pharmacol
, vol.4
, pp. 589-596
-
-
Holst, J.J.1
Deacon, C.F.2
-
8
-
-
0036298693
-
Metformin effects on dipeptidylpeptidase IV degradation of glucagon-like peptide-1
-
Hinke, S.A.; Kuhn-Wache, K.; Hoffmann, T.; Pederson, R.A.; McIntosh, C.H.S.; Demuth, H.-U. Metformin effects on dipeptidylpeptidase IV degradation of glucagon-like peptide-1. Biochem. Biophys. Res. Comm. 2002, 291, 1302-1308.
-
(2002)
Biochem. Biophys. Res. Comm
, vol.291
, pp. 1302-1308
-
-
Hinke, S.A.1
Kuhn-Wache, K.2
Hoffmann, T.3
Pederson, R.A.4
McIntosh, C.H.S.5
Demuth, H.-U.6
-
9
-
-
0036290037
-
Dipeptidyl peptidase IV inhibition as an approach to the treatment and prevention of type 2 diabetes: A historical perspective
-
Deacon, C.F.; Holst, J.J. Dipeptidyl peptidase IV inhibition as an approach to the treatment and prevention of type 2 diabetes: a historical perspective. Biochem. Biophys. Res. Comm. 2002, 294, 1-4.
-
(2002)
Biochem. Biophys. Res. Comm
, vol.294
, pp. 1-4
-
-
Deacon, C.F.1
Holst, J.J.2
-
10
-
-
0036391928
-
Rebuttal to Deacon and Holst: "Metformin effects on dipeptidyl peptidase IV degradation of glucagon-like peptide-1" versus "Dipeptidyl peptidase inhibition as an approach to the treatment and prevention of type 2 diabetes: a historical perspective." Biochem
-
Demuth, H.-U.; Hinke, S.A.; Pederson, R.A.; McIntosh, C.H.S. Rebuttal to Deacon and Holst: "Metformin effects on dipeptidyl peptidase IV degradation of glucagon-like peptide-1" versus "Dipeptidyl peptidase inhibition as an approach to the treatment and prevention of type 2 diabetes: a historical perspective." Biochem. Biophys. Res. Comm. 2002, 296, 229-232.
-
(2002)
Biophys. Res. Comm
, vol.296
, pp. 229-232
-
-
Demuth, H.-U.1
Hinke, S.A.2
Pederson, R.A.3
McIntosh, C.H.S.4
-
11
-
-
35448997033
-
DPP-IV inhibition and therapeutic potential
-
Villhauer, E.B.; Coppola, G.M.; Hughes, T.E. DPP-IV inhibition and therapeutic potential. Ann. Rep. Med. Chem. 2001, 36, 191-200.
-
(2001)
Ann. Rep. Med. Chem
, vol.36
, pp. 191-200
-
-
Villhauer, E.B.1
Coppola, G.M.2
Hughes, T.E.3
-
12
-
-
0037869031
-
Dipeptidyl peptidase IV inhibitors for the treatment of impaired glucose tolerance and type 2 diabetes
-
Wiedeman, P.E.; Trevillyan, J.M. Dipeptidyl peptidase IV inhibitors for the treatment of impaired glucose tolerance and type 2 diabetes. Curr. Opin. Investig. Drugs 2003, 4, 412-420.
-
(2003)
Curr. Opin. Investig. Drugs
, vol.4
, pp. 412-420
-
-
Wiedeman, P.E.1
Trevillyan, J.M.2
-
13
-
-
4544232468
-
Inhibitors of dipeptidyl peptidase IV: A novel approach for the prevention and treatment of type 2 diabetes?
-
Deacon, C.F.; Ahrén, B.; Holst, J.J. Inhibitors of dipeptidyl peptidase IV: a novel approach for the prevention and treatment of type 2 diabetes? Exp. Opin. Investig. Drugs 2004, 13, 1091-1102.
-
(2004)
Exp. Opin. Investig. Drugs
, vol.13
, pp. 1091-1102
-
-
Deacon, C.F.1
Ahrén, B.2
Holst, J.J.3
-
14
-
-
3843072211
-
Dipeptidyl peptidase IV inhibitors for the treatment of diabetes
-
Weber, A.E. Dipeptidyl peptidase IV inhibitors for the treatment of diabetes. J. Med. Chem. 2004, 47, 4135-4141.
-
(2004)
J. Med. Chem
, vol.47
, pp. 4135-4141
-
-
Weber, A.E.1
-
15
-
-
33747605803
-
-
Gwaltney, II, S. L.; Stafford, J. A. Inhibitors of Dipeptidyl Peptidase 4. Ann. Reports Med. Chem. 2005, 40, 149-165.
-
Gwaltney, II, S. L.; Stafford, J. A. Inhibitors of Dipeptidyl Peptidase 4. Ann. Reports Med. Chem. 2005, 40, 149-165.
-
-
-
-
16
-
-
60349089942
-
-
Okubo, A.; Nishioka, H.; Arai, H.; Tanaka, Y.; Kato, H.; Nakata, N. World Patent 1991/18877, 1991.
-
Okubo, A.; Nishioka, H.; Arai, H.; Tanaka, Y.; Kato, H.; Nakata, N. World Patent 1991/18877, 1991.
-
-
-
-
17
-
-
0028803516
-
Aminoacylpyrrolidine-2-nitriles: Potent and stable inhibitors of dipeptidyl-peptidase IV (CD26)
-
Li, J.; Wilk, E.; Wilk, S. Aminoacylpyrrolidine-2-nitriles: potent and stable inhibitors of dipeptidyl-peptidase IV (CD26). Arch. Biochem. Biophys. 1995, 323, 148-154.
-
(1995)
Arch. Biochem. Biophys
, vol.323
, pp. 148-154
-
-
Li, J.1
Wilk, E.2
Wilk, S.3
-
18
-
-
0029992827
-
2-Cyanopyrrolidides as potent, stable inhibitors of dipeptidyl peptidase IV
-
Ashworth, D.M.; Atrash, B.; Baker, G.R.; Baxter, A.J.; Jenkins, P.D.; Jones, D.M.; Szelke, M. 2-Cyanopyrrolidides as potent, stable inhibitors of dipeptidyl peptidase IV. Bioorg. Med. Chem. Lett. 1996, 6, 1163-1166.
-
(1996)
Bioorg. Med. Chem. Lett
, vol.6
, pp. 1163-1166
-
-
Ashworth, D.M.1
Atrash, B.2
Baker, G.R.3
Baxter, A.J.4
Jenkins, P.D.5
Jones, D.M.6
Szelke, M.7
-
19
-
-
0037030602
-
1-[2-[(5-Cyanopyridin-2-yl)amino]-ethylamino]acetyl-2-(S)pyrrolidine- carbonitrile: A potent, selective, and orally bioavailable dipeptidyl peptidase IV inhibitor with antihyperglycemic properties
-
Villhauer, E.B.; Brinkman, J.A.; Naderi, G.B.; Dunning, B.E.; Mangold, B.L.; Mone, M.D.; Russell, M.E.; Weldon, S.C.; Hughes, T.E. 1-[2-[(5-Cyanopyridin-2-yl)amino]-ethylamino]acetyl-2-(S)pyrrolidine- carbonitrile: a potent, selective, and orally bioavailable dipeptidyl peptidase IV inhibitor with antihyperglycemic properties. J. Med. Chem. 2002, 45, 2362-2365.
-
(2002)
J. Med. Chem
, vol.45
, pp. 2362-2365
-
-
Villhauer, E.B.1
Brinkman, J.A.2
Naderi, G.B.3
Dunning, B.E.4
Mangold, B.L.5
Mone, M.D.6
Russell, M.E.7
Weldon, S.C.8
Hughes, T.E.9
-
20
-
-
0036583164
-
Inhibition of dipeptidyl peptidase IV improves metabolic control over a 4-week study period in type 2 diabetes
-
Ahrén, B.; Simonsson, E.; Larsson, H.; Landin-olsson, M.; Torgeirsson, H.; Jansson, P.-A.; Sandqvist, M.; Bavenholm, P.; Efendic, S.; Eriksson, J.W.; Dickinson, S.; Holmes, D. Inhibition of dipeptidyl peptidase IV improves metabolic control over a 4-week study period in type 2 diabetes. Diabetes Care 2002, 25, 869-875.
-
(2002)
Diabetes Care
, vol.25
, pp. 869-875
-
-
Ahrén, B.1
Simonsson, E.2
Larsson, H.3
Landin-olsson, M.4
Torgeirsson, H.5
Jansson, P.-A.6
Sandqvist, M.7
Bavenholm, P.8
Efendic, S.9
Eriksson, J.W.10
Dickinson, S.11
Holmes, D.12
-
21
-
-
0037777695
-
1- (3-Hydroxy-1-adamantyl)amino]acetyl]-2-cyano-(S)pyrrolidine: A potent, selective, and orally bioavailable dipeptidyl peptidase IV inhibitor with antihyperglycemic properties
-
Villhauer, E.B.; Brinkman, J.A.; Naderi, G.B.; Burkey, B.F.; Dunning, B.E.; Prasad, K.; Mangold, B.L.; Russell, M.E.; Hughes, T.E. 1- (3-Hydroxy-1-adamantyl)amino]acetyl]-2-cyano-(S)pyrrolidine: a potent, selective, and orally bioavailable dipeptidyl peptidase IV inhibitor with antihyperglycemic properties. J. Med. Chem. 2003, 46, 2774-2789.
-
(2003)
J. Med. Chem
, vol.46
, pp. 2774-2789
-
-
Villhauer, E.B.1
Brinkman, J.A.2
Naderi, G.B.3
Burkey, B.F.4
Dunning, B.E.5
Prasad, K.6
Mangold, B.L.7
Russell, M.E.8
Hughes, T.E.9
-
22
-
-
2442482515
-
Inhibition of dipeptidyl peptidase-4 reduces glycemia, sustains insulin levels, and reduces glucagon levels in type 2 diabetes
-
Ahrén, B.; Landin-Olsson, M.; Jansson, P.-A.; Svensson, M.; Holmes, D.; Schweizer, A. Inhibition of dipeptidyl peptidase-4 reduces glycemia, sustains insulin levels, and reduces glucagon levels in type 2 diabetes. J. Clin. Endocrinol. Metab. 2004, 89, 2078-2084.
-
(2004)
J. Clin. Endocrinol. Metab
, vol.89
, pp. 2078-2084
-
-
Ahrén, B.1
Landin-Olsson, M.2
Jansson, P.-A.3
Svensson, M.4
Holmes, D.5
Schweizer, A.6
-
23
-
-
9444285818
-
Twelve- and 52-week efficacy of the dipeptidyl peptidase IV inhibitor LAF237 in metformin-treated patients with type 2 diabetes
-
Ahrén, B.; Gomis, R.; Standl, E.; Mills, D.; Schweizer, A. Twelve- and 52-week efficacy of the dipeptidyl peptidase IV inhibitor LAF237 in metformin-treated patients with type 2 diabetes. Diabetes Care 2004, 27, 2874-2880.
-
(2004)
Diabetes Care
, vol.27
, pp. 2874-2880
-
-
Ahrén, B.1
Gomis, R.2
Standl, E.3
Mills, D.4
Schweizer, A.5
-
24
-
-
60349087112
-
-
Novartis press release, November 13, 2006.
-
Novartis press release, November 13, 2006.
-
-
-
-
25
-
-
60349130948
-
-
Novartis press release, February 26, 2007.
-
Novartis press release, February 26, 2007.
-
-
-
-
26
-
-
0032544133
-
Probing the importance of spacial and conformational domains in captopril analogs for angiotensin converting enzyme activity
-
Hanessian, S.; Reinhold, U.; Saulnier, M.; Claridge, S. Probing the importance of spacial and conformational domains in captopril analogs for angiotensin converting enzyme activity. Bioorg. Med. Chem. Lett. 1998, 8, 2123-2128.
-
(1998)
Bioorg. Med. Chem. Lett
, vol.8
, pp. 2123-2128
-
-
Hanessian, S.1
Reinhold, U.2
Saulnier, M.3
Claridge, S.4
-
27
-
-
0030820238
-
The synthesis of enantiopure ω-methanoprolines and ω-methanopipecolic acids by a novel cyclopropanation reaction: The "flattening" of proline
-
Hanessian, S.; Reinhold, U.; Gentile, G. The synthesis of enantiopure ω-methanoprolines and ω-methanopipecolic acids by a novel cyclopropanation reaction: the "flattening" of proline. Angew. Chem., Int. Ed. Engl. 1997, 36, 1881-1884.
-
(1881)
Angew. Chem., Int. Ed. Engl
, vol.1997
, pp. 36
-
-
Hanessian, S.1
Reinhold, U.2
Gentile, G.3
-
28
-
-
2342565117
-
-
Magnin, D.R.; Robl, J.A.; Sulsky, R.B.; Augeri, D.J.; Huang, Y; Simpkins, L.M.; Taunk, P.C.; Betebenner, D.A.; Robertson, J.G.; Abboa-Offei, B.E.; Wang, A; Cap, M.; Xin, L.; Tao, L.; Sitkoff, D.F.; Malley, M.F.; Gougoutas, J.Z.; Khanna, A.; Huang, Q.; Han, S.-P.; Parker, R.A.; Hamann, L.G. Synthesis of novel potent dipeptidyl peptidase IV inhibitors with enhanced chemical stability: interplay between the N-terminal amino acid alkyl side chain and the cyclopropyl group of α-aminoacyl-L-cis-4,5-methanoprolinenitrile-based inhbitors. J. Med. Chem. 2004, 47, 2587-2598.
-
Magnin, D.R.; Robl, J.A.; Sulsky, R.B.; Augeri, D.J.; Huang, Y; Simpkins, L.M.; Taunk, P.C.; Betebenner, D.A.; Robertson, J.G.; Abboa-Offei, B.E.; Wang, A; Cap, M.; Xin, L.; Tao, L.; Sitkoff, D.F.; Malley, M.F.; Gougoutas, J.Z.; Khanna, A.; Huang, Q.; Han, S.-P.; Parker, R.A.; Hamann, L.G. Synthesis of novel potent dipeptidyl peptidase IV inhibitors with enhanced chemical stability: interplay between the N-terminal amino acid alkyl side chain and the cyclopropyl group of α-aminoacyl-L-cis-4,5-methanoprolinenitrile-based inhbitors. J. Med. Chem. 2004, 47, 2587-2598.
-
-
-
-
29
-
-
22744449063
-
-
Augeri, D.J.; Robl, J.A.; Betebenner, D.A.; Magnin, D.R.; Khanna, A.; Robertson, J.G.; Wang, A; Simpkins, L.M.; Taunk, P.C.; Huang, Q.; Han, S.-P.; Abboa-Offei, B.E.; Cap, M.; Xin, L.; Tao, L.; Tozzo, E.; Welzel, G.E.; Egan, D.M.; Marcinkeviciene, J.; Chang, S.Y.; Biller, S.A.; Kirby, M.S.; Parker, R.A.; Hamann, L.G. Discovery and preclinical profile of saxagliptin (BMS-477118): a highly potent, long-acting, orally active dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetes. J. Med. Chem. 2005, 48, 5025-5037.
-
Augeri, D.J.; Robl, J.A.; Betebenner, D.A.; Magnin, D.R.; Khanna, A.; Robertson, J.G.; Wang, A; Simpkins, L.M.; Taunk, P.C.; Huang, Q.; Han, S.-P.; Abboa-Offei, B.E.; Cap, M.; Xin, L.; Tao, L.; Tozzo, E.; Welzel, G.E.; Egan, D.M.; Marcinkeviciene, J.; Chang, S.Y.; Biller, S.A.; Kirby, M.S.; Parker, R.A.; Hamann, L.G. Discovery and preclinical profile of saxagliptin (BMS-477118): a highly potent, long-acting, orally active dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetes. J. Med. Chem. 2005, 48, 5025-5037.
-
-
-
-
30
-
-
42149194313
-
Glucose-lowering activity of the dipeptidyl peptidase-4 inhibitor saxagliptin in drug-naïve patients with type 2 diabetes
-
Rosenstock, J.; Sankoh, S.; List, J.F. Glucose-lowering activity of the dipeptidyl peptidase-4 inhibitor saxagliptin in drug-naïve patients with type 2 diabetes. Diabetes, Obesity Metab. 2008, 10, 376-386.
-
(2008)
Diabetes, Obesity Metab
, vol.10
, pp. 376-386
-
-
Rosenstock, J.1
Sankoh, S.2
List, J.F.3
-
32
-
-
35748965263
-
-
Weber, A. E.; Thornberry, N. Case history: Januvia™ (sitagliptin), a selective dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetes. Ann. Reports Med. Chem. 2007, 42, 95-109.
-
Weber, A. E.; Thornberry, N. Case history: Januvia™ (sitagliptin), a selective dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetes. Ann. Reports Med. Chem. 2007, 42, 95-109.
-
-
-
-
33
-
-
33947690115
-
Discovery of Januvia™ (sitagliptin), a selective dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetes
-
Thornberry, N.A.; Weber, A. E. Discovery of Januvia™ (sitagliptin), a selective dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetes. Curr. Top. Med. Chem. 2007, 7, 557-568.
-
(2007)
Curr. Top. Med. Chem
, vol.7
, pp. 557-568
-
-
Thornberry, N.A.1
Weber, A.E.2
-
34
-
-
19944427998
-
-
Kim, D.; Wang, L.; Beconi, M.; Eiermann, G.J.; Fisher, M.H.; He, H.; Hickey, G.J.; Kowalchick, J.E.; Leiting, B.; Lyons, K.; Marsilio, F.; McCann, M.E.; Patel, R.A.; Petrov, A.; Scapin, G.; Patel, S.B.; Roy, R.S.; Wu, J.K.; Wyvratt, M.J.; Zhang, B.B.; Zhu, L.; Thornberry, N.A.; Weber, A.E. (2R)-4-Oxo-4-[3-(trifluoromethyl)-5, 6-dihydro[1,2,4]triazolo[4,3-α]pyrazin-7(8H)-yl]-1-(2,4, 5-trifluorophenyl)butan-2-amine: a potent, orally active dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetes. J. Med. Chem. 2005, 48, 141-151.
-
Kim, D.; Wang, L.; Beconi, M.; Eiermann, G.J.; Fisher, M.H.; He, H.; Hickey, G.J.; Kowalchick, J.E.; Leiting, B.; Lyons, K.; Marsilio, F.; McCann, M.E.; Patel, R.A.; Petrov, A.; Scapin, G.; Patel, S.B.; Roy, R.S.; Wu, J.K.; Wyvratt, M.J.; Zhang, B.B.; Zhu, L.; Thornberry, N.A.; Weber, A.E. (2R)-4-Oxo-4-[3-(trifluoromethyl)-5, 6-dihydro[1,2,4]triazolo[4,3-α]pyrazin-7(8H)-yl]-1-(2,4, 5-trifluorophenyl)butan-2-amine: a potent, orally active dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetes. J. Med. Chem. 2005, 48, 141-151.
-
-
-
-
35
-
-
60349112706
-
-
Himmelsbach, F., Mark, M., Eckhardt, M., Langkopf, E., Maier, R., Lotz, R. World Patent 2002/068420, 2002.
-
Himmelsbach, F., Mark, M., Eckhardt, M., Langkopf, E., Maier, R., Lotz, R. World Patent 2002/068420, 2002.
-
-
-
-
36
-
-
60349088903
-
-
Kanstrup, A.B.; Christiansen, L.B.; Lundbeck, J.M.; Sams, C.K.; Kristiansen, M. World Patent 2002/02560, 2002.
-
Kanstrup, A.B.; Christiansen, L.B.; Lundbeck, J.M.; Sams, C.K.; Kristiansen, M. World Patent 2002/02560, 2002.
-
-
-
-
37
-
-
37349073397
-
8-(3-(R)-Aminopiperidin-1-yl)-7-but-2-ynyl-3-methyl -1-(4-methyl-quinazolin-2-ylmethyl)-3,7-dihydropurine-2,6-dione (BI 1356), a highly potent, selective, long-acting, and orally bioavailable DPP-4 inhibitor for the treatment of type 2 diabetes
-
Eckhardt,M.; Langkopf, E.; Mark,M.; Tadayyon,M.; Thomas,L.; Nar, H.; Pfrengle, W.; Guth, B.; Lotz, R.; Sieger, P.; Fuchs, H.; Himmelsbach, F. 8-(3-(R)-Aminopiperidin-1-yl)-7-but-2-ynyl-3-methyl -1-(4-methyl-quinazolin-2-ylmethyl)-3,7-dihydropurine-2,6-dione (BI 1356), a highly potent, selective, long-acting, and orally bioavailable DPP-4 inhibitor for the treatment of type 2 diabetes. J. Med. Chem. 2007, 50, 6450-6453.
-
(2007)
J. Med. Chem
, vol.50
, pp. 6450-6453
-
-
Eckhardt, M.1
Langkopf, E.2
Mark, M.3
Tadayyon, M.4
Thomas, L.5
Nar, H.6
Pfrengle, W.7
Guth, B.8
Lotz, R.9
Sieger, P.10
Fuchs, H.11
Himmelsbach, F.12
-
38
-
-
25844459084
-
Dipeptidyl peptidase IV inhibition for the treatment of type 2 diabetes
-
Lankas, G.R.; Leiting, B.; Roy, R.S.; Eiermann, G.J.; Beconi, M.G.; Biftu, T.; Chan, C.-C.; Edmondson, S.; Feeney, W.P.; He, H.; Ippolito, D.E.; Kim, D.; Lyons, K.A.; Ok, H.O.; Patel, R.A.; Petrov, A.N.; Pryor, K.A.; Qian, X.; Reigle, L.; Woods, A.; Wu, J.K.; Zaller, D.; Zhang, X.; Zhu, L.; Weber, A.E.; Thornberry, N.A. Dipeptidyl peptidase IV inhibition for the treatment of type 2 diabetes. Diabetes, 2005, 54, 2988-2994.
-
(2005)
Diabetes
, vol.54
, pp. 2988-2994
-
-
Lankas, G.R.1
Leiting, B.2
Roy, R.S.3
Eiermann, G.J.4
Beconi, M.G.5
Biftu, T.6
Chan, C.-C.7
Edmondson, S.8
Feeney, W.P.9
He, H.10
Ippolito, D.E.11
Kim, D.12
Lyons, K.A.13
Ok, H.O.14
Patel, R.A.15
Petrov, A.N.16
Pryor, K.A.17
Qian, X.18
Reigle, L.19
Woods, A.20
Wu, J.K.21
Zaller, D.22
Zhang, X.23
Zhu, L.24
Weber, A.E.25
Thornberry, N.A.26
more..
-
39
-
-
60349086667
-
-
Forst, T.; Uhlig-Laske, B; Ring, A; Ritzhaupt, A; Graefe-Mody, U; Dugi, K.A. The novel, potent, and selective DPP-IV inhibitor BI 1356 significantly lowers HbA1c after only 4 weeks of treatment in patients with type 2 diabetes. Presented at the 2007 American Diabetes Association Meeting, Chicago, IL, United States, June 22-26, 2007; 594-P.
-
Forst, T.; Uhlig-Laske, B; Ring, A; Ritzhaupt, A; Graefe-Mody, U; Dugi, K.A. The novel, potent, and selective DPP-IV inhibitor BI 1356 significantly lowers HbA1c after only 4 weeks of treatment in patients with type 2 diabetes. Presented at the 2007 American Diabetes Association Meeting, Chicago, IL, United States, June 22-26, 2007; 594-P.
-
-
-
-
40
-
-
0037394499
-
A fully integrated protein crystallization platform for small-molecule drug discovery
-
Hosfield, D., Palan, J., Hilgers, M., Scheibe, D., McRee , D.E., and Stevens, R.C. A fully integrated protein crystallization platform for small-molecule drug discovery. J. Struct. Biol., 2003, 142, 207-217.
-
(2003)
J. Struct. Biol
, vol.142
, pp. 207-217
-
-
Hosfield, D.1
Palan, J.2
Hilgers, M.3
Scheibe, D.4
McRee, D.E.5
Stevens, R.C.6
-
41
-
-
0037325440
-
Structural Genomix, and Syrrx. I can see clearly now: Structural biology and drug discovery
-
Mountain, V. Astex, Structural Genomix, and Syrrx. I can see clearly now: structural biology and drug discovery. Chem. Biol. 2003, 10, 95-98.
-
(2003)
Chem. Biol
, vol.10
, pp. 95-98
-
-
Mountain, V.A.1
-
42
-
-
34248999413
-
Discovery of alogliptin: A potent, selective, bioavailable, and efficacious inhibitor of dipeptidyl peptidase IV
-
Feng, J.; Zhang, Z.; Wallace, M. B.; Stafford, J. A.; Kaldor, S. W.; Kassel, D. B.; Navre, M.; Shi, L.; Skene, R. J.; Asakawa, T.; Takeuchi, K.; Xu, R.; Webb, D. R.; Gwaltney, S. L. Discovery of alogliptin: A potent, selective, bioavailable, and efficacious inhibitor of dipeptidyl peptidase IV. J. Med. Chem. 2007, 50, 2297-2300.
-
(2007)
J. Med. Chem
, vol.50
, pp. 2297-2300
-
-
Feng, J.1
Zhang, Z.2
Wallace, M.B.3
Stafford, J.A.4
Kaldor, S.W.5
Kassel, D.B.6
Navre, M.7
Shi, L.8
Skene, R.J.9
Asakawa, T.10
Takeuchi, K.11
Xu, R.12
Webb, D.R.13
Gwaltney, S.L.14
-
43
-
-
20244385394
-
Double incretin receptor knockout (DIRKO) mice reveal an essential role for the enteroinsular axis in transducing the glucoregulatory actions of DPP-IV inhibitors
-
Hansotia, T.; Baggio, L.L.; Delmeire, D.; Hinke, S.A.; Yamada, Y.; Tsukiyama, K.; Seino, Y.; Holst, J.J.; Schuit, F.; Drucker, D.J. Double incretin receptor knockout (DIRKO) mice reveal an essential role for the enteroinsular axis in transducing the glucoregulatory actions of DPP-IV inhibitors. Diabetes, 2004, 53, 1326-1335.
-
(2004)
Diabetes
, vol.53
, pp. 1326-1335
-
-
Hansotia, T.1
Baggio, L.L.2
Delmeire, D.3
Hinke, S.A.4
Yamada, Y.5
Tsukiyama, K.6
Seino, Y.7
Holst, J.J.8
Schuit, F.9
Drucker, D.J.10
-
44
-
-
60349120536
-
-
Christopher, R.; Covington, P.; Davenport, M.; Fleck, P.; Mekki, Q.; Wann, E.; Karim, A.; Pharmacokinetics, pharmacodynamics and tolerability of multiple doses of alogliptin benzoate (SYR-322), a dipeptidyl peptidase-IV inhibitor, in patients with type 2 diabetes. Presented at the 2007 American Diabetes Association Meeting, Chicago, IL, United States, June 22-26, 2007; 499-P.
-
Christopher, R.; Covington, P.; Davenport, M.; Fleck, P.; Mekki, Q.; Wann, E.; Karim, A.; Pharmacokinetics, pharmacodynamics and tolerability of multiple doses of alogliptin benzoate (SYR-322), a dipeptidyl peptidase-IV inhibitor, in patients with type 2 diabetes. Presented at the 2007 American Diabetes Association Meeting, Chicago, IL, United States, June 22-26, 2007; 499-P.
-
-
-
-
45
-
-
60349112285
-
-
DeFronzo, R.; Fleck, P.; Wilson, C.; Mekki, Q. Alogliptin monotherapy improves glycemic control in patients with type 2 diabetes. Presented at the 2008 American Diabetes Association Meeting, San Francisco, CA, United States, June 6-10, 2008; 446-P.
-
DeFronzo, R.; Fleck, P.; Wilson, C.; Mekki, Q. Alogliptin monotherapy improves glycemic control in patients with type 2 diabetes. Presented at the 2008 American Diabetes Association Meeting, San Francisco, CA, United States, June 6-10, 2008; 446-P.
-
-
-
-
46
-
-
60349110359
-
-
Fleck, P.; Christopher, R.; Covington, P.; Wilson, C.; Mekki, Q. Efficacy and safety of alogliptin monotherapy in patients with type 2 diabetes. Presented at the 2008 American Diabetes Association Meeting, San Francisco, CA, United States, June 6-10, 2008; 479-P.
-
Fleck, P.; Christopher, R.; Covington, P.; Wilson, C.; Mekki, Q. Efficacy and safety of alogliptin monotherapy in patients with type 2 diabetes. Presented at the 2008 American Diabetes Association Meeting, San Francisco, CA, United States, June 6-10, 2008; 479-P.
-
-
-
-
47
-
-
60349123530
-
-
Rosenstock, J.; Rendell, M.; Gross, J.L.; Fleck, P.; Wilson, C.; Mekki, Q. Alogliptin added to insulin therapy in patients with type 2 diabetes reduces HbA1c without increasing weight gain or hypoglycemia. Presented at the 2008 American Diabetes Association Meeting, San Francisco, CA, United States, June 6-10, 2008; 444-P.
-
Rosenstock, J.; Rendell, M.; Gross, J.L.; Fleck, P.; Wilson, C.; Mekki, Q. Alogliptin added to insulin therapy in patients with type 2 diabetes reduces HbA1c without increasing weight gain or hypoglycemia. Presented at the 2008 American Diabetes Association Meeting, San Francisco, CA, United States, June 6-10, 2008; 444-P.
-
-
-
-
48
-
-
60349084079
-
-
Pratley, R.; Kipnes, M.; Fleck, P.; Wilson, C.; Mekki, Q. Alogliptin added to sulfonylurea therapy in patients with type 2 diabetes reduces HbA1c without increasing hypoglycemia. Presented at the 2008 American Diabetes Association Meeting, San Francisco, CA, United States, June 6-10, 2008; 445-P.
-
Pratley, R.; Kipnes, M.; Fleck, P.; Wilson, C.; Mekki, Q. Alogliptin added to sulfonylurea therapy in patients with type 2 diabetes reduces HbA1c without increasing hypoglycemia. Presented at the 2008 American Diabetes Association Meeting, San Francisco, CA, United States, June 6-10, 2008; 445-P.
-
-
-
-
49
-
-
60349083167
-
-
Nauck, M.; Ellis, G.; Fleck, P.; Wilson, C.; Mekki, Q. Efficacy and safety of alogliptin added to metformin therapy in patients with type 2 diabetes. Presented at the 2008 American Diabetes Association Meeting, San Francisco, CA, United States, June 6-10, 2008; 447-P.
-
Nauck, M.; Ellis, G.; Fleck, P.; Wilson, C.; Mekki, Q. Efficacy and safety of alogliptin added to metformin therapy in patients with type 2 diabetes. Presented at the 2008 American Diabetes Association Meeting, San Francisco, CA, United States, June 6-10, 2008; 447-P.
-
-
-
-
50
-
-
60349128487
-
-
Pratley, R.; Reusch, J.; Fleck, P.; Wilson, C.; Mekki, Q. Efficacy and safety of alogliptin added to pioglitazone therapy in patients with type 2 diabetes. Presented at the 2008 American Diabetes Association Meeting, San Francisco, CA, United States, June 6-10, 2008; 448-P.
-
Pratley, R.; Reusch, J.; Fleck, P.; Wilson, C.; Mekki, Q. Efficacy and safety of alogliptin added to pioglitazone therapy in patients with type 2 diabetes. Presented at the 2008 American Diabetes Association Meeting, San Francisco, CA, United States, June 6-10, 2008; 448-P.
-
-
-
|