-
1
-
-
77953106887
-
Type 2 diabetes comorbidities and treatment challenges: Rationale for DPP-4 inhibitors
-
P.A. Hollander, and P. Kushner Type 2 diabetes comorbidities and treatment challenges: rationale for DPP-4 inhibitors Postgrad. Med. 122 2010 71 80
-
(2010)
Postgrad. Med.
, vol.122
, pp. 71-80
-
-
Hollander, P.A.1
Kushner, P.2
-
2
-
-
77953208938
-
A new therapeutic possibility for type 2 diabetes: DPP-4 inhibitors (sitagliptin)
-
T. Abel, and J. Feher A new therapeutic possibility for type 2 diabetes: DPP-4 inhibitors (sitagliptin) Orv Hetil 151 2010 1012 1016
-
(2010)
Orv Hetil
, vol.151
, pp. 1012-1016
-
-
Abel, T.1
Feher, J.2
-
3
-
-
0032963903
-
Glucagon-like peptide-1: A basis for new approaches to the management of diabetes
-
C.F. Deacon, J.J. Holst, and R.D. Carr Glucagon-like peptide-1: a basis for new approaches to the management of diabetes Drugs Today (Barc) 35 1999 159 170
-
(1999)
Drugs Today (Barc)
, vol.35
, pp. 159-170
-
-
Deacon, C.F.1
Holst, J.J.2
Carr, R.D.3
-
4
-
-
77953145811
-
Diabetes therapy-novel drugs to come (DPP-4 inhibitors, GLP-1 agonists, SGLT-2 inhibitors)
-
B. Gallwitz Diabetes therapy-novel drugs to come (DPP-4 inhibitors, GLP-1 agonists, SGLT-2 inhibitors) MMW Fortschr Med. 152 2010 43 44
-
(2010)
MMW Fortschr Med.
, vol.152
, pp. 43-44
-
-
Gallwitz, B.1
-
5
-
-
19944427998
-
(2R)-4-oxo-4-[3-(trifluoromethyl)-5,6-dihydro[1,2,4]triazolo[4,3-a] 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
-
D. Kim, L. Wang, M. Beconi, G.J. Eiermann, M.H. Fisher, H. He, G.J. Hickey, J.E. Kowalchick, B. Leiting, K. Lyons, F. Marsilio, M.E. McCann, R.A. Patel, A. Petrov, G. Scapin, S.B. Patel, R.S. Roy, J.K. Wu, M.J. Wyvratt, B.B. Zhang, L. Zhu, N.A. Thornberry, and A.E. Weber (2R)-4-oxo-4-[3-(trifluoromethyl) -5,6-dihydro[1,2,4]triazolo[4,3-a]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. 48 2005 141 151
-
(2005)
J. Med. Chem.
, vol.48
, pp. 141-151
-
-
Kim, D.1
Wang, L.2
Beconi, M.3
Eiermann, G.J.4
Fisher, M.H.5
He, H.6
Hickey, G.J.7
Kowalchick, J.E.8
Leiting, B.9
Lyons, K.10
Marsilio, F.11
McCann, M.E.12
Patel, R.A.13
Petrov, A.14
Scapin, G.15
Patel, S.B.16
Roy, R.S.17
Wu, J.K.18
Wyvratt, M.J.19
Zhang, B.B.20
Zhu, L.21
Thornberry, N.A.22
Weber, A.E.23
more..
-
6
-
-
39149121870
-
Discovery of potent and selective dipeptidyl peptidase IV inhibitors derived from beta-aminoamides bearing subsituted triazolopiperazines
-
D. Kim, J.E. Kowalchick, L.L. Brockunier, E.R. Parmee, G.J. Eiermann, M.H. Fisher, H. He, B. Leiting, K. Lyons, G. Scapin, S.B. Patel, A. Petrov, K.D. Pryor, R.S. Roy, J.K. Wu, X. Zhang, M.J. Wyvratt, B.B. Zhang, L. Zhu, N.A. Thornberry, and A.E. Weber Discovery of potent and selective dipeptidyl peptidase IV inhibitors derived from beta-aminoamides bearing subsituted triazolopiperazines J. Med. Chem. 51 2008 589 602
-
(2008)
J. Med. Chem.
, vol.51
, pp. 589-602
-
-
Kim, D.1
Kowalchick, J.E.2
Brockunier, L.L.3
Parmee, E.R.4
Eiermann, G.J.5
Fisher, M.H.6
He, H.7
Leiting, B.8
Lyons, K.9
Scapin, G.10
Patel, S.B.11
Petrov, A.12
Pryor, K.D.13
Roy, R.S.14
Wu, J.K.15
Zhang, X.16
Wyvratt, M.J.17
Zhang, B.B.18
Zhu, L.19
Thornberry, N.A.20
Weber, A.E.21
more..
-
7
-
-
0037030602
-
1-[2-[(5-Cyanopyridin-2-yl)amino]ethylamino]acetyl-2-(S) -pyrrolidinecarbon itrile: A potent, selective, and orally bioavailable dipeptidyl peptidase IV inhibitor with antihyperglycemic properties
-
E.B. Villhauer, J.A. Brinkman, G.B. Naderi, B.E. Dunning, B.L. Mangold, M.D. Mone, M.E. Russell, S.C. Weldon, and T.E. Hughes 1-[2-[(5-Cyanopyridin-2- yl)amino]ethylamino]acetyl-2-(S)-pyrrolidinecarbon itrile: a potent, selective, and orally bioavailable dipeptidyl peptidase IV inhibitor with antihyperglycemic properties J. Med. Chem. 45 2002 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
-
8
-
-
34147093268
-
Effects of vildagliptin on glucose control over 24 weeks in patients with type 2 diabetes inadequately controlled with metformin
-
E. Bosi, R.P. Camisasca, C. Collober, E. Rochotte, and A.J. Garber Effects of vildagliptin on glucose control over 24 weeks in patients with type 2 diabetes inadequately controlled with metformin Diabetes Care 30 2007 890 895
-
(2007)
Diabetes Care
, vol.30
, pp. 890-895
-
-
Bosi, E.1
Camisasca, R.P.2
Collober, C.3
Rochotte, E.4
Garber, A.J.5
-
9
-
-
34247874561
-
Addition of vildagliptin to insulin improves glycaemic control in type 2 diabetes
-
V. Fonseca, A. Schweizer, D. Albrecht, M.A. Baron, I. Chang, and S. Dejager Addition of vildagliptin to insulin improves glycaemic control in type 2 diabetes Diabetologia 50 2007 1148 1155
-
(2007)
Diabetologia
, vol.50
, pp. 1148-1155
-
-
Fonseca, V.1
Schweizer, A.2
Albrecht, D.3
Baron, M.A.4
Chang, I.5
Dejager, S.6
-
10
-
-
22744449063
-
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
-
D.J. Augeri, J.A. Robl, D.A. Betebenner, D.R. Magnin, A. Khanna, J.G. Robertson, A. Wang, L.M. Simpkins, P. Taunk, Q. Huang, S.P. Han, B. Abboa-Offei, M. Cap, L. Xin, L. Tao, E. Tozzo, G.E. Welzel, D.M. Egan, J. Marcinkeviciene, S.Y. Chang, S.A. Biller, M.S. Kirby, R.A. Parker, and L.G. Hamann 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. 48 2005 5025 5037
-
(2005)
J. Med. Chem.
, vol.48
, pp. 5025-5037
-
-
Augeri, D.J.1
Robl, J.A.2
Betebenner, D.A.3
Magnin, D.R.4
Khanna, A.5
Robertson, J.G.6
Wang, A.7
Simpkins, L.M.8
Taunk, P.9
Huang, Q.10
Han, S.P.11
Abboa-Offei, B.12
Cap, M.13
Xin, L.14
Tao, L.15
Tozzo, E.16
Welzel, G.E.17
Egan, D.M.18
Marcinkeviciene, J.19
Chang, S.Y.20
Biller, S.A.21
Kirby, M.S.22
Parker, R.A.23
Hamann, L.G.24
more..
-
11
-
-
34248999413
-
Discovery of alogliptin: A potent, selective, bioavailable, and efficacious inhibitor of dipeptidyl peptidase IV
-
J. Feng, Z. Zhang, M.B. Wallace, J.A. Stafford, S.W. Kaldor, D.B. Kassel, M. Navre, L. Shi, R.J. Skene, T. Asakawa, K. Takeuchi, R. Xu, D.R. Webb, and S.L. Gwaltney 2nd Discovery of alogliptin: a potent, selective, bioavailable, and efficacious inhibitor of dipeptidyl peptidase IV J. Med. Chem. 50 2007 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 II, S.L.14
-
12
-
-
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
-
M. Eckhardt, E. Langkop, M. Mark, M. Tadayyon, L. Thomas, H. Nar, W. Pfrengle, B. Guth, R. Lotz, P. Sieger, H. Fuchs, and F. Himmelsbach 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. 50 2007 6450 6453
-
(2007)
J. Med. Chem.
, vol.50
, pp. 6450-6453
-
-
Eckhardt, M.1
Langkop, 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
-
13
-
-
78650513267
-
The highly potent and selective dipeptidyl peptidase IV inhibitors bearing a thienopyrimidine scaffold effectively treat type 2 diabetes
-
J. Deng, L. Peng, G. Zhang, X. Lan, C. Li, F. Chen, Y. Zhou, Z. Lin, L. Chen, R. Dai, H. Xu, L. Yang, X. Zhang, and W. Hu The highly potent and selective dipeptidyl peptidase IV inhibitors bearing a thienopyrimidine scaffold effectively treat type 2 diabetes Eur. J. Med. Chem. 46 2011 71 76
-
(2011)
Eur. J. Med. Chem.
, vol.46
, pp. 71-76
-
-
Deng, J.1
Peng, L.2
Zhang, G.3
Lan, X.4
Li, C.5
Chen, F.6
Zhou, Y.7
Lin, Z.8
Chen, L.9
Dai, R.10
Xu, H.11
Yang, L.12
Zhang, X.13
Hu, W.14
-
14
-
-
84860333739
-
-
WO(2009)/062258
-
D.G. Bourke, C.J. Burns, A.N. Cuzzupe, J.T. Feutrill, M.R. Kling, T.L. Nero, N-Containing Heterocyclic Compounds, WO(2009)/062258.
-
N-Containing Heterocyclic Compounds
-
-
Bourke, D.G.1
Burns, C.J.2
Cuzzupe, A.N.3
Feutrill, J.T.4
Kling, M.R.5
Nero, T.L.6
-
16
-
-
78751651182
-
Design and synthesis of pyrimidinone and pyrimidinedione inhibitors of dipeptidyl peptidase IV
-
Z. Zhang, M.B. Wallace, J. Feng, J.A. Stafford, R.J. Skene, L. Shi, B. Lee, K. Aertgeerts, A. Jennings, R. Xu, D.B. Kassel, S.W. Kaldor, M. Navre, D.R. Webb, and S.L. Gwaltney Design and synthesis of pyrimidinone and pyrimidinedione inhibitors of dipeptidyl peptidase IV J. Med. Chem. 54 2011 510 524
-
(2011)
J. Med. Chem.
, vol.54
, pp. 510-524
-
-
Zhang, Z.1
Wallace, M.B.2
Feng, J.3
Stafford, J.A.4
Skene, R.J.5
Shi, L.6
Lee, B.7
Aertgeerts, K.8
Jennings, A.9
Xu, R.10
Kassel, D.B.11
Kaldor, S.W.12
Navre, M.13
Webb, D.R.14
Gwaltney, S.L.15
-
17
-
-
34547102733
-
Carbohydrate-based macrolides prepared via a convergent ring closing metathesis approach: In search for novel antibiotics
-
B. Ruttens, P. Blom, S. Van Hoof, I. Hubrecht, J. Van der Eycken, B. Sas, J. Van Hemel, and J. Vandenkerckhove Carbohydrate-based macrolides prepared via a convergent ring closing metathesis approach: in search for novel antibiotics J. Org. Chem. 72 2007 5514 5522
-
(2007)
J. Org. Chem.
, vol.72
, pp. 5514-5522
-
-
Ruttens, B.1
Blom, P.2
Van Hoof, S.3
Hubrecht, I.4
Van Der Eycken, J.5
Sas, B.6
Van Hemel, J.7
Vandenkerckhove, J.8
-
18
-
-
7044239576
-
Highly efficient stereoconservative amidation and deamidation of alpha-amino acids
-
D.M. Shendage, R. Frohlich, and G. Haufe Highly efficient stereoconservative amidation and deamidation of alpha-amino acids Org. Lett. 6 2004 3675 3678
-
(2004)
Org. Lett.
, vol.6
, pp. 3675-3678
-
-
Shendage, D.M.1
Frohlich, R.2
Haufe, G.3
-
19
-
-
0028838528
-
Selective N-Functionalization of 6-Substituted-2-Pyridones
-
H. Liu, S.B. Ko, H. Josien, and D.P. Curran Selective N-Functionalization of 6-Substituted-2-Pyridones Tetrahedron Lett. 36 1995 8917 8920
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 8917-8920
-
-
Liu, H.1
Ko, S.B.2
Josien, H.3
Curran, D.P.4
-
20
-
-
0037012681
-
Double elimination protocol for synthesis of 5,6,11,12- tetradehydrodibenzo[a, e]cyclooctene
-
A. Orita, D. Hasegawa, T. Nakano, and J. Otera Double elimination protocol for synthesis of 5,6,11,12-tetradehydrodibenzo[a, e]cyclooctene Chemistry 8 2002 2000 2004
-
(2002)
Chemistry
, vol.8
, pp. 2000-2004
-
-
Orita, A.1
Hasegawa, D.2
Nakano, T.3
Otera, J.4
-
21
-
-
39749179066
-
Non-conventional methodologies for transition-metal catalysed carbon-carbon coupling: A critical overview. Part 2: The Suzuki reaction
-
F. Alonso, I.P. Beletskaya, and M. Yus Non-conventional methodologies for transition-metal catalysed carbon-carbon coupling: a critical overview. Part 2: the Suzuki reaction Tetrahedron 64 2008 3047 3101
-
(2008)
Tetrahedron
, vol.64
, pp. 3047-3101
-
-
Alonso, F.1
Beletskaya, I.P.2
Yus, M.3
-
22
-
-
28444484982
-
Expression and function of efflux drug transporters in the intestine
-
M. Takano, R. Yumoto, and T. Murakami Expression and function of efflux drug transporters in the intestine Pharmacol. Ther. 109 2006 137 161
-
(2006)
Pharmacol. Ther.
, vol.109
, pp. 137-161
-
-
Takano, M.1
Yumoto, R.2
Murakami, T.3
-
24
-
-
24344439264
-
Transporters and drug therapy: Implications for drug disposition and disease
-
R.H. Ho, and R.B. Kim Transporters and drug therapy: implications for drug disposition and disease Clin. Pharmacol. Ther. 78 2005 260 277
-
(2005)
Clin. Pharmacol. Ther.
, vol.78
, pp. 260-277
-
-
Ho, R.H.1
Kim, R.B.2
-
25
-
-
0346728729
-
The ABCs of drug transport in intestine and liver: Efflux proteins limiting drug absorption and bioavailability
-
L.M. Chan, S. Lowes, and B.H. Hirst The ABCs of drug transport in intestine and liver: efflux proteins limiting drug absorption and bioavailability Eur. J. Pharm. Sci. 21 2004 25 51
-
(2004)
Eur. J. Pharm. Sci.
, vol.21
, pp. 25-51
-
-
Chan, L.M.1
Lowes, S.2
Hirst, B.H.3
-
26
-
-
14044262453
-
Development of computational models for enzymes, transporters, channels, and receptors relevant to ADME/Tox
-
S. Ekins, and P.W. Swaan Development of computational models for enzymes, transporters, channels, and receptors relevant to ADME/Tox Rev. Comp. Ch. 20 2004 333 415
-
(2004)
Rev. Comp. Ch.
, vol.20
, pp. 333-415
-
-
Ekins, S.1
Swaan, P.W.2
-
27
-
-
0037204543
-
Progress in understanding the structure-activity relationships of P-glycoprotein
-
T.R. Stouch, and O. Gudmundsson Progress in understanding the structure-activity relationships of P-glycoprotein Adv. Drug Deliv. Rev. 54 2002 315 328
-
(2002)
Adv. Drug Deliv. Rev.
, vol.54
, pp. 315-328
-
-
Stouch, T.R.1
Gudmundsson, O.2
-
28
-
-
33746057821
-
Functional role of P-glycoprotein in limiting peroral drug absorption: Optimizing drug delivery
-
M.V. Varma, O.P. Perumal, and R. Panchagnula Functional role of P-glycoprotein in limiting peroral drug absorption: optimizing drug delivery Curr. Opin. Chem. Biol. 10 2006 367 373
-
(2006)
Curr. Opin. Chem. Biol.
, vol.10
, pp. 367-373
-
-
Varma, M.V.1
Perumal, O.P.2
Panchagnula, R.3
-
29
-
-
2342533129
-
Structure-function relationships of multidrug resistance P-glycoprotein
-
I.K. Pajeva, C. Globisch, and M. Wiese Structure-function relationships of multidrug resistance P-glycoprotein J. Med. Chem. 47 2004 2523 2533
-
(2004)
J. Med. Chem.
, vol.47
, pp. 2523-2533
-
-
Pajeva, I.K.1
Globisch, C.2
Wiese, M.3
-
30
-
-
0032480901
-
Correlation of human jejunal permeability (in vivo) of drugs with experimentally and theoretically derived parameters. A multivariate data analysis approach
-
S. Winiwarter, N.M. Bonham, F. Ax, A. Hallberg, H. Lennernas, and A. Karlen Correlation of human jejunal permeability (in vivo) of drugs with experimentally and theoretically derived parameters. A multivariate data analysis approach J. Med. Chem. 41 1998 4939 4949
-
(1998)
J. Med. Chem.
, vol.41
, pp. 4939-4949
-
-
Winiwarter, S.1
Bonham, N.M.2
Ax, F.3
Hallberg, A.4
Lennernas, H.5
Karlen, A.6
-
31
-
-
0030914681
-
Polar molecular surface properties predict the intestinal absorption of drugs in humans
-
K. Palm, P. Stenberg, K. Luthman, and P. Artursson Polar molecular surface properties predict the intestinal absorption of drugs in humans Pharm. Res. 14 1997 568 571
-
(1997)
Pharm. Res.
, vol.14
, pp. 568-571
-
-
Palm, K.1
Stenberg, P.2
Luthman, K.3
Artursson, P.4
-
32
-
-
0035289779
-
Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
-
C.A. Lipinski, F. Lombardo, B.W. Dominy, and P.J. Feeney Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings Adv. Drug Deliv. Rev. 46 2001 3 26
-
(2001)
Adv. Drug Deliv. Rev.
, vol.46
, pp. 3-26
-
-
Lipinski, C.A.1
Lombardo, F.2
Dominy, B.W.3
Feeney, P.J.4
-
34
-
-
41549099967
-
The hERG K+ channel: Target and antitarget strategies in drug development
-
E. Raschi, V. Vasina, E. Poluzzi, and F. De Ponti The hERG K+ channel: target and antitarget strategies in drug development Pharmacol. Res. 57 2008 181 195
-
(2008)
Pharmacol. Res.
, vol.57
, pp. 181-195
-
-
Raschi, E.1
Vasina, V.2
Poluzzi, E.3
De Ponti, F.4
-
35
-
-
0038248920
-
Understanding the structure-activity relationship of the human ether-a-go-go-related gene cardiac K+ channel. A model for bad behavior
-
R. Pearlstein, R. Vaz, and D. Rampe Understanding the structure-activity relationship of the human ether-a-go-go-related gene cardiac K+ channel. A model for bad behavior J. Med. Chem. 46 2003 2017 2022
-
(2003)
J. Med. Chem.
, vol.46
, pp. 2017-2022
-
-
Pearlstein, R.1
Vaz, R.2
Rampe, D.3
-
36
-
-
46549083771
-
Pharmacokinetic, pharmacodynamic, and efficacy profiles of alogliptin, a novel inhibitor of dipeptidyl peptidase-4, in rats, dogs, and monkeys
-
B. Lee, L. Shi, D.B. Kassel, T. Asakawa, K. Takeuchi, and R.J. Christopher Pharmacokinetic, pharmacodynamic, and efficacy profiles of alogliptin, a novel inhibitor of dipeptidyl peptidase-4, in rats, dogs, and monkeys Eur. J. Pharmacol. 589 2008 306 314
-
(2008)
Eur. J. Pharmacol.
, vol.589
, pp. 306-314
-
-
Lee, B.1
Shi, L.2
Kassel, D.B.3
Asakawa, T.4
Takeuchi, K.5
Christopher, R.J.6
|