-
1
-
-
59849124635
-
Type 1 diabetes mellitus in pediatrics
-
quiz 85
-
Cooke DW, Plotnick L. Type 1 diabetes mellitus in pediatrics. Pediatr Rev 2008; 29: 374-84; quiz 85.
-
(2008)
Pediatr Rev
, vol.29
, pp. 374-384
-
-
Cooke, D.W.1
Plotnick, L.2
-
2
-
-
0028779842
-
The pathogenesis of insulindependent diabetes mellitus
-
Atkinson MA, Maclaren NK. The pathogenesis of insulindependent diabetes mellitus. N Engl J Med 1994; 331: 1428-36.
-
(1994)
N Engl J Med
, vol.331
, pp. 1428-1436
-
-
Atkinson, M.A.1
McLaren, N.K.2
-
4
-
-
57649195613
-
Dietary fats and prevention of type 2 diabetes
-
Riserus U, Willett WC, Hu FB. Dietary fats and prevention of type 2 diabetes. Prog Lipid Res 2009; 48: 44-51.
-
(2009)
Prog Lipid Res
, vol.48
, pp. 44-51
-
-
Riserus, U.1
Willett, W.C.2
Hu, F.B.3
-
5
-
-
0029043139
-
Cell and molecular biology of the incretin hormones glucagon-like peptide-I and glucose-dependent insulin releasing polypeptide
-
Fehmann HC, Goke R, Goke B. Cell and molecular biology of the incretin hormones glucagon-like peptide-I and glucose-dependent insulin releasing polypeptide. Endocr Rev 1995; 16: 390-410.
-
(1995)
Endocr Rev
, vol.16
, pp. 390-410
-
-
Fehmann, H.C.1
Goke, R.2
Goke, B.3
-
6
-
-
0037964447
-
Catalytic properties and inhibition of proline-specific dipeptidyl peptidases II, IV and VII
-
Leiting B, Pryor KD, Wu JK, et al. Catalytic properties and inhibition of proline-specific dipeptidyl peptidases II, IV and VII. Biochem J 2003; 371: 525-32.
-
(2003)
Biochem J
, vol.371
, pp. 525-532
-
-
Leiting, B.1
Pryor, K.D.2
Wu, J.K.3
-
7
-
-
0036158954
-
Biological actions and therapeutic potential of the glucagon-like peptides
-
Drucker DJ. Biological actions and therapeutic potential of the glucagon-like peptides. Gastroenterology 2002; 122: 531-44.
-
(2002)
Gastroenterology
, vol.122
, pp. 531-544
-
-
Drucker, D.J.1
-
9
-
-
0027157849
-
Biological effects and metabolic rates of glucagonlike peptide-1 7-36 amide and glucagonlike peptide-1 7-37 in healthy subjects are indistinguishable
-
Orskov C, Wettergren A, Holst JJ. Biological effects and metabolic rates of glucagonlike peptide-1 7-36 amide and glucagonlike peptide-1 7-37 in healthy subjects are indistinguishable. Diabetes 1993; 42: 658-61.
-
(1993)
Diabetes
, vol.42
, pp. 658-661
-
-
Orskov, C.1
Wettergren, A.2
Holst, J.J.3
-
10
-
-
0027215348
-
Dipeptidyl-peptidase IV hydrolyses gastric inhibitory polypeptide, glucagon-like peptide-1(7-36)amide, peptide histidine methionine and is responsible for their degradation in human serum
-
Mentlein R, Gallwitz B, Schmidt WE. Dipeptidyl-peptidase IV hydrolyses gastric inhibitory polypeptide, glucagon-like peptide-1(7-36)amide, peptide histidine methionine and is responsible for their degradation in human serum. Eur J Biochem 1993; 214: 829-35.
-
(1993)
Eur J Biochem
, vol.214
, pp. 829-835
-
-
Mentlein, R.1
Gallwitz, B.2
Schmidt, W.E.3
-
11
-
-
0023107555
-
Insulinotropin: Glucagon-like peptide I (7-37) co-encoded in the glucagon gene is a potent stimulator of insulin release in the perfused rat pancreas
-
Mojsov S, Weir GC, Habener JF. Insulinotropin: glucagon-like peptide I (7-37) co-encoded in the glucagon gene is a potent stimulator of insulin release in the perfused rat pancreas. J Clin Invest 1987; 79: 616-9.
-
(1987)
J Clin Invest
, vol.79
, pp. 616-619
-
-
Mojsov, S.1
Weir, G.C.2
Habener, J.F.3
-
12
-
-
0023781471
-
Glucagon-like peptide-1 (7-36 amide): A potent glucagonostatic and insulinotropic hormone
-
Matsuyama T, Komatsu R, Namba M, et al. Glucagon-like peptide-1 (7-36 amide): a potent glucagonostatic and insulinotropic hormone. Diabetes Res Clin Pract 1988; 5: 281-4.
-
(1988)
Diabetes Res Clin Pract
, vol.5
, pp. 281-284
-
-
Matsuyama, T.1
Komatsu, R.2
Namba, M.3
-
13
-
-
0344357096
-
Glucagon-like peptide I stimulates insulin gene expression and increases cyclic AMP levels in a rat islet cell line
-
Drucker DJ, Philippe J, Mojsov S, Chick WL, Habener JF. Glucagon-like peptide I stimulates insulin gene expression and increases cyclic AMP levels in a rat islet cell line. Proc Natl Acad Sci USA 1987; 84: 3434-8.
-
(1987)
Proc Natl Acad Sci USA
, vol.84
, pp. 3434-3438
-
-
Drucker, D.J.1
Philippe, J.2
Mojsov, S.3
Chick, W.L.4
Habener, J.F.5
-
14
-
-
0027533758
-
Truncated GLP-1 (proglucagon 78-107-amide) inhibits gastric and pancreatic functions in man
-
Wettergren A, Schjoldager B, Mortensen PE, et al. Truncated GLP-1 (proglucagon 78-107-amide) inhibits gastric and pancreatic functions in man. Dig Dis Sci 1993; 38: 665-73.
-
(1993)
Dig Dis Sci
, vol.38
, pp. 665-673
-
-
Wettergren, A.1
Schjoldager, B.2
Mortensen, P.E.3
-
15
-
-
0037414781
-
Glucagon-like peptide-1 receptor signaling modulates beta cell apoptosis
-
Li Y, Hansotia T, Yusta B, et al. Glucagon-like peptide-1 receptor signaling modulates beta cell apoptosis. J Biol Chem 2003; 278: 471-8.
-
(2003)
J Biol Chem
, vol.278
, pp. 471-478
-
-
Li, Y.1
Hansotia, T.2
Yusta, B.3
-
16
-
-
77951675095
-
Glucose-dependent insulinotropic polypeptide is expressed in pancreatic islet alphacells and promotes insulin secretion
-
Fujita Y, Wideman RD, Asadi A, et al. Glucose-dependent insulinotropic polypeptide is expressed in pancreatic islet alphacells and promotes insulin secretion. Gastroenterology 2010; 138: 1966-75.
-
(2010)
Gastroenterology
, vol.138
, pp. 1966-1975
-
-
Fujita, Y.1
Wideman, R.D.2
Asadi, A.3
-
17
-
-
66049137664
-
Glucosedependent insulinotropic polypeptide (GIP) and its receptor (GIPR): Cellular localization, lesion-affected expression, and impaired regenerative axonal growth
-
Buhren BA, Gasis M, Thorens B, Muller HW, Bosse F. Glucosedependent insulinotropic polypeptide (GIP) and its receptor (GIPR): cellular localization, lesion-affected expression, and impaired regenerative axonal growth. J Neurosci Res 2009; 87: 1858-70.
-
(2009)
J Neurosci Res
, vol.87
, pp. 1858-1870
-
-
Buhren, B.A.1
Gasis, M.2
Thorens, B.3
Muller, H.W.4
Bosse, F.5
-
18
-
-
0029118049
-
Degradation of glucosedependent insulinotropic polypeptide and truncated glucagon-like peptide 1 in vitro and in vivo by dipeptidyl peptidase IV
-
Kieffer TJ, McIntosh CH, Pederson RA. Degradation of glucosedependent insulinotropic polypeptide and truncated glucagon-like peptide 1 in vitro and in vivo by dipeptidyl peptidase IV. Endocrinology 1995; 136: 3585-96.
-
(1995)
Endocrinology
, vol.136
, pp. 3585-3596
-
-
Kieffer, T.J.1
McIntosh, C.H.2
Pederson, R.A.3
-
19
-
-
0033520869
-
GIP biology and fat metabolism
-
Yip RG, Wolfe MM. GIP biology and fat metabolism. Life Sci 2000; 66: 91-103.
-
(2000)
Life Sci
, vol.66
, pp. 91-103
-
-
Yip, R.G.1
Wolfe, M.M.2
-
20
-
-
17744374566
-
Osteoblast-derived cells express functional glucose-dependent insulinotropic peptide receptors
-
Bollag RJ, Zhong Q, Phillips P, et al. Osteoblast-derived cells express functional glucose-dependent insulinotropic peptide receptors. Endocrinology 2000; 141: 1228-35.
-
(2000)
Endocrinology
, vol.141
, pp. 1228-1235
-
-
Bollag, R.J.1
Zhong, Q.2
Phillips, P.3
-
21
-
-
0036068322
-
Inhibition of gastric inhibitory polypeptide signaling prevents obesity
-
Miyawaki K, Yamada Y, Ban N, et al. Inhibition of gastric inhibitory polypeptide signaling prevents obesity. Nat Med 2002; 8: 738-42.
-
(2002)
Nat Med
, vol.8
, pp. 738-742
-
-
Miyawaki, K.1
Yamada, Y.2
Ban, N.3
-
22
-
-
0038363953
-
Dipeptidyl peptidase IV substrates. An update on in vitro peptide hydrolysis by human DPPIV
-
de Meester I, Lambeir AM, Proost P, Scharpe S. Dipeptidyl peptidase IV substrates. An update on in vitro peptide hydrolysis by human DPPIV. Adv Exp Med Biol 2003; 524: 3-17.
-
(2003)
Adv Exp Med Biol
, vol.524
, pp. 3-17
-
-
de Meester, I.1
Lambeir, A.M.2
Proost, P.3
Scharpe, S.4
-
23
-
-
3042766378
-
Evolutionary relationships of the prolyl oligopeptidase family enzymes
-
Venalainen JI, Juvonen RO, Mannisto PT. Evolutionary relationships of the prolyl oligopeptidase family enzymes. Eur J Biochem 2004; 271: 2705-15.
-
(2004)
Eur J Biochem
, vol.271
, pp. 2705-2715
-
-
Venalainen, J.I.1
Juvonen, R.O.2
Mannisto, P.T.3
-
24
-
-
0033780088
-
Cloning, expression and chromosomal localization of a novel human dipeptidyl peptidase (DPP) IV homolog, DPP8
-
Abbott CA, Yu DM, Woollatt E, et al. Cloning, expression and chromosomal localization of a novel human dipeptidyl peptidase (DPP) IV homolog, DPP8. Eur J Biochem 2000; 267: 6140-50.
-
(2000)
Eur J Biochem
, vol.267
, pp. 6140-6150
-
-
Abbott, C.A.1
Yu, D.M.2
Woollatt, E.3
-
25
-
-
0037121086
-
Identification and characterization of human DPP9, a novel homologue of dipeptidyl peptidase IV
-
Olsen C, Wagtmann N. Identification and characterization of human DPP9, a novel homologue of dipeptidyl peptidase IV. Gene 2002; 299: 185-93.
-
(2002)
Gene
, vol.299
, pp. 185-193
-
-
Olsen, C.1
Wagtmann, N.2
-
26
-
-
0642277907
-
DPPIV, seprase, and related serine peptidases in multiple cellular functions
-
Chen WT, Kelly T, Ghersi G. DPPIV, seprase, and related serine peptidases in multiple cellular functions. Curr Top Dev Biol 2003; 54: 207-32.
-
(2003)
Curr Top Dev Biol
, vol.54
, pp. 207-232
-
-
Chen, W.T.1
Kelly, T.2
Ghersi, G.3
-
27
-
-
33646416468
-
The protease complex consisting of dipeptidyl peptidase IV and seprase plays a role in the migration and invasion of human endothelial cells in collagenous matrices
-
Ghersi G, Zhao Q, Salamone M, et al. The protease complex consisting of dipeptidyl peptidase IV and seprase plays a role in the migration and invasion of human endothelial cells in collagenous matrices. Cancer Res 2006; 66: 4652-61.
-
(2006)
Cancer Res
, vol.66
, pp. 4652-4661
-
-
Ghersi, G.1
Zhao, Q.2
Salamone, M.3
-
28
-
-
0035723325
-
CD26: A multifunctional integral membrane and secreted protein of activated lymphocytes
-
Gorrell MD, Gysbers V, McCaughan GW. CD26: a multifunctional integral membrane and secreted protein of activated lymphocytes. Scand J Immunol 2001; 54: 249-64.
-
(2001)
Scand J Immunol
, vol.54
, pp. 249-264
-
-
Gorrell, M.D.1
Gysbers, V.2
McCaughan, G.W.3
-
29
-
-
0038560496
-
CD26, let it cut or cut it down
-
De Meester I, Korom S, Van Damme J, Scharpe S. CD26, let it cut or cut it down. Immunol Today 1999; 20: 367-75.
-
(1999)
Immunol Today
, vol.20
, pp. 367-375
-
-
De Meester, I.1
Korom, S.2
Van Damme, J.3
Scharpe, S.4
-
30
-
-
0028038115
-
Components of biological variation in prolyl endopeptidase and dipeptidyl-peptidase IV activity in plasma of healthy subjects
-
Maes M, Scharpe S, De Meester I, et al. Components of biological variation in prolyl endopeptidase and dipeptidyl-peptidase IV activity in plasma of healthy subjects. Clin Chem 1994; 40: 1686-91.
-
(1994)
Clin Chem
, vol.40
, pp. 1686-1691
-
-
Maes, M.1
Scharpe, S.2
De Meester, I.3
-
31
-
-
0344117581
-
Prostate specific origin of dipeptidylpeptidase IV (CD-26) in human seminal plasma
-
Wilson MJ, Ruhland AR, Pryor JL, et al. Prostate specific origin of dipeptidylpeptidase IV (CD-26) in human seminal plasma. J Urol 1998; 160: 1905-9.
-
(1998)
J Urol
, vol.160
, pp. 1905-1909
-
-
Wilson, M.J.1
Ruhland, A.R.2
Pryor, J.L.3
-
32
-
-
0037966007
-
The crystal structure of dipeptidyl peptidase IV (CD26) reveals its functional regulation and enzymatic mechanism
-
Engel M, Hoffmann T, Wagner L, et al. The crystal structure of dipeptidyl peptidase IV (CD26) reveals its functional regulation and enzymatic mechanism. Proc Natl Acad Sci USA 2003; 100: 5063-8.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 5063-5068
-
-
Engel, M.1
Hoffmann, T.2
Wagner, L.3
-
33
-
-
0026633296
-
Cloning and functional expression of the T cell activation antigen CD26
-
Tanaka T, Camerini D, Seed B, et al. Cloning and functional expression of the T cell activation antigen CD26. J Immunol 1992; 149: 481-6.
-
(1992)
J Immunol
, vol.149
, pp. 481-486
-
-
Tanaka, T.1
Camerini, D.2
Seed, B.3
-
34
-
-
84876703878
-
Homology Modeling and Molecular Docking studies of Human DPP8 and DPP9
-
Janardhan S, Padmanabha Reddy Y. Homology Modeling and Molecular Docking studies of Human DPP8 and DPP9. Int J Pharm Res Dev 2011; 2: 131-46.
-
(2011)
Int J Pharm Res Dev
, vol.2
, pp. 131-146
-
-
Janardhan, S.1
Padmanabha Reddy, Y.2
-
35
-
-
10644296948
-
One site mutation disrupts dimer formation in human DPP-IV proteins
-
Chien CH, Huang LH, Chou CY, et al. One site mutation disrupts dimer formation in human DPP-IV proteins. J Biol Chem 2004; 279: 52338-45.
-
(2004)
J Biol Chem
, vol.279
, pp. 52338-52345
-
-
Chien, C.H.1
Huang, L.H.2
Chou, C.Y.3
-
36
-
-
0042131827
-
Structural basis of prolinespecific exopeptidase activity as observed in human dipeptidyl peptidase-IV
-
Thoma R, Loffler B, Stihle M, et al. Structural basis of prolinespecific exopeptidase activity as observed in human dipeptidyl peptidase-IV. Structure 2003; 11: 947-59.
-
(2003)
Structure
, vol.11
, pp. 947-959
-
-
Thoma, R.1
Loffler, B.2
Stihle, M.3
-
37
-
-
4544237622
-
Tyrosine 547 constitutes an essential part of the catalytic mechanism of dipeptidyl peptidase IV
-
Bjelke JR, Christensen J, Branner S, et al. Tyrosine 547 constitutes an essential part of the catalytic mechanism of dipeptidyl peptidase IV. J Biol Chem 2004; 279: 34691-7.
-
(2004)
J Biol Chem
, vol.279
, pp. 34691-34697
-
-
Bjelke, J.R.1
Christensen, J.2
Branner, S.3
-
38
-
-
0347367026
-
Structural requirements for catalysis, expression, and dimerization in the CD26/DPIV gene family
-
Ajami K, Abbott CA, Obradovic M, et al. Structural requirements for catalysis, expression, and dimerization in the CD26/DPIV gene family. Biochemistry (Mosc) 2003; 42: 694-701.
-
(2003)
Biochemistry (Mosc)
, vol.42
, pp. 694-701
-
-
Ajami, K.1
Abbott, C.A.2
Obradovic, M.3
-
39
-
-
77955387970
-
Discovery of 6-(aminomethyl)-5-(2,4-dichlorophenyl)-7-methylimidazo[1,2-a]pyrimidine-2-carboxa mides as potent, selective dipeptidyl peptidase-4 (DPP4) inhibitors
-
Meng W, Brigance RP, Chao HJ, et al. Discovery of 6-(aminomethyl)-5-(2,4-dichlorophenyl)-7-methylimidazo[1,2-a]pyrimidine-2-carboxa mides as potent, selective dipeptidyl peptidase-4 (DPP4) inhibitors. J Med Chem 2010; 53: 5620-8.
-
(2010)
J Med Chem
, vol.53
, pp. 5620-5628
-
-
Meng, W.1
Brigance, R.P.2
Chao, H.J.3
-
40
-
-
0037219684
-
Crystal structure of human dipeptidyl peptidase IV/CD26 in complex with a substrate analog
-
Rasmussen HB, Branner S, Wiberg FC, Wagtmann N. Crystal structure of human dipeptidyl peptidase IV/CD26 in complex with a substrate analog. Nat Struct Biol 2003; 10: 19-25.
-
(2003)
Nat Struct Biol
, vol.10
, pp. 19-25
-
-
Rasmussen, H.B.1
Branner, S.2
Wiberg, F.C.3
Wagtmann, N.4
-
41
-
-
0031570721
-
CD26/dipeptidyl peptidase IV does not work as an adenosine deaminase-binding protein in rat cells
-
Iwaki-Egawa S, Watanabe Y, Fujimoto Y. CD26/dipeptidyl peptidase IV does not work as an adenosine deaminase-binding protein in rat cells. Cell Immunol 1997; 178: 180-6.
-
(1997)
Cell Immunol
, vol.178
, pp. 180-186
-
-
Iwaki-Egawa, S.1
Watanabe, Y.2
Fujimoto, Y.3
-
42
-
-
0037205466
-
Clustered charged amino acids of human adenosine deaminase comprise a functional epitope for binding the adenosine deaminase complexing protein CD26/dipeptidyl peptidase IV
-
Richard E, Alam SM, Arredondo-Vega FX, Patel DD, Hershfield MS. Clustered charged amino acids of human adenosine deaminase comprise a functional epitope for binding the adenosine deaminase complexing protein CD26/dipeptidyl peptidase IV. J Biol Chem 2002; 277: 19720-6.
-
(2002)
J Biol Chem
, vol.277
, pp. 19720-19726
-
-
Richard, E.1
Alam, S.M.2
Arredondo-Vega, F.X.3
Patel, D.D.4
Hershfield, M.S.5
-
43
-
-
0025976294
-
Are diprotin A (Ile-Pro-Ile) and diprotin B (Val-Pro-Leu) inhibitors or substrates of dipeptidyl peptidase IV?
-
Rahfeld J, Schierhorn M, Hartrodt B, Neubert K, Heins J. Are diprotin A (Ile-Pro-Ile) and diprotin B (Val-Pro-Leu) inhibitors or substrates of dipeptidyl peptidase IV? Biochim Biophys Acta 1991; 1076: 314-6.
-
(1991)
Biochim Biophys Acta
, vol.1076
, pp. 314-316
-
-
Rahfeld, J.1
Schierhorn, M.2
Hartrodt, B.3
Neubert, K.4
Heins, J.5
-
44
-
-
0014405092
-
On the active site of proteases. 3. Mapping the active site of papain; specific peptide inhibitors of papain
-
Schechter I, Berger A. On the active site of proteases. 3. Mapping the active site of papain; specific peptide inhibitors of papain. Biochem Biophys Res Commun 1968; 32: 898-902.
-
(1968)
Biochem Biophys Res Commun
, vol.32
, pp. 898-902
-
-
Schechter, I.1
Berger, A.2
-
45
-
-
0032961099
-
The unique properties of dipeptidyl-peptidase IV (DPP IV / CD26) and the therapeutic potential of DPP IV inhibitors
-
Augustyns K, Bal G, Thonus G, et al. The unique properties of dipeptidyl-peptidase IV (DPP IV / CD26) and the therapeutic potential of DPP IV inhibitors. Curr Med Chem 1999; 6: 311-27.
-
(1999)
Curr Med Chem
, vol.6
, pp. 311-327
-
-
Augustyns, K.1
Bal, G.2
Thonus, G.3
-
46
-
-
0034612348
-
Enhanced insulin secretion and improved glucose tolerance in mice lacking CD26
-
Marguet D, Baggio L, Kobayashi T, et al. Enhanced insulin secretion and improved glucose tolerance in mice lacking CD26. Proc Natl Acad Sci USA 2000; 97: 6874-9.
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 6874-6879
-
-
Marguet, D.1
Baggio, L.2
Kobayashi, T.3
-
47
-
-
0030819309
-
Regulation of the receptor specificity and function of the chemokine RANTES (regulated on activation, normal T cell expressed and secreted) by dipeptidyl peptidase IV (CD26)-mediated cleavage
-
Oravecz T, Pall M, Roderiquez G, et al. Regulation of the receptor specificity and function of the chemokine RANTES (regulated on activation, normal T cell expressed and secreted) by dipeptidyl peptidase IV (CD26)-mediated cleavage. J Exp Med 1997; 186: 1865-72.
-
(1997)
J Exp Med
, vol.186
, pp. 1865-1872
-
-
Oravecz, T.1
Pall, M.2
Roderiquez, G.3
-
48
-
-
0035895070
-
Amino-terminal truncation of CXCR3 agonists impairs receptor signaling and lymphocyte chemotaxis, while preserving antiangiogenic properties
-
Proost P, Schutyser E, Menten P, et al. Amino-terminal truncation of CXCR3 agonists impairs receptor signaling and lymphocyte chemotaxis, while preserving antiangiogenic properties. Blood 2001; 98: 3554-61.
-
(2001)
Blood
, vol.98
, pp. 3554-3561
-
-
Proost, P.1
Schutyser, E.2
Menten, P.3
-
49
-
-
0032584761
-
Processing by CD26/dipeptidylpeptidase IV reduces the chemotactic and anti-HIV-1 activity of stromal-cell-derived factor-1alpha
-
Proost P, Struyf S, Schols D, et al. Processing by CD26/dipeptidylpeptidase IV reduces the chemotactic and anti-HIV-1 activity of stromal-cell-derived factor-1alpha. FEBS Lett 1998; 432: 73-6.
-
(1998)
FEBS Lett
, vol.432
, pp. 73-76
-
-
Proost, P.1
Struyf, S.2
Schols, D.3
-
50
-
-
0142039133
-
Degradation of endomorphin-2 at the supraspinal level in mice is initiated by dipeptidyl peptidase IV: An in vitro and in vivo study
-
Sakurada C, Sakurada S, Hayashi T, et al. Degradation of endomorphin-2 at the supraspinal level in mice is initiated by dipeptidyl peptidase IV: an in vitro and in vivo study. Biochem Pharmacol 2003; 66: 653-61.
-
(2003)
Biochem Pharmacol
, vol.66
, pp. 653-661
-
-
Sakurada, C.1
Sakurada, S.2
Hayashi, T.3
-
51
-
-
0037928769
-
The role of dipeptidyl peptidase IV in the cleavage of glucagon family peptides: In vivo metabolism of pituitary adenylate cyclase activating polypeptide-(1-38)
-
Zhu L, Tamvakopoulos C, Xie D, et al. The role of dipeptidyl peptidase IV in the cleavage of glucagon family peptides: in vivo metabolism of pituitary adenylate cyclase activating polypeptide-(1-38). J Biol Chem 2003; 278: 22418-23.
-
(2003)
J Biol Chem
, vol.278
, pp. 22418-22423
-
-
Zhu, L.1
Tamvakopoulos, C.2
Xie, D.3
-
52
-
-
0030795767
-
Intestinal function in mice with small bowel growth induced by glucagon-like peptide-2
-
Brubaker PL, Izzo A, Hill M, Drucker DJ. Intestinal function in mice with small bowel growth induced by glucagon-like peptide-2. Am J Physiol 1997; 272: E1050-8.
-
(1997)
Am J Physiol
, vol.272
-
-
Brubaker, P.L.1
Izzo, A.2
Hill, M.3
Drucker, D.J.4
-
53
-
-
0035798196
-
Kinetic study of the processing by dipeptidyl-peptidase IV/CD26 of neuropeptides involved in pancreatic insulin secretion
-
Lambeir AM, Durinx C, Proost P, et al. Kinetic study of the processing by dipeptidyl-peptidase IV/CD26 of neuropeptides involved in pancreatic insulin secretion. FEBS Lett 2001; 507: 327-30.
-
(2001)
FEBS Lett
, vol.507
, pp. 327-330
-
-
Lambeir, A.M.1
Durinx, C.2
Proost, P.3
-
54
-
-
0025201877
-
The degradation of bioactive peptides and proteins by dipeptidyl peptidase IV from human placenta
-
Nausch I, Mentlein R, Heymann E. The degradation of bioactive peptides and proteins by dipeptidyl peptidase IV from human placenta. Biol Chem Hoppe Seyler 1990; 371: 1113-8.
-
(1990)
Biol Chem Hoppe Seyler
, vol.371
, pp. 1113-1118
-
-
Nausch, I.1
Mentlein, R.2
Heymann, E.3
-
55
-
-
0033619675
-
Dipeptidyl-peptidase IV (CD26)--role in the inactivation of regulatory peptides
-
Mentlein R. Dipeptidyl-peptidase IV (CD26)--role in the inactivation of regulatory peptides. Regul Pept 1999; 85: 9-24.
-
(1999)
Regul Pept
, vol.85
, pp. 9-24
-
-
Mentlein, R.1
-
56
-
-
0027494070
-
Proteolytic processing of neuropeptide Y and peptide YY by dipeptidyl peptidase IV
-
Mentlein R, Dahms P, Grandt D, Kruger R. Proteolytic processing of neuropeptide Y and peptide YY by dipeptidyl peptidase IV. Regul Pept 1993; 49: 133-44.
-
(1993)
Regul Pept
, vol.49
, pp. 133-144
-
-
Mentlein, R.1
Dahms, P.2
Grandt, D.3
Kruger, R.4
-
57
-
-
0032933109
-
Study of the enzymatic degradation of vasostatin I and II and their precursor chromogranin A by dipeptidyl peptidase IV using highperformance liquid chromatography/electrospray mass spectrometry
-
Zhang XY, De Meester I, Lambeir AM, et al. Study of the enzymatic degradation of vasostatin I and II and their precursor chromogranin A by dipeptidyl peptidase IV using highperformance liquid chromatography/electrospray mass spectrometry. J Mass Spectrom 1999; 34: 255-63.
-
(1999)
J Mass Spectrom
, vol.34
, pp. 255-263
-
-
Zhang, X.Y.1
De Meester, I.2
Lambeir, A.M.3
-
58
-
-
0030037462
-
Dipeptidyl-peptidase IVbeta, a novel form of cell-surface-expressed protein with dipeptidyl-peptidase IV activity
-
Jacotot E, Callebaut C, Blanco J, et al. Dipeptidyl-peptidase IVbeta, a novel form of cell-surface-expressed protein with dipeptidyl-peptidase IV activity. Eur J Biochem 1996; 239: 248-58.
-
(1996)
Eur J Biochem
, vol.239
, pp. 248-258
-
-
Jacotot, E.1
Callebaut, C.2
Blanco, J.3
-
59
-
-
0032828216
-
Two highly conserved glutamic acid residues in the predicted beta propeller domain of dipeptidyl peptidase IV are required for its enzyme activity
-
Abbott CA, McCaughan GW, Gorrell MD. Two highly conserved glutamic acid residues in the predicted beta propeller domain of dipeptidyl peptidase IV are required for its enzyme activity. FEBS Lett 1999; 458: 278-84.
-
(1999)
FEBS Lett
, vol.458
, pp. 278-284
-
-
Abbott, C.A.1
McCaughan, G.W.2
Gorrell, M.D.3
-
60
-
-
21244503095
-
Structural and kinetic analysis of the substrate specificity of human fibroblast activation protein alpha
-
Aertgeerts K, Levin I, Shi L, et al. Structural and kinetic analysis of the substrate specificity of human fibroblast activation protein alpha. J Biol Chem 2005; 280: 19441-4.
-
(2005)
J Biol Chem
, vol.280
, pp. 19441-19444
-
-
Aertgeerts, K.1
Levin, I.2
Shi, L.3
-
61
-
-
5144227957
-
Structure of a human A-type potassium channel interacting protein DPPX, a member of the dipeptidyl aminopeptidase family
-
Strop P, Bankovich AJ, Hansen KC, Garcia KC, Brunger AT. Structure of a human A-type potassium channel interacting protein DPPX, a member of the dipeptidyl aminopeptidase family. J Mol Biol 2004; 343: 1055-65.
-
(2004)
J Mol Biol
, vol.343
, pp. 1055-1065
-
-
Strop, P.1
Bankovich, A.J.2
Hansen, K.C.3
Garcia, K.C.4
Brunger, A.T.5
-
62
-
-
0032563162
-
Prolyl oligopeptidase: An unusual beta-propeller domain regulates proteolysis
-
Fulop V, Bocskei Z, Polgar L. Prolyl oligopeptidase: an unusual beta-propeller domain regulates proteolysis. Cell 1998; 94: 161-70.
-
(1998)
Cell
, vol.94
, pp. 161-170
-
-
Fulop, V.1
Bocskei, Z.2
Polgar, L.3
-
63
-
-
34247898818
-
Dipeptidyl peptidase 8/9-like activity in human leukocytes
-
Maes MB, Dubois V, Brandt I, et al. Dipeptidyl peptidase 8/9-like activity in human leukocytes. J Leukoc Biol 2007; 81: 1252-7.
-
(2007)
J Leukoc Biol
, vol.81
, pp. 1252-1257
-
-
Maes, M.B.1
Dubois, V.2
Brandt, I.3
-
64
-
-
3042734543
-
Dipeptidyl peptidase 9 has two forms, a broad tissue distribution, cytoplasmic localization and DPIV-like peptidase activity
-
Ajami K, Abbott CA, McCaughan GW, Gorrell MD. Dipeptidyl peptidase 9 has two forms, a broad tissue distribution, cytoplasmic localization and DPIV-like peptidase activity. Biochim Biophys Acta 2004; 1679: 18-28.
-
(2004)
Biochim Biophys Acta
, vol.1679
, pp. 18-28
-
-
Ajami, K.1
Abbott, C.A.2
McCaughan, G.W.3
Gorrell, M.D.4
-
65
-
-
33744814340
-
Dipeptidyl peptidases 8 and 9: Specificity and molecular characterization compared with dipeptidyl peptidase IV
-
Bjelke JR, Christensen J, Nielsen PF, et al. Dipeptidyl peptidases 8 and 9: specificity and molecular characterization compared with dipeptidyl peptidase IV. Biochem J 2006; 396: 391-9.
-
(2006)
Biochem J
, vol.396
, pp. 391-399
-
-
Bjelke, J.R.1
Christensen, J.2
Nielsen, P.F.3
-
66
-
-
38449101374
-
Fibroblast activation protein and chronic liver disease
-
Wang XM, Yao TW, Nadvi NA, et al. Fibroblast activation protein and chronic liver disease. Front Biosci 2008; 13: 3168-80.
-
(2008)
Front Biosci
, vol.13
, pp. 3168-3180
-
-
Wang, X.M.1
Yao, T.W.2
Nadvi, N.A.3
-
67
-
-
0033579444
-
Fibroblast activation protein, a dual specificity serine protease expressed in reactive human tumor stromal fibroblasts
-
Park JE, Lenter MC, Zimmermann RN, et al. Fibroblast activation protein, a dual specificity serine protease expressed in reactive human tumor stromal fibroblasts. J Biol Chem 1999; 274: 36505-12.
-
(1999)
J Biol Chem
, vol.274
, pp. 36505-36512
-
-
Park, J.E.1
Lenter, M.C.2
Zimmermann, R.N.3
-
68
-
-
0031688228
-
Dipeptidyl-peptidase IVbeta--further characterization and comparison to dipeptidylpeptidase IV activity of CD26
-
Blanco J, Nguyen C, Callebaut C, et al. Dipeptidyl-peptidase IVbeta--further characterization and comparison to dipeptidylpeptidase IV activity of CD26. Eur J Biochem 1998; 256: 369-78.
-
(1998)
Eur J Biochem
, vol.256
, pp. 369-378
-
-
Blanco, J.1
Nguyen, C.2
Callebaut, C.3
-
69
-
-
0034470259
-
Attractin: A cub-family protease involved in T cell-monocyte/macrophage interactions
-
Duke-Cohan JS, Tang W, Schlossman SF. Attractin: a cub-family protease involved in T cell-monocyte/macrophage interactions. Adv Exp Med Biol 2000; 477: 173-85.
-
(2000)
Adv Exp Med Biol
, vol.477
, pp. 173-185
-
-
Duke-Cohan, J.S.1
Tang, W.2
Schlossman, S.F.3
-
70
-
-
34047215607
-
Does human attractin have DP4 activity?
-
Friedrich D, Hoffmann T, Bar J, et al. Does human attractin have DP4 activity? Biol Chem 2007; 388: 155-62.
-
(2007)
Biol Chem
, vol.388
, pp. 155-162
-
-
Friedrich, D.1
Hoffmann, T.2
Bar, J.3
-
71
-
-
84934444391
-
Expression of dipeptidyl peptidase IV-like enzymes in human peripheral blood mononuclear cells
-
Wrenger S, Guth B, Schultze B, et al. Expression of dipeptidyl peptidase IV-like enzymes in human peripheral blood mononuclear cells. Adv Exp Med Biol 2006; 575: 87-91.
-
(2006)
Adv Exp Med Biol
, vol.575
, pp. 87-91
-
-
Wrenger, S.1
Guth, B.2
Schultze, B.3
-
72
-
-
14844329054
-
Kinetic investigation of human dipeptidyl peptidase II (DPPII)-mediated hydrolysis of dipeptide derivatives and its identification as quiescent cell proline dipeptidase (QPP)/dipeptidyl peptidase 7 (DPP7)
-
Maes MB, Lambeir AM, Gilany K, et al. Kinetic investigation of human dipeptidyl peptidase II (DPPII)-mediated hydrolysis of dipeptide derivatives and its identification as quiescent cell proline dipeptidase (QPP)/dipeptidyl peptidase 7 (DPP7). Biochem J 2005; 386: 315-24.
-
(2005)
Biochem J
, vol.386
, pp. 315-324
-
-
Maes, M.B.1
Lambeir, A.M.2
Gilany, K.3
-
74
-
-
25844459084
-
Dipeptidyl peptidase IV inhibition for the treatment of type 2 diabetes: Potential importance of selectivity over dipeptidyl peptidases 8 and 9
-
Lankas GR, Leiting B, Roy RS, et al. Dipeptidyl peptidase IV inhibition for the treatment of type 2 diabetes: potential importance of selectivity over dipeptidyl peptidases 8 and 9. Diabetes 2005; 54: 2988-94.
-
(2005)
Diabetes
, vol.54
, pp. 2988-2994
-
-
Lankas, G.R.1
Leiting, B.2
Roy, R.S.3
-
75
-
-
0043073112
-
Prolyl peptidases: A serine protease subfamily with high potential for drug discovery
-
Rosenblum JS, Kozarich JW. Prolyl peptidases: a serine protease subfamily with high potential for drug discovery. Curr Opin Chem Biol 2003; 7: 496-504.
-
(2003)
Curr Opin Chem Biol
, vol.7
, pp. 496-504
-
-
Rosenblum, J.S.1
Kozarich, J.W.2
-
76
-
-
79953286743
-
Aromatic-Aromatic Interactions Database, A(2)ID: An analysis of aromatic pi-networks in proteins
-
Chourasia M, Sastry GM, Sastry GN. Aromatic-Aromatic Interactions Database, A(2)ID: an analysis of aromatic pi-networks in proteins. Int J Biol Macromol 2011; 48: 540-52.
-
(2011)
Int J Biol Macromol
, vol.48
, pp. 540-552
-
-
Chourasia, M.1
Sastry, G.M.2
Sastry, G.N.3
-
77
-
-
49949100432
-
Protein ligand interaction database (PLID)
-
Reddy AS, Amarnath HS, Bapi RS, Sastry GM, Sastry GN. Protein ligand interaction database (PLID). Comput Biol Chem 2008; 32: 387-90.
-
(2008)
Comput Biol Chem
, vol.32
, pp. 387-390
-
-
Reddy, A.S.1
Amarnath, H.S.2
Bapi, R.S.3
Sastry, G.M.4
Sastry, G.N.5
-
79
-
-
84871046431
-
Cation-pi interaction: Its role and relevance in chemistry, biology, and material science
-
Mahadevi AS, Sastry GN. Cation-pi interaction: its role and relevance in chemistry, biology, and material science. Chem Rev 2013; 113: 2100-38.
-
(2013)
Chem Rev
, vol.113
, pp. 2100-2138
-
-
Mahadevi, A.S.1
Sastry, G.N.2
-
80
-
-
38349134195
-
Exploring the size dependence of cyclic and acyclic pi-systems on cation-pi binding
-
Vijay D, Sastry GN. Exploring the size dependence of cyclic and acyclic pi-systems on cation-pi binding. Phys Chem Chem Phys 2008; 10: 582-90.
-
(2008)
Phys Chem Chem Phys
, vol.10
, pp. 582-590
-
-
Vijay, D.1
Sastry, G.N.2
-
81
-
-
49349111901
-
On the cooperativity of cation-pi and hydrogen bonding interactions
-
Vijay D, Zipse H, Sastry GN. On the cooperativity of cation-pi and hydrogen bonding interactions. J Phys Chem B 2008; 112: 8863-7.
-
(2008)
J Phys Chem B
, vol.112
, pp. 8863-8867
-
-
Vijay, D.1
Zipse, H.2
Sastry, G.N.3
-
82
-
-
0033214997
-
Vasoactive intestinal peptide and pituitary adenylate cyclase-activating polypeptide stimulate the induction of Th2 responses by up-regulating B7.2 expression
-
Delgado M, Leceta J, Gomariz RP, Ganea D. Vasoactive intestinal peptide and pituitary adenylate cyclase-activating polypeptide stimulate the induction of Th2 responses by up-regulating B7.2 expression. J Immunol 1999; 163: 3629-35.
-
(1999)
J Immunol
, vol.163
, pp. 3629-3635
-
-
Delgado, M.1
Leceta, J.2
Gomariz, R.P.3
Ganea, D.4
-
84
-
-
39749184723
-
Efficacy and safety of sitagliptin added to ongoing metformin therapy in patients with type 2 diabetes
-
Raz I, Chen Y, Wu M, et al. Efficacy and safety of sitagliptin added to ongoing metformin therapy in patients with type 2 diabetes. Curr Med Res Opin 2008; 24: 537-50.
-
(2008)
Curr Med Res Opin
, vol.24
, pp. 537-550
-
-
Raz, I.1
Chen, Y.2
Wu, M.3
-
85
-
-
84883419226
-
Implications of DPP4 modification of proteins that regulate stem/progenitor and more mature cell types
-
Ou X, O'Leary HA, Broxmeyer HE. Implications of DPP4 modification of proteins that regulate stem/progenitor and more mature cell types. Blood 2013; 122: 161-9.
-
(2013)
Blood
, vol.122
, pp. 161-169
-
-
Ou, X.1
O'Leary, H.A.2
Broxmeyer, H.E.3
-
86
-
-
0041589485
-
A role for interleukin-12 in the regulation of T cell plasma membrane compartmentation
-
Salgado FJ, Lojo J, Alonso-Lebrero JL, et al. A role for interleukin-12 in the regulation of T cell plasma membrane compartmentation. J Biol Chem 2003; 278: 24849-57.
-
(2003)
J Biol Chem
, vol.278
, pp. 24849-24857
-
-
Salgado, F.J.1
Lojo, J.2
Alonso-Lebrero, J.L.3
-
87
-
-
33947686803
-
TGF-beta1-mediated control of central nervous system inflammation and autoimmunity through the inhibitory receptor CD26
-
Preller V, Gerber A, Wrenger S, et al. TGF-beta1-mediated control of central nervous system inflammation and autoimmunity through the inhibitory receptor CD26. J Immunol 2007; 178: 4632-40.
-
(2007)
J Immunol
, vol.178
, pp. 4632-4640
-
-
Preller, V.1
Gerber, A.2
Wrenger, S.3
-
88
-
-
0035839639
-
Kinetic investigation of chemokine truncation by CD26/dipeptidyl peptidase IV reveals a striking selectivity within the chemokine family
-
Lambeir AM, Proost P, Durinx C, et al. Kinetic investigation of chemokine truncation by CD26/dipeptidyl peptidase IV reveals a striking selectivity within the chemokine family. J Biol Chem 2001; 276: 29839-45.
-
(2001)
J Biol Chem
, vol.276
, pp. 29839-29845
-
-
Lambeir, A.M.1
Proost, P.2
Durinx, C.3
-
89
-
-
0037777665
-
Cell surface peptidase CD26/DPPIV mediates G-CSF mobilization of mouse progenitor cells
-
Christopherson KW, 2nd, Cooper S, Broxmeyer HE. Cell surface peptidase CD26/DPPIV mediates G-CSF mobilization of mouse progenitor cells. Blood 2003; 101: 4680-6.
-
(2003)
Blood
, vol.101
, pp. 4680-4686
-
-
Christopherson II, K.W.1
Cooper, S.2
Broxmeyer, H.E.3
-
90
-
-
4043117769
-
Modulation of hematopoietic stem cell homing and engraftment by CD26
-
Christopherson KW, 2nd, Hangoc G, Mantel CR, Broxmeyer HE. Modulation of hematopoietic stem cell homing and engraftment by CD26. Science 2004; 305: 1000-3.
-
(2004)
Science
, vol.305
, pp. 1000-1003
-
-
Christopherson II, K.W.1
Hangoc, G.2
Mantel, C.R.3
Broxmeyer, H.E.4
-
91
-
-
0038118637
-
Increased adhesion potency of ovarian carcinoma cells to mesothelial cells by overexpression of dipeptidyl peptidase IV
-
Kikkawa F, Kajiyama H, Ino K, Shibata K, Mizutani S. Increased adhesion potency of ovarian carcinoma cells to mesothelial cells by overexpression of dipeptidyl peptidase IV. Int J Cancer 2003; 105: 779-83.
-
(2003)
Int J Cancer
, vol.105
, pp. 779-783
-
-
Kikkawa, F.1
Kajiyama, H.2
Ino, K.3
Shibata, K.4
Mizutani, S.5
-
92
-
-
0033517124
-
A role for dipeptidyl peptidase IV in suppressing the malignant phenotype of melanocytic cells
-
Wesley UV, Albino AP, Tiwari S, Houghton AN. A role for dipeptidyl peptidase IV in suppressing the malignant phenotype of melanocytic cells. J Exp Med 1999; 190: 311-22.
-
(1999)
J Exp Med
, vol.190
, pp. 311-322
-
-
Wesley, U.V.1
Albino, A.P.2
Tiwari, S.3
Houghton, A.N.4
-
93
-
-
3442900472
-
PT-100, a small molecule dipeptidyl peptidase inhibitor, has potent antitumor effects and augments antibody-mediated cytotoxicity via a novel immune mechanism
-
Adams S, Miller GT, Jesson MI, et al. PT-100, a small molecule dipeptidyl peptidase inhibitor, has potent antitumor effects and augments antibody-mediated cytotoxicity via a novel immune mechanism. Cancer Res 2004; 64: 5471-80.
-
(2004)
Cancer Res
, vol.64
, pp. 5471-5480
-
-
Adams, S.1
Miller, G.T.2
Jesson, M.I.3
-
94
-
-
2442678894
-
Cell surface adenosine deaminase binds and stimulates plasminogen activation on 1-LN human prostate cancer cells
-
Gonzalez-Gronow M, Hershfield MS, Arredondo-Vega FX, Pizzo SV. Cell surface adenosine deaminase binds and stimulates plasminogen activation on 1-LN human prostate cancer cells. J Biol Chem 2004; 279: 20993-8.
-
(2004)
J Biol Chem
, vol.279
, pp. 20993-20998
-
-
Gonzalez-Gronow, M.1
Hershfield, M.S.2
Arredondo-Vega, F.X.3
Pizzo, S.V.4
-
95
-
-
79953213304
-
Diet-induced adipose tissue inflammation and liver steatosis are prevented by DPP-4 inhibition in diabetic mice
-
Shirakawa J, Fujii H, Ohnuma K, et al. Diet-induced adipose tissue inflammation and liver steatosis are prevented by DPP-4 inhibition in diabetic mice. Diabetes 2011; 60: 1246-57.
-
(2011)
Diabetes
, vol.60
, pp. 1246-1257
-
-
Shirakawa, J.1
Fujii, H.2
Ohnuma, K.3
-
96
-
-
77951725805
-
Inhibition of fibroblast activation protein and dipeptidylpeptidase 4 increases cartilage invasion by rheumatoid arthritis synovial fibroblasts
-
Ospelt C, Mertens JC, Jungel A, et al. Inhibition of fibroblast activation protein and dipeptidylpeptidase 4 increases cartilage invasion by rheumatoid arthritis synovial fibroblasts. Arthritis Rheum 2010; 62: 1224-35.
-
(2010)
Arthritis Rheum
, vol.62
, pp. 1224-1235
-
-
Ospelt, C.1
Mertens, J.C.2
Jungel, A.3
-
97
-
-
28144441354
-
Active metabolite of GLP-1 mediates myocardial glucose uptake and improves left ventricular performance in conscious dogs with dilated cardiomyopathy
-
Nikolaidis LA, Elahi D, Shen YT, Shannon RP. Active metabolite of GLP-1 mediates myocardial glucose uptake and improves left ventricular performance in conscious dogs with dilated cardiomyopathy. Am J Physiol Heart Circ Physiol 2005; 289: H2401-8.
-
(2005)
Am J Physiol Heart Circ Physiol
, vol.289
-
-
Nikolaidis, L.A.1
Elahi, D.2
Shen, Y.T.3
Shannon, R.P.4
-
98
-
-
45849115827
-
Sitagliptin augments sympathetic enhancement of the renovascular effects of angiotensin II in genetic hypertension
-
Jackson EK, Mi Z. Sitagliptin augments sympathetic enhancement of the renovascular effects of angiotensin II in genetic hypertension. Hypertension 2008; 51: 1637-42.
-
(2008)
Hypertension
, vol.51
, pp. 1637-1642
-
-
Jackson, E.K.1
Mi, Z.2
-
99
-
-
33750116634
-
Discovery of 2-[4-{{2-(2S,5R)-2-cyano-5-ethynyl-1-pyrrolidinyl]-2-oxoethyl]amino]-4-methyl-1-piperidinyl]-4-pyridinecarboxylic acid (ABT-279): A very potent, selective, effective, and well-tolerated inhibitor of dipeptidyl peptidase-IV, useful for the treatment of diabetes
-
Madar DJ, Kopecka H, Pireh D, et al. Discovery of 2-[4-{{2-(2S,5R)-2-cyano-5-ethynyl-1-pyrrolidinyl]-2-oxoethyl]amino]-4-methyl-1-piperidinyl]-4-pyridinecarboxylic acid (ABT-279): a very potent, selective, effective, and well-tolerated inhibitor of dipeptidyl peptidase-IV, useful for the treatment of diabetes. J Med Chem 2006; 49: 6416-20.
-
(2006)
J Med Chem
, vol.49
, pp. 6416-6420
-
-
Madar, D.J.1
Kopecka, H.2
Pireh, D.3
-
100
-
-
33750456573
-
Discovery of (4R,5S)-5-amino-4-(2,4,5-trifluorophenyl)cyclohex-1-enyl)-(3-(trifluoromethyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone (ABT-341), a highly potent, selective, orally efficacious, and safe dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetes
-
Pei Z, Li X, von Geldern TW, et al. Discovery of (4R,5S)-5-amino-4-(2,4,5-trifluorophenyl)cyclohex-1-enyl)-(3-(trifluoromethyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone (ABT-341), a highly potent, selective, orally efficacious, and safe dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetes. J Med Chem 2006; 49: 6439-42.
-
(2006)
J Med Chem
, vol.49
, pp. 6439-6442
-
-
Pei, Z.1
Li, X.2
von Geldern, T.W.3
-
101
-
-
34248999413
-
Discovery of alogliptin: A potent, selective, bioavailable, and efficacious inhibitor of dipeptidyl peptidase IV
-
Feng J, Zhang Z, Wallace MB, et al. Discovery of alogliptin: a potent, selective, bioavailable, and efficacious inhibitor of dipeptidyl peptidase IV. J Med Chem 2007; 50: 2297-300.
-
(2007)
J Med Chem
, vol.50
, pp. 2297-2300
-
-
Feng, J.1
Zhang, Z.2
Wallace, M.B.3
-
102
-
-
74049162952
-
Discovery of carmegliptin: A potent and long-acting dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetes
-
Mattei P, Boehringer M, Di Giorgio P, et al. Discovery of carmegliptin: a potent and long-acting dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetes. Bioorg Med Chem Lett 2010; 20: 1109-13.
-
(2010)
Bioorg Med Chem Lett
, vol.20
, pp. 1109-1113
-
-
Mattei, P.1
Boehringer, M.2
Di Giorgio, P.3
-
103
-
-
63049125578
-
Emerging drug candidates of dipeptidyl peptidase IV (DPP IV) inhibitor class for the treatment of Type 2 Diabetes
-
Gupta R, Walunj SS, Tokala RK, et al. Emerging drug candidates of dipeptidyl peptidase IV (DPP IV) inhibitor class for the treatment of Type 2 Diabetes. Curr Drug Targets 2009; 10: 71-87.
-
(2009)
Curr Drug Targets
, vol.10
, pp. 71-87
-
-
Gupta, R.1
Walunj, S.S.2
Tokala, R.K.3
-
104
-
-
33748708415
-
E3024, 3-but-2-ynyl-5-methyl-2-piperazin-1-yl-3,5-dihydro-4H-imidazo[4,5-d]pyridazin-4-o ne tosylate, is a novel, selective and competitive dipeptidyl peptidase-IV inhibitor
-
Yasuda N, Nagakura T, Inoue T, et al. E3024, 3-but-2-ynyl-5-methyl-2-piperazin-1-yl-3,5-dihydro-4H-imidazo[4,5-d]pyridazin-4-o ne tosylate, is a novel, selective and competitive dipeptidyl peptidase-IV inhibitor. Eur J Pharmacol 2006; 548: 181-7.
-
(2006)
Eur J Pharmacol
, vol.548
, pp. 181-187
-
-
Yasuda, N.1
Nagakura, T.2
Inoue, T.3
-
105
-
-
37349073397
-
8-(3-(R)-aminopiperidin-1-yl)-7-but-2-ynyl-3-methyl-1-(4-methyl-quinazolin-2-ylme thyl)-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, et al. 8-(3-(R)-aminopiperidin-1-yl)-7-but-2-ynyl-3-methyl-1-(4-methyl-quinazolin-2-ylme thyl)-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: 6450-3.
-
(2007)
J Med Chem
, vol.50
, pp. 6450-6453
-
-
Eckhardt, M.1
Langkopf, E.2
Mark, M.3
-
106
-
-
0036312876
-
Chronic inhibition of circulating dipeptidyl peptidase IV by FE 999011 delays the occurrence of diabetes in male zucker diabetic fatty rats
-
Sudre B, Broqua P, White RB, et al. Chronic inhibition of circulating dipeptidyl peptidase IV by FE 999011 delays the occurrence of diabetes in male zucker diabetic fatty rats. Diabetes 2002; 51: 1461-9.
-
(2002)
Diabetes
, vol.51
, pp. 1461-1469
-
-
Sudre, B.1
Broqua, P.2
White, R.B.3
-
107
-
-
40849096097
-
Enzymatic C-demethylation of 1-[2-(5-tert-butyl-[1,3,4]oxadiazole-2-carbonyl)-4-fluoro-pyrrolidin-1-yl]-2-(2-hydroxy-1,1-dimethyl-ethyla mino)-ethanone (LC15-0133) in rat liver microsomes
-
Yoo HH, Chung HJ, Lee J, et al. Enzymatic C-demethylation of 1-[2-(5-tert-butyl-[1,3,4]oxadiazole-2-carbonyl)-4-fluoro-pyrrolidin-1-yl]-2-(2-hydroxy-1,1-dimethyl-ethyla mino)-ethanone (LC15-0133) in rat liver microsomes. Drug Metab Dispos 2008; 36: 485-9.
-
(2008)
Drug Metab Dispos
, vol.36
, pp. 485-489
-
-
Yoo, H.H.1
Chung, H.J.2
Lee, J.3
-
108
-
-
79952528360
-
Efficacy and safety of the dipeptidyl peptidase-4 inhibitor PF-734200 added to metformin in Type 2 diabetes
-
Rosenstock J, Lewin AJ, Norwood P, et al. Efficacy and safety of the dipeptidyl peptidase-4 inhibitor PF-734200 added to metformin in Type 2 diabetes. Diabet Med 2011; 28: 464-9.
-
(2011)
Diabet Med
, vol.28
, pp. 464-469
-
-
Rosenstock, J.1
Lewin, A.J.2
Norwood, P.3
-
109
-
-
1242314693
-
K579, a slow-binding inhibitor of dipeptidyl peptidase IV, is a long-acting hypoglycemic agent
-
Takasaki K, Iwase M, Nakajima T, et al. K579, a slow-binding inhibitor of dipeptidyl peptidase IV, is a long-acting hypoglycemic agent. Eur J Pharmacol 2004; 486: 335-42.
-
(2004)
Eur J Pharmacol
, vol.486
, pp. 335-342
-
-
Takasaki, K.1
Iwase, M.2
Nakajima, T.3
-
110
-
-
18144366970
-
1-(S)-gamma-substituted prolyl)-(S)-2-cyanopyrrolidine as a novel series of highly potent DPP-IV inhibitors
-
Sakashita H, Kitajima H, Nakamura M, Akahoshi F, Hayashi Y. 1-(S)-gamma-substituted prolyl)-(S)-2-cyanopyrrolidine as a novel series of highly potent DPP-IV inhibitors. Bioorg Med Chem Lett 2005; 15: 2441-5.
-
(2005)
Bioorg Med Chem Lett
, vol.15
, pp. 2441-2445
-
-
Sakashita, H.1
Kitajima, H.2
Nakamura, M.3
Akahoshi, F.4
Hayashi, Y.5
-
111
-
-
41149118550
-
(R)-8-(3-aminopiperidin-1-yl)-7-but-2-ynyl-3-methyl-1-(4-methyl-quinazolin-2-ylm ethyl)-3,7-dihydro-purine-2,6-dione (BI 1356), a novel xanthine-based dipeptidyl peptidase 4 inhibitor, has a superior potency and longer duration of action compared with other dipeptidyl peptidase-4 inhibitors
-
Thomas L, Eckhardt M, Langkopf E, et al. (R)-8-(3-aminopiperidin-1-yl)-7-but-2-ynyl-3-methyl-1-(4-methyl-quinazolin-2-ylm ethyl)-3,7-dihydro-purine-2,6-dione (BI 1356), a novel xanthine-based dipeptidyl peptidase 4 inhibitor, has a superior potency and longer duration of action compared with other dipeptidyl peptidase-4 inhibitors. J Pharmacol Exp Ther 2008; 325: 175-82.
-
(2008)
J Pharmacol Exp Ther
, vol.325
, pp. 175-182
-
-
Thomas, L.1
Eckhardt, M.2
Langkopf, E.3
-
112
-
-
0033533402
-
NVP-DPP728 (1-[2-[(5-cyanopyridin-2-yl)amino]ethyl]amino] acetyl]-2-cyano-(S)-pyrrolidine), a slow-binding inhibitor of dipeptidyl peptidase IV
-
Hughes TE, Mone MD, Russell ME, Weldon SC, Villhauer EB. NVP-DPP728 (1-[2-[(5-cyanopyridin-2-yl)amino]ethyl]amino] acetyl]-2-cyano-(S)-pyrrolidine), a slow-binding inhibitor of dipeptidyl peptidase IV. Biochemistry (Mosc) 1999; 38: 11597-603.
-
(1999)
Biochemistry (Mosc)
, vol.38
, pp. 11597-11603
-
-
Hughes, T.E.1
Mone, M.D.2
Russell, M.E.3
Weldon, S.C.4
Villhauer, E.B.5
-
113
-
-
0036228243
-
Long-term treatment with the dipeptidyl peptidase IV inhibitor P32/98 causes sustained improvements in glucose tolerance, insulin sensitivity, hyperinsulinemia, and beta-cell glucose responsiveness in VDF (fa/fa) Zucker rats
-
Pospisilik JA, Stafford SG, Demuth HU, et al. Long-term treatment with the dipeptidyl peptidase IV inhibitor P32/98 causes sustained improvements in glucose tolerance, insulin sensitivity, hyperinsulinemia, and beta-cell glucose responsiveness in VDF (fa/fa) Zucker rats. Diabetes 2002; 51: 943-50.
-
(2002)
Diabetes
, vol.51
, pp. 943-950
-
-
Pospisilik, J.A.1
Stafford, S.G.2
Demuth, H.U.3
-
114
-
-
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
-
Augeri DJ, Robl JA, Betebenner DA, et al. 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: 5025-37.
-
(2005)
J Med Chem
, vol.48
, pp. 5025-5037
-
-
Augeri, D.J.1
Robl, J.A.2
Betebenner, D.A.3
-
115
-
-
34249330949
-
Triazolopiperazineamides as dipeptidyl peptidase IV inhibitors: Close analogs of JANUVIA (sitagliptin phosphate)
-
Kim D, Kowalchick JE, Edmondson SD, et al. Triazolopiperazineamides as dipeptidyl peptidase IV inhibitors: close analogs of JANUVIA (sitagliptin phosphate). Bioorg Med Chem Lett 2007; 17: 3373-7.
-
(2007)
Bioorg Med Chem Lett
, vol.17
, pp. 3373-3377
-
-
Kim, D.1
Kowalchick, J.E.2
Edmondson, S.D.3
-
116
-
-
27744540889
-
Improved glycaemic control with dipeptidyl peptidase-4 inhibition in patients with type 2 diabetes: Vildagliptin (LAF237) dose response
-
Ristic S, Byiers S, Foley J, Holmes D. Improved glycaemic control with dipeptidyl peptidase-4 inhibition in patients with type 2 diabetes: vildagliptin (LAF237) dose response. Diabetes Obes Metab 2005; 7: 692-8.
-
(2005)
Diabetes Obes Metab
, vol.7
, pp. 692-698
-
-
Ristic, S.1
Byiers, S.2
Foley, J.3
Holmes, D.4
-
117
-
-
33947643014
-
Aromatic heterocyclebased DPP-IV inhibitors: Xanthines and related structural types
-
Szczepankiewicz BG, Kurukulasuriya R. Aromatic heterocyclebased DPP-IV inhibitors: xanthines and related structural types. Curr Top Med Chem 2007; 7: 569-78.
-
(2007)
Curr Top Med Chem
, vol.7
, pp. 569-578
-
-
Szczepankiewicz, B.G.1
Kurukulasuriya, R.2
-
118
-
-
45049086968
-
ASP8497 is a novel selective and competitive dipeptidyl peptidase-IV inhibitor with antihyperglycemic activity
-
Matsuyama-Yokono A, Tahara A, Nakano R, et al. ASP8497 is a novel selective and competitive dipeptidyl peptidase-IV inhibitor with antihyperglycemic activity. Biochem Pharmacol 2008; 76: 98-107.
-
(2008)
Biochem Pharmacol
, vol.76
, pp. 98-107
-
-
Matsuyama-Yokono, A.1
Tahara, A.2
Nakano, R.3
-
119
-
-
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 EB, Brinkman JA, Naderi GB, et al. 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: 2774-89.
-
(2003)
J Med Chem
, vol.46
, pp. 2774-2789
-
-
Villhauer, E.B.1
Brinkman, J.A.2
Naderi, G.B.3
-
120
-
-
22744442874
-
Type 2 diabetes--therapy with dipeptidyl peptidase IV inhibitors
-
Demuth HU, McIntosh CH, Pederson RA. Type 2 diabetes--therapy with dipeptidyl peptidase IV inhibitors. Biochim Biophys Acta 2005; 1751: 33-44.
-
(2005)
Biochim Biophys Acta
, vol.1751
, pp. 33-44
-
-
Demuth, H.U.1
McIntosh, C.H.2
Pederson, R.A.3
-
121
-
-
75849142837
-
The dipeptidyl peptidase IV inhibitor NVP-DPP728 reduces plasma glucagon concentration in cats
-
Furrer D, Kaufmann K, Tschuor F, Reusch CE, Lutz TA. The dipeptidyl peptidase IV inhibitor NVP-DPP728 reduces plasma glucagon concentration in cats. Vet J 2010; 183: 355-7.
-
(2010)
Vet J
, vol.183
, pp. 355-357
-
-
Furrer, D.1
Kaufmann, K.2
Tschuor, F.3
Reusch, C.E.4
Lutz, T.A.5
-
122
-
-
0000135759
-
Inhibition of dipeptidyl peptidase IV with NVP-DPP728 increases plasma GLP-1 (7-36 amide) concentrations and improves oral glucose tolerance in obese Zucker rats
-
Balkan B, Kwasnik L, Miserendino R, Holst JJ, Li X. Inhibition of dipeptidyl peptidase IV with NVP-DPP728 increases plasma GLP-1 (7-36 amide) concentrations and improves oral glucose tolerance in obese Zucker rats. Diabetologia 1999; 42: 1324-31.
-
(1999)
Diabetologia
, vol.42
, pp. 1324-1331
-
-
Balkan, B.1
Kwasnik, L.2
Miserendino, R.3
Holst, J.J.4
Li, X.5
-
123
-
-
0036583164
-
Inhibition of dipeptidyl peptidase IV improves metabolic control over a 4-week study period in type 2 diabetes
-
Ahren B, Simonsson E, Larsson H, et al. Inhibition of dipeptidyl peptidase IV improves metabolic control over a 4-week study period in type 2 diabetes. Diabetes Care 2002; 25: 869-75.
-
(2002)
Diabetes Care
, vol.25
, pp. 869-875
-
-
Ahren, B.1
Simonsson, E.2
Larsson, H.3
-
124
-
-
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
-
Kim D, Wang L, Beconi M, et al. (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 2005; 48: 141-51.
-
(2005)
J Med Chem
, vol.48
, pp. 141-151
-
-
Kim, D.1
Wang, L.2
Beconi, M.3
-
125
-
-
33846817233
-
Efficacy and safety of the dipeptidyl peptidase-4 inhibitor, sitagliptin, compared with the sulfonylurea, glipizide, in patients with type 2 diabetes inadequately controlled on metformin alone: A randomized, double-blind, non-inferiority trial
-
Nauck MA, Meininger G, Sheng D, Terranella L, Stein PP. Efficacy and safety of the dipeptidyl peptidase-4 inhibitor, sitagliptin, compared with the sulfonylurea, glipizide, in patients with type 2 diabetes inadequately controlled on metformin alone: a randomized, double-blind, non-inferiority trial. Diabetes Obes Metab 2007; 9: 194-205.
-
(2007)
Diabetes Obes Metab
, vol.9
, pp. 194-205
-
-
Nauck, M.A.1
Meininger, G.2
Sheng, D.3
Terranella, L.4
Stein, P.P.5
-
126
-
-
70349755766
-
Linagliptin, a dipeptidyl peptidase-4 inhibitor for the treatment of type 2 diabetes
-
Tiwari A. Linagliptin, a dipeptidyl peptidase-4 inhibitor for the treatment of type 2 diabetes. Curr Opin Investig Drugs 2009; 10: 1091-104.
-
(2009)
Curr Opin Investig Drugs
, vol.10
, pp. 1091-1104
-
-
Tiwari, A.1
-
127
-
-
78649691630
-
Safety and efficacy of linagliptin as add-on therapy to metformin in patients with type 2 diabetes: A randomized, double-blind, placebo-controlled study
-
Taskinen MR, Rosenstock J, Tamminen I, et al. Safety and efficacy of linagliptin as add-on therapy to metformin in patients with type 2 diabetes: a randomized, double-blind, placebo-controlled study. Diabetes Obes Metab 2011; 13: 65-74.
-
(2011)
Diabetes Obes Metab
, vol.13
, pp. 65-74
-
-
Taskinen, M.R.1
Rosenstock, J.2
Tamminen, I.3
-
128
-
-
74049094040
-
Saxagliptin
-
Dhillon S, Weber J. Saxagliptin. Drugs 2009; 69: 2103-14.
-
(2009)
Drugs
, vol.69
, pp. 2103-2114
-
-
Dhillon, S.1
Weber, J.2
-
129
-
-
3442890045
-
Role for dipeptidyl peptidase IV in tumor suppression of human non small cell lung carcinoma cells
-
Wesley UV, Tiwari S, Houghton AN. Role for dipeptidyl peptidase IV in tumor suppression of human non small cell lung carcinoma cells. Int J Cancer 2004; 109: 855-66.
-
(2004)
Int J Cancer
, vol.109
, pp. 855-866
-
-
Wesley, U.V.1
Tiwari, S.2
Houghton, A.N.3
-
130
-
-
73449117555
-
Saxagliptin: A new DPP-4 inhibitor for the treatment of type 2 diabetes mellitus
-
Tahrani AA, Piya MK, Barnett AH. Saxagliptin: a new DPP-4 inhibitor for the treatment of type 2 diabetes mellitus. Adv Ther 2009; 26: 249-62.
-
(2009)
Adv Ther
, vol.26
, pp. 249-262
-
-
Tahrani, A.A.1
Piya, M.K.2
Barnett, A.H.3
-
131
-
-
20444406121
-
Inhibition of dipeptidylpeptidase IV catalyzed peptide truncation by Vildagliptin (2S)-{[(3-hydroxyadamantan-1-yl)amino]acetyl}-pyrrolidine-2-carbonitrile)
-
Brandt I, Joossens J, Chen X, et al. Inhibition of dipeptidylpeptidase IV catalyzed peptide truncation by Vildagliptin (2S)-{[(3-hydroxyadamantan-1-yl)amino]acetyl}-pyrrolidine-2-carbonitrile). Biochem Pharmacol 2005; 70: 134-43.
-
(2005)
Biochem Pharmacol
, vol.70
, pp. 134-143
-
-
Brandt, I.1
Joossens, J.2
Chen, X.3
-
132
-
-
34548324787
-
The absolute oral bioavailability and population-based pharmacokinetic modelling of a novel dipeptidylpeptidase-IV inhibitor, vildagliptin, in healthy volunteers
-
He YL, Sadler BM, Sabo R, et al. The absolute oral bioavailability and population-based pharmacokinetic modelling of a novel dipeptidylpeptidase-IV inhibitor, vildagliptin, in healthy volunteers. Clin Pharmacokinet 2007; 46: 787-802.
-
(2007)
Clin Pharmacokinet
, vol.46
, pp. 787-802
-
-
He, Y.L.1
Sadler, B.M.2
Sabo, R.3
-
133
-
-
2442482515
-
Inhibition of dipeptidyl peptidase-4 reduces glycemia, sustains insulin levels, and reduces glucagon levels in type 2 diabetes
-
Ahren B, Landin-Olsson M, Jansson PA, et al. Inhibition of dipeptidyl peptidase-4 reduces glycemia, sustains insulin levels, and reduces glucagon levels in type 2 diabetes. J Clin Endocrinol Metab 2004; 89: 2078-84.
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 2078-2084
-
-
Ahren, B.1
Landin-Olsson, M.2
Jansson, P.A.3
-
134
-
-
34848834456
-
Pharmacokinetic and pharmacodynamic assessments of the dipeptidyl peptidase-4 inhibitor PHX1149: Double-blind, placebo-controlled, single-and multiple-dose studies in healthy subjects
-
O'Farrell AM, van Vliet A, Abou Farha K, et al. Pharmacokinetic and pharmacodynamic assessments of the dipeptidyl peptidase-4 inhibitor PHX1149: double-blind, placebo-controlled, single-and multiple-dose studies in healthy subjects. Clin Ther 2007; 29: 1692-705.
-
(2007)
Clin Ther
, vol.29
, pp. 1692-1705
-
-
O'Farrell, A.M.1
van Vliet, A.2
Abou Farha, K.3
-
135
-
-
77950122844
-
Dutogliptin, a selective DPP4 inhibitor, improves glycaemic control in patients with type 2 diabetes: A 12-week, double-blind, randomized, placebo-controlled, multicentre trial
-
Pattzi HM, Pitale S, Alpizar M, et al. Dutogliptin, a selective DPP4 inhibitor, improves glycaemic control in patients with type 2 diabetes: a 12-week, double-blind, randomized, placebo-controlled, multicentre trial. Diabetes Obes Metab 2010; 12: 348-55.
-
(2010)
Diabetes Obes Metab
, vol.12
, pp. 348-355
-
-
Pattzi, H.M.1
Pitale, S.2
Alpizar, M.3
-
136
-
-
84899846092
-
-
Chicago American Diabetes Association, Abstract: 604
-
Sanford DG, Wang p, Lai JH, Kiritsy C, Bachovchin WW. ARI2243, a Highly Potent and Selective Dipeptidyl Peptidase IV (DPP4) Inhibitor with exceptional anti-hyperglycemic activity for the Treatment of Type 2 Diabetes. Chicago American Diabetes Association 2007; Abstract: 604.
-
(2007)
ARI2243, a Highly Potent and Selective Dipeptidyl Peptidase IV (DPP4) Inhibitor with exceptional anti-hyperglycemic activity for the Treatment of Type 2 Diabetes
-
-
Sanford, D.G.1
Wang, P.2
Lai, J.H.3
Kiritsy, C.4
Bachovchin, W.W.5
-
137
-
-
78249267588
-
Pharmacokinetics and metabolism of the dipeptidyl peptidase IV inhibitor carmegliptin in rats, dogs, and monkeys
-
Kuhlmann O, Paehler A, Weick I, et al. Pharmacokinetics and metabolism of the dipeptidyl peptidase IV inhibitor carmegliptin in rats, dogs, and monkeys. Xenobiotica 2010; 40: 840-52.
-
(2010)
Xenobiotica
, vol.40
, pp. 840-852
-
-
Kuhlmann, O.1
Paehler, A.2
Weick, I.3
-
138
-
-
84899841730
-
Synthesis and biological evaluation of potent, selective, orally active 4-fluoro-2-cyanopyrrolidine inhibitors of DPP-IV
-
Philadelphia, USA
-
Haffner CD, McDougald DL, Reister SM. Synthesis and biological evaluation of potent, selective, orally active 4-fluoro-2-cyanopyrrolidine inhibitors of DPP-IV. 228th ACSl Meeting, Philadelphia, USA 2004.
-
(2004)
228th ACSl Meeting
-
-
Haffner, C.D.1
McDougald, D.L.2
Reister, S.M.3
-
139
-
-
80053950689
-
Target-mediated metabolism and target-mediated drug disposition of the DPPIV inhibitor AMG 222
-
Greene RJ, Tu H, Gibbs JP, Greg Slatter J. Target-mediated metabolism and target-mediated drug disposition of the DPPIV inhibitor AMG 222. Xenobiotica 2011; 41(11): 945-57.
-
(2011)
Xenobiotica
, vol.41
, Issue.11
, pp. 945-957
-
-
Greene, R.J.1
Tu, H.2
Gibbs, J.P.3
Greg Slatter, J.4
-
140
-
-
34249719258
-
Dipeptidyl peptidase IV inhibitors: An evolving treatment for type 2 diabetes from the incretin concept
-
Chyan YJ, Chuang LM. Dipeptidyl peptidase IV inhibitors: an evolving treatment for type 2 diabetes from the incretin concept. Recent Patents Endocr, Metab Immun Drug Discov 2007; 1: 15-24.
-
(2007)
Recent Patents Endocr, Metab Immun Drug Discov
, vol.1
, pp. 15-24
-
-
Chyan, Y.J.1
Chuang, L.M.2
-
141
-
-
3242730474
-
Role of incretin hormones in the regulation of insulin secretion in diabetic and nondiabetic humans
-
Holst JJ, Gromada J. Role of incretin hormones in the regulation of insulin secretion in diabetic and nondiabetic humans. Am J Physiol Endocrinol Metab 2004; 287: E199-206.
-
(2004)
Am J Physiol Endocrinol Metab
, vol.287
-
-
Holst, J.J.1
Gromada, J.2
-
142
-
-
65949122087
-
One-year treatment with exenatide improves beta-cell function, compared with insulin glargine, in metformin-treated type 2 diabetic patients: A randomized, controlled trial
-
Bunck MC, Diamant M, Corner A, et al. One-year treatment with exenatide improves beta-cell function, compared with insulin glargine, in metformin-treated type 2 diabetic patients: a randomized, controlled trial. Diabetes Care 2009; 32: 762-8.
-
(2009)
Diabetes Care
, vol.32
, pp. 762-768
-
-
Bunck, M.C.1
Diamant, M.2
Corner, A.3
-
143
-
-
77955456705
-
Pharmacokinetics of dipeptidylpeptidase-4 inhibitors
-
Scheen AJ. Pharmacokinetics of dipeptidylpeptidase-4 inhibitors. Diabetes Obes Metab 2010; 12: 648-58.
-
(2010)
Diabetes Obes Metab
, vol.12
, pp. 648-658
-
-
Scheen, A.J.1
-
144
-
-
58149177392
-
Pharmacokinetics and pharmacodynamics of vildagliptin in healthy Chinese volunteers
-
Hu P, Yin Q, Deckert F, et al. Pharmacokinetics and pharmacodynamics of vildagliptin in healthy Chinese volunteers. J Clin Pharmacol 2009; 49: 39-49.
-
(2009)
J Clin Pharmacol
, vol.49
, pp. 39-49
-
-
Hu, P.1
Yin, Q.2
Deckert, F.3
-
145
-
-
34447120048
-
Effect of renal insufficiency on the pharmacokinetics of sitagliptin, a dipeptidyl peptidase-4 inhibitor
-
Bergman AJ, Cote J, Yi B, et al. Effect of renal insufficiency on the pharmacokinetics of sitagliptin, a dipeptidyl peptidase-4 inhibitor. Diabetes Care 2007; 30: 1862-4.
-
(2007)
Diabetes Care
, vol.30
, pp. 1862-1864
-
-
Bergman, A.J.1
Cote, J.2
Yi, B.3
-
146
-
-
79960530809
-
Preclinical development of dipeptidyl peptidase IV inhibitor alogliptin: A brief overview
-
Parsa KV, Pal M. Preclinical development of dipeptidyl peptidase IV inhibitor alogliptin: a brief overview. Expert Opin Drug Discov 2011; 6: 855-69.
-
(2011)
Expert Opin Drug Discov
, vol.6
, pp. 855-869
-
-
Parsa, K.V.1
Pal, M.2
-
147
-
-
77957696165
-
Alogliptin: A review of its use in the management of type 2 diabetes mellitus
-
Scott LJ. Alogliptin: a review of its use in the management of type 2 diabetes mellitus. Drugs 2010; 70: 2051-72.
-
(2010)
Drugs
, vol.70
, pp. 2051-2072
-
-
Scott, L.J.1
-
148
-
-
84878200007
-
Alogliptin (nesina) for type 2 diabetes
-
Alogliptin (nesina) for type 2 diabetes. Med Lett Drugs Ther 2013; 55: 41-3.
-
(2013)
Med Lett Drugs Ther
, vol.55
, pp. 41-43
-
-
-
149
-
-
84875907876
-
Efficacy and safety of linagliptin in type 2 diabetes subjects at high risk for renal and cardiovascular disease: A pooled analysis of six phase III clinical trials
-
von Eynatten M, Gong Y, Emser A, Woerle HJ. Efficacy and safety of linagliptin in type 2 diabetes subjects at high risk for renal and cardiovascular disease: a pooled analysis of six phase III clinical trials. Cardiovasc Diabetol 2013; 12: 60.
-
(2013)
Cardiovasc Diabetol
, vol.12
, pp. 60
-
-
von Eynatten, M.1
Gong, Y.2
Emser, A.3
Woerle, H.J.4
-
150
-
-
84860708230
-
Review of linagliptin for the treatment of type 2 diabetes mellitus
-
Neumiller JJ, Setter SM. Review of linagliptin for the treatment of type 2 diabetes mellitus. Clin Ther 2012; 34: 993-1005.
-
(2012)
Clin Ther
, vol.34
, pp. 993-1005
-
-
Neumiller, J.J.1
Setter, S.M.2
-
151
-
-
34250206962
-
Docking-based 3DQSAR study for selectivity of DPP4, DPP8, and DPP9 inhibitors
-
Kang NS, Ahn JH, Kim SS, Chae CH, Yoo SE. Docking-based 3DQSAR study for selectivity of DPP4, DPP8, and DPP9 inhibitors. Bioorg Med Chem Lett 2007; 17: 3716-21.
-
(2007)
Bioorg Med Chem Lett
, vol.17
, pp. 3716-3721
-
-
Kang, N.S.1
Ahn, J.H.2
Kim, S.S.3
Chae, C.H.4
Yoo, S.E.5
-
152
-
-
34250346390
-
Modeling assisted rational design of novel, potent, and selective pyrrolopyrimidine DPP-4 inhibitors
-
Gao YD, Feng D, Sheridan RP, et al. Modeling assisted rational design of novel, potent, and selective pyrrolopyrimidine DPP-4 inhibitors. Bioorg Med Chem Lett 2007; 17: 3877-9.
-
(2007)
Bioorg Med Chem Lett
, vol.17
, pp. 3877-3879
-
-
Gao, Y.D.1
Feng, D.2
Sheridan, R.P.3
-
153
-
-
84882408604
-
3D QSAR and Docking Studies of Various Amido and Benzyl-Substituted 3-amino-4-(2-cyanopyrrolidide)Pyrrolidinyl Analogs as DPP-IV Inhibitors
-
Agrawal R, Jain P, Dikshit SN, Jain S. 3D QSAR and Docking Studies of Various Amido and Benzyl-Substituted 3-amino-4-(2-cyanopyrrolidide)Pyrrolidinyl Analogs as DPP-IV Inhibitors. Protein Pept Lett 2013; 20(9): 1066-78.
-
(2013)
Protein Pept Lett
, vol.20
, Issue.9
, pp. 1066-1078
-
-
Agrawal, R.1
Jain, P.2
Dikshit, S.N.3
Jain, S.4
-
154
-
-
79851489024
-
Development of a robust QSAR model to predict the affinity of pyrrolidine analogs for dipeptidyl peptidase IV (DPP-IV)
-
Paliwal S, Seth D, Yadav D, Yadav R. Development of a robust QSAR model to predict the affinity of pyrrolidine analogs for dipeptidyl peptidase IV (DPP-IV). J Enzyme Inhib Med Chem 2011; 26: 129-40.
-
(2011)
J Enzyme Inhib Med Chem
, vol.26
, pp. 129-140
-
-
Paliwal, S.1
Seth, D.2
Yadav, D.3
Yadav, R.4
-
155
-
-
80051564797
-
CoMFA and CoMSIA of diverse pyrrolidine analogues as dipeptidyl peptidase IV inhibitors: Active site requirements
-
Murugesan V, Sethi N, Prabhakar YS, Katti SB. CoMFA and CoMSIA of diverse pyrrolidine analogues as dipeptidyl peptidase IV inhibitors: active site requirements. Mol Divers 2011; 15: 457-66.
-
(2011)
Mol Divers
, vol.15
, pp. 457-466
-
-
Murugesan, V.1
Sethi, N.2
Prabhakar, Y.S.3
Katti, S.B.4
-
156
-
-
70649098188
-
3D-QSAR studies on triazolopiperazine amide inhibitors of dipeptidyl peptidase-IV as anti-diabetic agents
-
Saqib U, Siddiqi MI. 3D-QSAR studies on triazolopiperazine amide inhibitors of dipeptidyl peptidase-IV as anti-diabetic agents. SAR QSAR Environ Res 2009; 20: 519-35.
-
(2009)
SAR QSAR Environ Res
, vol.20
, pp. 519-535
-
-
Saqib, U.1
Siddiqi, M.I.2
-
157
-
-
77955095737
-
Molecular docking and 3D-QSAR studies on betaphenylalanine derivatives as dipeptidyl peptidase IV inhibitors
-
Jiang YK. Molecular docking and 3D-QSAR studies on betaphenylalanine derivatives as dipeptidyl peptidase IV inhibitors. J Mol Model 2010; 16: 1239-49.
-
(2010)
J Mol Model
, vol.16
, pp. 1239-1249
-
-
Jiang, Y.K.1
-
158
-
-
84880720439
-
Synthesis, Evaluation and Molecular Docking of Prolyl-Fluoropyrrolidine Derivatives as Dipeptidyl Peptidase IV Inhibitors
-
Sharma M, Gupta M, Singh D, Kumar M, Kaur P. Synthesis, Evaluation and Molecular Docking of Prolyl-Fluoropyrrolidine Derivatives as Dipeptidyl Peptidase IV Inhibitors. Chem Biol Drug Des 2013; 82: 156-66.
-
(2013)
Chem Biol Drug Des
, vol.82
, pp. 156-166
-
-
Sharma, M.1
Gupta, M.2
Singh, D.3
Kumar, M.4
Kaur, P.5
-
159
-
-
77957837734
-
Synthesis, biological assay in vitro and molecular docking studies of new imidazopyrazinone derivatives as potential dipeptidyl peptidase IV inhibitors
-
Zhu Y, Xia S, Zhu M, et al. Synthesis, biological assay in vitro and molecular docking studies of new imidazopyrazinone derivatives as potential dipeptidyl peptidase IV inhibitors. Eur J Med Chem 2010; 45: 4953-62.
-
(2010)
Eur J Med Chem
, vol.45
, pp. 4953-4962
-
-
Zhu, Y.1
Xia, S.2
Zhu, M.3
-
160
-
-
84862796538
-
Synthesis, structure-activity relationship, and pharmacophore modeling studies of pyrazole-3-carbohydrazone derivatives as dipeptidyl peptidase IV inhibitors
-
Wu D, Jin F, Lu W, et al. Synthesis, structure-activity relationship, and pharmacophore modeling studies of pyrazole-3-carbohydrazone derivatives as dipeptidyl peptidase IV inhibitors. Chem Biol Drug Des 2012; 79: 897-906.
-
(2012)
Chem Biol Drug Des
, vol.79
, pp. 897-906
-
-
Wu, D.1
Jin, F.2
Lu, W.3
-
161
-
-
56049116069
-
Discovery of DPP IV inhibitors by pharmacophore modeling and QSAR analysis followed by in silico screening
-
Al-Masri IM, Mohammad MK, Taha MO. Discovery of DPP IV inhibitors by pharmacophore modeling and QSAR analysis followed by in silico screening. Chem Med Chem 2008; 3: 1763-79.
-
(2008)
Chem Med Chem
, vol.3
, pp. 1763-1779
-
-
Al-Masri, I.M.1
Mohammad, M.K.2
Taha, M.O.3
-
162
-
-
33645962844
-
Choline kinase: An important target for cancer
-
Janardhan S, Srivani P, Sastry GN. Choline kinase: an important target for cancer. Curr Med Chem 2006; 13: 1169-86.
-
(2006)
Curr Med Chem
, vol.13
, pp. 1169-1186
-
-
Janardhan, S.1
Srivani, P.2
Sastry, G.N.3
-
164
-
-
84856481598
-
Virtual screening filters for the design of type II p38 MAP kinase inhibitors: A fragment based library generation approach
-
Badrinarayan P, Sastry GN. Virtual screening filters for the design of type II p38 MAP kinase inhibitors: a fragment based library generation approach. J Mol Graph Model 2012; 34: 89-100.
-
(2012)
J Mol Graph Model
, vol.34
, pp. 89-100
-
-
Badrinarayan, P.1
Sastry, G.N.2
-
165
-
-
34548288600
-
Virtual screening in drug discovery--a computational perspective
-
Reddy AS, Pati SP, Kumar PP, Pradeep HN, Sastry GN. Virtual screening in drug discovery--a computational perspective. Curr Protein Pept Sci 2007; 8: 329-51.
-
(2007)
Curr Protein Pept Sci
, vol.8
, pp. 329-351
-
-
Reddy, A.S.1
Pati, S.P.2
Kumar, P.P.3
Pradeep, H.N.4
Sastry, G.N.5
-
166
-
-
33744796586
-
Active site acidic residues and structural analysis of modelled human aromatase: A potential drug target for breast cancer
-
Murthy JN, Nagaraju M, Sastry GM, Rao AR, Sastry GN. Active site acidic residues and structural analysis of modelled human aromatase: a potential drug target for breast cancer. J Comput Aided Mol Des 2005; 19: 857-70.
-
(2005)
J Comput Aided Mol Des
, vol.19
, pp. 857-870
-
-
Murthy, J.N.1
Nagaraju, M.2
Sastry, G.M.3
Rao, A.R.4
Sastry, G.N.5
-
167
-
-
33645843948
-
Homology modeling of membrane proteins: A critical assessment
-
Reddy Ch S, Vijayasarathy K, Srinivas E, Sastry GM, Sastry GN. Homology modeling of membrane proteins: a critical assessment. Comput Biol Chem 2006; 30: 120-6.
-
(2006)
Comput Biol Chem
, vol.30
, pp. 120-126
-
-
Reddy Ch, S.1
Vijayasarathy, K.2
Srinivas, E.3
Sastry, G.M.4
Sastry, G.N.5
-
168
-
-
33750330064
-
2D and 3D Quantitative Structure-Activity Relationship Studies on a Series of bis-Pyridinium Compounds as Choline Kinase Inhibitors
-
Janardhan S, Srivani P, Sastry GN. 2D and 3D Quantitative Structure-Activity Relationship Studies on a Series of bis-Pyridinium Compounds as Choline Kinase Inhibitors. QSAR Comb Sci 2006; 25: 860-72.
-
(2006)
QSAR Comb Sci
, vol.25
, pp. 860-872
-
-
Janardhan, S.1
Srivani, P.2
Sastry, G.N.3
-
169
-
-
84887467606
-
Molecular Modeling Studies of--aminoacyl containing Homopiperazine derivatives as DPP4 Inhibitors
-
Janardhan S, Padmanabha Reddy Y. Molecular Modeling Studies of--aminoacyl containing Homopiperazine derivatives as DPP4 Inhibitors. Int J Drug Des Discov 2011; 2: 533-47.
-
(2011)
Int J Drug Des Discov
, vol.2
, pp. 533-547
-
-
Janardhan, S.1
Padmanabha Reddy, Y.2
-
170
-
-
41249089027
-
Molecular modeling studies of phenoxypyrimidinyl imidazoles as p38 kinase inhibitors using QSAR and docking
-
Ravindra GK, Achaiah G, Sastry GN. Molecular modeling studies of phenoxypyrimidinyl imidazoles as p38 kinase inhibitors using QSAR and docking. Eur J Med Chem 2008; 43: 830-8.
-
(2008)
Eur J Med Chem
, vol.43
, pp. 830-838
-
-
Ravindra, G.K.1
Achaiah, G.2
Sastry, G.N.3
-
171
-
-
84867582901
-
FDA approved drugs complexed to their targets: Evaluating pose prediction accuracy of docking protocols
-
Bohari MH, Sastry GN. FDA approved drugs complexed to their targets: evaluating pose prediction accuracy of docking protocols. J Mol Model 2012; 18: 4263-74.
-
(2012)
J Mol Model
, vol.18
, pp. 4263-4274
-
-
Bohari, M.H.1
Sastry, G.N.2
-
172
-
-
84881329806
-
Rational approaches towards lead optimization of kinase inhibitors: The issue of specificity
-
Badrinarayan P, Sastry GN. Rational approaches towards lead optimization of kinase inhibitors: the issue of specificity. Curr Pharm Des 2013; 19: 4714-38.
-
(2013)
Curr Pharm Des
, vol.19
, pp. 4714-4738
-
-
Badrinarayan, P.1
Sastry, G.N.2
-
173
-
-
84870038810
-
Molecular dynamics investigation on a series of HIV protease inhibitors: Assessing the performance of MM-PBSA and MM-GBSA approaches
-
Srivastava HK, Sastry GN. Molecular dynamics investigation on a series of HIV protease inhibitors: assessing the performance of MM-PBSA and MM-GBSA approaches. J Chem Inf Model 2012; 52: 3088-98.
-
(2012)
J Chem Inf Model
, vol.52
, pp. 3088-3098
-
-
Srivastava, H.K.1
Sastry, G.N.2
|