The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
22959556 |
57 |
Discovery and preclinical profile of teneligliptin (3-[(2S,4S)-4-[4-(3-methyl-1-phenyl-1H-pyrazol-5-yl)piperazin-1-yl]pyrrolidin-2-ylcarbonyl]thiazolidine): a highly potent, selective, long-lasting and orally active dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetes. |
Mitsubishi Tanabe Pharma |
22824762 |
39 |
Fused bicyclic heteroarylpiperazine-substituted L-prolylthiazolidines as highly potent DPP-4 inhibitors lacking the electrophilic nitrile group. |
Mitsubishi Tanabe Pharma |
21764322 |
33 |
Identification of 3-aminomethyl-1,2-dihydro-4-phenyl-1-isoquinolones: a new class of potent, selective, and orally active non-peptide dipeptidyl peptidase IV inhibitors that form a unique interaction with Lys554. |
Takeda Pharmaceutical |
19217790 |
68 |
Medicinal chemistry approaches to the inhibition of dipeptidyl peptidase-4 for the treatment of type 2 diabetes. |
Matrix Laboratories |
18039579 |
59 |
Design and synthesis of DPP-IV inhibitors lacking the electrophilic nitrile group. |
Ono Pharmaceutical |
17113301 |
83 |
Lead optimization of [(S)-gamma-(arylamino)prolyl]thiazolidine focused on gamma-substituent: Indoline compounds as potent DPP-IV inhibitors. |
Mitsubishi Pharma |
15713382 |
16 |
Synthesis and evaluation of pyrazolidine derivatives as dipeptidyl peptidase IV (DP-IV) inhibitors. |
Korea Research Institute of Chemical Technology |
15357972 |
30 |
Synthesis and DP-IV inhibition of cyano-pyrazoline derivatives as potent anti-diabetic agents. |
Korea Research Institute of Chemical Technology |
21324688 |
36 |
1-((3S,4S)-4-amino-1-(4-substituted-1,3,5-triazin-2-yl) pyrrolidin-3-yl)-5,5-difluoropiperidin-2-one inhibitors of DPP-4 for the treatment of type 2 diabetes. |
Pfizer |
19275964 |
64 |
(3,3-Difluoro-pyrrolidin-1-yl)-[(2S,4S)-(4-(4-pyrimidin-2-yl-piperazin-1-yl)-pyrrolidin-2-yl]-methanone: a potent, selective, orally active dipeptidyl peptidase IV inhibitor. |
Pfizer |
17317162 |
60 |
[(S)-gamma-(4-Aryl-1-piperazinyl)-l-prolyl]thiazolidines as a novel series of highly potent and long-lasting DPP-IV inhibitors. |
Mitsubishi Pharma |
16722626 |
94 |
cis-2,5-dicyanopyrrolidine inhibitors of dipeptidyl peptidase IV: synthesis and in vitro, in vivo, and X-ray crystallographic characterization. |
Pfizer |
15863294 |
36 |
1-((S)-gamma-substituted prolyl)-(S)-2-cyanopyrrolidine as a novel series of highly potent DPP-IV inhibitors. |
Mitsubishi Pharma |
12801240 |
105 |
1-[[(3-hydroxy-1-adamantyl)amino]acetyl]-2-cyano-(S)-pyrrolidine: a potent, selective, and orally bioavailable dipeptidyl peptidase IV inhibitor with antihyperglycemic properties. |
Novartis Institute For Biomedical Research |
12036346 |
12 |
1-[2-[(5-Cyanopyridin-2-yl)amino]ethylamino]acetyl-2-(S)-pyrrolidinecarbonitrile: a potent, selective, and orally bioavailable dipeptidyl peptidase IV inhibitor with antihyperglycemic properties. |
TBA |
15217282 |
4 |
First synthesis and determination of the absolute configuration of sulphostin, a novel inhibitor of dipeptidyl peptidase IV. |
Microbial Chemistry Research Center |
28442252 |
62 |
Approaches towards the development of chimeric DPP4/ACE inhibitors for treating metabolic syndrome. |
Ranbaxy Laboratories |
9195869 |
28 |
Molecular recognition at the thrombin active site: structure-based design and synthesis of potent and selective thrombin inhibitors and the X-ray crystal structures of two thrombin-inhibitor complexes. |
Laboratorium FÜR Organische Chemie |
19328688 |
12 |
Identification of an N-oxide pyridine GW4064 analog as a potent FXR agonist. |
Roche R & D Center(China) |