Pornthip Arayarat . Synthesis and affinity of 4H-[1,2,4]-triazolo-[4,3-a]-[1,4]-benzodiazepines as selective, cholecystikinin ligands. (). Khon Kaen University. Instructional Resource Center. : , 2002.
| Title | Contributor | Type |
|---|---|---|
| Process development : Synthesis of benzofuranyl-imidazoline (2-BFI) as a selective and highly potent 1-2 ligand with potential antidepressant activity
มหาวิทยาลัยขอนแก่น Lattmann, Eric ;Pornthip Arayarat | บทความ/Article | |
| Small organic molecules as cholecystokinin antagonists
มหาวิทยาลัยขอนแก่น Lattmann, Eric ;Arayarat, Pornthip ;Singh, Harjit | บทความ/Article | |
| Synthesis and affinity of 4H-[1,2,4]-triazolo-[4,3-a]-[1,4]-benzodiazepines as selective, cholecystikinin ligands
มหาวิทยาลัยขอนแก่น Lattmann, Eric ;Offel, Michael ;Poyner, David R. ;Pornthip Arayarat | บทความ/Article | |
| From CNS-Drugs to anti-neoplastic agents : Cholecystokinin (CCK)-antagonists as modern anti-cancer agents
มหาวิทยาลัยขอนแก่น Lattmann, Eric ;Pornthip Lattmann | บทความ/Article |
| Title | Contributor | Type |
|---|---|---|
| Synthesis and affinity of 4H-[1,2,4]-triazolo-[4,3-a]-[1,4]-benzodiazepines as selective, cholecystikinin ligands
มหาวิทยาลัยขอนแก่น Lattmann, Eric ;Offel, Michael ;Poyner, David R. ;Pornthip Arayarat | บทความ/Article |
| Title | Contributor | Type |
|---|---|---|
| Synthesis and affinity of 4H-[1,2,4]-triazolo-[4,3-a]-[1,4]-benzodiazepines as selective, cholecystikinin ligands
มหาวิทยาลัยขอนแก่น Lattmann, Eric ;Offel, Michael ;Poyner, David R. ;Pornthip Arayarat | บทความ/Article |
| Title | Contributor | Type |
|---|---|---|
| Process development : Synthesis of benzofuranyl-imidazoline (2-BFI) as a selective and highly potent 1-2 ligand with potential antidepressant activity
มหาวิทยาลัยขอนแก่น Lattmann, Eric ;Pornthip Arayarat | บทความ/Article | |
| Synthesis and affinity of 4H-[1,2,4]-triazolo-[4,3-a]-[1,4]-benzodiazepines as selective, cholecystikinin ligands
มหาวิทยาลัยขอนแก่น Lattmann, Eric ;Offel, Michael ;Poyner, David R. ;Pornthip Arayarat | บทความ/Article |