| Tài liệu tham khảo |
Loại |
Chi tiết |
| 3. Jin CY, Burgess JP, Rehder KS, Brine GA (2007) Synthesis of N 6 -[endo-2 ’ -(endo-5 ’ - hydroxy)norbornyl]-8-(N-methylisopropyl-amino)-9-methyladenine (WRC-0571): a potent and selective adenosine A1 receptor antagonist. Synthesis 2007(2):219 – 224 |
Sách, tạp chí |
| Tiêu đề: |
Synthesis of N 6 -[endo-2 ’ -(endo-5 ’ - hydroxy)norbornyl]-8-(N-methylisopropyl-amino)-9-methyladenine (WRC-0571): a potent and selective adenosine A1 receptor antagonist |
| Tác giả: |
Jin CY, Burgess JP, Rehder KS, Brine GA |
| Nhà XB: |
Synthesis |
| Năm: |
2007 |
|
| 4. Eckhardt M, Langkopf E, Mark M, Tadayyon M, Thomas L, Nar H, Pfrengle W, Guth B, Lotz R, Sieger P, Fuchs H, Himmelsbach F (2007) 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(26):6450 – 6453 |
Sách, tạp chí |
| Tiêu đề: |
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 |
| Tác giả: |
Eckhardt M, Langkopf E, Mark M, Tadayyon M, Thomas L, Nar H, Pfrengle W, Guth B, Lotz R, Sieger P, Fuchs H, Himmelsbach F |
| Nhà XB: |
J Med Chem |
| Năm: |
2007 |
|
| 5. Bansal Y, Silakari O (2012) The therapeutic journey of benzimidazoles: a review. Bioorgan Med Chem 20(21):6208 – 6236 |
Sách, tạp chí |
| Tiêu đề: |
The therapeutic journey of benzimidazoles: a review |
| Tác giả: |
Bansal Y, Silakari O |
| Nhà XB: |
Bioorgan Med Chem |
| Năm: |
2012 |
|
| 6. Gallardo-Godoy A, Gever J, Fife KL, Silber BM, Prusiner SB, Renslo AR (2011) 2-Aminothiazoles as therapeutic leads for prion diseases. J Med Chem 54(4):1010 – 1021 7. Zhang TZ, Yan ZH, Sromek A, Knapp BI, Scrimale T, Bidlack JM, Neumeyer JL (2011)Aminothiazolomorphinans with mixed j and l opioid activity. J Med Chem 54(6):1903 – 1913 |
Sách, tạp chí |
| Tiêu đề: |
2-Aminothiazoles as therapeutic leads for prion diseases |
| Tác giả: |
Gallardo-Godoy A, Gever J, Fife KL, Silber BM, Prusiner SB, Renslo AR |
| Nhà XB: |
J Med Chem |
| Năm: |
2011 |
|
| 11. Guram AS, Buchwald SL (1994) Palladium-catalyzed aromatic aminations with in situ generated aminostannanes. J Am Chem Soc 116(17):7901 – 79024.5 Supplemental Information 137 |
Sách, tạp chí |
| Tiêu đề: |
Palladium-catalyzed aromatic aminations with in situ generated aminostannanes |
| Tác giả: |
Guram AS, Buchwald SL |
| Nhà XB: |
J Am Chem Soc |
| Năm: |
1994 |
|
| 1. Orjales A, Mosquera R, Labeaga L, Rodes R (1997) New 2-piperazinylbenzimidazole derivatives as 5-HT 3 antagonists. Synthesis and pharmacological evaluation. J Med Chem 40 (4):586 – 593 |
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| 2. Massari S, Daelemans D, Barreca ML, Knezevich A, Sabatini S, Cecchetti V, Marcello A, Pannecouque C, Tabarrini O (2010) A 1,8-naphthyridone derivative targets the HIV-1 Tat-mediated transcription and potently inhibits the HIV-1 replication. J Med Chem 53 (2):641 – 648 |
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| 10. Kosugi M, Kameyama M, Migita T (1983) Palladium-catalyzed aromatic aminaiton of aryl bromides with N,N-diethylamino-tributyltin. Chem Lett 12(6):927 – 928 |
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