| Tài liệu tham khảo |
Loại |
Chi tiết |
| 1. a) N. Noolvia, H.M. Patel, M. Kaur, Benzothiazoles: Search for anticancer agents, Eur. J. Med. Chem. 2012, 54, 447– 462. b) D.-F. Shi, T.D. Bradshaw, S.Wrigley, C.J. McCall, P. Lelieveld, I. Fichtner, M.F.G. Stevens, Antitumor benzothiazoles. 3. Synthesis of 2-(4-Aminophenyl)benzothiazoles and evaluation of their activities against breast cancer cell Lines in vitro and in vivo, J. Med. Chem., 1996, 39, 3375-3384 |
Sách, tạp chí |
| Tiêu đề: |
Benzothiazoles: Search for anticanceragents", Eur. J. Med. Chem. 2012, 54, 447– 462. b) D.-F. Shi, T.D. Bradshaw, S.Wrigley, C.J. McCall, P. Lelieveld, I. Fichtner, M.F.G. Stevens, "Antitumorbenzothiazoles. 3. Synthesis of 2-(4-Aminophenyl)benzothiazoles and evaluation oftheir activities against breast cancer cell Lines in vitro and in vivo |
|
| 2. H.R. Hendriks, A.S. Govaerts, I. Fichtner, S. Burtles, A.D. Westwell, G.J. Peters, Pharmacologically directed strategies in academic anticancer drug discovery based on the European NCI compounds initiative, Brit. J. Cancer., 2017, 117, 195–202 |
Sách, tạp chí |
| Tiêu đề: |
Pharmacologically directed strategies in academic anticancer drug discovery basedon the European NCI compounds initiative |
|
| 3. M. Ueki, K. Ueno, S. Miyadoh, K. Abe, K. Shibata, M. Taniguchi, S. Oi, UK-1, a novel cytotoxic metabolite from Streptomyces sp. 517-02.J. Antibiot. 1993, 46, 1089–1094 |
Sách, tạp chí |
| Tiêu đề: |
UK-1, anovel cytotoxic metabolite from Streptomyces sp. 517-02 |
|
| 4. M.A. Abdelgawad, A. Belal, H.A. Omar, L. Hegazy, M.E. Rateb, Synthesis, anti- breast cancer activity and molecular modeling of some benzothiazole and benzoxazole derivatives, Arch. Pharm. Chem. Life Sci., 2013, 346, 534-541 |
Sách, tạp chí |
| Tiêu đề: |
Synthesis, anti-breast cancer activity and molecular modeling of some benzothiazole andbenzoxazole derivatives |
|
| 5. M. Ueki, M. Taniguchi, J. J. Antibiot, a Novel Cytotoxic Metabolite from Streptomyces sp. 517-02, J. Antibiot., 1997, 50, 788–790 |
Sách, tạp chí |
| Tiêu đề: |
a Novel Cytotoxic Metabolite from Streptomyces sp. 517-02 |
|
| 6. M. Yang, X. Yang, H. Sun, A. Li, Total Synthesis of Ileabethoxazole, Pseudopteroxazole, and seco‐Pseudopteroxazole, Angew. Chem. Int. Ed., 2016, 55, 8, 2851-2855 |
Sách, tạp chí |
| Tiêu đề: |
Total Synthesis of Ileabethoxazole,Pseudopteroxazole, and seco‐Pseudopteroxazole |
|
| 7. Khaled R. A. Abdellatif, Noha H., Amin Asma, A. Mohammed, Synthesis of some benzoxazole derivatives and their anti-inflammatory evaluation, J. Chem. Pharm.Res., 2016, 8 (4), 1253-1261 |
Sách, tạp chí |
| Tiêu đề: |
Synthesis of somebenzoxazole derivatives and their anti-inflammatory evaluation |
|
| 8. S. Sato, T. Kajiura, M. Noguchi, K. Takehana, T. Kobayasho, T. Tsuji, AJI9561, a new cytotoxic benzoxazole derivative produced by Streptomyces sp., J. Antibiot., 2001, 54, 102 |
Sách, tạp chí |
| Tiêu đề: |
AJI9561, anew cytotoxic benzoxazole derivative produced by Streptomyces sp |
|
| 9. M.J. Don, C.C. Shen, Y.L. Lin, W.J. Syu, Y.H. Ding, C.M. Sun, Nitrogen- Containing Compounds from Salvia miltiorrhiza, J. Nat. Prod., 2005, 68, 1066-1070 |
Sách, tạp chí |
| Tiêu đề: |
Nitrogen-Containing Compounds from Salvia miltiorrhiza |
|
| 10. J. Kobayashi, T. Madona, H. Shigemori, Nakijinol, a novel sesquiterpenoid containing a benzoxazole ring from an Okinawan sponge., Tetrahedron Lett., 1995, 36, 5589–5590 |
Sách, tạp chí |
| Tiêu đề: |
Nakijinol, a novel sesquiterpenoidcontaining a benzoxazole ring from an Okinawan sponge |
|
| 11. A.D. Rodríguez, C. Ramírez, I.I. Rodríguez, E. González, Novel Antimycobacterial Benzoxazole Alkaloids, from the West Indian Sea Whip Pseudopterogorgia elisabethae., Org. Lett., 1999, 1, 3, 527–530 |
Sách, tạp chí |
| Tiêu đề: |
NovelAntimycobacterial Benzoxazole Alkaloids, from the West Indian Sea WhipPseudopterogorgia elisabethae |
|
| 12. M.F.G. Stevens, C.J. McCall, P. Lelieveld, P. Alexander, A. Richter, D.E. Davies, Structural studies on bioactive compounds. 23. Synthesis of polyhydroxylated 2- phenylbenzothiazoles and a comparison of their cytotoxicities and pharmacological properties with genistein and quercetin, J. Med. Chem., 1994, 37 1689-1695 |
Sách, tạp chí |
| Tiêu đề: |
Synthesis of polyhydroxylated 2-phenylbenzothiazoles and a comparison of their cytotoxicities and pharmacologicalproperties with genistein and quercetin |
|
| 13. C. Hohmann, K. Schneider, C. Bruntner, El. Irran, Gr. Nicholson, A.T. Bull, A.L. Jones, R. Brown, J.E. M. Stach, M. Goodfellow, W. Beil, M. Krọmer, J.F. Imhoff, R. D. Süssmuth, H.P. Fiedler, Caboxamycin, a new antibiotic of the benzoxazole family produced by the deep-sea strain Streptomyces sp. NTK 937. J. Antibiot., 2009, 62, 99–104 |
Sách, tạp chí |
| Tiêu đề: |
Caboxamycin, a new antibiotic of the benzoxazolefamily produced by the deep-sea strain Streptomyces sp. NTK 937 |
|
| 14. A. Mohsen, M.E. Omar, O.M. Aboul, M.S. El-Shoukrofy, M.E. Amr, Benzoxazole derivatives as new generation of anti-breast cancer agents, Bioorg.Chem., 2020, 96, 103593 |
Sách, tạp chí |
| Tiêu đề: |
Benzoxazole derivatives as new generation of anti-breast cancer agents |
|
| 15. M.J. Akhtar, A.A. Siddiqui, A.A. Khan, Z. Ali, R.P. Dewangan, S. Pasha, M.S.Yar, Design, synthesis, docking and QSAR study of substituted benzimidazole linked oxadiazole as cytotoxic agents, EGFR and erbB2 receptor inhibitors, Eur. J. Med |
Sách, tạp chí |
| Tiêu đề: |
Design, synthesis, docking and QSAR study of substituted benzimidazole linkedoxadiazole as cytotoxic agents, EGFR and erbB2 receptor inhibitors |
|