| Tài liệu tham khảo |
Loại |
Chi tiết |
| 7. Nguyễn Văn Tuyến (2012), Hóa hữu cơ nâng cao - Các phương pháp tổng hợp hữu cơ hiện đại- NXB Khoa học và kỹ thuật.II. Tài liệu tiếng Anh |
Sách, tạp chí |
| Tiêu đề: |
Hóa hữu cơ nâng cao - Các phương pháp tổng hợp hữu cơ hiện đạ |
| Tác giả: |
Nguyễn Văn Tuyến |
| Nhà XB: |
NXB Khoa học và kỹ thuật. II. Tài liệu tiếng Anh |
| Năm: |
2012 |
|
| 8. Andrew Morell, Michael Placzek, SethParmley, SmithaAntony, Thomas S. Dexheimer, Yves Pommier and Mark Cushman, “Nitrated Indenoisoquinolines as TopoisomeraseI Inhibitors: A Systematic Study and optimization”, Journal of Medicinal Chemistry, 2007, 50, 4419 - 4430 |
Sách, tạp chí |
| Tiêu đề: |
Nitrated Indenoisoquinolines as TopoisomeraseI Inhibitors: A Systematic Study and optimization”, "Journal of Medicinal Chemistry", 2007, "50 |
|
| 9. Brian M. Fox, Xiangshu Xiao, Smitha Antony, Glenda Kohlhagen, Yves Pommier, Bart L. Staker, Lance Stewart, và Mark Cushman, “Design, Synthesis, and Biological Evaluation of Cytotoxic 11- Alkenylindenoisoquinoline Topoisomerase I Inhibitors and Indenoisoquinoline - Camptothecin Hybrids”, Journal of Medicinal Chemistry, 2003, 46, 3275 - 3282 |
Sách, tạp chí |
| Tiêu đề: |
Design, Synthesis, and Biological Evaluation of Cytotoxic 11- Alkenylindenoisoquinoline Topoisomerase I Inhibitors and Indenoisoquinoline - Camptothecin Hybrids”, "Journal of Medicinal Chemistry", 2003, "46 |
|
| 11. Katherine E. Peterson, Maris A. Cinelli, Andrew E. Morrell, Akhil Mehta, Thomas S. Dexheimer, Keli Agama, Smitha Antony, Yves Pommier, và Mark Cushman, “Alcohol-, Diol-, and Carbohydrate- Substituted Indeooisoquinolines as Topoisomerase I Inhibitors:Investigating the Relationships Involving Stereochemistry, Hydrogen Bonding, and Biological Activity”, Journal of Medicinal Chemistry, 2011, 54, 4937 - 4953 |
Sách, tạp chí |
| Tiêu đề: |
Alcohol-, Diol-, and Carbohydrate- Substituted Indeooisoquinolines as Topoisomerase I Inhibitors: Investigating the Relationships Involving Stereochemistry, Hydrogen Bonding, and Biological Activity”, "Journal of Medicinal Chemistry," 2011, "54 |
|
| 12. Gang Ahn, Nadège Schifano-Faux, Jean-Francois Goossens, Brigitte Baldeyrou, Axel Couture, Pierre Grandclaudon, Amélie Lansiaux, Adina Ryckebusch, “Synthesis, cytotoxicity and topoisomerase inhibition properties of multifarious aminoalkylated indeno[1,2-c]isoquinolin-5,11- diones”, Bioorganic & Medicinal Chemistry Letters, 2011, 21, 2259 - 2263 |
Sách, tạp chí |
| Tiêu đề: |
Synthesis, cytotoxicity and topoisomerase inhibition properties of multifarious aminoalkylated indeno[1,2-c]isoquinolin-5,11-diones”, "Bioorganic & Medicinal Chemistry Letters", 2011, "21 |
|
| 13. Xiaoyun Zhang, Rubing Wang, Li Zhao, Na Lu, Jubo Wang, Qidong You, Zhiyu Li, Qinglong Guo, “Synthesis and biological evaluations of novel indenoisoquinolines as topoisomerase I inhibitors”, Bioorganic &Medicinal Chemistry Letters, 2012, 22, 1276-1281 |
Sách, tạp chí |
| Tiêu đề: |
Synthesis and biological evaluations of novel indenoisoquinolines as topoisomerase I inhibitors”, "Bioorganic & "Medicinal Chemistry Letters," 2012, "22 |
|
| 14. Xiangshu Xiao, Andrew Morrell, Phillip E. Fanwick and Mark Cushmana, “On the mechanism of conversion of 4-carboxy-3,4-dihydro-3-phenyl-1(2H) isoquinolones to indeno[1,2-c]isoquinolines by thionyl chloride”, Tetrahedron, 2006, 62, 9705-9712 |
Sách, tạp chí |
| Tiêu đề: |
On the mechanism of conversion of 4-carboxy-3,4-dihydro-3-phenyl-1(2H) isoquinolones to indeno[1,2-c]isoquinolines by thionyl chloride”, "Tetrahedron", 2006, "62 |
|
| 16. Andrew Morrell, Smitha Antony, Glenda Kohlhagen,Yves Pommier and Mark Cushman, “Synthesis of benz[d]indeno[1,2-b]pyran-5,11-diones:Versatile intermediates for the design and synthesis of topoisomerase I inhibitors”, Bioorganic & Medicinal Chemistry Letters, 2006, 16, 1846- 1849 |
Sách, tạp chí |
| Tiêu đề: |
Synthesis of benz[d]indeno[1,2-b]pyran-5,11-diones: Versatile intermediates for the design and synthesis of topoisomerase I inhibitors”, "Bioorganic & Medicinal Chemistry Letters, "2006, "16 |
|
| 17. Mark Cushman, Muthusamy Jayaraman, Jeffrey A. Vroman, Anna K. Fukunaga, Brian M. Fox, Glenda Kohlhagen, Dirk Strumberg, and Yves Pommier, “Synthesis of New Indeno[1,2-c]isoquinolines: Cytotoxic Non-Camptothecin Topoisomerase I Inhibitors”, Journal of Medicinal Chemistry, 2000, 43, 3688-3698 |
Sách, tạp chí |
| Tiêu đề: |
Synthesis of New Indeno[1,2-"c"]isoquinolines: Cytotoxic Non-Camptothecin Topoisomerase I Inhibitors”, "Journal of Medicinal Chemistry, "2000, "43 |
|
| 18. Muthusamy Jayaraman, Brian M. Fox, Melinda Hollingshead, Glenda Kohlhagen, Yves Pommier, và Mark Cushman, “Synthesis of New Dihydroindeno[1-2]isoquinoline and Indenoisoquinolineium Chloride Topoisomerase I Inhibitors Having High in Vivo Anticancer Activity in the Hollow Fiber Animal Model”, Journal of Medicinal Chemistry, 2002, 45, 242- 249 |
Sách, tạp chí |
| Tiêu đề: |
Synthesis of New Dihydroindeno[1-2]isoquinoline and Indenoisoquinolineium Chloride Topoisomerase I Inhibitors Having High in Vivo Anticancer Activity in the Hollow Fiber Animal Model”, "Journal of Medicinal Chemistry", 2002, "45 |
|
| 19. Muthukaman Nagarajan, Andrew Morrell, Brian C. Fort, Marintha Rae Meckley, Smitha Antony, Glenda Kohlhagen, Yves Pommier, and Mark Cushman, “Synthesis and Anticancer Activity of Simplified Indenoisoquinoline Topoisomerase I Inhibitors Lacking Substituents on the Aromatic Rings”, Journal of Medicinal Chemistry, 2004, 47, 5651- 5661 |
Sách, tạp chí |
| Tiêu đề: |
Synthesis and Anticancer Activity of Simplified Indenoisoquinoline Topoisomerase I Inhibitors Lacking Substituents on the Aromatic Rings”, "Journal of Medicinal Chemistry", 2004, "47 |
|
| 20. Dirk strumberg, Yves Pommier, Kenneth Paull, Muthusamy Jayaraman, Pamela Nagafuji, and Mark Cushman, “Synthesis of Cytotoxic Indenoisoquinoline Topoisomerase I Poisons”, Journal of Medicinal Chemistry, 1999, 42, 446-457 |
Sách, tạp chí |
| Tiêu đề: |
Synthesis of Cytotoxic Indenoisoquinoline Topoisomerase I Poisons”, "Journal of Medicinal Chemistry", 1999, "42 |
|
| 21. Daulat Bikram Khadka, Won-Jea Cho, “3-Arylisoquinolines as novel topoisomerase I inhibitors”, Bioorganic & Medicinal Chemistry, 2011, 19, 724-734 |
Sách, tạp chí |
| Tiêu đề: |
3-Arylisoquinolines as novel topoisomerase I inhibitors”, "Bioorganic & Medicinal Chemistry", 2011, "19 |
|
| 22. Daniel E. Beck, Keli Agama, Christophe Marchand, Adel Chergui, Yves Pommier, and Mark Cushman, Synthesis and Biological Evaluation of New Carbohydrate-Substituted Indenoisoquinoline Topoisomerase I Inhibitors and Improved Syntheses of the Experimental Anticancer Agents Indotecan (LMP400) and Indimitecan (LMP776), Journal of Medicinal Chemistry, 2014, 57, 1495−1512 |
Sách, tạp chí |
| Tiêu đề: |
Journal of Medicinal Chemistry", 2014, "57 |
|
| 23. Hue Thi My Van, Quynh Manh Le, Kwang Youl Lee, Eung-Seok Lee, Youngjoo Kwon, Tae Sung Kim, Thanh Nguyen Le, Suh-Hee Lee and Won-Jea Cho, “Convenient synthesis of indeno[1,2-c]isoquinolines as constrained forms of 3-arylisoquinolines and docking study of a topoisomerase I inhibitor into DNA-topoisomerase I complex”, Bioorganic & Medicinal Chemistry Letters, 2007, 17, 5763-5767 |
Sách, tạp chí |
| Tiêu đề: |
Convenient synthesis of indeno[1,2-c]isoquinolines as constrained forms of 3-arylisoquinolines and docking study of a topoisomerase I inhibitor into DNA-topoisomerase I complex”, "Bioorganic & Medicinal Chemistry Letters," 2007, "17 |
|
| 24. Won-Jea Cho, Quynh Manh Le, Hue Thi My Van, Kwang Youl Lee, Bok Yun Kang, Eung-Seok Lee, Sang Kook Lee and Youngjoo Kwon,“Design, docking, and synthesis of novel indeno[1,2-c]isoquinolines for the development of antitumor agents as topoisomerase I inhibitors”, Bioorganic & Medicinal Chemistry Letters, 2007, 17, 3531-3534 |
Sách, tạp chí |
| Tiêu đề: |
Design, docking, and synthesis of novel indeno[1,2-c]isoquinolines for the development of antitumor agents as topoisomerase I inhibitors”, "Bioorganic & Medicinal Chemistry Letters", 2007, "17 |
|
| 25. Prakash G.jagtap, Erkan Baloglu, Garry J. Southan,Jon G. Mabley, Hongshan Li, Jing Zhou, John van Duzer, Andrew L. Salzman, va Csaba Szabó, Discovery of Potent Poly(ADP-ribose) Polymerase-1 Inhibitors from the Modification of Indeno[1,2-c]isoquinolinone, Journal of Medicinal Chemistry, 2005, 48, 5100-5103 |
Sách, tạp chí |
| Tiêu đề: |
c"]isoquinolinone, "Journal of Medicinal Chemistry, "2005, "48 |
|
| 26. Daulat Bikram Khadka, Quynh Manh Le, Su Hui Yang, Hue Thi My Van, Thanh Nguyen Le, Suk Hee Cho, Youngjoo Kwon, Kyung- Tae Lee, Eung- seok Lee, Won- Jea Cho,Design, synthesis and docking study of 5-amino substituted indeno[1,2-c]isoquinolines as novel topoisomerase I inhibitors, Bioorganic & Medicinal Chemistry, 2011, 19, 1924-1929 |
Sách, tạp chí |
| Tiêu đề: |
Bioorganic & Medicinal Chemistry," 2011, "19 |
|
| 27.Alexandra Ioanoviciu, Smitha Antony, Yves Pommier, Bart L. Staker, Lance Stewart and Mark Cushman, “Synthesis and Mechanism of Action Studies of a Series of Norindenoisoquinoline Topoisomerase I Poisons Reveal an Inhibitor with a Flipped Orientation in the Ternary DNA- Enzyme-Inhibitor Complex As Determined by X-ray Crystallographic Analysis”, Journal of Medicinal Chemistry, 2005, 48, 4803-4814 |
Sách, tạp chí |
| Tiêu đề: |
Synthesis and Mechanism of Action Studies of a Series of Norindenoisoquinoline Topoisomerase I Poisons Reveal an Inhibitor with a Flipped Orientation in the Ternary DNA-Enzyme-Inhibitor Complex As Determined by X-ray Crystallographic Analysis”, "Journal of Medicinal Chemistry", 2005, "48 |
|
| 28. Meslanie Dubois, Stéphane Lebrun, Axel Couture, Eric Deniau, Pierre Grandclaudon, “Alternative synthetic approaches to biologically active indeno[1,2-c]isoquinoline-5,11-diones”,15thinternational electronic conterence on synthetic organic chemistry, 2011 |
Sách, tạp chí |
| Tiêu đề: |
Alternative synthetic approaches to biologically active indeno[1,2-c]isoquinoline-5,11-diones”, "15"th" international electronic conterence on synthetic organic chemistry |
|