Tài liệu tham khảo |
Loại |
Chi tiết |
12. Kim H.J., Bae S.C., “Histonedeacetylase inhibitors: molecular mechanisms of action and clinical trials as anti-cancer drugs”, Am J Transl Res (2011) 3, 166-179 |
Sách, tạp chí |
Tiêu đề: |
Histonedeacetylase inhibitors: molecular mechanisms of action and clinical trials as anti-cancer drugs |
|
13. Milos Dokmanovic and Paul A. Marks, “ Prospects: Histone Deacetylase Inhibitors”, Journal of Cellular Biochemistry, (2005) 293-304 |
Sách, tạp chí |
Tiêu đề: |
Prospects: Histone Deacetylase Inhibitors”, Journal of Cellular Biochemistry |
|
14. Welch WM., Ewing FE., Huang J., Menniti FS., Pagnozzi MJ., Kelly K., et al. "Atropisomeric quinazolin-4-one derivatives are potent noncompetitive (- amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor antagonists". Bioorg Med Chem Lett (2001) 11,177-181 |
Sách, tạp chí |
Tiêu đề: |
Atropisomeric quinazolin-4-one derivatives are potent noncompetitive (-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor antagonists |
|
15. Holmes MA, Matthews BW: “Binding of hydroxamic acid inhibitors to crystalline thermolysin suggests a pentacoordinate zinc intermediate in catalysis”. Biochemistry (1981) 24, 6912-6920 |
Sách, tạp chí |
Tiêu đề: |
Binding of hydroxamic acid inhibitors to crystalline thermolysin suggests a pentacoordinate zinc intermediate in catalysis” |
|
16. Mei S, Ho AD, Mahlknecht U: “Role of histone deacetylase inhibitors in the treatment of cancer”. Int J Oncol (2004) 1, 1509-1519 |
Sách, tạp chí |
Tiêu đề: |
Role of histone deacetylase inhibitors in the treatment of cancer” |
|
17. Bolden JE, Peart MJ, Johnstone RW: “Anticancer activities of histone deacetylase inhibitors”. Nat Rev Drug Discov (2006) 5,769–784 |
Sách, tạp chí |
Tiêu đề: |
“Anticancer activities of histone deacetylase inhibitors” |
|
18. Bressi JC, Jennings AJ, Skene R, Wu Y, Melkus R, De Jong R,O’Connell S, Grimshaw CE, Navre M, Gangloff AR: “Exploration of the HDAC2 foot pocket: synthesis and SAR of substituted N- (2-aminophenyl)benzamides”.Bioorg Med Chem Lett (2010) 10, 3142-3145 |
Sách, tạp chí |
Tiêu đề: |
“Exploration of the HDAC2 foot pocket: synthesis and SAR of substituted N- (2-aminophenyl)benzamides” |
|
19. Marson CM,Mahadevan T,Dines J, et al. ‘’Structure-activity relationships of aryloxyalkanoic acid hydroxyamides as potent inhibitors of histone deacetylase’’. Bioorg Med Chem Lett (2007)17, 136 – 41 |
Sách, tạp chí |
Tiêu đề: |
’Structure-activity relationships of aryloxyalkanoic acid hydroxyamides as potent inhibitors of histone deacetylase’’ |
|
20. Kozikowski A.P., et. Al. ‘’Use of the nitril oxide cycloaddition (NOC) recation for molecular probe generation: A new class of enzyme selective of histone deacetylase inhibitors showing picomola activity at HDAC6’’, J. Med.Chem (2008) 51, 4370 - 4373 |
Sách, tạp chí |
Tiêu đề: |
’Use of the nitril oxide cycloaddition (NOC) recation for molecular probe generation: A new class of enzyme selective of histone deacetylase inhibitors showing picomola activity at HDAC6’’ |
|
21. Marson C.M., et al. “Structure-activity relationships of aryloxyalkanoic and hydroxamides as potent inhibitors of histone deacetylase”, Bioorganic and Medicinal Chemistry Letters (2007) 17, 136-141 |
Sách, tạp chí |
Tiêu đề: |
Structure-activity relationships of aryloxyalkanoic and hydroxamides as potent inhibitors of histone deacetylase |
|
22. Griess P. ‘’ĩber die Einwirkung des Cyans auf Anthranilsọure’’. Eur J Inorg Chem (1968)2, 415–418 |
Sách, tạp chí |
Tiêu đề: |
ĩber die Einwirkung des Cyans auf Anthranilsọure’’ |
|
23. Arora Rashmi, Kapoor Ashish et al “Quniazolinon: an overview” international research journal of pharmacy, 2011 |
Sách, tạp chí |
Tiêu đề: |
Quniazolinon: an overview |
|
24. Connolly DJ, Cusack D, Sullivan TPO, Guiry PJ. “Synthesis of quinazolinones and quinazolines”. Tetrahedron (2005) 61, 10153–10202 |
Sách, tạp chí |
Tiêu đề: |
Synthesis of quinazolinones and quinazolines |
|
25. Mhaske SB, Argade NP. “The chemistry of recently isolated naturally occurring quinazolinone alkaloids”. Tetrahedron (2006) 62, 9787–9826 |
Sách, tạp chí |
Tiêu đề: |
The chemistry of recently isolated naturally occurring quinazolinone alkaloids |
|
26. Jianguang Zhou and Jie Fang. One-Pot “Synthesis of Quinazolinones via Iridium-Catalyzed Hydrogen Transfers”. J. Org. Chem (2011) 76, 7730–7736 |
Sách, tạp chí |
Tiêu đề: |
Synthesis of Quinazolinones via Iridium-Catalyzed Hydrogen Transfers” |
|
27. Bipransh Kumar Tiwary, Kiran Pradhan et al “Implication of Quinazoline- 4(3H)-ones in Medicinal Chemistry: A Brief Review”, J. chem Bio ther, (2015) |
Sách, tạp chí |
Tiêu đề: |
Implication of Quinazoline-4(3H)-ones in Medicinal Chemistry: A Brief Review |
|
28. Welch WM, Ewing FE, Huang J, Menniti FS, Pagnozzi MJ, Kelly K, et al. “Atropisomeric quinazolin-4-one derivatives are potent noncompetitive (- amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor antagonists”. Bioorg Med Chem Lett (2001) 11,177–181 |
Sách, tạp chí |
Tiêu đề: |
Atropisomeric quinazolin-4-one derivatives are potent noncompetitive (-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor antagonists |
|
29. Alagarsamy, V. Ra Solomon, K. Dhanabal, “Synthesis and pharmacological evaluation of some 3-phenyl-2-substituted-3H- quinazolin-4-one as analgesic, anti-inflammatory agents”. Bioorganic & Medicinal Chemistry (2007)1, 235-241 |
Sách, tạp chí |
Tiêu đề: |
Synthesis and pharmacological evaluation of some 3-phenyl-2-substituted-3H- quinazolin-4-one as analgesic, anti-inflammatory agents” |
|
30. P. M. Chandrika, T. Yakaiah, A. R. R. Rao et al., “Synthesis of novel 4,6- disubstituted quinazoline derivatives, their anti-inflammatory and anti-cancer activity (cytotoxic) against U937 leukemia cell lines,” European Journal of edicinal Chemistry (2008) 4, 846–852 |
Sách, tạp chí |
Tiêu đề: |
Synthesis of novel 4,6-disubstituted quinazoline derivatives, their anti-inflammatory and anti-cancer activity (cytotoxic) against U937 leukemia cell lines |
|
31. A. S. El-Azab, M. A. Al-Omar, A. A. M. Abdel-Aziz et al., “Design, synthesis and biological evaluation of novel quinazoline derivatives as potential antitumor agents: Molecular docking study,” European Journal of Medicinal Chemistry (2010) 9, 4188–4198 |
Sách, tạp chí |
Tiêu đề: |
Design, synthesis and biological evaluation of novel quinazoline derivatives as potential antitumor agents: Molecular docking study |
|