Privileged structure-based quinazolinone natural product-templated libraries: identification of novel tubulin polymerization inhibitors.
暂无分享,去创建一个
Kevin Sprague | Daniel Yohannes | Christopher J. Wilson | S. Ng | D. Yohannes | Shi-Chung Ng | Ying-Ying Si | Jifeng Liu | Ping Ye | Christopher J Wilson | Ying Si | Ji-Feng Liu | Ping Ye | Katie Sargent | Galina Beletsky | Kevin J. Sprague | K. Sargent | Galina Beletsky
[1] A. Al-Shamma,et al. Antimicrobial agents from higher plants. Antimicrobial agents from Peganum harmala seeds. , 1981, Journal of natural products.
[2] R. M. Desai,et al. Vasicinone. A Bronchodilator Principle from Adhatoda Vasica Nees (N. O. Acanthaceae) , 1963 .
[3] R. Desimone,et al. Privileged structures: applications in drug discovery. , 2004, Combinatorial chemistry & high throughput screening.
[4] W. Greenlee,et al. A potent, orally active, balanced affinity angiotensin II AT1 antagonist and AT2 binding inhibitor. , 1993, Journal of medicinal chemistry.
[5] D. Dexter,et al. Synthesis and biological evaluation of 2-styrylquinazolin-4(3H)-ones, a new class of antimitotic anticancer agents which inhibit tubulin polymerization. , 1990, Journal of medicinal chemistry.
[6] S. Kuo,et al. Antitumor agents. Part 204: synthesis and biological evaluation of substituted 2-aryl quinazolinones. , 2001, Bioorganic & medicinal chemistry letters.
[7] D. Cherrak,et al. High throughput HPLC/MS purification in support of drug discovery , 2004 .
[8] Mimi Shirasu-Hiza,et al. Dynamics of the mitotic spindle--potential therapeutic targets. , 2003, Progress in cell cycle research.
[9] P. Molina,et al. Inhibition of leukocyte functions by the alkaloid isaindigotone from Isatis indigotica and some new synthetic derivatives. , 2001, Journal of natural products.
[10] A. Ganesan,et al. Total synthesis of the fumiquinazoline alkaloids: solution-phase studies. , 2000, The Journal of organic chemistry.
[11] S. Ng,et al. A-204197, a new tubulin-binding agent with antimitotic activity in tumor cell lines resistant to known microtubule inhibitors. , 2001, Cancer research.
[12] J. Fremlin. Sub-surface Temperatures on the Moon , 1959, Nature.
[13] M. Jordan,et al. Microtubules as a target for anticancer drugs , 2004, Nature Reviews Cancer.
[14] W. Goetzinger,et al. High-throughput techniques for compound characterization and purification. , 2001, Current opinion in drug discovery & development.
[15] T. Nomura,et al. TWO NEW PYRROLOQUINAZOLINOQUINOLINE ALKALOIDS FROM PEGANUM NIGELLASTRUM , 1997 .
[16] Libing Yu,et al. Three-component one-pot total syntheses of glyantrypine, fumiquinazoline F, and fiscalin B promoted by microwave irradiation. , 2005, The Journal of organic chemistry.
[17] E. Hamel,et al. Synthesis, cytotoxicity, and inhibitory effects on tubulin polymerization of a new 3-heterocyclo substituted 2-styrylquinazolinones. , 2004, European journal of medicinal chemistry.
[18] K. Wood,et al. Past and future of the mitotic spindle as an oncology target. , 2001, Current opinion in pharmacology.
[19] P. Schultz,et al. Identification of a novel protein regulating microtubule stability through a chemical approach. , 2004, Chemistry & biology.
[20] S. Koul,et al. Novel nor-harmal alkaloid from Adhatoda vasica , 1980 .
[21] Stefan Dimitrov,et al. Histone H3 phosphorylation and cell division , 2001, Oncogene.
[22] Christopher J. Wilson,et al. Novel one-pot total syntheses of deoxyvasicinone, mackinazolinone, isaindigotone, and their derivatives promoted by microwave irradiation. , 2005, Organic Letters.
[23] S. Hecht,et al. Luotonin A. A naturally occurring human DNA topoisomerase I poison. , 2003, Journal of the American Chemical Society.
[24] Douglas A. Horton,et al. The combinatorial synthesis of bicyclic privileged structures or privileged substructures. , 2003, Chemical reviews.
[25] Libing Yu,et al. Microwave-assisted one-pot synthesis of 2,3-disubstituted 3 H-quinazolin-4-ones , 2005 .
[26] D. Mehta,et al. A Bronchodilator Alkaloid (Vasicinone) from Adhatoda vasica Nees , 1959, Nature.
[27] B. E. Evans,et al. Methods for drug discovery: development of potent, selective, orally effective cholecystokinin antagonists. , 1988, Journal of Medicinal Chemistry.