Year |
Citation |
Score |
2002 |
Liu X, Lynn BC, Zhang J, Song L, Bom D, Du W, Curran DP, Burke TG. A versatile prodrug approach for liposomal core-loading of water-insoluble camptothecin anticancer drugs. Journal of the American Chemical Society. 124: 7650-1. PMID 12083906 DOI: 10.1021/Ja0256212 |
0.523 |
|
2000 |
Du W, Gabarda AE, Bom D, Curran DP. The combinatorial synthesis of racemic homosilatecan libraries via a cascade radical annulation. Annals of the New York Academy of Sciences. 922: 317-9. PMID 11193911 DOI: 10.1111/J.1749-6632.2000.Tb07053.X |
0.554 |
|
2000 |
Curran DP, Josien H, Bom D, Gabarda AE, Du W. The cascade radical annulation approach to new analogues of camptothecins. Combinatorial synthesis of silatecans and homosilatecans. Annals of the New York Academy of Sciences. 922: 112-21. PMID 11193887 DOI: 10.1111/J.1749-6632.2000.Tb07030.X |
0.592 |
|
2000 |
Bom D, Curran DP, Kruszewski S, Zimmer SG, Thompson Strode J, Kohlhagen G, Du W, Chavan AJ, Fraley KA, Bingcang AL, Latus LJ, Pommier Y, Burke TG. The novel silatecan 7-tert-butyldimethylsilyl-10-hydroxycamptothecin displays high lipophilicity, improved human blood stability, and potent anticancer activity. Journal of Medicinal Chemistry. 43: 3970-80. PMID 11052802 DOI: 10.1021/Jm000144O |
0.555 |
|
1999 |
Bom D, Curran DP, Chavan AJ, Kruszewski S, Zimmer SG, Fraley KA, Burke TG. Novel A,B,E-ring-modified camptothecins displaying high lipophilicity and markedly improved human blood stabilities. Journal of Medicinal Chemistry. 42: 3018-22. PMID 10447944 DOI: 10.1021/Jm9902279 |
0.477 |
|
1998 |
Josien H, Ko S, Bom D, Curran DP. A General Synthetic Approach to the (20S)-Camptothecin Family of Antitumor Agents by a Regiocontrolled Cascade Radical Cyclization of Aryl Isonitriles Chemistry - a European Journal. 4: 67-83. DOI: 10.1002/(Sici)1521-3765(199801)4:1<67::Aid-Chem67>3.0.Co;2-F |
0.519 |
|
1997 |
Josien H, Bom D, Curran DP, Zheng Y, Chou T. 7-Silylcamptothecins (silatecans): A new family of camptothecin antitumor agents Bioorganic & Medicinal Chemistry Letters. 7: 3189-3194. DOI: 10.1016/S0960-894X(97)10181-0 |
0.494 |
|
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