H. X. Chen

发表

Terfenadine (Seldane): a new drug for restoring sensitivity to multidrug resistant cancer cells.

M. Reiss, W. Hait, J. Yang, 1993, Biochemical pharmacology.

Rapid stimulation of rhodamine 123 efflux from multidrug-resistant KB cells by progesterone.

R. Hochberg, R. Carbone, H. X. Chen, 1993, Biochemical pharmacology.

Antitumor agents. 144. New gamma-lactone ring-modified arylamino etoposide analogs as inhibitors of human DNA topoisomerase II.

K. J. Lee, Y. Cheng, K. Lee, 1994, Journal of medicinal chemistry.

Antitumor agents. 120. New 4-substituted benzylamine and benzyl ether derivatives of 4'-O-demethylepipodophyllotoxin as potent inhibitors of human DNA topoisomerase II.

Y. Cheng, K. Lee, J. Chang, 1991, Journal of medicinal chemistry.

Unique biochemical, cytotoxic, and antitumor activity of camptothecin and 4beta-amino-4'-O-demethylepipodophyllotoxin conjugates.

Y. Cheng, K. Lee, J. Chang, 2000, Biochemical pharmacology.

Activities of novel nonglycosidic epipodophyllotoxins in etoposide-sensitive and -resistant variants of human KB cells, P-388 cells, and in vivo multidrug-resistant murine leukemia cells.

Y. Cheng, K. Lee, H. X. Chen, 1996, Molecular pharmacology.

BIBW 22, a dipyridamole analogue, acts as a bifunctional modulator on tumor cells by influencing both P-glycoprotein and nucleoside transport.

Y. Cheng, A. Heckel, H. X. Chen, 1993, Cancer research.

Degradation of topoisomerase I induced by topoisomerase I inhibitors is dependent on inhibitor structure but independent of cell death.

Y. Cheng, H. X. Chen, S. Grill, 1999, Molecular pharmacology.

5-Fluoro-2-pyrimidinone, a liver aldehyde oxidase-activated prodrug of 5-fluorouracil.

Y. Cheng, T. Lin, H. X. Chen, 1995, Biochemical pharmacology.