H. Suda

A water soluble prodrug of a novel camptothecin analog is efficacious against breast cancer resistance protein-expressing tumor xenografts

H. Yamada-Okabe, S. Niizuma, N. Shimma, 2009, Cancer Chemotherapy and Pharmacology.

Synthesis and structure-activity relationships of novel fungal chitin synthase inhibitors.

Y. Isshiki, N. Shimma, M. Sudoh, 2000, Bioorganic & medicinal chemistry letters.

Design and synthesis of the tumor-activated prodrug of dihydropyrimidine dehydrogenase (DPD) inhibitor, RO0094889 for combination therapy with capecitabine.

H. Ishitsuka, I. Horii, N. Shimma, 2003, Bioorganic & medicinal chemistry letters.

Synthesis and biological activities of topoisomerase I inhibitors, 6-N-amino analogues of NB-506.

S. Nishimura, T. Yoshinari, M. Ohkubo, 1999, Bioorganic & medicinal chemistry letters.

Synthesis and biological activities of a pH-dependently activated water-soluble prodrug of a novel hexacyclic camptothecin analog.

S. Niizuma, Kazuko Kobayashi, N. Shimma, 2009, Bioorganic & medicinal chemistry letters.

Synthesis of new camptothecin analogs with improved antitumor activities.

S. Niizuma, Kazuko Kobayashi, K. Morikami, 2009, Bioorganic & medicinal chemistry letters.