867064-26-4Relevant academic research and scientific papers
Synthesis and biological activities of a pH-dependently activated water-soluble prodrug of a novel hexacyclic camptothecin analog
Ohwada, Jun,Ozawa, Sawako,Kohchi, Masami,Fukuda, Hiroshi,Murasaki, Chikako,Suda, Hitomi,Murata, Takeshi,Niizuma, Satoshi,Tsukazaki, Masao,Ori, Kazutomo,Yoshinari, Kiyoshi,Itezono, Yoshiko,Endo, Mika,Ura, Masako,Tanimura, Hiromi,Miyazaki, Yoko,Kawashima, Akira,Nagao, Shunsuke,Namba, Eitarou,Ogawa, Koutarou,Kobayashi, Kazuko,Okabe, Hisafumi,Umeda, Isao,Shimma, Nobuo
scheme or table, p. 2772 - 2776 (2009/12/31)
CH0793076 (1) is a novel hexacyclic camptothecin analog showing potent antitumor activity in various human caner xenograft models. To improve the water solubility of 1, water-soluble prodrugs were designed to generate an active drug 1 nonenzymatically, th
AGENT FOR PREVENTING OR TREATING PANCREAS CANCER, OVARY CANCER OR LIVER CANCER CONTAINING NOVEL WATER-SOLUBLE PRODRUG
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, (2008/12/06)
Preventive or therapeutic agents for pancreatic cancer, ovarian cancer, or liver cancer of the present invention comprise a water-soluble prodrug represented by formula 1 described below, or a pharmaceutically acceptable salt, or a hydrate or solvate of t
NOVEL ANTICANCER CONCOMITANT DRUG
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Page/Page column 46-47, (2008/12/05)
A cancer therapeutic agent according to the present invention comprises a combination of compound A described below, or a pharmaceutically acceptable salt thereof, and compound B described below, or a pharmaceutically acceptable salt thereof: Compound A:
NOVEL WATER-SOLUBLE PRODRUG
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Page/Page column 48-49, (2010/11/25)
An objective of the present invention is to provide water-soluble prodrugs that can be administered parenterally, and which show excellent water solubility and small interspecies or individual differences and are rapidly converted to the active form by ch
