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IST 622
Known as:
IST-622
National Institutes of Health
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2004
2004
Antitumor effects of IST-622, a novel synthetic derivative of chartreusin, against murine and human tumor lines following oral administration
T. Tashiro
,
K. Kon
,
Masashi Yamamoto
,
N. Yamada
,
T. Tsuruo
,
S. Tsukagoshi
Cancer Chemotherapy and Pharmacology
2004
Corpus ID: 24422963
The antitumor effects of 6-O-(3-ethoxypropionyl)-3′,4′-O-exo-benzylidenechartreusin (IST-622), a new synthetic derivative of…
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2003
2003
Pharmacokinetic and pharmacodynamic study of IST-622, a novel synthetic derivative of chartreusin, by oral administration in a phase 2 study of patients with breast cancer
浅井 暁
2003
Corpus ID: 56581614
Review
1993
Review
1993
[Topoisomerase inhibitors developing in Japan].
H. Furue
Gan to kagaku ryoho. Cancer & chemotherapy
1993
Corpus ID: 24454242
Irinotecan hydrochloride (CPT-11), topotecan, sobuzoxane, NC-190, and IST-622 are unique topoisomerase inhibitors and are…
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Review
1993
Review
1993
[DNA topoisomerase inhibitor].
M. Hino
,
H. Niitani
Nihon rinsho. Japanese journal of clinical…
1993
Corpus ID: 32718421
DNA topoisomerases are enzymes involved in various aspects of genetic processes by catalyzing a topological change of DNA…
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Review
1992
Review
1992
[DNA topoisomerase inhibitor].
T. Sugiura
,
Y. Ariyoshi
Gan to kagaku ryoho. Cancer & chemotherapy
1992
Corpus ID: 43663335
CPT-11 and Topotecan are a new semisynthetic derivative of CPT, and have been shown to inhibit DNA topoisomerase I and to have a…
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