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J 107088
Known as:
J-107088
, J107088
National Institutes of Health
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Related topics
Related topics
2 relations
PHA-782615
Broader (1)
edotecarin
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2010
2010
A phase I dose-escalation study of edotecarin (J-107088) combined with infusional 5-fluorouracil and leucovorin in patients with advanced/metastatic solid tumors
M. Saif
,
S. Sellers
,
R. Diasio
,
J. Douillard
Anti-Cancer Drugs
2010
Corpus ID: 9907680
Edotecarin (J-107088), a novel inhibitor of topoisomerase I has an additive effect on colon cell lines (HCT-116) when combined…
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2007
2007
Antitumor activity of edotecarin in breast carcinoma models
M. Ciomei
,
V. Croci
,
F. Stellari
,
N. Amboldi
,
Rosa Giavarini
,
E. Pesenti
Cancer Chemotherapy and Pharmacology
2007
Corpus ID: 21601279
PurposeEdotecarin (J-107088, formerly ED-749) is a potent indolocarbazole topoisomerase-I inhibitor that has the potential to…
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2006
2006
A phase I study of the safety and pharmacokinetics of edotecarin (J-107088), a novel topoisomerase I inhibitor, in patients with advanced solid tumors
Herbert I. Hurwitz
,
Roger B. Cohen
,
+4 authors
T. Yoshinari
Cancer Chemotherapy and Pharmacology
2006
Corpus ID: 19956430
PurposeTo assess the maximum tolerated dose, safety, and pharmacokinetic (PK) profile of escalating doses of the novel…
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2006
2006
Antitumor Efficacy of Edotecarin as a Single Agent and in Combination with Chemotherapy Agents in a Xenograft Model
M. Ciomei
,
V. Croci
,
A. Ciavolella
,
D. Ballinari
,
E. Pesenti
Clinical Cancer Research
2006
Corpus ID: 16629024
The novel indolocarbazole edotecarin (J-107088, formerly ED-749) differs from other topoisomerase I inhibitors both…
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2005
2005
Pharmacokinetics (PK) of edotecarin (J-107088), a topoisomerase I inhibitor, in patients with metastatic breast cancer (mBC) or glioblastoma multiforme (GBM)
D. Yin
,
S. Toler
,
F. Guo
,
B. Duncan
,
A. Sharma
2005
Corpus ID: 74756428
2073 Background: Edotecarin is an indolocarbazole topoisomerase I inhibitor currently under clinical development for cancer…
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2003
2003
Plasma stability of two glycosyl indolocarbazole antitumor agents.
J. Goossens
,
J. Kluza
,
+5 authors
C. Bailly
Biochemical Pharmacology
2003
Corpus ID: 20429595
2001
2001
Therapeutic activity of the topoisomerase I inhibitor J-107088 [6-N-(1-hydroxymethyla-2-hydroxy) ethylamino-12,13-dihydro-13-(β-D-gluco pyranosyl)-5H-indolo[2,3-a]-pyrrolo[3,4-c]-carbazole-5,7(6H…
Christina M. Cavazos
,
S. Keir
,
T. Yoshinari
,
D. Bigner
,
H. Friedman
Cancer Chemotherapy and Pharmacology
2001
Corpus ID: 25959257
Abstract. Purpose: The in vivo antitumor activity of a novel topoisomerase I inhibitor, J-107088, was tested in athymic nude mice…
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Review
2000
Review
2000
Preclinical and Clinical Trials of Topoisomerase Inhibitors
N. Saijo
Annals of the New York Academy of Sciences
2000
Corpus ID: 5638704
Abstract: CPT‐11, developed by Yakult Honsha, has achieved the position of standard chemotherapy for colorectal cancer in the…
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Highly Cited
1999
Highly Cited
1999
Mode of action of a new indolocarbazole anticancer agent, J-107088, targeting topoisomerase I.
T. Yoshinari
,
Mitsuru Ohkubo
,
+7 authors
Susumu Nishimura
Cancer Research
1999
Corpus ID: 16735675
J-107088 [6-N-(1-hydroxymethyl-2-hydroxy)ethylamino-12,13-dihydro-2,10-dihydroxy- 13-(beta-D-glucopyranosyl)-5H-indolo[2,3-a…
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1999
1999
In vivo Anti‐tumor Activity of a Novel Indolocarbazole Compound, J‐107088, on Murine and Human Tumors Transplanted into Mice
H. Arakawa
,
M. Morita
,
+4 authors
S. Nishimura
Japanese journal of cancer research : Gann
1999
Corpus ID: 13721989
J‐107088 (6‐N‐(1‐hydroxymethyl‐2‐hydroxy)ethylamino‐12,13‐dihydro‐2,10‐dihydroxy‐13‐(β‐D‐glu‐copyranosyl)‐5H‐indolo[2,3‐a…
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