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UCN 01
Known as:
(+)-UCN-01
, UCN-01
National Institutes of Health
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Related topics
Related topics
1 relation
Broader (1)
7-hydroxystaurosporine
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2007
2007
ATR signaling mediates an S-phase checkpoint after inhibition of poly(ADP-ribose) polymerase activity.
J. Horton
,
Donna F. Stefanick
,
P. Kedar
,
Samuel H. Wilson
DNA Repair
2007
Corpus ID: 25407410
Highly Cited
2006
Highly Cited
2006
Phase I trial of UCN-01 in combination with topotecan in patients with advanced solid cancers: a Princess Margaret Hospital Phase II Consortium study.
S. Hotte
,
A. Oza
,
+6 authors
H. Hirte
Annals of Oncology
2006
Corpus ID: 38454136
BACKGROUND 7-Hydroxystaurosporine (UCN-01) inhibits serine-threonine kinases including the Ca2+ and phospholipid-dependent…
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Highly Cited
2005
Highly Cited
2005
A phase I and pharmacokinetic study of short infusions of UCN-01 in patients with refractory solid tumors.
E. Dees
,
S. Baker
,
+7 authors
R. Donehower
Clinical Cancer Research
2005
Corpus ID: 2594570
Purpose: To define the maximum tolerated dose and the dose-limiting toxicity of the kinase modulator UCN-01 administered as a…
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Highly Cited
2005
Highly Cited
2005
Phase I trial of the cyclin-dependent kinase inhibitor and protein kinase C inhibitor 7-hydroxystaurosporine in combination with Fluorouracil in patients with advanced solid tumors.
J. Kortmansky
,
M. Shah
,
+12 authors
G. Schwartz
Journal of Clinical Oncology
2005
Corpus ID: 27546440
PURPOSE Preclinical studies indicate that the cyclin-dependent kinase and protein kinase C inhibitor 7-hydroxystaurosporine (UCN…
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2005
2005
Involvement of poly(ADP-ribose) polymerase activity in regulating Chk1-dependent apoptotic cell death.
J. Horton
,
Donna F. Stefanick
,
Samuel H. Wilson
DNA Repair
2005
Corpus ID: 37907642
2005
2005
The Farnesyltransferase Inhibitor L744832 Potentiates UCN-01–Induced Apoptosis in Human Multiple Myeloma Cells
X. Pei
,
Yun Dai
,
M. Rahmani
,
Weiqun Li
,
P. Dent
,
S. Grant
Clinical Cancer Research
2005
Corpus ID: 44503989
Purpose: The purpose of this study was to characterize interactions between the farnesyltransferase inhibitor L744832 and the…
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Highly Cited
2004
Highly Cited
2004
7-Hydroxystaurosporine (UCN-01) Inhibition of Akt Thr308 but not Ser473 Phosphorylation
S. Kondapaka
,
M. Zarnowski
,
Dena R. Yver
,
E. Sausville
,
S. Cushman
Clinical Cancer Research
2004
Corpus ID: 10852059
7-Hydroxystaurosporine (UCN-01) infused for 72 hours by continuous i.v. infusion induced insulin resistance during phase I…
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Highly Cited
2002
Highly Cited
2002
Abrogation of the S Phase DNA Damage Checkpoint Results in S Phase Progression or Premature Mitosis Depending on the Concentration of 7-Hydroxystaurosporine and the Kinetics of Cdc25C Activation*
Ethan A. Kohn
,
Nicola D Ruth
,
Mary Kay Brown
,
M. Livingstone
,
A. Eastman
Journal of Biological Chemistry
2002
Corpus ID: 43612817
DNA damage causes cell cycle arrest in G1, S, or G2 to prevent replication on damaged DNA or to prevent aberrant mitosis. The G1…
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2000
2000
Physiological Modeling of Altered Pharmacokinetics of a Novel Anticancer Drug, UCN-01 (7-Hydroxystaurosporine), Caused by Slow Dissociation of UCN-01 from Human α1-Acid Glycoprotein
E. Fuse
,
Akitoshi Hashimoto
,
+4 authors
Y. Sugiyama
Pharmaceutical Research
2000
Corpus ID: 22402592
AbstractPurpose. The extremely low clearance and small distribution volumeof UCN-01 in humans could be partly due to the high…
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1999
1999
Pharmacokinetics and pharmacodynamics of a novel protein kinase inhibitor, UCN-01
N. Kurata
,
T. Kuwabara
,
+6 authors
Satoshi Kobayashi
Cancer Chemotherapy and Pharmacology
1999
Corpus ID: 12691220
Purpose: 7-Hydroxystaurosporine (UCN-01) is a potent protein kinase inhibitor and is being developed as a novel anticancer agent…
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