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ZD 9331
Known as:
BGC 9331
, ZD9331
, ZD-9331
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National Institutes of Health
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Alert
Related topics
Related topics
4 relations
Broader (2)
Antineoplastic Agents
Quinazolines
Plevitrexed
topotecan/ZD9331
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2004
Review
2004
Antifolates targeted specifically to the folate receptor.
A. Jackman
,
D. Theti
,
David D Gibbs
Advanced Drug Delivery Reviews
2004
Corpus ID: 29620264
Highly Cited
2004
Highly Cited
2004
Characterization of a Folate Transporter in HeLa Cells with a Low pH Optimum and High Affinity for Pemetrexed Distinct from the Reduced Folate Carrier
Yanhua Wang
,
R. Zhao
,
I. Goldman
Clinical Cancer Research
2004
Corpus ID: 23789942
Studies were undertaken to characterize a low pH transport activity in a reduced folate carrier (RFC)-null HeLa-derived cell line…
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Review
2003
Review
2003
Novel antifolate drugs
W. Purcell
,
D. Ettinger
Current Oncology Reports
2003
Corpus ID: 26063243
Antimetabolites are active chemotherapeutic agents for many solid tumor and hematologic malignancies. Folate antagonists, purine…
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Review
2003
Review
2003
Thymidylate synthase inhibitors as anticancer agents: from bench to bedside
E. Chu
,
M. Callender
,
Michael P. Farrell
,
J. C. Schmitz
Cancer Chemotherapy and Pharmacology
2003
Corpus ID: 1362857
Thymidylate synthase (TS) is a folate-dependent enzyme that catalyzes the reductive methylation of 2′-deoxyuridine-5…
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Highly Cited
2002
Highly Cited
2002
The role of thymidylate synthase induction in modulating p53-regulated gene expression in response to 5-fluorouracil and antifolates.
D. Longley
,
J. Boyer
,
+7 authors
P. Johnston
Cancer Research
2002
Corpus ID: 18392671
Thymidylate synthase (TS) is a critical target for chemotherapeutic agents such as 5-fluorouracil (5-FU) and antifolates such as…
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Highly Cited
2002
Highly Cited
2002
Resistance to multiple novel antifolates is mediated via defective drug transport resulting from clustered mutations in the reduced folate carrier gene in human leukaemia cell lines.
L. Rothem
,
I. Ifergan
,
Yotam Kaufman
,
D. Priest
,
G. Jansen
,
Y. Assaraf
Biochemical Journal
2002
Corpus ID: 8268103
We have studied the molecular basis of resistance of multiple human leukaemia CCRF-CEM sublines to the novel antifolates ZD9331…
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Highly Cited
2001
Highly Cited
2001
Marked suppression of the activity of some, but not all, antifolate compounds by augmentation of folate cofactor pools within tumor cells.
R. Zhao
,
F. Gao
,
I. Goldman
Biochemical Pharmacology
2001
Corpus ID: 22993533
Highly Cited
2001
Highly Cited
2001
Characterization of a thymidylate synthase (TS)-inducible cell line: a model system for studying sensitivity to TS- and non-TS-targeted chemotherapies.
D. Longley
,
P. Ferguson
,
+5 authors
P. Johnston
Clinical Cancer Research
2001
Corpus ID: 385348
Thymidylate synthase (TS) is responsible for the de novo synthesis of thymidylate, which is required for DNA synthesis and repair…
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Highly Cited
1997
Highly Cited
1997
Cellular pharmacology and in vivo activity of a new anticancer agent, ZD9331: a water-soluble, nonpolyglutamatable, quinazoline-based inhibitor of thymidylate synthase.
A. Jackman
,
R. Kimbell
,
+6 authors
F. T. Boyle
Clinical Cancer Research
1997
Corpus ID: 1141201
ZD9331 is a drug that was developed from a potent class of water-soluble, C7-methyl-substituted, quinazoline-based inhibitors of…
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Review
1996
Review
1996
Thymidylate synthase inhibitors.
N. Touroutoglou
,
R. Pazdur
Clinical Cancer Research
1996
Corpus ID: 17372280
Folate analogues that inhibit thymidylate synthase (TS) selectively were developed based on TS and folate molecular structures…
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