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laromustine
A sulfonyl hydrazine prodrug with antineoplastic activity. Laromustine releases the DNA chloroethylating agent 90CE after entering the blood stream…
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National Institutes of Health
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Related topics
Related topics
6 relations
Narrower (3)
Cloretazine
Onrigin
VNP 40101M
Broader (2)
Hydrazines
Sulfonamides
NCIt Antineoplastic Agent Terminology
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Carbamoylating Activity Associated with the Activation of the Antitumor Agent Laromustine Inhibits Angiogenesis by Inducing ASK1-Dependent Endothelial Cell Death
Weidong Ji
,
Mei Yang
,
+7 authors
W. Min
PLoS ONE
2014
Corpus ID: 474448
The anticancer agent 1,2-bis(methylsulfonyl)-1-(2-chloroethyl)-2-[(methylamino)carbonyl]hydrazine (laromustine), upon…
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2014
2014
Influence of Phosphate and Phosphoesters on the Decomposition Pathway of 1,2-Bis(methylsulfonyl)-1-(2-chloroethyhydrazine (90CE), the Active Anticancer Moiety Generated by Laromustine, KS119, and…
P. Penketh
,
K. Shyam
,
Rui-fang Zhu
,
R. Baumann
,
K. Ishiguro
,
A. Sartorelli
Chemical Research in Toxicology
2014
Corpus ID: 9427322
Prodrugs of the short-lived chloroethylating agent 1,2-bis(methylsulfonyl)-1-(2-chloroethyl)hydrazine (90CE) and its methylating…
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2012
2012
Thioredoxin reductase is inhibited by the carbamoylating activity of the anticancer sulfonylhydrazine drug laromustine
K. P. Rice
,
Edmund J. Klinkerch
,
S. Gerber
,
Tyler R. Schleicher
,
T. Kraus
,
Christopher Buros
Molecular and Cellular Biochemistry
2012
Corpus ID: 16527105
The thioredoxin system facilitates proliferative processes in cells and is upregulated in many cancers. The activities of both…
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2012
2012
Preclinical evaluation of Laromustine for use in combination with radiation therapy in the treatment of solid tumors
S. Rockwell
,
Yanfeng Liu
,
+7 authors
A. Sartorelli
International Journal of Radiation Biology
2012
Corpus ID: 19840400
Purpose: These studies explored questions related to the potential use of Laromustine in the treatment of solid tumors and in…
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2011
2011
Characterization of short-lived electrophilic metabolites of the anticancer agent laromustine (VNP40101M).
A-E. F. Nassar
,
I. King
,
J. Du
Chemical Research in Toxicology
2011
Corpus ID: 6988488
Laromustine (VNP40101M; 1,2-bis(methylsulfonyl)-1-(2-chloroethyl)-2-(methylamino) carbonylhydrazine) is a novel sulfonylhydrazine…
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2010
2010
In Vitro Profiling and Mass Balance of the Anti-Cancer Agent Laromustine [14C]-VNP40101M by Rat, Dog, Monkey and Human Liver Microsomes
A-E. F. Nassar
,
J. Du
,
M. Belcourt
,
X. Lin
,
I. King
2010
Corpus ID: 18014225
Laromustine (VNP40101M; 1,2-bis(methylsulfonyl)-1-(2-chloroethyl)-2-(methylamino) carbonylhydrazine) is a novel sulfonylhydrazine…
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Highly Cited
2009
Highly Cited
2009
Phase 3 randomized, placebo-controlled, double-blind study of high-dose continuous infusion cytarabine alone or with laromustine (VNP40101M) in patients with acute myeloid leukemia in first relapse.
F. Giles
,
N. Vey
,
+14 authors
S. O'brien
Blood
2009
Corpus ID: 24664789
Laromustine is a sulfonylhdrazine alkylator with significant antileukemia activity. An international, randomized (2:1), double…
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2009
2009
An in Vitro Evaluation of the Victim and Perpetrator Potential of the Anticancer Agent Laromustine (VNP40101M), Based on Reaction Phenotyping and Inhibition and Induction of Cytochrome P450 Enzymes
A. Nassar
,
I. King
,
+8 authors
A. Parkinson
Drug Metabolism And Disposition
2009
Corpus ID: 10582337
Laromustine (VNP40101M, also known as Cloretazine) is a novel sulfonylhydrazine alkylating (anticancer) agent. Laromustine…
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2009
2009
Effect of cloretazine (VNP40101M) on acute myeloid leukaemia blast cells in vitro as a single agent and combined with cytarabine and daunorubicin.
K. Morris
,
Julie Adams
,
J. L. Liu Yin
Leukemia research : a Forum for Studies on…
2009
Corpus ID: 9871062
Review
2009
Review
2009
Laromustine, a sulfonyl hydrolyzing alkylating prodrug for cancer therapy.
A. Pigneux
IDrugs : the investigational drugs journal
2009
Corpus ID: 22839407
Laromustine (Onrigin), under development by Vion Pharmaceuticals Inc, belongs to the sulfonylhydrazine class of alkylating agents…
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