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temozolomide/VNP40101M
Known as:
TMZ/VNP-40101M
National Institutes of Health
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2 relations
VNP 40101M
temozolomide
Papers overview
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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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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
2007
2007
Activity of VNP40101M (Cloretazine) in the treatment of CNS tumor xenografts in athymic mice.
M. Badruddoja
,
S. Keir
,
+5 authors
H. Friedman
Neuro-Oncology
2007
Corpus ID: 207138864
VNP40101M, or 1,2-bis(methylsulfonyl)-1-(2-choloroethyl)-2-(methylamino)carbonylhydrazine (Cloretazine), is a bifunctional…
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2007
2007
Determination of Cloretazine (VNP40101M) and its active metabolite (VNP4090CE) in human plasma by liquid chromatography electrospray tandem mass spectrometry (LC-ESI-MS/MS).
Feng Bai
,
Patton Minkin
,
Charles H. Fraga
,
M. O'Shaughnessy
,
S. Gururangan
,
C. Stewart
Journal of chromatography. B, Analytical…
2007
Corpus ID: 25115049
2005
2005
A phase I and pharmacokinetic study of VNP40101M, a new alkylating agent, in patients with advanced or metastatic cancer
J. Murren
,
M. Modiano
,
+4 authors
M. Sznol
Investigational new drugs
2005
Corpus ID: 12204754
SummaryPurpose: VNP40101M is a new alkylating agent that demonstrated broad anti-tumor activity in murine tumor models. A phase I…
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2005
2005
Role of O6-alkylguanine-DNA alkyltransferase in the cytotoxic activity of cloretazine
K. Ishiguro
,
K. Shyam
,
P. Penketh
,
A. Sartorelli
Molecular Cancer Therapeutics
2005
Corpus ID: 7285849
Cloretazine (VNP40101M; 101M; 1,2-bis(methylsulfonyl)-1-(2-chloroethyl)-2-[(methylamino)carbonyl]hydrazine) is a…
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2004
2004
1,2-Bis(methylsulfonyl)-1-(2-chloroethyl)-2-[(methylamino)carbonyl]hydrazine (VNP40101M): I. Direct inhibition of O6-alkylguanine-DNA alkyltransferase (AGT) by electrophilic species generated by…
P. Penketh
,
K. Shyam
,
R. Baumann
,
J. Remack
,
Thomas P. Brent
,
Alan C. Sartorelli
Cancer Chemotherapy and Pharmacology
2004
Corpus ID: 25368729
PurposeTo investigate the interaction of the electrophilic species generated by the decomposition of the antineoplastic prodrug 1…
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Highly Cited
2004
Highly Cited
2004
A Phase I and Pharmacokinetic Study of VNP40101M, a Novel Sulfonylhydrazine Alkylating Agent, in Patients with Refractory Leukemia
F. Giles
,
D. Thomas
,
+12 authors
H. Kantarjian
Clinical Cancer Research
2004
Corpus ID: 11925229
Purpose: VNP40101M is a novel sulfonylhydrazine alkylating agent with broad antitumor activity in animal models. As alkylating…
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2002
2002
Toxicological Evaluation of 1,2-Bis(methylsulfonyl)-1-(2-chloroethyl)-2-(methylaminocarbonyl)hydrazine (VNP40101M), a Novel Alkylating Agent with Potential Antitumor Activity, with Intravenous…
K. Lee
,
B. Almassian
,
J. Noveroske
International journal of toxicology
2002
Corpus ID: 41673226
These studies investigated the toxicological effects of 1,2-bis (methylsulfonyl)-1-(2-chloroethyl)-2-(methylaminocarbonyl…
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2001
2001
Pharmaceutical development and manufacturing of a parenteral formulation of a novel antitumor agent, VNP40101M
G. Krishna
,
W. F. Hodnick
,
+4 authors
B. Almassian
AAPS PharmSciTech
2001
Corpus ID: 24878359
The objective of this study was to develop and manufacture a stable parenteral formulation for Phase I clinical trials of…
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