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fotemustine
Known as:
1-[N-(2-chloroethyl)-N-nitrosoureido]ethylphosphonic acid diethyl ester
, diethyl[1-[3-(2-chloroethyl)-3-nitrosoureido]ethyl]phosphonate
, diethyl-1-(3-(2-chloroethyl)-3-nitrosoureido)ethylphosphonate
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A chloroethylating nitrosourea with antineoplastic activity. Fotemustine alkylates guanine by forming chloroethyl adducts at the 6 position of…
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National Institutes of Health
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Related topics
Related topics
6 relations
Broader (3)
Antineoplastic Agents
Nitrosourea Compounds
Organophosphorus Compounds
Narrower (2)
Muphoran
S 10036
NCIt Antineoplastic Agent Terminology
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2016
Review
2016
Treatment patterns of advanced malignant melanoma (stage III-IV) - A review of current standards in Europe.
M. Harries
,
J. Malvehy
,
+4 authors
D. Schadendorf
European Journal of Cancer
2016
Corpus ID: 26278691
Review
2013
Review
2013
Advances in therapy for melanoma brain metastases.
Jaclyn C Flanigan
,
Lucia B. Jilaveanu
,
V. Chiang
,
H. Kluger
Clinical Dermatology
2013
Corpus ID: 1253322
2004
2004
Positive phase II study in the treatment of advanced malignant melanoma with fotemustine
K. Schallreuter
,
E. Wenzel
,
F. Brassow
,
J. Berger
,
E. Breitbart
,
W. Teichmann
Cancer Chemotherapy and Pharmacology
2004
Corpus ID: 7689982
SummaryTo date, dacarbazine (DTIC) has been the most effective drug in the treatment of advanced metastatic melanoma, achieving…
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1999
1999
Sequential administration of temozolomide and fotemustine: depletion of O6-alkyl guanine-DNA transferase in blood lymphocytes and in tumours.
M. Gander
,
S. Leyvraz
,
+11 authors
M. D’Incalci
Annals of Oncology
1999
Corpus ID: 16931591
BACKGROUND The DNA repair protein O6-alkylguanine-DNA alkyl transferase (AT) mediates resistance to chloroethylnitrosoureas…
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Highly Cited
1999
Highly Cited
1999
Expression of DNA repair proteins hMSH2, hMSH6, hMLH1, O6‐methylguanine‐DNA methyltransferase and N‐methylpurine‐DNA glycosylase in melanoma cells with acquired drug resistance
H. Lage
,
M. Christmann
,
+4 authors
D. Schadendorf
International Journal of Cancer
1999
Corpus ID: 25374275
Malignant melanoma is well known for its primary unresponsiveness to chemotherapy. The mechanisms conferring this intrinsic…
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1998
1998
Modulation of O6-alkylating agent induced clastogenicity by enhanced DNA repair capacity of bone marrow cells.
N. Chinnasamy
,
L. Fairbairn
,
J. Laher
,
M. Willington
,
J. Rafferty
Mutation research
1998
Corpus ID: 21448687
Highly Cited
1997
Highly Cited
1997
Human melanoma cell lines selected in vitro displaying various levels of drug resistance against cisplatin, fotemustine, vindesine or etoposide: modulation of proto-oncogene expression.
M. A. Kern
,
H. Helmbach
,
M. Artuc
,
D. Karmann
,
K. Jurgovsky
,
D. Schadendorf
Anticancer Research
1997
Corpus ID: 11973328
Melanoma cells often display a multidrug-resistant phenotype, but the mechanisms involved are largely unknown. In order to…
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Highly Cited
1995
Highly Cited
1995
Palliative therapy of melanoma patients with fotemustine. Inverse relationship between tumour load and treatment effectiveness. A multicentre phase II trial of the EORTC‐Melanoma Cooperative Group…
U. Kleeberg
,
E. Engel
,
+7 authors
M. Lentz
Melanoma research
1995
Corpus ID: 29860730
Fotemustine (FM) is a new chloronitrosurea (CNU), chemically characterized by the graft of an aminophosphonic acid on the CNU…
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Review
1994
Review
1994
Fotemustine in the treatment of brain primary tumors and metastases.
D. Khayat
,
B. Giroux
,
+5 authors
J. Bizzari
Cancer Investigation
1994
Corpus ID: 24015612
Fotemustine is a new chloroethylnitrosourea characterized by the grafting of a phosphonoalanine group onto a nitrosourea radical…
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1991
1991
Liver targeting of autologous erythrocytes loaded with doxorubicin.
M. Tonetti
,
C. Polvani
,
+8 authors
A. De Flora
European Journal of Cancer
1991
Corpus ID: 7698343
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