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MB07133
Known as:
Cytarabine Monophosphate Prodrug MB07133
, MB-07133
, MB 07133
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A prodrug of the monophosphate (MP) form of the antimetabolite cytarabine (araCMP), an analogue of cytidine with a modified sugar moiety (arabinose…
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National Institutes of Health
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Efficacy of the hypoxia-activated prodrug evofosfamide (TH-302) in nasopharyngeal carcinoma in vitro and in vivo
Yan Huang
,
Ying Tian
,
+5 authors
Li Zhang
Cancer Communications
2018
Corpus ID: 19205101
BackgroundTumor hypoxia is considered an important factor in metastasis and disease relapse. Evofosfamide is a hypoxia-activated…
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2017
2017
Antineoplastic effects of CPPTL via the ROS/JNK pathway in acute myeloid leukemia
Huier Gao
,
Yue Sun
,
+8 authors
Yingdai Gao
OncoTarget
2017
Corpus ID: 33876227
Drug resistance and human leukocyte antigen (HLA) matching limit conventional treatment of acute myeloid leukemia (AML). Although…
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2016
2016
Dual-drug loaded nanoformulation with a galactosamine homing moiety for liver-targeted anticancer therapy.
Nafees Muhammad
,
Xiaoyong Wang
,
+4 authors
Zijian Guo
Dalton Transactions
2016
Corpus ID: 27763025
Drug resistance and unfavorable pharmacokinetics are the major obstacles for conventional anticancer drugs. A combination of…
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2007
2007
Novel Cyclic Phosphate Prodrug Approach for Cytochrome P450-activated Drugs Containing an Alcohol Functionality
K. Huttunen
,
Niina Mähönen
,
+6 authors
J. Rautio
Pharmaceutical Research
2007
Corpus ID: 24979701
PurposeA cyclic phosphate prodrug of a descriptive molecule containing an alcohol functionality was designed, synthesized and…
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2006
2006
A phase I/II study to assess the safety, tolerability and pharmacokinetics (PK) of intravenous (IV) infusion of MB07133 in subjects with unresectable hepatocellular carcinoma (HCC).
B. Ma
,
W. Forbes
,
+4 authors
D. Bullough
Journal of Clinical Oncology
2006
Corpus ID: 43796673
2054 Background: MB07133 is a novel cytarabine (araC) prodrug that uses the HepDirect technology to target production of the…
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2002
2002
Inhibition of endothelin-converting enzyme for protection against neointimal proliferation following balloon angioplasty of the rat carotid artery.
D. Pham
,
A. Jeng
,
S. Plante
,
E. Escher
,
B. Battistini
Canadian Journal of Physiology and Pharmacology
2002
Corpus ID: 13636870
Clinical success of percutaneous transluminal coronary angioplasty is limited by restenosis within months of the initial…
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Highly Cited
2000
Highly Cited
2000
Hypoxia-dependent retinal toxicity of bioreductive anticancer prodrugs in mice.
Alan E. Lee
,
W. Wilson
Toxicology and Applied Pharmacology
2000
Corpus ID: 25295634
The bioreductive anticancer prodrug CI-1010 ((2R)-1-[(2-bromoethyl)amino]-3-(2-nitro-1H-imidazol-1-yl)-2-propanol hydrobromide…
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1998
1998
Comparative pharmacology of the novel cyclopropylpyrroloindole-prodrug carzelesin in mice, rats, and humans.
O. van Tellingen
,
W. Nooijen
,
+4 authors
J. Beijnen
Cancer Research
1998
Corpus ID: 15705682
Carzelesin is a novel cyclopropylpyrroloindole prodrug analogue that has recently been tested in Phase I clinical trials. To…
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1992
1992
A comparative study of the antitumor activities off 5‐deoxy‐5‐fluorouridine and its prodrug trimethoxy benzoyl‐5‐deoxy‐5‐fluorocytidine (Ro09–1390) on human digestive organ cancer xenograft lines…
Y. Nio
,
Hiroko Kimura
,
+7 authors
M. Fukumoto
Anti-Cancer Drugs
1992
Corpus ID: 22771643
5'-Deoxy-5-fluorouridine (5'-DFUR) is one of the oral fluoropyrimidines widely used in the treatment of gastric, colorectal and…
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1991
1991
In vitro and in vivo activities of monoclonal antibody-alkaline phosphatase conjugates in combination with phenol mustard phosphate.
P. Wallace
,
P. Senter
Bioconjugate chemistry
1991
Corpus ID: 32603033
The prodrug p-[N,N-bis(2-chloroethyl)amino]phenyl phosphate (phenol mustard phosphate, POMP) was prepared from p-[N,N-bis(2…
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