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T 98
Known as:
T-98
National Institutes of Health
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2018
2018
Comparison of a ceramidase inhibitor (ceranib-2) with C2 ceramide and cisplatin on cytotoxicity and apoptosis of glioma cells.
G. Kus
,
Mete Özkurt
,
Pınar Öztopcu Vatan
,
N. Erkasap
,
R. Uyar
,
S. Kabadere
Turkish journal of biology = Turk biyoloji…
2018
Corpus ID: 73472957
Inhibiting ceramidase activity in cancer cells has been identified as a promising target for cancer therapy in recent studies…
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2014
2014
Modulation of uPA, MMPs and their inhibitors by a novel nutrient mixture in human glioblastoma cell lines.
M. W. Roomi
,
T. Kalinovsky
,
A. Niedzwiecki
,
M. Rath
International Journal of Oncology
2014
Corpus ID: 15868750
Brain tumors are highly aggressive tumors that are characterized by high levels of matrix metalloproteinase (MMP)-2 and -9…
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2011
2011
Three novel members of angucycline group from Streptomyces sp. N05WA963
Xiao Ren
,
Xinhua Lu
,
+8 authors
Hua Zhang
Journal of antibiotics (Tokyo. )
2011
Corpus ID: 23721218
Three novel members of angucycline family named N05WA963A (1), B (2) and D (4), together with a new anthracycline named N05WA963C…
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2005
2005
Effect of a cytotoxic analog of LH-RH (T-98) on the growth of estrogendependent MXT mouse mammary cancers: Correlations between growth characteristics and EGF receptor content of tumors
K. Szepesházi
,
A. Schally
,
G. Halmos
,
B. Szoke
,
K. Groot
,
A. Nagy
Breast Cancer Research and Treatment
2005
Corpus ID: 23080904
SummaryFemale BDF mice bearing estrogen-dependent MXT mouse mammary cancers were treated for 4 weeks with a cytotoxic analog of…
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2005
2005
Effect of treatment with LHRH analogs containing cytotoxic radicals on the binding characteristics of receptors for luteinizing-hormone-releasing hormone in MXT mouse mammary carcinoma
S. Milovanović
,
E. Monje
,
K. Szepesházi
,
S. Radulović
,
A. Schally
Journal of Cancer Research and Clinical Oncology
2005
Corpus ID: 20116175
Binding capacities and apparent dissociation constants of receptors for luteinizing-hormone-releasing hormone (LHRH) were…
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1994
1994
LH-RH analogue carrying a cytotoxic radical is internalized by rat pituitary cells in vitro
B. Szöke
,
J. Horváth
,
+4 authors
A. Schally
Peptides
1994
Corpus ID: 41001354
1993
1993
Inhibition of growth of experimental prostate cancer in rats by LH‐RH analogs linked to cytotoxic radicals
J. Pinski
,
A. Schally
,
+6 authors
A. Nagy
The Prostate
1993
Corpus ID: 40905662
The effects of hybrid cytotoxic LH‐RH analogs, produced by linking anthraquinone or methotrexate to carrier LH‐RH agonist [D‐Lys6…
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1992
1992
Effect of luteinizing hormone‐releasing hormone analogs containing cytotoxic radicals on growth of estrogen‐independent MXT mouse mammary carcinoma in vivo
K. Szepesházi
,
A. V. Schally
,
Attila Juhasz
,
A. Nagy
,
T. Janáky
Anti-Cancer Drugs
1992
Corpus ID: 262429528
Cytotoxic luteinizing hormone-releasing hormone (LH-RH) analogs, AJ-004 (agonist [D-Lys6]LH-RH linked to methotrexate (MTX)), T…
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1989
1989
Plant antimutagenic agents, 7. Structure and antimutagenic properties of cymobarbatol and 4-isocymobarbatol, new cymopols from green alga (Cymopolia barbata).
M. Wall
,
M. Wani
,
+6 authors
D. McPhail
Journal of Natural Products
1989
Corpus ID: 21096645
Two new compounds, cymobarbatol and 4-isocymobarbatol, were isolated from the marine alga Cymopolia barbata. The complete…
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1988
1988
Plant antimutagenic agents, 4. Isolation and structure elucidation of maesol, an inactive constituent of Maesa spp.
M. Wall
,
M. Wani
,
K. Gaetano
,
G. Manikumar
,
H. Taylor
,
R. McGivney
Journal of Natural Products
1988
Corpus ID: 20556169
Maesol, a novel dimeric phenol, was isolated from seeds of Maesa montana and Maesa indica. Maesol was shown to have the formula…
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