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SM 108
Known as:
SM-108
National Institutes of Health
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Related topics
Related topics
1 relation
Broader (1)
4-carbamoylimidazolium 5-olate
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
1991
1991
Induction of erythroid differentiation of K562 cells by 4-carbamoylimidazolium 5-olate (SM-108).
Y. Hata
,
Y. Yamaji
,
+5 authors
S. Irino
Biochemical Pharmacology
1991
Corpus ID: 28467119
1989
1989
[Phase II study of SM-108 (4-carbamoylimidazolium-5-olate) in hematological malignancies].
K. Kimura
,
K. Yamada
,
+4 authors
M. Ogawa
Gan to kagaku ryoho. Cancer & chemotherapy
1989
Corpus ID: 11214245
A total of 165 patients were entered into this study and 140 were evaluate for effects and 165 for toxicities. Of 39 patients…
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1989
1989
[Phase I study and early phase II of SM-108 (4-carbamoylimidazolium-5-olate) in lung cancer. SM-108 Study Group].
K. Kimura
,
Y. Suzuoki
,
+7 authors
T. Yoshida
Gan to kagaku ryoho. Cancer & chemotherapy
1989
Corpus ID: 1218514
Phase I study with a new oral purine antagonist, SM-108, was conducted in a total of 73 cases in a 5-day consecutive schedule…
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1988
1988
[Treatment of myelodysplastic syndrome using SM-108 in relation to stem cell kinetics].
Y. Uzuka
,
Y. Saito
Gan to kagaku ryoho. Cancer & chemotherapy
1988
Corpus ID: 35519101
Eighteen patients in a high-blast group of myelodysplastic syndrome were treated with low-dose SM-108 (4-carbamoylimidazolium 5…
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1988
1988
177 TWO DISTINCT TARGET SITES ON IMP DEHYDROGENASE IN CHEMOTHERAPY
Yasukazu Yamada
,
Y. Natsumeda
,
Y. Yamaji
,
G. Weber
Pediatric Research
1988
Corpus ID: 1708302
The inhibitory mechanisms of ribavirin 5′-monophosphate, (RMP), SM-108 nucleotide (bredinin 5′-monophosphate, BMP) and thiazole-4…
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1987
1987
[Clinical trial of SM-108 in myeloproliferative disorders].
M. Nishikawa
,
K. Morita
,
+7 authors
N. Minami
Gan to kagaku ryoho. Cancer & chemotherapy
1987
Corpus ID: 29061065
SM-108 (4-carbamoylimidazolium-5-olate) is a new purine antagonist which blocks IMP dehydrogenase, the key enzyme of de novo GMP…
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1986
1986
Selective reduction of intracellular guanosine 5'-triphosphate pool by 4-carbamoylimidazolium 5-olate in murine tumor cells.
M. Fukui
,
M. Inaba
,
S. Tsukagoshi
,
Y. Sakurai
Cancer Research
1986
Corpus ID: 43811097
Ehrlich carcinoma and P388 leukemia cells were rendered resistant to 4-carbamoylimidazolium 5-olate (SM-108), and assessments…
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1983
1983
Optimal treatment schedule and antitumor spectrum of 4-carbamoylimidazolium 5-olate (SM-108) in murine tumors.
N. Yoshida
,
M. Nakamura
,
+5 authors
Y. Sakurai
Cancer Research
1983
Corpus ID: 6829899
By designing optimal administration schedules, it was found that 4-carbamoylimidazolium 5-olate (SM-108) showed an excellent…
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1982
1982
New antitumor imidazole derivative, 5-carbamoyl-1H-imidazol-4-yl piperonylate, as an inhibitor of purine synthesis and its activation by adenine phosphoribosyltransferase.
M. Fukui
,
M. Inaba
,
S. Tsukagoshi
,
Y. Sakurai
Cancer Research
1982
Corpus ID: 32798718
The mechanism of action of 5-carbamoyl-1H-imidazol-4-yl piperonylate (SL-1250), which has a broad antitumor spectrum, was…
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1982
1982
Collateral sensitivity of 6-mercaptopurine-resistant sublines of P388 and L1210 leukemia to the new purine antagonists, 5-carbamoyl-1H-imidazol-4-yl piperonylate and 4-carbamoylimidazolium 5-olate.
M. Inaba
,
M. Fukui
,
N. Yoshida
,
S. Tsukagoshi
,
Y. Sakurai
Cancer Research
1982
Corpus ID: 25828307
Two new purine antagonists, 5-carbamoyl-1H-imidazol-4-yl piperonylate (SL-1250) and 4-carbamoylimidazolium 5-olate (SM-108), were…
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