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   <subfield code="a">Deoxyribonucleoside triphosphate pools and ara-ctp levels in P388 murine leukemic cells treated with 1-B-D-Arabinofuranosylcytosine-5′ -stearylphosphate which is a newly synthesized derivative OF 1-B-D-arabinofuranosylcytosine</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Masamune Higashigawa, Hiroki Hori, Toshiki Ohkubo, Hajime Kawasaki, Tamotu Yoshizumi, Minoru Sakurai]</subfield>
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   <subfield code="a">1-B-D-arabinofuranosylcytosine-573′-stearylphosphate (C18PCA), which is an Ara-CMP ester and one of the most promising orally effective anti-leukemic drugs, is a newly synthesized derivative of Ara-C. The antitumor effect of C18PCA and Ara-C was investigated against the P388 ascites tumor in BDF1 mice. Treatment with C18PCA (100 mg kg-1, orally) and Ara-C (40 mg kg-1, subcutaneously) was administered on days 1, 3 and 5 after tumor inoculation. The percentage increase in lifespans of the mice treated with C18PCA or Ara-C were 84.4% and 53.9%, respectively. The determination of the plasma Ara-C concentration revealed that the plasma concentration of Ara-C was retained much longer in mice which orally received C18PCA than in those which received Ara-C. By using high-performance liquid chromatography, it was revealed that the deoxyribonucleo-side triphosphate pools increased gradually but Ara-CTP concentration once increased, then decreased rapidly when Ara-C was administered subcutaneously. On the other hand, both the intracellular deoxyribonucleoside triphosphate (dNTP) pools and Ara-CTP level increased gradually after oral administration of C18PCA. We concluded that these longer-term biochemical effects, even if the plasma concentration of Ara-C and Ara-CTP level were low, might be correlated with antitumor effects of C18PCA.</subfield>
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