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Steven S. Matsumoto

Publications -  7
Citations -  213

Steven S. Matsumoto is an academic researcher. The author has contributed to research in topics: Myeloid leukemia & Cellular differentiation. The author has an hindex of 6, co-authored 7 publications receiving 207 citations.

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Growth inhibition and induction of cellular differentiation of human myeloid leukemia cells in culture by carbamoyl congeners of ribavirin.

TL;DR: These compounds were found to be inducers of cellular differentiation of HL-60 cells in the range of 30-60 microM and were comparable to ribavirin in this regard.
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Antitumor and antiviral activity of synthetic alpha- and beta-ribonucleosides of certain substituted pyrimido[5,4-d]pyrimidines: a new synthetic strategy for exocyclic aminonucleosides.

TL;DR: A novel and direct synthesis of the antiviral and antitumor agent 4-amino-8-(beta-D-ribofuranosylamino)pyrimido[5,4-d]pyrimidine (ARPP, 8) and its alpha-anomer (11) has been developed.
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Synthesis of Tubercidin, 6-Chlorotubercidin and Related Nucleosides

TL;DR: Tubercidin (7-deazaadenosine, 1a) and several 6-chlorotuber-Cidin derivatives were synthesized including 4-amino-6-chloro-7-β-D-ribofuranosylpyrrolo[2,3-d]pyrimidine-3′,5′-cycyclic phosphate 9 as discussed by the authors.
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Activation of the respiratory burst in murine phagocytes by certain guanine ribonucleosides modified at the 7 and 8 positions: possible involvement of a pertussis toxin-sensitive G-protein.

TL;DR: Observations establish these low-molecular-weight compounds as interesting probes for the study of stimulus-response coupling in phagocytes as well as suggesting an important role for cytokines/lymphokines in the nucleoside-induced phagocyte activation in vivo.
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Analysis of the in vitro antitumor activity of novel purine-6-sulfenamide, -sulfinamide, and -sulfonamide nucleosides and certain related compounds using a computer-aided receptor modeling procedure

TL;DR: The comparative antileukemic activities of 21 novel nucleosides were determined in vitro by using cultured L1210 cells and analyzed for structure-related efficacy by a computer-aided receptor modeling method (REMOTEDISC), thereby establishing the major contributions of these three molecular entities to overall antitumor activity.