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Cancer Research Institute Kanazawa University | 論文
- In Vitro Antitumor Activity of Polymyxin Acylase from Pseudomonas sp. M-6-3
- Purealidins J-R, New Bromotyrosine Alkaloids from the Okinawan Marine Sponge Psammaplysilla purea
- Untenospongin C, a New C_ Furanoterpene from the Okinawan Marine Sponge Hippospongia Sp.
- Agelasine G, a New Antileukemic Alkaloid from the Okinawan Marine Sponge Agelas sp.
- 末梢血単核球と多核白血球によるインターロイキン8の産生と熱帯熱マラリア原虫の発育阻害作用
- IL1,IL2の測定法(リンパ球の検査-3-)
- Marine Natural Products. XXXII. Absolute Configurations of C-4 of the Manoalide Family, Biologically Active Sesterterpenes from the Marine Sponge Hyrtions erecta
- Marine Natural Products. XXXI. Structure-Activity Correlation of a Potent Cytotoxic Dimeric Macrolide Swinholide A, from the Okinawan Marine Sponge Theonella swinhoei, and Its Isomers
- THE DESIGN, SYNTHESIS AND ANTILEUKEMIC ACTIVITY OF 5-ALKYNYL-1-β-D-RIBOFURANOSYLIMIDAZOLE-4-CARBOXAMIDES
- Antitumor Activity and Pharmacokinetics of TAS-106, 1-(3-C-Ethyny1-β-D-ribo-pentofuranosyl)cytosine
- Alkyl Addition Reaction of Pyrimidine 2'-Ketonucleosides : Synthesis of 2'-Branched-Chain Sugar Pyrimidine Nucleosides : Nucleosides and Nucleotides. LXXXI^1
- Antitumor Polysaccharides from Some Polyporaceae, Ganoderma applanatum (PERS.) PAT and Phellinus linteus (BERK. et CURT) AOSHIMA
- Nucleosides and Nucleotides. 186. Synthesis and Biological Activities of Pyrimidine Carbocyclic Nucleosides with a Hydroxyamino Group Instead of a Hydroxymethyl Group at the 4'-Position of the Sugar Moiety
- New Neplanocin Anallogues. VIII. Synthesis and Biological Activity of 6'-C-Ethyl, -Ethenyl, and -Ethynyl Derivatives of Neplanocin A
- Cytotoxic Principles of a Bangladeshi Crude Drug, Akond Mul (Roots of Calotropis gigantea L.)
- Purealidins A-R, New Bromotyrosine Alkaloids from an Okinawan Marine Sponge Psammaplysilla purea
- Synthesis of Lanosterol Derivatives with a Functional Group at C-32,Including an Antineoplastic Sterol, 3β-Hydroxylanost-7-en-32-oic Acid
- Sensitivity, of Human Cancer Cells to the New Anticancer Ribo-nucleoside TAS-106 Is Correlated with Expression of Uridine-cytidine Kinase 2
- Cellular and Biochemical Mechanisms of the Resistance of Human Cancer Cells to a New Anticancer Ribo-nucleoside, TAS-106
- Selective Acylation of the Amino or the Primary Hydroxyl Group of Cytidine
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