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[Design and synthesis of 3'-methyl-furanonucleosides and their anti-tumor activities].
- Source :
-
Yao xue xue bao = Acta pharmaceutica Sinica [Yao Xue Xue Bao] 2009 Jul; Vol. 44 (7), pp. 747-53. - Publication Year :
- 2009
-
Abstract
- Taking 3'-Me-Ado (3'-methyladenosine) and Cladribine as the leading compounds, seventeen 3'-C-methyl-furanonucleosides were designed and synthesized. All the structures were confirmed by 1H NMR and MS. The target compounds were tested in vitro against human pulmonary carcinoma A549, human colon carcinoma LOVO and human leukemia CEM by MTT assay. The results showed that these compounds possessed moderate cytotoxicities.
- Subjects :
- Adenosine analogs & derivatives
Adenosine chemical synthesis
Adenosine pharmacology
Cell Line, Tumor
Cladribine chemical synthesis
Cladribine pharmacology
Drug Screening Assays, Antitumor
Humans
Molecular Structure
Antineoplastic Agents chemical synthesis
Antineoplastic Agents pharmacology
Subjects
Details
- Language :
- Chinese
- ISSN :
- 0513-4870
- Volume :
- 44
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Yao xue xue bao = Acta pharmaceutica Sinica
- Publication Type :
- Academic Journal
- Accession number :
- 19806914