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Volumn 20, Issue 3, 2010, Pages 862-865

Structural diversity of nucleoside phosphonic acids as a key factor in the discovery of potent inhibitors of rat T-cell lymphoma thymidine phosphorylase

Author keywords

Nucleotide analogues; Phosphonate; Pyrrolidine; Rat T cell lymphomas; Thymidine phosphorylase

Indexed keywords

ANTINEOPLASTIC AGENT; ENZYME INHIBITOR; NUCLEOTIDE; PHOSPHONIC ACID DERIVATIVE; PROLINOL NUCLEOTIDE; PYRROLIDINE DERIVATIVE; SUGAR; THYMIDINE PHOSPHORYLASE; THYMINE; UNCLASSIFIED DRUG; NUCLEOSIDE;

EID: 74049150566     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2009.12.081     Document Type: Article
Times cited : (19)

References (45)
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  • 34
    • 84924233418 scopus 로고    scopus 로고
    • Li, Y. Studies in Nucleoside Chemistry. Synthesis of Purine and Pyrimidine Nucleoside Phosphorylase Inhibitors. Total Synthesis of the Sulfated Nucleoside Glycoside HF-7, 2000, Ph.D. Dissertation, Cornell University, Ithaca, NY.
    • Li, Y. Studies in Nucleoside Chemistry. Synthesis of Purine and Pyrimidine Nucleoside Phosphorylase Inhibitors. Total Synthesis of the Sulfated Nucleoside Glycoside HF-7, 2000, Ph.D. Dissertation, Cornell University, Ithaca, NY.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.