Synthesis and biological evaluation of enantiomeric rhamnose analogues of the antitumour agent spicamycin - Is the mode of action by modification of N-linked glycoproteins?

Tetrahedron Asymmetry

Volumn 10, Issue 12, 1999, Pages 2343-2360

  Martín, Angeles ^a   Butters, Terry D ^b   Fleet, George W J ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b UNIVERSITY OF OXFORD   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

6 [4' DEOXY 4' (DODECANOYLGLYCYL)AMINO BETA RHAMNOPYRANOSYLAMINO] 9H PURINE; ANTINEOPLASTIC AGENT; GLYCOPROTEIN; RHAMNOSE DERIVATIVE; SPICAMYCIN; UNCLASSIFIED DRUG;

ANTINEOPLASTIC ACTIVITY; ARTICLE; DRUG CYTOTOXICITY; DRUG PROTEIN BINDING; DRUG SYNTHESIS; ENANTIOMER; HUMAN; HUMAN CELL; MYELOMA CELL; PRIORITY JOURNAL; PROTEIN MODIFICATION; STRUCTURE ANALYSIS;

EID: 0033580751     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(99)00240-2     Document Type: Article

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