Diastereoselective synthesis and bioactivity of long-chain anti-2-amino-3-alkanols

European Journal of Medicinal Chemistry

Volumn 46, Issue 11, 2011, Pages 5480-5486

  Chen, Bi Shuang ^a   Yang, Long He ^a   Ye, Jian Liang ^a   Huang, Tao ^a   Ruan, Yuan Ping ^a   Fu, Jin ^a   Huang, Pei Qiang ^a  

^a XIAMEN UNIVERSITY   (China)

Author keywords

1 Deoxy sphingoid bases; Cell proliferation; Enantioselective synthesis; Marine compound; One pot reaction

Indexed keywords

1 (TERT BUTYLDIMETHYLSILYLOXY) 2 (DIBENZYLAMINO)DODECAN 3 OL; 2 (DIBENZYLAMINO) 11 METHYLDODECAN 3 OL; 2 (DIBENZYLAMINO)DODEC 8 EN 3 OL; 2 (DIBENZYLAMINO)DODECAN 3 OL; 2 (DIBENZYLAMINO)OCTADECAN 3 OL; 2 (DIBENZYLAMINO)TETRADECAN 3 OL; 2 AMINO 11 METHYLDODECAN 3 OL; 2 AMINODODECAN 3 OL; ALCOHOL DERIVATIVE; AMINOLDODECAN 1,3 DIOL; ANTINEOPLASTIC AGENT; CLAVAMINOL A; CLAVAMINOL B; CLAVAMINOL H; CLAVAMINOL N; SPHINGOSINE; SPISULOSINE; UNCLASSIFIED DRUG; XESTOAMINOL C;

ANTINEOPLASTIC ACTIVITY; ARTICLE; CELL DEATH; CELL PROLIFERATION; CELL VIABILITY; CYTOTOXICITY; DOSE RESPONSE; DRUG SYNTHESIS; GLIOBLASTOMA; HUMAN; HUMAN CELL; IC 50; IN VITRO STUDY; STEREOCHEMISTRY; STRUCTURE ACTIVITY RELATION; TREATMENT OUTCOME;

ALCOHOLS; ANTINEOPLASTIC AGENTS; CELL LINE, TUMOR; CELL PROLIFERATION; CHEMISTRY TECHNIQUES, SYNTHETIC; DOSE-RESPONSE RELATIONSHIP, DRUG; HUMANS; STEREOISOMERISM; SUBSTRATE SPECIFICITY;

EID: 80054917605     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2011.09.010     Document Type: Article

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