SCOPUS 정보 검색 플랫폼

Volumn 20, Issue 1, 2012, Pages 183-194

Design, synthesis and biological activity of sphingosine kinase 2 selective inhibitors

(6) Raje, Mithun R a Knott, Kenneth a Kharel, Yugesh b Bissel, Philippe a Lynch, Kevin R b Santos, Webster L a

a VIRGINIA POLYTECHNIC INSTITUTE AND STATE UNIVERSITY (United States)

b UNIVERSITY OF VIRGINIA (United States)

Author keywords

Cancer; FTY720; Kinase inhibitor; Lipid; Reductive amination; Sphingosine; Sphingosine kinase; Sphingosine 1 phosphate; Structure activity relationships

Indexed keywords

1 (NITROMETHYL) 4 (4 OCTYLPHENYL)CYCLOHEXANOL; 1 AMINO 4 (4 OCTYLPHENYL)CYCLOHEXANECARBONITRILE; 2 [4 (4 OCTYLPHENYL)CYCLOHEXYLIDENE]ETHANOL; 2 [[4 (4 OCTYLPHENYL)CYCLOHEXYL]AMINO]ETHANOL; 4 (4 OCTYLPHENYL) N (PYRIDIN 4 YLMETHYL)CYCLOHEXANAMINE; 4 (4 OCTYLPHENYL) N PROPYLCYCLOHEXANAMINE; 4 (4 OCTYLPHENYL)CYCLOHEXANOL; 4 (4 OCTYLPHENYL)CYCLOHEXANONE; 4 (4 OCTYLPHENYL)CYCLOHEXANONE OXIME; 8 (4 OCTYLPHENYL) 1,4 DIOXASPIRO[4.5]DECAN 8 OL; ANTINEOPLASTIC AGENT; FINGOLIMOD; METHYL 2 [4 (4 OCTYLPHENYL)CYCLOHEXYLIDENE]ACETATE; N (PROP 2 YNYL) 4 (4 OCTYLPHENYL)CYCLOHEXANAMINE; N ALLYL 4 (4 OCTYLPHENYL)CYCLOHEXANAMINE; N BENZYL 4 (4 OCTYLPHENYL)CYCLOHEXANAMINE; N BENZYL N,N DIMETHYL 4 (4 OCTYLPHENYL)CYCLOHEXANAMINIUM IODIDE; N BUTYL 4 (4 OCTYLPHENYL)CYCLOHEXANAMINE; N CYCLOPROPYL 4 (4 OCTYLPHENYL)CYCLOHEXANAMINE; N ISOPROPYL 4 (4 OCTYLPHENYL)CYCLOHEXANAMINE; N ISOPROPYL N METHYL 4 (4 OCTYLPHENYL)CYCLOHEXANAMINE; N ISOPROPYL N,N DIMETHYL 4 (4 OCTYLPHENYL)CYCLOHEXANAMINIUM IODIDE; N METHYL 4 (4 OCTYLPHENYL) N PROPYLCYCLOHEXANAMINE; N METHYL 4 (4 OCTYLPHENYL)CYCLOHEXANAMINE; N,N DIMETHYL 4 (4 OCTYLPHENYL) N PROPYLCYCLOHEXANAMINIUM IODIDE; N,N DIMETHYL 4 (4 OCTYLPHENYL)CYCLOHEXANAMINE; N,N,N TRIMETHYL 4 (4 OCTYLPHENYL)CYCLOHEXANAMINIUM IODIDE; SPHINGOSINE KINASE 2; SPHINGOSINE KINASE 2 SELECTIVE INHIBITOR DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

AMINATION; ANTINEOPLASTIC ACTIVITY; ARTICLE; CANCER CELL; CANCER GROWTH; CANCER SURVIVAL; CONTROLLED STUDY; DRUG DESIGN; DRUG POTENCY; DRUG SOLUBILITY; DRUG STRUCTURE; DRUG SYNTHESIS; HUMAN; HUMAN CELL; HYDROGENATION; IMMUNOMODULATION; PROTEIN PHOSPHORYLATION; STRUCTURE ACTIVITY RELATION;

ANTINEOPLASTIC AGENTS; CELL LINE, TUMOR; DRUG DESIGN; ENZYME ACTIVATION; ENZYME INHIBITORS; HUMANS; KINETICS; LYSOPHOSPHOLIPIDS; PHOSPHORYLATION; PHOSPHOTRANSFERASES (ALCOHOL GROUP ACCEPTOR); PROPYLENE GLYCOLS; SPHINGOSINE; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 84855206931 PISSN: 09680896 EISSN: 14643391 Source Type: Journal
DOI: 10.1016/j.bmc.2011.11.011 Document Type: Article

Times cited : (37)

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