Total synthesis of two photoactivatable analogues of the growth-factor-like mediator sphingosine 1-phosphate: Differential interaction with protein targets

Journal of Organic Chemistry

Volumn 68, Issue 18, 2003, Pages 7046-7050

  Lu, Xuequan ^a   Cseh, Sandor ^b   Byun, Hoe Sup ^a   Tigyi, Gabor ^b   Bittman, Robert ^a  

^a CITY UNIVERSITY OF NEW YORK   (United States)

^b UNIVERSITY OF TENNESSEE HEALTH SCIENCE CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CELLS; PLASMAS; PROTEINS;

PLASMA PROTEINS;

SYNTHESIS (CHEMICAL);

14 O [(4' TRIFLUOROMETHYLDIAZIRINYL)PHENYL]TETRADECENYL 2 AMINO 3 HYDROXY 1 PHOSPHATE; BENZOPHENONE DERIVATIVE; CARRIER PROTEIN; PHOSPHATE; PHOSPHORUS 32; PLASMA PROTEIN; SPHINGOSINE 1 PHOSPHATE; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; CONCENTRATION (PARAMETERS); HEPATOMA CELL; ISOTOPE LABELING; NONHUMAN; PHOTOACTIVATION; PROTEIN EXPRESSION; PROTEIN INTERACTION; PROTEIN SYNTHESIS; PROTEIN TARGETING; RAT;

ANIMALS; CELL LINE, TUMOR; INDICATORS AND REAGENTS; LIVER NEOPLASMS, EXPERIMENTAL; LYSOPHOSPHOLIPIDS; PHOTOAFFINITY LABELS; PHOTOCHEMISTRY; PROTEINS; RADIOLIGAND ASSAY; RATS; RATS, SPRAGUE-DAWLEY; RECEPTORS, G-PROTEIN-COUPLED; SPHINGOSINE;

EID: 0042839476     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo034828q     Document Type: Article

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