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Chemistry and Biodiversity

Volumn 9, Issue 3, 2012, Pages 557-566

Synthesis and in vitro inhibition properties of siRNA conjugates carrying acridine and quindoline moieties

(4) Aviñó, Anna a Ocampo, Sandra M a Perales, José C b Eritja, Ramon a

a BIOMATERIALES Y NANOMEDICINA CIBER BBN (Spain)

b UNIVERSITY OF BARCELONA (Spain)

Author keywords

Acridine; Inhibitors; Oligoribonucleotides; Quindoline; RNA; siRNA; Threoninol; Tumor necrosis factor

Indexed keywords

ACRIDINE DERIVATIVE; INDOLE DERIVATIVE; OLIGOFECTAMINE; OLIGONUCLEOTIDE; PHOSPHORAMIDOUS ACID; QUINDOLINE DERIVATIVE; SMALL INTERFERING RNA; TUMOR NECROSIS FACTOR ALPHA; TUMOR NECROSIS FACTOR ALPHA INHIBITOR; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL MODIFICATION; CONJUGATE; CONTROLLED STUDY; DRUG EFFECT; DRUG STRUCTURE; DRUG SYNTHESIS; GENE SILENCING; GENETIC TRANSFECTION; HELA CELL; MATRIX ASSISTED LASER DESORPTION IONIZATION TIME OF FLIGHT MASS SPECTROMETRY; NUCLEOTIDE SEQUENCE; REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;

ACRIDINES; ALKALOIDS; HELA CELLS; HUMANS; INDOLES; MICROSCOPY, FLUORESCENCE; NUCLEIC ACID DENATURATION; OLIGONUCLEOTIDES; QUINOLINES; RNA; RNA INTERFERENCE; RNA, SMALL INTERFERING; SPECTROMETRY, MASS, MATRIX-ASSISTED LASER DESORPTION-IONIZATION; TRANSFECTION; TUMOR NECROSIS FACTORS;

EID: 84859053208 PISSN: 16121872 EISSN: 16121880 Source Type: Journal
DOI: 10.1002/cbdv.201100321 Document Type: Article

Times cited : (11)

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