Synthesis and biological study of a flavone acetic acid analogue containing an azido reporting group designed as a multifunctional binding site probe

Bioorganic and Medicinal Chemistry

Volumn 13, Issue 8, 2005, Pages 2717-2722

  Malolanarasimhan, Krishnan ^a   Lai, Christopher C ^a   Kelley, James A ^a   Iaccarino, Lynn ^a   Reynolds, Della ^a   Young, Howard A ^a   Marquez, Victor E ^a  

^a NATIONAL CANCER INSTITUTE   (United States)

Author keywords

Affinity label; Azide modified flavone acetic acid; Flavone acetic acid; Immunomodulatory small molecules; Staudinger reaction

Indexed keywords

2 [2 (4 AZIDOPHENYL) 4 OXOCHROMEN 8 YL]ACETIC ACID; ASPARTYLTYROSYLLYSYLASPARTYLASPARTYLASPARTYLASPARTYLLYSINE; AZIDE; CHEMOKINE; FUNCTIONAL GROUP; MITOFLAXONE; PEPTIDE ANTIBODY; PEPTIDE DERIVATIVE; PHOSPHINE; RANTES; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; ANIMAL CELL; ARTICLE; CHEMICAL REACTION; CONTROLLED STUDY; DRUG BINDING SITE; DRUG PROTEIN BINDING; DRUG SYNTHESIS; GENE EXPRESSION; GENE FUNCTION; GENE INDUCTION; GENE PROBE; MOLECULE; MOUSE; NONHUMAN; PROTEIN ANALYSIS; REPORTER GENE;

EID: 15244344612     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmc.2005.02.035     Document Type: Article

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