Synthesis and evaluation of cyclic RGD-boron cluster conjugates to develop tumor-selective boron carriers for boron neutron capture therapy

Bioorganic and Medicinal Chemistry

Volumn 19, Issue 5, 2011, Pages 1721-1728

  Kimura, Sadaaki ^a,c   Masunaga, Shin Ichiro ^b   Harada, Tomohiro ^a   Kawamura, Yasuo ^a   Ueda, Satoshi ^a   Okuda, Kensuke ^a   Nagasawa, Hideko ^a  

^a GIFU PHARMACEUTICAL UNIVERSITY   (Japan)

^b KYOTO UNIVERSITY   (Japan)

^c NATIONAL CANCER CENTER HOSPITAL EAST   (Japan)

Author keywords

Boron neutron capture therapy (BNCT); Cyclic RGD; Integrin v 3; o Carborane

Indexed keywords

ARGINYLGLYCYLASPARTIC ACID; ARGINYLGLYCYLASPARTIC ACID BORON; BORON; CARBORANE DERIVATIVE; DISODIUM MERCAPTODODECABORATE; DRUG CARRIER; UNCLASSIFIED DRUG; VITRONECTIN RECEPTOR;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BINDING AFFINITY; CELL ADHESION; CONTROLLED STUDY; DRUG CONJUGATION; DRUG DESIGN; DRUG DISTRIBUTION; DRUG SELECTIVITY; DRUG SYNTHESIS; FEMALE; MOUSE; NEUTRON CAPTURE THERAPY; NONHUMAN;

ANIMALS; BORON; BORON NEUTRON CAPTURE THERAPY; CELL LINE, TUMOR; DRUG DELIVERY SYSTEMS; INJECTIONS, INTRAVENOUS; MICE; MOLECULAR STRUCTURE; PEPTIDES, CYCLIC; TISSUE DISTRIBUTION;

MUS;

EID: 79952196352     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmc.2011.01.020     Document Type: Article

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