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Title: Oligonucleoside alkyl or arylphosphonate derivatives capable of crosslinking with or cleaving nucleic acids

Patent ·
OSTI ID:872330

A composition for inactivating a target nucleic acid which comprises an oligonucleoside alkyl or arylphosphonate analogue which is complementary to the sequence of the target nucleic acid and includes a functional group which reacts with the target nucleic acid to render the target nucleic acid inactive or nonfunctional.

Research Organization:
Sandia National Laboratories (SNL), Albuquerque, NM, and Livermore, CA (United States)
Sponsoring Organization:
USDOE
DOE Contract Number:
FG02-88ER60636
Assignee:
Johns Hopkins University (Baltimore, MD)
Patent Number(s):
US 5912339
Application Number:
08/342005
OSTI ID:
872330
Country of Publication:
United States
Language:
English

References (12)

Effects of pendant groups at phosphorus on binding properties of d-ApA analogues journal January 1986
Sequence-specific cleavage of single-stranded DNA: oligodeoxynucleotide-EDTA X Fe(II). journal February 1985
Antiviral effect of oligo(nucleoside methylphosphonates) complementary to the herpes simplex virus type 1 immediate early mRNAs 4 and 5 journal February 1993
Oligonucleotide Analogues as Potential Chemotherapeutic Agents journal January 1988
Chemical synthesis of natural and modified oligodeoxynucleotides journal July 1985
Nonenzymatic sequence-specific cleavage of single-stranded DNA. journal February 1985
Molecular Biology: Antisense Has Growing Pains journal October 1995
CpG motifs in bacterial DNA trigger direct B-cell activation journal April 1995
Oligodeoxynucleotides covalently linked to intercalating agents: a new class of gene regulatory substances journal July 1985
Interaction of psoralen-derivatized oligodeoxyribonucleoside methylphosphonates with single-stranded DNA journal May 1988
Synthesis of porphyrin(Fe)-intercalators which cause DNA scission journal January 1983
Hybridization triggered cross-linking of deoxyoligonucleotides journal January 1986