2-aminopurine derivatives

Organic compounds -- part of the class 532-570 series – Organic compounds – Carbohydrates or derivatives

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

C536S026700, C536S027800, C514S04400A, C435S006120, C435S091500

Reexamination Certificate

active

06900307

ABSTRACT:
There are provided 2-aminopurine derivatives represented by the following general formula (1):where R represents any species selected from the group consisting of hydrogen and acyl groups, X represents any species selected from the group consisting of phosphoramidite and oligonucleotides, Y represents any species selected from the group consisting of dimethyltrityl groups and oligonucleotides, and Z1, Z2, Z3, Z4and Z5are the same or different and represent any species selected from the group consisting of hydrogen and hydroxyl, amino, lower alkyl, alkoxy, carboxyl and sulfonic acid groups, provided that Z1, Z2, Z3, Z4and Z5are not all hydrogen, as well as gene expression-regulating compositions characterized by comprising the derivatives. By introducing the 2-aminopurine derivatives into oligonucleotides it is possible to achieve crosslinking reaction with high reactivity for target nucleic acids and notably high base sequence specificity.

REFERENCES:
patent: 9-67392 (1997-03-01), None
patent: 9-124687 (1997-05-01), None
patent: WO 01/34619 (2001-05-01), None
Nagatsugi et al. (I), “New Design of Artificial Nucleobases as Cross-Linking Agents based on the ‘Prodrug’ Strategy,”Abstracts, Symposium on Biofunctional Chemistry, 11, 34-36 (1996);JICST File on Science Technology and Medicine in Japan,JST (Japan Science and Technology Agency) on STN as 970364213 (1997); only JICST abstract supplied.*
Nagatsugi et al. (II), “Synthesis and Cross-Linking of the Oligonucleotides Incorporating New Artifical Bases with Selective Reactivity to Cytidine,”Abstracts, Symposium on Biofunctional Chemistry, 12, 189-191 (1997);JICST File on Science Technology and Medicine in Japan,JST on STN as 980230686 (1998); only JICST abstract supplied.*
Nagatsugi et al., ‘Structural Analysis of Cross-linked Adducts With The Oligonucleotides Incorporating 2-Amino-6-Vinylpurin’, Nucleic Acids Symposium Series No. 39, 1998 Oxford University Press, pp. 103-104.
Nagatsugi et al., ‘Highly Effected and Selective Cross-Linking to Cytidine Based on a New Strategy for Auto-Activation Within a Duplex,’ J. Am. Chem. Soc. 1999, 121, pp. 6753-6754, (Web Pub: Jul. 3, 1999).
Woolf, Tod M., ‘Therapeutic Repair of Mutated Nucleic Acid Sequences’, Nature Biotechnology, vol. 16, Apr. 1998, pp. 341-344.
Grant et al., ‘Sequence-Specific Alkylation and Cleavage of DNA Mediated by Purine Motif Triple Helix Formation’, Biochemistry 1996, 35, pp. 12313-12319, (Abstr Pub Sep. 15, 1996).
Shaw et al., ‘Specific, High-Efficiency, Triple-Helix-Mediated Cross-Linking to Duplex DNA’, J. Am. Chem. Soc. 1991, 113, pp. 7765-7766.
Chang et al., ‘Antisense Inhibition of ras p21 Expression That is Sensitive to a Point Mutation’, Biochemistry (Am. Chem. Soc.), vol. 30, No. 34, Aug. 1991, pp. 8283-8286, (Aug. 27, 1991).
Nagatsugi et al., ‘2-Aminopurine Derivatives with C6-Substituted Olefin as Novel Cross-Linking Agents and the Synthesis of the Corresponding β-Phosphoramidite Precursors’,Tetrahedron,vol. 53, No. 9, 1997, pp 3035-3044.

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

2-aminopurine derivatives does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with 2-aminopurine derivatives, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and 2-aminopurine derivatives will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-3421977

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.