Purine and isosteric antibacterial compounds

Compositions: coating or plastic – Coating or plastic compositions – Contains fireproofing or biocidal agent

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

C544S276000, C544S118000, C514S234200, C514S263200, C514S263370

Reexamination Certificate

active

06926763

ABSTRACT:
The invention features compounds of the formula:or a pharmaceutically acceptable salt thereof, wherein A is CR2and B is N; wherein n is 0-3; wherein R1is (CH2)m—{(G)o—(CH2)p}q—L, in which G is CH2, CH═CH, C≡C, CO, O, S, or NR5, where R5is H or C1-6alkyl, CHR6, where R6is OH or C1-6alkyl, CH(CR7R8), where each of R7and R8is, independently, H, halo, or C1-6alkyl, OCO, CONR9, NR10CO, where each of R9and R10is, independently, H or C1-6alkyl, SO2NH, or NHSO2; in which m is 1-4, o is 0-4, p is 0-4, and q is 0-4. The compounds disclosed herein have potent anti-microbial, e.g., both Gram-positive and Gram-negative anti-bacterial properties. The compounds inhibit DNA polymerase IIIC and DNA polymerase IIIE enzymes and thus act therapeutically by inhibiting the growth of a broad array of bacteria. The compounds can be administered to prevent or to treat Gram-positive or Gram-negative bacterial infections, e.g., in eukaryotic cell cultures, animals, or humans.

REFERENCES:
patent: 5516905 (1996-05-01), Brown et al.
patent: 6492384 (2002-12-01), Mederski et al.
patent: 2003/0181719 (2003-09-01), Zhi et al.
patent: WO 01/28561 (2001-04-01), None
patent: WO 01/29010 (2001-04-01), None
patent: WO 01/29045 (2001-04-01), None
patent: WO 2002102792 (2002-12-01), None
George E. Wright, J Med. Chem 30, pp 109-116 1987.
Ali et al. Design and Synthesis of Novel Antibacterial Agents with Inhibitory Activity against DNA Polymerase III,Bioorg. Med. Chem. Lett.,2001, 11:2185-2188.
Braithewaite et al. Compilation, Alignment, and Phylogenetic Relationships of DNA Polymerases,Nucl. Acids Res.,1993, 21:787-802.
Brown et al. Inhibitors ofBacillus subtilisDNA Polymerase III. 6-(Arylalkylamino)uracils and 6-Anilinouracils,J. Med. Chem.,1977, 20:1186-1189.
Butler et al. Development of Novel Inhibitor Probes of DNA Polymerase III Based on dGTP Analogs of the HPUra Type: Base, Nucleoside and Nucleotide Derivatives of N2-(3,4-Dichlorobenzyl)guanine,Nucl. Acids Res.,1990, 18:7381-7387.
De Bode et al. Deazapurine Derivatives XII Investigations on the Synthesis of 3-deazaguanine,Recl. Trav. Chim. Pays-Bas,1974, 93:3-6.
Earl et al. The Synthesis of 8-aza-3-deazaguanosine [6-amino-1-(β-D-ribofuranosyl)-v-triazolo[4,5-c]pyridin-4-one] via a Novel 1, 3-dipolar Cycloaddition Reaction,Can. J. Chem.,1980, 58:2550-2561.
Mederski et al. Non-peptide Angiotensin II Receptor Antagonists: Synthesis and Biological Activity of a Series of Novel 4, 5-Dihydro-4-oxo-3H-imidazo[4,5-c]pyridine Derivatives,J. Med. Chem.,1994, 37:1632-1645.
Medveczky et al. Haloanilino Derivatives of Pyrimidines, Purines, and Purine Nucleoside Analogs: Synthesis and Activity against Human Cytomegalovirus,J. Med. Chem.,1995, 38:1811-1819.
Rousseau et al. The Synthesis of Various Chloroimidazo[4,5-c]pyridines and Related Derivatives,J. Heterocycl. Chem.,1965, 2:196-201.
Stimac et al. The Synthesis of v-Triazolo[4,5-c]pyridine Nucleosides,Nucleosides&Nucleotides,1991, 10:727-728.
Tarantino et al. 6-Anilinouracil-based Inhibitors ofBacillus subtilisDNA Polymerase III: Antipolymerase and Antimicrobial Structure-activity Relationships Based on Substitution at Uracil N3,J. Med. Chem.,1999, 42:2035-2040.
Wright et al., Inhibition ofBacillus subtilisDNA Polymerase III by Arylhydrazinopyrimidines,Biochim. Biophys. Acta.,1976, 432:37-48.
Wright et al. DNA Polymerase III: A New Target for Antibiotic Development,Curr. Opin. Anti-Infect. Invest. Drugs,1999, 1:45-48.
Xu et al. Synthesis, Properties, and Pharmacokinetic Studies of N2-Phenylguanine Derivatives as Inhibitors of Herpes Simplex Virus Thymidine Kinases,J. Med. Chem.,1995, 38:49-57.

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

Purine and isosteric antibacterial compounds does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Purine and isosteric antibacterial compounds, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Purine and isosteric antibacterial compounds will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-3521153

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