Peptoid compounds

Details Peptoid compounds Peptoid compounds

2006-11-03

2009-11-03

Tsang, Cecilia (Department: 1654)

Drug, bio-affecting and body treating compositions

Designated organic active ingredient containing

Peptide containing doai

C514S009100

Reexamination Certificate

active

07612036

ABSTRACT:
The invention relates to new peptoid compounds of formula (I), as well as their use in the treatment of bacterial infections, such as those caused by vancomycin resistant microorganisms, and to compositions thereof.

REFERENCES:
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STN: search report-two pages.
Bremner, J., et al., “The Synthesis of a Novel Carbazole-linked Cyclic Peptoid with Antibacterial Activity,”Synlett, No. 2:219-222, 2002.
Ezaki, M., et al., “Biphenomycin C, a Precursor of Biphenomycin A in Mixed Culture,”J. Antibiot. (Tokyo), 46(1):135-140, Jan. 1993.
Popieniek, P., et al., “A Fluorescent Ligand for Binding Studies with Glycopeptide Antibiotics of the Vancomycin Class,”Anal Biochem., 165(1):108-113, Aug. 15, 1987.
Uchida, I., et al., “Biphenomycins A and B, Novel Peptide Antibiotics. II. Structural Elucidation of Biphenomycins A and B,”J. Antibiot. (Tokyo), 38(11):1462-1468, Nov. 1985.
Park, C., et al., “Facile Macrocyclizations to β-Turn Mimics with Diverse Structural, Physical, and Conformational Properties,”J. Comb. Chem., 3(3):257-266, 2001.
Feng, Y., et al., “Solid Phase SNAr Macrocyclizations to Give Turn-Extended-Turn Peptidomimetics,”Chem. Eur. J., 5(11):3261-3272, 1999.
Ezaki, M., et al., “Biphenomycins A and B, Novel Peptide Antibiotics. I. Taxonomy, Fermentation, Isolation, and Characterization,”J. Antibiot., 38(11):1453-1461, 1985.

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