Decladinosyl-macrolides with anti-inflammatory activity

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Carbohydrate doai

Reexamination Certificate

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Details

C536S007200, C536S007400

Reexamination Certificate

active

07910559

ABSTRACT:
The present invention relates to novel semi-synthetic macrolides having anti-inflammatory activity. More particularly, the invention relates to 14- and 15-membered macrolides lacking cladinose sugar substituted at the C-3 position, to their pharmaceutically acceptable derivatives, to processes and intermediates for their preparation, to pharmaceutical compositions containing them and to their activity and use in the treatment of inflammatory diseases and conditions in humans and animals, especially those diseases associated with excessive secretion of TNF-α, IL-1, IL-6, IL-8, IL-2 or IL-5; and/or inhibitor of excessive lymphocyte proliferation; and/or excessive granulocyte degranulation.

REFERENCES:
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patent: 7488811 (2009-02-01), Napoletano et al.
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patent: 0 771 564 (1997-05-01), None
patent: 0 775 489 (1997-05-01), None
patent: 02/12260 (2002-02-01), None
patent: 2004/039821 (2004-05-01), None
Tanikawa et al., “Synthesis and Antibacterial Activity of Acylides (3-0-Acyl-Erythromycin Derivatives): A Novel Class of Macrolide Antibiotics,” Journal of Medicinal Chemistry, V44 N24, 2001, pp. 4027-4030.

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