Tri-substituted ureas as cytokine inhibitors

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

Reexamination Certificate

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C544S323000

Reexamination Certificate

active

07449474

ABSTRACT:
The present invention relates to 1,1,3-tri-substituted ureas which inhibit the extracellular release of inflammatory cytokines, said cytokines responsible for one or more human or higher mammalian disease states. The present invention further relates to compositions comprising said 1,1,3-tri-substituted ureas which inhibit the extracellular release of inflammatory cytokines, and methods for preventing, abating, or otherwise controlling enzymes which are understood to be the active components responsible for the herein described disease states.

REFERENCES:
patent: WO 99/23091 (1999-05-01), None
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Aleman et al., PubMed Abstract (Antivir Ther. 4(2):109-15), 1999.
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Green et al., PubMed Abstract (Immunol Rev 169:11-22), 1999.
Van Deventer, PubMed Abstract (Intensive Care Med. 26 Suppl 1:S98-102), 2000.
Holzheimer, PubMed Abstract (J Chemother. 13 Spec No. 1(1): 159-72), 2001.
Lesher, George Y., et al., “Novel orally active inhibitors of passive cutaneous anaphylaxis in rats: N-[2-(4-pyridinyl)-4-pyrimidinyl]ureas and dialkyl[[[2-(4-pyridinyl)-4-pyrimidinyl]amino]methyler,” Journal of Medical Chemistry, 25(7), 837-42. 1982, p. 841; Table IV.

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